Crystallography Open Database

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7121620 CIFC28 H27 N O3 SP 21 21 218.2814; 12.1086; 23.3936
90; 90; 90
2345.8Nguyen, Thi Le Nhon; Incerti-Pradillos, Celia A; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations.
Chemical communications (Cambridge, England), 2018, 54, 5622-5625
7121621 CIFC26 H27 N O3 SP 1 21 112.3854; 8.06169; 23.0268
90; 94.441; 90
2292.26Nguyen, Thi Le Nhon; Incerti-Pradillos, Celia A; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations.
Chemical communications (Cambridge, England), 2018, 54, 5622-5625
7121622 CIFC23.5 H26.5 N O3 S2P 1 21 115.72773; 8.01122; 18.9065
90; 111.479; 90
2216.75Nguyen, Thi Le Nhon; Incerti-Pradillos, Celia A; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations.
Chemical communications (Cambridge, England), 2018, 54, 5622-5625
7121623 CIFC25 H27 N O3 SP 21 21 217.977; 15.2993; 18.0186
90; 90; 90
2199Nguyen, Thi Le Nhon; Incerti-Pradillos, Celia A; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations.
Chemical communications (Cambridge, England), 2018, 54, 5622-5625
7121624 CIFC70 H76 Ag Au2 Cl N2 O3 P2P -113.8956; 16.1336; 16.6738
78.941; 78.141; 65.151
3296.1Zhang, Fan; Cao, Xiao-Ming; Wang, Jiwei; Jiao, Jiajun; Huang, Yongming; Shi, Min; Braunstein, Pierre; Zhang, Jun
A tritopic carbanionic N-heterocyclic dicarbene and its homo- and heterometallic coinage metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 5736-5739
7121625 CIFC64 H64 Au2 Br Cu N2 O P2P 1 21/c 118.6441; 14.8478; 24.59
90; 107.238; 90
6501.3Zhang, Fan; Cao, Xiao-Ming; Wang, Jiwei; Jiao, Jiajun; Huang, Yongming; Shi, Min; Braunstein, Pierre; Zhang, Jun
A tritopic carbanionic N-heterocyclic dicarbene and its homo- and heterometallic coinage metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 5736-5739
7121626 CIFC82 H79 Au3 Cl0.25 N2 O P3P 1 21/c 113.9827; 14.8116; 36.774
90; 90.166; 90
7616.1Zhang, Fan; Cao, Xiao-Ming; Wang, Jiwei; Jiao, Jiajun; Huang, Yongming; Shi, Min; Braunstein, Pierre; Zhang, Jun
A tritopic carbanionic N-heterocyclic dicarbene and its homo- and heterometallic coinage metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 5736-5739
7121627 CIFC12 H12 O3P -16.7868; 8.5848; 9.4383
87.679; 83.576; 73.938
525.1Shen, Guo; Zhou, Wen-Jun; Zhang, Xiao-Bo; Cao, Guang-Mei; Zhang, Zhen; Ye, Jian-Heng; Liao, Li-Li; Li, Jing; Yu, Da-Gang
Synthesis of tetronic acids from propargylic alcohols and CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 5610-5613
7121628 CIFC20 H16 N2P 1 21/n 111.883; 6.3386; 20.211
90; 92.61; 90
1520.7Li, Ni-Ya; Liu, Dong; Abrahams, Brendan F.; Lang, Jian-Ping
Covalent switching, involving divinylbenzene ligands within 3D coordination polymers, indicated by changes in fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 5831-5834
7121629 CIFC32 H22 N2 O4 ZnP 1 21/n 110.553; 13.677; 17.241
90; 93.47; 90
2483.9Li, Ni-Ya; Liu, Dong; Abrahams, Brendan F.; Lang, Jian-Ping
Covalent switching, involving divinylbenzene ligands within 3D coordination polymers, indicated by changes in fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 5831-5834
7121630 CIFC36 H22 N2 O8 Zn2P -110.502; 11.871; 13.571
94.67; 108.33; 104.03
1535.1Li, Ni-Ya; Liu, Dong; Abrahams, Brendan F.; Lang, Jian-Ping
Covalent switching, involving divinylbenzene ligands within 3D coordination polymers, indicated by changes in fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 5831-5834
7121631 CIFC36 H22 N2 O8 Zn2P -110.324; 12.009; 13.22
94.44; 111.17; 97.2
1503Li, Ni-Ya; Liu, Dong; Abrahams, Brendan F.; Lang, Jian-Ping
Covalent switching, involving divinylbenzene ligands within 3D coordination polymers, indicated by changes in fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 5831-5834
7121632 CIFC32 H22 N2 O4 ZnP 1 21/n 110.923; 13.139; 17.004
90; 94.47; 90
2432.9Li, Ni-Ya; Liu, Dong; Abrahams, Brendan F.; Lang, Jian-Ping
Covalent switching, involving divinylbenzene ligands within 3D coordination polymers, indicated by changes in fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 5831-5834
7121633 CIFC22 H28 O4P 659.0951; 9.0951; 38.8243
90; 90; 120
2781.31Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121634 CIFC20 H24 O4C 1 2/c 140.9654; 8.6677; 9.9042
90; 102.185; 90
3437.51Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121635 CIFC19 H22 O4P b c n7.4984; 10.1051; 20.5483
90; 90; 90
1556.99Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121636 CIFC17 H18 O4C 1 2/c 111.1202; 11.2585; 11.2577
90; 99.472; 90
1390.21Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121637 CIFC18 H20 O4P c a 2148.377; 7.5624; 21.0775
90; 90; 90
7711.1Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121638 CIFC21 H26 O4P -110.9041; 11.813; 15.392
67.718; 79.863; 89.142
1803.04Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121639 CIFC24 H0 In3 O15C m c m21.892; 37.916; 7.257
90; 90; 90
6024Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121640 CIFC24 H12 In3 O15C m c m21.851; 37.882; 7.246
90; 90; 90
5998Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121641 CIFC24 H12 In3 O15C m c m21.884; 37.906; 7.253
90; 90; 90
6017Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121642 CIFC24 H12 In3 O15C m c m21.841; 37.87; 7.246
90; 90; 90
5993Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121643 CIFC24 H12 In3 O15C m c m21.86; 37.89; 7.248
90; 90; 90
6003Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121644 CIFC24 H12 In3 O15C m c m21.872; 37.897; 7.25
90; 90; 90
6009Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121645 CIFC30 H45 Cl6 N2 P Pt RuP -110.0388; 11.4072; 15.5551
92.9312; 90.6096; 94.4168
1773.48Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121646 CIFC28 H53 Cl2 N2 O5 P PtP -19.4929; 13.9948; 14.1277
110.137; 105.007; 92.6871
1682.79Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121647 CIFC28 H45 Cl2 N2 O P PtP -19.674; 10.329; 15.976
90.696; 106.253; 99.069
1510.7Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121648 CIFC44 H81 Cl4 O P3 Pt RuP 1 21/n 115.8062; 16.5261; 19.3331
90; 91.648; 90
5048Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121649 CIFC79 H98 B Cl2 N3 P2 Pt RuP -112.9504; 14.9184; 20.154
104.998; 99.652; 97.274
3648.3Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121650 CIFC51 H44 Cl4 P4 Pt RuC 1 2/c 118.9; 21.5155; 16.337
90; 120.935; 90
5698.3Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121651 CIFC51.5 H75.5 Cl21.5 N P2 RuP 1 21/c 116.7297; 19.5656; 21.1868
90; 94.149; 90
6916.8Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121652 CIFC54 H96.5 Cl4 N1.5 P4 Pt RuP 1 21/c 114.6472; 19.8469; 21.394
90; 97.1342; 90
6171.1Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121653 CIFC28 H46 Cl13 N4 O P Pt RuP 1 21/n 114.4348; 11.4929; 27.5886
90; 104.657; 90
4427.9Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121654 CIFC56.33 H80.33 Cl7.33 N3 P2 Pt RuP -328.4392; 28.4392; 13.8884
90; 90; 120
9727.9Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121655 CIFC55.16 H52.08 Cl5.23 N O0.38 P4 Pt RuP -113.1006; 13.1671; 18.1048
72.0661; 72.0477; 63.5052
2605.1Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121656 CIFC100 H60 B12 F60 N O12P -113.3889; 13.8983; 29.7778
97.621; 100.29; 93.583
5382.7Wixtrom, Alex I.; Parvez, Zeeshan A.; Savage, Miles D.; Qian, Elaine A.; Jung, Dahee; Khan, Saeed I.; Rheingold, Arnold L.; Spokoyny, Alexander M.
Tuning the electrochemical potential of perfunctionalized dodecaborate clusters through vertex differentiation.
Chemical communications (Cambridge, England), 2018, 54, 5867-5870
7121657 CIFC93 H58 B12 F55 N2 O13P -114.125; 27.2616; 29.4644
110.44; 91.699; 97.139
10516.5Wixtrom, Alex I.; Parvez, Zeeshan A.; Savage, Miles D.; Qian, Elaine A.; Jung, Dahee; Khan, Saeed I.; Rheingold, Arnold L.; Spokoyny, Alexander M.
Tuning the electrochemical potential of perfunctionalized dodecaborate clusters through vertex differentiation.
Chemical communications (Cambridge, England), 2018, 54, 5867-5870
7121658 CIFC52 H39 B F15 O2 PP 1 21/n 113.04; 17.682; 20.467
90; 99.613; 90
4653Liu, Liu Leo; Cao, Levy L.; Zhu, Diya; Zhou, Jiliang; Stephan, Douglas W.
Homolytic cleavage of peroxide bonds via a single electron transfer of a frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 7431-7434
7121659 CIFC34.67 H25.33 B0.67 Br0.67 F10 O1.33 P0.67P -112.6688; 18.7187; 20.0531
90.811; 91.169; 97.947
4708.1Liu, Liu Leo; Cao, Levy L.; Zhu, Diya; Zhou, Jiliang; Stephan, Douglas W.
Homolytic cleavage of peroxide bonds via a single electron transfer of a frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 7431-7434
7121660 CIFC35.33 H27.33 B0.67 F10 O1.33 P0.67P 1 21/c 112.4203; 20.1153; 18.9334
90; 97.534; 90
4689.4Liu, Liu Leo; Cao, Levy L.; Zhu, Diya; Zhou, Jiliang; Stephan, Douglas W.
Homolytic cleavage of peroxide bonds via a single electron transfer of a frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 7431-7434
7121661 CIFC56 H63 F18 N8 P3 RuI -424.9906; 24.9906; 20.6467
90; 90; 90
12894.5Rota Martir, Diego; Cordes, David B.; Slawin, Alexandra M. Z.; Escudero, Daniel; Jacquemin, Denis; Warriner, Stuart L.; Zysman-Colman, Eli
A luminescent [Pd<sub>4</sub>Ru<sub>8</sub>]<sup>24+</sup> supramolecular cage.
Chemical communications (Cambridge, England), 2018, 54, 6016-6019
7121662 CIFC448 H496 F144 N64 P24 Pd4 Ru8P 4/m n c26.7344; 26.7344; 51.852
90; 90; 90
37060Rota Martir, Diego; Cordes, David B.; Slawin, Alexandra M. Z.; Escudero, Daniel; Jacquemin, Denis; Warriner, Stuart L.; Zysman-Colman, Eli
A luminescent [Pd<sub>4</sub>Ru<sub>8</sub>]<sup>24+</sup> supramolecular cage.
Chemical communications (Cambridge, England), 2018, 54, 6016-6019
7121663 CIFC50 H54 Cl2 O2 P4 Rh2 Si2P 21 21 2113.6107; 19.3024; 19.5658
90; 90; 90
5140.3Newland, Robert J.; Lynam, Jason M.; Mansell, Stephen M.
Small bite-angle 2-phosphinophosphinine ligands enable rhodium-catalysed hydroboration of carbonyls.
Chemical communications (Cambridge, England), 2018, 54, 5482-5485
7121664 CIFC61 H48 B F24 P2 Rh SiP -113.2396; 14.6179; 18.0412
98.298; 102.651; 110.657
3092.5Newland, Robert J.; Lynam, Jason M.; Mansell, Stephen M.
Small bite-angle 2-phosphinophosphinine ligands enable rhodium-catalysed hydroboration of carbonyls.
Chemical communications (Cambridge, England), 2018, 54, 5482-5485
7121665 CIFC53 H49 B F20 Mg N4 O2P 1 21 19.435; 27.598; 10.589
90; 105.636; 90
2655.2Banerjee, Sumanta; Ankur, ?; Andrews, Alex; Venugopal, Ajay
A disguised hydride in a butylmagnesium cation.
Chemical communications (Cambridge, England), 2018, 54, 5788-5791
7121666 CIFC82 H78 B2 F40 Mg2 N8 O4P 1 21/n 112.2624; 22.472; 15.7828
90; 92.505; 90
4345Banerjee, Sumanta; Ankur, ?; Andrews, Alex; Venugopal, Ajay
A disguised hydride in a butylmagnesium cation.
Chemical communications (Cambridge, England), 2018, 54, 5788-5791
7121667 CIFC40 H39 B F20 Mg N4P -112.305; 12.709; 15.464
69.721; 70.14; 83.743
2133.4Banerjee, Sumanta; Ankur, ?; Andrews, Alex; Venugopal, Ajay
A disguised hydride in a butylmagnesium cation.
Chemical communications (Cambridge, England), 2018, 54, 5788-5791
7121668 CIFC16 H9 B F2 I N O2P -18.1072; 10.316; 18.661
85.33; 85.74; 82.69
1539.6Tao, Yi-Chen; Li, Zhi-Zhou; Wang, Xue-Dong; Xiao, Lu; Fu, Hongbing; Liao, Liang-Sheng
Fluorescence/phosphorescence-conversion in self-assembled organic microcrystals.
Chemical communications (Cambridge, England), 2018, 54, 5895-5898
7121669 CIFC18 H17 Cl N2 OP -18.075; 8.096; 13.744
94.419; 104.016; 113.589
783.5Fan, Zhoulong; Lu, Heng; Cheng, Zhen; Zhang, Ao
Ligand-promoted ruthenium-catalyzed meta C-H chlorination of arenes using N-chloro-2,10-camphorsultam.
Chemical communications (Cambridge, England), 2018, 54, 6008-6011
7121670 CIFC15 H15 Cl N4P 1 21/c 113.886; 14.758; 6.953
90; 102.04; 90
1394Fan, Zhoulong; Lu, Heng; Cheng, Zhen; Zhang, Ao
Ligand-promoted ruthenium-catalyzed meta C-H chlorination of arenes using N-chloro-2,10-camphorsultam.
Chemical communications (Cambridge, England), 2018, 54, 6008-6011
7121671 CIFC12 H6 F6 N2 O8 Ru2P 1 21/c 114.2908; 8.8234; 15.2802
90; 101.799; 90
1886Fan, Zhoulong; Lu, Heng; Cheng, Zhen; Zhang, Ao
Ligand-promoted ruthenium-catalyzed meta C-H chlorination of arenes using N-chloro-2,10-camphorsultam.
Chemical communications (Cambridge, England), 2018, 54, 6008-6011
7121672 CIFC17 H16 Br2 Co N4 OP 1 21/c 18.8812; 17.0462; 11.8893
90; 96.1423; 90
1789.6Shee, Sujan; Ganguli, Kasturi; Jana, Kalipada; Kundu, Sabuj
Cobalt complex catalyzed atom-economical synthesis of quinoxaline, quinoline and 2-alkylaminoquinoline derivatives.
Chemical communications (Cambridge, England), 2018, 54, 6883-6886
7121673 CIFC30 H28 Br PP 1 21/c 118.8856; 8.5457; 15.9422
90; 107.321; 90
2456.24Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121674 CIFC59 H46 B F10 PP 1 2/c 122.7843; 8.4334; 27.6135
90; 113.888; 90
4851.4Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121675 CIFC42 H30 B F10 PP -111.8477; 12.3022; 14.0634
67.621; 72.281; 67.99
1725.74Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121676 CIFC47 H36 B F10 PP 1 21/n 113.0923; 11.9735; 24.9266
90; 98.327; 90
3866.32Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121677 CIFC42 H28 B F10 O2 PC 1 2/c 120.1789; 14.4682; 23.7982
90; 98.115; 90
6878.4Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121678 CIFC54 H42 B F10 PC 1 2/c 141.3837; 8.811; 24.2497
90; 96.346; 90
8788Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121679 CIFC53 H48 B F10 N2 PP -111.6758; 12.5018; 19.7217
90.855; 106.41; 104.165
2666.56Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121680 CIFC50 H40 B Cl6 F10 PP -111.5136; 14.6603; 16.4813
77.324; 70.587; 67.496
2410.36Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121681 CIFC50 H34 B F10 PP -113.3724; 14.8949; 23.4627
75.958; 83.414; 65.374
4120.83Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121682 CIFC52 H38 B F10 PP 1 21/n 114.5964; 18.8664; 15.7176
90; 104.493; 90
4190.6Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121683 CIFC48 H144 B12 Er2 P6P 1 21/n 114.7928; 12.1704; 24.504
90; 91.557; 90
4409.9Blake, Anastasia V.; Fetrow, Taylor V.; Theiler, Zachary J.; Vlaisavljevich, Bess; Daly, Scott R.
Homoleptic uranium and lanthanide phosphinodiboranates.
Chemical communications (Cambridge, England), 2018, 54, 5602-5605
7121684 CIFC52 H154 B12 O P6 U2P 1 21/n 115.0395; 12.0078; 24.766
90; 90.114; 90
4472.5Blake, Anastasia V.; Fetrow, Taylor V.; Theiler, Zachary J.; Vlaisavljevich, Bess; Daly, Scott R.
Homoleptic uranium and lanthanide phosphinodiboranates.
Chemical communications (Cambridge, England), 2018, 54, 5602-5605
7121685 CIFC52 H154 B12 Nd2 O P6P 1 21/n 115.0204; 11.9884; 24.771
90; 90.05; 90
4460.5Blake, Anastasia V.; Fetrow, Taylor V.; Theiler, Zachary J.; Vlaisavljevich, Bess; Daly, Scott R.
Homoleptic uranium and lanthanide phosphinodiboranates.
Chemical communications (Cambridge, England), 2018, 54, 5602-5605
7121686 CIFC23 H26 F N O2 SP -18.7586; 12.203; 19.973
91.534; 96.604; 90.138
2119.8Zhu, Xin-Qi; Sun, Qing; Zhang, Zhi-Xin; Zhou, Bo; Xie, Pei-Xi; Shen, Wen-Bo; Lu, Xin; Zhou, Jin-Mei; Ye, Long-Wu
Zinc-catalyzed reaction of isoxazoles with thioynol ethers involving an unprecedented 1,2-sulfur migration.
Chemical communications (Cambridge, England), 2018, 54, 7435-7438
7121687 CIFC40 H54 B4 O8P 1 21/n 112.331; 10.794; 15.681
90; 109.944; 90
1962Wakchaure, Vivek C.; Ranjeesh, Kayaramkodath C.; Goudappagouda, ?; Das, Tamal; Vanka, Kumar; Gonnade, Rajesh; Babu, Sukumaran S.
Mechano-responsive room temperature luminescence variations of boron conjugated pyrene in air.
Chemical communications (Cambridge, England), 2018, 54, 6028-6031
7121688 CIFC336 H Np24 O184F m -3 m27.6042; 27.6042; 27.6042
90; 90; 90
21034.2Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121689 CIFC22 H22 N2 Np O10C 1 2/c 115.345; 11.4621; 13.3406
90; 101.43; 90
2299.89Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121690 CIFC168 O70 Th12F m -3 m27.9879; 27.9879; 27.9879
90; 90; 90
21923.6Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121691 CIFC168 O70 Th12F m -3 m27.996; 27.996; 27.996
90; 90; 90
21943Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121692 CIFC192 Np12 O76F m -3 m33.3917; 33.3917; 33.3917
90; 90; 90
37231.9Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121693 CIFC168 Np12 O86F m -3 m27.5467; 27.5467; 27.5467
90; 90; 90
20903Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121694 CIFC43 H39 N6 O12 S2P -15.097; 11.161; 20.474
76.969; 86.696; 84.67
1129Chen, Cheng; Xiang, Yang; Liu, Ya; Hu, Xiangdong; Yang, Ke-Wu
Mercaptoacetate thioesters and their hydrolysate mercaptoacetic acids jointly inhibit metallo-β-lactamase L1.
MedChemComm, 2018, 9, 1172-1177
7121695 CIFC28 H20 B2 N2 S2P n a 2112.195; 12.807; 30.751
90; 90; 90
4803Zhang, Jinyun; Liu, Fude; Sun, Zhe; Li, Chenglong; Zhang, Qian; Zhang, Chen; Liu, Zhiqiang; Liu, Xuguang
Synthesis, characterization and properties of aryl-fused bis-BN dihydropyrenes.
Chemical communications (Cambridge, England), 2018, 54, 8178-8181
7121696 CIFC28 H20 B2 N2 O S2P 1 21 113.257; 8.073; 13.405
90; 104.92; 90
1386.3Zhang, Jinyun; Liu, Fude; Sun, Zhe; Li, Chenglong; Zhang, Qian; Zhang, Chen; Liu, Zhiqiang; Liu, Xuguang
Synthesis, characterization and properties of aryl-fused bis-BN dihydropyrenes.
Chemical communications (Cambridge, England), 2018, 54, 8178-8181
7121697 CIFC33 H26 B2 Cl2 N2P 21 21 217.742; 14.293; 25.54
90; 90; 90
2826.2Zhang, Jinyun; Liu, Fude; Sun, Zhe; Li, Chenglong; Zhang, Qian; Zhang, Chen; Liu, Zhiqiang; Liu, Xuguang
Synthesis, characterization and properties of aryl-fused bis-BN dihydropyrenes.
Chemical communications (Cambridge, England), 2018, 54, 8178-8181
7121698 CIFC22 H24 N2 O2P 1 21/c 114.8982; 5.9496; 21.2447
90; 97.139; 90
1868.5Zhou, Meng-Guang; Dai, Rui-Han; Tian, Shi-Kai
Nucleophilic addition of tertiary propargylic amines to arynes followed by a [2,3]-sigmatropic rearrangement.
Chemical communications (Cambridge, England), 2018, 54, 6036-6039
7121699 CIFBa2 H3 N O6P -6 2 m6.9069; 6.9069; 3.8028
90; 90; 120
157.109Dong, Xuehua; Huang, Ling; Liu, Qingyu; Zeng, Hongmei; Lin, Zhien; Xu, Dingguo; Zou, Guohong
Perfect balance harmony in Ba<sub>2</sub>NO<sub>3</sub>(OH)<sub>3</sub>: a beryllium-free nitrate as a UV nonlinear optical material.
Chemical communications (Cambridge, England), 2018, 54, 5792-5795
7121700 CIFC26 H28 N O2 P SP -19.3068; 11.0204; 12.97
76.267; 79.407; 66.841
1181.99Takeda, Youhei; Kaihara, Takahito; Okazaki, Masato; Higginbotham, Heather; Data, Przemyslaw; Tohnai, Norimitsu; Minakata, Satoshi
Conformationally-flexible and moderately electron-donating units-installed D–A–D triad enabling multicolor-changing mechanochromic luminescence, TADF and room-temperature phosphorescence
Chemical Communications, 2018
7121701 CIFC62 H48 N4 P2 S2P 4/n31.7603; 31.7603; 11.0024
90; 90; 90
11098.3Takeda, Youhei; Kaihara, Takahito; Okazaki, Masato; Higginbotham, Heather; Data, Przemyslaw; Tohnai, Norimitsu; Minakata, Satoshi
Conformationally-flexible and moderately electron-donating units-installed D‒A‒D triad enabling multicolor-changing mechanochromic luminescence, TADF and room-temperature phosphorescence
Chemical Communications, 2018
7121702 CIFC21 H20 N P SP 1 21/c 112.1594; 8.63342; 16.6826
90; 95.5524; 90
1743.08Takeda, Youhei; Kaihara, Takahito; Okazaki, Masato; Higginbotham, Heather; Data, Przemyslaw; Tohnai, Norimitsu; Minakata, Satoshi
Conformationally-flexible and moderately electron-donating units-installed D–A–D triad enabling multicolor-changing mechanochromic luminescence, TADF and room-temperature phosphorescence
Chemical Communications, 2018
7121703 CIFC64 H50 Cl6 N4 P2 S2P 42/n31.6082; 31.6082; 12.9408
90; 90; 90
12928.9Takeda, Youhei; Kaihara, Takahito; Okazaki, Masato; Higginbotham, Heather; Data, Przemyslaw; Tohnai, Norimitsu; Minakata, Satoshi
Conformationally-flexible and moderately electron-donating units-installed D–A–D triad enabling multicolor-changing mechanochromic luminescence, TADF and room-temperature phosphorescence
Chemical Communications, 2018
7121704 CIFC74 H72 N6 O3P 21 21 2135.034; 10.393; 17.979
90; 90; 90
6546Jeon, Hae-Geun; Lee, Hyun Kyung; Lee, Seungwon; Jeong, Kyu-Sung
Foldamer-based helicate displaying reversible switching between two distinct conformers.
Chemical communications (Cambridge, England), 2018, 54, 5740-5743
7121705 CIFC74 H68 Cl2 N6 O PdC 1 2/c 131.021; 22.132; 29.199
90; 119.15; 90
17508Jeon, Hae-Geun; Lee, Hyun Kyung; Lee, Seungwon; Jeong, Kyu-Sung
Foldamer-based helicate displaying reversible switching between two distinct conformers.
Chemical communications (Cambridge, England), 2018, 54, 5740-5743
7121706 CIFC148 H136 Cl4 N12 O2 Pd2P -116.792; 23.687; 39.551
73.077; 84.189; 81.24
14848Jeon, Hae-Geun; Lee, Hyun Kyung; Lee, Seungwon; Jeong, Kyu-Sung
Foldamer-based helicate displaying reversible switching between two distinct conformers.
Chemical communications (Cambridge, England), 2018, 54, 5740-5743
7121707 CIFC23 H21 B2 F8 N O2 Pd3P -110.1815; 10.931; 11.5703
110.912; 92.099; 98.047
1185.81Sugawa, Tsuyoshi; Yamamoto, Koji; Murahashi, Tetsuro
Bimodal coordination of fused arenes to a Pd<sub>3</sub> cluster site.
Chemical communications (Cambridge, England), 2018, 54, 5875-5878
7121708 CIFC46 H46 B2 F8 N O P Pd4P 1 21/c 115.662; 30.042; 9.1348
90; 90.782; 90
4297.7Sugawa, Tsuyoshi; Yamamoto, Koji; Murahashi, Tetsuro
Bimodal coordination of fused arenes to a Pd<sub>3</sub> cluster site.
Chemical communications (Cambridge, England), 2018, 54, 5875-5878
7121709 CIFC28 H23 B2 F8 N Pd3P 1 21/n 110.6819; 11.6177; 21.577
90; 100.429; 90
2633.5Sugawa, Tsuyoshi; Yamamoto, Koji; Murahashi, Tetsuro
Bimodal coordination of fused arenes to a Pd<sub>3</sub> cluster site.
Chemical communications (Cambridge, England), 2018, 54, 5875-5878
7121710 CIFC39.5 H34.5 B2 F8 N3.5 O Pd3P 1 21/c 118.3607; 14.2059; 15.0826
90; 102.778; 90
3836.6Sugawa, Tsuyoshi; Yamamoto, Koji; Murahashi, Tetsuro
Bimodal coordination of fused arenes to a Pd<sub>3</sub> cluster site.
Chemical communications (Cambridge, England), 2018, 54, 5875-5878
7121711 CIFC38 H56 Ge2 Ru2P -111.4301; 11.9637; 13.1386
87.895; 84.249; 88.71
1786.09Fujimori, Shiori; Mizuhata, Yoshiyuki; Tokitoh, Norihiro
Ru-Complexes of an anionic germabenzenyl ligand.
Chemical communications (Cambridge, England), 2018, 54, 8044-8047
7121712 CIFC60 H87 Ge3 Ru3P -112.3082; 13.0253; 19.5207
74.599; 89.993; 71.829
2854.97Fujimori, Shiori; Mizuhata, Yoshiyuki; Tokitoh, Norihiro
Ru-Complexes of an anionic germabenzenyl ligand.
Chemical communications (Cambridge, England), 2018, 54, 8044-8047
7121713 CIFC14 H18 Cu3 O15 P2P 1 21 18.872; 9.054; 13.255
90; 102.344; 90
1040.1Wang, Peng-Fei; Bao, Song-Song; Huang, Xin-Da; Akutagawa, T.; Zheng, Li-Min
Temperature controlled formation of polar copper phosphonates showing large dielectric anisotropy and a dehydration-induced switch from ferromagnetic to antiferromagnetic interactions.
Chemical communications (Cambridge, England), 2018, 54, 6276-6279
7121714 CIFC14 H12 Cu3 O12 P2P b c n22.65; 8.8845; 8.9245
90; 90; 90
1795.9Wang, Peng-Fei; Bao, Song-Song; Huang, Xin-Da; Akutagawa, T.; Zheng, Li-Min
Temperature controlled formation of polar copper phosphonates showing large dielectric anisotropy and a dehydration-induced switch from ferromagnetic to antiferromagnetic interactions.
Chemical communications (Cambridge, England), 2018, 54, 6276-6279
7121715 CIFC26 H28P 1 21/n 115.0392; 7.6824; 15.9139
90; 91.082; 90
1838.3Alonso, José M; Quiroga, Sabela; Codony, Sandra; Turcu, Andreea L.; Barniol-Xicota, Marta; Pérez, Dolores; Guitián, Enrique; Vázquez, Santiago; Peña, Diego
Palladium-catalyzed cocyclotrimerization of arynes with a pyramidalized alkene.
Chemical communications (Cambridge, England), 2018, 54, 5996-5999
7121716 CIFC35 H33 Cl3P -19.5957; 12.2865; 13.243
73.4435; 72.2898; 73.1598
1389.97Alonso, José M; Quiroga, Sabela; Codony, Sandra; Turcu, Andreea L.; Barniol-Xicota, Marta; Pérez, Dolores; Guitián, Enrique; Vázquez, Santiago; Peña, Diego
Palladium-catalyzed cocyclotrimerization of arynes with a pyramidalized alkene.
Chemical communications (Cambridge, England), 2018, 54, 5996-5999
7121717 CIFC51.2 H86.4 O71.2 Zr12P -112.5793; 15.7491; 16.7679
116.322; 93.693; 106.969
2774.1Fidelli, Athena M.; Karadeniz, Bahar; Howarth, Ashlee J.; Huskić, Igor; Germann, Luzia S.; Halasz, Ivan; Etter, Martin; Moon, Su-Young; Dinnebier, Robert E.; Stilinović, Vladimir; Farha, Omar K.; Friščić, Tomislav; UŽarević, Krunoslav
Green and rapid mechanosynthesis of high-porosity NU- and UiO-type metal-organic frameworks.
Chemical communications (Cambridge, England), 2018, 54, 6999-7002
7121718 CIFC60 H92 N4 O36 Zr6I -416.0037; 16.0037; 16.2833
90; 90; 90
4170.5Fidelli, Athena M.; Karadeniz, Bahar; Howarth, Ashlee J.; Huskić, Igor; Germann, Luzia S.; Halasz, Ivan; Etter, Martin; Moon, Su-Young; Dinnebier, Robert E.; Stilinović, Vladimir; Farha, Omar K.; Friščić, Tomislav; UŽarević, Krunoslav
Green and rapid mechanosynthesis of high-porosity NU- and UiO-type metal-organic frameworks.
Chemical communications (Cambridge, England), 2018, 54, 6999-7002
7121719 CIFC20 H17 N3 O2P 1 21/n 19.949; 15.604; 11.098
90; 104.703; 90
1666.5Sun, Wuji; Fang, Shubiao; Yan, Hong
Discovery of novel picolinamide-based derivatives as novel VEGFR-2 kinase inhibitors: synthesis, <i>in vitro</i> biological evaluation and molecular docking.
MedChemComm, 2018, 9, 1054-1058
7121720 CIFC25 H19 N3 O2P 21 21 215.4568; 7.5939; 45.622
90; 90; 90
1890.5Sun, Wuji; Fang, Shubiao; Yan, Hong
Discovery of novel picolinamide-based derivatives as novel VEGFR-2 kinase inhibitors: synthesis, <i>in vitro</i> biological evaluation and molecular docking.
MedChemComm, 2018, 9, 1054-1058
7121721 CIFC42 H32 N4 OP -17.7635; 18.657; 21.765
97.536; 90.005; 100.929
3067.6Xie, Ghaozan; Hahn, Sebastian; Rominger, Frank -; Freudenberg, Jan; Bunz, Uwe H. F.
Synthesis and characterization of two different azarubrenes
Chemical Communications, 2018
7121722 CIFC40 H26 N2 O2P 1 21/n 113.9299; 11.201; 18.2839
90; 96.8662; 90
2832.4Xie, Ghaozan; Hahn, Sebastian; Rominger, Frank -; Freudenberg, Jan; Bunz, Uwe H. F.
Synthesis and characterization of two different azarubrenes
Chemical Communications, 2018
7121723 CIFC38 H24 N4 O2P 4/n29.9853; 29.9853; 14.2542
90; 90; 90
12816.2Xie, Ghaozan; Hahn, Sebastian; Rominger, Frank -; Freudenberg, Jan; Bunz, Uwe H. F.
Synthesis and characterization of two different azarubrenes
Chemical Communications, 2018
7121724 CIFC40 H26 N2P -17.0727; 8.2696; 11.855
90.402; 106.039; 97.605
659.84Xie, Ghaozan; Hahn, Sebastian; Rominger, Frank -; Freudenberg, Jan; Bunz, Uwe H. F.
Synthesis and characterization of two different azarubrenes
Chemical Communications, 2018
7121725 CIFC36 H36 Cl6 N6 O10R -3 :H22.3483; 22.3483; 8.0031
90; 90; 120
3461.61Kosiorek, Sandra; Butkiewicz, Helena; Danylyuk, Oksana; Sashuk, Volodymyr
Pillar[6]pyridinium: a hexagonally shaped molecular box that selectively recognizes multicharged anionic species.
Chemical communications (Cambridge, England), 2018, 54, 6316-6319
7121726 CIFC8 H19 NP b c m4.8201; 7.003; 26.028
90; 90; 90
878.6Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121727 CIFC12 H27 NP b c m4.856; 7.056; 36.24
90; 90; 90
1241.7Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121728 CIFC4 H11 NC 1 2/c 18.0789; 15.538; 13.319
90; 98.065; 90
1655.4Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121729 CIFC5 H13 NP 1 21/n 18.933; 9.062; 15.56
90; 99.55; 90
1242Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121730 CIFC4 H11 NC 1 2/c 115.168; 8.902; 15.176
90; 90.67; 90
2049Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121731 CIFC6 H15 NC 1 c 114.348; 8.94; 17.768
90; 105.637; 90
2194.8Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121732 CIFC8 H19 NC 1 2/c 117.442; 11.612; 18.375
90; 90.08; 90
3722Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121733 CIFC6 H15 NC 1 2/c 114.527; 7.293; 14.148
90; 104.794; 90
1449.2Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121734 CIFC6 H15 NP 1 21/c 18.158; 10.492; 26.09
90; 90.156; 90
2233.1Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121735 CIFC3 H9 NP 1 21/n 17.761; 16.084; 14.231
90; 99.851; 90
1750Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121736 CIFC4 H11 NP 1 21/n 17.989; 15.32; 13.213
90; 96.29; 90
1607.4Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121737 CIFC66 H82 B2 F4 N8 P2 PtP -110.503; 11.094; 14.692
106.564; 90.122; 95.097
1633.7Dhindsa, Jasveer S.; Maar, Ryan R.; Barbon, Stephanie M.; Olivia Avilés, María; Powell, Zachary K.; Lagugné-Labarthet, François; Gilroy, Joe B.
A π-conjugated inorganic polymer constructed from boron difluoride formazanates and platinum(ii) diynes.
Chemical communications (Cambridge, England), 2018, 54, 6899-6902
7121738 CIFC7 H6 N2P 1 21/c 17.3184; 5.7059; 15.844
90; 113.439; 90
607Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121739 CIFC7 H6 N2P 1 21/c 17.243; 5.4842; 16.0426
90; 101.797; 90
623.79Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121740 CIFC7 H6 N2P 1 21/c 17.3198; 5.5097; 16.0906
90; 102.034; 90
634.67Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121741 CIFC7 H6 N2P 1 21/c 17.2662; 5.4906; 16.0552
90; 101.835; 90
626.92Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121742 CIFC7 H6 N2P 1 21/c 17.3414; 5.5181; 16.1043
90; 102.118; 90
637.86Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121743 CIFC7 H6 N2P 1 21/c 17.3002; 5.5022; 16.0771
90; 101.968; 90
631.73Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121744 CIFC7 H6 N2P 1 21/c 17.3645; 5.5357; 16.147
90; 102.119; 90
643.6Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121745 CIFC7 H6 N2P 1 21/c 17.3455; 5.7043; 15.878
90; 113.224; 90
611.4Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121746 CIFC7 H6 N2P 1 21/c 17.2228; 5.4765; 16.0273
90; 101.74; 90
620.71Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121747 CIFC7 H6 N2P 1 21/c 17.332; 5.7057; 15.859
90; 113.341; 90
609.2Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121748 CIFC7 H6 N2P 1 21/c 17.368; 5.7105; 15.915
90; 113.088; 90
616Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121749 CIFC7 H6 N2P 1 21/c 17.2815; 5.4951; 16.0633
90; 101.903; 90
628.91Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121750 CIFC11 H7 F N2 O5 SP -18.2004; 11.919; 12.4
93.86; 93.52; 95.79
1200.2Smedley, Christopher J.; Giel, Marie-Claire; Molino, Andrew; Barrow, Andrew S.; Wilson, David J. D.; Moses, John E.
1-Bromoethene-1-sulfonyl fluoride (BESF) is another good connective hub for SuFEx click chemistry.
Chemical communications (Cambridge, England), 2018, 54, 6020-6023
7121751 CIFC27 H23 Br N2 O6P b c n16.1053; 20.5425; 16.542
90; 90; 90
5472.8Gurubrahamam, Ramani; Nagaraju, Koppanathi; Chen, Kwunmin
Organocatalytic synthesis of densely functionalized oxa-bridged 2,6-epoxybenzo[b][1,5]oxazocine heterocycles.
Chemical communications (Cambridge, England), 2018, 54, 6048-6051
7121752 CIFC26 H37 I N2P 1 21/n 19.4821; 14.8496; 17.729
90; 100.901; 90
2451.3Teng, Qiaoqiao; Wu, Wenqin; Duong, Hung A.; Huynh, Han Vinh
Ring-expanded N-heterocyclic carbenes as ligands in iron-catalysed cross-coupling reactions of arylmagnesium reagents and aryl chlorides.
Chemical communications (Cambridge, England), 2018, 54, 6044-6047
7121753 CIFC23 H31 B F4 N2P 1 21/c 115.5061; 15.3089; 9.2595
90; 90.915; 90
2197.75Teng, Qiaoqiao; Wu, Wenqin; Duong, Hung A.; Huynh, Han Vinh
Ring-expanded N-heterocyclic carbenes as ligands in iron-catalysed cross-coupling reactions of arylmagnesium reagents and aryl chlorides.
Chemical communications (Cambridge, England), 2018, 54, 6044-6047
7121754 CIFC17 H20 I N2 O0.5C 1 2 117.5096; 10.5339; 11.1338
90; 126.315; 90
1654.71Teng, Qiaoqiao; Wu, Wenqin; Duong, Hung A.; Huynh, Han Vinh
Ring-expanded N-heterocyclic carbenes as ligands in iron-catalysed cross-coupling reactions of arylmagnesium reagents and aryl chlorides.
Chemical communications (Cambridge, England), 2018, 54, 6044-6047
7121755 CIFC9 H9 I2 N O2P b c a12.08; 11.704; 16.182
90; 90; 90
2287.88Li, Jing; Lear, Martin J.; Hayashi, Yujiro
Autoinductive conversion of α,α-diiodonitroalkanes to amides and esters catalysed by iodine byproducts under O<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 6360-6363
7121756 CIFC34 H56 Cl2 P2 Rh2 S2P 21 21 2114.121; 14.5253; 18.8086
90; 90; 90
3857.9Vlahopoulou, G.; Möller, S; Haak, J.; Hasche, P.; Drexler, H.-J.; Heller, D.; Beweries, T.
Synthesis of Rh(iii) thiophosphinito pincer hydrido complexes by base-free C-H bond activation at room temperature.
Chemical communications (Cambridge, England), 2018, 54, 6292-6295
7121757 CIFC76 H70 Cl6 P4 Rh4 S4P 1 21/c 112.0429; 13.0157; 45.0034
90; 90.985; 90
7053.1Vlahopoulou, G.; Möller, S; Haak, J.; Hasche, P.; Drexler, H.-J.; Heller, D.; Beweries, T.
Synthesis of Rh(iii) thiophosphinito pincer hydrido complexes by base-free C-H bond activation at room temperature.
Chemical communications (Cambridge, England), 2018, 54, 6292-6295
7121758 CIFC34 H56 Cl2 O2 P2 Rh2P b c a16.0812; 15.1354; 29.4358
90; 90; 90
7164.5Vlahopoulou, G.; Möller, S; Haak, J.; Hasche, P.; Drexler, H.-J.; Heller, D.; Beweries, T.
Synthesis of Rh(iii) thiophosphinito pincer hydrido complexes by base-free C-H bond activation at room temperature.
Chemical communications (Cambridge, England), 2018, 54, 6292-6295
7121759 CIFC78 H76 Cl8 O4 P4 Rh4P -112.2267; 13.3049; 13.5035
73.906; 69.569; 68.304
1884.77Vlahopoulou, G.; Möller, S; Haak, J.; Hasche, P.; Drexler, H.-J.; Heller, D.; Beweries, T.
Synthesis of Rh(iii) thiophosphinito pincer hydrido complexes by base-free C-H bond activation at room temperature.
Chemical communications (Cambridge, England), 2018, 54, 6292-6295
7121760 CIFC76 H72 Cl4 P4 Rh4 S4P -110.7617; 17.854; 19.459
78.973; 84.819; 78.382
3589.4Vlahopoulou, G.; Möller, S; Haak, J.; Hasche, P.; Drexler, H.-J.; Heller, D.; Beweries, T.
Synthesis of Rh(iii) thiophosphinito pincer hydrido complexes by base-free C-H bond activation at room temperature.
Chemical communications (Cambridge, England), 2018, 54, 6292-6295
7121761 CIFC21 H22 F O5 PP 21 21 218.7032; 13.2565; 18.0076
90; 90; 90
2077.61Sun, Jun; He, Fangcheng; Wang, Zhongyao; Pan, Dingwu; Zheng, Pengcheng; Mou, Chengli; Jin, Zhichao; Chi, Yonggui Robin
Carbene-catalyzed enal γ-carbon addition to α-ketophosphonates for enantioselective access to bioactive 2-pyranylphosphonates.
Chemical communications (Cambridge, England), 2018, 54, 6040-6043
7121762 CIFC17 H13 F3 OP 1 21/c 112.9659; 8.4037; 12.8931
90; 113.171; 90
1291.5Yokoo, Kazuma; Mori, Keiji
Divergent synthesis of CF<sub>3</sub>-substituted polycyclic skeletons based on control of activation site of acid catalysts.
Chemical communications (Cambridge, England), 2018, 54, 6927-6930
7121763 CIFC57 H43 B F20 N O2 PP -112.7541; 13.627; 17.1282
100.157; 95.562; 112.012
2672.94Volodarsky, Solomon; Dobrovetsky, Roman
Ambiphilic geometrically constrained phosphenium cation.
Chemical communications (Cambridge, England), 2018, 54, 6931-6934
7121764 CIFC21 H23 N O5P 21 21 217.1336; 12.7135; 20.4017
90; 90; 90
1850.3Abe, Hideki; Fujimaki, Mitsuru; Nakagawa, Eri; Kobayashi, Toyoharu; Ito, Hisanaka
Enantioselective total synthesis of sagittacin E and related natural products.
Chemical communications (Cambridge, England), 2018, 54, 6165-6168
7121765 CIFC16 H20 O5P 1 21 18.5141; 7.7265; 22.836
90; 94.095; 90
1498.4Abe, Hideki; Fujimaki, Mitsuru; Nakagawa, Eri; Kobayashi, Toyoharu; Ito, Hisanaka
Enantioselective total synthesis of sagittacin E and related natural products.
Chemical communications (Cambridge, England), 2018, 54, 6165-6168
7121766 CIFC16 H20 O4P 21 21 217.102; 8.451; 24.298
90; 90; 90
1458.3Abe, Hideki; Fujimaki, Mitsuru; Nakagawa, Eri; Kobayashi, Toyoharu; Ito, Hisanaka
Enantioselective total synthesis of sagittacin E and related natural products.
Chemical communications (Cambridge, England), 2018, 54, 6165-6168
7121767 CIFC62 H60 Cr2 N4 Ni O14P -18.831; 13.443; 13.675
118; 103.9; 92.2
1369.6Fotopoulou, Eirini; Martínez-Lillo, Jose; Siczek, Milosz; Lis, Tadeusz; Tangoulis, Vassilis; Evangelisti, Marco; Brechin, Euan K.; Milios, Constantinos J.
A [Cr<sub>2</sub>Ni] coordination polymer: slow relaxation of magnetization in quasi-one-dimensional ferromagnetic chains.
Chemical communications (Cambridge, England), 2018, 54, 6153-6156
7121768 CIFC80 H84 N6 O12 SnP 19.756; 13.413; 14.922
112.87; 100.33; 94.47
1746.4Natali, Mirco; Amati, Agnese; Demitri, Nicola; Iengo, Elisabetta
Formation of a long-lived radical pair in a Sn(iv) porphyrin-di(l-tyrosinato) conjugate driven by proton-coupled electron-transfer.
Chemical communications (Cambridge, England), 2018, 54, 6148-6152
7121769 CIFC19 H15 N O3 SP 1 21/n 117.529; 10.184; 18.2727
90; 99.753; 90
3214.81Huang, Yuanqiong; Guo, Zhonglin; Song, Hongjian; Liu, Yuxiu; Wang, Qingmin
Silver-copper co-catalyzed cascade intramolecular cyclization/desulfinamide/dehydrogenation: one-pot synthesis of substituted carbazoles.
Chemical communications (Cambridge, England), 2018, 54, 7143-7146
7121770 CIFC108 H187 Cu7 N30 O96 P4P 1 21 115.3831; 35.7449; 16.8107
90; 94.964; 90
9209Bruno, Rosaria; Marino, Nadia; Bartella, Lucia; Di Donna, Leonardo; De Munno, Giovanni; Pardo, Emilio; Armentano, Donatella
Highly efficient temperature-dependent chiral separation with a nucleotide-based coordination polymer.
Chemical communications (Cambridge, England), 2018, 54, 6356-6359
7121771 CIFC112 H172 Cu7 N31 O89 P4P 1 21 115.2378; 35.525; 16.7521
90; 95.389; 90
9028.2Bruno, Rosaria; Marino, Nadia; Bartella, Lucia; Di Donna, Leonardo; De Munno, Giovanni; Pardo, Emilio; Armentano, Donatella
Highly efficient temperature-dependent chiral separation with a nucleotide-based coordination polymer.
Chemical communications (Cambridge, England), 2018, 54, 6356-6359
7121772 CIFC32 H30 N2 O2P -17.925; 12.453; 13.592
83.497; 82.328; 88.609
1320.8Li, Feng; Hu, Peng; Sun, Mingming; Li, Chunju; Jia, Xueshun; Li, Jian
Ytterbium and silver co-catalyzed synthesis of pyrrole-fused bicyclic skeletons from enynones and isocyanides.
Chemical communications (Cambridge, England), 2018, 54, 6412-6415
7121773 CIFC30 H26 N2 O2C 1 2/c 131.48; 7.4853; 20.361
90; 104.443; 90
4646.2Li, Feng; Hu, Peng; Sun, Mingming; Li, Chunju; Jia, Xueshun; Li, Jian
Ytterbium and silver co-catalyzed synthesis of pyrrole-fused bicyclic skeletons from enynones and isocyanides.
Chemical communications (Cambridge, England), 2018, 54, 6412-6415
7121774 CIFC55.76 H31.5 D19.56 Fe4 N3 O22.22F m -3 m40.251; 40.251; 40.251
90; 90; 90
65212Gosselin, Eric J.; Lorzing, Gregory R.; Trump, Benjamin A.; Brown, Craig M.; Bloch, Eric D.
Gas adsorption in an isostructural series of pillared coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 6392-6395
7121775 CIFC56.86 H30.78 D17.44 Fe4 N3 O22.28F m -3 m40.216; 40.216; 40.216
90; 90; 90
65042Gosselin, Eric J.; Lorzing, Gregory R.; Trump, Benjamin A.; Brown, Craig M.; Bloch, Eric D.
Gas adsorption in an isostructural series of pillared coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 6392-6395
7121776 CIFC61.56 H40.32 D8.74 Fe4 N2.96 O23.3F m -3 m40.302; 40.302; 40.302
90; 90; 90
65461Gosselin, Eric J.; Lorzing, Gregory R.; Trump, Benjamin A.; Brown, Craig M.; Bloch, Eric D.
Gas adsorption in an isostructural series of pillared coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 6392-6395
7121777 CIFC34.9 Cu4 N2.71 O17.78F m -3 m39.9765; 39.9765; 39.9765
90; 90; 90
63887Gosselin, Eric J.; Lorzing, Gregory R.; Trump, Benjamin A.; Brown, Craig M.; Bloch, Eric D.
Gas adsorption in an isostructural series of pillared coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 6392-6395
7121778 CIFC50.24 H12.6 Cu4 D23.48 N1.56 O18.84F m -3 m39.942; 39.942; 39.942
90; 90; 90
63722Gosselin, Eric J.; Lorzing, Gregory R.; Trump, Benjamin A.; Brown, Craig M.; Bloch, Eric D.
Gas adsorption in an isostructural series of pillared coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 6392-6395
7121779 CIFC36 H61 Dy Si2P -19.6968; 12.7898; 16.0392
71.948; 75.157; 80.771
1821.04Kilpatrick, Alexander F. R.; Guo, Fu-Sheng; Day, Benjamin M.; Mansikkamäki, Akseli; Layfield, Richard A.; Cloke, F Geoffrey N
Single-molecule magnet properties of a monometallic dysprosium pentalene complex.
Chemical communications (Cambridge, England), 2018, 54, 7085-7088
7121780 CIFC36 H61 Si2 YP -19.7114; 12.7624; 15.9778
72.103; 75.026; 80.722
1813.26Kilpatrick, Alexander F. R.; Guo, Fu-Sheng; Day, Benjamin M.; Mansikkamäki, Akseli; Layfield, Richard A.; Cloke, F Geoffrey N
Single-molecule magnet properties of a monometallic dysprosium pentalene complex.
Chemical communications (Cambridge, England), 2018, 54, 7085-7088
7121781 CIFC22 H16 Co N6 S2C 1 2/c 112.099; 11.399; 16.538
90; 99.939; 90
2246.6Wang, Shi-Qiang; Yang, Qing-Yuan; Mukherjee, Soumya; O'Nolan, Daniel; Patyk-Kaźmierczak, Ewa; Chen, Kai-Jie; Shivanna, Mohana; Murray, Claire; Tang, Chiu C.; Zaworotko, Michael J.
Recyclable switching between nonporous and porous phases of a square lattice (sql) topology coordination network.
Chemical communications (Cambridge, England), 2018, 54, 7042-7045
7121782 CIFC22 H16 Co N6 S2C 1 2/c 112.605016; 11.467969; 19.683948
90; 92.9158; 90
2841.71Wang, Shi-Qiang; Yang, Qing-Yuan; Mukherjee, Soumya; O'Nolan, Daniel; Patyk-Kaźmierczak, Ewa; Chen, Kai-Jie; Shivanna, Mohana; Murray, Claire; Tang, Chiu C.; Zaworotko, Michael J.
Recyclable switching between nonporous and porous phases of a square lattice (sql) topology coordination network.
Chemical communications (Cambridge, England), 2018, 54, 7042-7045
7121783 CIFC36 H26 Co F6 N6 S2C 1 2/c 123.3527; 11.5209; 13.7802
90; 108.764; 90
3510.4Wang, Shi-Qiang; Yang, Qing-Yuan; Mukherjee, Soumya; O'Nolan, Daniel; Patyk-Kaźmierczak, Ewa; Chen, Kai-Jie; Shivanna, Mohana; Murray, Claire; Tang, Chiu C.; Zaworotko, Michael J.
Recyclable switching between nonporous and porous phases of a square lattice (sql) topology coordination network.
Chemical communications (Cambridge, England), 2018, 54, 7042-7045
7121784 CIFC29 H21 N O3P -19.7087; 10.8041; 11.9237
78.551; 66.373; 74.278
1097.26Zheng, Zhong; Wang, Ye; Xu, Murong; Kong, Lingkai; Wang, Mengdan; Li, Yanzhong
Transition-metal-free insertion reactions of alkynes into the C-N σ-bonds of imides: synthesis of substituted enamides or chromones.
