Crystallography Open Database

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7124620 CIFC39 H54 N3 NbP 19.6363; 10.354; 10.4978
107.019; 113.605; 91.585		905.11Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124621 CIFC39 H55 N6 NbP 1 21/n 111.649; 18.9555; 17.0768
90; 97.526; 90		3738.3Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124622 CIFC38 H49 N3 NbP n n m12.4801; 13.772; 19.2824
90; 90; 90		3314.2Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124623 CIFC67 H72 B F15 N5 NbP -112.5396; 17.4757; 29.99
84.127; 82.987; 73.602		6241.6Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124624 CIFC57 H55 B F15 N6 NbP -112.2684; 12.7008; 19.2268
79.4526; 83.1067; 68.923		2743.4Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124625 CIFC121 H118 B2 F30 N8 Nb2P b c a19.3473; 22.4336; 25.5172
90; 90; 90		11075.2Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124626 CIFC15 H32 Cu3 N12 O16P -112.6421; 14.2612; 17.0125
90.192; 96.38; 113.941		2782Kennedy, Zachary C.; Cardenas, Allan Jay P.; Corbey, Jordan F.; Warner, Marvin G.
2,6-Diiminopiperidin-1-ol: an overlooked motif relevant to uranyl and transition metal binding on poly(amidoxime) adsorbents.
Chemical communications (Cambridge, England), 2016, 52, 8802-8805
7124627 CIFC15 H44 Cl3 N9 Ni3 O13P 1 21/c 117.1605; 13.4761; 14.8097
90; 111.774; 90		3180.5Kennedy, Zachary C.; Cardenas, Allan Jay P.; Corbey, Jordan F.; Warner, Marvin G.
2,6-Diiminopiperidin-1-ol: an overlooked motif relevant to uranyl and transition metal binding on poly(amidoxime) adsorbents.
Chemical communications (Cambridge, England), 2016, 52, 8802-8805
7124628 CIFC18 H32 N8 O14 U2P 1 21/n 18.3529; 21.2854; 8.9198
90; 111.884; 90		1471.61Kennedy, Zachary C.; Cardenas, Allan Jay P.; Corbey, Jordan F.; Warner, Marvin G.
2,6-Diiminopiperidin-1-ol: an overlooked motif relevant to uranyl and transition metal binding on poly(amidoxime) adsorbents.
Chemical communications (Cambridge, England), 2016, 52, 8802-8805
7124629 CIFC31 H32 F2 I N O4 SP 1 21/c 114.4081; 22.6704; 19.5045
90; 109.072; 90		6021.2Yu, Liu-Zhu; Zhu, Zi-Zhong; Hu, Xu-Bo; Tang, Xiang-Ying; Shi, Min
Palladium-catalyzed cascade cyclization of allylamine-tethered alkylidenecyclopropanes: facile access to iodine/difluoromethylene- and perfluoroalkyl-containing 1-benzazepine scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 6581-6584
7124630 CIFC30 H36 B F2 PP -19.9138; 10.3236; 13.6951
76.806; 71.844; 82.615		1294.2Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124631 CIFC54 H32 B2 F25 PP 1 21 110.7299; 19.7985; 12.1281
90; 95.89; 90		2562.84Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124632 CIFC30 H32 B F6 PP 1 21/n 111.4351; 9.5654; 24.6131
90; 92.863; 90		2688.9Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124633 CIFC54 H36 B2 F21 PP -19.9916; 15.7747; 16.8287
86.925; 79.345; 75.871		2527.8Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124634 CIFC11 H13 N O2P 1 21/n 18.9638; 10.52; 11.467
90; 109.75; 90		1017.7Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124635 CIFC11 H12 F N O2P 1 21/c 17.7034; 22.119; 12.573
90; 105.27; 90		2066.7Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124636 CIFC12 H15 N O3P 1 21/n 17.4266; 11.889; 13.141
90; 102.2; 90		1134.1Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124637 CIFC11 H12 F N O2P 1 21/n 19.0682; 10.39; 11.58
90; 109.17; 90		1030.6Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124638 CIFC158 H178 Au24 Pd S18P -116.1244; 17.6398; 17.7651
65.152; 64.342; 81.391		4129.8Tian, Shubo; Liao, Lingwen; Yuan, Jinyun; Yao, Chuanhao; Chen, Jishi; Yang, Jinlong; Wu, Zhikun
Structures and magnetism of mono-palladium and mono-platinum doped Au25(PET)18 nanoclusters.
Chemical communications (Cambridge, England), 2016, 52, 9873-9876
7124639 CIFC158 H178 Au24 Pt S18P -116.19; 17.714; 17.8666
65.106; 64.289; 81.343		4184.5Tian, Shubo; Liao, Lingwen; Yuan, Jinyun; Yao, Chuanhao; Chen, Jishi; Yang, Jinlong; Wu, Zhikun
Structures and magnetism of mono-palladium and mono-platinum doped Au25(PET)18 nanoclusters.
Chemical communications (Cambridge, England), 2016, 52, 9873-9876
7124640 CIFC44 H42 Co4 N4 O14P 42/m b c25.569; 25.569; 16.707
90; 90; 90		10923Su, Lei; Song, Wei-Chao; Zhao, Jiong-Peng; Liu, Fu-Chen
Crystal engineering to control the magnetic interaction between weak ferromagnetic single-chain magnets assembled in a 3D framework.
Chemical communications (Cambridge, England), 2016, 52, 8722-8725
7124641 CIFC43 H51 Cl3 Co N2 O2 S2P 1 21/c 119.3263; 9.6193; 25.4228
90; 108.384; 90		4485Sarkar, Prasenjit; Tiwari, Archana; Sarmah, Amrit; Bhandary, Subhrajyoti; Roy, Ram Kinkar; Mukherjee, Chandan
An elusive vinyl radical isolated as an appended unit in a five-coordinate Co(iii)-bis(iminobenzosemiquinone) complex formed via ligand-centered C-S bond cleavage.
Chemical communications (Cambridge, England), 2016, 52, 10613-10616
7124642 CIFC21 H15 O7 PP 1 21/n 17.7879; 20.327; 11.9549
90; 93.558; 90		1888.9Feng, Genfeng; Liu, Wei; Peng, Yuxin; Zhao, Bo; Huang, Wei; Dai, Yafei
Cavity partition and functionalization of a [2+3] organic molecular cage by inserting polar P[double bond, length as m-dash]O bonds.
Chemical communications (Cambridge, England), 2016, 52, 9267-9270
7124643 CIFC60 H60 N6 O8 P2P 21 319.1327; 19.1327; 19.1327
90; 90; 90		7003.7Feng, Genfeng; Liu, Wei; Peng, Yuxin; Zhao, Bo; Huang, Wei; Dai, Yafei
Cavity partition and functionalization of a [2+3] organic molecular cage by inserting polar P[double bond, length as m-dash]O bonds.
Chemical communications (Cambridge, England), 2016, 52, 9267-9270
7124644 CIFC38 H32 F12 N4 P2P -18.8259; 9.7216; 12.7688
104.695; 100.791; 108.868		958.4Wang, Zhaoyang; Bai, Wei; Tong, Jiaqi; Wang, Yi Jia; Qin, Anjun; Sun, Jing Zhi; Tang, Ben Zhong
A macrocyclic 1,4-bis(4-pyridylethynyl)benzene showing unique aggregation-induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10365-10368
7124645 CIFC21 H27 N3 O4I 1 2 116.8244; 6.0896; 41.9414
90; 101.245; 90		4214.6Li, Dan; Wang, Yijie; Wang, Linqing; Wang, Jie; Wang, Pengxin; Wang, Kezhou; Lin, Li; Liu, Dongsheng; Jiang, Xianxing; Yang, Dongxu
Simple magnesium catalyst mediated γ-butyrolactams in desymmetrization of meso-aziridines.
Chemical communications (Cambridge, England), 2016, 52, 9640-9643
7124646 CIFC18 H13 N OP 1 21/c 110.016; 9.223; 13.978
90; 94.662; 90		1287Wu, Shanchao; Liu, Na; Dong, Guoqiang; Ma, Lin; Wang, Shengzheng; Shi, Wencai; Fang, Kun; Chen, Shuqiang; Li, Jian; Zhang, Wannian; Sheng, Chunquan; Wang, Wei
Facile construction of pyrrolo[1,2-b]isoquinolin-10(5H)-ones via a redox-amination-aromatization-Friedel-Crafts acylation cascade reaction and discovery of novel topoisomerase inhibitors.
Chemical communications (Cambridge, England), 2016, 52, 9593-9596
7124647 CIFC36 H45 F12 N7 O4 P2 RuP -18.4109; 11.4169; 11.725
74.801; 76.758; 87.087		1057.59He, Lei; Chen, Xiang; Meng, Zhenyu; Wang, Jintao; Tian, Keyin; Li, Tianhu; Shao, Fangwei
Octahedral ruthenium complexes selectively stabilize G-quadruplexes.
Chemical communications (Cambridge, England), 2016, 52, 8095-8098
7124648 CIFC29 H32 F12 N6 O3 P2 Ru SP 1 21/c 111.5273; 12.9572; 24.0256
90; 97.6261; 90		3556.8He, Lei; Chen, Xiang; Meng, Zhenyu; Wang, Jintao; Tian, Keyin; Li, Tianhu; Shao, Fangwei
Octahedral ruthenium complexes selectively stabilize G-quadruplexes.
Chemical communications (Cambridge, England), 2016, 52, 8095-8098
7124649 CIFC64 H59 Cl2 N6 O14P 21 21 2115.8312; 18.6954; 21.7724
90; 90; 90		6444Liu, Kang; Xiong, Yong; Wang, Zuo-Fei; Tao, Hai-Yan; Wang, Chun-Jiang
Ligand-controlled stereodivergent 1,3-dipolar cycloaddition of azomethine ylides with 3-methyl-4-nitro-5-styrylisoxazoles.
Chemical communications (Cambridge, England), 2016, 52, 9458-9461
7124650 CIFC29 H24 Cl N3 O8P 15.8187; 11.7632; 11.9555
79.413; 87.509; 78.478		788.2Liu, Kang; Xiong, Yong; Wang, Zuo-Fei; Tao, Hai-Yan; Wang, Chun-Jiang
Ligand-controlled stereodivergent 1,3-dipolar cycloaddition of azomethine ylides with 3-methyl-4-nitro-5-styrylisoxazoles.
Chemical communications (Cambridge, England), 2016, 52, 9458-9461
7124651 CIFC25 H31 B Br4 Ga PP 1 21/n 112.2483; 15.51; 15.3013
90; 90.094; 90		2906.8Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124652 CIFC18 H21 B F6 N O4 P S2P b c n30.337; 7.7017; 19.3533
90; 90; 90		4521.8Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124653 CIFC34 H26 B Br4 Ga N PP 1 21/n 112.5932; 14.1435; 19.2716
90; 107.068; 90		3281.3Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124654 CIFC31 H29 B N PP 1 21/n 16.9184; 22.8078; 16.1979
90; 101.927; 90		2500.7Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124655 CIFC33 H30 B F6 N2 O4 P S2P -18.9898; 12.2194; 15.5624
91.453; 91.387; 106.552		1637.28Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124656 CIFC12 H10 N4 O4 ZnP 43 21 27.8691; 7.8691; 22.353
90; 90; 90		1384.2Cepeda, Javier; Sebastian, Eider San; Padro, Daniel; Rodríguez-Diéguez, Antonio; García, Jose A; Ugalde, Jesus M.; Seco, Jose M.
A Zn based coordination polymer exhibiting long-lasting phosphorescence.
Chemical communications (Cambridge, England), 2016, 52, 8671-8674
7124657 CIFC21 H19 B O2P 1 21/a 114.9097; 6.6345; 16.6553
90; 92.822; 90		1645.52Wang, Taisheng; Zhang, Na; Zhang, Ke; Dai, Jingwen; Bai, Wei; Bai, Ruke
Pyrene boronic acid cyclic ester: a new fast self-recovering mechanoluminescent material at room temperature.
Chemical communications (Cambridge, England), 2016, 52, 9679-9682
7124658 CIFC22 H21 B O2P 1 21/c 111.7096; 10.8168; 14.2151
90; 91.551; 90		1799.8Wang, Taisheng; Zhang, Na; Zhang, Ke; Dai, Jingwen; Bai, Wei; Bai, Ruke
Pyrene boronic acid cyclic ester: a new fast self-recovering mechanoluminescent material at room temperature.
Chemical communications (Cambridge, England), 2016, 52, 9679-9682
7124659 CIFC42 F28P 21 21 218.45; 11.0004; 42.68
90; 90; 90		3967.3Zhang, Zhuoran; Ogden, William A.; Young, Victor G.; Douglas, Christopher J.
Synthesis, electrochemical properties, and crystal packing of perfluororubrene.
Chemical communications (Cambridge, England), 2016, 52, 8127-8130
7124660 CIFC42 F28P 1 21/n 116.6651; 11.1489; 19.1918
90; 90.213; 90		3565.8Zhang, Zhuoran; Ogden, William A.; Young, Victor G.; Douglas, Christopher J.
Synthesis, electrochemical properties, and crystal packing of perfluororubrene.
Chemical communications (Cambridge, England), 2016, 52, 8127-8130
7124661 CIFC42 F28P -112.5285; 17.8163; 24.7339
90.202; 101.264; 90.695		5414Zhang, Zhuoran; Ogden, William A.; Young, Victor G.; Douglas, Christopher J.
Synthesis, electrochemical properties, and crystal packing of perfluororubrene.
Chemical communications (Cambridge, England), 2016, 52, 8127-8130
7124662 CIFC44 H61 N O10P -112.0803; 12.3966; 14.483
106.375; 96.145; 108.074		1932.7Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Kalenius, Elina; Ras, Robin H. A.; Rissanen, Kari
2-Methylresorcinarene: a very high packing coefficient in a mono-anion based dimeric capsule and the X-ray crystal structure of the tetra-anion.
Chemical communications (Cambridge, England), 2016, 52, 8115-8118
7124663 CIFC125 H227 N10 O31.5P -113.3506; 15.7389; 17.8889
69.234; 75.125; 87.036		3393.7Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Kalenius, Elina; Ras, Robin H. A.; Rissanen, Kari
2-Methylresorcinarene: a very high packing coefficient in a mono-anion based dimeric capsule and the X-ray crystal structure of the tetra-anion.
Chemical communications (Cambridge, England), 2016, 52, 8115-8118
7124664 CIFC98 H120 N16 O18P 43 21 215.4204; 15.4204; 43.9852
90; 90; 90		10459.2Chung, Mee-Kyung; Lee, Stephen J.; Waters, Marcey L.; Gagné, Michel R
Tetrameric psuedo-peptide receptors with allosteric properties.
Chemical communications (Cambridge, England), 2016, 52, 8103-8106
7124665 CIFC68 H80 N16 O12P 21 21 2122.2194; 26.8073; 30.7909
90; 90; 90		18340.4Chung, Mee-Kyung; Lee, Stephen J.; Waters, Marcey L.; Gagné, Michel R
Tetrameric psuedo-peptide receptors with allosteric properties.
Chemical communications (Cambridge, England), 2016, 52, 8103-8106
7124666 CIFC31 H35 N O2 SiP 1 21/n 110.5604; 12.5871; 20.6289
90; 103.411; 90		2667.3Shinde, Popat S.; Shaikh, Aslam C.; Patil, Nitin T.
Efficient access to alkynylated quinalizinones via the gold(i)-catalyzed aminoalkynylation of alkynes.
Chemical communications (Cambridge, England), 2016, 52, 8152-8155
7124667 CIFC31 H33 N O2 SiP 1 21/c 117.0259; 19.7058; 8.2013
90; 101.746; 90		2694Shinde, Popat S.; Shaikh, Aslam C.; Patil, Nitin T.
Efficient access to alkynylated quinalizinones via the gold(i)-catalyzed aminoalkynylation of alkynes.
Chemical communications (Cambridge, England), 2016, 52, 8152-8155
7124668 CIFC78 H68 Cl2 F6 N4 Pt2 S2P 1 21/c 112.1203; 21.6638; 27.3069
90; 91.372; 90		7168Boixel, Julien; Zhu, Yifan; Le Bozec, Hubert; Benmensour, Mohamed Ali; Boucekkine, Abdou; Wong, Keith Man-Chung; Colombo, Alessia; Roberto, Dominique; Guerchais, Véronique; Jacquemin, Denis
Contrasted photochromic and luminescent properties in dinuclear Pt(ii) complexes linked through a central dithienylethene unit.