Chemical communications (Cambridge, England), 2018, 54, 6192-6195
7121785 CIFC29 H18 F N O3P 1 2/n 17.5691; 11.0082; 26.381
90; 93.532; 90
2193.9Zheng, Zhong; Wang, Ye; Xu, Murong; Kong, Lingkai; Wang, Mengdan; Li, Yanzhong
Transition-metal-free insertion reactions of alkynes into the C-N σ-bonds of imides: synthesis of substituted enamides or chromones.
Chemical communications (Cambridge, England), 2018, 54, 6192-6195
7121786 CIFC13 H8 Br2 O2P 1 21/n 115.484; 4.021; 19.824
90; 90.285; 90
1234.3Saha, Subhankar; Desiraju, Gautam R.
Trimorphs of 4-bromophenyl 4-bromobenzoate. Elastic, brittle, plastic.
Chemical communications (Cambridge, England), 2018, 54, 6348-6351
7121787 CIFC13 H8 Br2 O2P n a 217.859; 6.118; 24.872
90; 90; 90
1195.9Saha, Subhankar; Desiraju, Gautam R.
Trimorphs of 4-bromophenyl 4-bromobenzoate. Elastic, brittle, plastic.
Chemical communications (Cambridge, England), 2018, 54, 6348-6351
7121788 CIFC13 H8 Br2 O2P 21 21 213.8549; 11.732; 27.48
90; 90; 90
1242.8Saha, Subhankar; Desiraju, Gautam R.
Trimorphs of 4-bromophenyl 4-bromobenzoate. Elastic, brittle, plastic.
Chemical communications (Cambridge, England), 2018, 54, 6348-6351
7121789 CIFC28 H28 Br2 N2 O4P 21 21 218.3572; 15.2648; 20.6156
90; 90; 90
2629.95Jia, Hao; Guo, Zhenyan; Liu, Honglei; Mao, Biming; Shi, Xueyan; Guo, Hongchao
Tandem nucleophilic addition-cycloaddition of arynes with α-iminoesters: two concurrent pathways to imidazolidines.
Chemical communications (Cambridge, England), 2018, 54, 7050-7053
7121790 CIFC30 H27 N O4P 21 21 219.49079; 9.73586; 26.0784
90; 90; 90
2409.67Pawliczek, Martin; Shimazaki, Yuto; Kimura, Hidenori; Oberg, Kevin M.; Zakpur, Saman; Hashimoto, Takuya; Maruoka, Keiji
Phase-transfer-catalysed asymmetric synthesis of 2,2-disubstituted 1,4-benzoxazin-3-ones.
Chemical communications (Cambridge, England), 2018, 54, 7078-7080
7121791 CIFC36 H32 F3 N4 Nd O10P -110.1306; 11.4102; 17.3413
70.926; 88.066; 72.035
1797.08Sun, Si-Si; Zhang, Jian-Hua; Wang, Zheng; Yu, Yong-Qin; Zhu, Cheng-Yi; Pan, Mei; Su, Cheng-Yong
Anomalous thermally-activated NIR emission of ESIPT modulated Nd-complexes for optical fiber sensing devices.
Chemical communications (Cambridge, England), 2018, 54, 6304-6307
7121792 CIFC53 H41 B F20 Mg N2P -115.0751; 18.2135; 19.1996
79.2972; 86.7245; 72.6916
4945.36Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121793 CIFC65 H61 B F21 Mg N2 O PP -112.6579; 15.3343; 17.5503
92.793; 107.979; 99.369
3179.12Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121794 CIFC65 H53 B F20 Mg N2P -112.6783; 13.1414; 19.5127
100.801; 101.644; 110.656
2858.36Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121795 CIFC65 H53 B Ca F20 N2P 1 21/c 115.4894; 16.6388; 22.8557
90; 94.347; 90
5873.54Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121796 CIFC65 H71 B F20 Mg N2 O2 P2P -112.9094; 15.1447; 16.9144
94.761; 92.981; 96.921
3265.1Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121797 CIFC59 H51 B F20 Mg N2P 1 21/c 114.3528; 20.156; 19.2715
90; 100.557; 90
5480.8Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121798 CIFB5 F O8 PbP b c a10.885; 9.108; 13.576
90; 90; 90
1345.9Mutailipu, Miriding; Zhang, Min; Zhang, Bingbing; Yang, Zhihua; Pan, Shilie
The first lead fluorooxoborate PbB<sub>5</sub>O<sub>8</sub>F: achieving the coexistence of large birefringence and deep-ultraviolet cut-off edge.
Chemical communications (Cambridge, England), 2018, 54, 6308-6311
7121799 CIFBi7 Nd3I m m m4.2996; 15.2; 19.121
90; 90; 90
1249.6Ovchinnikov, Alexander; Makongo, Julien P. A.; Bobev, Svilen
Yet again, new compounds found in systems with known binary phase diagrams. Synthesis, crystal and electronic structure of Nd<sub>3</sub>Bi<sub>7</sub> and Sm<sub>3</sub>Bi<sub>7</sub>.
Chemical communications (Cambridge, England), 2018, 54, 7089-7092
7121800 CIFBi7 Sm3I m m m4.2762; 15.05; 19.034
90; 90; 90
1225Ovchinnikov, Alexander; Makongo, Julien P. A.; Bobev, Svilen
Yet again, new compounds found in systems with known binary phase diagrams. Synthesis, crystal and electronic structure of Nd<sub>3</sub>Bi<sub>7</sub> and Sm<sub>3</sub>Bi<sub>7</sub>.
Chemical communications (Cambridge, England), 2018, 54, 7089-7092
7121801 CIFC20 H15 N OP 1 21/n 113.107; 5.8099; 19.648
90; 102.575; 90
1460.3Jaiswal, Yogesh; Kumar, Yogesh; Pal, Jagannath; Subramanian, Ranga; Kumar, Amit
Rapid synthesis of polysubstituted phenanthridines from simple aliphatic/aromatic nitriles and iodo arenes via Pd(ii) catalyzed domino C-C/C-C/C-N bond formation.
Chemical communications (Cambridge, England), 2018, 54, 7207-7210
7121802 CIFC42 H72 Lu N3 Si3P 1 21/c 112.4709; 20.2287; 36.0755
90; 90.1168; 90
9100.8Boteju, Kasuni C.; Wan, Suchen; Venkatesh, Amrit; Ellern, Arkady; Rossini, Aaron J.; Sadow, Aaron D.
Rare earth arylsilazido compounds with inequivalent secondary interactions.
Chemical communications (Cambridge, England), 2018, 54, 7318-7321
7121803 CIFC57.5 H98 N3 O Si3 YP 1 21/n 118.7125; 31.04; 20.6586
90; 93.071; 90
11982Boteju, Kasuni C.; Wan, Suchen; Venkatesh, Amrit; Ellern, Arkady; Rossini, Aaron J.; Sadow, Aaron D.
Rare earth arylsilazido compounds with inequivalent secondary interactions.
Chemical communications (Cambridge, England), 2018, 54, 7318-7321
7121804 CIFC42 H72 N3 Sc Si3P 1 21/c 112.3546; 20.0869; 35.9838
90; 90.113; 90
8929.9Boteju, Kasuni C.; Wan, Suchen; Venkatesh, Amrit; Ellern, Arkady; Rossini, Aaron J.; Sadow, Aaron D.
Rare earth arylsilazido compounds with inequivalent secondary interactions.
Chemical communications (Cambridge, England), 2018, 54, 7318-7321
7121805 CIFC42 H72 N3 Si3 YP 1 21/c 112.5095; 20.2927; 36.0731
90; 90.412; 90
9157Boteju, Kasuni C.; Wan, Suchen; Venkatesh, Amrit; Ellern, Arkady; Rossini, Aaron J.; Sadow, Aaron D.
Rare earth arylsilazido compounds with inequivalent secondary interactions.
Chemical communications (Cambridge, England), 2018, 54, 7318-7321
7121806 CIFC55 H60 N3 O38.5 Y6I m -325.1402; 25.1402; 25.1402
90; 90; 90
15889.4Xue, Dong-Xu; Cadiau, Amandine; Weseliński, Łukasz J.; Jiang, Hao; Bhatt, Prashant M.; Shkurenko, Aleksander; Wojtas, Lukasz; Zhijie, Chen; Belmabkhout, Youssef; Adil, Karim; Eddaoudi, Mohamed
Topology meets MOF chemistry for pore-aperture fine tuning: ftw-MOF platform for energy-efficient separations via adsorption kinetics or molecular sieving
Chemical Communications, 2018
7121807 CIFC56.5 H59 N9.5 O36.75 Tb6R -3 c18.232; 18.232; 45.607
90; 90; 120
13129Xue, Dong-Xu; Cadiau, Amandine; Weseliński, Łukasz J.; Jiang, Hao; Bhatt, Prashant M.; Shkurenko, Aleksander; Wojtas, Lukasz; Zhijie, Chen; Belmabkhout, Youssef; Adil, Karim; Eddaoudi, Mohamed
Topology meets MOF chemistry for pore-aperture fine tuning: ftw-MOF platform for energy-efficient separations via adsorption kinetics or molecular sieving
Chemical Communications, 2018
7121808 CIFC24 H35 B N6 O2 Si WP 1 21/c 19.3555; 14.6772; 20.6011
90; 89.668; 90
2828.74Frogley, Benjamin J.; Hill, Anthony F.
Bis(alkylidynyl)arsines.
Chemical communications (Cambridge, England), 2018, 54, 7649-7652
7121809 CIFC25 H37 B N6 O2 Si WP 1 21/c 112.636; 14.8272; 16.3046
90; 109.839; 90
2873.47Frogley, Benjamin J.; Hill, Anthony F.
Bis(alkylidynyl)arsines.
Chemical communications (Cambridge, England), 2018, 54, 7649-7652
7121810 CIFC53 H80 B2 N12 O4 Si2 W2P -111.0937; 13.1532; 22.7516
91.059; 98.161; 108.441
3110.38Frogley, Benjamin J.; Hill, Anthony F.
Bis(alkylidynyl)arsines.
Chemical communications (Cambridge, England), 2018, 54, 7649-7652
7121811 CIFC19 H18 Cl N OC 1 2/c 120.1159; 8.9951; 17.9253
90; 93.382; 90
3237.8Gupta, Sonu; Chandna, Nisha; Dubey, Pooja; Singh, Ajai K.; Jain, Nidhi
GO-Cu<sub>7</sub>S<sub>4</sub> catalyzed ortho-aminomethylation of phenol derivatives with N,N-dimethylbenzylamines: site-selective oxidative CDC.
Chemical communications (Cambridge, England), 2018, 54, 7511-7514
7121812 CIFC12 H14 N2 OP 21 21 215.7386; 9.5416; 18.3137
90; 90; 90
1002.77Wu, Kui; Du, Yuliu; Wei, Zheng; Wang, Ting
Synthesis of functionalized pyrroloindolines via a visible-light-induced radical cascade reaction: rapid synthesis of (±)-flustraminol B.
Chemical communications (Cambridge, England), 2018, 54, 7443-7446
7121813 CIFC13 H16 N2 O2C 1 2/c 128.7011; 9.388; 8.9139
90; 99.23; 90
2370.7Wu, Kui; Du, Yuliu; Wei, Zheng; Wang, Ting
Synthesis of functionalized pyrroloindolines via a visible-light-induced radical cascade reaction: rapid synthesis of (±)-flustraminol B.
Chemical communications (Cambridge, England), 2018, 54, 7443-7446
7121814 CIFC26 H37 N O PP -110.0822; 10.8747; 12.0033
106.883; 90.592; 103.9
1217.9Mai, Juri; Arkhypchuk, Anna I.; Gupta, Arvind Kumar; Ott, Sascha
Reductive coupling of two aldehydes to unsymmetrical E-alkenes via phosphaalkene and phosphinate intermediates.
Chemical communications (Cambridge, England), 2018, 54, 7163-7166
7121815 CIFC57 H85 Cl3 N2 O6 P2P -110.7916; 17.0045; 17.0443
90.205; 96.705; 106.832
2971Mai, Juri; Arkhypchuk, Anna I.; Gupta, Arvind Kumar; Ott, Sascha
Reductive coupling of two aldehydes to unsymmetrical E-alkenes via phosphaalkene and phosphinate intermediates.
Chemical communications (Cambridge, England), 2018, 54, 7163-7166
7121816 CIFC209 H298 N36 O33 P2P -119.83; 22.082; 27.967
86.839; 77.529; 75.246
11563Zuo, Wei; Huang, Zhe; Zhao, Yanxia; Xu, Wenhua; Liu, Zhihua; Yang, Xiao-Juan; Jia, Chuandong; Wu, Biao
Chirality sensing of choline derivatives by a triple anion helicate cage through induced circular dichroism.
Chemical communications (Cambridge, England), 2018, 54, 7378-7381
7121817 CIFC22 H29 I N2 O3P -19.0399; 10.7529; 12.1907
84.915; 70.321; 80.746
1100.51Tam, Teck Lip Dexter; Ng, Chee Koon; Lu, Xuefeng; Lim, Zheng Long; Wu, Jishan
Anion-π interactions of highly π-acidic dipyridinium-naphthalene diimide salts.
Chemical communications (Cambridge, England), 2018, 54, 7374-7377
7121818 CIFC44 H58 Cl2 N4 O6P -17.9255; 9.259; 15.1784
96.993; 98.728; 98.758
1076.06Tam, Teck Lip Dexter; Ng, Chee Koon; Lu, Xuefeng; Lim, Zheng Long; Wu, Jishan
Anion-π interactions of highly π-acidic dipyridinium-naphthalene diimide salts.
Chemical communications (Cambridge, England), 2018, 54, 7374-7377
7121819 CIFC46 H55 F12 N7 O4 P2P 1 21/c 112.698; 17.0155; 23.0412
90; 96.201; 90
4949.2Tam, Teck Lip Dexter; Ng, Chee Koon; Lu, Xuefeng; Lim, Zheng Long; Wu, Jishan
Anion-π interactions of highly π-acidic dipyridinium-naphthalene diimide salts.
Chemical communications (Cambridge, England), 2018, 54, 7374-7377
7121820 CIFC44 H58 Br2 N4 O6P 1 21/c 18.303; 28.106; 9.5912
90; 104.697; 90
2165Tam, Teck Lip Dexter; Ng, Chee Koon; Lu, Xuefeng; Lim, Zheng Long; Wu, Jishan
Anion-π interactions of highly π-acidic dipyridinium-naphthalene diimide salts.
Chemical communications (Cambridge, England), 2018, 54, 7374-7377
7121821 CIFCe2 Cl12 Ni4F m -3 m10.1404; 10.1404; 10.1404
90; 90; 90
1042.7Baldo, Bianca; Rubio, Francisco; Flores, Erwin; Vega, Andres; Audebrand, Nathalie; Venegas-Yazigi, Diego; Paredes-García, Verónica
Ni<sub>2</sub>[LnCl<sub>6</sub>] (Ln = Eu<sup>II</sup>, Ce<sup>II</sup>, Gd<sup>II</sup>): the first Ln<sup>II</sup> compounds stabilized in a pure inorganic lattice.
Chemical communications (Cambridge, England), 2018, 54, 7531-7534
7121822 CIFCl12 Eu2 Ni4F m -3 m10.1666; 10.1666; 10.1666
90; 90; 90
1050.8Baldo, Bianca; Rubio, Francisco; Flores, Erwin; Vega, Andres; Audebrand, Nathalie; Venegas-Yazigi, Diego; Paredes-García, Verónica
Ni<sub>2</sub>[LnCl<sub>6</sub>] (Ln = Eu<sup>II</sup>, Ce<sup>II</sup>, Gd<sup>II</sup>): the first Ln<sup>II</sup> compounds stabilized in a pure inorganic lattice.
Chemical communications (Cambridge, England), 2018, 54, 7531-7534
7121823 CIFCl12 Gd2 Ni4F m -3 m10.1164; 10.1164; 10.1164
90; 90; 90
1035.33Baldo, Bianca; Rubio, Francisco; Flores, Erwin; Vega, Andres; Audebrand, Nathalie; Venegas-Yazigi, Diego; Paredes-García, Verónica
Ni<sub>2</sub>[LnCl<sub>6</sub>] (Ln = Eu<sup>II</sup>, Ce<sup>II</sup>, Gd<sup>II</sup>): the first Ln<sup>II</sup> compounds stabilized in a pure inorganic lattice.
Chemical communications (Cambridge, England), 2018, 54, 7531-7534
7121824 CIFC57 H71 B N4P -110.344; 15.31; 15.375
96.097; 93.5; 101.648
2363Winner, Lena; Hermann, Alexander; Bélanger-Chabot, Guillaume; González-Belman, Oscar F; Jiménez-Halla, J Oscar C; Kelch, Hauke; Braunschweig, Holger
Cleavage of BN triple bonds by main group reagents.
Chemical communications (Cambridge, England), 2018, 54, 8210-8213
7121825 CIFC34 H56 B N5 SiP 1 21/n 119.1168; 17.0388; 21.9556
90; 105.534; 90
6890.3Winner, Lena; Hermann, Alexander; Bélanger-Chabot, Guillaume; González-Belman, Oscar F; Jiménez-Halla, J Oscar C; Kelch, Hauke; Braunschweig, Holger
Cleavage of BN triple bonds by main group reagents.
Chemical communications (Cambridge, England), 2018, 54, 8210-8213
7121826 CIFC50 H59 B N4P -113.134; 16.944; 19.889
79.28; 81.864; 73.209
4145Winner, Lena; Hermann, Alexander; Bélanger-Chabot, Guillaume; González-Belman, Oscar F; Jiménez-Halla, J Oscar C; Kelch, Hauke; Braunschweig, Holger
Cleavage of BN triple bonds by main group reagents.
Chemical communications (Cambridge, England), 2018, 54, 8210-8213
7121827 CIFC27 H29 N7 O2P 1 21/n 19.814; 9.916; 25.156
90; 90.477; 90
2448Karvande, Anirudha; Khan, Shahnawaz; Khan, Irfan; Singh, Deepti; Khedgikar, Vikram; Kushwaha, Priyanka; Ahmad, Naseer; Kothari, Priyanka; Dhasmana, Anupam; Kant, Ruchir; Trivedi, Ritu; Chauhan, Prem M. S.
Discovery of a tetrazolyl β-carboline with <i>in vitro</i> and <i>in vivo</i> osteoprotective activity under estrogen-deficient conditions.
MedChemComm, 2018, 9, 1213-1225
7121828 CIFC17 H13 F2 N O2P b c a8.3324; 18.0049; 18.9382
90; 90; 90
2841.2Ma, Xingxing; Mai, Shaoyu; Zhou, Yao; Cheng, Gui-Juan; Song, Qiuling
Dual role of ethyl bromodifluoroacetate in the formation of fluorine-containing heteroaromatic compounds.
Chemical communications (Cambridge, England), 2018, 54, 8960-8963
7121829 CIFC34 H40 N2 O14 S12 ZnP 1 21/c 114.0234; 10.7448; 15.7641
90; 94.765; 90
2367.1Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121830 CIFC34 H40 Mn N2 O14 S12P 1 21/c 113.904; 10.668; 15.757
90; 95.34; 90
2327.1Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121831 CIFC34 H40 N2 O14 S12 ZnP 1 21/c 113.956; 10.755; 15.612
90; 94.237; 90
2336.9Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121832 CIFC34 H40 Mn N2 O14 S12P 1 21/c 113.957; 10.7952; 15.701
90; 94.815; 90
2357.3Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121833 CIFC34 H42 N2 O14 S12 ZnP 1 21/c 114.2765; 10.2073; 16.037
90; 92.05; 90
2335.5Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121834 CIFC34 H42 Mn N2 O14 S12P 1 21/c 114.0309; 10.3024; 16.0378
90; 93.634; 90
2313.6Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121835 CIFC7 H11 N O4P 1 21/n 19.7222; 7.91107; 11.6743
90; 102.086; 90
878Riemer, Martin; Uzunova, Veselina V.; Riemer, Nastja; Clarkson, Guy J.; Pereira, Nicole; Napier, Richard; Shipman, Michael
Phyllostictine A: total synthesis, structural verification and determination of substructure responsible for plant growth inhibition.
Chemical communications (Cambridge, England), 2018, 54, 7211-7214
7121836 CIFC14 H25 N O5P 1 21/c 115.5057; 9.2475; 11.6104
90; 108.886; 90
1575.17Hayashi, Hirohito; Kaga, Atsushi; Wang, Bin; Gagosz, Fabien; Chiba, Shunsuke
Use of a benzyl ether as a traceless hydrogen donor in the anti-Markovnikov hydrofunctionalization of alkenes with xanthates.
Chemical communications (Cambridge, England), 2018, 54, 7535-7538
7121837 CIFC H4 Cl3 K N2 O ZnP 1 21/m 16.8599; 7.353; 8.4999
90; 99.069; 90
423.38Casali, Lucia; Mazzei, Luca; Shemchuk, Oleksii; Honer, Kenneth; Grepioni, Fabrizia; Ciurli, Stefano; Braga, Dario; Baltrusaitis, Jonas
Smart urea ionic co-crystals with enhanced urease inhibition activity for improved nitrogen cycle management.
Chemical communications (Cambridge, England), 2018, 54, 7637-7640
7121838 CIFC H4 Cl3 K N2 O ZnP 1 21/n 17.422; 13.553; 8.4219
90; 92.089; 90
846.6Casali, Lucia; Mazzei, Luca; Shemchuk, Oleksii; Honer, Kenneth; Grepioni, Fabrizia; Ciurli, Stefano; Braga, Dario; Baltrusaitis, Jonas
Smart urea ionic co-crystals with enhanced urease inhibition activity for improved nitrogen cycle management.
Chemical communications (Cambridge, England), 2018, 54, 7637-7640
7121839 CIFC14 H16 N2 O2 SP 1 21 19.955; 5.5629; 12.732
90; 92.902; 90
704.2Wang, Miao; Tang, Bo-Cheng; Wang, Jun-Gang; Xiang, Jia-Chen; Guan, Ao-Yu; Huang, Ping-Ping; Guo, Wu-Yinzheng; Wu, Yan-Dong; Wu, An-Xin
The triple role of rongalite in aminosulfonylation of aryldiazonium tetrafluoroborates: synthesis of N-aminosulfonamides via a radical coupling reaction.
Chemical communications (Cambridge, England), 2018, 54, 7641-7644
7121840 CIFC17 H18 O4P 1 21 17.69761; 12.2794; 8.18769
90; 110.677; 90
724.07Shu, Tao; Li, Sun; Chen, Xiang-Yu; Liu, Qiang; von Essen, Carolina; Rissanen, Kari; Enders, Dieter
Asymmetric synthesis of functionalized tetrahydrofluorenones via an NHC-catalyzed homoenolate Michael addition.
Chemical communications (Cambridge, England), 2018, 54, 7661-7664
7121841 CIFC25 H34 N4 SP 1 21/n 115.443; 11.2028; 15.4669
90; 117.896; 90
2364.9Ruamps, Mirko; Bastin, Stéphanie; Rechignat, Lionel; Sournia-Saquet, Alix; Valyaev, Dmitry A.; Mouesca, Jean-Marie; Lugan, Noël; Maurel, Vincent; César, Vincent
Unveiling the redox-active character of imidazolin-2-thiones derived from amino-substituted N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2018, 54, 7653-7656
7121842 CIFC27 H37 F12 N5 S Sb2P -111.9044; 12.9628; 13.2255
60.88; 78.818; 80.295
1742.51Ruamps, Mirko; Bastin, Stéphanie; Rechignat, Lionel; Sournia-Saquet, Alix; Valyaev, Dmitry A.; Mouesca, Jean-Marie; Lugan, Noël; Maurel, Vincent; César, Vincent
Unveiling the redox-active character of imidazolin-2-thiones derived from amino-substituted N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2018, 54, 7653-7656
7121843 CIFC17 H28 O6P 21 21 217.6651; 12.4842; 18.5353
90; 90; 90
1773.69Feng, Jing; Yu, Tianzi; Zhang, Zhijiang; Li, Jinpeng; Fu, Shaomin; Chen, Juan; Liu, Bo
Asymmetric synthesis of the fully functionalized six-membered ring of trigoxyphin A.
Chemical communications (Cambridge, England), 2018, 54, 7665-7668
7121844 CIFC17 H26 O7P 21 21 218.9598; 11.7903; 17.2249
90; 90; 90
1819.62Feng, Jing; Yu, Tianzi; Zhang, Zhijiang; Li, Jinpeng; Fu, Shaomin; Chen, Juan; Liu, Bo
Asymmetric synthesis of the fully functionalized six-membered ring of trigoxyphin A.
Chemical communications (Cambridge, England), 2018, 54, 7665-7668
7121845 CIFC19 H18 N2P b c a10.619; 9.676; 28.661
90; 90; 90
2944.9Liu, Siyuan; Qu, Jingping; Wang, Baomin
Substrate-controlled divergent synthesis of polycyclic indoloazepines and indolodiazepines via 1,5-hydride shift/7-cyclization cascades.
Chemical communications (Cambridge, England), 2018, 54, 7928-7931
7121846 CIFC20 H20 N2P 1 21/n 19.4242; 7.9644; 19.9745
90; 99.582; 90
1478.33Liu, Siyuan; Qu, Jingping; Wang, Baomin
Substrate-controlled divergent synthesis of polycyclic indoloazepines and indolodiazepines via 1,5-hydride shift/7-cyclization cascades.
Chemical communications (Cambridge, England), 2018, 54, 7928-7931
7121847 CIFC41 H43 N4P 1 21/c 120.821; 9.5022; 17.881
90; 110.124; 90
3321.7Liu, Siyuan; Qu, Jingping; Wang, Baomin
Substrate-controlled divergent synthesis of polycyclic indoloazepines and indolodiazepines via 1,5-hydride shift/7-cyclization cascades.
Chemical communications (Cambridge, England), 2018, 54, 7928-7931
7121848 CIFC33 H30 N2 O2 SP 1 21/n 17.7368; 16.8658; 20.2866
90; 96.461; 90
2630.3Pradhan, Sajan; Shahi, Chandan Kumar; Bhattacharyya, Aditya; Ghorai, Manas K.
Stereoselective synthesis of 3-spiropiperidino indolenines via S<sub>N</sub>2-type ring opening of activated aziridines with 1H-indoles/Pd-catalyzed spirocyclization with propargyl carbonates.
Chemical communications (Cambridge, England), 2018, 54, 8583-8586
7121849 CIFC66 H64 O12P -19.3274; 12.0859; 12.4207
110.921; 90.774; 98.445
1290.4Chai, Hongxin; Yang, Liu-Pan; Ke, Hua; Pang, Xin-Yu; Jiang, Wei
Allosteric cooperativity in ternary complexes with low symmetry.
Chemical communications (Cambridge, England), 2018, 54, 7677-7680
7121850 CIFC67 H66 Cl2 O12P -112.3158; 12.769; 19.5858
85.884; 73.714; 80.961
2918.52Chai, Hongxin; Yang, Liu-Pan; Ke, Hua; Pang, Xin-Yu; Jiang, Wei
Allosteric cooperativity in ternary complexes with low symmetry.
Chemical communications (Cambridge, England), 2018, 54, 7677-7680
7121851 CIFC22 H23 F OP 1 21/c 112.6134; 8.4407; 17.1212
90; 94.76; 90
1816.54Xu, Ming-Hui; Dai, Kun-Long; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
A catalytic allylic cation-induced intermolecular allylation-semipinacol rearrangement.
Chemical communications (Cambridge, England), 2018, 54, 7685-7688
7121852 CIFC28 H28 OP n a 2118.308; 19.0516; 6.2276
90; 90; 90
2172.17Xu, Ming-Hui; Dai, Kun-Long; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
A catalytic allylic cation-induced intermolecular allylation-semipinacol rearrangement.
Chemical communications (Cambridge, England), 2018, 54, 7685-7688
7121853 CIFC17 H21 Br Cl N2 O RhP b c a15.4304; 14.9823; 16.4747
90; 90; 90
3808.7He, Shuang; Tan, Guangying; Luo, Anping; You, Jingsong
Rhodium-catalyzed oxidative C-H/C-H cross-coupling of aniline with heteroarene: N-nitroso group enabled mild conditions.
Chemical communications (Cambridge, England), 2018, 54, 7794-7797
7121854 CIFC65 H64 B Cl F20 Mg N2 O Si2P -113.3518; 14.4685; 17.3377
98.233; 97.872; 90.686
3281.8Pahl, Jürgen; Elsen, Holger; Friedrich, Alexander; Harder, Sjoerd
Unsupported metal silyl ether coordination.
Chemical communications (Cambridge, England), 2018, 54, 7846-7849
7121855 CIFC44 H42 N2 O4 S2P -17.2994; 9.0319; 14.3088
84.935; 77.163; 84.614
913.49Hu, Yingyuan; Wang, Zhenfeng; Jiang, Xiaofang; Cai, Xinyi; Su, Shi-Jian; Huang, Fei; Cao, Yong
One-step synthesis of cyclic compounds towards easy room-temperature phosphorescence and deep blue thermally activated delayed fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 7850-7853
7121856 CIFC38 H30 N2 O6 S2P 1 21/c 113.5501; 4.9755; 23.1851
90; 100.243; 90
1538.19Hu, Yingyuan; Wang, Zhenfeng; Jiang, Xiaofang; Cai, Xinyi; Su, Shi-Jian; Huang, Fei; Cao, Yong
One-step synthesis of cyclic compounds towards easy room-temperature phosphorescence and deep blue thermally activated delayed fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 7850-7853
7121857 CIFC30 H28 F12 N8 Ni P2P 1 21/c 110.7258; 18.871; 16.3402
90; 93.244; 90
3302.1Yang, Chu-Fan; Lu, Taotao; Chen, Xue-Tai; Xue, Zi-Ling
Unusual rearrangement of an N-heterocyclic carbene via a ring-opening and ring-closing process.
Chemical communications (Cambridge, England), 2018, 54, 7830-7833
7121858 CIFC30 H28 F12 N8 Ni P2P 21 21 2111.199; 15.1982; 19.638
90; 90; 90
3342.5Yang, Chu-Fan; Lu, Taotao; Chen, Xue-Tai; Xue, Zi-Ling
Unusual rearrangement of an N-heterocyclic carbene via a ring-opening and ring-closing process.
Chemical communications (Cambridge, England), 2018, 54, 7830-7833
7121859 CIFC28 H24 F6 N7 Ni PP 1 21/n 18.3433; 28.32; 11.5936
90; 90.533; 90
2739.2Yang, Chu-Fan; Lu, Taotao; Chen, Xue-Tai; Xue, Zi-Ling
Unusual rearrangement of an N-heterocyclic carbene via a ring-opening and ring-closing process.
Chemical communications (Cambridge, England), 2018, 54, 7830-7833
7121860 CIFC32 H31 F12 N9 P2 PdP 1 21/c 114.6723; 13.3927; 19.2473
90; 108.953; 90
3577.1Yang, Chu-Fan; Lu, Taotao; Chen, Xue-Tai; Xue, Zi-Ling
Unusual rearrangement of an N-heterocyclic carbene via a ring-opening and ring-closing process.
Chemical communications (Cambridge, England), 2018, 54, 7830-7833
7121861 CIFC42 H40 N4R -3 :H26.1757; 26.1757; 31.6025
90; 90; 120
18752Dutta, Ranjan; Firmansyah, Dikhi; Kim, Jihoon; Jo, Hongil; Ok, Kang Min; Lee, Chang-Hee
Unexpected halide anion binding modes in meso-bis-ethynyl picket-calix[4]pyrroles: effects of meso-π (ethynyl) extension.
Chemical communications (Cambridge, England), 2018, 54, 7936-7939
7121862 CIFC60 H77 F3 N6 O0.29P -111.5785; 13.3678; 19.1989
80.99; 73.141; 82.786
2798.7Dutta, Ranjan; Firmansyah, Dikhi; Kim, Jihoon; Jo, Hongil; Ok, Kang Min; Lee, Chang-Hee
Unexpected halide anion binding modes in meso-bis-ethynyl picket-calix[4]pyrroles: effects of meso-π (ethynyl) extension.
Chemical communications (Cambridge, England), 2018, 54, 7936-7939
7121863 CIFC46 H46 N6P 1 21/c 111.27; 14.844; 12.708
90; 114.23; 90
1938.7Dutta, Ranjan; Firmansyah, Dikhi; Kim, Jihoon; Jo, Hongil; Ok, Kang Min; Lee, Chang-Hee
Unexpected halide anion binding modes in meso-bis-ethynyl picket-calix[4]pyrroles: effects of meso-π (ethynyl) extension.
Chemical communications (Cambridge, England), 2018, 54, 7936-7939
7121864 CIFC18 H24 O7P 1 21/c 17.31; 24.5621; 10.1151
90; 91.383; 90
1815.6Burnie, Andrew J.; Evans, P. Andrew
Rhodium-catalyzed [(3+2)+1] carbocyclizations of alkynylidenecyclopropanes with carbon monoxide: construction of polysubstituted bicyclohexa-2,5-dienones.
Chemical communications (Cambridge, England), 2018, 54, 7621-7624
7121865 CIFC57.18 H44.44 O40 S4 Zr6I 4/m m m23.3559; 23.3559; 26.7429
90; 90; 90
14588.2Du, Pei-Yao; Lustig, William P.; Teat, Simon J.; Gu, Wen; Liu, Xin; Li, Jing
A robust two-dimensional zirconium-based luminescent coordination polymer built on a V-shaped dicarboxylate ligand for vapor phase sensing of volatile organic compounds.
Chemical communications (Cambridge, England), 2018, 54, 8088-8091
7121866 CIFC18 H30 Cl F2 N O10P c a 2114.558; 11.247; 14.392
90; 90; 90
2356.5Wei, Yan-Li; Jing, Jing; Shi, Chao; Ye, Heng-Yun; Wang, Zhong-Xia; Zhang, Yi
Unusual high-temperature reversible phase transition containing dielectric and nonlinear optical switches in host-guest supramolecular crown ether clathrates.
Chemical communications (Cambridge, England), 2018, 54, 8076-8079
7121867 CIFC18 H30 Cl F2 N O10P c a 2114.5486; 11.2914; 14.5674
90; 90; 90
2393Wei, Yan-Li; Jing, Jing; Shi, Chao; Ye, Heng-Yun; Wang, Zhong-Xia; Zhang, Yi
Unusual high-temperature reversible phase transition containing dielectric and nonlinear optical switches in host-guest supramolecular crown ether clathrates.
Chemical communications (Cambridge, England), 2018, 54, 8076-8079
7121868 CIFC5 H9 I2 N2 PC 1 2/m 113.4578; 8.6203; 9.8671
90; 116.365; 90
1025.62Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121869 CIFC18 H32 I N4 PI 1 2/a 19.4547; 19.5345; 11.8695
90; 94.891; 90
2184.2Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121870 CIFC9 H17 I2 N2 PP -17.7774; 8.4078; 11.6208
84.753; 79.435; 78.409
730.6Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121871 CIFC27 H37 I4 N2 PC 1 c 112.5136; 16.67; 16.872
90; 108.146; 90
3344.5Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121872 CIFC21 H25 I2 N2 PP 21 21 219.253; 15.3097; 16.0029
90; 90; 90
2267Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121873 CIFC28 H39 Cl2 I2 N2 PP 1 21/n 110.7558; 18.7258; 16.3345
90; 102.309; 90
3214.3Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121874 CIFC23 H30 O4P 1 21/n 117.18; 6.536; 17.28
90; 91.34; 90
1940Yao, Sheng; Zhang, Kai; Zhou, Quan-Quan; Zhao, Yu; Shi, De-Qing; Xiao, Wen-Jing
Photoredox-promoted alkyl radical addition/semipinacol rearrangement sequences of alkenylcyclobutanols: rapid access to cyclic ketones.
Chemical communications (Cambridge, England), 2018, 54, 8096-8099
7121875 CIFC14 H16 Cl2 N2 O6P -14.9143; 7.458; 11.698
73.27; 89.528; 69.737
383.2Donoshita, Masaki; Hayashi, Mikihiro; Ikeda, Ryuichi; Yoshida, Yukihiro; Morikawa, Shota; Sugimoto, Kunihisa; Kitagawa, Hiroshi
Drastic rearrangement of self-assembled hydrogen-bonded tapes in a molecular crystal.
Chemical communications (Cambridge, England), 2018, 54, 8571-8574
7121876 CIFC14 H16 Cl2 N2 O6P -14.987; 7.592; 11.718
72.926; 89.449; 71.157
399.6Donoshita, Masaki; Hayashi, Mikihiro; Ikeda, Ryuichi; Yoshida, Yukihiro; Morikawa, Shota; Sugimoto, Kunihisa; Kitagawa, Hiroshi
Drastic rearrangement of self-assembled hydrogen-bonded tapes in a molecular crystal.
Chemical communications (Cambridge, England), 2018, 54, 8571-8574
7121877 CIFC14 H16 Cl2 N2 O6P -14.6904; 8.921; 9.833
103.357; 96.447; 93.984
395.8Donoshita, Masaki; Hayashi, Mikihiro; Ikeda, Ryuichi; Yoshida, Yukihiro; Morikawa, Shota; Sugimoto, Kunihisa; Kitagawa, Hiroshi
Drastic rearrangement of self-assembled hydrogen-bonded tapes in a molecular crystal.
Chemical communications (Cambridge, England), 2018, 54, 8571-8574
7121878 CIFC14 H16 Cl2 N2 O6P -18.1575; 10.3671; 11.0921
74.29; 75.655; 67.442
822.93Donoshita, Masaki; Hayashi, Mikihiro; Ikeda, Ryuichi; Yoshida, Yukihiro; Morikawa, Shota; Sugimoto, Kunihisa; Kitagawa, Hiroshi
Drastic rearrangement of self-assembled hydrogen-bonded tapes in a molecular crystal.
Chemical communications (Cambridge, England), 2018, 54, 8571-8574
7121879 CIFC68 H98 Si3P 1 21/n 119.538; 14.015; 24.33
90; 108.596; 90
6314Zhao, Hui; Klemmer, Lukas; Cowley, Michael J.; Majumdar, Moumita; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Phenylene-bridged cross-conjugated 1,2,3-trisilacyclopentadienes.
Chemical communications (Cambridge, England), 2018, 54, 8399-8402
7121880 CIFC135 H202 Si6C 1 2/c 140.86; 14.207; 23.479
90; 96.47; 90
13543Zhao, Hui; Klemmer, Lukas; Cowley, Michael J.; Majumdar, Moumita; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Phenylene-bridged cross-conjugated 1,2,3-trisilacyclopentadienes.
Chemical communications (Cambridge, England), 2018, 54, 8399-8402
7121881 CIFC74 H102 Si3P -118.411; 20.736; 22.03
110.122; 100.632; 100.34
7488Zhao, Hui; Klemmer, Lukas; Cowley, Michael J.; Majumdar, Moumita; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Phenylene-bridged cross-conjugated 1,2,3-trisilacyclopentadienes.
Chemical communications (Cambridge, England), 2018, 54, 8399-8402
7121882 CIFC36 H24P 1 21/c 111.1772; 10.312; 11.2725
90; 106.329; 90
1246.85Spisak, Sarah N.; Wei, Zheng; Darzi, Evan; Jasti, Ramesh; Petrukhina, Marina A.
Highly strained [6]cycloparaphenylene: crystallization of an unsolvated polymorph and the first mono- and dianions.
Chemical communications (Cambridge, England), 2018, 54, 7818-7821
7121883 CIFC64 H80 Na O10P 1 21/c 110.1288; 17.237; 16.0129
90; 102.514; 90
2729.28Spisak, Sarah N.; Wei, Zheng; Darzi, Evan; Jasti, Ramesh; Petrukhina, Marina A.
Highly strained [6]cycloparaphenylene: crystallization of an unsolvated polymorph and the first mono- and dianions.
Chemical communications (Cambridge, England), 2018, 54, 7818-7821
7121884 CIFC76 H104 K2 O16P 1 21/n 110.1496; 23.2584; 15.4171
90; 98.784; 90
3596.73Spisak, Sarah N.; Wei, Zheng; Darzi, Evan; Jasti, Ramesh; Petrukhina, Marina A.
Highly strained [6]cycloparaphenylene: crystallization of an unsolvated polymorph and the first mono- and dianions.
Chemical communications (Cambridge, England), 2018, 54, 7818-7821
7121885 CIFC8 H14 Br3 N3 OP 1 21/c 16.4062; 20.4294; 9.5955
90; 92.369; 90
1254.74Weinberger, Craig; Hines, Rachel; Zeller, Matthias; Rosokha, Sergiy V.
Continuum of covalent to intermolecular bonding in the halogen-bonded complexes of 1,4-diazabicyclo[2.2.2]octane with bromine-containing electrophiles.
Chemical communications (Cambridge, England), 2018, 54, 8060-8063
7121886 CIFC19 H28 Br N5 O3 SP 32 2 19.8558; 9.8558; 18.9035
90; 90; 120
1590.22Weinberger, Craig; Hines, Rachel; Zeller, Matthias; Rosokha, Sergiy V.
Continuum of covalent to intermolecular bonding in the halogen-bonded complexes of 1,4-diazabicyclo[2.2.2]octane with bromine-containing electrophiles.
Chemical communications (Cambridge, England), 2018, 54, 8060-8063
7121887 CIFC8 H13 Br3 Cl3 N3 O2P n a 2114.314; 18.26; 6.4262
90; 90; 90
1679.6Weinberger, Craig; Hines, Rachel; Zeller, Matthias; Rosokha, Sergiy V.
Continuum of covalent to intermolecular bonding in the halogen-bonded complexes of 1,4-diazabicyclo[2.2.2]octane with bromine-containing electrophiles.
Chemical communications (Cambridge, England), 2018, 54, 8060-8063
7121888 CIFC7 H14 Br4 Cl2 N2P 1 21/m 17.7632; 7.428; 12.8269
90; 98.7339; 90
731.09Weinberger, Craig; Hines, Rachel; Zeller, Matthias; Rosokha, Sergiy V.
Continuum of covalent to intermolecular bonding in the halogen-bonded complexes of 1,4-diazabicyclo[2.2.2]octane with bromine-containing electrophiles.
Chemical communications (Cambridge, England), 2018, 54, 8060-8063
7121889 CIFC7 H12 Br Cl3 N2P 1 21/m 15.8771; 16.4201; 11.9239
90; 100.625; 90
1130.96Weinberger, Craig; Hines, Rachel; Zeller, Matthias; Rosokha, Sergiy V.
Continuum of covalent to intermolecular bonding in the halogen-bonded complexes of 1,4-diazabicyclo[2.2.2]octane with bromine-containing electrophiles.
Chemical communications (Cambridge, England), 2018, 54, 8060-8063
7121890 CIFC7 H13 Br3 N2P 1 21/n 16.0754; 15.7428; 12.0401
90; 101.885; 90
1126.88Weinberger, Craig; Hines, Rachel; Zeller, Matthias; Rosokha, Sergiy V.
Continuum of covalent to intermolecular bonding in the halogen-bonded complexes of 1,4-diazabicyclo[2.2.2]octane with bromine-containing electrophiles.
Chemical communications (Cambridge, England), 2018, 54, 8060-8063
7121891 CIFC7 H12 Br3 F N2P -16.5248; 14.6823; 19.4306
72.579; 85.379; 85.795
1767.91Weinberger, Craig; Hines, Rachel; Zeller, Matthias; Rosokha, Sergiy V.
Continuum of covalent to intermolecular bonding in the halogen-bonded complexes of 1,4-diazabicyclo[2.2.2]octane with bromine-containing electrophiles.
Chemical communications (Cambridge, England), 2018, 54, 8060-8063
7121892 CIFC32 H39 B2 Cl2 N O6P 1 21/c 121.0386; 12.0671; 12.7442
90; 91.25; 90
3234.66Odyniec, Maria L.; Sedgwick, Adam C.; Swan, Alexander H.; Weber, Maria; Tang, T. M. Simon; Gardiner, Jordan E.; Zhang, Miao; Jiang, Yun-Bao; Kociok-Kohn, Gabriele; Elmes, Robert B. P.; Bull, Steven D.; He, Xiao-Peng; James, Tony D.
'AND'-based fluorescence scaffold for the detection of ROS/RNS and a second analyte.
Chemical communications (Cambridge, England), 2018, 54, 8466-8469
7121893 CIFC33 H51 N3 SiP 1 21 112.0057; 8.9498; 15.48
90; 106.694; 90
1593.2Bai, Yunping; Zhang, Jianying; Cui, Chunming
An arene-tethered silylene ligand enabling reversible dinitrogen binding to iron and catalytic silylation.
Chemical communications (Cambridge, England), 2018, 54, 8124-8127
7121894 CIFC33 H51 Fe N5 SiP 1 21/c 119.752; 8.725; 19.801
90; 103.4; 90
3320Bai, Yunping; Zhang, Jianying; Cui, Chunming
An arene-tethered silylene ligand enabling reversible dinitrogen binding to iron and catalytic silylation.
Chemical communications (Cambridge, England), 2018, 54, 8124-8127
7121895 CIFC40 H59 Br2 Fe N3 SiP 1 21/n 112.408; 19.199; 17.68
90; 97.503; 90
4176Bai, Yunping; Zhang, Jianying; Cui, Chunming
An arene-tethered silylene ligand enabling reversible dinitrogen binding to iron and catalytic silylation.
Chemical communications (Cambridge, England), 2018, 54, 8124-8127
7121896 CIFC66 H102 Fe N6 Si2P -110.351; 12.058; 26.098
86.591; 82.254; 87.814
3220.4Bai, Yunping; Zhang, Jianying; Cui, Chunming
An arene-tethered silylene ligand enabling reversible dinitrogen binding to iron and catalytic silylation.
Chemical communications (Cambridge, England), 2018, 54, 8124-8127
7121897 CIFC45 H87 Fe N5 Si5P b c a20.912; 16.921; 30.492
90; 90; 90
10790Bai, Yunping; Zhang, Jianying; Cui, Chunming
An arene-tethered silylene ligand enabling reversible dinitrogen binding to iron and catalytic silylation.
Chemical communications (Cambridge, England), 2018, 54, 8124-8127
7121898 CIFC28 H40 Cl N2 O3 RhP 21 21 2110.0564; 15.7574; 17.1733
90; 90; 90
2721.33Thongpaen, Jompol; E Schmid, Thibault; Toupet, Loic; Dorcet, Vincent; Mauduit, Marc; Baslé, Olivier
Directed ortho C-H borylation catalyzed using Cp*Rh(iii)-NHC complexes.
Chemical communications (Cambridge, England), 2018, 54, 8202-8205
7121899 CIFC27 H36 Cl N2 O3 RhP 21 21 219.8757; 15.8497; 17.3332
90; 90; 90
2713.11Thongpaen, Jompol; E Schmid, Thibault; Toupet, Loic; Dorcet, Vincent; Mauduit, Marc; Baslé, Olivier
Directed ortho C-H borylation catalyzed using Cp*Rh(iii)-NHC complexes.
Chemical communications (Cambridge, England), 2018, 54, 8202-8205
7121900 CIFC12 H12 N2 O2R -328.7013; 28.7013; 6.9232
90; 90; 120
4939Bao, Wen; Wang, Jun-Qi; Xu, Xuetao; Zhang, Bang-Hong; Liu, Wei-Ting; Lei, Lin-Sheng; Liang, Huan; Zhang, Kun; Wang, Shao-Hua
Copper-Catalyzed Cyclization of 2-Cyanobenzaldehydes and 2-Isocyanoacetates: an Efficient Strategy for the Synthesis of Substituted 1-Aminoisoquinolines
Chemical Communications, 2018
7121901 CIFC18 H17 N O4P -17.9181; 8.0407; 12.3418
80.124; 76.501; 85.004
751.83Maier, Josef M.; Li, Ping; Ritchey, Jackson S.; Yehl, Christopher J.; Shimizu, Ken D.
Anion-enhanced solvophobic effects in organic solvent.
Chemical communications (Cambridge, England), 2018, 54, 8502-8505
7121902 CIFC66 H44 Cu3 Eu2 N18 O31R -3 c :H14.0021; 14.0021; 63.523
90; 90; 120
10785.7Yi, Fei-Yan; Chen, Jinlei; Wang, Shi-Cheng; Gu, Minli; Han, Lei
A heterobimetallic metal-organic framework as a "turn-on" sensor toward DMF.
Chemical communications (Cambridge, England), 2018, 54, 8233-8236
7121903 CIFHg Na7 S12 Sb5R -3 :H14.537; 14.537; 9.815
90; 90; 120
1796Wu, Kui; Zhang, Bingbing; Yang, Zhihua; Pan, Shilie
Remarkable multimember-ring configurations in a new family of Na<sub>7</sub>M<sup>II</sup>Sb<sub>5</sub>S<sub>12</sub> (M<sup>II</sup> = Zn, Cd, Hg) exhibiting various three-dimensional tunnel structures.
Chemical communications (Cambridge, England), 2018, 54, 8269-8272
7121904 CIFCd Na7 S12 Sb5R -3 :H14.531; 14.531; 9.845
90; 90; 120
1800.3Wu, Kui; Zhang, Bingbing; Yang, Zhihua; Pan, Shilie
Remarkable multimember-ring configurations in a new family of Na<sub>7</sub>M<sup>II</sup>Sb<sub>5</sub>S<sub>12</sub> (M<sup>II</sup> = Zn, Cd, Hg) exhibiting various three-dimensional tunnel structures.
Chemical communications (Cambridge, England), 2018, 54, 8269-8272
7121905 CIFNa7 S12 Sb5 ZnR -3 :H14.4964; 14.4964; 9.8156
90; 90; 120
1786.4Wu, Kui; Zhang, Bingbing; Yang, Zhihua; Pan, Shilie
Remarkable multimember-ring configurations in a new family of Na<sub>7</sub>M<sup>II</sup>Sb<sub>5</sub>S<sub>12</sub> (M<sup>II</sup> = Zn, Cd, Hg) exhibiting various three-dimensional tunnel structures.
Chemical communications (Cambridge, England), 2018, 54, 8269-8272
7121906 CIFC44 H71 Al N2P -111.9225; 13.3038; 13.3821
79.775; 80.203; 79.872
2035.1Cao, Levy L.; Stephan, Douglas W.
Reversible 1,1-hydroaluminations and C-H activation in reactions of a cyclic (alkyl)(amino) carbene with alane.
Chemical communications (Cambridge, England), 2018, 54, 8407-8410
7121907 CIFC44 H73 Al N2P -19.4074; 11.461; 19.1698
92.871; 98.051; 101.38
1999.8Cao, Levy L.; Stephan, Douglas W.
Reversible 1,1-hydroaluminations and C-H activation in reactions of a cyclic (alkyl)(amino) carbene with alane.
Chemical communications (Cambridge, England), 2018, 54, 8407-8410
7121908 CIFC74 H135 Al3 N5P -111.636; 18.707; 19.303
66.586; 76.109; 86.462
3740.3Cao, Levy L.; Stephan, Douglas W.
Reversible 1,1-hydroaluminations and C-H activation in reactions of a cyclic (alkyl)(amino) carbene with alane.
Chemical communications (Cambridge, England), 2018, 54, 8407-8410
7121909 CIFC20 H23 N O4P 1 21/n 110.4449; 8.4856; 21.461
90; 99.489; 90
1876.1Yu, Yang; Zhang, Yan; Xiao, Li-Yun; Peng, Qin-Qin; Zhao, Yu-Long
Thermally induced formal [4+2] cycloaddition of 3-aminocyclobutenones with electron-deficient alkynes: facile and efficient synthesis of 4-pyridones.
Chemical communications (Cambridge, England), 2018, 54, 8229-8232
7121910 CIFC36.75 H51.75 Co N4 O3P -110.455; 14.036; 14.199
107.28; 110.92; 97.29
1793.9Leconte, Nicolas; du Moulinet d'Hardemare, Amaury; Philouze, Christian; Thomas, Fabrice
A highly active diradical cobalt(iii) catalyst for the cycloisomerization of alkynoic acids.
Chemical communications (Cambridge, England), 2018, 54, 8241-8244
7121911 CIFC16 H14 O2P n a 2117.365; 12.283; 5.6968
90; 90; 90
1215.1Leconte, Nicolas; du Moulinet d'Hardemare, Amaury; Philouze, Christian; Thomas, Fabrice
A highly active diradical cobalt(iii) catalyst for the cycloisomerization of alkynoic acids.
Chemical communications (Cambridge, England), 2018, 54, 8241-8244
7121912 CIFC36 H49 Cl Co N5P 1 21/n 114.519; 16.983; 14.819
90; 108.83; 90
3458.5Leconte, Nicolas; du Moulinet d'Hardemare, Amaury; Philouze, Christian; Thomas, Fabrice
A highly active diradical cobalt(iii) catalyst for the cycloisomerization of alkynoic acids.