Chemical communications (Cambridge, England), 2016, 52, 9833-9836
7124669 CIFC34 H58 F4 Mo N6 P4P 1 n 110.2417; 18.3288; 21.5881
90; 95.3341; 90		4034.93Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124670 CIFC34 H58 Cr F4 N6 P4P 1 21/c 110.8985; 13.441; 13.4741
90; 101.392; 90		1934.89Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124671 CIFC34 H58 Cr F4 N6 P4P 1 21/n 110.301; 18.8047; 20.7192
90; 93.77; 90		4004.77Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124672 CIFC34 H58 F4 N6 P4 WP 1 n 110.2469; 18.3292; 21.5498
90; 95.426; 90		4029.29Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124673 CIFC105 H105 N5P b c a32.7165; 16.1948; 39.103
90; 90; 90		20718.2Qiao, Bo; Anderson, Joseph R.; Pink, Maren; Flood, Amar H.
Size-matched recognition of large anions by cyanostar macrocycles is saved when solvent-bias is avoided.
Chemical communications (Cambridge, England), 2016, 52, 8683-8686
7124674 CIFC17 H13 N O2P 1 21/c 18.9419; 20.446; 7.9832
90; 111.874; 90		1354.5Li, Jiu-Ling; Li, Wei-Ze; Wang, Ying-Chun; Ren, Qiu; Wang, Heng-Shan; Pan, Ying-Ming
Palladium(ii)-catalyzed C-C and C-O bond formation for the synthesis of C1-benzoyl isoquinolines from isoquinoline N-oxides and nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 10028-10031
7124675 CIFC9 H9 N O3P 21 21 215.43; 7.8748; 20.6997
90; 90; 90		885.12Vidal-Albalat, A; Swiderek, K.; Izquierdo, J.; Rodríguez, S; Moliner, V.; González, F V
Catalytic enantioselective epoxidation of nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 10060-10063
7124676 CIFC14 H11 N O3P 1 21 18.6028; 6.2292; 11.4861
90; 94.415; 90		613.7Vidal-Albalat, A; Swiderek, K.; Izquierdo, J.; Rodríguez, S; Moliner, V.; González, F V
Catalytic enantioselective epoxidation of nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 10060-10063
7124677 CIFC42 H76 Cl3 Dy O35P -112.741; 13.235; 17.923
89.94; 85.741; 86.594		3008.6Al Hareri, M.; Gavey, E. L.; Regier, J.; Ras Ali, Z.; Carlos, L. D.; Ferreira, R. A. S.; Pilkington, M.
Encapsulation of a [Dy(OH2)8](3+) cation: magneto-optical and theoretical studies of a caged, emissive SMM.
Chemical communications (Cambridge, England), 2016, 52, 11335-11338
7124678 CIFC19 H20 N2 O4P 1 21/n 17.791; 13.1164; 16.9526
90; 96.895; 90		1719.86Briones, John F.; Basarab, Gregory S.
Expedient synthesis of tetrahydroquinoline-3-spirohydantoin derivatives via the Lewis acid-catalyzed tert-amino effect reaction.
Chemical communications (Cambridge, England), 2016, 52, 8541-8544
7124679 CIFC52 H62 F12 N2 O14 P2P -113.595; 20.8235; 23.687
74.639; 84.656; 76.364		6280.5Cheng, Ming; Yao, Chenhao; Cao, Yihan; Wang, Qi; Pan, Yi; Jiang, Juli; Wang, Leyong
4-Methylcoumarin-bridged fluorescent responsive cryptand: from [2+2] photodimerization to supramolecular polymer.
Chemical communications (Cambridge, England), 2016, 52, 8715-8718
7124680 CIFC26 H24 N2 O3P 1 21/n 19.1828; 9.0675; 26.107
90; 91.376; 90		2173.2An, Yuanyuan; Xia, Hongguang; Wu, Jie
Base-controlled [3+3] cycloaddition of isoquinoline N-oxides with azaoxyallyl cations.
Chemical communications (Cambridge, England), 2016, 52, 10415-10418
7124681 CIFC26 H24 N2 O3C 1 2/c 138.327; 12.158; 9.715
90; 95.51; 90		4506An, Yuanyuan; Xia, Hongguang; Wu, Jie
Base-controlled [3+3] cycloaddition of isoquinoline N-oxides with azaoxyallyl cations.
Chemical communications (Cambridge, England), 2016, 52, 10415-10418
7124682 CIFC66 H57 Ce F15 N3 O2 P2 S6 Si3P -113.5981; 14.8764; 21.2531
75.799; 87.413; 75.372		4032.2Yin, Haolin; Carroll, Patrick J.; Schelter, Eric J.
Reactions of a cerium(iii) amide with heteroallenes: insertion, silyl-migration and de-insertion.
Chemical communications (Cambridge, England), 2016, 52, 9813-9816
7124683 CIFC48 H69 Ce F15 N9 Si3C 1 2/c 123.8; 12.7595; 40.727
90; 97.599; 90		12259.2Yin, Haolin; Carroll, Patrick J.; Schelter, Eric J.
Reactions of a cerium(iii) amide with heteroallenes: insertion, silyl-migration and de-insertion.
Chemical communications (Cambridge, England), 2016, 52, 9813-9816
7124684 CIFC21 H16 OP 1 21/c 113.33; 15.13; 7.59
90; 100.77; 90		1504Jin, Ruiwen; Chen, Yiyong; Liu, Wangsheng; Xu, Dawen; Li, Yawei; Ding, Aishun; Guo, Hao
Merging photoredox catalysis with Lewis acid catalysis: activation of carbon-carbon triple bonds.
Chemical communications (Cambridge, England), 2016, 52, 9909-9912
7124685 CIFC16 H14 O5P 1 21/c 18.4933; 10.7736; 14.1815
90; 92.817; 90		1296.1Chen, Dong; Xu, Wen-Dan; Liu, Hao-Miao; Li, Ming-Ming; Yan, Yong-Min; Li, Xiao-Nian; Li, Yan; Cheng, Yong-Xian; Qin, Hong-Bo
Enantioselective total synthesis of (+)-Lingzhiol via tandem semipinacol rearrangement/Friedel-Crafts type cyclization.
Chemical communications (Cambridge, England), 2016, 52, 8561-8564
7124686 CIFC16 H13 Br O5P 21 21 218.1765; 10.7366; 16.4944
90; 90; 90		1448Chen, Dong; Xu, Wen-Dan; Liu, Hao-Miao; Li, Ming-Ming; Yan, Yong-Min; Li, Xiao-Nian; Li, Yan; Cheng, Yong-Xian; Qin, Hong-Bo
Enantioselective total synthesis of (+)-Lingzhiol via tandem semipinacol rearrangement/Friedel-Crafts type cyclization.
Chemical communications (Cambridge, England), 2016, 52, 8561-8564
7124687 CIFC15 H14 N2 O3P 1 21/c 19.7836; 19.184; 7.2536
90; 110.113; 90		1278.4Alcaide, Benito; Almendros, Pedro; Cembellín, Sara; Fernández, Israel; Martínez Del Campo, Teresa
Stereoselective synthesis of strained cage compounds via gold-catalyzed allene functionalization.
Chemical communications (Cambridge, England), 2016, 52, 10265-10268
7124688 CIFC2 H4 N6 O2C 1 2/c 112.8179; 4.8463; 18.2472
90; 100.494; 90		1114.55He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124689 CIFC3 H4 N6 O4P n a 2112.7338; 9.977; 5.136
90; 90; 90		652.5He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124690 CIFC2 H4 N6 O2P 1 21 13.5852; 16.3937; 9.4278
90; 98.448; 90		548.1He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124691 CIFC2 H4 N6 O2P 1 21/n 18.0055; 6.4742; 10.7844
90; 96.224; 90		555.65He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124692 CIFC H N O SP 1 21/c 115.924; 8.289; 15.498
90; 99.13; 90		2019.7Wang, Sasa; Chen, Xinzheng; Ao, Qiaoqiao; Wang, Huifei; Zhai, Hongbin
Decarboxylative Csp(3)-Csp(3) coupling for benzylation of unstable ketone enolates: synthesis of p-(acylethyl)phenols.
Chemical communications (Cambridge, England), 2016, 52, 9454-9457
7124693 CIFC22 H26 F6 N2 Rh SbP 1 21/n 112.6576; 14.5099; 13.416
90; 106.523; 90		2362.24Hou, Wei; Yang, Yaxi; Wu, Yunxiang; Feng, Huijin; Li, Yuanchao; Zhou, Bing
Rhodium(iii)-catalyzed alkylation of primary C(sp(3))-H bonds with α-diazocarbonyl compounds.
Chemical communications (Cambridge, England), 2016, 52, 9672-9675
7124694 CIFC64 H256 Co16 N64 Nb32 O205 S4 V39P n m a23.9036; 21.2261; 18.0968
90; 90; 90		9182Hu, Ju-Fang; Han, Tian; Chi, Ying-Nan; Lin, Zheng-Guo; Xu, Yan-Qing; Yang, Song; Wei, Ding; Zheng, Yan-Zhen; Hu, Chang-Wen
Sulfur-centred polyoxoniobate-based 3D organic-inorganic hybrid compound and its magnetic behavior.
Chemical communications (Cambridge, England), 2016, 52, 10846-10849
7124695 CIFC21 H30 Li N3P 1 21 110.1048; 12.9834; 15.341
90; 102.567; 90		1964.4Blair, V. L.; Stevens, M. A.; Thompson, C. D.
The importance of the Lewis base in lithium mediated metallation and bond cleavage reaction of allyl amines and allyl phosphines.
Chemical communications (Cambridge, England), 2016, 52, 8111-8114
7124696 CIFC38 H48 Li2 O2 P2C 1 c 110.592; 18.626; 9.119
90; 95.24; 90		1791.5Blair, V. L.; Stevens, M. A.; Thompson, C. D.
The importance of the Lewis base in lithium mediated metallation and bond cleavage reaction of allyl amines and allyl phosphines.
Chemical communications (Cambridge, England), 2016, 52, 8111-8114
7124697 CIFC24 H37 Li N4P 1 21/c 110.1275; 8.6095; 27.5008
90; 91.558; 90		2396.98Blair, V. L.; Stevens, M. A.; Thompson, C. D.
The importance of the Lewis base in lithium mediated metallation and bond cleavage reaction of allyl amines and allyl phosphines.
Chemical communications (Cambridge, England), 2016, 52, 8111-8114
7124698 CIFC51 H57 N9 O6P 1 21/c 126.8526; 13.8261; 26.9848
90; 111.812; 90		9301.3Pfletscher, Michael; Wölper, Christoph; Gutmann, Jochen S.; Mezger, Markus; Giese, Michael
A modular approach towards functional supramolecular aggregates - subtle structural differences inducing liquid crystallinity.
Chemical communications (Cambridge, England), 2016, 52, 8549-8552
7124699 CIFC25 H39 Br Co P2 SiP 1 21/n 112.1709; 14.4443; 15.9292
90; 97.855; 90		2774.1Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124700 CIFC30 H41 Br Co P2 SiP 1 21/c 111.0181; 18.0167; 15.4914
90; 98.734; 90		3039.5Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124701 CIFC25 H42 Br4 Co P2 SiP b c a17.6793; 16.195; 23.2286
90; 90; 90		6650.7Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124702 CIFC30 H42 P2 SiP 1 21/c 113.1415; 14.3471; 16.6192
90; 112.798; 90		2888.6Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124703 CIFC25 H40 Br2 Co P2 SiP 1 21/c 117.1233; 9.7303; 17.9002
90; 110.977; 90		2784.8Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124704 CIFC12 H32 Br4 Co N2P b c a12.3228; 13.1299; 26.5742
90; 90; 90		4299.6Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124705 CIFC30 H42 Br2 Co P2 SiP 1 21/c 117.387; 11.5644; 15.641
90; 92.891; 90		3140.9Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124706 CIFC62 H59 F12 N11 O11 P2 Ru3P -115.8008; 16.2412; 19.6284
107.027; 102.696; 109.127		4263.5Zhang, Biaobiao; Li, Fei; Zhang, Rong; Ma, Chengbing; Chen, Lin; Sun, Licheng
Characterization of a trinuclear ruthenium species in catalytic water oxidation by Ru(bda)(pic)2 in neutral media.
Chemical communications (Cambridge, England), 2016, 52, 8619-8622
7124707 CIFC47 H34 N6 O3P c a 2126.853; 10.1988; 27.005
90; 90; 90		7395.8Luciano, M.; Tardie, W.; Zeller, M.; Brückner, C
Supersizing pyrrole-modified porphyrins by reversal of the 'breaking and mending' strategy.
Chemical communications (Cambridge, England), 2016, 52, 10133-10136
7124708 CIFC24 H20 O3P 1 21/c 111.887; 10.4572; 14.8193
90; 100.36; 90		1812.08Ma, Ben; Wu, Ziang; Huang, Ben; Liu, Lu; Zhang, Junliang
Gold-catalysed facile access to indene scaffolds via sequential C-H functionalization and 5-endo-dig carbocyclization.
Chemical communications (Cambridge, England), 2016, 52, 9351-9354
7124709 CIFC24 H20 O4P 1 21/n 112.6203; 10.0898; 15.4768
90; 106.857; 90		1886.08Ma, Ben; Wu, Ziang; Huang, Ben; Liu, Lu; Zhang, Junliang
Gold-catalysed facile access to indene scaffolds via sequential C-H functionalization and 5-endo-dig carbocyclization.
Chemical communications (Cambridge, England), 2016, 52, 9351-9354
7124710 CIFC23 H16 Br2 O4P -18.0971; 11.2035; 12.1077
87.795; 71.122; 74.233		998.7Ma, Ben; Wu, Ziang; Huang, Ben; Liu, Lu; Zhang, Junliang
Gold-catalysed facile access to indene scaffolds via sequential C-H functionalization and 5-endo-dig carbocyclization.
Chemical communications (Cambridge, England), 2016, 52, 9351-9354
7124711 CIFC18 H22 Cl2 O6P c a 2112.3202; 4.6501; 32.022
90; 90; 90		1834.5Kaufmann, Lena; Kennedy, Stuart R.; Jones, Christopher D.; Steed, Jonathan W.
Cavity-containing supramolecular gels as a crystallization tool for hydrophobic pharmaceuticals.
Chemical communications (Cambridge, England), 2016, 52, 10113-10116
7124712 CIFC19 H24 N O6 P SP 319.7393; 9.7393; 18.532
90; 90; 120		1522.3Yan, Zhong; Wu, Bo; Gao, Xiang; Zhou, Yong-Gui
Enantioselective synthesis of quaternary α-aminophosphonates by Pd-catalyzed arylation of cyclic α-ketiminophosphonates with arylboronic acids.
Chemical communications (Cambridge, England), 2016, 52, 10882-10885
7124713 CIFC36 H41 N3 O10 S3P 6314.5223; 14.5223; 10.2703
90; 90; 120		1875.8Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124714 CIFC288 H264 Ag12 N24 O96 Re12 S24F 4 3 235.7237; 35.7237; 35.7237
90; 90; 90		45590Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124715 CIFC288 H264 Ag12 B12 F48 N24 O48 S24F 4 3 235.4548; 35.4548; 35.4548
90; 90; 90		44568.2Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124716 CIFC39 H42 N6 O12 S3R 3 :H28.138; 28.138; 4.4445
90; 90; 120		3047.5Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124717 CIFC42.98 H46.96 Ag Cl3.96 N3 O4 PP 21 21 2114.018; 17.0222; 19.3743
90; 90; 90		4623.04de la Campa, Raquel; Gammack Yamagata, Adam D.; Ortín, Irene; Franchino, Allegra; Thompson, Amber L.; Odell, Barbara; Dixon, Darren J.
Catalytic enantio- and diastereoselective Mannich reaction of α-substituted isocyanoacetates and ketimines.
Chemical communications (Cambridge, England), 2016, 52, 10632-10635
7124718 CIFC28 H20 O2P 1 21 19.4569; 19.807; 21.941
90; 96.83; 90		4080.7Zhang, Xin; Chen, Lin; Chen, Xiang-Yu; Zhang, Hanzhi; Yang, Liuqing; Yang, Fengchun
Effective separation of single-walled carbon nanotubes and their very different electrochemical behaviours.
Chemical communications (Cambridge, England), 2016, 52, 9287-9290
7124719 CIFC20 H14 O2P 3110.784; 10.784; 10.863
90; 90; 120		1094.1Zhang, Xin; Chen, Lin; Chen, Xiang-Yu; Zhang, Hanzhi; Yang, Liuqing; Yang, Fengchun
Effective separation of single-walled carbon nanotubes and their very different electrochemical behaviours.
Chemical communications (Cambridge, England), 2016, 52, 9287-9290
7124720 CIFC39 H84 Ge10 N7 O12 Rb2P -110.8759; 13.4395; 21.2985
85.907; 88.885; 88.995		3104.2Bentlohner, Manuel M.; Fischer, Christina; Fässler, Thomas F
Synthesis and characterization of pristine closo-[Ge10](2.).
Chemical communications (Cambridge, England), 2016, 52, 9841-9843
7124721 CIFC38 H32 N4 O2P 1 21/n 111.4777; 15.9325; 17.0968
90; 103.233; 90		3043.4Krick, Marcel; Holstein, Julian; Würtele, Christian; Clever, Guido H.
Endohedral dynamics of push-pull rotor-functionalized cages.
Chemical communications (Cambridge, England), 2016, 52, 10411-10414
7124722 CIFC46 H32 D8 N4 O3P -19.7141; 13.7175; 13.8642
92.206; 97.198; 98.744		1808.46Krick, Marcel; Holstein, Julian; Würtele, Christian; Clever, Guido H.
Endohedral dynamics of push-pull rotor-functionalized cages.
Chemical communications (Cambridge, England), 2016, 52, 10411-10414
7124723 CIFC40 H43 Br6 N9 P2P 1 21/c 115.79; 17.796; 16.457
90; 104.672; 90		4473.6Đorđević, Nemanja; Ganguly, Rakesh; Petković, Milena; Vidović, Dragoslav
Bis(carbodicarbene)phosphenium trication: the case against hypervalency.
Chemical communications (Cambridge, England), 2016, 52, 9789-9792
7124724 CIFC84 H93.9 Br2 F24 N19.05 O0.47 P2 Sb4P -112.1048; 13.7318; 16.1379
108.884; 98.2298; 102.753		2407.61Đorđević, Nemanja; Ganguly, Rakesh; Petković, Milena; Vidović, Dragoslav
Bis(carbodicarbene)phosphenium trication: the case against hypervalency.
Chemical communications (Cambridge, England), 2016, 52, 9789-9792
7124725 CIFC38 H26 F2P -19.3318; 16.3035; 18.6019
94.673; 90.768; 100.362		2773.6Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124726 CIFC37 H28 Cl2 N2P 1 21/n 110.2875; 9.5469; 30.516
90; 90.739; 90		2996.8Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124727 CIFC40 H32 S2P 1 21/c 19.6317; 9.5173; 33.0419
90; 96.269; 90		3010.8Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124728 CIFC40 H32 S2P 1 21/c 116.2653; 11.5962; 18.2995
90; 115.9; 90		3104.9Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124729 CIFC35 H36 Br Cl4 Ir N2P 1 21/n 111.5187; 12.8279; 23.1283
90; 96.529; 90		3395.29Hellou, Nora; Jahier-Diallo, Claire; Baslé, Olivier; Srebro-Hooper, Monika; Toupet, Loïc; Roisnel, Thierry; Caytan, Elsa; Roussel, Christian; Vanthuyne, Nicolas; Autschbach, Jochen; Mauduit, Marc; Crassous, Jeanne
Electronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligands.
Chemical communications (Cambridge, England), 2016, 52, 9243-9246
7124730 CIFC41 H36 Br Ir N2P 21 21 2113.7643; 14.1122; 16.9238
90; 90; 90		3287.4Hellou, Nora; Jahier-Diallo, Claire; Baslé, Olivier; Srebro-Hooper, Monika; Toupet, Loïc; Roisnel, Thierry; Caytan, Elsa; Roussel, Christian; Vanthuyne, Nicolas; Autschbach, Jochen; Mauduit, Marc; Crassous, Jeanne
Electronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligands.
Chemical communications (Cambridge, England), 2016, 52, 9243-9246
7124731 CIFC33 H32 Br Ir N2P 21 21 219.2873; 16.9087; 17.495
90; 90; 90		2747.3Hellou, Nora; Jahier-Diallo, Claire; Baslé, Olivier; Srebro-Hooper, Monika; Toupet, Loïc; Roisnel, Thierry; Caytan, Elsa; Roussel, Christian; Vanthuyne, Nicolas; Autschbach, Jochen; Mauduit, Marc; Crassous, Jeanne
Electronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligands.
Chemical communications (Cambridge, England), 2016, 52, 9243-9246
7124732 CIFC20 H20 N2 O2P 1 21/n 19.797; 9.3477; 19.3037
90; 103.385; 90		1719.8Kim, Won Young; Shi, Hu; Jung, Hyo Sung; Cho, Daeheum; Verwilst, Peter; Lee, Jin Yong; Kim, Jong Seung
Coumarin-decorated Schiff base hydrolysis as an efficient driving force for the fluorescence detection of water in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 8675-8678
7124733 CIFC19 H19 N3 O2P 1 21/c 17.9685; 10.0372; 20.628
90; 91.778; 90		1649.1Kim, Won Young; Shi, Hu; Jung, Hyo Sung; Cho, Daeheum; Verwilst, Peter; Lee, Jin Yong; Kim, Jong Seung
Coumarin-decorated Schiff base hydrolysis as an efficient driving force for the fluorescence detection of water in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 8675-8678
7124734 CIFC14 H14 F N O3P 21 21 218.2754; 12.082; 13.332
90; 90; 90		1333Liu, Jianchao; Xu, Xiaobing; Li, Jiuyi; Liu, Bo; Jiang, Huanfeng; Yin, Biaolin
Palladium-catalyzed dearomatizing 2,5-alkoxyarylation of furan rings: diastereospecific access to spirooxindoles.
Chemical communications (Cambridge, England), 2016, 52, 9550-9553
7124735 CIFC17 H19 N O4P 1 21/n 114.349; 7.2477; 14.692
90; 105.12; 90		1475Liu, Jianchao; Xu, Xiaobing; Li, Jiuyi; Liu, Bo; Jiang, Huanfeng; Yin, Biaolin
Palladium-catalyzed dearomatizing 2,5-alkoxyarylation of furan rings: diastereospecific access to spirooxindoles.
Chemical communications (Cambridge, England), 2016, 52, 9550-9553
7124736 CIFC14 H12 N2 O2P -16.0661; 7.8841; 12.8564
91.07; 94.098; 97.33		608.04Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124737 CIFC16 H16 N2 O2P -19.2837; 9.9699; 9.9836
92.401; 112.162; 116.147		743.75Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124738 CIFC18 H16 N2 O2 SP 1 21/c 18.4209; 28.5775; 6.9049
90; 101.544; 90		1628.04Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124739 CIFC18 H17 N O4 SP -16.5556; 11.4813; 12.6356
113.781; 98.198; 93.092		854.85Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124740 CIFC162 H66 Cl8 N2 O14P -116.2768; 16.3003; 23.6077
94.242; 95.588; 115.579		5575.6Hisaki, Ichiro; Nakagawa, Shoichi; Sato, Hiroyasu; Tohnai, Norimitsu
Alignment of paired molecules of C60 within a hexagonal platform networked through hydrogen-bonds.
Chemical communications (Cambridge, England), 2016, 52, 9781-9784
7124741 CIFC156 H51 Cl8 O12P -113.8208; 17.4812; 24.2884
76.082; 87.204; 70.991		5382.5Hisaki, Ichiro; Nakagawa, Shoichi; Sato, Hiroyasu; Tohnai, Norimitsu
Alignment of paired molecules of C60 within a hexagonal platform networked through hydrogen-bonds.
Chemical communications (Cambridge, England), 2016, 52, 9781-9784
7124742 CIFC93 H55 Cl6 N O13P -112.0893; 17.1939; 24.6711
104.88; 90.051; 98.347		4899.8Hisaki, Ichiro; Nakagawa, Shoichi; Sato, Hiroyasu; Tohnai, Norimitsu
Alignment of paired molecules of C60 within a hexagonal platform networked through hydrogen-bonds.
Chemical communications (Cambridge, England), 2016, 52, 9781-9784
7124743 CIFC18 H23 Cl2 N O2 RuP 1 21/n 113.7506; 7.06591; 19.8176
90; 109.476; 90		1815.31Ma, Lili; Ma, Rong; Wang, Zhigang; Yiu, Shek-Man; Zhu, Guangyu
Heterodinuclear Pt(iv)-Ru(ii) anticancer prodrugs to combat both drug resistance and tumor metastasis.
Chemical communications (Cambridge, England), 2016, 52, 10735-10738
7124744 CIFC9.5 H20 Cl3 N3 O4 Pt S0.5P -18.8701; 12.497; 17.2431
92.445; 103.722; 104.921		1783.24Ma, Lili; Ma, Rong; Wang, Zhigang; Yiu, Shek-Man; Zhu, Guangyu
Heterodinuclear Pt(iv)-Ru(ii) anticancer prodrugs to combat both drug resistance and tumor metastasis.
Chemical communications (Cambridge, England), 2016, 52, 10735-10738
7124745 CIFC28 H46 Ir O2 P3P 1 21/c 112.8054; 12.7662; 20.774
90; 104.821; 90		3283.1Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124746 CIFC29 H48 Ir O2 P3P -110.2215; 11.864; 16.0253
103.712; 100.633; 93.622		1843.9Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124747 CIFC31 H52 Ir O2 P3C 1 2/c 110.5197; 20.993; 30.334
90; 99.463; 90		6607.8Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124748 CIFC28 H48 Ir O2 P3P 1 21/c 112.8121; 12.7747; 20.771
90; 104.573; 90		3290.2Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124749 CIFC29 H50 Ir O2 P3P -110.23; 11.9105; 15.9818
103.735; 100.957; 93.714		1844.8Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124750 CIFC36 H66 Ir O2 P3P -110.901; 12.686; 15.2272
78.184; 72.973; 73.418		1912.8Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124751 CIFC40 H30 N2 O2P -17.2874; 14.4206; 15.0229
64.011; 79.684; 83.373		1394.93Das, Amrita; Ghosh, Indrajit; König, Burkhard
Synthesis of pyrrolo[1,2-a]quinolines and ullazines by visible light mediated one- and twofold annulation of N-arylpyrroles with arylalkynes.
Chemical communications (Cambridge, England), 2016, 52, 8695-8698
7124752 CIFC20 H14 Cl N OP 1 21/c 116.4245; 7.25848; 13.1153
90; 108.39; 90		1483.72Das, Amrita; Ghosh, Indrajit; König, Burkhard
Synthesis of pyrrolo[1,2-a]quinolines and ullazines by visible light mediated one- and twofold annulation of N-arylpyrroles with arylalkynes.
Chemical communications (Cambridge, England), 2016, 52, 8695-8698
7124753 CIFC25 H24 Cl N3 OP 21 21 2110.3206; 11.6585; 18.3971
90; 90; 90		2213.59Ma, Jiajia; Harms, Klaus; Meggers, Eric
Enantioselective rhodium/ruthenium photoredox catalysis en route to chiral 1,2-aminoalcohols.
Chemical communications (Cambridge, England), 2016, 52, 10183-10186
7124754 CIFC48.4 H49.6 Cl2 F6 N4 O P Rh S2P -117.1583; 17.7095; 18.8292
66.918; 69.054; 76.796		4889.7Ma, Jiajia; Harms, Klaus; Meggers, Eric
Enantioselective rhodium/ruthenium photoredox catalysis en route to chiral 1,2-aminoalcohols.
Chemical communications (Cambridge, England), 2016, 52, 10183-10186
7124755 CIFC16 H46 Mo2 N2 Ni2 O16P 1 21/n 112.0683; 10.1464; 12.6315
90; 91.893; 90		1545.88Kuznetsov, Denis A.; Konev, Dmitry V.; Komarova, Natal'ya S.; Ionov, Andrey M.; Mozhchil, Rais N.; Fedyanin, Ivan V.
Ni-based heterogeneous catalyst from a designed molecular precursor for the efficient electrochemical water oxidation.
Chemical communications (Cambridge, England), 2016, 52, 9255-9258
7124756 CIFC106 H74.5 B3.5 F13.88 I0.5 N21 O4 Pd2C 1 2/c 142.9184; 20.7337; 28.9827
90; 125.086; 90		21104.1Li, Yu-Hao; Jiang, Ji-Jun; Fan, Yan-Zhong; Wei, Zhang-Wen; Chen, Cheng-Xia; Yu, Hui-Juan; Zheng, Shao-Ping; Fenske, Dieter; Su, Cheng-Yong; Barboiu, Mihail
Solvent- and anion-induced interconversions of metal-organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8745-8748
7124757 CIFC98 H75 B4 F16 N17 O4 Pd2C 1 2/c 143.0462; 20.744; 28.9748
90; 125.766; 90		20993.7Li, Yu-Hao; Jiang, Ji-Jun; Fan, Yan-Zhong; Wei, Zhang-Wen; Chen, Cheng-Xia; Yu, Hui-Juan; Zheng, Shao-Ping; Fenske, Dieter; Su, Cheng-Yong; Barboiu, Mihail
Solvent- and anion-induced interconversions of metal-organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8745-8748
7124758 CIFC106 H56 N6 O2P -116.792; 19.978; 23.171
102.93; 101.11; 112.55		6654Burgun, Alexandre; Valente, Peter; Evans, Jack D.; Huang, David M.; Sumby, Christopher J.; Doonan, Christian J.
Endohedrally functionalised porous organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8850-8853
7124759 CIFC110 H60 N2 O2P b c n31.58; 18.296; 20.075
90; 90; 90		11599Burgun, Alexandre; Valente, Peter; Evans, Jack D.; Huang, David M.; Sumby, Christopher J.; Doonan, Christian J.
Endohedrally functionalised porous organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8850-8853
7124760 CIFC116 H66 N2 O2I 41/a c d :239.28; 39.28; 39.78
90; 90; 90		61377Burgun, Alexandre; Valente, Peter; Evans, Jack D.; Huang, David M.; Sumby, Christopher J.; Doonan, Christian J.
Endohedrally functionalised porous organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8850-8853
7124761 CIFC17 H21 N O3P -18.0877; 8.9461; 10.5339
93.626; 92.834; 94.652		756.99Kaishap, Partha Pratim; Sarma, Bipul; Gogoi, Sanjib
The amide C-N bond of isatins as the directing group and the internal oxidant in Ru-catalyzed C-H activation and annulation reactions: access to 8-amido isocoumarins.
Chemical communications (Cambridge, England), 2016, 52, 9809-9812
7124762 CIFC798 H638 Ca17 N72 O322P 1 21/c 144.593; 51.642; 38.959
90; 107.1; 90		85751Mandal, Pradeep K.; Kauffmann, Brice; Destecroix, Harry; Ferrand, Yann; Davis, Anthony P.; Huc, Ivan
Crystal structure of a complex between β-glucopyranose and a macrocyclic receptor with dendritic multicharged water solubilizing chains.
Chemical communications (Cambridge, England), 2016, 52, 9355-9358
7124763 CIFC54 H72 Br N9 O8P 1 21/n 112.865; 18.623; 22.483
90; 90.143; 90		5387Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124764 CIFC54 H72 Cl N9 O8P 1 21/n 113.0109; 18.833; 22.702
90; 90.423; 90		5562.6Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124765 CIFC54 H72 I N9 O8P c a 2121.335; 15.168; 37.948
90; 90; 90		12280Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124766 CIFC54 H72 Cl0.63 F0.37 N9 O8P 1 21/n 112.9168; 18.9009; 22.5896
90; 90.65; 90		5514.7Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124767 CIFC72 H116 Cl3 N10 O18 P2P -118.5581; 19.3272; 23.1017
86.218; 87.845; 81.721		8178.5Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124768 CIFC58 H60 Cl6 N10 O14P -111.224; 13.636; 22.374
101.011; 98.751; 91.381		3317Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124769 CIFC70 H110 N10 O16 S2P 1 21/n 114.239; 21.245; 24.51
90; 92.19; 90		7409Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124770 CIFC54 H72 N10 O11P 1 21/n 112.8705; 18.6776; 23.141
90; 90.418; 90		5562.7Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124771 CIFC56 H75 N9 O10P 1 21/n 112.773; 19.067; 23.221
90; 91.69; 90		5653Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124772 CIFC87 H129 N4 O16 Zn2P -114.3039; 17.603; 20.104
64.648; 74.715; 86.046		4407.1Gonawala, Sunalee; Leopoldino, Verônica R; Kpogo, Kenneth; Verani, Cláudio N
Langmuir-Blodgett films of salophen-based metallosurfactants as surface pretreatment coatings for corrosion mitigation.