Chemical communications (Cambridge, England), 2018, 54, 8241-8244
7121913 CIFC28 H34 B NP 1 21/c 18.4716; 27.7566; 11.7695
90; 100.257; 90
2723.29Li, Hai-Jun; Mellerup, Soren K.; Wang, Xiang; Wang, Suning
Transforming benzylideneamine N,C-chelate boron compounds to BN-cycloocta-/cyclohepta-trienes bearing a tetrasubstituted B[double bond, length as m-dash]N unit via photoisomerization.
Chemical communications (Cambridge, England), 2018, 54, 8245-8248
7121914 CIFC22 H22 B NP b c a19.0048; 7.986; 23.0446
90; 90; 90
3497.5Li, Hai-Jun; Mellerup, Soren K.; Wang, Xiang; Wang, Suning
Transforming benzylideneamine N,C-chelate boron compounds to BN-cycloocta-/cyclohepta-trienes bearing a tetrasubstituted B[double bond, length as m-dash]N unit via photoisomerization.
Chemical communications (Cambridge, England), 2018, 54, 8245-8248
7121915 CIFC22 H22 B NP 1 21/c 114.0764; 13.7022; 9.8458
90; 110.47; 90
1779.1Li, Hai-Jun; Mellerup, Soren K.; Wang, Xiang; Wang, Suning
Transforming benzylideneamine N,C-chelate boron compounds to BN-cycloocta-/cyclohepta-trienes bearing a tetrasubstituted B[double bond, length as m-dash]N unit via photoisomerization.
Chemical communications (Cambridge, England), 2018, 54, 8245-8248
7121916 CIFC34 H41 B NP 1 21/c 17.9902; 21.3281; 17.0355
90; 102.778; 90
2831.2Li, Hai-Jun; Mellerup, Soren K.; Wang, Xiang; Wang, Suning
Transforming benzylideneamine N,C-chelate boron compounds to BN-cycloocta-/cyclohepta-trienes bearing a tetrasubstituted B[double bond, length as m-dash]N unit via photoisomerization.
Chemical communications (Cambridge, England), 2018, 54, 8245-8248
7121917 CIFC18 H22 Cl N3 OP c a 2137.512; 7.28; 12.978
90; 90; 90
3544Castriconi, Federica; Paolino, Marco; Grisci, Giorgio; Francini, Cinzia Maria; Reale, Annalisa; Giuliani, Germano; Anzini, Maurizio; Giorgi, Gianluca; Mennuni, Laura; Sabatini, Chiara; Lanza, Marco; Caselli, Gianfranco; Cappelli, Andrea
Development of subnanomolar-affinity serotonin 5-HT<sub>4</sub> receptor ligands based on quinoline structures.
MedChemComm, 2018, 9, 1466-1471
7121918 CIFC20 H29 N3 O3P 1 21/c 111.3833; 11.7128; 15.0977
90; 103.83; 90
1954.62Castriconi, Federica; Paolino, Marco; Grisci, Giorgio; Francini, Cinzia Maria; Reale, Annalisa; Giuliani, Germano; Anzini, Maurizio; Giorgi, Gianluca; Mennuni, Laura; Sabatini, Chiara; Lanza, Marco; Caselli, Gianfranco; Cappelli, Andrea
Development of subnanomolar-affinity serotonin 5-HT<sub>4</sub> receptor ligands based on quinoline structures.
MedChemComm, 2018, 9, 1466-1471
7121919 CIFC39 H40 N2 O7P 17.035; 8.4308; 15.21
98.594; 99.03; 105.311
841.9Zhao, Mengting; Yue, Yuxin; Liu, Chang; Hui, Peiyi; He, Song; Zhao, Liancheng; Zeng, Xianshun
A colorimetric and fluorometric dual-modal sensor for methanol based on a functionalized pentacenequinone derivative.
Chemical communications (Cambridge, England), 2018, 54, 8339-8342
7121920 CIFC25 H29 N O5 SP -19.0009; 9.4814; 14.6222
92.269; 102.45; 100.774
1192.89Wang, Sasa; Liu, Miao; Chen, Xinzheng; Wang, Huifei; Zhai, Hongbin
Copper-catalyzed decarboxylative propargylation/hydroamination reactions: access to C3 β-ketoester-functionalized indoles.
Chemical communications (Cambridge, England), 2018, 54, 8375-8378
7121921 CIFC22 H34 N2 O3P 21 21 217.9398; 12.1284; 22.1403
90; 90; 90
2132Liang, Xiao; Huang, Xin; Xiong, Mingteng; Shen, Kexin; Pan, Yuanjiang
Copper(i)-catalyzed N-H olefination of sulfonamides for N-sulfonyl enaminone synthesis.
Chemical communications (Cambridge, England), 2018, 54, 8403-8406
7121922 CIFC18 H13 NF d d 212.7887; 38.195; 10.823
90; 90; 90
5286.7Sun, Qikun; Zhang, Kai; Zhang, Zhenzhen; Tang, Linagliang; Xie, Zongliang; Chi, Zhenguo; Xue, Shanfeng; Zhang, Haichang; Yang, Wenjun
A simple and versatile strategy for realizing bright multicolor mechanoluminescence.
Chemical communications (Cambridge, England), 2018, 54, 8206-8209
7121923 CIFC26 H31 B Br2 F5 NP 1 21/n 111.6404; 15.7259; 14.2888
90; 99.812; 90
2577.39Roy, Dipak Kumar; Krummenacher, Ivo; Stennett, Tom E.; Lenczyk, Carsten; Thiess, Torsten; Welz, Eileen; Engels, Bernd; Braunschweig, Holger
Selective one- and two-electron reductions of a haloborane enabled by a π-withdrawing carbene ligand.
Chemical communications (Cambridge, England), 2018, 54, 9015-9018
7121924 CIFC30 H28 B Br2 Cl0 F5 N2 O2P 21 21 218.492; 15.351; 22.229
90; 90; 90
2898Roy, Dipak Kumar; Krummenacher, Ivo; Stennett, Tom E.; Lenczyk, Carsten; Thiess, Torsten; Welz, Eileen; Engels, Bernd; Braunschweig, Holger
Selective one- and two-electron reductions of a haloborane enabled by a π-withdrawing carbene ligand.
Chemical communications (Cambridge, England), 2018, 54, 9015-9018
7121925 CIFC84 H104 B2 Br2 F10 Li2 N4 O10P 1 21/c 110.2637; 24.161; 16.6779
90; 97.972; 90
4095.8Roy, Dipak Kumar; Krummenacher, Ivo; Stennett, Tom E.; Lenczyk, Carsten; Thiess, Torsten; Welz, Eileen; Engels, Bernd; Braunschweig, Holger
Selective one- and two-electron reductions of a haloborane enabled by a π-withdrawing carbene ligand.
Chemical communications (Cambridge, England), 2018, 54, 9015-9018
7121926 CIFC30 H28 B Br F5 N2 O2P -17.394; 11.982; 16.917
104.9; 102.465; 99.493
1375.1Roy, Dipak Kumar; Krummenacher, Ivo; Stennett, Tom E.; Lenczyk, Carsten; Thiess, Torsten; Welz, Eileen; Engels, Bernd; Braunschweig, Holger
Selective one- and two-electron reductions of a haloborane enabled by a π-withdrawing carbene ligand.
Chemical communications (Cambridge, England), 2018, 54, 9015-9018
7121927 CIFC29 H34 B F5 NP 1 21/n 17.7509; 10.5075; 31.1985
90; 91.565; 90
2539.9Roy, Dipak Kumar; Krummenacher, Ivo; Stennett, Tom E.; Lenczyk, Carsten; Thiess, Torsten; Welz, Eileen; Engels, Bernd; Braunschweig, Holger
Selective one- and two-electron reductions of a haloborane enabled by a π-withdrawing carbene ligand.
Chemical communications (Cambridge, England), 2018, 54, 9015-9018
7121928 CIFC54 H60 Cl N26 Np O24P -115.2162; 15.3864; 15.665
73.052; 82.55; 67.868
3248.9Mei, Lei; Xu, Chao; Wu, Qun-Yan; Hu, Kong-Qiu; Yuan, Li-Yong; Chen, Jing; Xiao, Cheng-Liang; Wang, Shu-Ao; Chai, Zhi-Fang; Shi, Wei-Qun
A neptunium(v)-mediated interwoven transuranium-rotaxane network incorporating a mechanically interlocked [c2]daisy chain unit.
Chemical communications (Cambridge, England), 2018, 54, 8645-8648
7121929 CIFC108 H114 Cl4 N52 O62P -112.687; 15.9445; 35.622
86.375; 88.628; 67.119
6625.6Mei, Lei; Xu, Chao; Wu, Qun-Yan; Hu, Kong-Qiu; Yuan, Li-Yong; Chen, Jing; Xiao, Cheng-Liang; Wang, Shu-Ao; Chai, Zhi-Fang; Shi, Wei-Qun
A neptunium(v)-mediated interwoven transuranium-rotaxane network incorporating a mechanically interlocked [c2]daisy chain unit.
Chemical communications (Cambridge, England), 2018, 54, 8645-8648
7121930 CIFC54 H70 Cl2 N26 O30P -112.1092; 12.2; 12.804
106.917; 112.567; 92.559
1644.78Mei, Lei; Xu, Chao; Wu, Qun-Yan; Hu, Kong-Qiu; Yuan, Li-Yong; Chen, Jing; Xiao, Cheng-Liang; Wang, Shu-Ao; Chai, Zhi-Fang; Shi, Wei-Qun
A neptunium(v)-mediated interwoven transuranium-rotaxane network incorporating a mechanically interlocked [c2]daisy chain unit.
Chemical communications (Cambridge, England), 2018, 54, 8645-8648
7121931 CIFC108 H112 Cl2 N52 O42 UP -112.7487; 15.3678; 17.1021
90.328; 97.214; 95.183
3310Mei, Lei; Xu, Chao; Wu, Qun-Yan; Hu, Kong-Qiu; Yuan, Li-Yong; Chen, Jing; Xiao, Cheng-Liang; Wang, Shu-Ao; Chai, Zhi-Fang; Shi, Wei-Qun
A neptunium(v)-mediated interwoven transuranium-rotaxane network incorporating a mechanically interlocked [c2]daisy chain unit.
Chemical communications (Cambridge, England), 2018, 54, 8645-8648
7121932 CIFC36 H59 N6 O13 YbP -18.0215; 14.8835; 17.6485
106.991; 90.0945; 94.499
2008.17Mason, Kevin; Harnden, Alice C.; Patrick, Connor W.; Poh, Adeline W. J.; Batsanov, Andrei S.; Suturina, Elizaveta A.; Vonci, Michele; McInnes, Eric J. L.; Chilton, Nicholas F.; Parker, David
Exquisite sensitivity of the ligand field to solvation and donor polarisability in coordinatively saturated lanthanide complexes.
Chemical communications (Cambridge, England), 2018, 54, 8486-8489
7121933 CIFC27 H33 N6 O9 YbP 1 n 17.9466; 11.7823; 14.7072
90; 99.3301; 90
1358.81Mason, Kevin; Harnden, Alice C.; Patrick, Connor W.; Poh, Adeline W. J.; Batsanov, Andrei S.; Suturina, Elizaveta A.; Vonci, Michele; McInnes, Eric J. L.; Chilton, Nicholas F.; Parker, David
Exquisite sensitivity of the ligand field to solvation and donor polarisability in coordinatively saturated lanthanide complexes.
Chemical communications (Cambridge, England), 2018, 54, 8486-8489
7121934 CIFC34 H49 N6 O13 YbP -17.8898; 14.8884; 15.9436
95.4509; 93.4986; 96.4015
1847.88Mason, Kevin; Harnden, Alice C.; Patrick, Connor W.; Poh, Adeline W. J.; Batsanov, Andrei S.; Suturina, Elizaveta A.; Vonci, Michele; McInnes, Eric J. L.; Chilton, Nicholas F.; Parker, David
Exquisite sensitivity of the ligand field to solvation and donor polarisability in coordinatively saturated lanthanide complexes.
Chemical communications (Cambridge, England), 2018, 54, 8486-8489
7121935 CIFC40 H65 N6 O12 YbP -17.6574; 13.1494; 22.747
86.53; 86.957; 74.094
2197.08Mason, Kevin; Harnden, Alice C.; Patrick, Connor W.; Poh, Adeline W. J.; Batsanov, Andrei S.; Suturina, Elizaveta A.; Vonci, Michele; McInnes, Eric J. L.; Chilton, Nicholas F.; Parker, David
Exquisite sensitivity of the ligand field to solvation and donor polarisability in coordinatively saturated lanthanide complexes.
Chemical communications (Cambridge, England), 2018, 54, 8486-8489
7121936 CIFC27 H29 Cl3 Eu N6 O8.5P -18.037; 11.9227; 17.541
109.078; 90.559; 108.769
1491.6Mason, Kevin; Harnden, Alice C.; Patrick, Connor W.; Poh, Adeline W. J.; Batsanov, Andrei S.; Suturina, Elizaveta A.; Vonci, Michele; McInnes, Eric J. L.; Chilton, Nicholas F.; Parker, David
Exquisite sensitivity of the ligand field to solvation and donor polarisability in coordinatively saturated lanthanide complexes.
Chemical communications (Cambridge, England), 2018, 54, 8486-8489
7121937 CIFC27 H32 Cl3 N6 O10 YbP 21 21 217.8822; 17.4071; 22.7074
90; 90; 90
3115.6Mason, Kevin; Harnden, Alice C.; Patrick, Connor W.; Poh, Adeline W. J.; Batsanov, Andrei S.; Suturina, Elizaveta A.; Vonci, Michele; McInnes, Eric J. L.; Chilton, Nicholas F.; Parker, David
Exquisite sensitivity of the ligand field to solvation and donor polarisability in coordinatively saturated lanthanide complexes.
Chemical communications (Cambridge, England), 2018, 54, 8486-8489
7121938 CIFC39 H63 Eu N6 O12P -17.5667; 13.2216; 22.7804
87.639; 87.556; 74.19
2189.8Mason, Kevin; Harnden, Alice C.; Patrick, Connor W.; Poh, Adeline W. J.; Batsanov, Andrei S.; Suturina, Elizaveta A.; Vonci, Michele; McInnes, Eric J. L.; Chilton, Nicholas F.; Parker, David
Exquisite sensitivity of the ligand field to solvation and donor polarisability in coordinatively saturated lanthanide complexes.
Chemical communications (Cambridge, England), 2018, 54, 8486-8489
7121939 CIFC40 H65 N6 O12 YbP -17.6432; 13.1291; 22.7386
86.5326; 86.9081; 74.1063
2188.87Mason, Kevin; Harnden, Alice C.; Patrick, Connor W.; Poh, Adeline W. J.; Batsanov, Andrei S.; Suturina, Elizaveta A.; Vonci, Michele; McInnes, Eric J. L.; Chilton, Nicholas F.; Parker, David
Exquisite sensitivity of the ligand field to solvation and donor polarisability in coordinatively saturated lanthanide complexes.
Chemical communications (Cambridge, England), 2018, 54, 8486-8489
7121940 CIFC18 H66 Cl3 Dy N9 O9 P3P 1 21/c 111.3237; 38.167; 19.4676
90; 101.025; 90
8258.4Canaj, Angelos B.; Singh, Mukesh Kumar; Wilson, Claire; Rajaraman, Gopalan; Murrie, Mark
Chemical and in silico tuning of the magnetisation reversal barrier in pentagonal bipyramidal Dy(iii) single-ion magnets.
Chemical communications (Cambridge, England), 2018, 54, 8273-8276
7121941 CIFC24 H82 Dy I3 N12 O9 P4C 1 c 114.0512; 19.1355; 20.4829
90; 101.075; 90
5404.8Canaj, Angelos B.; Singh, Mukesh Kumar; Wilson, Claire; Rajaraman, Gopalan; Murrie, Mark
Chemical and in silico tuning of the magnetisation reversal barrier in pentagonal bipyramidal Dy(iii) single-ion magnets.
Chemical communications (Cambridge, England), 2018, 54, 8273-8276
7121942 CIFC24 H82 I3 N12 O9 P4 YC 1 c 114.096; 19.1099; 20.5439
90; 101.091; 90
5430.6Canaj, Angelos B.; Singh, Mukesh Kumar; Wilson, Claire; Rajaraman, Gopalan; Murrie, Mark
Chemical and in silico tuning of the magnetisation reversal barrier in pentagonal bipyramidal Dy(iii) single-ion magnets.
Chemical communications (Cambridge, England), 2018, 54, 8273-8276
7121943 CIFC18 H66 Cl3 N9 O9 P3 YP 1 21/c 111.4154; 38.613; 19.9862
90; 101.936; 90
8619.1Canaj, Angelos B.; Singh, Mukesh Kumar; Wilson, Claire; Rajaraman, Gopalan; Murrie, Mark
Chemical and in silico tuning of the magnetisation reversal barrier in pentagonal bipyramidal Dy(iii) single-ion magnets.
Chemical communications (Cambridge, England), 2018, 54, 8273-8276
7121944 CIFC58 H68 Ce Cl4 N8 O4C 1 2/c 115.12; 25.007; 15.405
90; 95.137; 90
5801Klamm, Bonnie E.; Windorff, Cory J.; Marsh, Matthew L.; Meeker, David S.; Albrecht-Schmitt, Thomas E
Schiff-base coordination complexes with plutonium(iv) and cerium(iv).
Chemical communications (Cambridge, England), 2018, 54, 8634-8636
7121945 CIFC58 H68 Cl4 N8 O4 PuC 1 2/c 115.0632; 24.9196; 15.354
90; 95.012; 90
5741.4Klamm, Bonnie E.; Windorff, Cory J.; Marsh, Matthew L.; Meeker, David S.; Albrecht-Schmitt, Thomas E
Schiff-base coordination complexes with plutonium(iv) and cerium(iv).
Chemical communications (Cambridge, England), 2018, 54, 8634-8636
7121946 CIFC28 H18 Co N4 O7P 1 21/c 111.386; 23.961; 14.85
90; 104.161; 90
3928.3Jiang, Min; Li, Pingping; Wu, Pengyan; Zhang, Fengjie; Tian, Xueqing; Deng, Chaofan; Wang, Jian
A squaramide-based metal-organic framework as a luminescent sensor for the detection of lactose in aqueous solution and in milk.
Chemical communications (Cambridge, England), 2018, 54, 9131-9134
7121947 CIFC19 H23 N O3 SP -19.1466; 10.045; 11.2749
78.594; 69.193; 70.534
909.29Yan, Xufei; Sun, Huihui; Xiang, Haifeng; Yu, Da-Gang; Luo, Daibing; Zhou, Xiangge
Palladium-catalyzed C(carbonyl)-C bond cleavage of amides: a facile access to phenylcarbamate derivatives with alcohols.
Chemical communications (Cambridge, England), 2018, 54, 8606-8609
7121948 CIFC22 H22 N2 O Pd SP 21 21 219.4594; 11.2077; 19.4065
90; 90; 90
2057.44Yan, Xufei; Sun, Huihui; Xiang, Haifeng; Yu, Da-Gang; Luo, Daibing; Zhou, Xiangge
Palladium-catalyzed C(carbonyl)-C bond cleavage of amides: a facile access to phenylcarbamate derivatives with alcohols.
Chemical communications (Cambridge, England), 2018, 54, 8606-8609
7121949 CIFC33 H36 N4 O10P 1 21/c 110.4543; 13.8322; 23.1289
90; 90.3385; 90
3344.52Zhao, Qian; Peng, Cheng; Huang, Hua; Liu, Shuai-Jiang; Zhong, Ya-Jun; Huang, Wei; He, Gu; Han, Bo
Asymmetric synthesis of tetrahydroisoquinoline-fused spirooxindoles as Ras-GTP inhibitors that inhibit colon adenocarcinoma cell proliferation and invasion.
Chemical communications (Cambridge, England), 2018, 54, 8359-8362
7121950 CIFC4 H3 F3 O2P 1 21/n 15.165; 11.201; 8.564
90; 101.626; 90
485.3Thomson, Connor J.; Zhang, Qingzhi; Al-Maharik, Nawaf; Bühl, Michael; Cordes, David B.; Slawin, Alexandra M. Z.; O'Hagan, David
Fluorinated cyclopropanes: synthesis and chemistry of the aryl α,β,β-trifluorocyclopropane motif.
Chemical communications (Cambridge, England), 2018, 54, 8415-8418
7121951 CIFC10 H8 F3 N OP 1 21/n 15.6878; 20.542; 8.921
90; 107.525; 90
993.9Thomson, Connor J.; Zhang, Qingzhi; Al-Maharik, Nawaf; Bühl, Michael; Cordes, David B.; Slawin, Alexandra M. Z.; O'Hagan, David
Fluorinated cyclopropanes: synthesis and chemistry of the aryl α,β,β-trifluorocyclopropane motif.
Chemical communications (Cambridge, England), 2018, 54, 8415-8418
7121952 CIFC11 H10 F3 N OP c a 2121.421; 8.828; 11.037
90; 90; 90
2087.1Thomson, Connor J.; Zhang, Qingzhi; Al-Maharik, Nawaf; Bühl, Michael; Cordes, David B.; Slawin, Alexandra M. Z.; O'Hagan, David
Fluorinated cyclopropanes: synthesis and chemistry of the aryl α,β,β-trifluorocyclopropane motif.
Chemical communications (Cambridge, England), 2018, 54, 8415-8418
7121953 CIFC16 H12 Br F2 N O2P 1 21/n 14.7918; 9.3365; 33.8797
90; 92.292; 90
1514.52Thomson, Connor J.; Zhang, Qingzhi; Al-Maharik, Nawaf; Bühl, Michael; Cordes, David B.; Slawin, Alexandra M. Z.; O'Hagan, David
Fluorinated cyclopropanes: synthesis and chemistry of the aryl α,β,β-trifluorocyclopropane motif.
Chemical communications (Cambridge, England), 2018, 54, 8415-8418
7121954 CIFC16 H12 Br F2 N O SP 1 21/n 14.81051; 9.39477; 34.2042
90; 92.9598; 90
1543.75Thomson, Connor J.; Zhang, Qingzhi; Al-Maharik, Nawaf; Bühl, Michael; Cordes, David B.; Slawin, Alexandra M. Z.; O'Hagan, David
Fluorinated cyclopropanes: synthesis and chemistry of the aryl α,β,β-trifluorocyclopropane motif.
Chemical communications (Cambridge, England), 2018, 54, 8415-8418
7121955 CIFC22 H20 F6 N2P 1 21/c 19.6136; 15.5641; 13.7093
90; 104.355; 90
1987.2Shi, Lou; Wang, Mingshan; Pan, Ling; Li, Yifei; Liu, Qun
Csp<sup>3</sup>-H bond functionalization of amines via tunable iminium ions: divergent synthesis of trifluoromethylated arylamines.
Chemical communications (Cambridge, England), 2018, 54, 8721-8724
7121956 CIFC84 H112 O6 Sm4P -112.252; 12.49; 12.826
84.442; 77.873; 80.73
1889.8Wolf, Benjamin M.; Stuhl, Christoph; Anwander, Reiner
Synthesis of homometallic divalent lanthanide organoimides from benzyl complexes.
Chemical communications (Cambridge, England), 2018, 54, 8826-8829
7121957 CIFC22 H34 O4 YbP 1 21/c 113.172; 12.265; 14.497
90; 90.35; 90
2342Wolf, Benjamin M.; Stuhl, Christoph; Anwander, Reiner
Synthesis of homometallic divalent lanthanide organoimides from benzyl complexes.
Chemical communications (Cambridge, England), 2018, 54, 8826-8829
7121958 CIFC72 H116 N4 O6 Yb4P 1 c 113.2322; 16.2283; 17.9608
90; 111.614; 90
3585.6Wolf, Benjamin M.; Stuhl, Christoph; Anwander, Reiner
Synthesis of homometallic divalent lanthanide organoimides from benzyl complexes.
Chemical communications (Cambridge, England), 2018, 54, 8826-8829
7121959 CIFC34 H54 O4 YbC 1 2/c 19.536; 16.441; 20.897
90; 96.14; 90
3257Wolf, Benjamin M.; Stuhl, Christoph; Anwander, Reiner
Synthesis of homometallic divalent lanthanide organoimides from benzyl complexes.
Chemical communications (Cambridge, England), 2018, 54, 8826-8829
7121960 CIFC32 H36 Eu2 OP -112.4889; 14.9634; 15.0111
94.734; 94.59; 90.111
2786.6Wolf, Benjamin M.; Stuhl, Christoph; Anwander, Reiner
Synthesis of homometallic divalent lanthanide organoimides from benzyl complexes.
Chemical communications (Cambridge, England), 2018, 54, 8826-8829
7121961 CIFC64 H100 Eu4 N4 O4P 1 21 112.8719; 24.3507; 13.4375
90; 118.609; 90
3697.61Wolf, Benjamin M.; Stuhl, Christoph; Anwander, Reiner
Synthesis of homometallic divalent lanthanide organoimides from benzyl complexes.
Chemical communications (Cambridge, England), 2018, 54, 8826-8829
7121962 CIFC204 H192 B5 F20 N36 Ni4I 2 2 219.7257; 25.1015; 25.7068
90; 90; 90
12728.6Bao, Ling-Yu; Hao, Si-Jia; Xi, Sai-Fei; Yan, Xiaodong; Zhang, Hai-Xia; Shen, Rui; Gu, Zhi-Guo
Chiral supramolecular coordination cages as high-performance inhibitors against amyloid-β aggregation.
Chemical communications (Cambridge, England), 2018, 54, 8725-8728
7121963 CIFC216 H216 Cl5 N36 Ni4 O20I 2 322.4671; 22.4671; 22.4671
90; 90; 90
11340.7Bao, Ling-Yu; Hao, Si-Jia; Xi, Sai-Fei; Yan, Xiaodong; Zhang, Hai-Xia; Shen, Rui; Gu, Zhi-Guo
Chiral supramolecular coordination cages as high-performance inhibitors against amyloid-β aggregation.
Chemical communications (Cambridge, England), 2018, 54, 8725-8728
7121964 CIFC228 H240 N36 Ni4I 2 323.8389; 23.8389; 23.8389
90; 90; 90
13547.5Bao, Ling-Yu; Hao, Si-Jia; Xi, Sai-Fei; Yan, Xiaodong; Zhang, Hai-Xia; Shen, Rui; Gu, Zhi-Guo
Chiral supramolecular coordination cages as high-performance inhibitors against amyloid-β aggregation.
Chemical communications (Cambridge, England), 2018, 54, 8725-8728
7121965 CIFC15 H11 Br F5 I OF d d 238.2117; 18.5754; 9.3073
90; 90; 90
6606.3Gruber, Stefan; Ametamey, Simon M.; Schibli, Roger
Unexpected reactivity of cyclic perfluorinated iodanes with electrophiles.
Chemical communications (Cambridge, England), 2018, 54, 8999-9002
7121966 CIFC17 H15 Br Cl F4 I O2P 1 21/n 111.3548; 8.0586; 21.0488
90; 95.611; 90
1916.82Gruber, Stefan; Ametamey, Simon M.; Schibli, Roger
Unexpected reactivity of cyclic perfluorinated iodanes with electrophiles.
Chemical communications (Cambridge, England), 2018, 54, 8999-9002
7121967 CIFC15 H9 Br Cl F4 I O3P -17.9867; 8.2391; 13.6897
74.798; 84.253; 86.584
864.41Gruber, Stefan; Ametamey, Simon M.; Schibli, Roger
Unexpected reactivity of cyclic perfluorinated iodanes with electrophiles.
Chemical communications (Cambridge, England), 2018, 54, 8999-9002
7121968 CIFC64.33 H58 N2.67 O7.67P 1 21/c 121.31; 22.284; 16.397
90; 95.97; 90
7744Wang, Linqin; Zhang, Jinbao; Liu, Peng; Xu, Bo; Zhang, Biaobiao; Chen, Hong; Inge, A. Ken; Li, Yuanyuan; Wang, Haoxin; Cheng, Yi-Bing; Kloo, Lars; Sun, Licheng
Design and synthesis of dopant-free organic hole-transport materials for perovskite solar cells.
Chemical communications (Cambridge, England), 2018, 54, 9571-9574
7121969 CIFC61 H46 N2 O5P -110.6341; 16.3753; 17.6369
64.812; 87.802; 88.57
2777Wang, Linqin; Zhang, Jinbao; Liu, Peng; Xu, Bo; Zhang, Biaobiao; Chen, Hong; Inge, A. Ken; Li, Yuanyuan; Wang, Haoxin; Cheng, Yi-Bing; Kloo, Lars; Sun, Licheng
Design and synthesis of dopant-free organic hole-transport materials for perovskite solar cells.
Chemical communications (Cambridge, England), 2018, 54, 9571-9574
7121970 CIFC28 H19 Cu2 I0.4 N9 O10.2F d -3 c :243.0555; 43.0555; 43.0555
90; 90; 90
79815.3Ye, Chun-Rong; Zheng, Ji; Li, Mian; Huang, Xiao-Chun
A zeolite-like MOF based on a heterotritopic linker of imidazolyl, carboxyl and pyridine with a long-sought uks net on Schwarz's D-surface.
Chemical communications (Cambridge, England), 2018, 54, 8769-8772
7121971 CIFC62 H78 B4 F16 N10 Ni2 O4P 1 21 116.5417; 9.9989; 20.3707
90; 92.563; 90
3365.92Shen, Junyu; Wang, Mei; He, Tianhao; Jiang, Jian; Hu, Maowei
Influence of the backbone of N<sub>5</sub>-pentadentate ligands on the catalytic performance of Ni(ii) complexes for electrochemical water oxidation in neutral aqueous solutions.
Chemical communications (Cambridge, England), 2018, 54, 9019-9022
7121972 CIFC33 H63 B3 Cl3 N9 Si6P -111.3419; 14.9551; 16.2731
98.833; 110.206; 102.878
2443.71Bawari, Deependra; Negi, Chandrakala; Jaiswal, Kuldeep; Prashanth, Billa; Choudhury, Angshuman Roy; Singh, Sanjay
Group 13 element containing conformationally rigid "N-E-N" heteroatomic bridged [3.3](2,6)pyridinophanes (E = B, Al).
Chemical communications (Cambridge, England), 2018, 54, 8857-8860
7121973 CIFC22 H44 B2 N6 Si4P -16.519; 14.118; 17.136
84.72; 89.46; 84.14
1562.2Bawari, Deependra; Negi, Chandrakala; Jaiswal, Kuldeep; Prashanth, Billa; Choudhury, Angshuman Roy; Singh, Sanjay
Group 13 element containing conformationally rigid "N-E-N" heteroatomic bridged [3.3](2,6)pyridinophanes (E = B, Al).
Chemical communications (Cambridge, England), 2018, 54, 8857-8860
7121974 CIFC11 H26 B N3 Si2P 1 21/c 17.1703; 18.86; 12.843
90; 98.818; 90
1716.3Bawari, Deependra; Negi, Chandrakala; Jaiswal, Kuldeep; Prashanth, Billa; Choudhury, Angshuman Roy; Singh, Sanjay
Group 13 element containing conformationally rigid "N-E-N" heteroatomic bridged [3.3](2,6)pyridinophanes (E = B, Al).
Chemical communications (Cambridge, England), 2018, 54, 8857-8860
7121975 CIFC12 H24 Al N3 Si2P 1 21/c 111.6602; 12.6412; 12.9228
90; 116.275; 90
1708Bawari, Deependra; Negi, Chandrakala; Jaiswal, Kuldeep; Prashanth, Billa; Choudhury, Angshuman Roy; Singh, Sanjay
Group 13 element containing conformationally rigid "N-E-N" heteroatomic bridged [3.3](2,6)pyridinophanes (E = B, Al).
Chemical communications (Cambridge, England), 2018, 54, 8857-8860
7121976 CIFC24 H48 Al2 N6 Si4P 1 21/c 117.2486; 12.6136; 16.1018
90; 91.704; 90
3501.7Bawari, Deependra; Negi, Chandrakala; Jaiswal, Kuldeep; Prashanth, Billa; Choudhury, Angshuman Roy; Singh, Sanjay
Group 13 element containing conformationally rigid "N-E-N" heteroatomic bridged [3.3](2,6)pyridinophanes (E = B, Al).
Chemical communications (Cambridge, England), 2018, 54, 8857-8860
7121977 CIFC10 H12 F11 N OP 1 21/c 17.4929; 10.3291; 18.055
90; 94.475; 90
1393.11Schaab, Jonas; Schwab, Miriam; Kratzert, Daniel; Schwabedissen, Jan; Stammler, Hans-Georg; Mitzel, Norbert W.; Krossing, Ingo
The perfluorinated alcohols c-C<sub>6</sub>F<sub>11</sub>OH, c-C<sub>6</sub>F<sub>10</sub>-1,1-(OH)<sub>2</sub> and c-C<sub>6</sub>F<sub>10</sub>-1-(CF<sub>3</sub>)OH.
Chemical communications (Cambridge, England), 2018, 54, 9294-9297
7121978 CIFC21 H7 F39 O5P 1 21/c 17.039; 22.2491; 21.3552
90; 93.561; 90
3338Schaab, Jonas; Schwab, Miriam; Kratzert, Daniel; Schwabedissen, Jan; Stammler, Hans-Georg; Mitzel, Norbert W.; Krossing, Ingo
The perfluorinated alcohols c-C<sub>6</sub>F<sub>11</sub>OH, c-C<sub>6</sub>F<sub>10</sub>-1,1-(OH)<sub>2</sub> and c-C<sub>6</sub>F<sub>10</sub>-1-(CF<sub>3</sub>)OH.
Chemical communications (Cambridge, England), 2018, 54, 9294-9297
7121979 CIFC11 H12 F13 N OP n n a14.4972; 14.78; 28.496
90; 90; 90
6105.8Schaab, Jonas; Schwab, Miriam; Kratzert, Daniel; Schwabedissen, Jan; Stammler, Hans-Georg; Mitzel, Norbert W.; Krossing, Ingo
The perfluorinated alcohols c-C<sub>6</sub>F<sub>11</sub>OH, c-C<sub>6</sub>F<sub>10</sub>-1,1-(OH)<sub>2</sub> and c-C<sub>6</sub>F<sub>10</sub>-1-(CF<sub>3</sub>)OH.
Chemical communications (Cambridge, England), 2018, 54, 9294-9297
7121980 CIFC6 H2 F10 O2P c a 2110.3768; 20.2598; 8.3401
90; 90; 90
1753.36Schaab, Jonas; Schwab, Miriam; Kratzert, Daniel; Schwabedissen, Jan; Stammler, Hans-Georg; Mitzel, Norbert W.; Krossing, Ingo
The perfluorinated alcohols c-C<sub>6</sub>F<sub>11</sub>OH, c-C<sub>6</sub>F<sub>10</sub>-1,1-(OH)<sub>2</sub> and c-C<sub>6</sub>F<sub>10</sub>-1-(CF<sub>3</sub>)OH.
Chemical communications (Cambridge, England), 2018, 54, 9294-9297
7121981 CIFC22 H20 F6 N4 O SP 112.62193; 13.55916; 20.6596
92.8838; 91.5768; 94.1281
3520.38Zabaleta, Nagore; Uria, Uxue; Reyes, Efraim; Carrillo, Luisa; Vicario, Jose L.
Ion-pairing catalysis in the enantioselective addition of hydrazones to N-acyldihydropyrrole derivatives.
Chemical communications (Cambridge, England), 2018, 54, 8905-8908
7121982 CIFC21 H18 F6 N4 O2I 1 2/a 123.7773; 5.4608; 31.7244
90; 92.002; 90
4116.7Zabaleta, Nagore; Uria, Uxue; Reyes, Efraim; Carrillo, Luisa; Vicario, Jose L.
Ion-pairing catalysis in the enantioselective addition of hydrazones to N-acyldihydropyrrole derivatives.
Chemical communications (Cambridge, England), 2018, 54, 8905-8908
7121983 CIFC24 H20 Br N O4P 1 21 15.71336; 14.1891; 12.7481
90; 97.421; 90
1024.8Liu, Wen; Cao, Weidi; Hu, Haipeng; Lin, Lili; Feng, Xiaoming
Dynamic kinetic asymmetric transformations of β-halo-α-keto esters by N,N'-dioxide/Ni(ii)-catalyzed carbonyl-ene reaction.
Chemical communications (Cambridge, England), 2018, 54, 8901-8904
7121984 CIFC57 H45 Dy2 F36 N6 O18P 1 2/c 110.927; 12.297; 30.796
90; 100.219; 90
4072.4Xiao, Zhao-Xin; Miao, Hao; Shao, Dong; Wei, Hai-Yan; Zhang, Yi-Quan; Wang, Xin-Yi
Single-molecule magnet behaviour in a dysprosium-triradical complex.
Chemical communications (Cambridge, England), 2018, 54, 9726-9729
7121985 CIFC28 H33 B F2 N2 Si2C 1 2/c 121.64; 8.223; 32.26
90; 97.4; 90
5693Zheng, Xianghui; Du, Wei; Gai, Lizhi; Xiao, Xuqiong; Li, Zhifang; Xu, Liwen; Tian, Yupeng; Kira, Mitsuo; Lu, Hua
Disilanylene-bridged BODIPY-based D-σ-A architectures: a novel promising series of NLO chromophores.
Chemical communications (Cambridge, England), 2018, 54, 8834-8837
7121986 CIFC30 H38 B F2 N3 Si2P -111.115; 11.547; 13.669
69.556; 82.496; 79.484
1612Zheng, Xianghui; Du, Wei; Gai, Lizhi; Xiao, Xuqiong; Li, Zhifang; Xu, Liwen; Tian, Yupeng; Kira, Mitsuo; Lu, Hua
Disilanylene-bridged BODIPY-based D-σ-A architectures: a novel promising series of NLO chromophores.
Chemical communications (Cambridge, England), 2018, 54, 8834-8837
7121987 CIFC106 H156 O6 Si12 U4P -112.6651; 16.1115; 19.1954
101.395; 104.401; 111.57
3341.6Tsoureas, Nikolaos; Cloke, F Geoffrey N
Activation of carbon suboxide (C<sub>3</sub>O<sub>2</sub>) by U(iii) to form a cyclobutane-1,3-dione ring.
Chemical communications (Cambridge, England), 2018, 54, 8830-8833
7121988 CIFC54 H90 O Si7 U2P -19.0648; 14.3955; 25.3043
87.99; 89.525; 72.969
3155.3Tsoureas, Nikolaos; Cloke, F Geoffrey N
Activation of carbon suboxide (C<sub>3</sub>O<sub>2</sub>) by U(iii) to form a cyclobutane-1,3-dione ring.
Chemical communications (Cambridge, England), 2018, 54, 8830-8833
7121989 CIFC56 H62 Cl2 Co3 N12 O8R -3 :H11.349; 11.349; 38.211
90; 90; 120
4262.2Mitsuhashi, Ryoji; Pedersen, Kasper S.; Ueda, Takaaki; Suzuki, Takayoshi; Bendix, Jesper; Mikuriya, Masahiro
Field-induced single-molecule magnet behavior in ideal trigonal antiprismatic cobalt(ii) complexes: precise geometrical control by a hydrogen-bonded rigid metalloligand.
Chemical communications (Cambridge, England), 2018, 54, 8869-8872
7121990 CIFC56 H62 Br2 Co3 N12 O8R -3 c :H11.0654; 11.0654; 87.132
90; 90; 120
9239.4Mitsuhashi, Ryoji; Pedersen, Kasper S.; Ueda, Takaaki; Suzuki, Takayoshi; Bendix, Jesper; Mikuriya, Masahiro
Field-induced single-molecule magnet behavior in ideal trigonal antiprismatic cobalt(ii) complexes: precise geometrical control by a hydrogen-bonded rigid metalloligand.
Chemical communications (Cambridge, England), 2018, 54, 8869-8872
7121991 CIFC56 H62 Co3 N14 O14R -3 c :H11.169; 11.169; 87.48
90; 90; 120
9451Mitsuhashi, Ryoji; Pedersen, Kasper S.; Ueda, Takaaki; Suzuki, Takayoshi; Bendix, Jesper; Mikuriya, Masahiro
Field-induced single-molecule magnet behavior in ideal trigonal antiprismatic cobalt(ii) complexes: precise geometrical control by a hydrogen-bonded rigid metalloligand.
Chemical communications (Cambridge, England), 2018, 54, 8869-8872
7121992 CIFC80 H140 B6 Br4 Mg2 N2 O2 P4 Si4P 1 21/c 110.1567; 25.514; 19.2566
90; 91.717; 90
4987.9Lu, Wei; Kinjo, Rei
Complexation of asymmetric diborenes with magnesium bromide.
Chemical communications (Cambridge, England), 2018, 54, 8842-8844
7121993 CIFC62.68 H123.36 B6 Br4 Mg2 N2 O2 P4 Si4P -116.6079; 16.8383; 17.897
107.011; 97.982; 109.327
4359.4Lu, Wei; Kinjo, Rei
Complexation of asymmetric diborenes with magnesium bromide.
Chemical communications (Cambridge, England), 2018, 54, 8842-8844
7121994 CIFC14 H10 Br N O2P 21 21 213.8787; 13.3741; 26.3417
90; 90; 90
1366.45Ding, Jun; Jiang, Wei; Bai, He-Yuan; Ding, Tong-Mei; Gao, Dafang; Bao, Xiaoguang; Zhang, Shu-Yu
Experimental and computational studies on H<sub>2</sub>O-promoted, Rh-catalyzed transient-ligand-free ortho-C(sp<sup>2</sup>)-H amidation of benzaldehydes with dioxazolones.
Chemical communications (Cambridge, England), 2018, 54, 8889-8892
7121995 CIFC18 H12 N O2P b c a11.6111; 8.5608; 26.6519
90; 90; 90
2649.21Ding, Jun; Jiang, Wei; Bai, He-Yuan; Ding, Tong-Mei; Gao, Dafang; Bao, Xiaoguang; Zhang, Shu-Yu
Experimental and computational studies on H<sub>2</sub>O-promoted, Rh-catalyzed transient-ligand-free ortho-C(sp<sup>2</sup>)-H amidation of benzaldehydes with dioxazolones.
Chemical communications (Cambridge, England), 2018, 54, 8889-8892
7121996 CIFC13 H8 Cl F N2 O2P -13.8145; 12.348; 13.349
71.5; 89.83; 89.58
596.2Mishra, Manish Kumar; Kadambi, Sourabh B.; Ramamurty, Upadrasta; Ghosh, Soumyajit
Elastic flexibility tuning via interaction factor modulation in molecular crystals.
Chemical communications (Cambridge, England), 2018, 54, 9047-9050
7121997 CIFC16 H15 Cl2 N O3P n a 2127.733; 4.024; 13.705
90; 90; 90
1529.44Mishra, Manish Kumar; Kadambi, Sourabh B.; Ramamurty, Upadrasta; Ghosh, Soumyajit
Elastic flexibility tuning via interaction factor modulation in molecular crystals.
Chemical communications (Cambridge, England), 2018, 54, 9047-9050
7121998 CIFC13 H8 Cl2 I NP 1 21/n 14.1; 22.199; 14.223
90; 96.954; 90
1285Mishra, Manish Kumar; Kadambi, Sourabh B.; Ramamurty, Upadrasta; Ghosh, Soumyajit
Elastic flexibility tuning via interaction factor modulation in molecular crystals.
Chemical communications (Cambridge, England), 2018, 54, 9047-9050
7121999 CIFC15 H9 NP 21 21 213.8727; 15.111; 17.132
90; 90; 90
1002.6Mishra, Manish Kumar; Kadambi, Sourabh B.; Ramamurty, Upadrasta; Ghosh, Soumyajit
Elastic flexibility tuning via interaction factor modulation in molecular crystals.
Chemical communications (Cambridge, England), 2018, 54, 9047-9050
7122000 CIFC40 H32 Cu2 F12 N12 O12 S8P -19.7479; 10.8987; 14.1786
67.525; 73.066; 83.669
1331.6Faulkner, Robert A.; Patmore, Nathan J.; Rice, Craig R.; Slater, Christopher
Dihydrogen phosphate-containing dinuclear double assemblies that demonstrate phosphate reactivity to the tetrafluoroborate anion.
Chemical communications (Cambridge, England), 2018, 54, 9159-9162
7122001 CIFC40 H34 Cu2 F9 N13.858 O15.743 P S7P -111.358; 16.28; 16.681
99.03; 108.218; 92.693
2878.3Faulkner, Robert A.; Patmore, Nathan J.; Rice, Craig R.; Slater, Christopher
Dihydrogen phosphate-containing dinuclear double assemblies that demonstrate phosphate reactivity to the tetrafluoroborate anion.
Chemical communications (Cambridge, England), 2018, 54, 9159-9162
7122002 CIFC43 H42 Cu2 F9 N12 O13 P S7P -114.629; 15.453; 17.397
93.102; 103.018; 95.287
3804Faulkner, Robert A.; Patmore, Nathan J.; Rice, Craig R.; Slater, Christopher
Dihydrogen phosphate-containing dinuclear double assemblies that demonstrate phosphate reactivity to the tetrafluoroborate anion.
Chemical communications (Cambridge, England), 2018, 54, 9159-9162
7122003 CIFC40 H40 B4 Cu2 F14 N12 O4.5 P S4I -4 2 d22.4423; 22.4423; 20.6438
90; 90; 90
10397.4Faulkner, Robert A.; Patmore, Nathan J.; Rice, Craig R.; Slater, Christopher
Dihydrogen phosphate-containing dinuclear double assemblies that demonstrate phosphate reactivity to the tetrafluoroborate anion.
Chemical communications (Cambridge, England), 2018, 54, 9159-9162
7122004 CIFC114 H114 B5 Cu6 F18 N42 O20 P2 S12P -112.3871; 24.199; 32.271
78.661; 85.813; 78.326
9282.8Faulkner, Robert A.; Patmore, Nathan J.; Rice, Craig R.; Slater, Christopher
Dihydrogen phosphate-containing dinuclear double assemblies that demonstrate phosphate reactivity to the tetrafluoroborate anion.
Chemical communications (Cambridge, England), 2018, 54, 9159-9162
7122005 CIFC28.67 H59.34 Cd N4 S6P 1 21/c 114.601; 16.214; 17.317
90; 111.59; 90
3812Macreadie, Lauren K.; Forsyth, Craig M.; Turner, David R.; Chesman, Anthony S. R.
Cadmium tris(dithiocarbamate) ionic liquids as single source, solvent-free cadmium sulfide precursors.
Chemical communications (Cambridge, England), 2018, 54, 8925-8928
7122006 CIFC33 H68 Cd N4 O S6P 1 21/c 115.564; 15.533; 18.558
90; 106.15; 90
4309.4Macreadie, Lauren K.; Forsyth, Craig M.; Turner, David R.; Chesman, Anthony S. R.
Cadmium tris(dithiocarbamate) ionic liquids as single source, solvent-free cadmium sulfide precursors.
Chemical communications (Cambridge, England), 2018, 54, 8925-8928
7122007 CIFC34 H67 Cd N5 S6P 1 21/c 19.672; 10.838; 40.33
90; 92.81; 90
4222.5Macreadie, Lauren K.; Forsyth, Craig M.; Turner, David R.; Chesman, Anthony S. R.
Cadmium tris(dithiocarbamate) ionic liquids as single source, solvent-free cadmium sulfide precursors.
Chemical communications (Cambridge, England), 2018, 54, 8925-8928
7122008 CIFC42 H88 Cd N4 O S6P n a 2121.093; 22.769; 10.847
90; 90; 90
5209.5Macreadie, Lauren K.; Forsyth, Craig M.; Turner, David R.; Chesman, Anthony S. R.
Cadmium tris(dithiocarbamate) ionic liquids as single source, solvent-free cadmium sulfide precursors.
Chemical communications (Cambridge, England), 2018, 54, 8925-8928
7122009 CIFC23 H22 Cl N3C 1 2/c 133.35; 5.917; 21.754
90; 119.191; 90
3748Chen, Xiuwen; Zhao, He; Chen, Chunlian; Jiang, Huanfeng; Zhang, Min
Transfer hydrogenative para-selective aminoalkylation of aniline derivatives with N-heteroarenes via ruthenium/acid dual catalysis.
Chemical communications (Cambridge, England), 2018, 54, 9087-9090
7122010 CIFC22 H28 Au Cl2 F7 N2 O TeP -19.5656; 9.886; 16.5307
94.667; 95.131; 116.737
1377.45Ellwanger, Mathias A.; von Randow, Clara; Steinhauer, Simon; Zhou, Yunfei; Wiesner, Anja; Beckers, Helmut; Braun, Thomas; Riedel, Sebastian
Tuning the Lewis acidity of difluorido gold(iii) complexes: the synthesis of [AuClF<sub>2</sub>(SIMes)] and [AuF<sub>2</sub>(OTeF<sub>5</sub>)(SIMes)].
Chemical communications (Cambridge, England), 2018, 54, 9301-9304
7122011 CIFC21 H26 Au Cl F2 N2P n m a14.7369; 20.2843; 7.0652
90; 90; 90
2112Ellwanger, Mathias A.; von Randow, Clara; Steinhauer, Simon; Zhou, Yunfei; Wiesner, Anja; Beckers, Helmut; Braun, Thomas; Riedel, Sebastian
Tuning the Lewis acidity of difluorido gold(iii) complexes: the synthesis of [AuClF<sub>2</sub>(SIMes)] and [AuF<sub>2</sub>(OTeF<sub>5</sub>)(SIMes)].
Chemical communications (Cambridge, England), 2018, 54, 9301-9304
7122012 CIFC3 H9 F5 O Si TeP 1 21/c 16.2372; 19.3447; 8.1649
90; 108.024; 90
936.81Ellwanger, Mathias A.; von Randow, Clara; Steinhauer, Simon; Zhou, Yunfei; Wiesner, Anja; Beckers, Helmut; Braun, Thomas; Riedel, Sebastian
Tuning the Lewis acidity of difluorido gold(iii) complexes: the synthesis of [AuClF<sub>2</sub>(SIMes)] and [AuF<sub>2</sub>(OTeF<sub>5</sub>)(SIMes)].
Chemical communications (Cambridge, England), 2018, 54, 9301-9304
7122013 CIFC23.25 H27.5 Au F9.62 N2 O1.38 Te1.38C 1 2/c 145.692; 10.1726; 33.134
90; 130.894; 90
11641.9Ellwanger, Mathias A.; von Randow, Clara; Steinhauer, Simon; Zhou, Yunfei; Wiesner, Anja; Beckers, Helmut; Braun, Thomas; Riedel, Sebastian
Tuning the Lewis acidity of difluorido gold(iii) complexes: the synthesis of [AuClF<sub>2</sub>(SIMes)] and [AuF<sub>2</sub>(OTeF<sub>5</sub>)(SIMes)].
Chemical communications (Cambridge, England), 2018, 54, 9301-9304
7122014 CIFC23 H18 N2 OP -110.0747; 10.1323; 10.7896
68.543; 62.333; 65.904
869.06Li, Qiuyun; Li, Bin; Wang, Baiquan
Rhodium-catalyzed intramolecular cascade sequence for the formation of fused carbazole-annulated medium-sized rings by cleavage of C(sp<sup>2</sup>)-H/C(sp<sup>3</sup>)-H bonds.
Chemical communications (Cambridge, England), 2018, 54, 9147-9150
7122015 CIFC44 H37 B F2 N2C 1 2/c 126.687; 11.1023; 23.908
90; 99.655; 90
6983.3Lv, Fan; Yu, Yang; Hao, Erhong; Yu, Changjiang; Wang, Hua; Jiao, Lijuan; Boens, Noël
Copper-catalyzed α-benzylation of BODIPYs via radical-triggered oxidative cross-coupling of two C-H bonds.
Chemical communications (Cambridge, England), 2018, 54, 9059-9062
7122016 CIFC20 H21 B F2 N2P 1 21/c 111.5066; 11.9871; 13.3556
90; 102.81; 90
1796.3Lv, Fan; Yu, Yang; Hao, Erhong; Yu, Changjiang; Wang, Hua; Jiao, Lijuan; Boens, Noël
Copper-catalyzed α-benzylation of BODIPYs via radical-triggered oxidative cross-coupling of two C-H bonds.
Chemical communications (Cambridge, England), 2018, 54, 9059-9062
7122017 CIFC22 H16 B F2 N3 O2P -18.1055; 10.403; 12.2541
73.386; 89.11; 85.852
987.5Lv, Fan; Yu, Yang; Hao, Erhong; Yu, Changjiang; Wang, Hua; Jiao, Lijuan; Boens, Noël
Copper-catalyzed α-benzylation of BODIPYs via radical-triggered oxidative cross-coupling of two C-H bonds.
Chemical communications (Cambridge, England), 2018, 54, 9059-9062
7122018 CIFC78 H194 Ba2 Cu6 N12 Ni4 O103P 4/m m m36.209; 36.209; 15.2135
90; 90; 90
19946Mon, Marta; Tiburcio, Estefanía; Ferrando-Soria, Jesús; Gil San Millán, Rodrigo; Navarro, Jorge A. R.; Armentano, Donatella; Pardo, Emilio
A post-synthetic approach triggers selective and reversible sulphur dioxide adsorption on a metal-organic framework.
Chemical communications (Cambridge, England), 2018, 54, 9063-9066
7122019 CIFC23 H15 Br Cl3 N O2P -19.9551; 10.2283; 11.7216
102.79; 98.7; 103.152
1107.55Li, Jin-Shan; Liu, Yong-Jie; Li, Shen; Ma, Jun-An
Chiral phosphoric acid-catalyzed direct asymmetric mannich reaction of cyclic C-acylimines with simple ketones: facile access to C2-quaternary indolin-3-ones.
Chemical communications (Cambridge, England), 2018, 54, 9151-9154
7122020 CIFC54 H80 Mo2 N4C 1 2/c 123.4539; 11.5987; 18.4225
90; 91.682; 90
5009.4Pérez-Jiménez, Marina; Campos, Jesús; López-Serrano, Joaquín; Carmona, Ernesto
Reactivity of a trans-[H-Mo[quadruple bond, length as m-dash]Mo-H] unit towards alkenes and alkynes: bimetallic migratory insertion, H-elimination and other reactions.
Chemical communications (Cambridge, England), 2018, 54, 9186-9189
7122021 CIFC122 H144 Mo2 N4 O2P -112.1566; 12.4253; 17.8335
99.015; 93.299; 101.706
2593.99Pérez-Jiménez, Marina; Campos, Jesús; López-Serrano, Joaquín; Carmona, Ernesto
Reactivity of a trans-[H-Mo[quadruple bond, length as m-dash]Mo-H] unit towards alkenes and alkynes: bimetallic migratory insertion, H-elimination and other reactions.
Chemical communications (Cambridge, England), 2018, 54, 9186-9189
7122022 CIFC60 H84 Mo2 N4P 1 21/c 112.1639; 19.6377; 23.5597
90; 101.505; 90
5514.7Pérez-Jiménez, Marina; Campos, Jesús; López-Serrano, Joaquín; Carmona, Ernesto
Reactivity of a trans-[H-Mo[quadruple bond, length as m-dash]Mo-H] unit towards alkenes and alkynes: bimetallic migratory insertion, H-elimination and other reactions.
Chemical communications (Cambridge, England), 2018, 54, 9186-9189
7122023 CIFC22 H34 Cl Cr N3 O2P 21 21 219.01882; 13.64803; 19.2371
90; 90; 90
2367.88Schiwek, Christian H.; Vasilenko, Vladislav; Wadepohl, Hubert; Gade, Lutz H.
The open d-shell enforces the active space in 3d metal catalysis: highly enantioselective chromium(ii) pincer catalysed hydrosilylation of ketones.
Chemical communications (Cambridge, England), 2018, 54, 9139-9142
7122024 CIFC26 H45 Cr N3 O2 SiP 21 21 2111.7996; 14.2516; 17.9837
90; 90; 90
3024.2Schiwek, Christian H.; Vasilenko, Vladislav; Wadepohl, Hubert; Gade, Lutz H.
The open d-shell enforces the active space in 3d metal catalysis: highly enantioselective chromium(ii) pincer catalysed hydrosilylation of ketones.
Chemical communications (Cambridge, England), 2018, 54, 9139-9142
7122025 CIFC12 H34.54 B2.63 I0.37 O3 TbP b c n9.1844; 14.3006; 14.7076
90; 90; 90
1931.73Goodwin, Conrad A. P.; Reta, Daniel; Ortu, Fabrizio; Liu, Jingjing; Chilton, Nicholas F.; Mills, David P.
Terbocenium: completing a heavy lanthanide metallocenium cation family with an alternative anion abstraction strategy.
Chemical communications (Cambridge, England), 2018, 54, 9182-9185
7122026 CIFC12 H34.42 B2.61 I0.4 O3 YP 1 21/c 18.9188; 12.5674; 16.2017
90; 91.122; 90
1815.64Goodwin, Conrad A. P.; Reta, Daniel; Ortu, Fabrizio; Liu, Jingjing; Chilton, Nicholas F.; Mills, David P.
Terbocenium: completing a heavy lanthanide metallocenium cation family with an alternative anion abstraction strategy.
Chemical communications (Cambridge, England), 2018, 54, 9182-9185
7122027 CIFC58 H58 B F20 TbP -111.7358; 12.4581; 19.971
82.81; 89.321; 79.728
2850.32Goodwin, Conrad A. P.; Reta, Daniel; Ortu, Fabrizio; Liu, Jingjing; Chilton, Nicholas F.; Mills, David P.
Terbocenium: completing a heavy lanthanide metallocenium cation family with an alternative anion abstraction strategy.
Chemical communications (Cambridge, England), 2018, 54, 9182-9185
7122028 CIFC34 H62 B TbP 1 21/c 110.332; 15.6294; 20.5234
90; 99.173; 90
3271.8Goodwin, Conrad A. P.; Reta, Daniel; Ortu, Fabrizio; Liu, Jingjing; Chilton, Nicholas F.; Mills, David P.
Terbocenium: completing a heavy lanthanide metallocenium cation family with an alternative anion abstraction strategy.
Chemical communications (Cambridge, England), 2018, 54, 9182-9185
7122029 CIFC34 H62 B YP 1 21/c 110.3453; 15.6331; 20.5613
90; 99.312; 90
3281.5Goodwin, Conrad A. P.; Reta, Daniel; Ortu, Fabrizio; Liu, Jingjing; Chilton, Nicholas F.; Mills, David P.
Terbocenium: completing a heavy lanthanide metallocenium cation family with an alternative anion abstraction strategy.
Chemical communications (Cambridge, England), 2018, 54, 9182-9185
7122030 CIFC28 H18 Al F36 Ga O4P 1 21/n 110.5553; 14.7194; 25.9642
90; 100.032; 90
3972.3Schorpp, Marcel; Rein, Stephan; Weber, Stefan; Scherer, Harald; Krossing, Ingo
Guilty and charged: a stable solution of the hexamethylbenzene radical cation as a ligand forming oxidising agent.
Chemical communications (Cambridge, England), 2018, 54, 10036-10039
7122031 CIFC40 H36 Ag Al F36 O4P 1 21 122.3404; 20.5472; 23.5734
90; 109.786; 90
10182.1Schorpp, Marcel; Rein, Stephan; Weber, Stefan; Scherer, Harald; Krossing, Ingo
Guilty and charged: a stable solution of the hexamethylbenzene radical cation as a ligand forming oxidising agent.
Chemical communications (Cambridge, England), 2018, 54, 10036-10039
7122032 CIFC25 H12 Al F36 In O4P 1 21 110.6026; 17.5964; 11.1567
90; 113.373; 90
1910.7Schorpp, Marcel; Rein, Stephan; Weber, Stefan; Scherer, Harald; Krossing, Ingo
Guilty and charged: a stable solution of the hexamethylbenzene radical cation as a ligand forming oxidising agent.
Chemical communications (Cambridge, England), 2018, 54, 10036-10039
7122033 CIFC28 H18 Al F36 In O4P 1 21/n 110.5712; 14.7281; 26.0049
90; 100.363; 90
3982.75Schorpp, Marcel; Rein, Stephan; Weber, Stefan; Scherer, Harald; Krossing, Ingo
Guilty and charged: a stable solution of the hexamethylbenzene radical cation as a ligand forming oxidising agent.
Chemical communications (Cambridge, England), 2018, 54, 10036-10039
7122034 CIFC87 H50 Cl5 F9 N12 O6 S16P 1 21/c 110.819; 23.7852; 35.167
90; 93.979; 90
9027.8Mckeown, George R.; Manion, Joseph G.; Lough, Alan J.; Seferos, Dwight S.
Synthesis of fused-ring aza-dipyrromethenes from aromatic nitriles.
Chemical communications (Cambridge, England), 2018, 54, 8893-8896
7122035 CIFC24 H17 N OP 1 21/n 116.0364; 7.5753; 16.754
90; 117.214; 90
1809.99Xu, Letian; Li, Guoping; Xu, Tao; Zhang, Weidong; Zhang, Sikun; Yin, Shiwei; An, Zhongfu; He, Gang
Chalcogen atom modulated persistent room-temperature phosphorescence through intramolecular electronic coupling.
Chemical communications (Cambridge, England), 2018, 54, 9226-9229
7122036 CIFC24 H17 N SP 1 21/c 114.7755; 16.6199; 7.5149
90; 100.035; 90
1817.18Xu, Letian; Li, Guoping; Xu, Tao; Zhang, Weidong; Zhang, Sikun; Yin, Shiwei; An, Zhongfu; He, Gang
Chalcogen atom modulated persistent room-temperature phosphorescence through intramolecular electronic coupling.
Chemical communications (Cambridge, England), 2018, 54, 9226-9229
7122037 CIFC24 H17 N SeP 1 21/c 114.9778; 16.6273; 7.5305
90; 99.679; 90
1848.7Xu, Letian; Li, Guoping; Xu, Tao; Zhang, Weidong; Zhang, Sikun; Yin, Shiwei; An, Zhongfu; He, Gang
Chalcogen atom modulated persistent room-temperature phosphorescence through intramolecular electronic coupling.
Chemical communications (Cambridge, England), 2018, 54, 9226-9229
7122038 CIFC30 H42 Cl Cu N6P 1 21/n 116.6483; 10.5534; 18.3838
90; 97.541; 90
3202.03Rasale, Dnyaneshwar; Patil, Kiran; Sauter, Basilius; Geigle, Stefanie; Zhanybekova, Saule; Gillingham, Dennis
A new water soluble copper N-heterocyclic carbene complex delivers mild O<sup>6</sup>G-selective RNA alkylation.
Chemical communications (Cambridge, England), 2018, 54, 9174-9177
7122039 CIFC42 H41 Cl5 N6 Pt2P -110.8699; 12.8241; 17.0041
109.788; 96.434; 99.529
2163.2Gee, Jack C.; Fuller, Beth A.; Lockett, Hannah-Marie; Sedghi, Gita; Robertson, Craig M.; Luzyanin, Konstantin V.
Visible light accelerated hydrosilylation of alkynes using platinum-[acyclic diaminocarbene] photocatalysts.
Chemical communications (Cambridge, England), 2018, 54, 9450-9453
7122040 CIFC26 H22 Cl N O3P -19.588; 14.091; 15.915
88.6; 78.027; 88.2
2102Zhao, Hong-Wu; Du, Juan; Guo, Jia-Ming; Feng, Ning-Ning; Wang, Li-Ru; Ding, Wan-Qiu; Song, Xiu-Qing
Formal [5+2] cycloaddition of vinylethylene carbonates to oxazol-5-(4H)-ones for the synthesis of 3,4-dihydrooxepin-2(7H)-ones.
Chemical communications (Cambridge, England), 2018, 54, 9178-9181
7122041 CIFC26 H18 B2 F15 NP b c a17.2304; 13.7966; 22.128
90; 90; 90
5260.3Winner, Lena; Bélanger-Chabot, Guillaume; Celik, Mehmet Ali; Schäfer, Marius; Braunschweig, Holger
Intriguing migrations in transient iminoborane adducts: two new pathways to aminoboranes.
Chemical communications (Cambridge, England), 2018, 54, 9349-9351
7122042 CIFC40 H56 B N3P 1 21/n 110.9215; 18.1709; 18.1668
90; 99.987; 90
3550.6Winner, Lena; Bélanger-Chabot, Guillaume; Celik, Mehmet Ali; Schäfer, Marius; Braunschweig, Holger
Intriguing migrations in transient iminoborane adducts: two new pathways to aminoboranes.
Chemical communications (Cambridge, England), 2018, 54, 9349-9351
7122043 CIFC24 H20 N2 OP -19.126; 9.491; 11.16
101.7; 96.75; 96.63
930.3Zhang, Lvye; Wu, Binqiang; Chen, Zhangtao; Hu, Jinjin; Zeng, Xiaofei; Zhong, Guofu
Chiral phosphoric acid catalyzed enantioselective N-alkylation of indoles with in situ generated cyclic N-acyl ketimines.
Chemical communications (Cambridge, England), 2018, 54, 9230-9233
7122044 CIFC36 H30 Cl8 N4 O4P -17.94286; 14.5267; 16.8597
75.958; 85.8331; 87.3903
1881.43Kersten, Kortney M.; Breen, Meghan E.; Mapp, Anna K.; Matzger, Adam J.
Pharmaceutical solvate formation for the incorporation of the antimicrobial agent hydrogen peroxide.
Chemical communications (Cambridge, England), 2018, 54, 9286-9289
7122045 CIFC32 H27 N O4P 1 21/c 111.6289; 10.409; 22.0032
90; 101.519; 90
2609.7Sha, Hong-Kai; Xu, Ting; Liu, Feng; Tang, Bu-Zheng; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
Metal-free naphthannulation reactions of yne-allenone esters for accessing polycyclic aromatic hydrocarbons.
Chemical communications (Cambridge, England), 2018, 54, 10415-10418
7122046 CIFC4 H6 N6 O6P b c a8.821; 9.509; 19.681
90; 90; 90
1650.8Yan, Chao; Yang, Hongwei; Qi, Xiujuan; Jin, Yunhe; Wang, Kangcai; Liu, Tianlin; Tian, Junjun; Nie, Fude; Cheng, Guangbin; Zhang, Qinghua
A simple and versatile strategy for taming FOX-7.
Chemical communications (Cambridge, England), 2018, 54, 9333-9336
7122047 CIFC4 H5 Cl N6 O6P 1 21/c 18.582; 11.47; 10.482
90; 110.736; 90
965Yan, Chao; Yang, Hongwei; Qi, Xiujuan; Jin, Yunhe; Wang, Kangcai; Liu, Tianlin; Tian, Junjun; Nie, Fude; Cheng, Guangbin; Zhang, Qinghua
A simple and versatile strategy for taming FOX-7.
Chemical communications (Cambridge, England), 2018, 54, 9333-9336
7122048 CIFC4 H5 N7 O8P -15.886; 8.134; 20.46
99.275; 90.656; 93.353
964.9Yan, Chao; Yang, Hongwei; Qi, Xiujuan; Jin, Yunhe; Wang, Kangcai; Liu, Tianlin; Tian, Junjun; Nie, Fude; Cheng, Guangbin; Zhang, Qinghua
A simple and versatile strategy for taming FOX-7.
Chemical communications (Cambridge, England), 2018, 54, 9333-9336
7122049 CIFC4 H6 N6 O6P n m a7.1223; 10.448; 11.389
90; 90; 90
847.5Yan, Chao; Yang, Hongwei; Qi, Xiujuan; Jin, Yunhe; Wang, Kangcai; Liu, Tianlin; Tian, Junjun; Nie, Fude; Cheng, Guangbin; Zhang, Qinghua
A simple and versatile strategy for taming FOX-7.
Chemical communications (Cambridge, England), 2018, 54, 9333-9336
7122050 CIFC4 H4 Cl N7 O7P 1 21/c 18.1381; 11.242; 11.677
90; 106.132; 90
1026.2Yan, Chao; Yang, Hongwei; Qi, Xiujuan; Jin, Yunhe; Wang, Kangcai; Liu, Tianlin; Tian, Junjun; Nie, Fude; Cheng, Guangbin; Zhang, Qinghua
A simple and versatile strategy for taming FOX-7.
Chemical communications (Cambridge, England), 2018, 54, 9333-9336
7122051 CIFC4 H5 N7 O8P 1 21/n 118.913; 5.827; 18.914
90; 102.724; 90
2033.2Yan, Chao; Yang, Hongwei; Qi, Xiujuan; Jin, Yunhe; Wang, Kangcai; Liu, Tianlin; Tian, Junjun; Nie, Fude; Cheng, Guangbin; Zhang, Qinghua
A simple and versatile strategy for taming FOX-7.
Chemical communications (Cambridge, England), 2018, 54, 9333-9336
7122052 CIFC4 H4 Cl N7 O8P b c a11.4945; 11.5752; 16.011
90; 90; 90
2130.3Yan, Chao; Yang, Hongwei; Qi, Xiujuan; Jin, Yunhe; Wang, Kangcai; Liu, Tianlin; Tian, Junjun; Nie, Fude; Cheng, Guangbin; Zhang, Qinghua
A simple and versatile strategy for taming FOX-7.
Chemical communications (Cambridge, England), 2018, 54, 9333-9336
7122053 CIFC43 H73 Cl N5 Ni O3.5 Si2C 1 2/c 132.1007; 12.451; 25.1623
90; 99.965; 90
9905.3Hadlington, Terrance J.; Szilvási, Tibor; Driess, Matthias
Metal nitrene-like reactivity of a Si[double bond, length as m-dash]N bond towards CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 9352-9355
7122054 CIFC44 H77 Cl N6 Ni O2 Si2P -111.2566; 12.7269; 17.1548
89.747; 85.046; 86.16
2442.94Hadlington, Terrance J.; Szilvási, Tibor; Driess, Matthias
Metal nitrene-like reactivity of a Si[double bond, length as m-dash]N bond towards CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 9352-9355
7122055 CIFC39 H66 Cl N5 Ni O5 Si2P 19.394; 11.9351; 20.7497
86.519; 79.694; 82.07
2265.4Hadlington, Terrance J.; Szilvási, Tibor; Driess, Matthias
Metal nitrene-like reactivity of a Si[double bond, length as m-dash]N bond towards CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 9352-9355
7122056 CIFC35 H50 N4 Ni OP 21 21 2110.2787; 15.5439; 21.1529
90; 90; 90
3379.62Hadlington, Terrance J.; Szilvási, Tibor; Driess, Matthias
Metal nitrene-like reactivity of a Si[double bond, length as m-dash]N bond towards CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 9352-9355
7122057 CIFC39 H66 Cl N5 Ni O5 Si2P 1 21/n 113.8284; 14.3306; 24.1972
90; 104.6; 90
4640.3Hadlington, Terrance J.; Szilvási, Tibor; Driess, Matthias
Metal nitrene-like reactivity of a Si[double bond, length as m-dash]N bond towards CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 9352-9355
7122058 CIFC24 H40 N4 Ni O2P 1 21/n 112.5272; 15.8955; 13.0261
90; 90.227; 90
2593.82Hadlington, Terrance J.; Szilvási, Tibor; Driess, Matthias
Metal nitrene-like reactivity of a Si[double bond, length as m-dash]N bond towards CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 9352-9355
7122059 CIFC13 H18 B2 N2 O3P 1 21/c 113.5677; 17.9941; 12.3197
90; 99.37; 90
2967.6Kamio, Shintaro; Kageyuki, Ikuo; Osaka, Itaru; Hatano, Sayaka; Abe, Manabu; Yoshida, Hiroto
Anthranilamide (aam)-substituted diboron: palladium-catalyzed selective B(aam) transfer.
Chemical communications (Cambridge, England), 2018, 54, 9290-9293
7122060 CIFC16 H20 B2 N2 O2P 1 21/c 113.217; 11.608; 10.778
90; 102.985; 90
1611.3Kamio, Shintaro; Kageyuki, Ikuo; Osaka, Itaru; Hatano, Sayaka; Abe, Manabu; Yoshida, Hiroto
Anthranilamide (aam)-substituted diboron: palladium-catalyzed selective B(aam) transfer.
Chemical communications (Cambridge, England), 2018, 54, 9290-9293
7122061 CIFC36 H54 N4 O6P -315.714; 15.714; 9.1939
90; 90; 120
1966.09Cole, Bren E.; Falcones, Ingemar B.; Cheisson, Thibault; Manor, Brian C.; Carroll, Patrick J.; Schelter, Eric J.
A molecular basis to rare earth separations for recycling: tuning the TriNOx ligand properties for improved performance.
Chemical communications (Cambridge, England), 2018, 54, 10276-10279
7122062 CIFC165 H228 N16 Nd4 O24P 1 21/n 115.0466; 21.7784; 25.24
90; 92.93; 90
8260.1Cole, Bren E.; Falcones, Ingemar B.; Cheisson, Thibault; Manor, Brian C.; Carroll, Patrick J.; Schelter, Eric J.
A molecular basis to rare earth separations for recycling: tuning the TriNOx ligand properties for improved performance.
Chemical communications (Cambridge, England), 2018, 54, 10276-10279
7122063 CIFC40 H59 N4 Nd O7P -110.1532; 16.0011; 16.825
73.266; 89.599; 74.177
2510.9Cole, Bren E.; Falcones, Ingemar B.; Cheisson, Thibault; Manor, Brian C.; Carroll, Patrick J.; Schelter, Eric J.
A molecular basis to rare earth separations for recycling: tuning the TriNOx ligand properties for improved performance.
Chemical communications (Cambridge, England), 2018, 54, 10276-10279
7122064 CIFC44 H67 Dy N4 O8P -110.0807; 15.9867; 16.7547
74.347; 89.439; 74.228
2496.2Cole, Bren E.; Falcones, Ingemar B.; Cheisson, Thibault; Manor, Brian C.; Carroll, Patrick J.; Schelter, Eric J.
A molecular basis to rare earth separations for recycling: tuning the TriNOx ligand properties for improved performance.
Chemical communications (Cambridge, England), 2018, 54, 10276-10279
7122065 CIFC44 H48 N6 O5P -111.1805; 12.0077; 16.8416
71.554; 78.981; 68.315
1985.98Lee, Juhoon; Brewster, James T.; Song, Bo; Lynch, Vincent M.; Hwang, Inhong; Li, Xiaopeng; Sessler, Jonathan L.
Uranyl dication mediated photoswitching of a calix[4]pyrrole-based metal coordination cage.
Chemical communications (Cambridge, England), 2018, 54, 9422-9425
7122066 CIFC192 H200 N24 O32 U4P 1 21/n 119.2663; 25.3809; 24.2879
90; 96.389; 90
11802.9Lee, Juhoon; Brewster, James T.; Song, Bo; Lynch, Vincent M.; Hwang, Inhong; Li, Xiaopeng; Sessler, Jonathan L.
Uranyl dication mediated photoswitching of a calix[4]pyrrole-based metal coordination cage.
Chemical communications (Cambridge, England), 2018, 54, 9422-9425
7122067 CIFC15 H26 N2 O3 S2 SiP 21 21 217.68141; 10.8441; 23.4756
90; 90; 90
1955.47Sohtome, Yoshihiro; Shimazu, Tadahiro; Barjau, Joaquin; Fujishiro, Shinya; Akakabe, Mai; Terayama, Naoki; Dodo, Kosuke; Ito, Akihiro; Yoshida, Minoru; Shinkai, Yoichi; Sodeoka, Mikiko
Unveiling epidithiodiketopiperazine as a non-histone arginine methyltransferase inhibitor by chemical protein methylome analyses.
Chemical communications (Cambridge, England), 2018, 54, 9202-9205
7122068 CIFC12 H16 O3P 1 21 112.8484; 6.1584; 13.6137
90; 97.415; 90
1068.18Wu, Xiang; Chen, Shu-Sen; Zhang, Ling; Wang, Hai-Jun; Gong, Liu-Zhu
Palladium-catalyzed enantioselective carboannulation of 1,3-dienes with aryl iodides enables access to chiral indanes.
Chemical communications (Cambridge, England), 2018, 54, 9595-9598
7122069 CIFC76 H59 N4 O8P 1 21 19.8509; 13.4787; 22.2482
90; 96.124; 90
2937.2Ling, Zheng; Xie, Fang; Gridnev, Ilya D.; Terada, Masahiro; Zhang, Wanbin
Cu-Catalyzed switchable synthesis of functionalized pyridines and pyrroles.
Chemical communications (Cambridge, England), 2018, 54, 9446-9449
7122070 CIFC38 H29 N2 O8 S2P 1 21/c 116.3964; 24.3356; 8.2487
90; 94.46; 90
3281.4Ling, Zheng; Xie, Fang; Gridnev, Ilya D.; Terada, Masahiro; Zhang, Wanbin
Cu-Catalyzed switchable synthesis of functionalized pyridines and pyrroles.
Chemical communications (Cambridge, England), 2018, 54, 9446-9449
7122071 CIFC36 H71 As Ge Si2P 21 21 2111.871; 17.675; 19.376
90; 90; 90
4065.5Lee, Vladimir Ya; Kawai, Manami; Gapurenko, Olga A.; Minkin, Vladimir I.; Gornitzka, Heinz; Sekiguchi, Akira
Arsagermene, a compound with an -As[double bond, length as m-dash]Ge[double bond splayed right] double bond.
Chemical communications (Cambridge, England), 2018, 54, 10947-10949
7122072 CIFC14 H14 N4 OP 1 21/c 17.753; 14.532; 11.144
90; 98.574; 90
1241.5Zhang, Ruizhong; Tong, Feng; Yang, Liuqing; Adsetts, Jonathan Ralph; Yan, Tianhao; Wang, Ruiyao; Ding, Zhifeng; Wang, Hong-Bo
Facile synthesis and efficient electrochemiluminescence of a readily accessible pyridopyrimidine.
Chemical communications (Cambridge, England), 2018, 54, 9897-9900
7122073 CIFC23 H24 Cl2 N O2 TaP n a 2116.827; 14.9556; 8.5588
90; 90; 90
2153.9Štarha, Pavel; Trávníček, Zdeněk; Dvořák, Zdeněk
A cytotoxic tantalum(v) half-sandwich complex: a new challenge for metal-based anticancer agents.
Chemical communications (Cambridge, England), 2018, 54, 9533-9536
7122074 CIFC17 H13 N O3C 1 c 110.914; 21.762; 5.713
90; 91.119; 90
1356.6Su, Shikuan; Li, Jianxiong; Sun, Mingming; Zhao, Hongbin; Chen, Yali; Li, Jian
A domino reaction of 2-isocyanophenyloxyacrylate and aryne to synthesize arenes with vicinal olefin and benzoxazole.
Chemical communications (Cambridge, England), 2018, 54, 9611-9614
7122075 CIFC17 H12 Cl N O3P -110.986; 11.502; 13.713
111.941; 101.876; 104.589
1466.1Su, Shikuan; Li, Jianxiong; Sun, Mingming; Zhao, Hongbin; Chen, Yali; Li, Jian
A domino reaction of 2-isocyanophenyloxyacrylate and aryne to synthesize arenes with vicinal olefin and benzoxazole.
Chemical communications (Cambridge, England), 2018, 54, 9611-9614
7122076 CIFC8 H8 F2 O SP 21 21 214.9111; 8.9793; 18.918
90; 90; 90
834.25Batisse, Chloé; Panossian, Armen; Hanquet, Gilles; Leroux, Frédéric R
Access towards enantiopure α,α-difluoromethyl alcohols by means of sulfoxides as traceless chiral auxiliaries.
Chemical communications (Cambridge, England), 2018, 54, 10423-10426
7122077 CIFC15 H15 F2 N3 O3P -112.5999; 12.8512; 13.5479
63.165; 62.666; 64.519
1668.7Wang, Xin-Gang; Li, Yuke; Zhang, Lu-Lu; Zhang, Bo-Sheng; Wang, Qiang; Ma, Jun-Wei; Liang, Yong-Min
Ruthenium(ii)-catalyzed selective C-H difluoroalkylation of aniline derivatives with pyrimidyl auxiliaries.
Chemical communications (Cambridge, England), 2018, 54, 9541-9544
7122078 CIFC42.5 H29 N3 O0.5R -3 :H21.982; 21.982; 10.3781
90; 90; 120
4342.93Ou, Arnold; Guédin, Aurore; Skelton, Brian W.; Amrane, Samir; Evans, Cameron W.; Norret, Marck; Iyer, K. Swaminathan; Mergny, Jean-Louis; Smith, Nicole M.
Multicarbazole scaffolds for selective G-quadruplex binding.
Chemical communications (Cambridge, England), 2018, 54, 9647-9650
7122079 CIFC26 H22 Mo N6 O3P 1 21/n 17.531; 21.121; 14.986
90; 91.728; 90
2382.6Manakin, Yu V.; Mironov, V. S.; Bazhenova, T. A.; Lyssenko, K. A.; Gilmutdinov, I. F.; Bikbaev, K. Sh; Masitov, A. A.; Yagubskii, E. B.
(Et<sub>4</sub>N)[Mo<sup>III</sup>(DAPBH)Cl<sub>2</sub>], the first pentagonal-bipyramidal Mo(iii) complex with a N<sub>3</sub>O<sub>2</sub>-type Schiff-base ligand: manifestation of unquenched orbital momentum and Ising-type magnetic anisotropy.
Chemical communications (Cambridge, England), 2018, 54, 10084-10087
7122080 CIFC31 H39 Cl2 Mo N6 O2P n a 2121.9939; 11.0133; 12.8402
90; 90; 90
3110.22Manakin, Yu V.; Mironov, V. S.; Bazhenova, T. A.; Lyssenko, K. A.; Gilmutdinov, I. F.; Bikbaev, K. Sh; Masitov, A. A.; Yagubskii, E. B.
(Et<sub>4</sub>N)[Mo<sup>III</sup>(DAPBH)Cl<sub>2</sub>], the first pentagonal-bipyramidal Mo(iii) complex with a N<sub>3</sub>O<sub>2</sub>-type Schiff-base ligand: manifestation of unquenched orbital momentum and Ising-type magnetic anisotropy.
Chemical communications (Cambridge, England), 2018, 54, 10084-10087
7122081 CIFC34 H28.62 Cl2 K3 N14 O24.31 Y3I a -3 d28.006; 28.006; 28.006
90; 90; 90
21966Mohideen, M Infas H; Belmabkhout, Youssef; Bhatt, Prashant M.; Shkurenko, Aleksander; Chen, Zhijie; Adil, Karim; Eddaoudi, Mohamed
Upgrading gasoline to high octane numbers using a zeolite-like metal-organic framework molecular sieve with ana-topology.
Chemical communications (Cambridge, England), 2018, 54, 9414-9417
7122082 CIFC63 H79 N3 O3 YP -110.266; 12.111; 23.973
87.84; 77.96; 76.14
2829.9Tolmachova, Nataliya A.; Kondratov, Ivan S.; Dolovanyuk, Violetta G.; Pridma, Stanislav O.; Chernykh, Anton V.; Daniliuc, Constantin G.; Haufe, Günter
Synthesis of new fluorinated proline analogues from polyfluoroalkyl β-ketoacetals and ethyl isocyanoacetate.
Chemical communications (Cambridge, England), 2018, 54, 9683-9686
7122083 CIFC7 H11 Cl F5 N O3P 1 21/c 111.579; 10.2974; 9.8109
90; 109.426; 90
1103.19Tolmachova, Nataliya A.; Kondratov, Ivan S.; Dolovanyuk, Violetta G.; Pridma, Stanislav O.; Chernykh, Anton V.; Daniliuc, Constantin G.; Haufe, Günter
Synthesis of new fluorinated proline analogues from polyfluoroalkyl β-ketoacetals and ethyl isocyanoacetate.
Chemical communications (Cambridge, England), 2018, 54, 9683-9686
7122084 CIFC18 H22 F3 N O3P 1 21/c 116.4371; 9.2127; 24.407
90; 109.415; 90
3485.8Inoue, Yuta; Hatayama, Takahiro; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Stereoselective aldol reactions using pseudo C<sub>2</sub> symmetric 1-benzyl-4-(trifluoromethyl)piperidine-2,6-dione.
Chemical communications (Cambridge, England), 2018, 54, 9913-9916
7122085 CIFC22 H22 F3 N O3P -19.8654; 10.7372; 11.1375
66.63; 79.912; 63.756
971.3Inoue, Yuta; Hatayama, Takahiro; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Stereoselective aldol reactions using pseudo C<sub>2</sub> symmetric 1-benzyl-4-(trifluoromethyl)piperidine-2,6-dione.
Chemical communications (Cambridge, England), 2018, 54, 9913-9916
7122086 CIFC18 H22 F3 N O3P 1 21/n 111.0908; 9.261; 16.8687
90; 94.711; 90
1726.8Inoue, Yuta; Hatayama, Takahiro; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Stereoselective aldol reactions using pseudo C<sub>2</sub> symmetric 1-benzyl-4-(trifluoromethyl)piperidine-2,6-dione.
Chemical communications (Cambridge, England), 2018, 54, 9913-9916
7122087 CIFC23 H24 F3 N O5P 1 21/c 19.9904; 10.9743; 19.9416
90; 98.589; 90
2161.83Inoue, Yuta; Hatayama, Takahiro; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Stereoselective aldol reactions using pseudo C<sub>2</sub> symmetric 1-benzyl-4-(trifluoromethyl)piperidine-2,6-dione.
Chemical communications (Cambridge, England), 2018, 54, 9913-9916
7122088 CIFC22 H22 F3 N O3P 1 21/c 19.9948; 23.4736; 16.9093
90; 92.259; 90
3964.1Inoue, Yuta; Hatayama, Takahiro; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Stereoselective aldol reactions using pseudo C<sub>2</sub> symmetric 1-benzyl-4-(trifluoromethyl)piperidine-2,6-dione.
Chemical communications (Cambridge, England), 2018, 54, 9913-9916
7122089 CIFC22 H22 F3 N O3P 1 21/n 110.8871; 9.3186; 19.1257
90; 101.892; 90
1898.71Inoue, Yuta; Hatayama, Takahiro; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Stereoselective aldol reactions using pseudo C<sub>2</sub> symmetric 1-benzyl-4-(trifluoromethyl)piperidine-2,6-dione.
Chemical communications (Cambridge, England), 2018, 54, 9913-9916
7122090 CIFC13 H15 F3 O3 S SeP n a 2123.29; 12.0766; 5.2849
90; 90; 90
1486.5Ghiazza, Clément; Khrouz, Lhoussain; Monnereau, Cyrille; Billard, Thierry; Tlili, Anis
Visible-light promoted fluoroalkylselenolation: toward the reactivity of unsaturated compounds.
Chemical communications (Cambridge, England), 2018, 54, 9909-9912
7122091 CIFC18 H19 F3 O3 S SeF d d 257.215; 23.058; 5.6571
90; 90; 90
7463Ghiazza, Clément; Khrouz, Lhoussain; Monnereau, Cyrille; Billard, Thierry; Tlili, Anis
Visible-light promoted fluoroalkylselenolation: toward the reactivity of unsaturated compounds.
Chemical communications (Cambridge, England), 2018, 54, 9909-9912
7122092 CIFC22 H17 F3 O2 S SeC 1 2/c 135.871; 5.8331; 19.33
90; 92.742; 90
4040Ghiazza, Clément; Khrouz, Lhoussain; Monnereau, Cyrille; Billard, Thierry; Tlili, Anis
Visible-light promoted fluoroalkylselenolation: toward the reactivity of unsaturated compounds.
Chemical communications (Cambridge, England), 2018, 54, 9909-9912
7122093 CIFC16 H22 F6 I N2 PP -18.0754; 8.355; 15.6634
99.537; 98.842; 98.269
1014.16Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122094 CIFC16 H22 F6 I N2 PP -17.9723; 8.2018; 15.4695
99.377; 97.639; 100.448
967.59Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122095 CIFC16 H22 Cl I N2 O4C 1 2/c 129.1018; 8.5668; 15.9883
90; 100.803; 90
3915.39Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122096 CIFC8 H12 Br NC 1 2/c 18.6217; 14.9357; 6.8943
90; 90.007; 90
887.79Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122097 CIFC16 H22 B Br F4 N2C 1 2/c 129.0149; 8.50144; 15.54176
90; 100.798; 90
3765.79Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122098 CIFC16 H22 Cl I N2 O4C 1 2/c 127.9017; 11.0678; 23.4625
90; 126.566; 90
5819.3Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122099 CIFC16 H22 Br Cl N2 O4C 1 2/c 126.7649; 10.8741; 23.3335
90; 126.93; 90
5428.59Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122100 CIFC16 H22 B Br F4 N2C 1 2/c 128.9753; 8.47823; 15.0337
90; 102.878; 90
3600.27Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122101 CIFC16 H22 Br Cl N2 O4C 1 2/c 128.8168; 8.5588; 15.2931
90; 102.549; 90
3681.7Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122102 CIFC16 H22 Br F6 N2 PP -17.9058; 8.2573; 15.1037
98.632; 98.087; 100.308
944.74Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122103 CIFC16 H22 Br Cl N2 O4C 1 2/c 127.3108; 11.0568; 23.5758
90; 127.217; 90
5669.4Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122104 CIFC16 H22 Cl I N2 O4C 1 2/c 127.2651; 10.9468; 23.2069
90; 126.137; 90
5593.9Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122105 CIFC16 H22 Br F6 N2 PP -18.0237; 8.3951; 15.2556
99.42; 98.926; 97.07
989.79Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122106 CIFC16 H22 Br Cl N2 O4C 1 2/c 128.8059; 8.5296; 15.8383
90; 99.565; 90
3837.4Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122107 CIFC16 H22 Cl I N2 O4C 1 2/c 129.0825; 8.5757; 15.4139
90; 102.602; 90
3751.66Morgan, Lewis C. F.; Kim, Yejin; Blandy, Jack N.; Murray, Claire A.; Christensen, Kirsten E.; Thompson, Amber L.
Unexpected behaviour in derivatives of Barluenga's reagent, Hal(Coll)<sub>2</sub>X (Coll = 2,4,6-trimethyl pyridine, collidine; Hal = I, Br; X = PF<sub>6</sub>, ClO<sub>4</sub> & BF<sub>4</sub>).
Chemical communications (Cambridge, England), 2018, 54, 9849-9852
7122108 CIFC48 H62 O8 P4 Pd2P 1 21 18.3653; 35.4662; 10.0227
90; 93.23; 90
2968.86Vasseur, Alexandre; Membrat, Romain; Palpacelli, Davide; Giorgi, Michel; Nuel, Didier; Giordano, Laurent; Martinez, Alexandre
Synthesis of chiral supramolecular bisphosphinite palladacycles through hydrogen transfer-promoted self-assembly process.
Chemical communications (Cambridge, England), 2018, 54, 10132-10135
7122109 CIFC25 H32 O5 P2 PdP 21 21 219.8492; 13.6242; 20.1945
90; 90; 90
2709.85Vasseur, Alexandre; Membrat, Romain; Palpacelli, Davide; Giorgi, Michel; Nuel, Didier; Giordano, Laurent; Martinez, Alexandre
Synthesis of chiral supramolecular bisphosphinite palladacycles through hydrogen transfer-promoted self-assembly process.
Chemical communications (Cambridge, England), 2018, 54, 10132-10135
7122110 CIFC29 H38 O4 P2 PdP 21 21 219.8856; 15.3472; 20.4744
90; 90; 90
3106.3Vasseur, Alexandre; Membrat, Romain; Palpacelli, Davide; Giorgi, Michel; Nuel, Didier; Giordano, Laurent; Martinez, Alexandre
Synthesis of chiral supramolecular bisphosphinite palladacycles through hydrogen transfer-promoted self-assembly process.
Chemical communications (Cambridge, England), 2018, 54, 10132-10135
7122111 CIFC27 H33 Br O4 P2 PdP 1 21 110.08802; 12.8237; 11.49841
90; 94.1533; 90
1483.59Vasseur, Alexandre; Membrat, Romain; Palpacelli, Davide; Giorgi, Michel; Nuel, Didier; Giordano, Laurent; Martinez, Alexandre
Synthesis of chiral supramolecular bisphosphinite palladacycles through hydrogen transfer-promoted self-assembly process.
Chemical communications (Cambridge, England), 2018, 54, 10132-10135
7122112 CIFC27 H33 Cl O4 P2 PdP 18.2891; 10.4836; 17.2528
77.456; 86.077; 84.648
1455.3Vasseur, Alexandre; Membrat, Romain; Palpacelli, Davide; Giorgi, Michel; Nuel, Didier; Giordano, Laurent; Martinez, Alexandre
Synthesis of chiral supramolecular bisphosphinite palladacycles through hydrogen transfer-promoted self-assembly process.
Chemical communications (Cambridge, England), 2018, 54, 10132-10135
7122113 CIFC27 H34 O4 P2 Pd SP 1 21 19.9564; 12.8239; 11.6231
90; 93.421; 90
1481.39Vasseur, Alexandre; Membrat, Romain; Palpacelli, Davide; Giorgi, Michel; Nuel, Didier; Giordano, Laurent; Martinez, Alexandre
Synthesis of chiral supramolecular bisphosphinite palladacycles through hydrogen transfer-promoted self-assembly process.
Chemical communications (Cambridge, England), 2018, 54, 10132-10135
7122114 CIFC34 H47 N O6 P2 PdP 21 21 218.18015; 10.09118; 45.8101
90; 90; 90
3781.5Vasseur, Alexandre; Membrat, Romain; Palpacelli, Davide; Giorgi, Michel; Nuel, Didier; Giordano, Laurent; Martinez, Alexandre
Synthesis of chiral supramolecular bisphosphinite palladacycles through hydrogen transfer-promoted self-assembly process.
Chemical communications (Cambridge, England), 2018, 54, 10132-10135
7122115 CIFC74 H76 O8 P4 Pd2I 1 2 116.0483; 41.2069; 22.6837
90; 101.452; 90
14702.1Vasseur, Alexandre; Membrat, Romain; Palpacelli, Davide; Giorgi, Michel; Nuel, Didier; Giordano, Laurent; Martinez, Alexandre
Synthesis of chiral supramolecular bisphosphinite palladacycles through hydrogen transfer-promoted self-assembly process.
Chemical communications (Cambridge, England), 2018, 54, 10132-10135
7122116 CIFC32 H46 Br2 N4 O4 Si2P 1 21 17.0818; 34.0727; 8.0223
90; 105.239; 90
1867.7Tsuchimochi, Izuru; Kitamura, Yuta; Aoyama, Hiroshi; Akai, Shuji; Nakai, Keiyo; Yoshimitsu, Takehiko
Total synthesis of (-)-agelastatin A: an S<sub>H</sub>2' radical azidation strategy.
Chemical communications (Cambridge, England), 2018, 54, 9893-9896
7122117 CIFC44 H18 Mg3 N4 O19P 63/m m c16.9671; 16.9671; 15.3079
90; 90; 120
3816.5Li, Yong-Peng; Li, Shu-Ni; Jiang, Yu-Cheng; Hu, Man-Cheng; Zhai, Quan-Guo
A semiconductor and fluorescence dual-mode room-temperature ammonia sensor achieved by decorating hydroquinone into a metal-organic framework.
Chemical communications (Cambridge, England), 2018, 54, 9789-9792
7122118 CIFC38.25 H47.5 Cl1.5 Co F7.5 N5 O10 S3C 1 2/c 142.0464; 9.0171; 29.4652
90; 124.455; 90
9211.5Call, Arnau; Lloret-Fillol, Julio
Enhancement and control of the selectivity in light-driven ketone versus water reduction using aminopyridine cobalt complexes.
Chemical communications (Cambridge, England), 2018, 54, 9643-9646
7122119 CIFC39 H30.89 B Br0.11P 1 21/n 110.71416; 18.5823; 14.07156
90; 95.4564; 90
2788.87Kahan, R. J.; Crossley, D. L.; Cid, J.; Radcliffe, J. E.; Woodward, A. W.; Fasano, V.; Endres, S.; Whitehead, G. F. S.; Ingleson, M. J.
Generation of a series of B<sub>n</sub> fused oligo-naphthalenes (n = 1 to 3) from a B<sub>1</sub>-polycyclic aromatic hydrocarbon.
Chemical communications (Cambridge, England), 2018, 54, 9490-9493
7122120 CIFC58 H45.87 B2 Br0.13P 1 21/c 117.545; 12.6207; 22.2518
90; 94.451; 90
4912.4Kahan, R. J.; Crossley, D. L.; Cid, J.; Radcliffe, J. E.; Woodward, A. W.; Fasano, V.; Endres, S.; Whitehead, G. F. S.; Ingleson, M. J.
Generation of a series of B<sub>n</sub> fused oligo-naphthalenes (n = 1 to 3) from a B<sub>1</sub>-polycyclic aromatic hydrocarbon.
Chemical communications (Cambridge, England), 2018, 54, 9490-9493
7122121 CIFC20 H18 Cl2 N3 O2 Pt SP 1 21/n 111.425; 15.9927; 11.939
90; 105.051; 90
2106.62Qin, Qi-Pin; Zou, Bi-Qun; Hu, Fei-Long; Huang, Guo-Bao; Wang, Shu-Long; Gu, Yun-Qiong; Tan, Ming-Xiong
Platinum(ii) complexes with rutaecarpine and tryptanthrin derivatives induce apoptosis by inhibiting telomerase activity and disrupting mitochondrial function.
MedChemComm, 2018, 9, 1639-1648
7122122 CIFC17 H14 Cl2 N2 O3 Pt SP -18.5196; 9.9538; 10.8961
95.033; 90.166; 98.338
910.61Qin, Qi-Pin; Zou, Bi-Qun; Hu, Fei-Long; Huang, Guo-Bao; Wang, Shu-Long; Gu, Yun-Qiong; Tan, Ming-Xiong
Platinum(ii) complexes with rutaecarpine and tryptanthrin derivatives induce apoptosis by inhibiting telomerase activity and disrupting mitochondrial function.
MedChemComm, 2018, 9, 1639-1648
7122123 CIFC17 H13 Cl2 I N2 O3 Pt SP 1 21/c 18.594; 11.5135; 21.0202
90; 108.188; 90
1975.97Qin, Qi-Pin; Zou, Bi-Qun; Hu, Fei-Long; Huang, Guo-Bao; Wang, Shu-Long; Gu, Yun-Qiong; Tan, Ming-Xiong
Platinum(ii) complexes with rutaecarpine and tryptanthrin derivatives induce apoptosis by inhibiting telomerase activity and disrupting mitochondrial function.
MedChemComm, 2018, 9, 1639-1648
7122124 CIFC18 H17 Br Cl2 N2 O4 Pt SC 1 2/c 123.8724; 7.916; 23.4616
90; 106.984; 90
4240.26Qin, Qi-Pin; Zou, Bi-Qun; Hu, Fei-Long; Huang, Guo-Bao; Wang, Shu-Long; Gu, Yun-Qiong; Tan, Ming-Xiong
Platinum(ii) complexes with rutaecarpine and tryptanthrin derivatives induce apoptosis by inhibiting telomerase activity and disrupting mitochondrial function.
MedChemComm, 2018, 9, 1639-1648
7122125 CIFC25 H26 F3 N3 O5 S3P 1 21/c 119.508; 8.2786; 17.511
90; 106.363; 90
2713.5Shinde, Sopan Valiba; Talukdar, Pinaki
An anion receptor that facilitates transmembrane proton-anion symport by deprotonating its sulfonamide N-H proton.
Chemical communications (Cambridge, England), 2018, 54, 10351-10354
7122126 CIFC23 H22 N4 O6 S2P -17.567; 12.628; 12.89
106.657; 91.327; 92.275
1178.3Shinde, Sopan Valiba; Talukdar, Pinaki
An anion receptor that facilitates transmembrane proton-anion symport by deprotonating its sulfonamide N-H proton.
Chemical communications (Cambridge, England), 2018, 54, 10351-10354
7122127 CIFC38 H52 Cl F3 N4 O4.5 SC 1 2/c 120.234; 13.246; 30.365
90; 101.943; 90
7962Shinde, Sopan Valiba; Talukdar, Pinaki
An anion receptor that facilitates transmembrane proton-anion symport by deprotonating its sulfonamide N-H proton.
Chemical communications (Cambridge, England), 2018, 54, 10351-10354
7122128 CIFC60 H135 K O20 Si5 Sm2P -113.9095; 15.4386; 21.897
80.979; 87.169; 80.361
4577.2Kelly, Rory P.; Toniolo, Davide; Tirani, Farzaneh Fadaei; Maron, Laurent; Mazzanti, Marinella
A tetranuclear samarium(ii) inverse sandwich from direct reduction of toluene by a samarium(ii) siloxide.
Chemical communications (Cambridge, England), 2018, 54, 10268-10271
7122129 CIFC56 H128 O20 Si4 Sm2P 6113.49276; 13.49276; 73.6861
90; 90; 120
11617.6Kelly, Rory P.; Toniolo, Davide; Tirani, Farzaneh Fadaei; Maron, Laurent; Mazzanti, Marinella
A tetranuclear samarium(ii) inverse sandwich from direct reduction of toluene by a samarium(ii) siloxide.
Chemical communications (Cambridge, England), 2018, 54, 10268-10271
7122130 CIFC79 H170 O24 Si6 Sm4P -113.2055; 13.2859; 19.3107
81.584; 73.829; 65.648
2962.5Kelly, Rory P.; Toniolo, Davide; Tirani, Farzaneh Fadaei; Maron, Laurent; Mazzanti, Marinella
A tetranuclear samarium(ii) inverse sandwich from direct reduction of toluene by a samarium(ii) siloxide.
Chemical communications (Cambridge, England), 2018, 54, 10268-10271
7122131 CIFC79 H169 K2 O24 Si6 Sm2P -113.3255; 13.457; 19.2064
80.512; 72.563; 64.969
2974.4Kelly, Rory P.; Toniolo, Davide; Tirani, Farzaneh Fadaei; Maron, Laurent; Mazzanti, Marinella
A tetranuclear samarium(ii) inverse sandwich from direct reduction of toluene by a samarium(ii) siloxide.
Chemical communications (Cambridge, England), 2018, 54, 10268-10271
7122132 CIFC54 H34 Cu Fe2 N6P 1 21/c 118.6124; 8.954; 15.5768
90; 113.979; 90
2371.91Patra, Bratati; Sobottka, Sebastian; Mondal, Sruti; Sarkar, Biprajit; Kar, Sanjib
Metal coordination induced ring contraction of porphyrin derivatives.
Chemical communications (Cambridge, England), 2018, 54, 9945-9948
7122133 CIFC129 H75 Ag3 Fe3 N18P -118.4767; 18.7775; 19.617
99.222; 104.379; 117.221
5558.5Patra, Bratati; Sobottka, Sebastian; Mondal, Sruti; Sarkar, Biprajit; Kar, Sanjib
Metal coordination induced ring contraction of porphyrin derivatives.
Chemical communications (Cambridge, England), 2018, 54, 9945-9948
7122134 CIFC54 H48.67 B2.67 Co1.33 Dy N18 O10I 2 320.9059; 20.9059; 20.9059
90; 90; 90
9137.1Alexandropoulos, Dimitris I.; Schulte, Kelsey A.; Vignesh, Kuduva R.; Dunbar, Kim R.
Slow magnetic dynamics in a family of mononuclear lanthanide complexes exhibiting the rare cubic coordination geometry.
Chemical communications (Cambridge, England), 2018, 54, 10136-10139
7122135 CIFC54 H48.67 B2.67 Co1.33 N18 O10 TbI 2 320.9135; 20.9135; 20.9135
90; 90; 90
9147Alexandropoulos, Dimitris I.; Schulte, Kelsey A.; Vignesh, Kuduva R.; Dunbar, Kim R.
Slow magnetic dynamics in a family of mononuclear lanthanide complexes exhibiting the rare cubic coordination geometry.
Chemical communications (Cambridge, England), 2018, 54, 10136-10139
7122136 CIFC54 H48.67 B2.67 Co1.33 N18 O10 YI 2 320.9091; 20.9091; 20.9091
90; 90; 90
9141.3Alexandropoulos, Dimitris I.; Schulte, Kelsey A.; Vignesh, Kuduva R.; Dunbar, Kim R.
Slow magnetic dynamics in a family of mononuclear lanthanide complexes exhibiting the rare cubic coordination geometry.
Chemical communications (Cambridge, England), 2018, 54, 10136-10139
7122137 CIFC54 H48.67 B2.67 Co1.33 Er N18 O10I 2 320.9076; 20.9076; 20.9076
90; 90; 90
9139.3Alexandropoulos, Dimitris I.; Schulte, Kelsey A.; Vignesh, Kuduva R.; Dunbar, Kim R.
Slow magnetic dynamics in a family of mononuclear lanthanide complexes exhibiting the rare cubic coordination geometry.
Chemical communications (Cambridge, England), 2018, 54, 10136-10139
7122138 CIFC60 H35 Dy3 N O24C m c 2127.7738; 10.6809; 19.1423
90; 90; 90
5678.5Wang, Mengmeng; Meng, Xixi; Song, Fen; He, Yanfei; Shi, Wei; Gao, Hongling; Tang, Jinkui; Peng, Cheng
Reversible structural transformation induced switchable single-molecule magnet behavior in lanthanide metal-organic frameworks.
Chemical communications (Cambridge, England), 2018, 54, 10183-10186
7122139 CIFC37 H42 Dy N3 O15P -19.4019; 13.8627; 16.5461
85.355; 76.826; 72.112
1998.15Wang, Mengmeng; Meng, Xixi; Song, Fen; He, Yanfei; Shi, Wei; Gao, Hongling; Tang, Jinkui; Peng, Cheng
Reversible structural transformation induced switchable single-molecule magnet behavior in lanthanide metal-organic frameworks.