Chemical communications (Cambridge, England), 2016, 52, 11155-11158
7124773 CIFC44 H28 Br4 N8 O12 Pb4 PdP -17.634; 13.084; 14.166
105.216; 105.376; 94.884		1298.1Dong, Ying; Li, Yue; Wei, Yong-Liang; Wang, Jian-Cheng; Ma, Jian-Ping; Ji, Jun; Yao, Bing-Jian; Dong, Yu-Bin
A N-heterocyclic tetracarbene Pd(ii) moiety containing a Pd(ii)-Pb(ii) bimetallic MOF for three-component cyclotrimerization via benzyne.
Chemical communications (Cambridge, England), 2016, 52, 10505-10508
7124774 CIFC126 H250 N10 O102 S4 V24I -4 3 m21.927; 21.927; 21.927
90; 90; 90		10542Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124775 CIFC123.5 H250.5 N15.5 O101.5 S4 V24I -4 3 m21.841; 21.841; 21.841
90; 90; 90		10419Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124776 CIFC121 H152 Br6 O101 S4 V24I -4 3 m22.108; 22.108; 22.108
90; 90; 90		10806Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124777 CIFC106.5 H221.5 N8.5 O100.5 S4 V24I -421.848; 21.848; 19.081
90; 90; 90		9108Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124778 CIFC183.5 H280.5 N9.5 O101.5 S4 V24I -428.983; 28.983; 25.744
90; 90; 90		21625Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124779 CIFC48 H69 N O6 Si2P 21 21 2110.50766; 14.738; 35.4339
90; 90; 90		5487.36Gan, Zubao; Chu, Zhiwen; Hu, Jia; Su, Zhishan; Hu, Changwei; Gao, Lu; Song, Zhenlei
Tunable reactivity of geminal bis(silyl) enol derivatives leading to selective exo-IEDDA or Sakurai allylation with a β,γ-unsaturated ketoester.
Chemical communications (Cambridge, England), 2016, 52, 10137-10140
7124780 CIFC226 H226 Cl16 F24 N26 O68 Pd4 S8P -117.8945; 19.5103; 20.507
90.134; 99.808; 110.635		6587.2Szalóki, György; Croué, Vincent; Allain, Magali; Goeb, Sébastien; Sallé, Marc
Neutral versus polycationic coordination cages: a comparison regarding neutral guest inclusion.
Chemical communications (Cambridge, England), 2016, 52, 10012-10015
7124781 CIFC210 H199 Cl16 F24 N21 O32 Pd4 S8P 1 21/c 116.3201; 29.0112; 27.2545
90; 105.883; 90		12411.4Szalóki, György; Croué, Vincent; Allain, Magali; Goeb, Sébastien; Sallé, Marc
Neutral versus polycationic coordination cages: a comparison regarding neutral guest inclusion.
Chemical communications (Cambridge, England), 2016, 52, 10012-10015
7124782 CIFC21 H28 B2 F8 N2 O2P -16.8103; 12.0335; 15.7289
70.566; 78.711; 88.033		1191.39Catalán, Aldo C; Tiburcio, Jorge
Self-assembly of pseudo-rotaxane and rotaxane complexes using an electrostatic slippage approach.
Chemical communications (Cambridge, England), 2016, 52, 9526-9529
7124783 CIFC24 H25 N3 O4I 1 2/a 122.3944; 10.7588; 19.4913
90; 105.44; 90		4526.69Ren, Shichao; Song, Shengjin; Ye, Lu; Feng, Chao; Loh, Teck-Peng
Copper-catalyzed oxyamination of electron-deficient alkenes with N-acyloxyamines.
Chemical communications (Cambridge, England), 2016, 52, 10373-10376
7124784 CIFC118 H108 Cl6 Co3 Ir2 N24 O29C 1 2/c 131.23; 17.481; 26.747
90; 102.845; 90		14237Li, Xuezhao; Wu, Jinguo; Chen, Liyong; Zhong, Xiaoming; He, Cheng; Zhang, Rong; Duan, Chunying
Engineering an iridium-containing metal-organic molecular capsule for induced-fit geometrical conversion and dual catalysis.
Chemical communications (Cambridge, England), 2016, 52, 9628-9631
7124785 CIFC121 H107 Cl4 Co3 Ir2 N25 O22P 43 21 220.973; 20.973; 30.067
90; 90; 90		13225Li, Xuezhao; Wu, Jinguo; Chen, Liyong; Zhong, Xiaoming; He, Cheng; Zhang, Rong; Duan, Chunying
Engineering an iridium-containing metal-organic molecular capsule for induced-fit geometrical conversion and dual catalysis.
Chemical communications (Cambridge, England), 2016, 52, 9628-9631
7124786 CIFC29 H20 OP -19.5812; 10.2719; 12.371
114.389; 96.569; 105.237		1034.9Chen, Ling; Cao, Jian; Xu, Zheng; Zheng, Zhan-Jiang; Cui, Yu-Ming; Xu, Li-Wen
Lewis acid catalyzed [2+2] cycloaddition of ynamides and propargyl silyl ethers: synthesis of alkylidenecyclobutenones and their reactivity in ring-opening and ring expansion.
Chemical communications (Cambridge, England), 2016, 52, 9574-9577
7124787 CIFC33 H31 N OP -19.688; 9.724; 14.142
92.269; 93.742; 99.428		1309.8Chen, Ling; Cao, Jian; Xu, Zheng; Zheng, Zhan-Jiang; Cui, Yu-Ming; Xu, Li-Wen
Lewis acid catalyzed [2+2] cycloaddition of ynamides and propargyl silyl ethers: synthesis of alkylidenecyclobutenones and their reactivity in ring-opening and ring expansion.
Chemical communications (Cambridge, England), 2016, 52, 9574-9577
7124788 CIFC29 H22 O2P -18.5465; 11.111; 12.403
109.873; 101.743; 90.448		1080.7Chen, Ling; Cao, Jian; Xu, Zheng; Zheng, Zhan-Jiang; Cui, Yu-Ming; Xu, Li-Wen
Lewis acid catalyzed [2+2] cycloaddition of ynamides and propargyl silyl ethers: synthesis of alkylidenecyclobutenones and their reactivity in ring-opening and ring expansion.
Chemical communications (Cambridge, England), 2016, 52, 9574-9577
7124789 CIFC21 H23 N O4C 1 c 18.12275; 19.6409; 11.31395
90; 92.5884; 90		1803.16Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124790 CIFC22 H25 N O4P 1 21/c 111.06181; 9.47232; 18.5215
90; 97.9172; 90		1922.2Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124791 CIFC21 H22 F3 N O4P -111.7112; 15.2229; 22.2156
78.173; 76.486; 89.949		3764.55Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124792 CIFC21 H23 N O4P b c n22.8332; 9.84289; 16.7747
90; 90; 90		3770.02Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124793 CIFC22 H28 N2 O4P 1 21/c 120.1612; 9.24516; 10.76938
90; 96.7643; 90		1993.37Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124794 CIFC22 H25 N O4P 1 21/n 19.8686; 23.9445; 33.107
90; 90.065; 90		7823.1Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124795 CIFC22 H28 N2 O4P 1 21 19.67334; 11.20885; 18.6086
90; 94.3265; 90		2011.93Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124796 CIFC14 H23 O6 P Si2 WP 21 21 219.7786; 9.9521; 21.9977
90; 90; 90		2140.76Kyri, A. W.; Schnakenburg, G.; Streubel, R.
A novel route to C-unsubstituted 1,2-oxaphosphetane and 1,2-oxaphospholane complexes.
Chemical communications (Cambridge, England), 2016, 52, 8593-8595
7124797 CIFC14 H24 I O6 P Si2 WP -19.179; 10.433; 14.066
86.293; 81.81; 65.584		1214Kyri, A. W.; Schnakenburg, G.; Streubel, R.
A novel route to C-unsubstituted 1,2-oxaphosphetane and 1,2-oxaphospholane complexes.
Chemical communications (Cambridge, England), 2016, 52, 8593-8595
7124798 CIFC15 H25 O6 P Si2 WP 21 21 219.2343; 10.3502; 23.1652
90; 90; 90		2214.06Kyri, A. W.; Schnakenburg, G.; Streubel, R.
A novel route to C-unsubstituted 1,2-oxaphosphetane and 1,2-oxaphospholane complexes.
Chemical communications (Cambridge, England), 2016, 52, 8593-8595
7124799 CIFC49 H71 Br2 Fe3 N6 O SP -111.9958; 12.5852; 17.0913
104.697; 102.692; 91.2459		2426.6Lee, Yousoon; Abboud, Khalil A.; García-Serres, Ricardo; Murray, Leslie J.
A three-coordinate Fe(ii) center within a [3Fe-(μ3-S)] cluster that provides an accessible coordination site.
Chemical communications (Cambridge, England), 2016, 52, 9295-9298
7124800 CIFC50.88 H74.76 Br1.03 Fe3 N6 O1.47 SP -111.651; 12.6465; 17.0493
94.401; 95.909; 96.266		2473.99Lee, Yousoon; Abboud, Khalil A.; García-Serres, Ricardo; Murray, Leslie J.
A three-coordinate Fe(ii) center within a [3Fe-(μ3-S)] cluster that provides an accessible coordination site.
Chemical communications (Cambridge, England), 2016, 52, 9295-9298
7124801 CIFC31 H29 Br2 N O4P 4312.339; 12.339; 18.0683
90; 90; 90		2750.9Li, Meng; Lu, Hai-Yan; Zhang, Chao; Shi, Lin; Tang, Zhiyong; Chen, Chuan-Feng
Helical aromatic imide based enantiomers with full-color circularly polarized luminescence.
Chemical communications (Cambridge, England), 2016, 52, 9921-9924
7124802 CIFC31 H29 Br2 N O4P 4112.347; 12.347; 18.073
90; 90; 90		2755.2Li, Meng; Lu, Hai-Yan; Zhang, Chao; Shi, Lin; Tang, Zhiyong; Chen, Chuan-Feng
Helical aromatic imide based enantiomers with full-color circularly polarized luminescence.
Chemical communications (Cambridge, England), 2016, 52, 9921-9924
7124803 CIFC23 H19 N O SP 21 21 215.6327; 14.2928; 21.544
90; 90; 90		1734.4León, Thierry; Fernández, Elena
The Pauson-Khand reaction using alkynylboronic esters: solving a long-standing regioselectivity issue.
Chemical communications (Cambridge, England), 2016, 52, 9363-9366
7124804 CIFC22 H25 B O3P -19.7865; 12.5627; 16.1123
90.4912; 102.202; 93.6195		1931.82León, Thierry; Fernández, Elena
The Pauson-Khand reaction using alkynylboronic esters: solving a long-standing regioselectivity issue.
Chemical communications (Cambridge, England), 2016, 52, 9363-9366
7124805 CIFC26 H21 B N2 OP 1 21/c 119.3909; 10.1233; 20.4987
90; 95.235; 90		4007.1León, Thierry; Fernández, Elena
The Pauson-Khand reaction using alkynylboronic esters: solving a long-standing regioselectivity issue.
Chemical communications (Cambridge, England), 2016, 52, 9363-9366
7124806 CIFC8 H4 In O5I 41 2 215.4625; 15.4625; 12.337
90; 90; 90		2949.6Peralta, Ricardo A.; Campos-Reales-Pineda, Alberto; Pfeiffer, Heriberto; Álvarez, J Raziel; Zárate, J Antonio; Balmaseda, Jorge; González-Zamora, Eduardo; Martínez, Ana; Martínez-Otero, Diego; Jancik, Vojtech; Ibarra, Ilich A.
CO2 capture enhancement in InOF-1 via the bottleneck effect of confined ethanol.
Chemical communications (Cambridge, England), 2016, 52, 10273-10276
7124807 CIFC10 H10 In O6I 41 2 215.483; 15.483; 12.308
90; 90; 90		2950.5Peralta, Ricardo A.; Campos-Reales-Pineda, Alberto; Pfeiffer, Heriberto; Álvarez, J Raziel; Zárate, J Antonio; Balmaseda, Jorge; González-Zamora, Eduardo; Martínez, Ana; Martínez-Otero, Diego; Jancik, Vojtech; Ibarra, Ilich A.
CO2 capture enhancement in InOF-1 via the bottleneck effect of confined ethanol.
Chemical communications (Cambridge, England), 2016, 52, 10273-10276
7124808 CIFC60 H62 Au Cl P S3P 1 21 19.8334; 21.319; 12.7266
90; 95.59; 90		2655.3Aillard, Paul; Dova, Davide; Magné, Valentin; Retailleau, Pascal; Cauteruccio, Silvia; Licandro, Emanuela; Voituriez, Arnaud; Marinetti, Angela
The synthesis of substituted phosphathiahelicenes via regioselective bromination of a preformed helical scaffold: a new approach to modular ligands for enantioselective gold-catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10984-10987
7124809 CIFC12 H6 Cl2 Cu2 N2 O10 PdR -3 m :H18.899; 18.899; 31.69
90; 90; 120		9802Spanopoulos, I.; Bratsos, I.; Tampaxis, C.; Vourloumis, D.; Klontzas, E.; Froudakis, G. E.; Charalambopoulou, G.; Steriotis, T. A.; Trikalitis, P. N.
Exceptional gravimetric and volumetric CO2 uptake in a palladated NbO-type MOF utilizing cooperative acidic and basic, metal-CO2 interactions.
Chemical communications (Cambridge, England), 2016, 52, 10559-10562
7124810 CIFC16 H34 Mg N2 O2 P2 S2P 1 21/n 113.2446; 10.2823; 17.0713
90; 97.7952; 90		2303.37Benson, Callum G. M.; Plajer, Alex J.; García-Rodríguez, Raúl; Bond, Andrew D.; Singh, Sanjay; Gade, Lutz H.; Wright, Dominic S.
A versatile hard-soft N/S-ligand for metal coordination and cluster formation.
Chemical communications (Cambridge, England), 2016, 52, 9683-9686
7124811 CIFC20 H28 N2 P2 S2 SnP -18.5948; 9.7615; 14.7996
85.955; 87.786; 73.175		1185.33Benson, Callum G. M.; Plajer, Alex J.; García-Rodríguez, Raúl; Bond, Andrew D.; Singh, Sanjay; Gade, Lutz H.; Wright, Dominic S.
A versatile hard-soft N/S-ligand for metal coordination and cluster formation.
Chemical communications (Cambridge, England), 2016, 52, 9683-9686
7124812 CIFC96 H209 N16 Na17 O8 P16 S17P 4 c c23.7918; 23.7918; 37.5449
90; 90; 90		21252.3Benson, Callum G. M.; Plajer, Alex J.; García-Rodríguez, Raúl; Bond, Andrew D.; Singh, Sanjay; Gade, Lutz H.; Wright, Dominic S.
A versatile hard-soft N/S-ligand for metal coordination and cluster formation.
Chemical communications (Cambridge, England), 2016, 52, 9683-9686
7124813 CIFC11 H9 N OP 1 21/c 15.8141; 23.591; 6.8413
90; 114.257; 90		855.5Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124814 CIFC17 H14 Cl N O3P 1 21/c 115.84; 13.517; 7.047
90; 101.395; 90		1479.1Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124815 CIFC24 H24 N2P 1 21/c 112.648; 5.914; 13.125
90; 94.02; 90		979Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124816 CIFC10 H13 N O4P 1 21 14.8503; 17.114; 6.4411
90; 105.911; 90		514.2Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124817 CIFC10 H13 N O3P -16.69; 8.863; 9.115
107.219; 111.191; 92.478		474.4Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124818 CIFC22 H16 N2P 1 21/c 120.26; 5.434; 16.088
90; 110.528; 90		1658.7Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124819 CIFC26 H28 N2I 1 2/a 118.301; 6.133; 18.738
90; 94.032; 90		2098Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124820 CIFC10 H13 N O3P 1 21/c 16.8201; 16.879; 9.0566
90; 106.25; 90		1000.9Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124821 CIFC77 H66 B4 Cl6P -112.3724; 16.262; 18.3411
68.034; 76.109; 68.507		3161.58Zhang, Zuolun; Wang, Zheng; Haehnel, Martin; Eichhorn, Antonius; Edkins, Robert M.; Steffen, Andreas; Krueger, Anke; Lin, Zhenyang; Marder, Todd B.
Synthesis and fluxional behaviour of novel chloroborole dimers.