Chemical communications (Cambridge, England), 2018, 54, 10183-10186
7122140 CIFC30 H44 B2 O5P 1 21/c 113.0983; 12.425; 18.235
90; 95.349; 90
2954.8Davenport, Elliot; Fernandez, Elena
Transition-metal-free synthesis of vicinal triborated compounds and selective functionalisation of the internal C-B bond.
Chemical communications (Cambridge, England), 2018, 54, 10104-10107
7122141 CIFC59 H34 F Mn3 N O19 P2C 1 2/c 117.796; 31.098; 15.1639
90; 106.338; 90
8053Reynolds, Joseph E.; Walsh, Kelly M.; Li, Bin; Kunal, Pranaw; Chen, Banglin; Humphrey, Simon M.
Highly selective room temperature acetylene sorption by an unusual triacetylenic phosphine MOF.
Chemical communications (Cambridge, England), 2018, 54, 9937-9940
7122142 CIFC19 H19 N O2P 21 21 217.7693; 12.582; 15.723
90; 90; 90
1537Wang, Peng-Zi; Yu, Xiao-Ye; Li, Chan-Yun; He, Bin-Qing; Chen, Jia-Rong; Xiao, Wen-Jing
A photocatalytic iminyl radical-mediated C-C bond cleavage/addition/cyclization cascade for the synthesis of 1,2,3,4-tetrahydrophenanthrenes.
Chemical communications (Cambridge, England), 2018, 54, 9925-9928
7122143 CIFC21 H21 N O4P 1 21/n 110.271; 18.417; 10.492
90; 114.416; 90
1807.2Wang, Peng-Zi; Yu, Xiao-Ye; Li, Chan-Yun; He, Bin-Qing; Chen, Jia-Rong; Xiao, Wen-Jing
A photocatalytic iminyl radical-mediated C-C bond cleavage/addition/cyclization cascade for the synthesis of 1,2,3,4-tetrahydrophenanthrenes.
Chemical communications (Cambridge, England), 2018, 54, 9925-9928
7122144 CIFC21 H21 N O4P 1 21/c 18.712; 23.551; 9.11
90; 106.515; 90
1792Wang, Peng-Zi; Yu, Xiao-Ye; Li, Chan-Yun; He, Bin-Qing; Chen, Jia-Rong; Xiao, Wen-Jing
A photocatalytic iminyl radical-mediated C-C bond cleavage/addition/cyclization cascade for the synthesis of 1,2,3,4-tetrahydrophenanthrenes.
Chemical communications (Cambridge, England), 2018, 54, 9925-9928
7122145 CIFC93 H99 B6 Fe3 N21 O18P 1 21/c 118.077; 49.704; 12.9398
90; 103.811; 90
11290.3Jansze, Suzanne M.; Ortiz, Daniel; Fadaei Tirani, Farzaneh; Scopelliti, Rosario; Menin, Laure; Severin, Kay
Inflating face-capped Pd<sub>6</sub>L<sub>8</sub> coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 9529-9532
7122146 CIFC75 H87 B6 Fe3 N21 O18P c a 2135.551; 9.273; 29.6345
90; 90; 90
9769.4Jansze, Suzanne M.; Ortiz, Daniel; Fadaei Tirani, Farzaneh; Scopelliti, Rosario; Menin, Laure; Severin, Kay
Inflating face-capped Pd<sub>6</sub>L<sub>8</sub> coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 9529-9532
7122147 CIFC600 H696 B48 Fe24 N168 O144 Pd6F 4 3 252.2358; 52.2358; 52.2358
90; 90; 90
142529Jansze, Suzanne M.; Ortiz, Daniel; Fadaei Tirani, Farzaneh; Scopelliti, Rosario; Menin, Laure; Severin, Kay
Inflating face-capped Pd<sub>6</sub>L<sub>8</sub> coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 9529-9532
7122148 CIFC14 H14 O2P 21 21 215.6861; 7.4078; 28.14
90; 90; 90
1185.3Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122149 CIFC14 H14 O2P 21 21 215.7075; 7.6016; 28.125
90; 90; 90
1220.2Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122150 CIFC14 H14 O2P 21 21 215.7073; 7.5909; 28.133
90; 90; 90
1218.8Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122151 CIFC18 H16 O2P 21 21 215.8843; 7.2086; 32.936
90; 90; 90
1397.06Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122152 CIFC18 H16 O2P 21 21 215.9264; 7.4922; 32.946
90; 90; 90
1462.9Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122153 CIFC14 H14 O2P 21 21 215.6915; 7.4628; 28.143
90; 90; 90
1195.36Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122154 CIFC18 H16 O2P 21 21 215.9061; 7.3412; 32.9746
90; 90; 90
1429.71Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122155 CIFC18 H16 O2P 21 21 215.8987; 7.2946; 32.966
90; 90; 90
1418.48Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122156 CIFC14 H14 O2P 21 21 215.709; 7.6146; 28.123
90; 90; 90
1222.6Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122157 CIFC18 H16 O2P 21 21 215.9146; 7.3912; 32.9799
90; 90; 90
1441.75Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122158 CIFC14 H14 O2P 21 21 215.6838; 7.3834; 28.139
90; 90; 90
1180.87Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122159 CIFC18 H16 O2P 21 21 215.9244; 7.4427; 32.968
90; 90; 90
1453.68Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122160 CIFC18 H16 O2P 21 21 215.8912; 7.2496; 32.95
90; 90; 90
1407.26Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122161 CIFC14 H14 O2P 21 21 215.6883; 7.4343; 28.14
90; 90; 90
1190Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122162 CIFC14 H14 O2P 21 21 215.6944; 7.4936; 28.143
90; 90; 90
1200.91Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122163 CIFC14 H14 O2P 21 21 215.6982; 7.5247; 28.143
90; 90; 90
1206.69Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122164 CIFC14 H14 O2P 21 21 215.7113; 7.6398; 28.117
90; 90; 90
1226.8Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122165 CIFC14 H14 O2P 21 21 215.7113; 7.6271; 28.122
90; 90; 90
1225Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122166 CIFC14 H14 O2P 21 21 215.713; 7.6527; 28.116
90; 90; 90
1229.2Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122167 CIFC14 H14 O2P 21 21 215.7057; 7.5595; 28.152
90; 90; 90
1214.26Negi, Lalita; Shrivastava, Ashutosh; Das, Dinabandhu
Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing.
Chemical communications (Cambridge, England), 2018, 54, 10675-10678
7122168 CIFC28 H20 Br N O7P -19.0255; 10.5951; 13.5639
80.012; 77.037; 72.625
1198.4Yu, Jhen-Kuei; Chien, Han-Wei; Lin, Yi-Jung; Karanam, Praneeth; Chen, Yu-Heng; Lin, Wenwei
Diversity-oriented synthesis of chromenopyrrolidines from azomethine ylides and 2-hydroxybenzylidene indandiones via base-controlled regiodivergent (3+2) cycloaddition.
Chemical communications (Cambridge, England), 2018, 54, 9921-9924
7122169 CIFC28 H20 Br N O7P -19.47; 10.6706; 13.3664
76.892; 69.377; 76.41
1213.24Yu, Jhen-Kuei; Chien, Han-Wei; Lin, Yi-Jung; Karanam, Praneeth; Chen, Yu-Heng; Lin, Wenwei
Diversity-oriented synthesis of chromenopyrrolidines from azomethine ylides and 2-hydroxybenzylidene indandiones via base-controlled regiodivergent (3+2) cycloaddition.
Chemical communications (Cambridge, England), 2018, 54, 9921-9924
7122170 CIFC29 H22 Br N O8P -19.3617; 12.1176; 13.2597
63.828; 82.131; 76.526
1311.82Yu, Jhen-Kuei; Chien, Han-Wei; Lin, Yi-Jung; Karanam, Praneeth; Chen, Yu-Heng; Lin, Wenwei
Diversity-oriented synthesis of chromenopyrrolidines from azomethine ylides and 2-hydroxybenzylidene indandiones via base-controlled regiodivergent (3+2) cycloaddition.
Chemical communications (Cambridge, England), 2018, 54, 9921-9924
7122171 CIFC12 H15 N3P 1 21/n 18.3134; 12.5189; 11.0332
90; 107.377; 90
1095.9Sawant, Devesh M.; Sharma, Shivani; Pathare, Ramdas S.; Joshi, Gaurav; Kalra, Sourav; Sukanya, Sukanya; Maurya, Antim K.; Metre, Ramesh K.; Agnihotri, Vijai K.; Khan, Shahnawaz; Kumar, Raj; Pardasani, R. T.
Relay tricyclic Pd(ii)/Ag(i) catalysis: design of a four-component reaction driven by nitrene-transfer on isocyanide yields inhibitors of EGFR.
Chemical communications (Cambridge, England), 2018, 54, 11530-11533
7122172 CIFC19 H22 N4 O2 SP -17.8633; 9.3267; 13.5742
84.166; 89.184; 79.543
973.9Sawant, Devesh M.; Sharma, Shivani; Pathare, Ramdas S.; Joshi, Gaurav; Kalra, Sourav; Sukanya, Sukanya; Maurya, Antim K.; Metre, Ramesh K.; Agnihotri, Vijai K.; Khan, Shahnawaz; Kumar, Raj; Pardasani, R. T.
Relay tricyclic Pd(ii)/Ag(i) catalysis: design of a four-component reaction driven by nitrene-transfer on isocyanide yields inhibitors of EGFR.
Chemical communications (Cambridge, England), 2018, 54, 11530-11533
7122173 CIFC19 H23 N4 O3 SC 1 2/c 134.877; 9.0455; 12.9419
90; 105.171; 90
3940.6Sawant, Devesh M.; Sharma, Shivani; Pathare, Ramdas S.; Joshi, Gaurav; Kalra, Sourav; Sukanya, Sukanya; Maurya, Antim K.; Metre, Ramesh K.; Agnihotri, Vijai K.; Khan, Shahnawaz; Kumar, Raj; Pardasani, R. T.
Relay tricyclic Pd(ii)/Ag(i) catalysis: design of a four-component reaction driven by nitrene-transfer on isocyanide yields inhibitors of EGFR.
Chemical communications (Cambridge, England), 2018, 54, 11530-11533
7122174 CIFC26 H28 N4 O4 SC 1 2/c 129.7473; 10.1292; 18.7181
90; 118.728; 90
4945.8Sawant, Devesh M.; Sharma, Shivani; Pathare, Ramdas S.; Joshi, Gaurav; Kalra, Sourav; Sukanya, Sukanya; Maurya, Antim K.; Metre, Ramesh K.; Agnihotri, Vijai K.; Khan, Shahnawaz; Kumar, Raj; Pardasani, R. T.
Relay tricyclic Pd(ii)/Ag(i) catalysis: design of a four-component reaction driven by nitrene-transfer on isocyanide yields inhibitors of EGFR.
Chemical communications (Cambridge, England), 2018, 54, 11530-11533
7122175 CIFC28 H31 F18 N3 O4 SP 1 21/c 118.835; 8.0827; 22.8945
90; 96.376; 90
3463.8Riccobono, Alessio; Parker, Rachel R.; Whitwood, Adrian C.; Slattery, John M.; Bruce, Duncan W.; Pibiri, Ivana; Pace, Andrea
1,2,4-Triazolium ions as flexible scaffolds for the construction of polyphilic ionic liquid crystals.
Chemical communications (Cambridge, England), 2018, 54, 9965-9968
7122176 CIFC63 H43 Cl3 O2P -18.1774; 15.6087; 20.2266
100.693; 99.58; 104.108
2398.9Qiu, Shuhai; Wang, Chaoqiang; Xie, Sheng; Huang, Xiaobo; Chen, Lanlan; Zhao, Yunhui; Zeng, Zebing
Toward helical-shaped diradicaloids: cyclobutenyl o-quinodimethane-bridged indeno[1,2-b]fluorenes.
Chemical communications (Cambridge, England), 2018, 54, 11383-11386
7122177 CIFC80 H64 OP b c n18.9589; 17.5568; 20.8566
90; 90; 90
6942.3Qiu, Shuhai; Wang, Chaoqiang; Xie, Sheng; Huang, Xiaobo; Chen, Lanlan; Zhao, Yunhui; Zeng, Zebing
Toward helical-shaped diradicaloids: cyclobutenyl o-quinodimethane-bridged indeno[1,2-b]fluorenes.
Chemical communications (Cambridge, England), 2018, 54, 11383-11386
7122178 CIFC62 H42 O2P -112.7002; 16.2234; 16.3308
116.444; 98.064; 105.765
2762.93Qiu, Shuhai; Wang, Chaoqiang; Xie, Sheng; Huang, Xiaobo; Chen, Lanlan; Zhao, Yunhui; Zeng, Zebing
Toward helical-shaped diradicaloids: cyclobutenyl o-quinodimethane-bridged indeno[1,2-b]fluorenes.
Chemical communications (Cambridge, England), 2018, 54, 11383-11386
7122179 CIFC19 H13 F O2P 1 21/c 17.508; 12.35; 14.7
90; 91.4; 90
1363Li, Ting; Wang, Huiyan; Qian, Pengcheng; Yang, Yuhan; Li, Bo; Zhang, Liming
Au(i)-Catalyzed expeditious access to naphtho[2,3-c]furan-1(3-H)-ones from readily available propargylic ynoates.
Chemical communications (Cambridge, England), 2018, 54, 10447-10450
7122180 CIFC22 H46 Cl3 La N2 O7C 1 2/c 113.8322; 16.2467; 13.1611
90; 106.058; 90
2842.3Huh, Daniel N.; Windorff, Cory J.; Ziller, Joseph W.; Evans, William J.
Synthesis of uranium-in-cryptand complexes.
Chemical communications (Cambridge, England), 2018, 54, 10272-10275
7122181 CIFC21 H42 Cl6 I3 N2 O6 UP 1 21/c 111.485; 26.766; 12.275
90; 101.244; 90
3701Huh, Daniel N.; Windorff, Cory J.; Ziller, Joseph W.; Evans, William J.
Synthesis of uranium-in-cryptand complexes.
Chemical communications (Cambridge, England), 2018, 54, 10272-10275
7122182 CIFC18 H38 I3 N2 O7 UP 1 21/n 110.8943; 19.313; 13.3229
90; 96.0099; 90
2787.8Huh, Daniel N.; Windorff, Cory J.; Ziller, Joseph W.; Evans, William J.
Synthesis of uranium-in-cryptand complexes.
Chemical communications (Cambridge, England), 2018, 54, 10272-10275
7122183 CIFC44 H61 B I2 N3 O7 UP 1 21/n 120.142; 9.6317; 26.979
90; 107.307; 90
4997Huh, Daniel N.; Windorff, Cory J.; Ziller, Joseph W.; Evans, William J.
Synthesis of uranium-in-cryptand complexes.
Chemical communications (Cambridge, England), 2018, 54, 10272-10275
7122184 CIFC18 H18 N2 OP 1 21/c 122.8586; 5.0654; 13.05
90; 98.008; 90
1496.3Huang, Huan-Ming; Adams, Ralph W.; Procter, David J.
Reductive cyclisations of amidines involving aminal radicals.
Chemical communications (Cambridge, England), 2018, 54, 10160-10163
7122185 CIFC19 H18 N2 O3P 1 21/n 111.001; 6.9737; 20.129
90; 93.637; 90
1541.1Huang, Huan-Ming; Adams, Ralph W.; Procter, David J.
Reductive cyclisations of amidines involving aminal radicals.
Chemical communications (Cambridge, England), 2018, 54, 10160-10163
7122186 CIFC19 H20 N2 OC m c 2141.133; 13.3359; 11.1564
90; 90; 90
6119.8Huang, Huan-Ming; Adams, Ralph W.; Procter, David J.
Reductive cyclisations of amidines involving aminal radicals.
Chemical communications (Cambridge, England), 2018, 54, 10160-10163
7122187 CIFC150 H132 O18P 1 21 116.42491; 18.47453; 20.7026
90; 108.584; 90
5954.49Zhao, Peng; Wu, Simeng; Ke, Chaoqi; Liu, Xiaohua; Feng, Xiaoming
Chiral Lewis acid-catalyzed enantioselective cyclopropanation and C-H insertion reactions of vinyl ketones with α-diazoesters.
Chemical communications (Cambridge, England), 2018, 54, 9837-9840
7122188 CIFC32 H30 N2 O4 SP 1 21 19.7057; 10.031; 14.8723
90; 97.782; 90
1434.6Zhao, Peng; Wu, Simeng; Ke, Chaoqi; Liu, Xiaohua; Feng, Xiaoming
Chiral Lewis acid-catalyzed enantioselective cyclopropanation and C-H insertion reactions of vinyl ketones with α-diazoesters.
Chemical communications (Cambridge, England), 2018, 54, 9837-9840
7122189 CIFC63 H101 N Na2 O64 S8 Y2R -3 :H47.5183; 47.5183; 25.9584
90; 90; 120
50761Ling, Irene; Kumari, Harshita; Mirzamani, Marzieh; Sobolev, Alexandre N.; Garvey, Christopher J.; Atwood, Jerry L.; Raston, Colin L.
Phase dependent structural perturbation of a robust multicomponent assembled icosahedral array.
Chemical communications (Cambridge, England), 2018, 54, 10824-10827
7122190 CIFC56 H106 Na2 O65 S8 Y2P -112.1783; 13.4788; 27.6293
89.078; 80.089; 88.413
4465.6Ling, Irene; Kumari, Harshita; Mirzamani, Marzieh; Sobolev, Alexandre N.; Garvey, Christopher J.; Atwood, Jerry L.; Raston, Colin L.
Phase dependent structural perturbation of a robust multicomponent assembled icosahedral array.
Chemical communications (Cambridge, England), 2018, 54, 10824-10827
7122191 CIFC8 H24 Cl5 N4 Np O2P -17.4041; 10.4454; 12.3566
76.494; 89.313; 71.795
880.8Payne, Maurice K.; Pyrch, Mikaela; Jubinsky, Matthew; Basile, Madeline; Forbes, Tori
Impacts of oxo interactions within actinyl metal organic materials: Highlight on thermal expansion behaviour
Chemical Communications, 2018
7122192 CIFC4 H6 N Np O6P m m n8.2246; 9.7709; 4.538
90; 90; 90
364.68Payne, Maurice K.; Pyrch, Mikaela; Jubinsky, Matthew; Basile, Madeline; Forbes, Tori
Impacts of oxo interactions within actinyl metal organic materials: Highlight on thermal expansion behaviour
Chemical Communications, 2018
7122193 CIFC89 H136 N2 O26 Ti6P 1 21/c 126.6207; 20.7575; 17.7843
90; 90.493; 90
9826.9Zou, Dan-Hong; Cui, Li-Na; Liu, Pei-Yi; Yang, Shen; Zhu, Qin-Yu; Dai, Jie
Triphenylamine derived titanium oxo clusters: an approach to effective organic-inorganic hybrid dyes for photoactive electrodes.
Chemical communications (Cambridge, England), 2018, 54, 9933-9936
7122194 CIFC70 H128 N2 O25 Ti6I 1 2/a 126.227; 25.66; 29.043
90; 105.67; 90
18819Zou, Dan-Hong; Cui, Li-Na; Liu, Pei-Yi; Yang, Shen; Zhu, Qin-Yu; Dai, Jie
Triphenylamine derived titanium oxo clusters: an approach to effective organic-inorganic hybrid dyes for photoactive electrodes.
Chemical communications (Cambridge, England), 2018, 54, 9933-9936
7122195 CIFC96 H122 N2 O30 Ti6P 1 21/c 115.5612; 15.6396; 21.2233
90; 95.892; 90
5137.8Zou, Dan-Hong; Cui, Li-Na; Liu, Pei-Yi; Yang, Shen; Zhu, Qin-Yu; Dai, Jie
Triphenylamine derived titanium oxo clusters: an approach to effective organic-inorganic hybrid dyes for photoactive electrodes.
Chemical communications (Cambridge, England), 2018, 54, 9933-9936
7122196 CIFC12 H2 Cl2 N8 O14P 1 21/c 111.43; 5.4511; 15.427
90; 98.6; 90
950.4Yang, Xiaoming; Lin, Xinyu; Yang, Li; Zhang, Tonglai
A novel method to synthesize stable nitrogen-rich polynitrobenzenes with π-stacking for high-energy-density energetic materials.
Chemical communications (Cambridge, England), 2018, 54, 10296-10299
7122197 CIFC12 N18 O8P b c a9.3869; 15.742; 25.114
90; 90; 90
3711.1Yang, Xiaoming; Lin, Xinyu; Yang, Li; Zhang, Tonglai
A novel method to synthesize stable nitrogen-rich polynitrobenzenes with π-stacking for high-energy-density energetic materials.
Chemical communications (Cambridge, England), 2018, 54, 10296-10299
7122198 CIFC25 H35 Cl3 O5 SiP 21 21 218.2183; 12.5178; 28.0079
90; 90; 90
2881.3Kobayashi, Toyoharu; Tanaka, Konomi; Ishida, Masako; Yamakita, Natsumi; Abe, Hideki; Ito, Hisanaka
Asymmetric total synthesis of pleurospiroketals A and B.
Chemical communications (Cambridge, England), 2018, 54, 10316-10319
7122199 CIFC15 H22 O5P 21 21 219.883; 10.008; 15.166
90; 90; 90
1500.1Kobayashi, Toyoharu; Tanaka, Konomi; Ishida, Masako; Yamakita, Natsumi; Abe, Hideki; Ito, Hisanaka
Asymmetric total synthesis of pleurospiroketals A and B.
Chemical communications (Cambridge, England), 2018, 54, 10316-10319
7122200 CIFC21 H41 N3 Ni P2P b c a11.1132; 15.6569; 28.295
90; 90; 90
4923.3Li, Huaifeng; Gonçalves, Théo P; Zhao, Qianyi; Gong, Dirong; Lai, Zhiping; Wang, Zhixiang; Zheng, Junrong; Huang, Kuo-Wei
Diverse catalytic reactivity of a dearomatized PN<sup>3</sup>P*-nickel hydride pincer complex towards CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2018, 54, 11395-11398
7122201 CIFC25 H41 N3 Ni P2I 41/a :220.386; 20.386; 24.639
90; 90; 90
10240Li, Huaifeng; Gonçalves, Théo P; Zhao, Qianyi; Gong, Dirong; Lai, Zhiping; Wang, Zhixiang; Zheng, Junrong; Huang, Kuo-Wei
Diverse catalytic reactivity of a dearomatized PN<sup>3</sup>P*-nickel hydride pincer complex towards CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2018, 54, 11395-11398
7122202 CIFC22 H43 N3 Ni P2P n a 2121.7707; 8.2148; 14.0657
90; 90; 90
2515.5Li, Huaifeng; Gonçalves, Théo P; Zhao, Qianyi; Gong, Dirong; Lai, Zhiping; Wang, Zhixiang; Zheng, Junrong; Huang, Kuo-Wei
Diverse catalytic reactivity of a dearomatized PN<sup>3</sup>P*-nickel hydride pincer complex towards CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2018, 54, 11395-11398
7122203 CIFC40 H56 N10 O14 S2P 1 21 18.9283; 13.9637; 18.7435
90; 101.484; 90
2290.01Williams, Neil J.; Seipp, Charles A.; Garrabrant, Kathleen A.; Custelcean, Radu; Holguin, Erick; Keum, Jong K.; Ellis, Ross J.; Moyer, Bruce A.
Surprisingly selective sulfate extraction by a simple monofunctional di(imino)guanidinium micelle-forming anion receptor.
Chemical communications (Cambridge, England), 2018, 54, 10048-10051
7122204 CIFC263 H194 Au40 Cl4 F24 P8 Sb4C 1 2/c 141.9547; 18.5701; 44.422
90; 117.333; 90
30745.3Wang, Ting; Zhang, Wen-Han; Yuan, Shang-Fu; Guan, Zong-Jie; Wang, Quan-Ming
An alkynyl-protected Au<sub>40</sub> nanocluster featuring PhC[triple bond, length as m-dash]C-Au-P^P motifs.
Chemical communications (Cambridge, England), 2018, 54, 10367-10370
7122205 CIFC24 H18 Cl F N2 O3P 1 21/c 110.474; 11.271; 17.518
90; 96.136; 90
2056.2Umar, Tarana; Shalini, Shruti; Raza, Md Kausar; Gusain, Siddharth; Kumar, Jitendra; Ahmed, Waqar; Tiwari, Manisha; Hoda, Nasimul
New amyloid beta-disaggregating agents: synthesis, pharmacological evaluation, crystal structure and molecular docking of <i>N</i>-(4-((7-chloroquinolin-4-yl)oxy)-3-ethoxybenzyl)amines.
MedChemComm, 2018, 9, 1891-1904
7122206 CIFC25 H23 Cl N2 O2P -15.35; 14.08; 14.717
101; 90.44; 97.24
1079Umar, Tarana; Shalini, Shruti; Raza, Md Kausar; Gusain, Siddharth; Kumar, Jitendra; Ahmed, Waqar; Tiwari, Manisha; Hoda, Nasimul
New amyloid beta-disaggregating agents: synthesis, pharmacological evaluation, crystal structure and molecular docking of <i>N</i>-(4-((7-chloroquinolin-4-yl)oxy)-3-ethoxybenzyl)amines.
MedChemComm, 2018, 9, 1891-1904
7122207 CIFC22 H17 Br F N O2 SP 21 21 2110.0581; 11.341; 17.3605
90; 90; 90
1980.3Fan, Xing; Wang, Qiang; Wei, Yin; Shi, Min
Catalyst-free geminal aminofluorination of ortho-sulfonamide-tethered alkylidenecyclopropanes via a Wagner-Meerwein rearrangement.
Chemical communications (Cambridge, England), 2018, 54, 10503-10506
7122208 CIFC25 H22 Br F3 N2 O3 SP 1 21/n 114.399; 9.6415; 17.024
90; 93.004; 90
2360.2Fan, Xing; Wang, Qiang; Wei, Yin; Shi, Min
Catalyst-free geminal aminofluorination of ortho-sulfonamide-tethered alkylidenecyclopropanes via a Wagner-Meerwein rearrangement.
Chemical communications (Cambridge, England), 2018, 54, 10503-10506
7122209 CIFC22 H19 F2 N O2 SP 1 21/c 114.943; 11.511; 11.392
90; 98.266; 90
1939.2Fan, Xing; Wang, Qiang; Wei, Yin; Shi, Min
Catalyst-free geminal aminofluorination of ortho-sulfonamide-tethered alkylidenecyclopropanes via a Wagner-Meerwein rearrangement.
Chemical communications (Cambridge, England), 2018, 54, 10503-10506
7122210 CIFC20 H19 N O5P 1 21 18.2648; 10.1169; 10.9096
90; 106.079; 90
876.51Wang, Zhe-Hao; Zhang, Huan-Huan; Xu, Peng-Fei; Luo, Yong-Chun
Synthesis of five-membered cyclic nitrones based on the Lewis acid-catalysed [3+2]-annulation reaction of donor-acceptor cyclopropanes with 1,4,2-dioxazoles.
Chemical communications (Cambridge, England), 2018, 54, 10128-10131
7122211 CIFC20 H19 N O5P -19.683; 9.746; 11.167
68.9; 72.87; 64.67
876.2Wang, Zhe-Hao; Zhang, Huan-Huan; Xu, Peng-Fei; Luo, Yong-Chun
Synthesis of five-membered cyclic nitrones based on the Lewis acid-catalysed [3+2]-annulation reaction of donor-acceptor cyclopropanes with 1,4,2-dioxazoles.
Chemical communications (Cambridge, England), 2018, 54, 10128-10131
7122212 CIFC42 H72 Lu2 Si6P 1 21/c 19.8651; 39.2173; 12.3474
90; 92.598; 90
4772.1Lorenz, Volker; Liebing, Phil; Bathelier, Adrien; Engelhardt, Felix; Maron, Laurent; Hilfert, Liane; Busse, Sabine; Edelmann, Frank T.
The "Wanderlust" of Me<sub>3</sub>Si groups in rare-earth triple-decker complexes: a combined experimental and computational study.
Chemical communications (Cambridge, England), 2018, 54, 10280-10283
7122213 CIFC42 H72 Si6 Tb2P 1 21/n 120.141; 12.664; 20.822
90; 116.07; 90
4770.6Lorenz, Volker; Liebing, Phil; Bathelier, Adrien; Engelhardt, Felix; Maron, Laurent; Hilfert, Liane; Busse, Sabine; Edelmann, Frank T.
The "Wanderlust" of Me<sub>3</sub>Si groups in rare-earth triple-decker complexes: a combined experimental and computational study.
Chemical communications (Cambridge, England), 2018, 54, 10280-10283
7122214 CIFC84 H144 Si12 Y4P -111.761; 13.119; 15.744
87.01; 81.33; 86.58
2395Lorenz, Volker; Liebing, Phil; Bathelier, Adrien; Engelhardt, Felix; Maron, Laurent; Hilfert, Liane; Busse, Sabine; Edelmann, Frank T.
The "Wanderlust" of Me<sub>3</sub>Si groups in rare-earth triple-decker complexes: a combined experimental and computational study.
Chemical communications (Cambridge, England), 2018, 54, 10280-10283
7122215 CIFC42 H72 La2 Si6P 1 21 111.747; 20.28; 20.734
90; 94.11; 90
4927Lorenz, Volker; Liebing, Phil; Bathelier, Adrien; Engelhardt, Felix; Maron, Laurent; Hilfert, Liane; Busse, Sabine; Edelmann, Frank T.
The "Wanderlust" of Me<sub>3</sub>Si groups in rare-earth triple-decker complexes: a combined experimental and computational study.
Chemical communications (Cambridge, England), 2018, 54, 10280-10283
7122216 CIFC42 H72 Si6 Tm2P -113.092; 18.108; 20.921
73.62; 86.142; 89.8
4747Lorenz, Volker; Liebing, Phil; Bathelier, Adrien; Engelhardt, Felix; Maron, Laurent; Hilfert, Liane; Busse, Sabine; Edelmann, Frank T.
The "Wanderlust" of Me<sub>3</sub>Si groups in rare-earth triple-decker complexes: a combined experimental and computational study.
Chemical communications (Cambridge, England), 2018, 54, 10280-10283
7122217 CIFC12 H10 Br I OC 1 2/c 121.7877; 5.806; 19.489
90; 100.565; 90
2423.6Yoshimura, Akira; Shea, Michael T.; Guselnikova, Olga; Postnikov, Pavel S.; Rohde, Gregory T.; Saito, Akio; Yusubov, Mekhman S.; Nemykin, Victor N.; Zhdankin, Viktor V.
Preparation and structure of phenolic aryliodonium salts.
Chemical communications (Cambridge, England), 2018, 54, 10363-10366
7122218 CIFC10 H8 Br I O SC 1 2/c 122.0476; 5.678; 18.9405
90; 100.965; 90
2327.8Yoshimura, Akira; Shea, Michael T.; Guselnikova, Olga; Postnikov, Pavel S.; Rohde, Gregory T.; Saito, Akio; Yusubov, Mekhman S.; Nemykin, Victor N.; Zhdankin, Viktor V.
Preparation and structure of phenolic aryliodonium salts.
Chemical communications (Cambridge, England), 2018, 54, 10363-10366
7122219 CIFC24 H19 Br I2 O2P b c n11.0912; 18.5647; 10.9748
90; 90; 90
2259.76Yoshimura, Akira; Shea, Michael T.; Guselnikova, Olga; Postnikov, Pavel S.; Rohde, Gregory T.; Saito, Akio; Yusubov, Mekhman S.; Nemykin, Victor N.; Zhdankin, Viktor V.
Preparation and structure of phenolic aryliodonium salts.
Chemical communications (Cambridge, England), 2018, 54, 10363-10366
7122220 CIFC13 H9 I O3P 6215.5268; 15.5268; 16.7336
90; 90; 120
3493.7Yoshimura, Akira; Shea, Michael T.; Guselnikova, Olga; Postnikov, Pavel S.; Rohde, Gregory T.; Saito, Akio; Yusubov, Mekhman S.; Nemykin, Victor N.; Zhdankin, Viktor V.
Preparation and structure of phenolic aryliodonium salts.
Chemical communications (Cambridge, England), 2018, 54, 10363-10366
7122221 CIFC11 H8 F3 I O4 S2P 1 21/c 112.296; 10.711; 12.599
90; 115.117; 90
1502.4Yoshimura, Akira; Shea, Michael T.; Guselnikova, Olga; Postnikov, Pavel S.; Rohde, Gregory T.; Saito, Akio; Yusubov, Mekhman S.; Nemykin, Victor N.; Zhdankin, Viktor V.
Preparation and structure of phenolic aryliodonium salts.
Chemical communications (Cambridge, England), 2018, 54, 10363-10366
7122222 CIFC11 H8 F3 I O4 S2P 1 21/c 112.4345; 10.6515; 12.6308
90; 115.594; 90
1508.8Yoshimura, Akira; Shea, Michael T.; Guselnikova, Olga; Postnikov, Pavel S.; Rohde, Gregory T.; Saito, Akio; Yusubov, Mekhman S.; Nemykin, Victor N.; Zhdankin, Viktor V.
Preparation and structure of phenolic aryliodonium salts.
Chemical communications (Cambridge, England), 2018, 54, 10363-10366
7122223 CIFC60 H140 Cl42 Np38 O76I 4/m19.562; 19.562; 29.3799
90; 90; 90
11242.9Martin, Nicolas P.; Volkringer, Christophe; Roussel, Pascal; März, Juliane; Hennig, Christoph; Loiseau, Thierry; Ikeda-Ohno, Atsushi
{Np<sub>38</sub>} clusters: the missing link in the largest poly-oxo cluster series of tetravalent actinides.
Chemical communications (Cambridge, England), 2018, 54, 10060-10063
7122224 CIFC200 H184 Cl18 Np38 O112I 4/m21.9347; 21.9347; 29.8559
90; 90; 90
14364.6Martin, Nicolas P.; Volkringer, Christophe; Roussel, Pascal; März, Juliane; Hennig, Christoph; Loiseau, Thierry; Ikeda-Ohno, Atsushi
{Np<sub>38</sub>} clusters: the missing link in the largest poly-oxo cluster series of tetravalent actinides.
Chemical communications (Cambridge, England), 2018, 54, 10060-10063
7122225 CIFC34 H31 N O6 SP 1 21 111.5709; 7.9832; 17.4107
90; 105.455; 90
1550.12Zhong, Xia; Tang, Qiong; Zhou, Pengfei; Zhong, Ziwei; Dong, Shunxi; Liu, Xiaohua; Feng, Xiaoming
Asymmetric synthesis of polysubstituted methylenecyclobutanes via catalytic [2+2] cycloaddition reactions of N-allenamides.
Chemical communications (Cambridge, England), 2018, 54, 10511-10514
7122226 CIFC42 H49 N O7 S SiP 1 21/c 114.938; 19.9785; 13.3618
90; 97.025; 90
3957.74Zhong, Xia; Tang, Qiong; Zhou, Pengfei; Zhong, Ziwei; Dong, Shunxi; Liu, Xiaohua; Feng, Xiaoming
Asymmetric synthesis of polysubstituted methylenecyclobutanes via catalytic [2+2] cycloaddition reactions of N-allenamides.
Chemical communications (Cambridge, England), 2018, 54, 10511-10514
7122227 CIFC27 H36 B Cl3 F4 Rh2 S2P -18.5593; 13.716; 13.8176
77.0026; 88.6155; 88.3987
1579.7Zhao, Xiangyu; Yang, Dawei; Zhang, Yahui; Wang, Baomin; Qu, Jingping
Terminal alkyne insertion into a thiolate-bridged dirhodium hydride complex derived from heterolytic cleavage of H<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 11112-11115
7122228 CIFC60 H64 B Cl5 Rh2 S2P -111.8882; 13.8454; 17.6084
88.5777; 76.6031; 79.8761
2775.14Zhao, Xiangyu; Yang, Dawei; Zhang, Yahui; Wang, Baomin; Qu, Jingping
Terminal alkyne insertion into a thiolate-bridged dirhodium hydride complex derived from heterolytic cleavage of H<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 11112-11115
7122229 CIFC52 H57 B Rh2 S2P -110.9219; 13.2492; 17.0937
106.757; 95.401; 108.677
2195.9Zhao, Xiangyu; Yang, Dawei; Zhang, Yahui; Wang, Baomin; Qu, Jingping
Terminal alkyne insertion into a thiolate-bridged dirhodium hydride complex derived from heterolytic cleavage of H<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 11112-11115
7122230 CIFC26 H34 Rh2 S2P -19.6295; 9.8207; 15.3103
100.996; 103.941; 106.208
1296.65Zhao, Xiangyu; Yang, Dawei; Zhang, Yahui; Wang, Baomin; Qu, Jingping
Terminal alkyne insertion into a thiolate-bridged dirhodium hydride complex derived from heterolytic cleavage of H<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 11112-11115
7122231 CIFC26 H35 F6 P Rh2 S2P -19.9962; 11.8993; 13.388
104.449; 90.0325; 95.9034
1533.36Zhao, Xiangyu; Yang, Dawei; Zhang, Yahui; Wang, Baomin; Qu, Jingping
Terminal alkyne insertion into a thiolate-bridged dirhodium hydride complex derived from heterolytic cleavage of H<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 11112-11115
7122232 CIFC55 H63 B Rh2 S2C 1 c 119.4748; 10.6687; 23.5138
90; 106.023; 90
4695.7Zhao, Xiangyu; Yang, Dawei; Zhang, Yahui; Wang, Baomin; Qu, Jingping
Terminal alkyne insertion into a thiolate-bridged dirhodium hydride complex derived from heterolytic cleavage of H<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 11112-11115
7122233 CIFC58 H69 B Cl2 Rh2 S2P -113.5617; 14.409; 15.3302
73.0429; 73.0526; 74.0362
2681.2Zhao, Xiangyu; Yang, Dawei; Zhang, Yahui; Wang, Baomin; Qu, Jingping
Terminal alkyne insertion into a thiolate-bridged dirhodium hydride complex derived from heterolytic cleavage of H<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 11112-11115
7122234 CIFC50 H54 B Cl Ir2 S2P -110.8763; 13.0712; 17.1848
106.971; 93.6316; 108.717
2179.6Zhao, Xiangyu; Yang, Dawei; Zhang, Yahui; Wang, Baomin; Qu, Jingping
Terminal alkyne insertion into a thiolate-bridged dirhodium hydride complex derived from heterolytic cleavage of H<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 11112-11115
7122235 CIFC26 H35 B F4 Ir2 S2P -19.921; 11.57; 13.212
74.619; 86.919; 83.718
1453Zhao, Xiangyu; Yang, Dawei; Zhang, Yahui; Wang, Baomin; Qu, Jingping
Terminal alkyne insertion into a thiolate-bridged dirhodium hydride complex derived from heterolytic cleavage of H<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 11112-11115
7122236 CIFC61 H67 B Cl4 Rh2 S2P -111.8737; 13.8883; 17.6708
88.3611; 76.5046; 80.2492
2792.4Zhao, Xiangyu; Yang, Dawei; Zhang, Yahui; Wang, Baomin; Qu, Jingping
Terminal alkyne insertion into a thiolate-bridged dirhodium hydride complex derived from heterolytic cleavage of H<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 11112-11115
7122237 CIFC52 H68 Ir4 S4P -110.7515; 15.4939; 16.0369
79.6888; 77.901; 87.8163
2569.9Zhao, Xiangyu; Yang, Dawei; Zhang, Yahui; Wang, Baomin; Qu, Jingping
Terminal alkyne insertion into a thiolate-bridged dirhodium hydride complex derived from heterolytic cleavage of H<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 11112-11115
7122238 CIFC13 Dy1.45 K6 N2 O63.75 Si W11P 1 21 110.6779; 20.1665; 15.5021
90; 103.346; 90
3248Arab Fashapoyeh, Marzieh; Mirzaei, Masoud; Eshtiagh-Hosseini, Hossein; Rajagopal, Ashwene; Lechner, Manuel; Liu, Rongji; Streb, Carsten
Photochemical and electrochemical hydrogen evolution reactivity of lanthanide-functionalized polyoxotungstates.
Chemical communications (Cambridge, England), 2018, 54, 10427-10430
7122239 CIFC14 K4 N2 O63.75 Pr2 Si W11P 1 21/n 111.4529; 30.495; 17.907
90; 101.994; 90
6117.6Arab Fashapoyeh, Marzieh; Mirzaei, Masoud; Eshtiagh-Hosseini, Hossein; Rajagopal, Ashwene; Lechner, Manuel; Liu, Rongji; Streb, Carsten
Photochemical and electrochemical hydrogen evolution reactivity of lanthanide-functionalized polyoxotungstates.
Chemical communications (Cambridge, England), 2018, 54, 10427-10430
7122240 CIFC14 K4.5 La2 N2 O63.5 Si W11P 1 21/n 111.5296; 30.702; 17.9958
90; 101.94; 90
6232.4Arab Fashapoyeh, Marzieh; Mirzaei, Masoud; Eshtiagh-Hosseini, Hossein; Rajagopal, Ashwene; Lechner, Manuel; Liu, Rongji; Streb, Carsten
Photochemical and electrochemical hydrogen evolution reactivity of lanthanide-functionalized polyoxotungstates.
Chemical communications (Cambridge, England), 2018, 54, 10427-10430
7122241 CIFC18 H18 Br Mn N2 O3 SP b c a16.5242; 9.503; 26.035
90; 90; 90
4088.3Das, Kalicharan; Mondal, Avijit; Srimani, Dipankar
Phosphine free Mn-complex catalysed dehydrogenative C-C and C-heteroatom bond formation: a sustainable approach to synthesize quinoxaline, pyrazine, benzothiazole and quinoline derivatives.
Chemical communications (Cambridge, England), 2018, 54, 10582-10585
7122242 CIFC17 H18 N2P 21 21 215.9134; 7.7193; 31.935
90; 90; 90
1457.7Baglai, Iaroslav; Leeman, Michel; Wurst, Klaus; Kaptein, Bernard; Kellogg, Richard M.; Noorduin, Willem L.
The Strecker reaction coupled to Viedma ripening: a simple route to highly hindered enantiomerically pure amino acids.
Chemical communications (Cambridge, England), 2018, 54, 10832-10834
7122243 CIFC18 H20 N2 OP 21 21 215.9479; 12.3654; 21.1408
90; 90; 90
1554.9Baglai, Iaroslav; Leeman, Michel; Wurst, Klaus; Kaptein, Bernard; Kellogg, Richard M.; Noorduin, Willem L.
The Strecker reaction coupled to Viedma ripening: a simple route to highly hindered enantiomerically pure amino acids.
Chemical communications (Cambridge, England), 2018, 54, 10832-10834
7122244 CIFC19 H21 F N2P 21 21 216.4325; 15.1525; 15.7404
90; 90; 90
1534.19Baglai, Iaroslav; Leeman, Michel; Wurst, Klaus; Kaptein, Bernard; Kellogg, Richard M.; Noorduin, Willem L.
The Strecker reaction coupled to Viedma ripening: a simple route to highly hindered enantiomerically pure amino acids.
Chemical communications (Cambridge, England), 2018, 54, 10832-10834
7122245 CIFC21 H22 O6C 1 2/c 156.225; 4.6615; 14.0454
90; 101.729; 90
3604.3Maguire, Casey J.; Chen, Zhi; Mocharla, Vani P.; Sriram, Madhavi; Strecker, Tracy E.; Hamel, Ernest; Zhou, Heling; Lopez, Ramona; Wang, Yifan; Mason, Ralph P.; Chaplin, David J.; Trawick, Mary Lynn; Pinney, Kevin G.
Synthesis of dihydronaphthalene analogues inspired by combretastatin A-4 and their biological evaluation as anticancer agents.
MedChemComm, 2018, 9, 1649-1662
7122246 CIFC20 H22 O5P 1 21/n 112.1996; 6.7253; 20.3499
90; 94.1342; 90
1665.28Maguire, Casey J.; Chen, Zhi; Mocharla, Vani P.; Sriram, Madhavi; Strecker, Tracy E.; Hamel, Ernest; Zhou, Heling; Lopez, Ramona; Wang, Yifan; Mason, Ralph P.; Chaplin, David J.; Trawick, Mary Lynn; Pinney, Kevin G.
Synthesis of dihydronaphthalene analogues inspired by combretastatin A-4 and their biological evaluation as anticancer agents.
MedChemComm, 2018, 9, 1649-1662
7122247 CIFC38 H50 SiP 21 21 2110.0265; 12.7798; 25.9558
90; 90; 90
3325.89Buffet, Jean-Charles; Turner, Zoë R; O'Hare, Dermot
Popcorn-shaped polyethylene synthesised using highly active supported permethylindenyl metallocene catalyst systems.
Chemical communications (Cambridge, England), 2018, 54, 10970-10973
7122248 CIFC44 H54 Cl2 Hf SiP -110.5667; 13.3377; 14.5723
94.961; 106.587; 94.008
1951.27Buffet, Jean-Charles; Turner, Zoë R; O'Hare, Dermot
Popcorn-shaped polyethylene synthesised using highly active supported permethylindenyl metallocene catalyst systems.
Chemical communications (Cambridge, England), 2018, 54, 10970-10973
7122249 CIFC85 H116 Cl4 Si2 Zr2P -113.8066; 15.6857; 19.9468
78.658; 76.378; 69.286
3896.2Buffet, Jean-Charles; Turner, Zoë R; O'Hare, Dermot
Popcorn-shaped polyethylene synthesised using highly active supported permethylindenyl metallocene catalyst systems.
Chemical communications (Cambridge, England), 2018, 54, 10970-10973
7122250 CIFC44 H54 Cl2 Si ZrP -110.5809; 13.3793; 14.5519
94.719; 106.544; 94.233
1957.84Buffet, Jean-Charles; Turner, Zoë R; O'Hare, Dermot
Popcorn-shaped polyethylene synthesised using highly active supported permethylindenyl metallocene catalyst systems.
Chemical communications (Cambridge, England), 2018, 54, 10970-10973
7122251 CIFC39 H50 Cl2 Si ZrP -111.1926; 12.9453; 13.5301
101.807; 108.951; 97.086
1776.35Buffet, Jean-Charles; Turner, Zoë R; O'Hare, Dermot
Popcorn-shaped polyethylene synthesised using highly active supported permethylindenyl metallocene catalyst systems.
Chemical communications (Cambridge, England), 2018, 54, 10970-10973
7122252 CIFC40 H52 Cl2 Si ZrP -115.4588; 16.8913; 19.2243
68.923; 84.784; 65.752
4261.2Buffet, Jean-Charles; Turner, Zoë R; O'Hare, Dermot
Popcorn-shaped polyethylene synthesised using highly active supported permethylindenyl metallocene catalyst systems.
Chemical communications (Cambridge, England), 2018, 54, 10970-10973
7122253 CIFC15 H21 Co Na O6R -3 c :H16.321; 16.321; 11.887
90; 90; 120
2742Li, Maofan; Yang, Kai; Liu, Jiajie; Hu, Xiaobing; Kong, Defei; Liu, Tongchao; Zhang, Mingjian; Pan, Feng
A heterobimetallic single-source precursor enabled layered oxide cathode for sodium-ion batteries.
Chemical communications (Cambridge, England), 2018, 54, 10714-10717
7122254 CIFC31 H34 O5P 1 21/c 116.8787; 21.4898; 15.3187
90; 91.028; 90
5555.5Shen, Zheng-Jia; Shi, Hao-Nan; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
Visible-light photocatalytic bicyclization of β-alkynyl propenones for accessing diastereoenriched syn-fluoren-9-ones.
Chemical communications (Cambridge, England), 2018, 54, 11542-11545
7122255 CIFC8 H9 Cl N2P -15.5421; 7.9319; 9.4933
82.068; 76.113; 80.977
397.91Richards, Josh E.; Hooper, Alexander J. J.; Bayfield, Oliver W.; Cockett, Martin C. R.; Dear, Gordon J.; Holmes, A. Jonathon; John, Richard O.; Mewis, Ryan E.; Pridmore, Natalie; Roberts, Andy D.; Whitwood, Adrian C.; Duckett, Simon B.
Using hyperpolarised NMR and DFT to rationalise the unexpected hydrogenation of quinazoline to 3,4-dihydroquinazoline.
Chemical communications (Cambridge, England), 2018, 54, 10375-10378
7122256 CIFC27 H34 O Si2P -19.2327; 9.5206; 17.1628
94.671; 104.862; 112.646
1318Zhou, Bo; Lu, Ailan; Shao, Changdong; Liang, Xinda; Zhang, Yanghui
Palladium-catalyzed sequential three-component reactions to access vinylsilanes.
Chemical communications (Cambridge, England), 2018, 54, 10598-10601
7122257 CIFC29 H28 O2 P2P -19.8918; 11.8798; 12.5977
117.242; 103.91; 98.15
1221.99Coles, N. T.; Mahon, M. F.; Webster, R. L.
1,1-Diphosphines and divinylphosphines via base catalyzed hydrophosphination.
Chemical communications (Cambridge, England), 2018, 54, 10443-10446
7122258 CIFC33 H28 O P2P 1 21/c 16.2505; 22.1889; 18.8017
90; 93.871; 90
2601.69Coles, N. T.; Mahon, M. F.; Webster, R. L.
1,1-Diphosphines and divinylphosphines via base catalyzed hydrophosphination.
Chemical communications (Cambridge, England), 2018, 54, 10443-10446
7122259 CIFC34 H31 N O P2C 1 c 117.0617; 10.7421; 17.4615
90; 117.433; 90
2840.44Coles, N. T.; Mahon, M. F.; Webster, R. L.
1,1-Diphosphines and divinylphosphines via base catalyzed hydrophosphination.
Chemical communications (Cambridge, England), 2018, 54, 10443-10446
7122260 CIFC41 H36 N2 P2P 1 21/n 110.1534; 18.1256; 18.7968
90; 99.266; 90
3414.16Coles, N. T.; Mahon, M. F.; Webster, R. L.
1,1-Diphosphines and divinylphosphines via base catalyzed hydrophosphination.
Chemical communications (Cambridge, England), 2018, 54, 10443-10446
7122261 CIFC22 H19 PP n a 2115.9327; 17.7483; 6.06371
90; 90; 90
1714.69Coles, N. T.; Mahon, M. F.; Webster, R. L.
1,1-Diphosphines and divinylphosphines via base catalyzed hydrophosphination.
Chemical communications (Cambridge, England), 2018, 54, 10443-10446
7122262 CIFC29 H22 Cl2 N2 O2P 21 21 217.1378; 16.682; 20.056
90; 90; 90
2388.1Niklas, Julie E.; Hardy, Emily E.; Gorden, Anne E. V.
Solid-state structural elucidation and electrochemical analysis of uranyl naphthylsalophen.
Chemical communications (Cambridge, England), 2018, 54, 11693-11696
7122263 CIFC60 H48 Cl8 N4 O10 U2P 1 21/n 115.4659; 19.3294; 22.2346
90; 106.655; 90
6368.1Niklas, Julie E.; Hardy, Emily E.; Gorden, Anne E. V.
Solid-state structural elucidation and electrochemical analysis of uranyl naphthylsalophen.
Chemical communications (Cambridge, England), 2018, 54, 11693-11696
7122264 CIFC8 H9 N9 O4P 1 21/n 17.7715; 29.4724; 11.6745
90; 96.989; 90
2654.1Tang, Yongxing; He, Chunlin; Imler, Gregory H.; Parrish, Damon A.; Shreeve, Jean'ne M.
A C-C bonded 5,6-fused bicyclic energetic molecule: exploring an advanced energetic compound with improved performance.
Chemical communications (Cambridge, England), 2018, 54, 10566-10569
7122265 CIFC12 H18 N16 O11P b c n10.847; 14.2197; 14.3756
90; 90; 90
2217.31Tang, Yongxing; He, Chunlin; Imler, Gregory H.; Parrish, Damon A.; Shreeve, Jean'ne M.
A C-C bonded 5,6-fused bicyclic energetic molecule: exploring an advanced energetic compound with improved performance.
Chemical communications (Cambridge, England), 2018, 54, 10566-10569
7122266 CIFC13 H15 N15 O12C 1 c 18.8353; 18.9345; 13.781
90; 90.062; 90
2305.45Tang, Yongxing; He, Chunlin; Imler, Gregory H.; Parrish, Damon A.; Shreeve, Jean'ne M.
A C-C bonded 5,6-fused bicyclic energetic molecule: exploring an advanced energetic compound with improved performance.
Chemical communications (Cambridge, England), 2018, 54, 10566-10569
7122267 CIFC32 H29 F3 N4 O3P 1 21 110.5588; 11.2682; 12.194
90; 90.698; 90
1450.72Li, Shi-Wu; Kang, Qiang
Catalytic asymmetric synthesis of diphenylbutazone analogues.