Chemical communications (Cambridge, England), 2016, 52, 9707-9710
7124822 CIFC38 H28 B2 Br4 Cl2P -110.7763; 11.4318; 15.5909
74.252; 81.811; 69.779		1732.1Zhang, Zuolun; Wang, Zheng; Haehnel, Martin; Eichhorn, Antonius; Edkins, Robert M.; Steffen, Andreas; Krueger, Anke; Lin, Zhenyang; Marder, Todd B.
Synthesis and fluxional behaviour of novel chloroborole dimers.
Chemical communications (Cambridge, England), 2016, 52, 9707-9710
7124823 CIFC14 H36 Cu N6 O8P -19.4885; 10.1789; 11.6397
85.237; 74.922; 77.744		1060.29Yu, Fengshou; Li, Fei; Hu, Jixiang; Bai, Lichen; Zhu, Yong; Sun, Licheng
Electrocatalytic water oxidation by a macrocyclic Cu(ii) complex in neutral phosphate buffer.
Chemical communications (Cambridge, England), 2016, 52, 10377-10380
7124824 CIFC41 H36 F16 N2P 1 21/c 112.7034; 15.8896; 29.1048
90; 94.795; 90		5854.3Kim, Youngsuk; Lee, Eunsung
Activation of C-F bonds in fluoroarenes by N-heterocyclic carbenes as an effective route to synthesize abnormal NHC complexes.
Chemical communications (Cambridge, England), 2016, 52, 10922-10925
7124825 CIFC45 H42 Au Cl F14 N2 OP 1 21/c 115.0816; 14.3924; 20.4104
90; 96.525; 90		4401.6Kim, Youngsuk; Lee, Eunsung
Activation of C-F bonds in fluoroarenes by N-heterocyclic carbenes as an effective route to synthesize abnormal NHC complexes.
Chemical communications (Cambridge, England), 2016, 52, 10922-10925
7124826 CIFC34 H41 F5 N2C 1 2/c 118.227; 17.04; 20.143
90; 101.779; 90		6124Kim, Youngsuk; Lee, Eunsung
Activation of C-F bonds in fluoroarenes by N-heterocyclic carbenes as an effective route to synthesize abnormal NHC complexes.
Chemical communications (Cambridge, England), 2016, 52, 10922-10925
7124827 CIFC29 H16P 1 21/c 111.856; 7.3071; 20.186
90; 96.412; 90		1737.8Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124828 CIFC30 H14 SP c a 219.2775; 26.8593; 7.3125
90; 90; 90		1822.18Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124829 CIFC29 H16 SP 1 21/n 114.111; 7.318; 18.169
90; 100.411; 90		1845.3Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124830 CIFC30 H19 NP 1 21/n 114.3543; 7.4826; 17.7472
90; 97.963; 90		1887.8Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124831 CIFC13 H12 Cd N2 O2I 41/a :224.583; 24.583; 10.8704
90; 90; 90		6569.2Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124832 CIFC13 H12 Cd N2 O2I 41/a :224.0666; 24.0666; 10.5856
90; 90; 90		6131.2Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124833 CIFC13 H12 Cd N2 O2I 41/a :224.6108; 24.6108; 10.76785
90; 90; 90		6521.99Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124834 CIFC13 H12 Cd N2 O2I 41/a :224.029; 24.029; 10.5501
90; 90; 90		6091.6Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124835 CIFC15 H9 Cd2 N13 O12P c c n9.1873; 12.5692; 20.0824
90; 90; 90		2319.1Frost, Jamie M.; Kobera, Libor; Pialat, Amélie; Zhang, Yixin; Southern, Scott A.; Gabidullin, Bulat; Bryce, David L.; Murugesu, Muralee
From discrete molecule, to polymer, to MOF: mapping the coordination chemistry of Cd(II) using (113)Cd solid-state NMR.
Chemical communications (Cambridge, England), 2016, 52, 10680-10683
7124836 CIFC10 H6 Cd N4 O4I m -3 m30.1172; 30.1172; 30.1172
90; 90; 90		27317.7Frost, Jamie M.; Kobera, Libor; Pialat, Amélie; Zhang, Yixin; Southern, Scott A.; Gabidullin, Bulat; Bryce, David L.; Murugesu, Muralee
From discrete molecule, to polymer, to MOF: mapping the coordination chemistry of Cd(II) using (113)Cd solid-state NMR.
Chemical communications (Cambridge, England), 2016, 52, 10680-10683
7124837 CIFC45 H51.47 F12 Mo N3 O3 P4P 1 21/c 115.3031; 15.9629; 20.6295
90; 104.622; 90		4876.2Pal, Raja; Laureanti, Joseph A.; Groy, Thomas L.; Jones, Anne K.; Trovitch, Ryan J.
Hydrogen production from water using a bis(imino)pyridine molybdenum electrocatalyst.
Chemical communications (Cambridge, England), 2016, 52, 11555-11558
7124838 CIFC39 H41 Mo N3 O P2P 1 21/c 111.1519; 16.9788; 18.245
90; 105.844; 90		3323.4Pal, Raja; Laureanti, Joseph A.; Groy, Thomas L.; Jones, Anne K.; Trovitch, Ryan J.
Hydrogen production from water using a bis(imino)pyridine molybdenum electrocatalyst.
Chemical communications (Cambridge, England), 2016, 52, 11555-11558
7124839 CIFC15 H10 O5C 1 2/c 127.783; 4.6822; 20.212
90; 118.891; 90		2302Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124840 CIFC15 H10 O5P 1 21/n 116.4721; 3.6915; 19.4294
90; 96.188; 90		1174.56Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124841 CIFC15 H10 O5P 1 21/n 112.6343; 3.6437; 31.2026
90; 95.706; 90		1429.31Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124842 CIFC15 H10 O5P 1 21/n 116.6384; 3.6887; 19.406
90; 95.544; 90		1185.45Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124843 CIFC44 H36 Cl F24 N7 P2P -112.175; 12.483; 18.276
75.34; 78.55; 71.31		2524.5Amendola, Valeria; Bergamaschi, Greta; Boiocchi, Massimo; Legnani, Laura; Presti, Eliana Lo; Miljkovic, Ana; Monzani, Enrico; Pancotti, Francesca
Chloride-binding in organic-water mixtures: the powerful synergy of C-H donor groups within a bowl-shaped cavity.
Chemical communications (Cambridge, England), 2016, 52, 10910-10913
7124844 CIFC44 H36 Br F24 N7 P2P -112.226; 12.514; 18.219
75.477; 78.586; 71.715		2540.5Amendola, Valeria; Bergamaschi, Greta; Boiocchi, Massimo; Legnani, Laura; Presti, Eliana Lo; Miljkovic, Ana; Monzani, Enrico; Pancotti, Francesca
Chloride-binding in organic-water mixtures: the powerful synergy of C-H donor groups within a bowl-shaped cavity.
Chemical communications (Cambridge, England), 2016, 52, 10910-10913
7124845 CIFC18 H17 Cl2 N O4 SP 1 21/c 113.725; 7.0845; 20.233
90; 108.593; 90		1864.7Xia, Dong; Li, Yang; Miao, Tao; Li, Pinhua; Wang, Lei
Direct synthesis of sulfonated dihydroisoquinolinones from N-allylbenzamide and arylsulfinic acids via TBHP-promoted cascade radical addition and cyclization.
Chemical communications (Cambridge, England), 2016, 52, 11559-11562
7124846 CIFC42 H40 Br2 N2 O6P 1 21 19.5936; 17.0134; 12.402
90; 111.095; 90		1888.6Li, Jun-Long; Yang, Kai-Chuan; Li, Yi; Li, Qiang; Zhu, Hong-Ping; Han, Bo; Peng, Cheng; Zhi, Yong-Gang; Gou, Xiao-Jun
Asymmetric synthesis of bicyclic dihydropyrans via organocatalytic inverse-electron-demand oxo-Diels-Alder reactions of enolizable aliphatic aldehydes.
Chemical communications (Cambridge, England), 2016, 52, 10617-10620
7124847 CIFC31 H27 I N2 O2 SP 1 21/c 19.6062; 11.1759; 25.6122
90; 92.1354; 90		2747.76Li, Honghe; Li, Xiaoxiao; Zhao, Zhigang; Ma, Ting; Sun, Chenyang; Yang, Bowen
Intermolecular iodofunctionalization of allenamides with indoles, pyrroles, and furans: synthesis of iodine-substituted Z-enamides.
Chemical communications (Cambridge, England), 2016, 52, 10167-10170
7124848 CIFC19 H18 I N3 O2 SP -18.421; 10; 11.8424
100.66; 103.744; 90.605		950.42Li, Honghe; Li, Xiaoxiao; Zhao, Zhigang; Ma, Ting; Sun, Chenyang; Yang, Bowen
Intermolecular iodofunctionalization of allenamides with indoles, pyrroles, and furans: synthesis of iodine-substituted Z-enamides.
Chemical communications (Cambridge, England), 2016, 52, 10167-10170
7124849 CIFC20 H13 F N4 SP -19.927; 13.059; 13.682
69.528; 89.026; 78.107		1623.1Yoshida, Suguru; Yano, Takahisa; Nishiyama, Yoshitake; Misawa, Yoshihiro; Kondo, Masakazu; Matsushita, Takeshi; Igawa, Kazunobu; Tomooka, Katsuhiko; Hosoya, Takamitsu
Thiazolobenzyne: a versatile intermediate for multisubstituted benzothiazoles.
Chemical communications (Cambridge, England), 2016, 52, 11199-11202
7124850 CIFC32 H64 B Li O8P 1 21/n 110.6111; 22.4729; 14.576
90; 92.676; 90		3472.03Basnet, Prakash; Thapa, Surendra; Dickie, Diane A.; Giri, Ramesh
The copper-catalysed Suzuki-Miyaura coupling of alkylboron reagents: disproportionation of anionic (alkyl)(alkoxy)borates to anionic dialkylborates prior to transmetalation.
Chemical communications (Cambridge, England), 2016, 52, 11072-11075
7124851 CIFC28 H56 B2 Li2 O6P -18.3308; 9.3831; 10.3351
98.43; 106.326; 90.671		765.74Basnet, Prakash; Thapa, Surendra; Dickie, Diane A.; Giri, Ramesh
The copper-catalysed Suzuki-Miyaura coupling of alkylboron reagents: disproportionation of anionic (alkyl)(alkoxy)borates to anionic dialkylborates prior to transmetalation.
Chemical communications (Cambridge, England), 2016, 52, 11072-11075
7124852 CIFC19 H27 N O9 ZnP -110.4273; 10.8211; 10.8805
85.208; 74.992; 67.508		1095.45Foster, Jonathan A.; Henke, Sebastian; Schneemann, Andreas; Fischer, Roland A.; Cheetham, Anthony K.
Liquid exfoliation of alkyl-ether functionalised layered metal-organic frameworks to nanosheets.
Chemical communications (Cambridge, England), 2016, 52, 10474-10477
7124853 CIFC27 H24 Au F5 N2P 1 21/c 122.2207; 12.08219; 20.7776
90; 114.995; 90		5055.81Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124854 CIFC11 H8 Au F5 N2P 1 21/c 112.1492; 7.1342; 13.5219
90; 97.48; 90		1162.03Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124855 CIFC15 H16 Au F5 N2P -19.2638; 9.9251; 10.7976
104.458; 104.138; 114.79		801.05Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124856 CIFC29 H32 Au F5 N2P 1 21/c 116.6316; 6.73754; 23.1802
90; 107.797; 90		2473.18Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124857 CIFC32 H20 F N3 OP 1 21/c 127.5965; 5.8463; 14.617
90; 93.918; 90		2352.76Yu, Ling; Wu, Zhongbin; Xie, Guohua; Zhong, Cheng; Zhu, Zece; Cong, Hengjiang; Ma, Dongge; Yang, Chuluo
Achieving a balance between small singlet-triplet energy splitting and high fluorescence radiative rate in a quinoxaline-based orange-red thermally activated delayed fluorescence emitter.
Chemical communications (Cambridge, England), 2016, 52, 11012-11015
7124858 CIFC55.18 H49.76 B2 Cl3.96 Cu2 F8 Mo4 N4.6 O8 P4P 31 2 113.2466; 13.2466; 38.4491
90; 90; 120		5842.9Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124859 CIFC28.2 H25.9 B Cl0.4 Cu F4 Mo2 N2.5 O4 P2P -112.15; 12.9837; 13.0995
112.581; 95.502; 112.579		1688.53Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124860 CIFC28.1 H22.2 B Cl0.2 Cu F4 Mo2 N2 O8 P2P -111.051; 12.9411; 14.5125
107.454; 109.734; 92.922		1836.64Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124861 CIFC57 H46 B2 Cl2 Cu2 F8 Mo4 N4 O16 P4C 1 2/c 123.3364; 15.9366; 20.1067
90; 116.735; 90		6678.3Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124862 CIFC36 H17 B2 F20 NP 1 21/n 114.9491; 11.0572; 20.4604
90; 102.897; 90		3296.69Körte, Leif A; Blomeyer, Sebastian; Heidemeyer, Shari; Mix, Andreas; Neumann, Beate; Mitzel, Norbert W.
Intramolecular cooperativity in frustrated Lewis pairs.
Chemical communications (Cambridge, England), 2016, 52, 9949-9952
7124863 CIFC13 H22 B10 O2P -17.0022; 11.1149; 12.7151
72.088; 85.357; 77.321		918.58Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124864 CIFC14 H24 B10 O2P -16.9249; 11.0485; 13.4241
70.985; 82.699; 79.375		951.9Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124865 CIFC15 H27 B10 N O2P -17.3998; 11.4524; 12.796
101.746; 102.967; 101.723		998.81Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124866 CIFC13 H21 B10 Cl O2P 1 21/n 114.2465; 6.9536; 19.296
90; 103.257; 90		1860.6Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124867 CIFC13 H21 B10 Br O2P 1 21/n 114.3765; 6.99225; 19.7177
90; 105.687; 90		1908.28Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124868 CIFC19 H26 B10 O2P 1 21/c 115.59137; 7.11207; 20.7564
90; 106.786; 90		2203.55Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124869 CIFC17 H24 B10 O2P -17.5123; 11.5047; 13.1285
109.896; 91.522; 105.035		1022.13Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124870 CIFC18 H26 B10 O3C 1 2/c 126.4656; 8.57309; 20.8506
90; 111.965; 90		4387.43Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124871 CIFC11 H20 B10 O3P 1 21/n 122.1533; 6.78019; 23.3341
90; 100.05; 90		3451.09Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124872 CIFC11 H20 B10 O2 SP 1 21/n 114.009; 7.0087; 17.9756
90; 100.292; 90		1736.5Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124873 CIFC11 H20 B10 O2 SP 1 21/n 114.1171; 7.06182; 17.8292
90; 100.102; 90		1749.88Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124874 CIFC12 H21 B10 N O2C 1 2/c 122.0219; 6.88628; 24.2999
90; 104.579; 90		3566.4Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124875 CIFC124 Cl12 N7 O73 Si2 Sn6 W18P 1 21 118.7517; 28.4384; 21.539
90; 115.122; 90		10399.6Suzuki, Kosuke; Hanaya, Takumi; Sato, Rinta; Minato, Takuo; Yamaguchi, Kazuya; Mizuno, Noritaka
Hexanuclear tin(ii) and mixed valence tin(ii,iv) oxide clusters within polyoxometalates.
Chemical communications (Cambridge, England), 2016, 52, 10688-10691
7124876 CIFC115 N10 O77 Si2 Sn6 W18P -117.6999; 18.7362; 29.8744
82.659; 88.278; 74.291		9458.9Suzuki, Kosuke; Hanaya, Takumi; Sato, Rinta; Minato, Takuo; Yamaguchi, Kazuya; Mizuno, Noritaka
Hexanuclear tin(ii) and mixed valence tin(ii,iv) oxide clusters within polyoxometalates.
Chemical communications (Cambridge, England), 2016, 52, 10688-10691
7124877 CIFC64 H36 F4 N2 O8 Zn2P -113.967; 15.48; 20.893
89.948; 83.096; 89.209		4484Wang, Fangming; Liu, Wei; Teat, Simon J.; Xu, Feng; Wang, Hao; Wang, Xinlong; An, Litao; Li, Jing
Chromophore-immobilized luminescent metal-organic frameworks as potential lighting phosphors and chemical sensors.