Chemical communications (Cambridge, England), 2018, 54, 10479-10482
7122268 CIFC49 H27 Eu F18 O8 P2P 1 21/c 123.1941; 13.4114; 16.7226
90; 91.6148; 90
5199.8Hasegawa, Yasuchika; Miura, Yui; Kitagawa, Yuichi; Wada, Satoshi; Nakanishi, Takayuki; Fushimi, Koji; Seki, Tomohiro; Ito, Hajime; Iwasa, Takeshi; Taketsugu, Tetsuya; Gon, Masayuki; Tanaka, Kazuo; Chujo, Yoshiki; Hattori, Shingo; Karasawa, Masanobu; Ishii, Kazuyuki
Spiral Eu(iii) coordination polymers with circularly polarized luminescence.
Chemical communications (Cambridge, England), 2018, 54, 10695-10697
7122269 CIFC98 H54 Eu2 F36 O16 P4P 1 21/n 112.5432; 30.3644; 12.9212
90; 90.378; 90
4921.1Hasegawa, Yasuchika; Miura, Yui; Kitagawa, Yuichi; Wada, Satoshi; Nakanishi, Takayuki; Fushimi, Koji; Seki, Tomohiro; Ito, Hajime; Iwasa, Takeshi; Taketsugu, Tetsuya; Gon, Masayuki; Tanaka, Kazuo; Chujo, Yoshiki; Hattori, Shingo; Karasawa, Masanobu; Ishii, Kazuyuki
Spiral Eu(iii) coordination polymers with circularly polarized luminescence.
Chemical communications (Cambridge, England), 2018, 54, 10695-10697
7122270 CIFC14 H11 N3P 1 21/c 110.5028; 4.8074; 23.494
90; 98.523; 90
1173.1An, Zhenyu; Jiang, Yong; Guan, Xin; Yan, Rulong
Copper-catalyzed tandem aerobic oxidative cyclization for the synthesis of 4-cyanoalkylpyrrolo[1,2-a]quinoxalines from 1-(2-aminophenyl)pyrroles and cyclobutanone oxime esters.
Chemical communications (Cambridge, England), 2018, 54, 10738-10741
7122271 CIFC7 H8 Cu4 I4 N5P n n a14.8153; 14.334; 11.4471
90; 90; 90
2430.9Zhao, Nian; Yang, Lun; Pan, Qiyun; Han, Juanjuan; Li, Xiang; Liu, Meifeng; Xie, Bo; Wang, Yu; Wang, Xiuzhang; Zhu, Guangshan
Organic amines as templates: pore imprints with exactly size matching in a series of metal-organic frameworks
Chemical Communications, 2018
7122272 CIFC40 H56 Cu16 I16 N20 OP m m n17.84; 31; 8.4707
90; 90; 90
4684.6Zhao, Nian; Yang, Lun; Pan, Qiyun; Han, Juanjuan; Li, Xiang; Liu, Meifeng; Xie, Bo; Wang, Yu; Wang, Xiuzhang; Zhu, Guangshan
Organic amines as templates: pore imprints with exactly size matching in a series of metal-organic frameworks
Chemical Communications, 2018
7122273 CIFC14 H23 Cu4 I4 N5P 1 21/n 111.3646; 14.8491; 14.7153
90; 98.85; 90
2453.7Zhao, Nian; Yang, Lun; Pan, Qiyun; Han, Juanjuan; Li, Xiang; Liu, Meifeng; Xie, Bo; Wang, Yu; Wang, Xiuzhang; Zhu, Guangshan
Organic amines as templates: pore imprints with exactly size matching in a series of metal-organic frameworks
Chemical Communications, 2018
7122274 CIFC18 H18 Cl2 F6 Ge2 N4 O6 S2P -18.3092; 13.8633; 13.868
64.284; 80.304; 73.576
1378.6Majumdar, Moumita; Raut, Ravindra K.; Sahoo, Padmini; Kumar, Vikas
Bis(chlorogermyliumylidene) and its significant role in elusive reductive cyclization.
Chemical communications (Cambridge, England), 2018, 54, 10839-10842
7122275 CIFC18 H22 F6 N4 O6 S2P 1 21/n 111.8024; 17.854; 12.5096
90; 113.836; 90
2411.2Majumdar, Moumita; Raut, Ravindra K.; Sahoo, Padmini; Kumar, Vikas
Bis(chlorogermyliumylidene) and its significant role in elusive reductive cyclization.
Chemical communications (Cambridge, England), 2018, 54, 10839-10842
7122276 CIFC18 H20 F6 Ge N4 O6 S2P 1 21/c 120.604; 13.372; 20.162
90; 118.5; 90
4882Majumdar, Moumita; Raut, Ravindra K.; Sahoo, Padmini; Kumar, Vikas
Bis(chlorogermyliumylidene) and its significant role in elusive reductive cyclization.
Chemical communications (Cambridge, England), 2018, 54, 10839-10842
7122277 CIFC40 H66 K2 N4 O12P 1 21 123.5972; 14.6704; 26.824
90; 104.411; 90
8993.8Majumdar, Moumita; Raut, Ravindra K.; Sahoo, Padmini; Kumar, Vikas
Bis(chlorogermyliumylidene) and its significant role in elusive reductive cyclization.
Chemical communications (Cambridge, England), 2018, 54, 10839-10842
7122278 CIFC10 H8.67 F4 I N O2.67P 1 21 118.049; 5.593; 18.384
90; 92.36; 90
1854.3Bergamaschi, Greta; Lascialfari, Luisa; Pizzi, Andrea; Martinez Espinoza, Maria Isabel; Demitri, Nicola; Milani, Alberto; Gori, Alessandro; Metrangolo, Pierangelo
A halogen bond-donor amino acid for organocatalysis in water.
Chemical communications (Cambridge, England), 2018, 54, 10718-10721
7122279 CIFC30 H22 F8 I4 N2 O2P 1 21/c 116.6735; 7.2738; 29.148
90; 96.23; 90
3514.18Bergamaschi, Greta; Lascialfari, Luisa; Pizzi, Andrea; Martinez Espinoza, Maria Isabel; Demitri, Nicola; Milani, Alberto; Gori, Alessandro; Metrangolo, Pierangelo
A halogen bond-donor amino acid for organocatalysis in water.
Chemical communications (Cambridge, England), 2018, 54, 10718-10721
7122280 CIFC78 H112 O6 Se2 UP 1 21 110.6644; 20.483; 17.7085
90; 104.649; 90
3742.5Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Behrle, Andrew C.; Vilanova, Sean P.; Kelley, Stephen P.; Lukens, Wayne W.; Walensky, Justin R.
Structure and properties of [(4,6-<sup>t</sup>Bu<sub>2</sub>C<sub>6</sub>H<sub>2</sub>O)<sub>2</sub>Se]<sub>2</sub>An(THF)<sub>2</sub>, An = U, Np, and their reaction with p-benzoquinone.
Chemical communications (Cambridge, England), 2018, 54, 10435-10438
7122281 CIFC78 H112 Np O6 Se2P 1 21 117.578; 20.5093; 21.1111
90; 104.991; 90
7351.8Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Behrle, Andrew C.; Vilanova, Sean P.; Kelley, Stephen P.; Lukens, Wayne W.; Walensky, Justin R.
Structure and properties of [(4,6-<sup>t</sup>Bu<sub>2</sub>C<sub>6</sub>H<sub>2</sub>O)<sub>2</sub>Se]<sub>2</sub>An(THF)<sub>2</sub>, An = U, Np, and their reaction with p-benzoquinone.
Chemical communications (Cambridge, England), 2018, 54, 10435-10438
7122282 CIFC154 H212 O12 Se4 U2P -114.3383; 14.4734; 21.5834
102.642; 98.558; 114.946
3812.7Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Behrle, Andrew C.; Vilanova, Sean P.; Kelley, Stephen P.; Lukens, Wayne W.; Walensky, Justin R.
Structure and properties of [(4,6-<sup>t</sup>Bu<sub>2</sub>C<sub>6</sub>H<sub>2</sub>O)<sub>2</sub>Se]<sub>2</sub>An(THF)<sub>2</sub>, An = U, Np, and their reaction with p-benzoquinone.
Chemical communications (Cambridge, England), 2018, 54, 10435-10438
7122283 CIFC37 H76 N6 Si6 UP 1 21/c 118.57; 11.24; 28.43
90; 122.98; 90
4978Ghatak, Tapas; Makarov, Konstantin; Fridman, Natalia; Eisen, Moris S.
Catalytic regeneration of a Th-H bond from a Th-O bond through a mild and chemoselective carbonyl hydroboration.
Chemical communications (Cambridge, England), 2018, 54, 11001-11004
7122284 CIFC37 H76 N6 Si6 ThP 1 21/c 118.619; 11.246; 28.548
90; 123.219; 90
5001Ghatak, Tapas; Makarov, Konstantin; Fridman, Natalia; Eisen, Moris S.
Catalytic regeneration of a Th-H bond from a Th-O bond through a mild and chemoselective carbonyl hydroboration.
Chemical communications (Cambridge, England), 2018, 54, 11001-11004
7122285 CIFC20 H18 N2 O3P 1 21/c 113.2268; 8.5916; 15.6448
90; 108.955; 90
1681.5Liao, Gang; Chen, Hao-Ming; Shi, Bing-Feng
Synthesis of phthalic acid derivatives via Pd-catalyzed alkoxycarbonylation of aromatic C-H bonds with alkyl chloroformates.
Chemical communications (Cambridge, England), 2018, 54, 10859-10862
7122286 CIFC10 H5 F3 N2 O3P 1 21/c 110.7939; 13.928; 6.9529
90; 92.479; 90
1044.3Luo, Beibei; Weng, Zhiqiang
Elemental tellurium mediated synthesis of 2-(trifluoromethyl)oxazoles using trifluoroacetic anhydride as reagent.
Chemical communications (Cambridge, England), 2018, 54, 10750-10753
7122287 CIFC22 H35 F14 N O2 P4 W3P b c a16.7303; 17.878; 24.095
90; 90; 90
7206.9Levason, William; Monzittu, Francesco M.; Reid, Gillian; Zhang, Wenjian
Neutral and cationic tungsten(vi) fluoride complexes with tertiary phosphine and arsine coordination.
Chemical communications (Cambridge, England), 2018, 54, 11681-11684
7122288 CIFC20 H32 As4 F12 W2F d d d :213.1003; 21.3132; 21.3804
90; 90; 90
5969.6Levason, William; Monzittu, Francesco M.; Reid, Gillian; Zhang, Wenjian
Neutral and cationic tungsten(vi) fluoride complexes with tertiary phosphine and arsine coordination.
Chemical communications (Cambridge, England), 2018, 54, 11681-11684
7122289 CIFC92 H69 F24 N7 P4P 1 21/c 112.8107; 27.467; 25.2827
90; 113.746; 90
8143.1Jacquot de Rouville, Henri-Pierre; Zorn, Nathalie; Leize-Wagner, Emmanuelle; Heitz, Valérie
Entwined dimer formation from self-complementary bis-acridiniums.
Chemical communications (Cambridge, England), 2018, 54, 10966-10969
7122290 CIFC40 H43 Cd N5 O12P 21 21 213.8223; 25.3271; 11.6674
90; 90; 90
4084.5Zhang, Qingfu; Lei, Mingyuan; Kong, Fang; Yang, Yan
A water-stable homochiral luminescent MOF constructed from an achiral acylamide-containing dicarboxylate ligand for enantioselective sensing of penicillamine.
Chemical communications (Cambridge, England), 2018, 54, 10901-10904
7122291 CIFC40 H43 Cd N5 O12P 21 21 213.8223; 25.3271; 11.6674
90; 90; 90
4084.5Wang, Hongyu; Man, Yunquan; Wang, Kaiye; Wan, Xiuyan; Tong, Lili; Li, Na; Tang, Bo
Hydrogen bond directed aerobic oxidation of amines via photoredox catalysis.
Chemical communications (Cambridge, England), 2018, 54, 10989-10992
7122292 CIFC29 H33 Cl N2 O2 OsP 1 21/n 111.0472; 19.7668; 12.2934
90; 113.161; 90
2468.1Ortega, Enrique; Yellol, Jyoti G.; Rothemund, Matthias; Ballester, Francisco J.; Rodríguez, Venancio; Yellol, Gorakh; Janiak, Christoph; Schobert, Rainer; Ruiz, José
A new C,N-cyclometalated osmium(ii) arene anticancer scaffold with a handle for functionalization and antioxidative properties.
Chemical communications (Cambridge, England), 2018, 54, 11120-11123
7122293 CIFC41 H45 Cl N2 O4 OsP -110.9559; 10.9932; 16.2594
105.966; 102.536; 103.578
1745.05Ortega, Enrique; Yellol, Jyoti G.; Rothemund, Matthias; Ballester, Francisco J.; Rodríguez, Venancio; Yellol, Gorakh; Janiak, Christoph; Schobert, Rainer; Ruiz, José
A new C,N-cyclometalated osmium(ii) arene anticancer scaffold with a handle for functionalization and antioxidative properties.
Chemical communications (Cambridge, England), 2018, 54, 11120-11123
7122294 CIFC17 H16 N2 O2P 1 21/n 111.026; 7.7415; 16.838
90; 96.29; 90
1428.6Iyer, Akila; Ahuja, Sapna; Jockusch, Steffen; Ugrinov, Angel; Sivaguru, Jayaraman
Conjugate addition from the excited state.
Chemical communications (Cambridge, England), 2018, 54, 11021-11024
7122295 CIFC19 H18 N3 O2P 1 21/c 114.7749; 12.4865; 8.8566
90; 93.211; 90
1631.36Iyer, Akila; Ahuja, Sapna; Jockusch, Steffen; Ugrinov, Angel; Sivaguru, Jayaraman
Conjugate addition from the excited state.
Chemical communications (Cambridge, England), 2018, 54, 11021-11024
7122296 CIFC16 H18 N2 O3P 1 21/n 19.4606; 12.6354; 12.7086
90; 105.269; 90
1465.54Iyer, Akila; Ahuja, Sapna; Jockusch, Steffen; Ugrinov, Angel; Sivaguru, Jayaraman
Conjugate addition from the excited state.
Chemical communications (Cambridge, England), 2018, 54, 11021-11024
7122297 CIFC19 H15 Cl3 N2 O3P 1 21/n 18.0186; 14.7308; 16.1335
90; 91.803; 90
1904.75Iyer, Akila; Ahuja, Sapna; Jockusch, Steffen; Ugrinov, Angel; Sivaguru, Jayaraman
Conjugate addition from the excited state.
Chemical communications (Cambridge, England), 2018, 54, 11021-11024
7122298 CIFC25 H23 N3 O2 SP -19.4533; 10.264; 11.7955
73.208; 79.209; 78.894
1064.58Iyer, Akila; Ahuja, Sapna; Jockusch, Steffen; Ugrinov, Angel; Sivaguru, Jayaraman
Conjugate addition from the excited state.
Chemical communications (Cambridge, England), 2018, 54, 11021-11024
7122299 CIFC50 H46 N6 O4 S2P 1 21/n 18.6439; 12.4156; 40.7123
90; 95.515; 90
4349Iyer, Akila; Ahuja, Sapna; Jockusch, Steffen; Ugrinov, Angel; Sivaguru, Jayaraman
Conjugate addition from the excited state.
Chemical communications (Cambridge, England), 2018, 54, 11021-11024
7122300 CIFC12 H15 N2 O2P 1 21/c 19.456; 10.7425; 11.1944
90; 99.483; 90
1121.6Iyer, Akila; Ahuja, Sapna; Jockusch, Steffen; Ugrinov, Angel; Sivaguru, Jayaraman
Conjugate addition from the excited state.
Chemical communications (Cambridge, England), 2018, 54, 11021-11024
7122301 CIFC19 H16 N2 O3P -18.2022; 8.6904; 12.6628
87.88; 75.115; 64.061
781.49Iyer, Akila; Ahuja, Sapna; Jockusch, Steffen; Ugrinov, Angel; Sivaguru, Jayaraman
Conjugate addition from the excited state.
Chemical communications (Cambridge, England), 2018, 54, 11021-11024
7122302 CIFC18 H16 N2 O4 SP 1 21/n 15.1019; 33.051; 9.41
90; 92.525; 90
1585.2Tsai, Meng-Han; Wang, Cheng-Yu; Kulandai Raj, Antony Sekar; Liu, Rai-Shung
Gold-catalyzed annulations of N-aryl ynamides with benzisoxazoles to construct 6H-indolo[2,3-b]quinoline cores.
Chemical communications (Cambridge, England), 2018, 54, 10866-10869
7122303 CIFC28 H28 Ce Fe N O3P n m a17.6116; 13.4206; 10.1455
90; 90; 90
2398Burns, Corey P.; Yang, Xin; Sung, Siyoung; Wofford, Joshua D.; Bhuvanesh, Nattamai S.; Hall, Michael B.; Nippe, Michael
Towards understanding of lanthanide-transition metal bonding: investigations of the first Ce-Fe bonded complex.
Chemical communications (Cambridge, England), 2018, 54, 10893-10896
7122304 CIFC22 H23 Ce F3 N O4 SP n a 2114.8353; 9.9906; 15.3663
90; 90; 90
2277.49Burns, Corey P.; Yang, Xin; Sung, Siyoung; Wofford, Joshua D.; Bhuvanesh, Nattamai S.; Hall, Michael B.; Nippe, Michael
Towards understanding of lanthanide-transition metal bonding: investigations of the first Ce-Fe bonded complex.
Chemical communications (Cambridge, England), 2018, 54, 10893-10896
7122305 CIFC36 H30 Ce2 F6 N2 O6 S2P 1 21/n 19.9043; 9.2078; 20.3459
90; 102.969; 90
1808.15Burns, Corey P.; Yang, Xin; Sung, Siyoung; Wofford, Joshua D.; Bhuvanesh, Nattamai S.; Hall, Michael B.; Nippe, Michael
Towards understanding of lanthanide-transition metal bonding: investigations of the first Ce-Fe bonded complex.
Chemical communications (Cambridge, England), 2018, 54, 10893-10896
7122306 CIFC44 H45.98 N10P 1 21/n 112.5203; 19.8938; 16.988
90; 102.163; 90
4136.3Kim, Hyeongcheol; Hong, Kyeong-Im; Lee, Jeong Heon; Kang, Philjae; Choi, Moon-Gun; Jang, Woo-Dong
Triazole-bearing calixpyrroles: strong halide binding affinities through multiple N-H and C-H hydrogen bonds.
Chemical communications (Cambridge, England), 2018, 54, 10863-10865
7122307 CIFC44 H46 N10P 1 21/c 112.546; 27.351; 11.169
90; 93.95; 90
3823.5Kim, Hyeongcheol; Hong, Kyeong-Im; Lee, Jeong Heon; Kang, Philjae; Choi, Moon-Gun; Jang, Woo-Dong
Triazole-bearing calixpyrroles: strong halide binding affinities through multiple N-H and C-H hydrogen bonds.
Chemical communications (Cambridge, England), 2018, 54, 10863-10865
7122308 CIFC30 H37 Dy Fe N10 O8 S2P -112.5138; 13.4439; 13.7508
111.405; 112.613; 98.389
1874.72Chen, Wen-Bin; Chen, Yan-Cong; Huang, Guo-Zhang; Liu, Jun-Liang; Jia, Jian-Hua; Tong, Ming-Liang
Cyclic OFF/Part/ON switching of single-molecule magnet behaviours via multistep single-crystal-to-single-crystal transformation between discrete Fe(ii)-Dy(iii) complexes.
Chemical communications (Cambridge, England), 2018, 54, 10886-10889
7122309 CIFC30 H35 Dy Fe N10 O7 S2P -112.617; 13.314; 13.742
111.14; 112.417; 98.797
1874Chen, Wen-Bin; Chen, Yan-Cong; Huang, Guo-Zhang; Liu, Jun-Liang; Jia, Jian-Hua; Tong, Ming-Liang
Cyclic OFF/Part/ON switching of single-molecule magnet behaviours via multistep single-crystal-to-single-crystal transformation between discrete Fe(ii)-Dy(iii) complexes.
Chemical communications (Cambridge, England), 2018, 54, 10886-10889
7122310 CIFC60 H58 Dy2 Fe2 N20 O8 S4P -114.4632; 15.3659; 15.8216
89.095; 83.157; 85.417
3479.9Chen, Wen-Bin; Chen, Yan-Cong; Huang, Guo-Zhang; Liu, Jun-Liang; Jia, Jian-Hua; Tong, Ming-Liang
Cyclic OFF/Part/ON switching of single-molecule magnet behaviours via multistep single-crystal-to-single-crystal transformation between discrete Fe(ii)-Dy(iii) complexes.
Chemical communications (Cambridge, England), 2018, 54, 10886-10889
7122311 CIFC16 H28 Cl2 N4 O4 ZnC 1 2/c 117.6678; 6.9371; 18.0628
90; 91.515; 90
2213.06Shemchuk, Oleksii; Song, Lixing; Robeyns, Koen; Braga, Dario; Grepioni, Fabrizia; Leyssens, Tom
Solid-state chiral resolution mediated by stoichiometry: crystallizing etiracetam with ZnCl<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 10890-10892
7122312 CIFC16 H28 Cl4 N4 O4 Zn2P 1 21 16.3692; 11.6771; 17.1077
90; 98.496; 90
1258.4Shemchuk, Oleksii; Song, Lixing; Robeyns, Koen; Braga, Dario; Grepioni, Fabrizia; Leyssens, Tom
Solid-state chiral resolution mediated by stoichiometry: crystallizing etiracetam with ZnCl<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 10890-10892
7122313 CIFC11 H12 Cl N2 OP 1 21/c 111.8906; 8.8166; 11.2785
90; 104.338; 90
1145.5Yuan, Zaifeng; Zhu, Chunyu; Ma, Zhixian; Xia, Chengfeng
Copper-catalyzed amination of an α-C(sp<sup>3</sup>)-H bond in inactivated ethers to synthesize α-aminonitriles.
Chemical communications (Cambridge, England), 2018, 54, 11033-11036
7122314 CIFC25 H25 N O5P 21 21 218.139; 15.8253; 17.185
90; 90; 90
2213.5Bedekar, Ashutosh; Khanvilkar, Aditya N.
Optically pure 2-(quinolin-8-yloxy)cyclohexan-1-ol as a practical agent for molecular recognition by NMR and fluorescence spectroscopy
Chemical Communications, 2018
7122315 CIFC23 H25 N O5I 1 2 110.7133; 12.3487; 15.4466
90; 98.908; 90
2018.9Bedekar, Ashutosh; Khanvilkar, Aditya N.
Optically pure 2-(quinolin-8-yloxy)cyclohexan-1-ol as a practical agent for molecular recognition by NMR and fluorescence spectroscopy
Chemical Communications, 2018
7122316 CIFC15 H18 N O2.5C 2 2 218.3581; 22.439; 14.0407
90; 90; 90
2633.3Bedekar, Ashutosh; Khanvilkar, Aditya N.
Optically pure 2-(quinolin-8-yloxy)cyclohexan-1-ol as a practical agent for molecular recognition by NMR and fluorescence spectroscopy
Chemical Communications, 2018
7122317 CIFC15 H18 N O2.5C 2 2 218.4035; 22.609; 14.0695
90; 90; 90
2673.1Bedekar, Ashutosh; Khanvilkar, Aditya N.
Optically pure 2-(quinolin-8-yloxy)cyclohexan-1-ol as a practical agent for molecular recognition by NMR and fluorescence spectroscopy
Chemical Communications, 2018
7122318 CIFC21 H23 Au F3 N O2P -18.7448; 9.6069; 12.4327
94.949; 95.354; 104.902
998.32Holmsen, Marte Sofie Martinsen; Nova, Ainara; Hylland, Knut; Wragg, David S.; Øien-Ødegaard, Sigurd; Heyn, Richard H.; Tilset, Mats
Synthesis of a (N,C,C) Au(iii) pincer complex via C<sub>sp<sup>3</sup></sub>-H bond activation: increasing catalyst robustness by rational catalyst design.
Chemical communications (Cambridge, England), 2018, 54, 11104-11107
7122319 CIFC24 H15 F3 I3 PP -19.164; 10.9788; 13.5101
87.947; 72.521; 76.29
1258.6Xu, Yijue; Huang, Jasmine; Gabidullin, Bulat; Bryce, David L.
A rare example of a phosphine as a halogen bond acceptor.
Chemical communications (Cambridge, England), 2018, 54, 11041-11043
7122320 CIFC24 H15 F3 I3 O PP 1 21/c 114.23; 10.1079; 17.79
90; 105.164; 90
2469.7Xu, Yijue; Huang, Jasmine; Gabidullin, Bulat; Bryce, David L.
A rare example of a phosphine as a halogen bond acceptor.
Chemical communications (Cambridge, England), 2018, 54, 11041-11043
7122321 CIFC99 H111P -112.352; 14.495; 24.02
98.958; 92.578; 111.662
3923.5Shimizu, Yuki; Shoji, Yoshiaki; Hashizume, Daisuke; Nagata, Yuuya; Fukushima, Takanori
Sensing the chirality of various organic solvents by helically arranged π-blades.
Chemical communications (Cambridge, England), 2018, 54, 12314-12317
7122322 CIFC139 H145 Cl3 O3 Si3P 21 21 2115.27587; 24.1176; 37.3535
90; 90; 90
13761.7Shimizu, Yuki; Shoji, Yoshiaki; Hashizume, Daisuke; Nagata, Yuuya; Fukushima, Takanori
Sensing the chirality of various organic solvents by helically arranged π-blades.
Chemical communications (Cambridge, England), 2018, 54, 12314-12317
7122323 CIFC20 H21 N O3 SP 1 21/c 113.5862; 9.993; 13.1956
90; 94.489; 90
1786.03Han, Xiang-Lei; Liu, Xu-Ge; Lin, E.; Chen, Yunyun; Chen, Zhuangzhong; Wang, Honggen; Li, Qingjiang
Cp*Co(iii)-Catalyzed oxidative [5+2] annulation: regioselective synthesis of 2-aminobenzoxepines via C-H/O-H functionalization of 2-vinylphenols with ynamides.
Chemical communications (Cambridge, England), 2018, 54, 11562-11565
7122324 CIFC15 H17 Cl N2 O5 SP 1 21/c 18.5374; 10.4577; 18.7809
90; 97.412; 90
1662.78Han, Xiang-Lei; Liu, Xu-Ge; Lin, E.; Chen, Yunyun; Chen, Zhuangzhong; Wang, Honggen; Li, Qingjiang
Cp*Co(iii)-Catalyzed oxidative [5+2] annulation: regioselective synthesis of 2-aminobenzoxepines via C-H/O-H functionalization of 2-vinylphenols with ynamides.
Chemical communications (Cambridge, England), 2018, 54, 11562-11565
7122325 CIFC13 H17 N5C 1 2/c 120.97; 7.2564; 17.3888
90; 106.224; 90
2540.6Li, Lian-Hua; Niu, Zhi-Jie; Li, Ying-Xiu; Liang, Yong-Min
Transition-metal-free multinitrogenation of amides by C-C bond cleavage: a new approach to tetrazoles.
Chemical communications (Cambridge, England), 2018, 54, 11148-11151
7122326 CIFC11 H13 N5P b c a10.2177; 11.0976; 19.154
90; 90; 90
2171.9Li, Lian-Hua; Niu, Zhi-Jie; Li, Ying-Xiu; Liang, Yong-Min
Transition-metal-free multinitrogenation of amides by C-C bond cleavage: a new approach to tetrazoles.
Chemical communications (Cambridge, England), 2018, 54, 11148-11151
7122327 CIFC13 H10 N4P 1 21/n 110.7182; 7.0388; 14.6427
90; 90.42; 90
1104.66Li, Lian-Hua; Niu, Zhi-Jie; Li, Ying-Xiu; Liang, Yong-Min
Transition-metal-free multinitrogenation of amides by C-C bond cleavage: a new approach to tetrazoles.
Chemical communications (Cambridge, England), 2018, 54, 11148-11151
7122328 CIFC11 H19 N5P -16.8335; 9.1979; 10.0075
94.814; 103.101; 96.922
604.13Li, Lian-Hua; Niu, Zhi-Jie; Li, Ying-Xiu; Liang, Yong-Min
Transition-metal-free multinitrogenation of amides by C-C bond cleavage: a new approach to tetrazoles.
Chemical communications (Cambridge, England), 2018, 54, 11148-11151
7122329 CIFC13 H15 N5P 1 21/c 112.0745; 9.2802; 11.0512
90; 96.656; 90
1229.98Li, Lian-Hua; Niu, Zhi-Jie; Li, Ying-Xiu; Liang, Yong-Min
Transition-metal-free multinitrogenation of amides by C-C bond cleavage: a new approach to tetrazoles.
Chemical communications (Cambridge, England), 2018, 54, 11148-11151
7122330 CIFC34 H40 N2 O6P 1 21/n 17.4062; 15.555; 27.3276
90; 96.466; 90
3128.21Núñez-Villanueva, Diego; Jinks, Michael A.; Gómez Magenti, Jorge; Hunter, Christopher A.
Ultrasound-induced gelation of a giant macrocycle.
Chemical communications (Cambridge, England), 2018, 54, 10874-10877
7122331 CIFC56 H74 N4 O2 Si2 YbP 1 21/c 115.0291; 19.9303; 18.7135
90; 110.869; 90
5237.6Schuhknecht, Danny; Truong, Khai-Nghi; Spaniol, Thomas P.; Maron, Laurent; Okuda, Jun
Molecular hydrides of divalent ytterbium supported by a macrocyclic ligand: synthesis, structure and olefin hydrofunctionalization catalysis.
Chemical communications (Cambridge, England), 2018, 54, 11280-11283
7122332 CIFC63 H95 B N4 O3 YbP -112.394; 13.0452; 19.0172
102.769; 92.103; 94.209
2986.2Schuhknecht, Danny; Truong, Khai-Nghi; Spaniol, Thomas P.; Maron, Laurent; Okuda, Jun
Molecular hydrides of divalent ytterbium supported by a macrocyclic ligand: synthesis, structure and olefin hydrofunctionalization catalysis.
Chemical communications (Cambridge, England), 2018, 54, 11280-11283
7122333 CIFC204 H316 B4 N16 O7 Yb4P 1 21/c 122.3771; 12.7674; 35.4193
90; 102.023; 90
9897.2Schuhknecht, Danny; Truong, Khai-Nghi; Spaniol, Thomas P.; Maron, Laurent; Okuda, Jun
Molecular hydrides of divalent ytterbium supported by a macrocyclic ligand: synthesis, structure and olefin hydrofunctionalization catalysis.
Chemical communications (Cambridge, England), 2018, 54, 11280-11283
7122334 CIFC57 H106 N11 UP -112.3599; 12.6609; 21.029
88.8639; 77.3174; 79.3741
3154.7Settineri, Nicholas S.; Shiau, Angela A.; Arnold, John
Two-electron oxidation of a homoleptic U(iii) guanidinate complex by diphenyldiazomethane.
Chemical communications (Cambridge, England), 2018, 54, 10913-10916
7122335 CIFC39 H84 N12 UP -113.0981; 13.2024; 17.7597
96.101; 103.866; 119.638
2497.88Settineri, Nicholas S.; Shiau, Angela A.; Arnold, John
Two-electron oxidation of a homoleptic U(iii) guanidinate complex by diphenyldiazomethane.
Chemical communications (Cambridge, England), 2018, 54, 10913-10916
7122336 CIFC39 H84 N9 UP 1 21/c 113.289; 19.9565; 18.7099
90; 110.091; 90
4660Settineri, Nicholas S.; Shiau, Angela A.; Arnold, John
Two-electron oxidation of a homoleptic U(iii) guanidinate complex by diphenyldiazomethane.
Chemical communications (Cambridge, England), 2018, 54, 10913-10916
7122337 CIFC48 H105 Cl N9 UP 1 21/c 111.6454; 37.8373; 13.3431
90; 109.795; 90
5532Settineri, Nicholas S.; Shiau, Angela A.; Arnold, John
Two-electron oxidation of a homoleptic U(iii) guanidinate complex by diphenyldiazomethane.
Chemical communications (Cambridge, England), 2018, 54, 10913-10916
7122338 CIFC49 H98 N10 UC 1 2/c 139.246; 14.3692; 19.965
90; 109.062; 90
10642Settineri, Nicholas S.; Shiau, Angela A.; Arnold, John
Two-electron oxidation of a homoleptic U(iii) guanidinate complex by diphenyldiazomethane.
Chemical communications (Cambridge, England), 2018, 54, 10913-10916
7122339 CIFC39 H84 N9 O UP 1 21/c 119.9133; 12.7998; 19.1902
90; 109.856; 90
4600.5Settineri, Nicholas S.; Shiau, Angela A.; Arnold, John
Two-electron oxidation of a homoleptic U(iii) guanidinate complex by diphenyldiazomethane.
Chemical communications (Cambridge, England), 2018, 54, 10913-10916
7122340 CIFC62 H46 F12 N8 O P2 S2 ZnP 1 21/n 121.356; 13.467; 22.171
90; 110.931; 90
5956Shen, Yu; Shao, Tao; Fang, Bin; Du, Wei; Zhang, Mingzhu; Liu, Jiejie; Liu, Tianyan; Tian, Xiaohe; Zhang, Qiong; Wang, Aidong; Yang, Jiaxiang; Wu, Jieying; Tian, Yupeng
Visualization of mitochondrial DNA in living cells with super-resolution microscopy using thiophene-based terpyridine Zn(ii) complexes.
Chemical communications (Cambridge, England), 2018, 54, 11288-11291
7122341 CIFC14 H14 Cl2 N2 O2P -14.4516; 6.7274; 11.4945
86.957; 83.772; 77.68
334.16Kolesnichenko, Igor V.; Escamilla, P. Rogelio; Michael, Jason A.; Lynch, Vincent M.; Vanden Bout, David A.; Anslyn, Eric V.
Hydrogen peroxide production via a redox reaction of N,N'-dimethyl-2,6-diaza-9,10-anthraquinonediium by addition of bisulfite.
Chemical communications (Cambridge, England), 2018, 54, 11204-11207
7122342 CIFC32 H23 N O2P b c a12.2322; 15.6754; 24.857
90; 90; 90
4766.2Kong, Lingkai; Wang, Mengdan; Wang, Ye; Song, Bo; Yang, Yajie; Yao, Qiyi; Li, Yanzhong
Merging base-promoted C-C bond cleavage and iron-catalyzed skeletal rearrangement involving C-C/C-H bond activation: synthesis of highly functionalized carbazoles.
Chemical communications (Cambridge, England), 2018, 54, 11009-11012
7122343 CIFC32 H23 N O2P 1 21/c 112.3437; 8.8269; 21.695
90; 90.191; 90
2363.8Kong, Lingkai; Wang, Mengdan; Wang, Ye; Song, Bo; Yang, Yajie; Yao, Qiyi; Li, Yanzhong
Merging base-promoted C-C bond cleavage and iron-catalyzed skeletal rearrangement involving C-C/C-H bond activation: synthesis of highly functionalized carbazoles.
Chemical communications (Cambridge, England), 2018, 54, 11009-11012
7122344 CIFC32 H25 N O2P 1 21/n 112.5424; 9.1677; 22.0679
90; 104.02; 90
2461.89Kong, Lingkai; Wang, Mengdan; Wang, Ye; Song, Bo; Yang, Yajie; Yao, Qiyi; Li, Yanzhong
Merging base-promoted C-C bond cleavage and iron-catalyzed skeletal rearrangement involving C-C/C-H bond activation: synthesis of highly functionalized carbazoles.
Chemical communications (Cambridge, England), 2018, 54, 11009-11012
7122345 CIFC32 H25 N O2P 1 21/c 113.1322; 18.0792; 11.7504
90; 102.654; 90
2722.01Kong, Lingkai; Wang, Mengdan; Wang, Ye; Song, Bo; Yang, Yajie; Yao, Qiyi; Li, Yanzhong
Merging base-promoted C-C bond cleavage and iron-catalyzed skeletal rearrangement involving C-C/C-H bond activation: synthesis of highly functionalized carbazoles.
Chemical communications (Cambridge, England), 2018, 54, 11009-11012
7122346 CIFC13 H27 B9 N2 OC 1 2/c 131.845; 10.2834; 15.723
90; 118.864; 90
4509.2Liang, Xuewei; Shen, Yunjun; Zhang, Kang; Liu, Jiyong; Duttwyler, Simon
Rhodium(iii)-catalyzed dehydrogenative dialkenylation of the monocarba-closo-decaborate cluster by regioselective B-H activation.
Chemical communications (Cambridge, England), 2018, 54, 12451-12454
7122347 CIFC19 H38 B9 N2 Na O6P 1 21/n 111.6821; 16.6672; 16.3779
90; 110.407; 90
2988.8Liang, Xuewei; Shen, Yunjun; Zhang, Kang; Liu, Jiyong; Duttwyler, Simon
Rhodium(iii)-catalyzed dehydrogenative dialkenylation of the monocarba-closo-decaborate cluster by regioselective B-H activation.
Chemical communications (Cambridge, England), 2018, 54, 12451-12454
7122348 CIFC29 H49 B9 N2 OC 1 c 17.9588; 22.66; 18.5609
90; 90.433; 90
3347.3Liang, Xuewei; Shen, Yunjun; Zhang, Kang; Liu, Jiyong; Duttwyler, Simon
Rhodium(iii)-catalyzed dehydrogenative dialkenylation of the monocarba-closo-decaborate cluster by regioselective B-H activation.
Chemical communications (Cambridge, England), 2018, 54, 12451-12454
7122349 CIFC11 H25 B9 N Na O5 S2P b c a14.3755; 11.2861; 51.571
90; 90; 90
8367.1Liang, Xuewei; Shen, Yunjun; Zhang, Kang; Liu, Jiyong; Duttwyler, Simon
Rhodium(iii)-catalyzed dehydrogenative dialkenylation of the monocarba-closo-decaborate cluster by regioselective B-H activation.
Chemical communications (Cambridge, England), 2018, 54, 12451-12454
7122350 CIFC52 H71 Cl3 Co N9 O14P -19.8881; 15.6504; 20.0289
69.061; 85.977; 75.978
2808.1Liu, Dong-Cheng; Wang, Hong-Juan; Wang, Jia-Wei; Zhong, Di-Chang; Jiang, Long; Lu, Tong-Bu
Highly efficient and selective visible-light driven CO<sub>2</sub>-to-CO conversion by a Co-based cryptate in H<sub>2</sub>O/CH<sub>3</sub>CN solution.
Chemical communications (Cambridge, England), 2018, 54, 11308-11311
7122351 CIFC14 H5 Au F5 N O2P -17.3857; 7.4524; 27.7545
82.335; 89.173; 60.856
1320.06Seki, Tomohiro; Kobayashi, Koh; Mashimo, Takaki; Ito, Hajime
A gold isocyanide complex with a pendant carboxy group: orthogonal molecular arrangements and hypsochromically shifted luminescent mechanochromism.
Chemical communications (Cambridge, England), 2018, 54, 11136-11139
7122352 CIFC13 H5 Au F5 NP -17.2397; 7.3439; 12.3992
77.44; 75.353; 71.305
597.43Seki, Tomohiro; Kobayashi, Koh; Mashimo, Takaki; Ito, Hajime
A gold isocyanide complex with a pendant carboxy group: orthogonal molecular arrangements and hypsochromically shifted luminescent mechanochromism.
Chemical communications (Cambridge, England), 2018, 54, 11136-11139
7122353 CIFC14 H5 Au F5 N O2P 1 2/c 113.4101; 7.7601; 13.0837
90; 97.493; 90
1349.91Seki, Tomohiro; Kobayashi, Koh; Mashimo, Takaki; Ito, Hajime
A gold isocyanide complex with a pendant carboxy group: orthogonal molecular arrangements and hypsochromically shifted luminescent mechanochromism.
Chemical communications (Cambridge, England), 2018, 54, 11136-11139
7122354 CIFC22 H16 Co N2 O2C 1 2/c 140.77; 8.4491; 43.181
90; 110.199; 90
13959.8Hickson, James R.; Horsewill, Samuel J.; McGuire, Jake; Wilson, Claire; Sproules, Stephen; Farnaby, Joy H.
The semiquinone radical anion of 1,10-phenanthroline-5,6-dione: synthesis and rare earth coordination chemistry.
Chemical communications (Cambridge, England), 2018, 54, 11284-11287
7122355 CIFC22 H17 Co N2 O2P 21 21 219.4592; 18.0502; 20.2671
90; 90; 90
3460.4Hickson, James R.; Horsewill, Samuel J.; McGuire, Jake; Wilson, Claire; Sproules, Stephen; Farnaby, Joy H.
The semiquinone radical anion of 1,10-phenanthroline-5,6-dione: synthesis and rare earth coordination chemistry.
Chemical communications (Cambridge, England), 2018, 54, 11284-11287
7122356 CIFC23 H19 N O4P 1 21/n 15.8882; 16.418; 18.894
90; 95.016; 90
1819.5Mayakrishnan, Sivakalai; Arun, Yuvaraj; Uma Maheswari, Narayanan; Perumal, Paramasivan Thirumalai
Rhodium(iii)-catalysed decarbonylative annulation through C-H activation: expedient access to aminoisocoumarins by weak coordination.
Chemical communications (Cambridge, England), 2018, 54, 11889-11892
7122357 CIFC18 H17 Br N2 O2P 1 21/c 112.569; 7.6182; 17.8411
90; 104.161; 90
1656.43Taneja, Neha; Peddinti, Rama Krishna
Metal-free direct C-arylation of 1,3-dicarbonyl compounds and ethyl cyanoacetate: a platform to access diverse arrays of meta-functionalized phenols.
Chemical communications (Cambridge, England), 2018, 54, 11423-11426
7122358 CIFMg7 N22 Si9 Sr8C 1 2/m 115.2798; 7.4691; 10.9358
90; 110.462; 90
1169.32Li, Chao; Zheng, Hong-Wei; Wei, Heng-Wei; Su, Jie; Liao, Fu-Hui; Zhang, Zhen-Yi; Xu, Ling; Yang, Zu-Pei; Wang, Xiao-Ming; Jiao, Huan
Narrow-band blue emitting nitridomagnesosilicate phosphor Sr<sub>8</sub>Mg<sub>7</sub>Si<sub>9</sub>N<sub>22</sub>:Eu<sup>2+</sup> for phosphor-converted LEDs.
Chemical communications (Cambridge, England), 2018, 54, 11598-11601
7122359 CIFC72 Mn12 O48 S3P m -3 m15.8573; 15.8573; 15.8573
90; 90; 90
3987.4Yang, Huajun; Luo, Min; Wu, Zhou; Wang, Wei; Xue, Chaozhuang; Wu, Tao
A semiconducting metal-chalcogenide-organic framework with square-planar tetra-coordinated sulfur.
Chemical communications (Cambridge, England), 2018, 54, 11272-11275
7122360 CIFC78 H66 Cu3 O15C 1 2/c 136.295; 25.304; 20.4575
90; 116.08; 90
16875.3Chen, Gong-Jun; Chen, Chao-Qun; Li, Xue-Tian; Ma, Hui-Chao; Dong, Yu-Bin
Cu<sub>3</sub>L<sub>2</sub> metal-organic cages for A<sup>3</sup>-coupling reactions: reversible coordination interaction triggered homogeneous catalysis and heterogeneous recovery.
Chemical communications (Cambridge, England), 2018, 54, 11550-11553
7122361 CIFC150 H103 Cl12 Cu6 O24P -119.5003; 22.2603; 22.4658
62.026; 88.05; 65.547
7682.9Chen, Gong-Jun; Chen, Chao-Qun; Li, Xue-Tian; Ma, Hui-Chao; Dong, Yu-Bin
Cu<sub>3</sub>L<sub>2</sub> metal-organic cages for A<sup>3</sup>-coupling reactions: reversible coordination interaction triggered homogeneous catalysis and heterogeneous recovery.
Chemical communications (Cambridge, England), 2018, 54, 11550-11553
7122362 CIFC82 H106 Au2 N4 O5P 1 21/n 113.7382; 33.2731; 18.3424
90; 110.79; 90
7838.6Fernandez-Cestau, Julio; Rocchigiani, Luca; Pintus, Anna; Rama, Raquel J.; Budzelaar, Peter H. M.; Bochmann, Manfred
Isocyanide insertion into Au-H bonds: first gold iminoformyl complexes.
Chemical communications (Cambridge, England), 2018, 54, 11447-11450
7122363 CIFC118 H100 D48 N6 O20 S8 U2P -114.1675; 15.6425; 15.7252
74.352; 89.153; 79.49
3297.3Chaudhry, Mohammad; Lelj, Francesco; MacLachlan, Mark
Expanded Campestarene Hosts for Tetra- and Dinuclear Uranyl(VI) Complexes
Chemical Communications, 2018
7122364 CIFC42 H49 N2 O5 UI 41/a29.7978; 29.7978; 21.0965
90; 90; 90
18731.8Chaudhry, Mohammad; Lelj, Francesco; MacLachlan, Mark
Expanded Campestarene Hosts for Tetra- and Dinuclear Uranyl(VI) Complexes
Chemical Communications, 2018
7122365 CIFC156 H206 N6 O22 U2P -114.0254; 16.697; 18
69.218; 72.211; 83.081
3752.2Chaudhry, Mohammad; Lelj, Francesco; MacLachlan, Mark
Expanded Campestarene Hosts for Tetra- and Dinuclear Uranyl(VI) Complexes
Chemical Communications, 2018
7122366 CIFC68 H68 N4 O10 U2I 41/a c d35.7713; 35.7713; 28.7439
90; 90; 90
36780Chaudhry, Mohammad; Lelj, Francesco; MacLachlan, Mark
Expanded Campestarene Hosts for Tetra- and Dinuclear Uranyl(VI) Complexes
Chemical Communications, 2018
7122367 CIFC31 H27 N O2 SP 1 21/n 16.8229; 24.8007; 15.1265
90; 100.932; 90
2513.1Gillbard, Simone M.; Chung, Chieh-Hsu; Karad, Somnath Narayan; Panchal, Heena; Lewis, William; Lam, Hon Wai
Synthesis of multisubstituted pyrroles by nickel-catalyzed arylative cyclizations of N-tosyl alkynamides.
Chemical communications (Cambridge, England), 2018, 54, 11769-11772
7122368 CIFC54 H42 N13.5 O8 Zn2C 1 2/c 130.9656; 15.6428; 29.8532
90; 113.368; 90
13274.4Fu, Hong-Ru; Wang, Ning; Qin, Jian-Hua; Han, Min-Le; Ma, Lu-Fang; Wang, Fei
Spatial confinement of a cationic MOF: a SC-SC approach for high capacity Cr(vi)-oxyanion capture in aqueous solution.
Chemical communications (Cambridge, England), 2018, 54, 11645-11648
7122369 CIFC108 H84 Cr3 N28 O14 Zn4C 1 2/c 130.349; 15.649; 30.83
90; 113.41; 90
13437Fu, Hong-Ru; Wang, Ning; Qin, Jian-Hua; Han, Min-Le; Ma, Lu-Fang; Wang, Fei
Spatial confinement of a cationic MOF: a SC-SC approach for high capacity Cr(vi)-oxyanion capture in aqueous solution.
Chemical communications (Cambridge, England), 2018, 54, 11645-11648
7122370 CIFC21 H28 B Fe N7 SP b c a15.19917; 13.84434; 21.58924
90; 90; 90
4542.86Fischer, Anne A.; Lindeman, Sergey V.; Fiedler, Adam T.
A synthetic model of the nonheme iron-superoxo intermediate of cysteine dioxygenase.
Chemical communications (Cambridge, England), 2018, 54, 11344-11347
7122371 CIFC97 H114 N10 O18P -115.635; 15.853; 20.76
76.822; 87.31; 85.63
4993Zeng, Xianqiang; Deng, Hongmei; Jia, Xueshun; Cui, Lei; Li, Jian; Li, Chunju; Fang, Jianhui
Construction of [2]rotaxane-based supramolecular polymers driven by wheel-stopper ππ interactions.
Chemical communications (Cambridge, England), 2018, 54, 11634-11637
7122372 CIFC27 H18 F3 N O4 SP -18.9248; 11.0144; 12.8073
107.95; 91.426; 100.556
1172.96Mule, Ravindra D.; Shaikh, Aslam C.; Gade, Amol B.; Patil, Nitin T.
A new class of N-doped ionic PAHs via intramolecular [4+2]-cycloaddition between arylpyridines and alkynes.
Chemical communications (Cambridge, England), 2018, 54, 11909-11912
7122373 CIFC31 H21 F3 N3 O3 SC 1 2/c 19.0551; 29.5519; 20.7844
90; 99.425; 90
5486.7Mule, Ravindra D.; Shaikh, Aslam C.; Gade, Amol B.; Patil, Nitin T.
A new class of N-doped ionic PAHs via intramolecular [4+2]-cycloaddition between arylpyridines and alkynes.
Chemical communications (Cambridge, England), 2018, 54, 11909-11912
7122374 CIFC80 H80 Ag18 ClP n -3 n23.686; 23.686; 23.686
90; 90; 90
13288Zhang, Shanshan; Su, Hai-Feng; Zhuang, Gui-lin; Wang, Xing-Po; Tung, Chen-Ho; Sun, Di; Zheng, Lansun
A Hexadecanuclear Silver Alkynyl Cluster Based NbO Framework with Triple Emissions from Visible to Near-Infrared II Region
Chemical Communications, 2018
7122375 CIFC9 H11 N3 SP 1 21/c 113.2482; 8.2243; 10.2827
90; 111.265; 90
1044.09Mathew, Bijo; Baek, Seung Cheol; Grace Thomas Parambi, Della; Pil Lee, Jae; Joy, Monu; Annie Rilda, P. R.; Randev, Rugma V.; Nithyamol, P.; Vijayan, Vijitha; Inasu, Sini T.; Mathew, Githa Elizabeth; Lohidakshan, Krishnakumar K.; Kumar Krishnan, Girish; Kim, Hoon
Selected aryl thiosemicarbazones as a new class of multi-targeted monoamine oxidase inhibitors.
MedChemComm, 2018, 9, 1871-1881
7122376 CIFC33 H74 Mo12 N2 O42 P Zn4C 1 2/c 126.704; 18.529; 17.539
90; 124.78; 90
7128Cheng, Weiwei; Xue, Yun-Shan; Luo, Xi-Ming; Xu, Yan
A rare three-dimensional POM-based inorganic metal polymer bonded by CO<sub>2</sub> with high catalytic performance for CO<sub>2</sub> cycloaddition.
Chemical communications (Cambridge, England), 2018, 54, 12808-12811
7122377 CIFC31 H28 Cl N O5 SP -110.9353; 12.3322; 12.6739
65.821; 76.706; 64.368
1402.9Chen, Renjie; Liu, Yu; Cui, Sunliang
1,4-Conjugate addition/esterification of ortho-quinone methides in a multicomponent reaction.
Chemical communications (Cambridge, England), 2018, 54, 11753-11756
7122378 CIFC68 H115 K2 N5 O12 Ru2 Sb6P -113.1437; 13.96; 23.484
88.5283; 84.7546; 79.2296
4215.2Wang, Yi; Zavalij, Peter; Eichhorn, Bryan
The cyclo-Sb<sub>6</sub> ring in the [Sb<sub>6</sub>(RuCp*)<sub>2</sub>]<sup>2-</sup> ion.
Chemical communications (Cambridge, England), 2018, 54, 11917-11920
7122379 CIFC70 H118 K2 N4 O12 Ru2 Sb6P -113.0477; 14.1374; 23.62
87.7781; 84.4934; 79.1444
4258.3Wang, Yi; Zavalij, Peter; Eichhorn, Bryan
The cyclo-Sb<sub>6</sub> ring in the [Sb<sub>6</sub>(RuCp*)<sub>2</sub>]<sup>2-</sup> ion.
Chemical communications (Cambridge, England), 2018, 54, 11917-11920
7122380 CIFC29 H18 Co3 N O16P -6 2 c14.5594; 14.5594; 13.7247
90; 90; 120
2519.54Zhang, Qing-Qing; Liu, Xiao-Fei; Ma, Lin; Wei, Yong-Sheng; Wang, Zhao-Yang; Xu, Hong; Zang, Shuang-Quan
Remoulding a MOF's pores by auxiliary ligand introduction for stability improvement and highly selective CO<sub>2</sub>-capture.
Chemical communications (Cambridge, England), 2018, 54, 12029-12032
7122381 CIFC50.01 H28 Co3 N4 O13P -6 2 c14.3406; 14.3406; 14.1626
90; 90; 120
2522.37Zhang, Qing-Qing; Liu, Xiao-Fei; Ma, Lin; Wei, Yong-Sheng; Wang, Zhao-Yang; Xu, Hong; Zang, Shuang-Quan
Remoulding a MOF's pores by auxiliary ligand introduction for stability improvement and highly selective CO<sub>2</sub>-capture.
Chemical communications (Cambridge, England), 2018, 54, 12029-12032
7122382 CIFC50.01 H28 Co3 N4 O13P -6 2 c14.339; 14.339; 14.359
90; 90; 120
2556.78Zhang, Qing-Qing; Liu, Xiao-Fei; Ma, Lin; Wei, Yong-Sheng; Wang, Zhao-Yang; Xu, Hong; Zang, Shuang-Quan
Remoulding a MOF's pores by auxiliary ligand introduction for stability improvement and highly selective CO<sub>2</sub>-capture.
Chemical communications (Cambridge, England), 2018, 54, 12029-12032
7122383 CIFC70 H67 O6 PP 1 21/n 110.6501; 37.3357; 14.6867
90; 97.195; 90
5793.9Gupta, Vivek; Santra, Biswajit; Mandal, Debdeep; Das, Shubhajit; Narayanan, Ramakirushnan Suriya; Kalita, Pankaj; Rao, D. Krishna; Schulzke, Carola; Pati, Swapan K.; Chandrasekhar, Vadapalli; Jana, Anukul
Neutral and anionic phosphate-diesters as molecular templates for the encapsulation of a water dimer.
Chemical communications (Cambridge, England), 2018, 54, 11913-11916
7122384 CIFC24 H35 O4 PP -18.6709; 11.8216; 12.5323
71.887; 79.512; 77.411
1182.52Gupta, Vivek; Santra, Biswajit; Mandal, Debdeep; Das, Shubhajit; Narayanan, Ramakirushnan Suriya; Kalita, Pankaj; Rao, D. Krishna; Schulzke, Carola; Pati, Swapan K.; Chandrasekhar, Vadapalli; Jana, Anukul
Neutral and anionic phosphate-diesters as molecular templates for the encapsulation of a water dimer.
Chemical communications (Cambridge, England), 2018, 54, 11913-11916
7122385 CIFC80 H88 N3 O6 PP 1 21/c 116.4577; 14.985; 27.7532
90; 96.392; 90
6801.9Gupta, Vivek; Santra, Biswajit; Mandal, Debdeep; Das, Shubhajit; Narayanan, Ramakirushnan Suriya; Kalita, Pankaj; Rao, D. Krishna; Schulzke, Carola; Pati, Swapan K.; Chandrasekhar, Vadapalli; Jana, Anukul
Neutral and anionic phosphate-diesters as molecular templates for the encapsulation of a water dimer.
Chemical communications (Cambridge, England), 2018, 54, 11913-11916
7122386 CIFC80 H84 N3 O4 PP -112.4315; 12.5478; 22.9017
90.892; 95.969; 108.698
3360.96Gupta, Vivek; Santra, Biswajit; Mandal, Debdeep; Das, Shubhajit; Narayanan, Ramakirushnan Suriya; Kalita, Pankaj; Rao, D. Krishna; Schulzke, Carola; Pati, Swapan K.; Chandrasekhar, Vadapalli; Jana, Anukul
Neutral and anionic phosphate-diesters as molecular templates for the encapsulation of a water dimer.
Chemical communications (Cambridge, England), 2018, 54, 11913-11916
7122387 CIFC10 H14 I2 N8 O20 PuP 1 21/n 18.7845; 12.3118; 12.6497
90; 96.447; 90
1359.45Surbella, Robert G.; Ducati, Lucas C.; Autschbach, Jochen; Pellegrini, Kristi L.; McNamara, Bruce K.; Schwantes, Jon M.; Cahill, Christopher L.
Plutonium chlorido nitrato complexes: ligand competition and computational metrics for assembly and bonding.
Chemical communications (Cambridge, England), 2018, 54, 12014-12017
7122388 CIFC10 H10 Cl4 I2 N4 O6 PuP -19.8096; 10.1402; 11.5033
73.416; 82.364; 87.1
1086.83Surbella, Robert G.; Ducati, Lucas C.; Autschbach, Jochen; Pellegrini, Kristi L.; McNamara, Bruce K.; Schwantes, Jon M.; Cahill, Christopher L.
Plutonium chlorido nitrato complexes: ligand competition and computational metrics for assembly and bonding.
Chemical communications (Cambridge, England), 2018, 54, 12014-12017
7122389 CIFC10 H12 Cl3 N5 O9 PuP 1 21/c 117.2683; 7.7622; 15.1117
90; 97.598; 90
2007.8Surbella, Robert G.; Ducati, Lucas C.; Autschbach, Jochen; Pellegrini, Kristi L.; McNamara, Bruce K.; Schwantes, Jon M.; Cahill, Christopher L.
Plutonium chlorido nitrato complexes: ligand competition and computational metrics for assembly and bonding.
Chemical communications (Cambridge, England), 2018, 54, 12014-12017
7122390 CIFC10 H10 Cl5 N3 O5 PuP -16.7493; 10.8107; 14.1715
73.657; 81.412; 75.206
955.99Surbella, Robert G.; Ducati, Lucas C.; Autschbach, Jochen; Pellegrini, Kristi L.; McNamara, Bruce K.; Schwantes, Jon M.; Cahill, Christopher L.
Plutonium chlorido nitrato complexes: ligand competition and computational metrics for assembly and bonding.
Chemical communications (Cambridge, England), 2018, 54, 12014-12017
7122391 CIFC147 H128 N6 O14P -118.348; 18.837; 21.554
97.9; 100.31; 114.63
6472Li, Lei; Hong, Yu-Jian; Lin, Yun; Xiao, Wang-Chuan; Lin, Mei-Jin
An electron-deficient nanosized polycyclic aromatic hydrocarbon with enhanced anion-π interactions.
Chemical communications (Cambridge, England), 2018, 54, 11941-11944
7122392 CIFC65 H59 Cl2 N3 O6P 1 21/c 122.793; 19.106; 14.475
90; 107.05; 90
6027Li, Lei; Hong, Yu-Jian; Lin, Yun; Xiao, Wang-Chuan; Lin, Mei-Jin
An electron-deficient nanosized polycyclic aromatic hydrocarbon with enhanced anion-π interactions.
Chemical communications (Cambridge, England), 2018, 54, 11941-11944
7122393 CIFC18 H13 N3 O SP 1 21/n 117.1396; 4.0692; 22.0699
90; 108.746; 90
1457.6Zhang, Xinyu; Jiang, Yuqian; Xiao, Nao
Monitoring ADP and ATP in vivo using a fluorescent Ga(iii)-probe complex.
Chemical communications (Cambridge, England), 2018, 54, 12812-12815
7122394 CIFC37 H73 Fe N4 P3P b c m8.8347; 21.828; 20.7072
90; 90; 90
3993.3Cavaillé, Anthony; Joyeux, Benjamin; Saffon-Merceron, Nathalie; Nebra, Noel; Fustier-Boutignon, Marie; Mézailles, Nicolas
Triphos-Fe dinitrogen and dinitrogen-hydride complexes: relevance to catalytic N<sub>2</sub> reductions.
Chemical communications (Cambridge, England), 2018, 54, 11953-11956
7122395 CIFC34 H59 Fe N2 P3P -19.9709; 18.7613; 19.3003
104.771; 90.189; 99.733
3436.8Cavaillé, Anthony; Joyeux, Benjamin; Saffon-Merceron, Nathalie; Nebra, Noel; Fustier-Boutignon, Marie; Mézailles, Nicolas
Triphos-Fe dinitrogen and dinitrogen-hydride complexes: relevance to catalytic N<sub>2</sub> reductions.
Chemical communications (Cambridge, England), 2018, 54, 11953-11956
7122396 CIFC36 H69 Cl2 Fe O P3C 1 2/c 124.9372; 14.9752; 23.2922
90; 116.275; 90
7799.5Cavaillé, Anthony; Joyeux, Benjamin; Saffon-Merceron, Nathalie; Nebra, Noel; Fustier-Boutignon, Marie; Mézailles, Nicolas
Triphos-Fe dinitrogen and dinitrogen-hydride complexes: relevance to catalytic N<sub>2</sub> reductions.
Chemical communications (Cambridge, England), 2018, 54, 11953-11956
7122397 CIFC36.5 H63 Cl Fe P3P 1 21/n 111.2863; 28.1832; 23.9028
90; 102.292; 90
7428.8Cavaillé, Anthony; Joyeux, Benjamin; Saffon-Merceron, Nathalie; Nebra, Noel; Fustier-Boutignon, Marie; Mézailles, Nicolas
Triphos-Fe dinitrogen and dinitrogen-hydride complexes: relevance to catalytic N<sub>2</sub> reductions.
Chemical communications (Cambridge, England), 2018, 54, 11953-11956
7122398 CIFC24 H17 Br N2 OP 1 21 113.08; 5.727; 14.056
90; 113.482; 90
965.7Li, Ling; Liu, Zhen-Ting; Hu, Xiang-Ping
Copper-catalyzed propargylic [3+3] cycloaddition with 1H-pyrazol-5(4H)-ones: enantioselective access to optically active dihydropyrano[2,3-c]pyrazoles.
Chemical communications (Cambridge, England), 2018, 54, 12033-12036
7122399 CIFC68 H64 Cd2 N4 O12P 1 21/n 117.222; 10.281; 36.345
90; 102.86; 90
6274Xu, Kui; Yu, Bing; Li, Yuanyuan; Su, Huifang; Wang, Bingnan; Sun, Kai; Liu, Yuanyuan; Peng, Qiuchen; Hou, Hongwei; Li, Kai
Photo-induced free radical production in a tetraphenylethylene ligand-based metal-organic framework.
Chemical communications (Cambridge, England), 2018, 54, 12942-12945
7122400 CIFC42 H47 B N PP b c a16.4464; 18.2277; 24.0228
90; 90; 90
7201.6Lee, Young Hoon; Jana, Saibal; Lee, Heechai; Lee, Sang Uck; Lee, Min Hyung
Rational design of time-resolved turn-on fluorescence sensors: exploiting delayed fluorescence for hydrogen peroxide sensing.
Chemical communications (Cambridge, England), 2018, 54, 12069-12072
7122401 CIFC36 H34 B NP 1 21/c 115.7787; 8.2376; 21.582
90; 100.292; 90
2760.06Lee, Young Hoon; Jana, Saibal; Lee, Heechai; Lee, Sang Uck; Lee, Min Hyung
Rational design of time-resolved turn-on fluorescence sensors: exploiting delayed fluorescence for hydrogen peroxide sensing.
Chemical communications (Cambridge, England), 2018, 54, 12069-12072
7122402 CIFC44 H50 B N2 O PP 1 21/c 18.7694; 26.1702; 17.0409
90; 95.5961; 90
3892.2Lee, Young Hoon; Jana, Saibal; Lee, Heechai; Lee, Sang Uck; Lee, Min Hyung
Rational design of time-resolved turn-on fluorescence sensors: exploiting delayed fluorescence for hydrogen peroxide sensing.
Chemical communications (Cambridge, England), 2018, 54, 12069-12072
7122403 CIFC51 H73 N O4P n a 2115.4381; 15.9969; 18.31405
90; 90; 90
4522.87Whiteside, R. E.; Gunaratne, H. Q. Nimal; Muzio, A. F. V.; Nockemann, P.
Selective monoalkylation of p-tert-butylcalix-[4]-arene in a methyl carbonate ionic liquid.
Chemical communications (Cambridge, England), 2018, 54, 12037-12040
7122404 CIFC64 H101 N3 O4P 1 21/c 115.3846; 15.7251; 24.2062
90; 105.073; 90
5654.59Whiteside, R. E.; Gunaratne, H. Q. Nimal; Muzio, A. F. V.; Nockemann, P.
Selective monoalkylation of p-tert-butylcalix-[4]-arene in a methyl carbonate ionic liquid.
Chemical communications (Cambridge, England), 2018, 54, 12037-12040
7122405 CIFC26 H17 F2 N O2P -18.821; 11.239; 11.41
81.907; 70.268; 69.729
998.4Zheng, Kailu; Zhuang, Shiyi; Shu, Wenming; Wu, Yandong; Yang, Chuluo; Wu, Anxin
Molecular iodine-mediated formal [2+1+1+1] cycloaddition access to pyrrolo[2,1-a]isoquinolines with DMSO as the methylene source.
Chemical communications (Cambridge, England), 2018, 54, 11897-11900
7122406 CIFC26 H18 N2 O4P 1 21/c 111.821; 9.242; 18.97
90; 92.57; 90
2070Zheng, Kailu; Zhuang, Shiyi; Shu, Wenming; Wu, Yandong; Yang, Chuluo; Wu, Anxin
Molecular iodine-mediated formal [2+1+1+1] cycloaddition access to pyrrolo[2,1-a]isoquinolines with DMSO as the methylene source.
Chemical communications (Cambridge, England), 2018, 54, 11897-11900
7122407 CIFC26 H17 Br2 N O2P 1 21/c 18.7349; 22.1152; 11.5746
90; 107.507; 90
2132.3Zheng, Kailu; Zhuang, Shiyi; Shu, Wenming; Wu, Yandong; Yang, Chuluo; Wu, Anxin
Molecular iodine-mediated formal [2+1+1+1] cycloaddition access to pyrrolo[2,1-a]isoquinolines with DMSO as the methylene source.
Chemical communications (Cambridge, England), 2018, 54, 11897-11900
7122408 CIFC28 H26 Cl2 Dy2 N8 O8P -19.292; 9.345; 21.486
80.32; 80.796; 65.327
1662.8Tian, Haiquan; Wang, Bao-Lin; Lu, Jing; Liu, Hou-Ting; Su, Jianhui; Li, Dacheng; Dou, Jianmin
Consecutive one-/two-step relaxation transformations of single-molecule magnets via coupling dinuclear dysprosium compounds with chloride bridges.
Chemical communications (Cambridge, England), 2018, 54, 12105-12108
7122409 CIFC14 H14 Cl Dy N4 O4P -19.159; 9.343; 11.151
88.62; 73.41; 67.12
838.5Tian, Haiquan; Wang, Bao-Lin; Lu, Jing; Liu, Hou-Ting; Su, Jianhui; Li, Dacheng; Dou, Jianmin
Consecutive one-/two-step relaxation transformations of single-molecule magnets via coupling dinuclear dysprosium compounds with chloride bridges.
Chemical communications (Cambridge, England), 2018, 54, 12105-12108
7122410 CIFC56 H56 Cl4 Dy4 N16 O16P 1 21/c 19.416; 21.374; 16.637
90; 104.907; 90
3236Tian, Haiquan; Wang, Bao-Lin; Lu, Jing; Liu, Hou-Ting; Su, Jianhui; Li, Dacheng; Dou, Jianmin
Consecutive one-/two-step relaxation transformations of single-molecule magnets via coupling dinuclear dysprosium compounds with chloride bridges.
Chemical communications (Cambridge, England), 2018, 54, 12105-12108
7122411 CIFC54.5 H50 Cl1.5 Cu3 N12.5 O10P 3 1 c15.064; 15.064; 29.042
90; 90; 120
5707.4Kintzel, Benjamin; Böhme, Michael; Liu, Junjie; Burkhardt, Anja; Mrozek, Jakub; Buchholz, Axel; Ardavan, Arzhang; Plass, Winfried
Molecular electronic spin qubits from a spin-frustrated trinuclear copper complex.
Chemical communications (Cambridge, England), 2018, 54, 12934-12937
7122412 CIFC160 H136 Br5.69 Dy4 N56 O27.25I a -3 d63.74; 63.74; 63.74
90; 90; 90
258962Wu, Jianfeng; Guo, Mei; Li, Xiao-Lei; Zhao, Lang; Sun, Qing-Fu; Layfield, Richard A.; Tang, Jinkui
From double-shelled grids to supramolecular frameworks.
Chemical communications (Cambridge, England), 2018, 54, 12097-12100
7122413 CIFC160 H128 Cl6 Cu4 Dy4 N56 O32I a -3 d63.821; 63.821; 63.821
90; 90; 90
259951Wu, Jianfeng; Guo, Mei; Li, Xiao-Lei; Zhao, Lang; Sun, Qing-Fu; Layfield, Richard A.; Tang, Jinkui
From double-shelled grids to supramolecular frameworks.
Chemical communications (Cambridge, England), 2018, 54, 12097-12100
7122414 CIFC17 H17 N OP 1 21/n 113.587; 6.23; 15.598
90; 92.11; 90
1319.4Yang, Yuwen; Yang, Weibo
Divergent synthesis of N-heterocycles by Pd-catalyzed controllable cyclization of vinylethylene carbonates.
Chemical communications (Cambridge, England), 2018, 54, 12182-12185
7122415 CIFC23 H20 Cl2 N2P b c a5.8417; 26.828; 28.4867
90; 90; 90
4464.5Yang, Yuwen; Yang, Weibo
Divergent synthesis of N-heterocycles by Pd-catalyzed controllable cyclization of vinylethylene carbonates.
Chemical communications (Cambridge, England), 2018, 54, 12182-12185
7122416 CIFC15 H19 N O3P 1 21 113.093; 7.5118; 14.149
90; 91.872; 90
1390.8Yoshida, Taira; Mori, Keiji
Expeditious synthesis of multisubstituted indoles via multiple hydrogen transfers.
Chemical communications (Cambridge, England), 2018, 54, 12686-12689
7122417 CIFC25 H29 Cl N O2 RhP 1 21/n 18.6375; 13.8673; 18.4717
90; 103.076; 90
2155.15Aboo, Ahmed H.; Bennett, Elliot L.; Deeprose, Mark; Robertson, Craig M.; Iggo, Jonathan A.; Xiao, Jianliang
Methanol as hydrogen source: transfer hydrogenation of aromatic aldehydes with a rhodacycle.
Chemical communications (Cambridge, England), 2018, 54, 11805-11808
7122418 CIFC212 H298 Br2 N12 O40 Si6F -4 3 m27.9568; 27.9568; 27.9568
90; 90; 90
21850.6Holmes, Jessica L.; Abrahams, Brendan F.; Ahveninen, Anna; Boughton, Berin A.; Hudson, Timothy A.; Robson, Richard; Thinagaran, Dinaiz
Self-assembly of a Si-based cage by the formation of 24 equivalent covalent bonds.
Chemical communications (Cambridge, England), 2018, 54, 11877-11880
7122419 CIFC152 H298 Br2 Cs4 N4 O94 Si6F -4 3 m27.7206; 27.7206; 27.7206
90; 90; 90
21301.4Holmes, Jessica L.; Abrahams, Brendan F.; Ahveninen, Anna; Boughton, Berin A.; Hudson, Timothy A.; Robson, Richard; Thinagaran, Dinaiz
Self-assembly of a Si-based cage by the formation of 24 equivalent covalent bonds.
Chemical communications (Cambridge, England), 2018, 54, 11877-11880
7122420 CIFC23 H33 Cl N2 O3P 1 21/c 110.753; 11.5829; 19.2555
90; 100.949; 90
2354.63Guo, Jing; Liu, Xiaohua; He, Changqiang; Tan, Fei; Dong, Shunxi; Feng, Xiaoming
Nickel(ii)-catalyzed enantioselective α-alkylation of β-ketoamides with phenyliodonium ylide via a radical process.
Chemical communications (Cambridge, England), 2018, 54, 12254-12257
7122421 CIFC43 H68 Cl2 N4 Ni O14P 43 21 212.9026; 12.9026; 29.8458
90; 90; 90
4968.64Guo, Jing; Liu, Xiaohua; He, Changqiang; Tan, Fei; Dong, Shunxi; Feng, Xiaoming
Nickel(ii)-catalyzed enantioselective α-alkylation of β-ketoamides with phenyliodonium ylide via a radical process.
Chemical communications (Cambridge, England), 2018, 54, 12254-12257
7122422 CIFC16 H12 Co F24 N O4P n m a17.216; 20.2934; 7.1911
90; 90; 90
2512.4Steele, Jennifer L.; Tahsini, Laleh; Sun, Chen; Elinburg, Jessica K.; Kotyk, Christopher M.; McNeely, James; Stoian, Sebastian A.; Dragulescu-Andrasi, Alina; Ozarowski, Andrew; Ozerov, M.; Krzystek, J.; Telser, Joshua; Bacon, Jeffrey W.; Golen, James A.; Rheingold, Arnold L.; Doerrer, Linda H.
Square-planar Co(iii) in {O<sub>4</sub>} coordination: large ZFS and reactivity with ROS.
Chemical communications (Cambridge, England), 2018, 54, 12045-12048
7122423 CIFC20 H30 Co F24 N2 O9P 1 21/c 118.9087; 9.8278; 18.7047
90; 90.009; 90
3475.9Steele, Jennifer L.; Tahsini, Laleh; Sun, Chen; Elinburg, Jessica K.; Kotyk, Christopher M.; McNeely, James; Stoian, Sebastian A.; Dragulescu-Andrasi, Alina; Ozarowski, Andrew; Ozerov, M.; Krzystek, J.; Telser, Joshua; Bacon, Jeffrey W.; Golen, James A.; Rheingold, Arnold L.; Doerrer, Linda H.
Square-planar Co(iii) in {O<sub>4</sub>} coordination: large ZFS and reactivity with ROS.
Chemical communications (Cambridge, England), 2018, 54, 12045-12048
7122424 CIFC52 H64 Mg2 N4P -110.5161; 13.651; 17.9616
78.981; 77.249; 69.307
2334.5Garçon, Martí; White, Andrew J. P.; Crimmin, Mark R.
Palladium-catalysed magnesiation of benzene.
Chemical communications (Cambridge, England), 2018, 54, 12326-12328
7122425 CIFC7 H0 N7 O1.17 S2 ZnR -3 :H23.39; 23.39; 13.909
90; 90; 120
6590Gai, Yanli; Chen, Xitong; Yang, Huajun; Wang, Yanxiang; Bu, Xianhui; Feng, Pingyun
A new strategy for constructing a disulfide-functionalized ZIF-8 analogue using structure-directing ligand-ligand covalent interaction.
Chemical communications (Cambridge, England), 2018, 54, 12109-12112
7122426 CIFC63 H45 F20 N9 S3 Th2P -111.1776; 12.1625; 25.368
81.4051; 86.7035; 74.0481
3278.2Gotthelf, Garret; Stuber, Matthew A.; Kornienko, Anna Y.; Emge, Thomas J.; Brennan, John G.
Organosoluble tetravalent actinide di- and trifluorides.
Chemical communications (Cambridge, England), 2018, 54, 12018-12020
7122427 CIFC30 H30 F2 I2 N6 UP 1 21/c 19.809; 38.747; 9.755
90; 117.859; 90
3277.9Gotthelf, Garret; Stuber, Matthew A.; Kornienko, Anna Y.; Emge, Thomas J.; Brennan, John G.
Organosoluble tetravalent actinide di- and trifluorides.
Chemical communications (Cambridge, England), 2018, 54, 12018-12020
7122428 CIFC48 H107 Ge4 K1.09 N8 O18 Rb1.91 ZnP b c n12.8668; 28.2571; 20.0883
90; 90; 90
7303.7Henneberger, Thomas; Klein, Wilhelm; Dums, Jasmin V.; Fässler, Thomas F
[(μ<sub>2</sub>-H)(η<sup>2</sup>-Ge<sub>4</sub>)ZnPh<sub>2</sub>]<sup>3-</sup>, an edge-on protonated E<sub>4</sub> cluster establishing the first three-center two-electron Ge-H-Ge bond.
Chemical communications (Cambridge, England), 2018, 54, 12381-12384
7122429 CIFC12 H37.5 Ge9 K0.45 N4.5 O6 Rb3.55C 1 2/c 138.5713; 9.997; 19.0042
90; 94.337; 90
7307Henneberger, Thomas; Klein, Wilhelm; Dums, Jasmin V.; Fässler, Thomas F
[(μ<sub>2</sub>-H)(η<sup>2</sup>-Ge<sub>4</sub>)ZnPh<sub>2</sub>]<sup>3-</sup>, an edge-on protonated E<sub>4</sub> cluster establishing the first three-center two-electron Ge-H-Ge bond.
Chemical communications (Cambridge, England), 2018, 54, 12381-12384
7122430 CIFC26 H34 B N6 O2 P WP b c a15.073; 20.533; 20.5731
90; 90; 90
6367.2Frogley, Benjamin J.; Hill, Anthony F.
Alkynylbis(alkylidynyl)phosphines: {L<sub>n</sub>M[triple bond, length as m-dash]C}<sub>2</sub>PC[triple bond, length as m-dash]CR.
Chemical communications (Cambridge, England), 2018, 54, 12373-12376
7122431 CIFC38 H45 B2 N12 O4 P W2I 1 2/a 115.285; 10.7644; 27.3927
90; 93.766; 90
4497.3Frogley, Benjamin J.; Hill, Anthony F.
Alkynylbis(alkylidynyl)phosphines: {L<sub>n</sub>M[triple bond, length as m-dash]C}<sub>2</sub>PC[triple bond, length as m-dash]CR.
Chemical communications (Cambridge, England), 2018, 54, 12373-12376
7122432 CIFC50 H54 As B2 N12 O4 P W2P -111.2582; 11.6958; 22.3488
83.656; 81.841; 71.23
2751.44Frogley, Benjamin J.; Hill, Anthony F.
Alkynylbis(alkylidynyl)phosphines: {L<sub>n</sub>M[triple bond, length as m-dash]C}<sub>2</sub>PC[triple bond, length as m-dash]CR.
Chemical communications (Cambridge, England), 2018, 54, 12373-12376
7122433 CIFC29 H36 B Mo N6 O2 P SiP n a 2117.0572; 10.5503; 17.9411
90; 90; 90
3228.65Frogley, Benjamin J.; Hill, Anthony F.
Alkynylbis(alkylidynyl)phosphines: {L<sub>n</sub>M[triple bond, length as m-dash]C}<sub>2</sub>PC[triple bond, length as m-dash]CR.
Chemical communications (Cambridge, England), 2018, 54, 12373-12376
7122434 CIFC41.67 H53.67 B2 Cl2 N12 O4 P Si W2C 1 2/c 121.7758; 10.976; 24.157
90; 115.485; 90
5212Frogley, Benjamin J.; Hill, Anthony F.
Alkynylbis(alkylidynyl)phosphines: {L<sub>n</sub>M[triple bond, length as m-dash]C}<sub>2</sub>PC[triple bond, length as m-dash]CR.
Chemical communications (Cambridge, England), 2018, 54, 12373-12376
7122435 CIFC29 H42 B Mo N6 O2 P SiP n a 2117.5232; 10.5308; 18.0406
90; 90; 90
3329.09Frogley, Benjamin J.; Hill, Anthony F.
Alkynylbis(alkylidynyl)phosphines: {L<sub>n</sub>M[triple bond, length as m-dash]C}<sub>2</sub>PC[triple bond, length as m-dash]CR.
Chemical communications (Cambridge, England), 2018, 54, 12373-12376
7122436 CIFC44 H49 B2 N12 O4 P W2C 1 2/c 122.4317; 10.8744; 23.8394
90; 117.336; 90
5165.8Frogley, Benjamin J.; Hill, Anthony F.
Alkynylbis(alkylidynyl)phosphines: {L<sub>n</sub>M[triple bond, length as m-dash]C}<sub>2</sub>PC[triple bond, length as m-dash]CR.
Chemical communications (Cambridge, England), 2018, 54, 12373-12376
7122437 CIFC41 H53 Au B2 Cl N12 O4 P Si W2C 1 2/c 122.114; 11.0992; 23.9715
90; 114.633; 90
5348.3Frogley, Benjamin J.; Hill, Anthony F.
Alkynylbis(alkylidynyl)phosphines: {L<sub>n</sub>M[triple bond, length as m-dash]C}<sub>2</sub>PC[triple bond, length as m-dash]CR.
Chemical communications (Cambridge, England), 2018, 54, 12373-12376
7122438 CIFC45 H51 B2 N12 O4 P W2P -110.7103; 12.8936; 19.5744
77.598; 78.252; 70.388
2461.3Frogley, Benjamin J.; Hill, Anthony F.
Alkynylbis(alkylidynyl)phosphines: {L<sub>n</sub>M[triple bond, length as m-dash]C}<sub>2</sub>PC[triple bond, length as m-dash]CR.
Chemical communications (Cambridge, England), 2018, 54, 12373-12376
7122439 CIFC43 H54 B2 Cl3 N12 O4 P W2C 1 2/c 121.415; 10.8991; 24.0583
90; 115.668; 90
5061.2Frogley, Benjamin J.; Hill, Anthony F.
Alkynylbis(alkylidynyl)phosphines: {L<sub>n</sub>M[triple bond, length as m-dash]C}<sub>2</sub>PC[triple bond, length as m-dash]CR.
Chemical communications (Cambridge, England), 2018, 54, 12373-12376
7122440 CIFC29 H36 B N6 O2 P Si WP n a 2117.0998; 10.5256; 17.8373
90; 90; 90
3210.46Frogley, Benjamin J.; Hill, Anthony F.
Alkynylbis(alkylidynyl)phosphines: {L<sub>n</sub>M[triple bond, length as m-dash]C}<sub>2</sub>PC[triple bond, length as m-dash]CR.
Chemical communications (Cambridge, England), 2018, 54, 12373-12376
7122441 CIFC18 H16 O2P -18.2469; 9.0265; 9.4627
95.548; 94.576; 92.972
697.61Panchal, Heena; Clarke, Christopher; Bell, Charles; Karad, Somnath Narayan; Lewis, William; Lam, Hon Wai
Nickel-catalyzed, ligand-free, diastereoselective synthesis of 3-methyleneindan-1-ols.
Chemical communications (Cambridge, England), 2018, 54, 12389-12392
7122442 CIFC14 H14 O3P c a 2123.9951; 14.2011; 6.8998
90; 90; 90
2351.15Panchal, Heena; Clarke, Christopher; Bell, Charles; Karad, Somnath Narayan; Lewis, William; Lam, Hon Wai
Nickel-catalyzed, ligand-free, diastereoselective synthesis of 3-methyleneindan-1-ols.
Chemical communications (Cambridge, England), 2018, 54, 12389-12392
7122443 CIFC16 H17 N O3P b c a18.5434; 8.2224; 18.7134
90; 90; 90
2853.26Panchal, Heena; Clarke, Christopher; Bell, Charles; Karad, Somnath Narayan; Lewis, William; Lam, Hon Wai
Nickel-catalyzed, ligand-free, diastereoselective synthesis of 3-methyleneindan-1-ols.
Chemical communications (Cambridge, England), 2018, 54, 12389-12392
7122444 CIFC13 H15 N O5P 21 21 215.12044; 14.66642; 16.34735
90; 90; 90
1227.66Luo, Zhonghua; Sun, Guodong; Zhou, Zihong; Liu, Guozhu; Luan, Baolei; Lin, Yicao; Zhang, Lei; Wang, Zhongqing
Stereogenic cis-2-substituted-N-acetyl-3-hydroxy-indolines via ruthenium(ii)-catalyzed dynamic kinetic resolution-asymmetric transfer hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13503-13506
7122445 CIFC23 H16 B Cl F4 OP 1 21/n 113.337; 10.087; 15.17
90; 93.785; 90
2036.4Fathimath Salfeena, C. T.; Basavaraja, ?; Ashitha, K. T.; Kumar, V. Praveen; Varughese, Sunil; Suresh, Cherumuttathu H.; Sasidhar, B. S.
Synthesis of symmetrical and unsymmetrical triarylpyrylium ions via an inverse electron demand Diels-Alder reaction.
Chemical communications (Cambridge, England), 2018, 54, 12463-12466
7122446 CIFC257 H240 F15 Fe4 N36 O27 S5P 120.155; 20.4279; 20.6157
114.452; 109.472; 91.124
7160.9Han, Wang-Kang; Zhang, Hai-Xia; Wang, Yong; Liu, Wei; Yan, Xiaodong; Li, Tao; Gu, Zhi-Guo
Tetrahedral metal-organic cages with cube-like cavities for selective encapsulation of fullerene guests and their spin-crossover properties.
Chemical communications (Cambridge, England), 2018, 54, 12646-12649
7122447 CIFC283 H252 F21 Fe4 N36 O33 S7P 3223.752; 23.752; 49.776
90; 90; 120
24319Han, Wang-Kang; Zhang, Hai-Xia; Wang, Yong; Liu, Wei; Yan, Xiaodong; Li, Tao; Gu, Zhi-Guo
Tetrahedral metal-organic cages with cube-like cavities for selective encapsulation of fullerene guests and their spin-crossover properties.
Chemical communications (Cambridge, England), 2018, 54, 12646-12649
7122448 CIFC40 H43 F9 O10 P3 S3P -113.755; 13.9164; 13.9779
87.306; 60.676; 88.417
2330.2Bayne, J. M.; Fasano, V.; Szkop, K. M.; Ingleson, M. J.; Stephan, D. W.
Phosphorous(v) Lewis acids: water/base tolerant P<sub>3</sub>-trimethylated trications.
Chemical communications (Cambridge, England), 2018, 54, 12467-12470
7122449 CIFC50 H55 F9 N O10 P3 S3P -112.7151; 14.6939; 15.3772
77.042; 81.897; 72.53
2662.3Bayne, J. M.; Fasano, V.; Szkop, K. M.; Ingleson, M. J.; Stephan, D. W.
Phosphorous(v) Lewis acids: water/base tolerant P<sub>3</sub>-trimethylated trications.
Chemical communications (Cambridge, England), 2018, 54, 12467-12470
7122450 CIFC32 H25 N O2 SP 1 21/c 110.6386; 19.7299; 12.606
90; 104.558; 90
2561.03Zhang, Jingyi; Li, Siqi; Qiao, Yan; Peng, Cheng; Wang, Xiao-Na; Chang, Junbiao
Metal-free cycloisomerizations of o-alkynylbiaryls.
Chemical communications (Cambridge, England), 2018, 54, 12455-12458
7122451 CIFC30 H34 B3 PP 1 21/n 111.7002; 17.2942; 12.6635
90; 91.842; 90
2561.08Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
A convenient route to internally phosphane-stabilized aryltriborane(7) compounds.
Chemical communications (Cambridge, England), 2018, 54, 12606-12609
7122452 CIFC24 H26 Br PP 21 21 217.9924; 15.6376; 33.0811
90; 90; 90
4134.5Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
A convenient route to internally phosphane-stabilized aryltriborane(7) compounds.
Chemical communications (Cambridge, England), 2018, 54, 12606-12609
7122453 CIFC42 H32 B3 F10 PP -115.0735; 15.1214; 19.54
84.907; 81.768; 86.11
4383.6Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
A convenient route to internally phosphane-stabilized aryltriborane(7) compounds.
Chemical communications (Cambridge, England), 2018, 54, 12606-12609
7122454 CIFC18 H20 I N3 O2P 21 21 216.5952; 8.1944; 34.4405
90; 90; 90
1861.29Zhang, Hang; Yao, Qian; Cao, Weidi; Ge, Shulin; Xu, Jinxiu; Liu, Xiaohua; Feng, Xiaoming
Catalytic enantioselective ene-type reactions of vinylogous hydrazone: construction of α-methylene-γ-butyrolactone derivatives.
Chemical communications (Cambridge, England), 2018, 54, 12511-12514
7122455 CIFC23.9 H24 I N3 O3P 112.05; 12.052; 16.964
90.01; 90.05; 90.012
2464Zhang, Hang; Yao, Qian; Cao, Weidi; Ge, Shulin; Xu, Jinxiu; Liu, Xiaohua; Feng, Xiaoming
Catalytic enantioselective ene-type reactions of vinylogous hydrazone: construction of α-methylene-γ-butyrolactone derivatives.
Chemical communications (Cambridge, England), 2018, 54, 12511-12514
7122456 CIFC34 H44 N4 O4P 18.1154; 9.9402; 10.784
78.245; 87.577; 69.347
796.54Zhang, Hang; Yao, Qian; Cao, Weidi; Ge, Shulin; Xu, Jinxiu; Liu, Xiaohua; Feng, Xiaoming
Catalytic enantioselective ene-type reactions of vinylogous hydrazone: construction of α-methylene-γ-butyrolactone derivatives.
Chemical communications (Cambridge, England), 2018, 54, 12511-12514
7122457 CIFC50 H74 F12 N8 O13 S4 ZnP 1 21 120.73104; 15.56761; 24.0468
90; 103.086; 90
7559.15Zhang, Hang; Yao, Qian; Cao, Weidi; Ge, Shulin; Xu, Jinxiu; Liu, Xiaohua; Feng, Xiaoming
Catalytic enantioselective ene-type reactions of vinylogous hydrazone: construction of α-methylene-γ-butyrolactone derivatives.
Chemical communications (Cambridge, England), 2018, 54, 12511-12514
7122458 CIFC295 H52 Br4 N8 S6P -114.3499; 16.3659; 18.7206
112.433; 94.237; 102.687
3903.5Liu, Tong-Xin; Yue, Shuaishuai; Wei, Changgeng; Ma, Nana; Zhang, Pengling; Liu, Qingfeng; Zhang, Guisheng
Solvent-promoted catalyst-free regioselective N-incorporation multicomponent domino reaction: rapid assembly of π-functionalized [60]fullerene-fused dihydrocarbolines.
Chemical communications (Cambridge, England), 2018, 54, 13331-13334
7122459 CIFC40 H60 Gd N79 Ni10 O17P -111.1561; 17.898; 28.868
105.722; 93.827; 103.427
5344.8Krause, Jasmin; Alexandropoulos, Dimitris I.; Carrella, Luca M.; Rentschler, Eva; Stamatatos, Theocharis C.
Increasing the nuclearity and spin ground state in a new family of ferromagnetically-coupled {Ni<sub>10</sub>} disk-like complexes bearing exclusively end-on bridging azido ligands.
Chemical communications (Cambridge, England), 2018, 54, 12499-12502
7122460 CIFC36 H54 N77 Ni10 O15 YP -111.0684; 14.2915; 16.0071
78.715; 84.321; 81.693
2450.5Krause, Jasmin; Alexandropoulos, Dimitris I.; Carrella, Luca M.; Rentschler, Eva; Stamatatos, Theocharis C.
Increasing the nuclearity and spin ground state in a new family of ferromagnetically-coupled {Ni<sub>10</sub>} disk-like complexes bearing exclusively end-on bridging azido ligands.
Chemical communications (Cambridge, England), 2018, 54, 12499-12502
7122461 CIFC36 H54 N77 Ni10 O17 TbP -111.16; 19.509; 23.698
106.432; 91.339; 94.085
4931.1Krause, Jasmin; Alexandropoulos, Dimitris I.; Carrella, Luca M.; Rentschler, Eva; Stamatatos, Theocharis C.
Increasing the nuclearity and spin ground state in a new family of ferromagnetically-coupled {Ni<sub>10</sub>} disk-like complexes bearing exclusively end-on bridging azido ligands.
Chemical communications (Cambridge, England), 2018, 54, 12499-12502
7122462 CIFC35 H52.5 Dy N77 Ni10 O16P -111.165; 19.456; 23.633
106.086; 91.383; 93.738
4917.4Krause, Jasmin; Alexandropoulos, Dimitris I.; Carrella, Luca M.; Rentschler, Eva; Stamatatos, Theocharis C.
Increasing the nuclearity and spin ground state in a new family of ferromagnetically-coupled {Ni<sub>10</sub>} disk-like complexes bearing exclusively end-on bridging azido ligands.
Chemical communications (Cambridge, England), 2018, 54, 12499-12502
7122463 CIFC32 H40 Cr2 K O6P -110.5276; 13.9902; 16.3421
111.959; 96.047; 92.045
2212.5Labrum, Nicholas S.; Losovyj, Yaroslav; Caulton, Kenneth G.
A new access route to dimetal sandwich complexes, including a radical anion.
Chemical communications (Cambridge, England), 2018, 54, 12397-12399
7122464 CIFC34.08 H23.17 Cl3.17 O5P 1 21 113.2268; 6.9147; 33.035
90; 99.015; 90
2984Chen, Yi-Ru; Ganapuram, Madhusudhan Reddy; Hsieh, Kai-Hong; Chen, Kai-Han; Karanam, Praneeth; Vagh, Sandip Sambhaji; Liou, Yan-Cheng; Lin, Wenwei
3-Homoacyl coumarin: an all carbon 1,3-dipole for enantioselective concerted (3+2) cycloaddition.
Chemical communications (Cambridge, England), 2018, 54, 12702-12705
7122465 CIFC16 H16 Au2 N10C 1 2/m 113.0911; 6.4907; 11.9991
90; 105.112; 90
984.31Liu, Qi; Xie, Mo; Chang, Xiaoyong; Gao, Qin; Chen, Yong; Lu, Wei
Correlating thermochromic and mechanochromic phosphorescence with polymorphs of a complex gold(i) double salt with infinite aurophilicity.
Chemical communications (Cambridge, England), 2018, 54, 12844-12847
7122466 CIFC16 H16 Au2 N10P m n 216.2753; 8.0957; 18.757
90; 90; 90
952.91Liu, Qi; Xie, Mo; Chang, Xiaoyong; Gao, Qin; Chen, Yong; Lu, Wei
Correlating thermochromic and mechanochromic phosphorescence with polymorphs of a complex gold(i) double salt with infinite aurophilicity.
Chemical communications (Cambridge, England), 2018, 54, 12844-12847
7122467 CIFC16 H16 Au2 N10P m n a6.3484; 8.1538; 18.6895
90; 90; 90
967.44Liu, Qi; Xie, Mo; Chang, Xiaoyong; Gao, Qin; Chen, Yong; Lu, Wei
Correlating thermochromic and mechanochromic phosphorescence with polymorphs of a complex gold(i) double salt with infinite aurophilicity.
Chemical communications (Cambridge, England), 2018, 54, 12844-12847
7122468 CIFC16 H16 Au2 N10P m n 216.3306; 8.141; 18.7077
90; 90; 90
964.15Liu, Qi; Xie, Mo; Chang, Xiaoyong; Gao, Qin; Chen, Yong; Lu, Wei
Correlating thermochromic and mechanochromic phosphorescence with polymorphs of a complex gold(i) double salt with infinite aurophilicity.
Chemical communications (Cambridge, England), 2018, 54, 12844-12847
7122469 CIFC16 H16 Au2 N10P m n 216.2961; 8.1146; 18.7357
90; 90; 90
957.21Liu, Qi; Xie, Mo; Chang, Xiaoyong; Gao, Qin; Chen, Yong; Lu, Wei
Correlating thermochromic and mechanochromic phosphorescence with polymorphs of a complex gold(i) double salt with infinite aurophilicity.
Chemical communications (Cambridge, England), 2018, 54, 12844-12847
7122470 CIFC16 H16 Au2 N10P m n a6.3929; 8.1734; 18.6898
90; 90; 90
976.57Liu, Qi; Xie, Mo; Chang, Xiaoyong; Gao, Qin; Chen, Yong; Lu, Wei
Correlating thermochromic and mechanochromic phosphorescence with polymorphs of a complex gold(i) double salt with infinite aurophilicity.
Chemical communications (Cambridge, England), 2018, 54, 12844-12847
7122471 CIFC16 H16 Au2 N10P m n a6.3632; 8.1603; 18.6843
90; 90; 90
970.19Liu, Qi; Xie, Mo; Chang, Xiaoyong; Gao, Qin; Chen, Yong; Lu, Wei
Correlating thermochromic and mechanochromic phosphorescence with polymorphs of a complex gold(i) double salt with infinite aurophilicity.
Chemical communications (Cambridge, England), 2018, 54, 12844-12847
7122472 CIFC76 H30 F24 O34 Zr6P 42/m m c24.3097; 24.3097; 14.977
90; 90; 90
8850.8Chen, Cheng-Xia; Qiu, Qian-Feng; Pan, Mei; Cao, Chen-Chen; Zhu, Neng-Xiu; Wang, Hai-Ping; Jiang, Ji-Jun; Wei, Zhang-Wen; Su, Cheng-Yong
Tunability of fluorescent metal-organic frameworks through dynamic spacer installation with multivariate fluorophores.
Chemical communications (Cambridge, England), 2018, 54, 13666-13669
7122473 CIFC80 H32 F24 O34 Zr6P 42/m m c24.3839; 24.3839; 14.8719
90; 90; 90
8842.5Chen, Cheng-Xia; Qiu, Qian-Feng; Pan, Mei; Cao, Chen-Chen; Zhu, Neng-Xiu; Wang, Hai-Ping; Jiang, Ji-Jun; Wei, Zhang-Wen; Su, Cheng-Yong
Tunability of fluorescent metal-organic frameworks through dynamic spacer installation with multivariate fluorophores.
Chemical communications (Cambridge, England), 2018, 54, 13666-13669
7122474 CIFC28 H24 F12 N8 P2 RuC 1 2/c 113.5829; 20.0799; 11.563
90; 90.845; 90
3153.39Havrylyuk, Dmytro; Deshpande, Megha; Parkin, Sean; Glazer, Edith C.
Ru(ii) complexes with diazine ligands: electronic modulation of the coordinating group is key to the design of "dual action" photoactivated agents.
Chemical communications (Cambridge, England), 2018, 54, 12487-12490
7122475 CIFC28 H24 F12 N8 P2 RuC 1 2/c 121.4835; 10.2495; 17.1972
90; 125.539; 90
3081.35Havrylyuk, Dmytro; Deshpande, Megha; Parkin, Sean; Glazer, Edith C.
Ru(ii) complexes with diazine ligands: electronic modulation of the coordinating group is key to the design of "dual action" photoactivated agents.
Chemical communications (Cambridge, England), 2018, 54, 12487-12490
7122476 CIFC40 H52 Cl2 Cu N5 SiP -111.7503; 12.5328; 15.207
89.784; 88.66; 68.23
2079.1Frisch, Philipp; Inoue, Shigeyoshi
Coinage metal complexes of NHC-stabilized silyliumylidene ions.
Chemical communications (Cambridge, England), 2018, 54, 13658-13661
7122477 CIFC42 H55 Au Cl2 N6 SiP -111.8216; 12.5459; 15.1586
89.892; 88.954; 68.401
2089.97Frisch, Philipp; Inoue, Shigeyoshi
Coinage metal complexes of NHC-stabilized silyliumylidene ions.
Chemical communications (Cambridge, England), 2018, 54, 13658-13661
7122478 CIFC16 H27 Au Cl N5P -19.656; 10.844; 19.427
76.21; 79.39; 88.399
1941.5Frisch, Philipp; Inoue, Shigeyoshi
Coinage metal complexes of NHC-stabilized silyliumylidene ions.
Chemical communications (Cambridge, England), 2018, 54, 13658-13661
7122479 CIFC74 H110 Ag2 Cl2 F6 N8 O6 S2 Si2P -19.2078; 15.2562; 17.3518
86.901; 74.733; 74.546
2266.13Frisch, Philipp; Inoue, Shigeyoshi
Coinage metal complexes of NHC-stabilized silyliumylidene ions.
Chemical communications (Cambridge, England), 2018, 54, 13658-13661
7122480 CIFC43 H55 Ag Cl F3 N6 O3 S SiC 1 2/c 128.241; 24.601; 17.0773
90; 125.378; 90
9673.8Frisch, Philipp; Inoue, Shigeyoshi
Coinage metal complexes of NHC-stabilized silyliumylidene ions.
Chemical communications (Cambridge, England), 2018, 54, 13658-13661
7122481 CIFC32 H28 N4 O2C 1 c 19.7923; 17.627; 15.121
90; 91.028; 90
2609.6Geng, Xiao; Wu, Xia; Wang, Can; Zhao, Peng; Zhou, You; Sun, Xuan; Wang, Ling-Jiao; Guan, Wen-Juan; Wu, Yan-Dong; Wu, An-Xin
NaHS·nH<sub>2</sub>O-induced umpolung: the synthesis of 2-acyl-3-aminoindoles from aryl methyl ketones and 2-aminobenzonitriles.
Chemical communications (Cambridge, England), 2018, 54, 12730-12733
7122482 CIFC16 H14 N2 O3 SP 1 21/n 15.7269; 28.551; 8.8421
90; 103.507; 90
1405.8Geng, Xiao; Wu, Xia; Wang, Can; Zhao, Peng; Zhou, You; Sun, Xuan; Wang, Ling-Jiao; Guan, Wen-Juan; Wu, Yan-Dong; Wu, An-Xin
NaHS·nH<sub>2</sub>O-induced umpolung: the synthesis of 2-acyl-3-aminoindoles from aryl methyl ketones and 2-aminobenzonitriles.
Chemical communications (Cambridge, England), 2018, 54, 12730-12733
7122483 CIFC25 H23 N O4P n a 2152.223; 15.6152; 7.4921
90; 90; 90
6109.6Mambrini, Antonin; Gori, Didier; Guillot, Régis; Kouklovsky, Cyrille; Alezra, Valérie
Oxidative coupling of enolates using memory of chirality: an original enantioselective synthesis of quaternary α-amino acid derivatives.
Chemical communications (Cambridge, England), 2018, 54, 12742-12745
7122484 CIFC96 H82 N24 O32 Tb4P 1 21/c 118.886; 32.064; 25.879
90; 104.04; 90
15203Wang, Xiaoning; Li, Jia-Luo; Jiang, Chenggang; Hu, Peng; Li, Bao; Zhang, Tianle; Zhou, Hong-Cai
An efficient strategy for improving the luminescent sensing performance of a terbium(iii) metal-organic framework towards multiple substances.
Chemical communications (Cambridge, England), 2018, 54, 13271-13274
7122485 CIFC32 H27 N O2P 1 21/c 118.041; 12.292; 11.066
90; 94.663; 90
2445.9Qiu, Huang; Arman, Hadi; Hu, Wenhao; Doyle, Michael P.
Intramolecular cycloaddition/rearrangement cascade from gold(iii)-catalysed reactions of propargyl aryldiazoesters with cinnamyl imines.
Chemical communications (Cambridge, England), 2018, 54, 12828-12831
7122486 CIFC52 H16 B Cu F16 N4I -423.5586; 23.5586; 24.6516
90; 90; 90
13681.8Thapa, Sheela; Hettiarachchi, Eshani; Dickie, Diane A.; Rubasinghege, Gayan; Qin, Yang
A charge-separated diamondoid metal-organic framework.
Chemical communications (Cambridge, England), 2018, 54, 12654-12657
7122487 CIFC13 H19 N O3P 21 21 217.3307; 20.5418; 8.597
90; 90; 90
1294.59Pańczyk, Katarzyna; Żelaszczyk, Dorota; Koczurkiewicz, Paulina; Słoczyńska, Karolina; Pękala, Elżbieta; Żesławska, Ewa; Nitek, Wojciech; Żmudzki, Paweł; Marona, Henryk; Waszkielewicz, Anna
Synthesis and anticonvulsant activity of phenoxyacetyl derivatives of amines, including aminoalkanols and amino acids.
MedChemComm, 2018, 9, 1933-1948
7122488 CIFC14 H20 N O3P n a 2121.431; 8.483; 7.516
90; 90; 90
1366.4Pańczyk, Katarzyna; Żelaszczyk, Dorota; Koczurkiewicz, Paulina; Słoczyńska, Karolina; Pękala, Elżbieta; Żesławska, Ewa; Nitek, Wojciech; Żmudzki, Paweł; Marona, Henryk; Waszkielewicz, Anna
Synthesis and anticonvulsant activity of phenoxyacetyl derivatives of amines, including aminoalkanols and amino acids.
MedChemComm, 2018, 9, 1933-1948
7122489 CIFC13 H19 N O3P 21 21 217.3182; 20.524; 8.5965
90; 90; 90
1291.2Pańczyk, Katarzyna; Żelaszczyk, Dorota; Koczurkiewicz, Paulina; Słoczyńska, Karolina; Pękala, Elżbieta; Żesławska, Ewa; Nitek, Wojciech; Żmudzki, Paweł; Marona, Henryk; Waszkielewicz, Anna
Synthesis and anticonvulsant activity of phenoxyacetyl derivatives of amines, including aminoalkanols and amino acids.
MedChemComm, 2018, 9, 1933-1948
7122490 CIFC99 H114 N18P -116.1763; 20.0396; 21.3747
66.358; 76.628; 78.423
6129.9Saini, Meenaxi; Verma, Ashish; Tomar, Kapil; Bharadwaj, Parimal K.; Sadhu, Kalyan K.
Regioisomeric cryptand stabilized gold supraspheres and elongated dodecahedron supraparticles for reversible host-guest chemistry.
Chemical communications (Cambridge, England), 2018, 54, 12836-12839
7122491 CIFC76 H88 N27 O21 Pu2P -116.109; 16.909; 18.673
63.434; 79.805; 88.801
4467.6Reilly, Sean D.; Su, Jing; Keith, Jason M.; Yang, Ping; Batista, Enrique R.; Gaunt, Andrew J.; Harwood, Laurence M.; Hudson, Michael J.; Lewis, Frank W.; Scott, Brian L.; Sharrad, Clint A.; Whittaker, Daniel M.