Chemical communications (Cambridge, England), 2016, 52, 10249-10252
7124878 CIFC66 H38 F4 N2 O8 Zn2P -116.317; 16.8197; 20.0452
89.982; 85.952; 85.919		5473.6Wang, Fangming; Liu, Wei; Teat, Simon J.; Xu, Feng; Wang, Hao; Wang, Xinlong; An, Litao; Li, Jing
Chromophore-immobilized luminescent metal-organic frameworks as potential lighting phosphors and chemical sensors.
Chemical communications (Cambridge, England), 2016, 52, 10249-10252
7124879 CIFC23 H22 S2P 1 21 110.023; 7.569; 13.421
90; 108.949; 90		963Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124880 CIFC15 H16 O S2P 1 21/c 115.567; 7.3046; 12.5049
90; 107.222; 90		1358.2Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124881 CIFC52 H40 O2 S4P 1 21 110.601; 19.272; 11.193
90; 117.501; 90		2028.4Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124882 CIFC26 H20 O S2C 1 2/c 122.945; 11.378; 16.575
90; 111.887; 90		4015Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124883 CIFC28 H38 Au F6 N O2 P SbP 1 21/n 112.9088; 13.5954; 18.3182
90; 93.268; 90		3209.6Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124884 CIFC26 H20 S2P 1 21/n 111.9307; 11.8029; 13.8044
90; 98.163; 90		1924.2Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124885 CIFC29 H20 S2P 1 21/c 115.8061; 6.3393; 21.023
90; 95.291; 90		2097.5Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124886 CIFC28 H24 O3 S2P -19.8628; 11.701; 12.236
108.538; 104.931; 90.24		1287.9Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124887 CIFC13 H11 Cl N4 OP 1 21 16.1447; 8.6445; 12.6178
90; 101.032; 90		657.84Vishwanath, Manjunatha; Sivamuthuraman, Koilpitchai; Kesavan, Venkitasamy
An efficient construction of N,N-bicyclic pyrazolidinones comprising enaminonitriles via asymmetric [3+2] cycloaddition.
Chemical communications (Cambridge, England), 2016, 52, 12314-12317
7124888 CIFC50 H96 Br8 Dy6 N14 O32P -111.225; 12.338; 18.269
72.433; 82.638; 89.18		2391.5Li, Xiao-Lei; Wu, Jianfeng; Tang, Jinkui; Le Guennic, Boris; Shi, Wei; Cheng, Peng
A planar triangular Dy3 + Dy3 single-molecule magnet with a toroidal magnetic moment.
Chemical communications (Cambridge, England), 2016, 52, 9570-9573
7124889 CIFC16 H16 Co Dy N8 O5P 1 21/m 16.897; 15.6685; 9.6096
90; 102.131; 90		1015.28Chorazy, Szymon; Wang, Junhao; Ohkoshi, Shin-Ichi
Yellow to greenish-blue colour-tunable photoluminescence and 4f-centered slow magnetic relaxation in a cyanido-bridged Dy(III)(4-hydroxypyridine)-Co(III) layered material.
Chemical communications (Cambridge, England), 2016, 52, 10795-10798
7124890 CIFC45 H62 Cl2 N4 O4 ZrP 1 21/n 112.9667; 18.0916; 18.8976
90; 95.342; 90		4413.9Schneider, Fabian; Zhao, Tiankun; Huhn, Thomas
Cytotoxic heteroleptic heptacoordinate salan zirconium(iv)-bis-chelates - synthesis, aqueous stability and X-ray structure analysis.
Chemical communications (Cambridge, England), 2016, 52, 10151-10154
7124891 CIFC29 H33 N3 O6 ZrP 1 21/n 19.4729; 22.863; 12.408
90; 93.774; 90		2681.5Schneider, Fabian; Zhao, Tiankun; Huhn, Thomas
Cytotoxic heteroleptic heptacoordinate salan zirconium(iv)-bis-chelates - synthesis, aqueous stability and X-ray structure analysis.
Chemical communications (Cambridge, England), 2016, 52, 10151-10154
7124892 CIFC31 H29 B2 F10 N O2P -19.8867; 10.3242; 16.1713
76.107; 86.224; 73.616		1537.3Fleige, Mirco; Möbus, Juri; Vom Stein, Thorsten; Glorius, Frank; Stephan, Douglas W.
Lewis acid catalysis: catalytic hydroboration of alkynes initiated by Piers' borane.
Chemical communications (Cambridge, England), 2016, 52, 10830-10833
7124893 CIFC20 H16 Br N2 O2P 1 21/n 121; 7.6152; 23.7899
90; 112.403; 90		3517.3Das, Tapas; Kayet, Anirban; Mishra, Ruchika; Singh, Vinod K.
Highly fluorescent 1,2-dihydropyrimido[1,6-α]indole: an efficient metal free synthesis and photophysical study.
Chemical communications (Cambridge, England), 2016, 52, 11231-11234
7124894 CIFC120 H101 B Cl6 N12 O5C m c 2126.6592; 23.6211; 19.6982
90; 90; 90		12404.3Zhang, Yuehong; Oh, Juwon; Wang, Kang; Shin, Dongju; Zhan, Xiaopeng; Zheng, Yingting; Kim, Dongho; Jiang, Jianzhuang
The first porphyrin-subphthalocyaninatoboron(iii)-fused hybrid with unique conformation and intramolecular charge transfer behavior.
Chemical communications (Cambridge, England), 2016, 52, 10517-10520
7124895 CIFC19 H16 O3P -17.0903; 10.2299; 11.0836
67.824; 77.107; 79.532		721.45Jiang, Chongguo; Xiong, Zhiling; Jin, Shengfei; Gao, Peng; Tang, Yingzhan; Wang, Yanshi; Du, Chuan; Wang, Xiaoyu; Liu, Yang; Lin, Bin; Liu, Yongxiang; Cheng, Maosheng
A Au(i)-catalyzed hydrogen bond-directed tandem strategy to synthesize indeno-chromen-4-one and indeno-quinolin-4-one derivatives.
Chemical communications (Cambridge, England), 2016, 52, 11516-11519
7124896 CIFC78 H66 Eu N7 O18P 21 320.898; 20.898; 20.898
90; 90; 90		9127Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124897 CIFC78 H60 Cd Eu N7.5 O26P 21 320.509; 20.509; 20.509
90; 90; 90		8626.48Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124898 CIFC26 H20 Cl4 Hg2 N2 O5C 1 2/c 120.25; 12.1502; 13.984
90; 123.951; 90		2854.1Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124899 CIFC52 H48 N8 O25 Pb2P 1 21/c 116.777; 12.3446; 13.27
90; 96.886; 90		2728.5Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124900 CIFC14 H12P 1 21/c 118.222; 5.648; 20.014
90; 97.925; 90		2040.1Chen, Gen-Qiang; Fang, Wei; Wei, Yin; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed dehydrogenative cycloisomerization of 1,5-enynes.
Chemical communications (Cambridge, England), 2016, 52, 10799-10802
7124901 CIFC41 H30 B Cl3 N4 O2P -19.821; 12.383; 15.111
79.156; 84.922; 73.193		1726.7Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124902 CIFC61.5 H46.5 B Cl4.5 N4 O6P -113.411; 20.416; 21.32
75.181; 83.052; 88.03		5602Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124903 CIFC40.5 H30 B Cl N4 O2P 19.887; 11.839; 15.495
77.762; 80.071; 66.473		1617.3Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124904 CIFC60 H42 B2 N4 O6P 1 21 111.4322; 16.3704; 12.5755
90; 100.994; 90		2310.31Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124905 CIFC62 H44 B2 Cl6 N4 O6P 1 21/n 127.3653; 13.783; 31.7984
90; 114.516; 90		10912.3Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124906 CIFC33 H53 B K N3 O SiP 21 21 2111.5483; 15.6266; 19.1969
90; 90; 90		3464.3Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124907 CIFC47 H59 N O3 Si ZnP -4 21 c21.1923; 21.1923; 18.9615
90; 90; 90		8515.9Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124908 CIFC33 H53 B Br N3 O Si ZnP 1 21/c 115.203; 11.974; 19.965
90; 100.3; 90		3575.9Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124909 CIFC84 H98 N2 O2 Si2 Zn2P -113.39; 14.317; 20.067
80.79; 79.66; 71.54		3567.7Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124910 CIFC42 H48.98 Br0.02 N Si ZnP -114.0869; 15.8901; 17.1769
72.101; 81.448; 81.036		3593.29Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124911 CIFC45 H54 Br N O3 Si ZnI 41/a :220.9835; 20.9835; 37.613
90; 90; 90		16561.3Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124912 CIFC55.75 H62 N O2 Si ZnP n a 2127.289; 12.855; 28.084
90; 90; 90		9852Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124913 CIFC44 H53 N Si ZnP b c a18.699; 10.648; 37.755
90; 90; 90		7517Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124914 CIFC38 H41 N Si ZnP -19.9787; 11.6997; 14.992
88.8; 85.337; 72.292		1661.8Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124915 CIFC28 H23 Br N2 O2P 1 21/c 18.1067; 15.997; 18.8373
90; 99.636; 90		2408.41Zhou, Xiaorong; Peng, Zhixing; Zhao, Hongyang; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Rh-Catalyzed annulations of N-methoxybenzamides with ketenimines: synthesis of 3-aminoisoindolinones and 3-diarylmethyleneisoindolinones with strong aggregation induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10676-10679
7124916 CIFC32 H23 N OP 1 21/n 113.2048; 9.7962; 36.3
90; 90.681; 90		4695.3Zhou, Xiaorong; Peng, Zhixing; Zhao, Hongyang; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Rh-Catalyzed annulations of N-methoxybenzamides with ketenimines: synthesis of 3-aminoisoindolinones and 3-diarylmethyleneisoindolinones with strong aggregation induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10676-10679
7124917 CIFC44 H31 N OP 1 21/n 19.7155; 11.1424; 33.67
90; 94.871; 90		3631.7Zhou, Xiaorong; Peng, Zhixing; Zhao, Hongyang; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Rh-Catalyzed annulations of N-methoxybenzamides with ketenimines: synthesis of 3-aminoisoindolinones and 3-diarylmethyleneisoindolinones with strong aggregation induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10676-10679
7124918 CIFC42 H90 Cl4 N6 O2 ReP -110.4031; 11.9265; 11.9819
64.8219; 75.0617; 82.2082		1299.34Feng, Xiaowen; Liu, Jun-Liang; Pedersen, Kasper S.; Nehrkorn, Joscha; Schnegg, Alexander; Holldack, Karsten; Bendix, Jesper; Sigrist, Marc; Mutka, Hannu; Samohvalov, Dumitru; Aguilà, David; Tong, Ming-Liang; Long, Jeffrey R.; Clérac, Rodolphe
Multifaceted magnetization dynamics in the mononuclear complex [Re<sup>IV</sup>Cl<sub>4</sub>(CN)<sub>2</sub>]<sup>2</sup>.
Chemical communications (Cambridge, England), 2016, 52, 12905-12908
7124919 CIFC13 H9 F3 N2 OP -15.617; 7.3899; 14.156
75.267; 80.383; 88.88		560.1Ragupathi, Ayyakkannu; Sagadevan, Arunachalam; Lin, Chun-Cheng; Hwu, Jih-Ru; Hwang, Kuo Chu
Copper(i)-catalysed oxidative C-N coupling of 2-aminopyridine with terminal alkynes featuring a C[triple bond, length as m-dash]C bond cleavage promoted by visible light.
Chemical communications (Cambridge, England), 2016, 52, 11756-11759
7124920 CIFC5 H16 Cl5 N2 SbP 21 21 217.662; 13.433; 13.883
90; 90; 90		1428.9Mei, Guang-Quan; Zhang, Han-Yue; Liao, Wei-Qiang
A symmetry breaking phase transition-triggered high-temperature solid-state quadratic nonlinear optical switch coupled with a switchable dielectric constant in an organic-inorganic hybrid compound.
Chemical communications (Cambridge, England), 2016, 52, 11135-11138
7124921 CIFC5 H16 Cl5 N2 SbP n m a13.514; 7.818; 13.8
90; 90; 90		1458Mei, Guang-Quan; Zhang, Han-Yue; Liao, Wei-Qiang
A symmetry breaking phase transition-triggered high-temperature solid-state quadratic nonlinear optical switch coupled with a switchable dielectric constant in an organic-inorganic hybrid compound.
Chemical communications (Cambridge, England), 2016, 52, 11135-11138
7124922 CIFC70 H78 N2 O2 Ti2P 1 21/c 111.09321; 22.0757; 28.1078
90; 92.8099; 90		6875.05Liu, Cham-Chuen; Chan, Michael C. W.; Lo, Po-Kam; Lau, Kai-Chung; Yiu, Shek-Man
Multifaceted chelating μ-(η(3):η(3)-antifacial)-(cis-C4R2H2) coordination motif in binuclear complexes.
Chemical communications (Cambridge, England), 2016, 52, 11056-11059
7124923 CIFC72 H83 N2 O2.5 Zr2P -111.3506; 15.5365; 19.1544
79.469; 79.993; 81.353		3245.81Liu, Cham-Chuen; Chan, Michael C. W.; Lo, Po-Kam; Lau, Kai-Chung; Yiu, Shek-Man
Multifaceted chelating μ-(η(3):η(3)-antifacial)-(cis-C4R2H2) coordination motif in binuclear complexes.
Chemical communications (Cambridge, England), 2016, 52, 11056-11059
7124924 CIFC73.5 H85.5 Hf2 N2 O2P 1 21/c 114.6909; 16.2174; 27.5623
90; 103.614; 90		6382.2Liu, Cham-Chuen; Chan, Michael C. W.; Lo, Po-Kam; Lau, Kai-Chung; Yiu, Shek-Man
Multifaceted chelating μ-(η(3):η(3)-antifacial)-(cis-C4R2H2) coordination motif in binuclear complexes.
Chemical communications (Cambridge, England), 2016, 52, 11056-11059
7124925 CIFC211 H82 Cl5 N6 Na2 O12 Sc6P 1 21/c 115.1344; 20.6079; 21.8351
90; 90.019; 90		6810.1Konarev, Dmitri V.; Zorina, Leokadiya V.; Khasanov, Salavat S.; Popov, Alexey A.; Otsuka, Akihiro; Yamochi, Hideki; Saito, Gunzi; Lyubovskaya, Rimma N.
A crystalline anionic complex of scandium nitride endometallofullerene: experimental observation of single-bonded (Sc3N@Ih-C80(-))2 dimers.
Chemical communications (Cambridge, England), 2016, 52, 10763-10766
7124926 CIFC67.5 H108 O13 S6 Zn4P -113.8362; 15.0709; 20.3113
89.161; 79.646; 73.544		3992.8Kelly, Rory P.; Kazeminejad, Neda; Lamsfus, Carlos A.; Maron, Laurent; Roesky, Peter W.
Activation of SO<sub>2</sub> by [Zn(Cp*)<sub>2</sub>] and [(Cp*)Zn<sup>I</sup>-Zn<sup>I</sup>(Cp*)].
Chemical communications (Cambridge, England), 2016, 52, 13090-13093
7124927 CIFC16 H40 N4 O8 S3 Zn2P 1 21/c 112.903; 15.8305; 13.4913
90; 103.699; 90		2677.4Kelly, Rory P.; Kazeminejad, Neda; Lamsfus, Carlos A.; Maron, Laurent; Roesky, Peter W.
Activation of SO<sub>2</sub> by [Zn(Cp*)<sub>2</sub>] and [(Cp*)Zn<sup>I</sup>-Zn<sup>I</sup>(Cp*)].
Chemical communications (Cambridge, England), 2016, 52, 13090-13093
7124928 CIFC29 H20 O2P -18.6037; 9.6242; 13.0214
79.03; 81.504; 74.717		1015.65Chen, Ling; Cui, Yu-Ming; Xu, Zheng; Cao, Jian; Zheng, Zhan-Jiang; Xu, Li-Wen
An efficient approach toward formation of polycyclic coumarin derivatives via carbocation-initiated [4+2] cycloaddition and atom-economical photo-irradiated cyclization.
Chemical communications (Cambridge, England), 2016, 52, 11131-11134
7124929 CIFC17 H14 O4P 1 21/n 18.1218; 27.7422; 12.2315
90; 95.062; 90		2745.2Ji, Wei; Liu, Guofeng; Wang, Fang; Zhu, Zhu; Feng, Chuanliang
Galactose-decorated light-responsive hydrogelator precursors for selectively killing cancer cells.
Chemical communications (Cambridge, England), 2016, 52, 12574-12577
7124930 CIFC29 H33 N3 O2P -19.6437; 11.6855; 12.1217
87.115; 71.784; 82.973		1287.7Quinodoz, P.; Wright, K.; Drouillat, B.; David, O.; Marrot, J.; Couty, F.
Synthesis of homopropargylamines from 2-cyanoazetidines.
Chemical communications (Cambridge, England), 2016, 52, 10072-10075
7124931 CIFC28 H26P c a 2120.325; 11.622; 8.52
90; 90; 90		2012.6Wang, Guohua; Chen, Chao; Peng, Jing
Copper-catalyzed intramolecular aryl-bicyclization of diynes with diaryliodonium salts via vinyl cations.
Chemical communications (Cambridge, England), 2016, 52, 10277-10280
7124932 CIFC192 H240 Cl4 N36 Ni4 O16I 2 323.432; 23.432; 23.432
90; 90; 90		12865.5Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124933 CIFC192 H240 Cl4 N36 Ni4 O16I 2 323.4359; 23.4359; 23.4359
90; 90; 90		12872Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124934 CIFC204 H264 B6 F24 N36 Ni4 O12P 118.9274; 19.8289; 22.328
110.839; 102.662; 108.564		6881.7Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124935 CIFC240 H276 Cl4 N36 Ni4 O6F 41 3 239.2624; 39.2624; 39.2624
90; 90; 90		60524Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124936 CIFC241 H264 F3 N36 Ni4 O3 SP 119.222; 20.854; 22.254
106.518; 103.878; 112.172		7289.5Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124937 CIFC29 H28 F4 N2 O5P 1 21/c 112.4966; 9.7777; 22.6334
90; 100.263; 90		2721.3Hua, Hui-Liang; Zhang, Bo-Sheng; He, Yu-Tao; Qiu, Yi-Feng; Hu, Jing-Yuan; Yang, Yu-Chen; Liang, Yong-Min
Copper-catalyzed difluoromethylation of propargylamide-substituted indoles: synthesis of mono- and bis-difluoromethylated indoloazepinone derivatives.
Chemical communications (Cambridge, England), 2016, 52, 10396-10399
7124938 CIFC24 H22 F2 N2 O3P b c a12.2175; 15.8782; 22.0697
90; 90; 90		4281.34Hua, Hui-Liang; Zhang, Bo-Sheng; He, Yu-Tao; Qiu, Yi-Feng; Hu, Jing-Yuan; Yang, Yu-Chen; Liang, Yong-Min
Copper-catalyzed difluoromethylation of propargylamide-substituted indoles: synthesis of mono- and bis-difluoromethylated indoloazepinone derivatives.
Chemical communications (Cambridge, England), 2016, 52, 10396-10399
7124939 CIFC28 H25 Cl F4 N2 O5P 1 21/c 112.8985; 14.8772; 27.961
90; 97.992; 90		5313.4Hua, Hui-Liang; Zhang, Bo-Sheng; He, Yu-Tao; Qiu, Yi-Feng; Hu, Jing-Yuan; Yang, Yu-Chen; Liang, Yong-Min
Copper-catalyzed difluoromethylation of propargylamide-substituted indoles: synthesis of mono- and bis-difluoromethylated indoloazepinone derivatives.
Chemical communications (Cambridge, England), 2016, 52, 10396-10399
7124940 CIFC29 H28 N2 OP 1 21 18.118; 16.336; 8.515
90; 91.597; 90		1128.8Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124941 CIFC41 H38 N4 O2R -3 :H24.722; 24.722; 13.524
90; 90; 120		7158Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124942 CIFC28 H27 B F4 N4P 1 21/c 16.691; 29.96; 12.952
90; 104.2; 90		2517Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124943 CIFC29 H31 N3 O SP 1 21 113.438; 14.165; 13.5796
90; 93.657; 90		2579.6Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124944 CIFC56 H82 N4 Na4 O6P 1 2/c 118.372; 10.659; 28.255
90; 100.193; 90		5446Lichtenberg, C.; Krummenacher, I.
Aminotroponiminates as tunable, redox-active ligands: reversible single electron transfer and reductive dimerisation.
Chemical communications (Cambridge, England), 2016, 52, 10044-10047
7124945 CIFC25 H39 Co N6 O4P 1 21/n 114.5396; 9.6307; 20.8295
90; 109.316; 90		2752.5Das, Debasree; Pattanayak, Santanu; Singh, Kundan K.; Garai, Bikash; Sen Gupta, Sayam
Electrocatalytic water oxidation by a molecular cobalt complex through a high valent cobalt oxo intermediate.
Chemical communications (Cambridge, England), 2016, 52, 11787-11790
7124946 CIFC167 H278 Al4 N8 O12I 1 2/a 129.9091; 11.0908; 25.9834
90; 108.075; 90		8193.8McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124947 CIFC33 H51 Al N2 O3P 1 21/c 112.1388; 19.0837; 14.1406
90; 102.663; 90		3196.04McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124948 CIFC38 H61 Al N2 O2P 1 21/c 113.8779; 13.002; 20.8532
90; 98.2288; 90		3724McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124949 CIFC43 H61 Al N2 O3P -110.9794; 14.2923; 15.1168
115.692; 100.605; 102.864		1974.85McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124950 CIFC23 H20 Br N O P TcC 1 2/c 122.001; 13.607; 17.541
90; 126.91; 90		4198.8Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124951 CIFC24 H20 B F4 N O2 P TcP 1 21/c 19.27; 17.374; 14.27
90; 100.29; 90		2261.3Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124952 CIFC29 H25 N O P TcP 1 21 19.179; 13.937; 10.048
90; 112.89; 90		1184.2Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124953 CIFC36.5 H31 Br3 Cl N O3 P2 TcP 1 21/c 112.551; 14.394; 44.488
90; 97.55; 90		7967.5Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124954 CIFC25 H28 N2 O4 SP 21 21 218.782; 10.8274; 26.0299
90; 90; 90		2475.08Rainoldi, G.; Faltracco, M.; Lo Presti, L.; Silvani, A.; Lesma, G.
Highly diastereoselective entry into chiral spirooxindole-based 4-methyleneazetidines via formal [2+2] annulation reaction.
Chemical communications (Cambridge, England), 2016, 52, 11575-11578
7124955 CIFC18 H12 Cu2 N0 O10 SiP 63/m m c18.5185; 18.5185; 19.1215
90; 90; 120		5678.9Gao, Chao-Ying; Tian, Hong-Rui; Ai, Jing; Li, Lei-Jiao; Dang, Song; Lan, Ya-Qian; Sun, Zhong-Ming
A microporous Cu-MOF with optimized open metal sites and pore spaces for high gas storage and active chemical fixation of CO2.
Chemical communications (Cambridge, England), 2016, 52, 11147-11150
7124956 CIFC8 H16 Cu F6 N4 O4 VP 4/n b m :29.7325; 9.7325; 8.2154
90; 90; 90		778.18Manson, Jamie L.; Schlueter, John A.; Garrett, Kerry E.; Goddard, Paul A.; Lancaster, Tom; Möller, Johannes S; Blundell, Stephen J.; Steele, Andrew J.; Franke, Isabel; Pratt, Francis L.; Singleton, John; Bendix, Jesper; Lapidus, Saul H.; Uhlarz, Marc; Ayala-Valenzuela, Oscar; McDonald, Ross D.; Gurak, Mary; Baines, Christopher
Bimetallic MOFs (H<sub>3</sub>O)<sub>x</sub>[Cu(MF<sub>6</sub>)(pyrazine)<sub>2</sub>]·(4 - x)H<sub>2</sub>O (M = V<sup>4+</sup>, x = 0; M = Ga<sup>3+</sup>, x = 1): co-existence of ordered and disordered quantum spins in the V<sup>4+</sup> system.
Chemical communications (Cambridge, England), 2016, 52, 12653-12656
7124957 CIFC8 H17 Cu F6 Ga N4 O4P 4/n b m :29.7134; 9.7134; 8.2415
90; 90; 90		777.59Manson, Jamie L.; Schlueter, John A.; Garrett, Kerry E.; Goddard, Paul A.; Lancaster, Tom; Möller, Johannes S; Blundell, Stephen J.; Steele, Andrew J.; Franke, Isabel; Pratt, Francis L.; Singleton, John; Bendix, Jesper; Lapidus, Saul H.; Uhlarz, Marc; Ayala-Valenzuela, Oscar; McDonald, Ross D.; Gurak, Mary; Baines, Christopher
Bimetallic MOFs (H<sub>3</sub>O)<sub>x</sub>[Cu(MF<sub>6</sub>)(pyrazine)<sub>2</sub>]·(4 - x)H<sub>2</sub>O (M = V<sup>4+</sup>, x = 0; M = Ga<sup>3+</sup>, x = 1): co-existence of ordered and disordered quantum spins in the V<sup>4+</sup> system.
Chemical communications (Cambridge, England), 2016, 52, 12653-12656
7124958 CIFC24 H20 N2 O2P 1 21/c 110.3006; 17.4826; 10.8631
90; 92.484; 90		1954.4Huo, Congde; Dong, Jie; Su, Yingpeng; Tang, Jing; Chen, Fengjuan
Iron-catalyzed oxidative sp<sup>3</sup> carbon-hydrogen bond functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones.
Chemical communications (Cambridge, England), 2016, 52, 13341-13344
7124959 CIFC19 H22 N2 O2 SP 1 21 19.5967; 9.265; 10.1709
90; 102.244; 90		883.76Zhao, Quan-Qing; Hu, Xiao-Qiang; Yang, Meng-Nan; Chen, Jia-Rong; Xiao, Wen-Jing
A visible-light photocatalytic N-radical cascade of hydrazones for the synthesis of dihydropyrazole-fused benzosultams.
Chemical communications (Cambridge, England), 2016, 52, 12749-12752
7124960 CIFC19 H20 N2 O2 SP -19.31; 13.2449; 14.8906
69.506; 77.927; 89.163		1678.5Zhao, Quan-Qing; Hu, Xiao-Qiang; Yang, Meng-Nan; Chen, Jia-Rong; Xiao, Wen-Jing
A visible-light photocatalytic N-radical cascade of hydrazones for the synthesis of dihydropyrazole-fused benzosultams.
Chemical communications (Cambridge, England), 2016, 52, 12749-12752
7124961 CIFC104 H92 Br8 Cl2 N4 OP -110.9254; 13.4449; 15.8457
95.9; 100.524; 95.947		2258.4Krzeszewski, Maciej; Swider, Paweł; Dobrzycki, Łukasz; Cyrański, Michał K; Danikiewicz, Witold; Gryko, Daniel T.
The role of steric hindrance in the intramolecular oxidative aromatic coupling of pyrrolo[3,2-b]pyrroles.
Chemical communications (Cambridge, England), 2016, 52, 11539-11542
7124962 CIFC46 H51 Ge N2 O PP 1 21/n 113.91699; 19.62321; 14.94628
90; 94.7717; 90		4067.62Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124963 CIFC46 H51 N2 O P SiP -19.4352; 12.6209; 17.8147
85.36; 78.369; 76.089		2015.71Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124964 CIFC46 H51 N2 O P SnP 1 21/n 114.0166; 19.8309; 14.945
90; 94.185; 90		4143.06Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124965 CIFC49 H61 N2 O P SnP -110.64809; 11.6076; 19.4163
91.4216; 92.8956; 110.289		2245.77Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124966 CIFC45 H51 Ge N2 PP 1 21/n 124.0628; 12.8152; 25.4632
90; 94.7933; 90		7824.62Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124967 CIFC160 H164 N8 O1.5 P4 Sn4P -113.0114; 17.0048; 18.7117
111.389; 94.838; 110.638		3498.2Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124968 CIFC51 H41 N7 O2P 1 21/c 111.998; 14.423; 21.871
90; 92.101; 90		3782Mosca, Lorenzo; Čejka, Jan; Dolenský, Bohumil; Havlík, Martin; Jakubek, Milan; Kaplánek, Robert; Král, Vladimír; Anzenbacher, Pavel
Bowl-shaped Tröger's bases and their recognition properties.
Chemical communications (Cambridge, England), 2016, 52, 10664-10667
7124969 CIFC69 H52 N8 O4P 1 21/c 121.3761; 12.4047; 21.2424
90; 113.697; 90		5157.8Mosca, Lorenzo; Čejka, Jan; Dolenský, Bohumil; Havlík, Martin; Jakubek, Milan; Kaplánek, Robert; Král, Vladimír; Anzenbacher, Pavel
Bowl-shaped Tröger's bases and their recognition properties.
Chemical communications (Cambridge, England), 2016, 52, 10664-10667
7124970 CIFC46 H38 Cl2 N6P -117.9422; 18.3629; 20.9128
107.088; 100.483; 116.305		5498.3Mosca, Lorenzo; Čejka, Jan; Dolenský, Bohumil; Havlík, Martin; Jakubek, Milan; Kaplánek, Robert; Král, Vladimír; Anzenbacher, Pavel
Bowl-shaped Tröger's bases and their recognition properties.
Chemical communications (Cambridge, England), 2016, 52, 10664-10667
7124971 CIFC17 H14 Ag N7 O4I 41/a :231.37; 31.37; 7.8467
90; 90; 90		7721.8Li, Cheng-Peng; Wang, Si; Guo, Wei; Yan, Yan; Du, Miao
Dual structure evolution of a Ag(i) supramolecular framework triggered by anion-exchange: replacement of terminal ligand and switching of network interpenetration degree.
Chemical communications (Cambridge, England), 2016, 52, 11060-11063
7124972 CIFC17 H15 Ag N7 O3.5I 41/a :231.065; 31.065; 8.0003
90; 90; 90		7720.6Li, Cheng-Peng; Wang, Si; Guo, Wei; Yan, Yan; Du, Miao
Dual structure evolution of a Ag(i) supramolecular framework triggered by anion-exchange: replacement of terminal ligand and switching of network interpenetration degree.
Chemical communications (Cambridge, England), 2016, 52, 11060-11063
7124973 CIFC19 H14 Ag F3 N6 O3P 42/n :222.8131; 22.8131; 7.7879
90; 90; 90		4053.1Li, Cheng-Peng; Wang, Si; Guo, Wei; Yan, Yan; Du, Miao
Dual structure evolution of a Ag(i) supramolecular framework triggered by anion-exchange: replacement of terminal ligand and switching of network interpenetration degree.
Chemical communications (Cambridge, England), 2016, 52, 11060-11063
7124974 CIFC29 H41 F6 Fe N4 O2 PP 1 21/c 121.0286; 8.7204; 17.6555
90; 99.237; 90		3195.6Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124975 CIFC29.5 H41 Cl Fe N4 O2P 1 21/c 19.6385; 13.7609; 23.41
90; 92.164; 90		3102.8Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124976 CIFC29 H44 Br3 Fe N5P -110.0331; 13.3181; 14.1
64.813; 81.091; 81.046		1675.9Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124977 CIFC27 H40 F6 Fe N6 O2 PP -18.4876; 12.8367; 16.0181
112.855; 90.553; 99.918		1578.52Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124978 CIFC25 H25 Cl Hg N2 O3P -19.4629; 11.35; 12.3473
103.843; 109.616; 99.745		1166.87Hong, Jung-Ho; Kurapati, Sathish; Jo, Yunhee; Shin, June-Ho; Cho, Dong-Gyu
Accelerated hydration reaction of an unsymmetrical tolan evidenced by a Hg(ii)-trapped macrocycle and its application as a Hg(ii)-selective indicator.
Chemical communications (Cambridge, England), 2016, 52, 10759-10762
7124979 CIFC127 H139 Cd2 Cr4 N8 Na5 O42F 2 2 240.623; 41.321; 51.868
90; 90; 90		87065Xia, Qingchun; Liu, Yan; Li, Zijian; Gong, Wei; Cui, Yong
A Cr(salen)-based metal-organic framework as a versatile catalyst for efficient asymmetric transformations.
Chemical communications (Cambridge, England), 2016, 52, 13167-13170
7124980 CIFC8 H8 N2 O4P 1 21/c 14.7242; 12.369; 13.831
90; 82.466; 90		801.2Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124981 CIFC12 H16 N2 O5P 1 21/c 122.309; 19.1478; 9.01
90; 91.398; 90		3847.6Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124982 CIFC10 H11 N3 O4P -113.3689; 15.143; 18.786
77.079; 74.563; 63.839		3265.5Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124983 CIFC11 H14 N2 O5P 1 21/n 114.6759; 31.285; 15.9269
90; 99.324; 90		7216Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124984 CIFC12.2 H11.5 N2.7 O5.4P -4 21 c17.707; 17.707; 7.3732
90; 90; 90		2311.8Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124985 CIFC20 H22 N4 O4P -14.5668; 20.531; 20.9009
76.149; 88.228; 88.156		1901.2Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124986 CIFC8 H10 N2 O5P 21 21 214.5426; 10.729; 18.692
90; 90; 90		911Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124987 CIFC28 H24 N4 O4 Pd2P 1 21/c 113.9426; 18.5793; 18.8456
90; 146.18; 90		2717.16Monas, Andrea; Užarević, Krunoslav; Halasz, Ivan; Kulcsár, Marina Juribašić; Ćurić, Manda
Vapour-induced solid-state C-H bond activation for the clean synthesis of an organopalladium biothiol sensor.