Plutonium coordination and redox chemistry with the CyMe<sub>4</sub>-BTPhen polydentate N-donor extractant ligand.
Chemical communications (Cambridge, England), 2018, 54, 12582-12585
7122492 CIFC24 H32 N2 O4C 1 2/c 113.47; 15.343; 12.671
90; 113.48; 90
2401.9Kishore, M. V. Nanda; Panda, Pradeepta K.
Revisiting the intense NIR active bronzaphyrin, a 26-π aromatic expanded porphyrin: synthesis and structural analysis.
Chemical communications (Cambridge, England), 2018, 54, 13135-13138
7122493 CIFC52 H54 F12 N4 O8 S2P 1 21/c 112.4875; 12.9069; 16.8517
90; 98.078; 90
2689.12Kishore, M. V. Nanda; Panda, Pradeepta K.
Revisiting the intense NIR active bronzaphyrin, a 26-π aromatic expanded porphyrin: synthesis and structural analysis.
Chemical communications (Cambridge, England), 2018, 54, 13135-13138
7122494 CIFC20 H19 Au Cl2 N4C 1 2/c 129.8651; 9.3064; 16.4107
90; 120.991; 90
3910.02Bente, Stefanie; Kampert, Florian; Tan, Tristan T. Y.; Hahn, F. Ekkehardt
Site-selective metallation of dicarbene precursors.
Chemical communications (Cambridge, England), 2018, 54, 12887-12890
7122495 CIFC20 H20 Cl I N4P 1 21/c 114.0786; 11.8861; 11.9437
90; 96.767; 90
1984.73Bente, Stefanie; Kampert, Florian; Tan, Tristan T. Y.; Hahn, F. Ekkehardt
Site-selective metallation of dicarbene precursors.
Chemical communications (Cambridge, England), 2018, 54, 12887-12890
7122496 CIFC27 H25 Au Cl2 N4P 1 21/n 110.7045; 14.7865; 15.7768
90; 90.904; 90
2496.87Bente, Stefanie; Kampert, Florian; Tan, Tristan T. Y.; Hahn, F. Ekkehardt
Site-selective metallation of dicarbene precursors.
Chemical communications (Cambridge, England), 2018, 54, 12887-12890
7122497 CIFC90 H80 Au Cl2 F6 N8 P3 Pd2C 1 2/c 138.16; 19.3493; 28.0802
90; 112.666; 90
19132.2Bente, Stefanie; Kampert, Florian; Tan, Tristan T. Y.; Hahn, F. Ekkehardt
Site-selective metallation of dicarbene precursors.
Chemical communications (Cambridge, England), 2018, 54, 12887-12890
7122498 CIFC25 H22 O4P 1 21/n 115.6081; 6.1955; 21.7106
90; 107.33; 90
2004.11Alavala, Gopi Krishna Reddy; Sajjad, Farrukh; Shi, Taoda; Kang, Zhenghui; Ma, Mingliang; Xing, Dong; Hu, Wenhao
Diastereoselective synthesis of isochromans via the Cu(ii)-catalysed intramolecular Michael-type trapping of oxonium ylides.
Chemical communications (Cambridge, England), 2018, 54, 12650-12653
7122499 CIFCs2 Na O14 Si4 U2C m m m8.3837; 11.4748; 7.49
90; 90; 90
720.55Pace, Kristen A.; Klepov, Vladislav V.; Morrison, Gregory; Zur Loye, Hans-Conrad
Moderate supercritical synthesis as a facile route to mixed-valent uranium(iv,v) and (v,vi) silicates.
Chemical communications (Cambridge, England), 2018, 54, 13794-13797
7122500 CIFCs2 Na O11 Si2 U2P c c n13.8327; 7.4187; 11.5783
90; 90; 90
1188.17Pace, Kristen A.; Klepov, Vladislav V.; Morrison, Gregory; Zur Loye, Hans-Conrad
Moderate supercritical synthesis as a facile route to mixed-valent uranium(iv,v) and (v,vi) silicates.
Chemical communications (Cambridge, England), 2018, 54, 13794-13797
7122501 CIFNa O14 Rb2 Si4 U2C m m m8.3008; 11.3013; 7.4374
90; 90; 90
697.7Pace, Kristen A.; Klepov, Vladislav V.; Morrison, Gregory; Zur Loye, Hans-Conrad
Moderate supercritical synthesis as a facile route to mixed-valent uranium(iv,v) and (v,vi) silicates.
Chemical communications (Cambridge, England), 2018, 54, 13794-13797
7122502 CIFK2 Na O14 Si4 U2I m m a8.3067; 11.1188; 14.7604
90; 90; 90
1363.28Pace, Kristen A.; Klepov, Vladislav V.; Morrison, Gregory; Zur Loye, Hans-Conrad
Moderate supercritical synthesis as a facile route to mixed-valent uranium(iv,v) and (v,vi) silicates.
Chemical communications (Cambridge, England), 2018, 54, 13794-13797
7122503 CIFNa O11 Rb2 Si2 U2P c c n13.6169; 7.3529; 11.4921
90; 90; 90
1150.63Pace, Kristen A.; Klepov, Vladislav V.; Morrison, Gregory; Zur Loye, Hans-Conrad
Moderate supercritical synthesis as a facile route to mixed-valent uranium(iv,v) and (v,vi) silicates.
Chemical communications (Cambridge, England), 2018, 54, 13794-13797
7122504 CIFC20 H12 F7 N3P -18.5757; 10.724; 11.5979
64.62; 77.985; 71.245
909.41Xie, Ting; Zhang, Yao-Wei; Liu, Li-Li; Shen, Zhi-Liang; Loh, Teck-Peng; Chu, Xue-Qiang
Polycyclic heteroaromatic ring construction driven by silver/cobalt co-catalyzed desulfonylative and defluorinative fragment-recombination of enol nonaflates with amidines.
Chemical communications (Cambridge, England), 2018, 54, 12722-12725
7122505 CIFMg Sb11 Yb13.82I 41/a c d16.553; 16.553; 22.1368
90; 90; 90
6065.5Kunz Wille, Elizabeth L.; Jo, Na Hyun; Fettinger, James C.; Canfield, Paul; Kauzlarich, Susan M.
Single crystal growth and magnetic properties of the mixed valent Yb containing Zintl phase, Yb14MgSb11
Chemical Communications, 2018
7122506 CIFC56 H66 Br2 N4 O8P -110.3142; 10.6819; 25.6534
100.702; 99.312; 92.569
2732.4Jonker, Sybrand J. T.; Diner, Colin; Schulz, Göran; Iwamoto, Hiroaki; Eriksson, Lars; Szabó, Kálmán J
Catalytic asymmetric propargyl- and allylboration of hydrazonoesters: a metal-free approach to sterically encumbered chiral α-amino acid derivatives.
Chemical communications (Cambridge, England), 2018, 54, 12852-12855
7122507 CIFC72 H50 N2 O10 Zn2P -17.3263; 19.7481; 20.1
82.056; 85.336; 80.416
2834.91Liang, Xiao; Guo, Zhifen; Wei, Hongxia; Liu, Xin; Lv, Hui; Xing, Hongzhu
Selective photooxidation of sulfides mediated by singlet oxygen using visible-light-responsive coordination polymers.
Chemical communications (Cambridge, England), 2018, 54, 13002-13005
7122508 CIFC10 H14 N3 O7 PC 1 2/c 119.532; 11.187; 27.511
90; 93.54; 90
6000Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Molecular design of high-temperature organic dielectric switches.
Chemical communications (Cambridge, England), 2018, 54, 13111-13114
7122509 CIFC12 H18 N3 O7 PP 1 21/c 17.0034; 19.672; 12.38
90; 105.85; 90
1640.8Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Molecular design of high-temperature organic dielectric switches.
Chemical communications (Cambridge, England), 2018, 54, 13111-13114
7122510 CIFC12 H16 N3 O7 PP c a b7.0408; 19.834; 23.634
90; 90; 90
3300.4Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Molecular design of high-temperature organic dielectric switches.
Chemical communications (Cambridge, England), 2018, 54, 13111-13114
7122511 CIFC11 H16 N3 O8 PP 1 21/c 16.8885; 19.726; 12.287
90; 107.24; 90
1594.6Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Molecular design of high-temperature organic dielectric switches.
Chemical communications (Cambridge, England), 2018, 54, 13111-13114
7122512 CIFC11 H16 N3 O8 PC m c m11.5686; 20.037; 7.0578
90; 90; 90
1636Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Molecular design of high-temperature organic dielectric switches.
Chemical communications (Cambridge, England), 2018, 54, 13111-13114
7122513 CIFC11 H16 N3 O8 PP 110.232; 9.883; 8.5961
102.92; 99.2; 68.34
784.6Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Molecular design of high-temperature organic dielectric switches.
Chemical communications (Cambridge, England), 2018, 54, 13111-13114
7122514 CIFC71 H84 F4 I2 N4 O10P -114.2852; 15.3486; 16.0133
87.769; 85.092; 79.626
3440Han, Chengyou; Zhao, Dezhi; Dong, Shengyi
Three-dimensional supramolecular polymerization based on pillar[n]arenes (n = 5, 6) and halogen bonding interactions.
Chemical communications (Cambridge, England), 2018, 54, 13099-13102
7122515 CIFC20 H24P 1 21/n 111.5971; 5.737; 12.137
90; 94.7502; 90
804.7Takahashi, Toshifumi; Kuroda, Daiki; Kuwano, Toru; Yoshida, Yuji; Kurahashi, Takuya; Matsubara, Seijiro
Nickel-catalyzed intermolecular carboiodination of alkynes with aryl iodides.
Chemical communications (Cambridge, England), 2018, 54, 12750-12753
7122516 CIFC20 H30 B I O2P 1 21/c 113.663; 10.672; 15.638
90; 105.433; 90
2198Takahashi, Toshifumi; Kuroda, Daiki; Kuwano, Toru; Yoshida, Yuji; Kurahashi, Takuya; Matsubara, Seijiro
Nickel-catalyzed intermolecular carboiodination of alkynes with aryl iodides.
Chemical communications (Cambridge, England), 2018, 54, 12750-12753
7122517 CIFC132 H129.5I 1 2/a 120.993; 17.0469; 30.788
90; 90.228; 90
11017.9Hu, Yunbin; Wang, Di; Baumgarten, Martin; Schollmeyer, Dieter; Müllen, Klaus; Narita, Akimitsu
Spiro-fused bis-hexa-peri-hexabenzocoronene.
Chemical communications (Cambridge, England), 2018, 54, 13575-13578
7122518 CIFC1.91 H2.26 N0.52 O0.52P 1 21/c 15.8179; 11.3981; 17.623
90; 92.653; 90
1167.4He, Kaixuan; Li, Pengfei; Zhang, Shuwei; Chen, Qian; Ji, Honghe; Yuan, Yu; Jia, Xiaodong
One-step construction of molecular complexity by tert-butyl nitrite (TBN)-initiated cascade α,β-sp<sup>3</sup> C-H bond difunctionalization and C-N bond cleavage.
Chemical communications (Cambridge, England), 2018, 54, 13232-13235
7122519 CIFC15 H18 O5P 21 21 218.2861; 9.8316; 18.092
90; 90; 90
1473.9Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122520 CIFC15 H18 O5P 21 21 218.1993; 9.5498; 18.6176
90; 90; 90
1457.79Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122521 CIFC14 H14 O5P 21 21 214.674; 12.9175; 21.3349
90; 90; 90
1288.12Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122522 CIFC15 H20 O5P 21 21 218.8306; 10.0761; 17.1204
90; 90; 90
1523.34Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122523 CIFC14 H16 O5P 1 21 17.6832; 7.5202; 11.6492
90; 91.533; 90
672.84Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122524 CIFC15 H20 O5P 21 21 2111.0585; 11.4256; 11.8876
90; 90; 90
1502Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122525 CIFC48 H70 N6 O10P 1 21 110.819; 14.713; 30.167
90; 96.24; 90
4773.5Kovaleva, Kseniya S.; Zubkov, Fedor I.; Bormotov, Nikolay I.; Novikov, Roman A.; Dorovatovskii, Pavel V.; Khrustalev, Victor N.; Gatilov, Yuriy V.; Zarubaev, Vladimir V.; Yarovaya, Olga I.; Shishkina, Larisa N.; Salakhutdinov, Nariman F.
Synthesis of d-(+)-camphor-based <i>N</i>-acylhydrazones and their antiviral activity.
MedChemComm, 2018, 9, 2072-2082
7122526 CIFC15 H20 N2 O2P 1 21 110.6401; 13.1077; 11.089
90; 111.31; 90
1440.8Kovaleva, Kseniya S.; Zubkov, Fedor I.; Bormotov, Nikolay I.; Novikov, Roman A.; Dorovatovskii, Pavel V.; Khrustalev, Victor N.; Gatilov, Yuriy V.; Zarubaev, Vladimir V.; Yarovaya, Olga I.; Shishkina, Larisa N.; Salakhutdinov, Nariman F.
Synthesis of d-(+)-camphor-based <i>N</i>-acylhydrazones and their antiviral activity.
MedChemComm, 2018, 9, 2072-2082
7122527 CIFC58 H74 N6 O8P 1 21 110.949; 15.752; 31.273
90; 98.92; 90
5328.4Kovaleva, Kseniya S.; Zubkov, Fedor I.; Bormotov, Nikolay I.; Novikov, Roman A.; Dorovatovskii, Pavel V.; Khrustalev, Victor N.; Gatilov, Yuriy V.; Zarubaev, Vladimir V.; Yarovaya, Olga I.; Shishkina, Larisa N.; Salakhutdinov, Nariman F.
Synthesis of d-(+)-camphor-based <i>N</i>-acylhydrazones and their antiviral activity.
MedChemComm, 2018, 9, 2072-2082
7122528 CIFC52 H54 Au2 Cl2 N2 O2 P2P 1 21 111.0336; 14.8166; 15.2675
90; 96.44; 90
2480.2Tabey, Alexis; Berlande, Murielle; Hermange, Philippe; Fouquet, Eric
Mechanistic and asymmetric investigations of the Au-catalysed cross-coupling between aryldiazonium salts and arylboronic acids using (P,N) gold complexes.
Chemical communications (Cambridge, England), 2018, 54, 12867-12870
7122529 CIFC23 H17 N OP 21 21 217.92466; 11.5149; 19.0209
90; 90; 90
1735.69Yuan, Tingting; Pi, Chao; You, Chang; Cui, Xiuling; Du, Sidong; Wan, Ting; Wu, Yangjie
Rapid Assembly of Cyclopentene Spiroisoindolinones via Rhodium-Catalysed Redox-Neutral Cascade Reaction
Chemical Communications, 2018
7122530 CIFC20 H36 Cl F6 Fe2 N3 P S2P b c a16.1521; 17.3762; 20.485
90; 90; 90
5749.4Su, Linan; Yang, Dawei; Zhang, Yixin; Wang, Baomin; Qu, Jingping
Methylene insertion into an Fe<sub>2</sub>S<sub>2</sub> cluster: formation of a thiolate-bridged diiron complex containing an Fe-CH<sub>2</sub>-S moiety.
Chemical communications (Cambridge, England), 2018, 54, 13119-13122
7122531 CIFC19 H35 Cl2 Fe2 N2 S2P 1 21/c 114.7655; 11.1673; 14.2254
90; 95.3012; 90
2335.6Su, Linan; Yang, Dawei; Zhang, Yixin; Wang, Baomin; Qu, Jingping
Methylene insertion into an Fe<sub>2</sub>S<sub>2</sub> cluster: formation of a thiolate-bridged diiron complex containing an Fe-CH<sub>2</sub>-S moiety.
Chemical communications (Cambridge, England), 2018, 54, 13119-13122
7122532 CIFC21 H38 Cl F6 Fe2 N3 P S2P b c a11.7179; 15.2415; 33.0452
90; 90; 90
5901.8Su, Linan; Yang, Dawei; Zhang, Yixin; Wang, Baomin; Qu, Jingping
Methylene insertion into an Fe<sub>2</sub>S<sub>2</sub> cluster: formation of a thiolate-bridged diiron complex containing an Fe-CH<sub>2</sub>-S moiety.
Chemical communications (Cambridge, England), 2018, 54, 13119-13122
7122533 CIFC36 H16 Cu3 F24 N8P -19.1317; 11.0607; 11.7651
72.527; 70.675; 69.17
1025.4Titov, Aleksei; Larionov, Vladimir A.; Smol’yakov, Alexander F.; Godovikova, Maria I.; Titova, Ekaterina M.; Maleev, Victor I.; Shubina, Elena
Interaction of the trinuclear copper(I) pyrazolate with alkynes and carbon-carbon triple bond activation
Chemical Communications, 2018
7122534 CIFC36 H32 Cu3 F24 N8P -18.55; 10.66; 13.468
107.62; 100.88; 95.18
1135Titov, Aleksei; Larionov, Vladimir A.; Smol’yakov, Alexander F.; Godovikova, Maria I.; Titova, Ekaterina M.; Maleev, Victor I.; Shubina, Elena
Interaction of the trinuclear copper(I) pyrazolate with alkynes and carbon-carbon triple bond activation
Chemical Communications, 2018
7122535 CIFC12 H12 N2 O6P 1 21/c 110.53644; 18.23475; 6.97824
90; 111.604; 90
1246.54Lukin, Stipe; Tireli, Martina; Lončarić, Ivor; Barišić, Dajana; Šket, PrimoŽ; Vrsaljko, Domagoj; di Michiel, Marco; Plavec, Janez; UŽarević, Krunoslav; Halasz, Ivan
Mechanochemical carbon-carbon bond formation that proceeds via a cocrystal intermediate.
Chemical communications (Cambridge, England), 2018, 54, 13216-13219
7122536 CIFC12 H11 N2 O5.5P 1 21/n 114.148; 14.7902; 12.1137
90; 115.972; 90
2278.8Lukin, Stipe; Tireli, Martina; Lončarić, Ivor; Barišić, Dajana; Šket, PrimoŽ; Vrsaljko, Domagoj; di Michiel, Marco; Plavec, Janez; UŽarević, Krunoslav; Halasz, Ivan
Mechanochemical carbon-carbon bond formation that proceeds via a cocrystal intermediate.
Chemical communications (Cambridge, England), 2018, 54, 13216-13219
7122537 CIFC20 H20 Br N O2P 1 21 110.901; 6.2481; 13.318
90; 98.052; 90
898.2Du, Juan; Jiang, Yang-Jie; Suo, Jia-Jia; Wu, Wen-Qiong; Liu, Xiu-Yan; Chen, Di; Ding, Chang-Hua; Wei, Yin; Hou, Xue-Long
Trisubstituted alkenes with a single activator as dipolarophiles in a highly diastereo- and enantioselective [3+2] cycloaddition with vinyl epoxides under Pd-catalysis.
Chemical communications (Cambridge, England), 2018, 54, 13143-13146
7122538 CIFC20 H21 Cl N2 O4P 21 21 2110.4038; 20.5233; 37.6117
90; 90; 90
8030.9Du, Juan; Jiang, Yang-Jie; Suo, Jia-Jia; Wu, Wen-Qiong; Liu, Xiu-Yan; Chen, Di; Ding, Chang-Hua; Wei, Yin; Hou, Xue-Long
Trisubstituted alkenes with a single activator as dipolarophiles in a highly diastereo- and enantioselective [3+2] cycloaddition with vinyl epoxides under Pd-catalysis.
Chemical communications (Cambridge, England), 2018, 54, 13143-13146
7122539 CIFC17 H23.4 Br N O2P 21 21 2110.2614; 21.747; 40.341
90; 90; 90
9002.3Du, Juan; Jiang, Yang-Jie; Suo, Jia-Jia; Wu, Wen-Qiong; Liu, Xiu-Yan; Chen, Di; Ding, Chang-Hua; Wei, Yin; Hou, Xue-Long
Trisubstituted alkenes with a single activator as dipolarophiles in a highly diastereo- and enantioselective [3+2] cycloaddition with vinyl epoxides under Pd-catalysis.
Chemical communications (Cambridge, England), 2018, 54, 13143-13146
7122540 CIFC112 H160 K2 N4 O10 Yb3P -113.294; 13.787; 15.741
105.839; 92.357; 112.705
2525.3Fedushkin, Igor L.; Lukina, Daria A.; Skatova, Alexandra A.; Lukoyanov, Anton N.; Cherkasov, Anton V.
Ca(ii), Yb(ii) and Tm(iii) complexes with tri- and tetra-anions of 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene.
Chemical communications (Cambridge, England), 2018, 54, 12950-12953
7122541 CIFC112 H160 Ca2 N4 Na4 O10P -113.0748; 13.2572; 15.9107
79.799; 85.246; 69.146
2535.9Fedushkin, Igor L.; Lukina, Daria A.; Skatova, Alexandra A.; Lukoyanov, Anton N.; Cherkasov, Anton V.
Ca(ii), Yb(ii) and Tm(iii) complexes with tri- and tetra-anions of 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene.
Chemical communications (Cambridge, England), 2018, 54, 12950-12953
7122542 CIFC80 H96 N4 Na2 O2 Tm2P 1 21/n 113.694; 16.73; 14.7
90; 91.656; 90
3366.4Fedushkin, Igor L.; Lukina, Daria A.; Skatova, Alexandra A.; Lukoyanov, Anton N.; Cherkasov, Anton V.
Ca(ii), Yb(ii) and Tm(iii) complexes with tri- and tetra-anions of 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene.
Chemical communications (Cambridge, England), 2018, 54, 12950-12953
7122543 CIFC9 H13 N17 O15P 1 21/n 17.7021; 25.8034; 11.7215
90; 91.931; 90
2328.21Zhang, Xiaopeng; Chen, Shusen; Wu, Yige; Jin, Shaohua; Wang, Xiaojun; Wang, Yuqiao; Shang, Fengqin; Chen, Kun; Du, Junyi; Shu, Qinghai
A novel cocrystal composed of CL-20 and an energetic ionic salt.
Chemical communications (Cambridge, England), 2018, 54, 13268-13270
7122544 CIFC36 H34 Cr F18 N10 P3P n a 2120.0625; 16.1756; 13.5227
90; 90; 90
4388.43Jiménez, Juan-Ramón; Doistau, Benjamin; Besnard, Céline; Piguet, Claude
Versatile heteroleptic bis-terdentate Cr(iii) chromophores displaying room temperature millisecond excited state lifetimes.
Chemical communications (Cambridge, England), 2018, 54, 13228-13231
7122545 CIFC17 H17 Br3 Cr N5P 1 21/n 19.35425; 15.1963; 13.72684
90; 95.8596; 90
1941.07Jiménez, Juan-Ramón; Doistau, Benjamin; Besnard, Céline; Piguet, Claude
Versatile heteroleptic bis-terdentate Cr(iii) chromophores displaying room temperature millisecond excited state lifetimes.
Chemical communications (Cambridge, England), 2018, 54, 13228-13231
7122546 CIFC42 H41 Cr F15 N11 O5 P2 SP -111.9089; 12.6435; 19.9341
74.089; 75.79; 69.487
2666Jiménez, Juan-Ramón; Doistau, Benjamin; Besnard, Céline; Piguet, Claude
Versatile heteroleptic bis-terdentate Cr(iii) chromophores displaying room temperature millisecond excited state lifetimes.
Chemical communications (Cambridge, England), 2018, 54, 13228-13231
7122547 CIFC36 H78 Cl6 N2 Pt2P 1 21/n 113.1677; 12.8495; 13.3831
90; 98.427; 90
2239.95Silalahi, Imelda H.; Sethi, Navpreet K.; Shafikov, Marsel Z.; Chechik, Victor; Whitwood, Adrian C.; Bruce, Duncan W.
Unexpected, photochemically induced activation of the tetrabutylammonium cation by hexachloroplatinate(iv).
Chemical communications (Cambridge, England), 2018, 54, 13682-13685
7122548 CIFC64 H60 Cl Dy N8 O22 Zn3P 32 2 116.9961; 16.9961; 19.8792
90; 90; 120
4973.1Liu, Cai-Ming; Zhang, De-Qing; Xiong, Ren-Gen; Hao, Xiang; Zhu, Dao-Ben
A homochiral Zn-Dy heterometallic left-handed helical chain complex without chiral ligands: anion-induced assembly and multifunctional integration.
Chemical communications (Cambridge, England), 2018, 54, 13379-13382
7122549 CIFC86 H64 Dy2 N12 O24 Zn3P b c a16.007; 21.007; 55.589
90; 90; 90
18692Liu, Cai-Ming; Zhang, De-Qing; Xiong, Ren-Gen; Hao, Xiang; Zhu, Dao-Ben
A homochiral Zn-Dy heterometallic left-handed helical chain complex without chiral ligands: anion-induced assembly and multifunctional integration.
Chemical communications (Cambridge, England), 2018, 54, 13379-13382
7122550 CIFC22 H16 N2 OP 1 21/n 111.1571; 12.454; 11.9
90; 90.045; 90
1653.51Aksenov, Alexander V.; Aksenov, Nicolai A.; Aksenov, Dmitrii A.; Khamraev, Vladislav F.; Rubin, Michael
Nitrostyrenes as 1,4-CCNO-dipoles: diastereoselective formal [4+1] cycloaddition of indoles.
Chemical communications (Cambridge, England), 2018, 54, 13260-13263
7122551 CIFC132 H136 F4 N26 O24 Pd2 S2P b c m21.3685; 26.9448; 41.0041
90; 90; 90
23608.9Lin, Qi; Gao, Lei; Kauffmann, Brice; Zhang, Jiajia; Ma, Chunmiao; Luo, Dan; Gan, Quan
Helicity adaptation within a quadruply stranded helicate by encapsulation.
Chemical communications (Cambridge, England), 2018, 54, 13447-13450
7122552 CIFC136 H140 B4 F20 N30 O14 Pd2P -117.0266; 17.8919; 18.1716
74.712; 66.581; 78.682
4873.8Lin, Qi; Gao, Lei; Kauffmann, Brice; Zhang, Jiajia; Ma, Chunmiao; Luo, Dan; Gan, Quan
Helicity adaptation within a quadruply stranded helicate by encapsulation.
Chemical communications (Cambridge, England), 2018, 54, 13447-13450
7122553 CIFC128 H124 F4 N24 O16 Pd2I 4/m18.9268; 18.9268; 24.7717
90; 90; 90
8873.8Lin, Qi; Gao, Lei; Kauffmann, Brice; Zhang, Jiajia; Ma, Chunmiao; Luo, Dan; Gan, Quan
Helicity adaptation within a quadruply stranded helicate by encapsulation.
Chemical communications (Cambridge, England), 2018, 54, 13447-13450
7122554 CIFC128 H124 B14 F24 N24 O16 Pd2P 1 21/n 119.8811; 22.8682; 44.582
90; 94.821; 90
20197.3Lin, Qi; Gao, Lei; Kauffmann, Brice; Zhang, Jiajia; Ma, Chunmiao; Luo, Dan; Gan, Quan
Helicity adaptation within a quadruply stranded helicate by encapsulation.
Chemical communications (Cambridge, England), 2018, 54, 13447-13450
7122555 CIFC19 H17 N O3P 1 21/n 18.3135; 7.8576; 24.136
90; 99.49; 90
1555.09Kumari, Pratibha; Verma, Sanjay Kumar; Mobin, Shaikh M.
A facile two-photon fluorescent probe: Endoplasmic Reticulum tracker, monitoring ER stress and vesicular transport to lysosomes
Chemical Communications, 2018
7122556 CIFC170 H176 Li4 N12 O8P -116.963; 17.366; 26.321
108.871; 105.372; 92.009
7012.1Diaz-Rodriguez, Roberto M; Robertson, Katherine N.; Thompson, Alison
Synthesis and reactivity of aza-dipyrrin alkali metal salts.
Chemical communications (Cambridge, England), 2018, 54, 13139-13142
7122557 CIFC56 H36 N6 ZnC 1 2/c 123.287; 11.257; 16.403
90; 108.675; 90
4073.5Diaz-Rodriguez, Roberto M; Robertson, Katherine N.; Thompson, Alison
Synthesis and reactivity of aza-dipyrrin alkali metal salts.
Chemical communications (Cambridge, England), 2018, 54, 13139-13142
7122558 CIFC36 H30 Cl N3 O ZnP -18.3304; 13.73; 26.735
103.459; 92.281; 97.662
2939.4Diaz-Rodriguez, Roberto M; Robertson, Katherine N.; Thompson, Alison
Synthesis and reactivity of aza-dipyrrin alkali metal salts.
Chemical communications (Cambridge, England), 2018, 54, 13139-13142
7122559 CIFC86 H136 Fe2 K N6 O10P -113.1435; 13.7367; 14.6446
66.914; 88.232; 68.744
2247.7McWilliams, Sean F.; Bunting, Philip C.; Kathiresan, Venkatesan; Mercado, Brandon Q.; Hoffman, Brian M.; Long, Jeffrey R.; Holland, Patrick L.
Isolation and characterization of a high-spin mixed-valent iron dinitrogen complex.
Chemical communications (Cambridge, England), 2018, 54, 13339-13342
7122560 CIFC60 H54 B4 F16 Fe2 N24 O6P 63/m14.3872; 14.3872; 24.9442
90; 90; 120
4471.5Wilson, Benjamin H.; Scott, Hayley S.; Qazvini, Omid T.; Telfer, Shane G.; Mathonière, Corine; Clérac, Rodolphe; Kruger, Paul E.
A supramolecular porous material comprising Fe(ii) mesocates.
Chemical communications (Cambridge, England), 2018, 54, 13391-13394
7122561 CIFC18 H18 N2 O3 SP 21 21 218.2292; 12.3415; 17.181
90; 90; 90
1744.9Lu, Yi-Nan; Lan, Jin-Ping; Mao, Yu-Jia; Wang, Ye-Xin; Mei, Guang-Jian; Shi, Feng
Catalytic asymmetric de novo construction of dihydroquinazolinone scaffolds via enantioselective decarboxylative [4+2] cycloadditions.
Chemical communications (Cambridge, England), 2018, 54, 13527-13530
7122562 CIFC21 H22 N PP 1 21/c 114.1544; 4.5958; 26.774
90; 96.099; 90
1731.8Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122563 CIFC73 H71 I Mo N3 O3 P3 UP -112.6048; 13.305; 21.6579
89.18; 75.294; 88.901
3512.4Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122564 CIFC80 H79 Cl Mo N3 O3 P3 UP -112.2335; 13.3432; 21.8523
89.2225; 74.9637; 89.8281
3444.59Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122565 CIFC73 H71 I Mo N3 O3 P3 ThP -112.7259; 13.3141; 21.7153
88.662; 75.262; 88.66
3556.7Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122566 CIFC77 H79 Cl N3 P3 UP 1 21/n 115.9544; 22.7597; 18.2868
90; 96.5882; 90
6596.4Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122567 CIFC29 H41 Li N O2 PP 1 21/c 119.3727; 9.1104; 16.222
90; 105.113; 90
2764Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122568 CIFC77 H79 I N3 P3 UP 1 21/n 112.496; 39.078; 13.949
90; 91.079; 90
6810Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122569 CIFC67 H63 Cl N3 O4 P3 U WP -113.639; 14.6571; 16.721
76.466; 88.965; 67.082
2983.3Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122570 CIFC63 H63 Cl N3 P3 ThP 1 21/n 113.04797; 25.46193; 16.86018
90; 97.423; 90
5554.46Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122571 CIFC80 H79 Cl Mo N3 O3 P3 ThP -112.326; 13.3087; 21.9496
88.897; 74.385; 89.611
3467.1Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122572 CIFC63 H63 I N3 P3 ThP 1 21/n 113.05887; 25.3036; 17.01612
90; 96.6633; 90
5584.77Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122573 CIFC67 H63 Cl Cr N3 O4 P3 UP -113.7659; 14.4077; 16.5607
76.698; 89.117; 67.671
2947.3Ayres, Alexander J.; Zegke, Markus; Ostrowski, Joseph P. A.; Tuna, Floriana; McInnes, Eric J. L.; Wooles, Ashley J.; Liddle, Stephen T.
Actinide-transition metal bonding in heterobimetallic uranium- and thorium-molybdenum paddlewheel complexes.
Chemical communications (Cambridge, England), 2018, 54, 13515-13518
7122574 CIFC39.2 H44.8 F4.8 N4.8 O4.8 S1.6 Si0.8P 1 21/n 112.8682; 24.121; 17.041
90; 97.415; 90
5245.19Hermannsdorfer, André; Stephan, Douglas W.; Driess, Matthias
Taming a silyldiium cation and its reactivity towards sodium phosphaethynolate.
Chemical communications (Cambridge, England), 2018, 54, 13523-13526
7122575 CIFC33.09 H43.64 Cl0.73 F2.18 N2.91 O2.18 P1.45 S0.73I 1 2/a 121.3898; 14.7759; 32.3467
90; 108.989; 90
9666.9Hermannsdorfer, André; Stephan, Douglas W.; Driess, Matthias
Taming a silyldiium cation and its reactivity towards sodium phosphaethynolate.
Chemical communications (Cambridge, England), 2018, 54, 13523-13526
7122576 CIFC38 H45 F3 N4 O3 P2 SP -19.2894; 11.9054; 18.4338
95.68; 101.636; 92.537
1982.6Hermannsdorfer, André; Stephan, Douglas W.; Driess, Matthias
Taming a silyldiium cation and its reactivity towards sodium phosphaethynolate.
Chemical communications (Cambridge, England), 2018, 54, 13523-13526
7122577 CIFC46 H53 F3 N5 O3 P S SiP 1 21/n 120.7909; 9.6113; 23.6415
90; 105.534; 90
4551.66Hermannsdorfer, André; Stephan, Douglas W.; Driess, Matthias
Taming a silyldiium cation and its reactivity towards sodium phosphaethynolate.
Chemical communications (Cambridge, England), 2018, 54, 13523-13526
7122578 CIFC16 H16 O5 SP -18.157; 9.8595; 10.2239
63.734; 75.835; 85.625
714.44Porcu, Stefania; Luridiana, Alberto; Martis, Alberto; Frongia, Angelo; Sarais, Giorgia; Aitken, David J.; Boddaert, Thomas; Guillot, Regis; Secci, Francesco
Acid-catalyzed synthesis of functionalized arylthio cyclopropane carbaldehydes and ketones.
Chemical communications (Cambridge, England), 2018, 54, 13547-13550
7122579 CIFC H N OP 1 21 16.9872; 15.5151; 19.425
90; 98.467; 90
2082.9Zhao, Fengyi; Lu, Wen; Su, Fan; Xu, Li; Jiang, Dong; Sun, Xu; Shi, Jiuzhou; Zhou, Mengyi; Lin, Feng; Cao, Fuliang
Synthesis and potential antineoplastic activity of dehydroabietylamine imidazole derivatives.
MedChemComm, 2018, 9, 2091-2099
7122580 CIFC25 H37 N3 O5P 1 21 110.3659; 7.0531; 16.9815
90; 92.543; 90
1240.32Zhao, Fengyi; Lu, Wen; Su, Fan; Xu, Li; Jiang, Dong; Sun, Xu; Shi, Jiuzhou; Zhou, Mengyi; Lin, Feng; Cao, Fuliang
Synthesis and potential antineoplastic activity of dehydroabietylamine imidazole derivatives.
MedChemComm, 2018, 9, 2091-2099
7122581 CIFC16 H56 Cl12 N8 O4 Pb2P n n m8.21; 25.782; 9.467
90; 90; 90
2003.9Ma, Yujie; Li, Jing; Ye, Jianxun; Liu, Delong; Zhang, Wanbin
Synthesis of chiral chromanols via a RuPHOX-Ru catalyzed asymmetric hydrogenation of chromones.
Chemical communications (Cambridge, England), 2018, 54, 13571-13574
7122582 CIFC10 H8 I2 N2 O2C 1 c 116.6999; 4.4334; 17.237
90; 101.316; 90
1251.37Ma, Yujie; Li, Jing; Ye, Jianxun; Liu, Delong; Zhang, Wanbin
Synthesis of chiral chromanols via a RuPHOX-Ru catalyzed asymmetric hydrogenation of chromones.
Chemical communications (Cambridge, England), 2018, 54, 13571-13574
7122583 CIFC10 H12 O2P 1 21 111.506; 4.84; 16.85
90; 103.13; 90
914Ma, Yujie; Li, Jing; Ye, Jianxun; Liu, Delong; Zhang, Wanbin
Synthesis of chiral chromanols via a RuPHOX-Ru catalyzed asymmetric hydrogenation of chromones.
Chemical communications (Cambridge, England), 2018, 54, 13571-13574
7122584 CIFC18 H15 N O3P 21 21 2110.598; 11.469; 12.275
90; 90; 90
1492Ma, Yujie; Li, Jing; Ye, Jianxun; Liu, Delong; Zhang, Wanbin
Synthesis of chiral chromanols via a RuPHOX-Ru catalyzed asymmetric hydrogenation of chromones.
Chemical communications (Cambridge, England), 2018, 54, 13571-13574
7122585 CIFC36 H36 N6P 1 21/c 113.0765; 13.7569; 8.1842
90; 101.42; 90
1443.13Longevial, Jean-François; Yamaji, Ayaka; Aggad, Dina; Kim, Gakhyun; Chia, Wen Xi; Nishimura, Tsubasa; Miyake, Yoshihiro; Clément, Sébastien; Oh, Juwon; Daurat, Morgane; Nguyen, Christophe; Kim, Dongho; Gary-Bobo, Magali; Richeter, Sébastien; Shinokubo, Hiroshi
Diazachlorin and diazabacteriochlorin for one- and two-photon photodynamic therapy.
Chemical communications (Cambridge, England), 2018, 54, 13829-13832
7122586 CIFC26 H24 N2 O3P -17.4591; 12.033; 12.1333
102.784; 94.976; 99.04
1040.5Wang, Shuai; An, Xiao-De; Li, Shuai-Shuai; Liu, Xicheng; Liu, Qing; Xiao, Jian
Hydride transfer initiated ring expansion of pyrrolidines toward highly functionalized tetrahydro-1-benzazepines.
Chemical communications (Cambridge, England), 2018, 54, 13833-13836
7122587 CIFC15 H20 B10 Cl N OP 1 21/n 19.7687; 12.8969; 15.702
90; 100.297; 90
1946.4Xu, Tao-Tao; Cao, Ke; Zhang, Cai-Yan; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed selective arylation of o-carboranes via B(4)-H activation: amide induced regioselectivity reversal.
Chemical communications (Cambridge, England), 2018, 54, 13603-13606
7122588 CIFC35 H31 B Cl F10 P SiP 1 21/n 110.9107; 17.0092; 18.4957
90; 97.954; 90
3399.5Ueno, Atsushi; Möricke, Jennifer; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Phosphirenium borate betaines from alkynylphosphanes and the halogeno-B(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub> reagents.
Chemical communications (Cambridge, England), 2018, 54, 13746-13749
7122589 CIFC35 H31 B Br F10 P SiP 1 21/c 19.6668; 20.0637; 19.4399
90; 95.326; 90
3754.13Ueno, Atsushi; Möricke, Jennifer; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Phosphirenium borate betaines from alkynylphosphanes and the halogeno-B(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub> reagents.
Chemical communications (Cambridge, England), 2018, 54, 13746-13749
7122590 CIFC28 H23 B Cl F10 PP 1 21/n 19.2115; 22.0031; 14.1968
90; 97.69; 90
2851.55Ueno, Atsushi; Möricke, Jennifer; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Phosphirenium borate betaines from alkynylphosphanes and the halogeno-B(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub> reagents.
Chemical communications (Cambridge, England), 2018, 54, 13746-13749
7122591 CIFC39.5 H35 B Br F10 PP -19.5895; 10.8563; 18.736
82.363; 76.153; 76.873
1837.99Ueno, Atsushi; Möricke, Jennifer; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Phosphirenium borate betaines from alkynylphosphanes and the halogeno-B(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub> reagents.
Chemical communications (Cambridge, England), 2018, 54, 13746-13749
7122592 CIFC28 H23 B Br F10 PP 1 21/n 18.9577; 18.6647; 16.594
90; 91.458; 90
2773.5Ueno, Atsushi; Möricke, Jennifer; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Phosphirenium borate betaines from alkynylphosphanes and the halogeno-B(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub> reagents.
Chemical communications (Cambridge, England), 2018, 54, 13746-13749
7122593 CIFC12 H14 N2 P2 S4P -14.6979; 7.2032; 12.158
91.108; 99.021; 104.05
393.47Begum, Imtiaz; Schnakenburg, Gregor; Kelemen, Zsolt; Nyulászi, László; Boeré, René T; Streubel, Rainer
Expanding the chemistry of ring-fused 1,4-diphosphinines by stable mono anion formation.
Chemical communications (Cambridge, England), 2018, 54, 13555-13558
7122594 CIFC30 H62 K N3 O3 P2 S4 Si2P -18.9737; 14.8907; 16.9261
77.937; 83.96; 88.797
2199.5Begum, Imtiaz; Schnakenburg, Gregor; Kelemen, Zsolt; Nyulászi, László; Boeré, René T; Streubel, Rainer
Expanding the chemistry of ring-fused 1,4-diphosphinines by stable mono anion formation.
Chemical communications (Cambridge, England), 2018, 54, 13555-13558
7122595 CIFC12 H14 Cl2 N2 P2 S4P -16.5353; 6.6119; 10.7915
84.231; 88.651; 88.674
463.72Begum, Imtiaz; Schnakenburg, Gregor; Kelemen, Zsolt; Nyulászi, László; Boeré, René T; Streubel, Rainer
Expanding the chemistry of ring-fused 1,4-diphosphinines by stable mono anion formation.
Chemical communications (Cambridge, England), 2018, 54, 13555-13558
7122596 CIFC36 H64 N6 P4 S8 Si4P 1 21/c 112.0838; 19.5676; 24.8575
90; 95.5499; 90
5850.03Begum, Imtiaz; Schnakenburg, Gregor; Kelemen, Zsolt; Nyulászi, László; Boeré, René T; Streubel, Rainer
Expanding the chemistry of ring-fused 1,4-diphosphinines by stable mono anion formation.
Chemical communications (Cambridge, England), 2018, 54, 13555-13558
7122597 CIFC30 H42 N3 P3 S4 Si2P c a 2118.7088; 11.7664; 33.3168
90; 90; 90
7334.2Begum, Imtiaz; Schnakenburg, Gregor; Kelemen, Zsolt; Nyulászi, László; Boeré, René T; Streubel, Rainer
Expanding the chemistry of ring-fused 1,4-diphosphinines by stable mono anion formation.
Chemical communications (Cambridge, England), 2018, 54, 13555-13558
7122598 CIFC24 H26 N2 O10 Zn2P 1 21/c 17.1598; 24.1618; 10.4735
90; 134.259; 90
1297.63Volodin, Alexander D.; Korlyukov, Alexander A.; Zorina-Tikhonova, Ekaterina N; Chistyakov, Aleksandr S.; Sidorov, Aleksei A.; Eremenko, Igor L.; Vologzhanina, Anna V.
Diastereoselective solid-state crossed photocycloaddition of olefins in a 3D Zn(ii) coordination polymer.
Chemical communications (Cambridge, England), 2018, 54, 13861-13864
7122599 CIFC24 H26 N2 O10 Zn2P 1 21/c 17.227; 25.3; 10.48
90; 134.6; 90
1364Volodin, Alexander D.; Korlyukov, Alexander A.; Zorina-Tikhonova, Ekaterina N; Chistyakov, Aleksandr S.; Sidorov, Aleksei A.; Eremenko, Igor L.; Vologzhanina, Anna V.
Diastereoselective solid-state crossed photocycloaddition of olefins in a 3D Zn(ii) coordination polymer.
Chemical communications (Cambridge, England), 2018, 54, 13861-13864
7122600 CIFC24 H26 N2 O10 Zn2P 1 21/c 17.1977; 24.7844; 10.4717
90; 134.483; 90
1332.78Volodin, Alexander D.; Korlyukov, Alexander A.; Zorina-Tikhonova, Ekaterina N; Chistyakov, Aleksandr S.; Sidorov, Aleksei A.; Eremenko, Igor L.; Vologzhanina, Anna V.
Diastereoselective solid-state crossed photocycloaddition of olefins in a 3D Zn(ii) coordination polymer.
Chemical communications (Cambridge, England), 2018, 54, 13861-13864
7122601 CIFC24 H26 N2 O10 Zn2P 1 n 17.1981; 24.07; 7.4585
90; 90.75; 90
1292.1Volodin, Alexander D.; Korlyukov, Alexander A.; Zorina-Tikhonova, Ekaterina N; Chistyakov, Aleksandr S.; Sidorov, Aleksei A.; Eremenko, Igor L.; Vologzhanina, Anna V.
Diastereoselective solid-state crossed photocycloaddition of olefins in a 3D Zn(ii) coordination polymer.
Chemical communications (Cambridge, England), 2018, 54, 13861-13864
7122602 CIFC169 H74.35 Cl15 N4 O10.68 S2P 1 21/c 117.719; 28.837; 23.889
90; 96.934; 90
12117Hashikawa, Yoshifumi; Hasegawa, Shota; Murata, Yasujiro
A single but hydrogen-bonded water molecule confined in an anisotropic subnanospace.
Chemical communications (Cambridge, England), 2018, 54, 13686-13689
7122603 CIFC130 H89.64 N6 Ni O4.67 SP -113.8823; 17.675; 21.013
91.943; 109.228; 108.323
4566.9Hashikawa, Yoshifumi; Hasegawa, Shota; Murata, Yasujiro
A single but hydrogen-bonded water molecule confined in an anisotropic subnanospace.
Chemical communications (Cambridge, England), 2018, 54, 13686-13689
7122604 CIFC14 H18 Mo9 N2 O28C 1 2/c 127.187; 5.4936; 24.825
90; 121.511; 90
3161Wei, Yong-Qin; Sun, Cai; Chen, Qing-Song; Wang, Ming-Sheng; Guo, Guo-Cong
Significant enhancement of conductance of a hybrid layered molybdate semiconductor by light or heat.
Chemical communications (Cambridge, England), 2018, 54, 14077-14080
7122605 CIFC19 H21 N O3 SC 1 2/c 135.236; 7.3453; 13.4985
90; 96.077; 90
3474Cao, Bo; Wei, Yin; Shi, Min
Palladium-catalyzed intramolecular transfer hydrogenation & cycloaddition of p-quinamine-tethered alkylidenecyclopropanes to synthesize perhydroindole scaffolds.
Chemical communications (Cambridge, England), 2018, 54, 14085-14088
7122606 CIFC19 H23 N O3 SP 1 21/n 17.0366; 20.3622; 12.3027
90; 96.424; 90
1751.7Cao, Bo; Wei, Yin; Shi, Min
Palladium-catalyzed intramolecular transfer hydrogenation & cycloaddition of p-quinamine-tethered alkylidenecyclopropanes to synthesize perhydroindole scaffolds.
Chemical communications (Cambridge, England), 2018, 54, 14085-14088
7122607 CIFC208 H224 N64 Ni16 O64I 41/a19.5487; 19.5487; 29.8878
90; 90; 90
11421.7Kivi, Charlie Eric William; Gelfand, Benjamin Sidney; Dureckova, Hana; Ho, Ha T. K.; Ma, Cindy; Shimizu, George K. H.; Woo, Tom; Song, Datong
3D Porous Metal‒Organic Framework for Selective Adsorption of Methane over Dinitrogen under Ambient Pressure
Chemical Communications, 2018
7122608 CIFC38 H22 N10 O0.84 SiP -4 n 29.7375; 9.7375; 15.684
90; 90; 90
1487.1Kocherga, Margaret; Castaneda, Jose; Walter, Michael G.; Zhang, Yong; Saleh, Nemah-Allah; Wang, Le; Jones, Daniel S.; Merkert, Jon; Donovan-Merkert, Bernadette; Li, Yanzeng; Hofmann, Tino; Schmedake, Thomas A.
Si(bzimpy)<sub>2</sub> - a hexacoordinate silicon pincer complex for electron transport and electroluminescence.
Chemical communications (Cambridge, England), 2018, 54, 14073-14076
7122609 CIFC29 H23 Br2 Mn N O2 P2P -113.2012; 15.1666; 16.3854
98.384; 111.38; 108.519
2766.6Wu, Yue; Zhang, Xu; Zhang, Yun-Qin; Yang, Ming; Chen, Zhong-Ning
Achievement of ligand-field induced thermochromic luminescence via two-step single-crystal to single-crystal transformations.
Chemical communications (Cambridge, England), 2018, 54, 13961-13964
7122610 CIFC29 H23 Br2 Mn N O2 P2P -113.0769; 15.2036; 16.9342
99.7454; 109.665; 107.534
2882.52Wu, Yue; Zhang, Xu; Zhang, Yun-Qin; Yang, Ming; Chen, Zhong-Ning
Achievement of ligand-field induced thermochromic luminescence via two-step single-crystal to single-crystal transformations.
Chemical communications (Cambridge, England), 2018, 54, 13961-13964
7122611 CIFC29 H23 Br2 Mn N O2 P2P -110.4577; 12.4576; 12.4979
85.451; 68.607; 82.521
1502.2Wu, Yue; Zhang, Xu; Zhang, Yun-Qin; Yang, Ming; Chen, Zhong-Ning
Achievement of ligand-field induced thermochromic luminescence via two-step single-crystal to single-crystal transformations.
Chemical communications (Cambridge, England), 2018, 54, 13961-13964
7122612 CIFC58 H46 Br4 Mn2 N2 O4 P4P -113.137; 15.1638; 16.736
99.164; 110.439; 107.866
2837.6Wu, Yue; Zhang, Xu; Zhang, Yun-Qin; Yang, Ming; Chen, Zhong-Ning
Achievement of ligand-field induced thermochromic luminescence via two-step single-crystal to single-crystal transformations.
Chemical communications (Cambridge, England), 2018, 54, 13961-13964
7122613 CIFC58 H46 Br4 Mn2 N2 O4 P4P -112.089; 15.242; 17.019
100.06; 104.032; 100.712
2908.8Wu, Yue; Zhang, Xu; Zhang, Yun-Qin; Yang, Ming; Chen, Zhong-Ning
Achievement of ligand-field induced thermochromic luminescence via two-step single-crystal to single-crystal transformations.
Chemical communications (Cambridge, England), 2018, 54, 13961-13964
7122614 CIFC58 H46 Br4 Mn2 N2 O4 P4P -113.2006; 15.1682; 16.4695
98.582; 111.11; 108.38
2787.9Wu, Yue; Zhang, Xu; Zhang, Yun-Qin; Yang, Ming; Chen, Zhong-Ning
Achievement of ligand-field induced thermochromic luminescence via two-step single-crystal to single-crystal transformations.
Chemical communications (Cambridge, England), 2018, 54, 13961-13964
7122615 CIFC29 H23 Br2 Mn N O2 P2P -113.182; 15.175; 16.539
98.923; 110.826; 108.11
2804.6Wu, Yue; Zhang, Xu; Zhang, Yun-Qin; Yang, Ming; Chen, Zhong-Ning
Achievement of ligand-field induced thermochromic luminescence via two-step single-crystal to single-crystal transformations.
Chemical communications (Cambridge, England), 2018, 54, 13961-13964
7122616 CIFC29 H23 Br2 Mn N O2 P2P -110.4868; 12.5077; 12.6045
85.095; 68.271; 82.281
1520.7Wu, Yue; Zhang, Xu; Zhang, Yun-Qin; Yang, Ming; Chen, Zhong-Ning
Achievement of ligand-field induced thermochromic luminescence via two-step single-crystal to single-crystal transformations.
Chemical communications (Cambridge, England), 2018, 54, 13961-13964
7122617 CIFC58 H47 Br4 Mn2 N2 O4 P4P -112.347; 15.1937; 17.255
100.149; 105.447; 100.713
2977.3Wu, Yue; Zhang, Xu; Zhang, Yun-Qin; Yang, Ming; Chen, Zhong-Ning
Achievement of ligand-field induced thermochromic luminescence via two-step single-crystal to single-crystal transformations.
Chemical communications (Cambridge, England), 2018, 54, 13961-13964
7122618 CIFC29 H23 Br2 Mn N O2 P2P -110.4487; 12.5208; 12.6339
84.869; 68.184; 82.196
1518.9Wu, Yue; Zhang, Xu; Zhang, Yun-Qin; Yang, Ming; Chen, Zhong-Ning
Achievement of ligand-field induced thermochromic luminescence via two-step single-crystal to single-crystal transformations.
Chemical communications (Cambridge, England), 2018, 54, 13961-13964
7122619 CIFC29 H23 Br2 Mn N O2 P2P -110.449; 12.532; 12.846
84.23; 67.331; 81.688
1534Wu, Yue; Zhang, Xu; Zhang, Yun-Qin; Yang, Ming; Chen, Zhong-Ning
Achievement of ligand-field induced thermochromic luminescence via two-step single-crystal to single-crystal transformations.
Chemical communications (Cambridge, England), 2018, 54, 13961-13964

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