Chemical communications (Cambridge, England), 2016, 52, 12960-12963
7124988 CIFC28 H24 N4 O4 Pd2P b c a15.7028; 12.1884; 27.7307
90; 90; 90		5307.4Monas, Andrea; Užarević, Krunoslav; Halasz, Ivan; Kulcsár, Marina Juribašić; Ćurić, Manda
Vapour-induced solid-state C-H bond activation for the clean synthesis of an organopalladium biothiol sensor.
Chemical communications (Cambridge, England), 2016, 52, 12960-12963
7124989 CIFC30 H36 B2 Br4 Fe N6 O6C 1 2/c 126.14; 8.4019; 18.4972
90; 117.658; 90		3598.3Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124990 CIFC50 H52 B2 Fe N10 O6P 1 21/c 18.84673; 38.91135; 14.15673
90; 105.312; 90		4700.3Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124991 CIFC408 H368 B8 F48 Fe4 N40 O72 P16 Pt8 S16P -128.3614; 28.8276; 41.0379
101.861; 92.914; 104.12		31663Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124992 CIFC24 H24 B2 Br4 Fe N6 O6I 1 2/a 114.7088; 12.8848; 18.6454
90; 102.859; 90		3445.05Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124993 CIFC44 H40 B2 Fe N10 O6P 1 21/c 19.4866; 10.6979; 47.959
90; 94.425; 90		4852.7Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124994 CIFC95 H34 O2P 1 21/c 110.8278; 30.7175; 16.9665
90; 102.171; 90		5516.3Vidal, Sara; Izquierdo, Marta; Law, Wai Kit; Jiang, Kui; Filippone, Salvatore; Perles, Josefina; Yan, He; Martín, Nazario
Photochemical site-selective synthesis of [70]methanofullerenes.
Chemical communications (Cambridge, England), 2016, 52, 12733-12736
7124995 CIFC140 H136 K4 O11P -113.3928; 15.4263; 15.9182
72.759; 71.007; 66.158		2792.2Sumy, Daniel P.; Finke, Aaron D.; Whalley, Adam C.
The reductive aromatization of tridecacyclene.
Chemical communications (Cambridge, England), 2016, 52, 12368-12371
7124996 CIFC93 H128.56 O3 UP 1 21/c 116.6756; 37.752; 12.3496
90; 93.136; 90		7762.9Hoerger, Christopher J.; La Pierre, Henry S.; Maron, Laurent; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Reductive disproportionation of nitric oxide mediated by low-valent uranium.
Chemical communications (Cambridge, England), 2016, 52, 10854-10857
7124997 CIFC81 H105 O4 UP 1 21/c 121.4453; 13.7404; 25.313
90; 119.622; 90		6484.1Hoerger, Christopher J.; La Pierre, Henry S.; Maron, Laurent; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Reductive disproportionation of nitric oxide mediated by low-valent uranium.
Chemical communications (Cambridge, England), 2016, 52, 10854-10857
7124998 CIFC9 H20 B N O2I b a 210.1195; 29.385; 7.4892
90; 90; 90		2227Romero, Erik A.; Peltier, Jesse L.; Jazzar, Rodolphe; Bertrand, Guy
Catalyst-free dehydrocoupling of amines, alcohols, and thiols with pinacol borane and 9-borabicyclononane (9-BBN).
Chemical communications (Cambridge, England), 2016, 52, 10563-10565
7124999 CIFC24 H18 Br PP 1 21/n 110.9091; 8.4128; 20.1396
90; 94.569; 90		1842.46Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125000 CIFC24 H18 As BrP 1 21/n 110.8919; 8.4344; 20.3175
90; 94.242; 90		1861.39Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125001 CIFC24 H18 Br SbP 1 21/n 110.9265; 8.5022; 20.5734
90; 93.534; 90		1907.62Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125002 CIFC33 H29 As TeP 1 21/n 112.0462; 8.7352; 25.0693
90; 98.504; 90		2608.94Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125003 CIFC33 H29 Sb TeP -18.7261; 11.7875; 14.189
79.576; 74.286; 75.358		1349.35Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125004 CIFC28 H26 Cl O P TeP 1 21/c 18.7067; 12.5095; 22.0558
90; 94.318; 90		2395.42Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125005 CIFC25 H20 Cl3 P TeP -18.5366; 11.678; 12.597
89.5; 87.76; 85.74		1251.4Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125006 CIFC48 H36 P2 TeP -111.7394; 12.5066; 14.3469
91.146; 101.003; 117.065		1827.45Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125007 CIFC18 H22 Cl P TeP 1 21/c 114.502; 8.33; 14.464
90; 91.826; 90		1746.4Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125008 CIFC18 H22 Br P TeP 1 21/n 17.786; 13.9267; 16.4054
90; 97.078; 90		1765.3Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125009 CIFC18 H22 I P TeP 1 21/n 17.9634; 14.047; 16.871
90; 99.976; 90		1858.7Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125010 CIFC38 H48 Cl4 I6 P2 Te3C 1 2/c 122.509; 11.4213; 22.101
90; 110.786; 90		5312Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125011 CIFC18 H22 I3 P TeP 1 21/n 19.8954; 15.5322; 14.5588
90; 93.366; 90		2233.8Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125012 CIFC25 H18 F3 O3 P S TeP 1 21/n 18.5859; 13.5523; 20.3142
90; 99.133; 90		2333.77Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125013 CIFC25 H18 As F3 O3 S TeP 1 21/n 18.6484; 13.5162; 20.5103
90; 99.069; 90		2367.55Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125014 CIFC28 H24 F3 O3 S Sb TeC 1 2/c 122.9864; 12.573; 20.1946
90; 115.397; 90		5272.4Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125015 CIFC40 H26 B F15 Na O7 PP 1 21/c 110.0891; 18.9802; 20.8742
90; 93.041; 90		3991.6Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125016 CIFC440 H572 Au92 S44C 1 2/c 145.325; 28.1243; 88.076
90; 91.544; 90		112233Liao, Lingwen; Chen, Jishi; Wang, Chengming; Zhuang, Shengli; Yan, Nan; Yao, Chuanhao; Xia, Nan; Li, Lingling; Bao, Xiaoli; Wu, Zhikun
Transition-sized Au<sub>92</sub> nanoparticle bridging non-fcc-structured gold nanoclusters and fcc-structured gold nanocrystals.
Chemical communications (Cambridge, England), 2016, 52, 12036-12039
7125017 CIFC15 H20 N2 O2 SP -16.2192; 9.1506; 13.4968
98.63; 96.96; 92.679		752.15Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125018 CIFC18 H24 N2 O2 SP 1 21/n 110.79743; 13.38129; 11.85342
90; 96.5156; 90		1701.56Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125019 CIFC19 H20 N2 O2 SP 1 21/c 115.7933; 8.92836; 12.9799
90; 110.209; 90		1717.6Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125020 CIFC30 H40 N4 O4 S2P 1 21/n 118.0343; 7.581; 23.5816
90; 109.174; 90		3045.18Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125021 CIFC12 H16 N2 O2 S2P 1 21/c 114.6626; 5.3944; 18.2386
90; 113.435; 90		1323.6Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125022 CIFC29 H21 Br N2 O4P 21 21 217.08473; 16.7619; 22.085
90; 90; 90		2622.67Wang, Kai-Kai; Wang, Pan; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
Substrate-controlled switchable asymmetric annulations to access polyheterocyclic skeletons.
Chemical communications (Cambridge, England), 2016, 52, 11104-11107
7125023 CIFC23 H17 N3 O2P 21 21 2110.06732; 10.59058; 22.9703
90; 90; 90		2449.06Wang, Kai-Kai; Wang, Pan; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
Substrate-controlled switchable asymmetric annulations to access polyheterocyclic skeletons.
Chemical communications (Cambridge, England), 2016, 52, 11104-11107
7125024 CIFC40 H38.4 Cl4 Cr2 F8 N4 O21.2 Tb2P -19.6481; 11.3861; 13.3598
67.617; 78.339; 87.41		1328.23Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125025 CIFC40 H37.2 Cl4 Cr2 Dy2 F8 N4 O20.6P -19.543; 11.414; 13.306
67.56; 77.95; 87.25		1309.3Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125026 CIFC40 H37.67 Cl4 Cr2 F8 Ho2 N4 O20.83P -19.667; 11.331; 13.316
67.54; 78.27; 87.69		1318.7Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125027 CIFC70 H114 Cr2 Dy2 N4 O23P -111.164; 11.907; 16.534
70.77; 73.76; 82.43		1990.5Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125028 CIFC12 H24 B10 O8P 1 21/n 111.7899; 13.5842; 13.728
90; 104.058; 90		2132.78Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125029 CIFC20 H32 B10 O8P -112.7205; 13.3454; 16.395
98.928; 92.479; 90.262		2746.7Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125030 CIFC6 H18 B10 O2P -17.3484; 7.6219; 12.005
83.262; 88.589; 88.161		667.2Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125031 CIFC6 H18 B10 O2P 1 21/n 17.7915; 21.7; 8.0127
90; 94.885; 90		1349.83Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125032 CIFC25 H28 F6 N4 O2 P RuC 1 2/c 130.6243; 19.9078; 11.5863
90; 102.813; 90		6887.83Xie, Jianhui; Lo, Po-Kam; Lam, William W. Y.; Man, Wai-Lun; Ma, Li; Yiu, Shek-Man; Lau, Kai-Chung; Lau, Tai-Chu
Oxidation of hydroquinones by a (salen)ruthenium(vi) nitrido complex.
Chemical communications (Cambridge, England), 2016, 52, 11430-11433
7125033 CIFC22 H16 Br Cl N2 OP 21 21 218.048; 9.69; 25.348
90; 90; 90		1976.8Bao, Xiaoze; Wei, Shiqiang; Zou, Liwei; He, Yuli; Xue, Fuzhao; Qu, Jingping; Wang, Baomin
Asymmetric chlorination of 4-substituted pyrazolones catalyzed by natural cinchona alkaloid.
Chemical communications (Cambridge, England), 2016, 52, 11426-11429
7125034 CIFC5.5 H12 F6 N2 O0.5 PC 1 2/c 116.155; 6.7318; 19.587
90; 109.09; 90		2013Regnier, Vianney; Molton, Florian; Philouze, Christian; Martin, David
An air-persistent oxyallyl radical cation with simple di(methyl)amino substituents.
Chemical communications (Cambridge, England), 2016, 52, 11422-11425
7125035 CIFC24 H17 N OP n a 2115.3015; 12.1976; 9.6252
90; 90; 90		1796.5Liu, Ren-Rong; Xu, Teng-Fei; Wang, Yong-Gang; Xiang, Bin; Gao, Jian-Rong; Jia, Yi-Xia
Palladium-catalyzed dearomative arylalkynylation of indoles.
Chemical communications (Cambridge, England), 2016, 52, 13664-13667
7125036 CIFC31 H30 Cl3 F6 N6 O P RuP -110.63; 12.402; 14.118
77.336; 74.113; 79.124		1730.1Ng, Chee Koon; Wu, Jie; Hor, T. S. Andy; Luo, He-Kuan
A binary catalyst system of a cationic Ru-CNC pincer complex with an alkali metal salt for selective hydroboration of carbon dioxide.
Chemical communications (Cambridge, England), 2016, 52, 11842-11845
7125037 CIFC31 H30 Cl4 F6 N5 O2 P RuP b c a16.6675; 11.1422; 38.2172
90; 90; 90		7097.4Ng, Chee Koon; Wu, Jie; Hor, T. S. Andy; Luo, He-Kuan
A binary catalyst system of a cationic Ru-CNC pincer complex with an alkali metal salt for selective hydroboration of carbon dioxide.
Chemical communications (Cambridge, England), 2016, 52, 11842-11845
7125038 CIFC27 H32 Br N3 O6 SP 1 21/n 113.4851; 8.5343; 25.6709
90; 103.401; 90		2873.9Fuentes de Arriba, Ángel L; Simón, Luis; Rubio, Omayra H.; Monleón, Laura M; Alcázar, Victoria; Sanz, Francisca; Raposo, César A; Morán, Joaquín R
A bio-inspired enantioselective small-molecule artificial receptor for β adrenergic agonists and antagonists and its application for enantioselective extraction.
Chemical communications (Cambridge, England), 2016, 52, 12582-12585
7125039 CIFC92 H108 Br2 N10 O15 S2P 1 21 18.3467; 25.1787; 22.297
90; 92.223; 90		4682.4Fuentes de Arriba, Ángel L; Simón, Luis; Rubio, Omayra H.; Monleón, Laura M; Alcázar, Victoria; Sanz, Francisca; Raposo, César A; Morán, Joaquín R
A bio-inspired enantioselective small-molecule artificial receptor for β adrenergic agonists and antagonists and its application for enantioselective extraction.
Chemical communications (Cambridge, England), 2016, 52, 12582-12585
7125040 CIFC44.16 N8 O76 Zr12C 1 2/m 121.28954; 14.55846; 8.10658
90; 84.173; 90		2499.59Waitschat, S.; Reinsch, H.; Stock, N.
Water-based synthesis and characterisation of a new Zr-MOF with a unique inorganic building unit.
Chemical communications (Cambridge, England), 2016, 52, 12698-12701
7125041 CIFC28 H21 Br O3P -17.336; 11.8041; 13.6969
104.265; 98.881; 96.225		1122.36Wu, Ya-Nan; Xu, Ting; Fu, Rong; Wang, Nan-Nan; Hao, Wen-Juan; Wang, Shu-Liang; Li, Guigen; Tu, Shu-Jiang; Jiang, Bo
Dual rhodium/copper catalysis: synthesis of benzo[b]fluorenes and 2-naphthalenylmethanones via de-diazotized cycloadditions.
Chemical communications (Cambridge, England), 2016, 52, 11943-11946
7125042 CIFC52 H42 B F2 Fe2 N3 O4P -112.567; 13.2195; 14.1831
114.172; 93.299; 97.933		2112Didukh, Natalia O.; Zatsikha, Yuriy V.; Rohde, Gregory T.; Blesener, Tanner S.; Yakubovskyi, Viktor P.; Kovtun, Yuriy P.; Nemykin, Victor N.
NIR absorbing diferrocene-containing meso-cyano-BODIPY with a UV-Vis-NIR spectrum remarkably close to that of magnesium tetracyanotetraferrocenyltetraazaporphyrin.
Chemical communications (Cambridge, England), 2016, 52, 11563-11566
7125043 CIFC29 H21 Br Cl3 F3 N2 O3P 21 21 2112.0262; 13.8263; 17.009
90; 90; 90		2828.2Wang, Zhen-Hua; Wu, Zhi-Jun; Yue, Deng-Feng; Hu, Wen-Fei; Zhang, Xiao-Mei; Xu, Xiao-Ying; Yuan, Wei-Cheng
Organocatalytic asymmetric [3+2] cycloaddition of N-2,2,2-trifluoroethylisatin ketimines with 3-alkenyl-5-arylfuran-2(3H)-ones.
Chemical communications (Cambridge, England), 2016, 52, 11708-11711
7125044 CIFC31 H30 Bi F6 Mn N3 O12 S2P -19.6023; 12.8674; 15.9332
96.095; 105.256; 104.605		1806.25Pearson, Tyler J.; Fataftah, Majed S.; Freedman, Danna E.
Enhancement of magnetic anisotropy in a Mn-Bi heterobimetallic complex.
Chemical communications (Cambridge, England), 2016, 52, 11394-11397
7125045 CIFC23 H31 BrC 1 2/c 122.7174; 6.5055; 25.667
90; 94.802; 90		3780Christopher Braddock, D.; Mahtey, Areeb; Rzepa, Henry S.; White, Andrew J. P.
Stable bromoallene oxides.
Chemical communications (Cambridge, England), 2016, 52, 11219-11222
7125046 CIFC17 H25 Br OP 1 21/n 110.8427; 6.8117; 21.255
90; 94.932; 90		1564.02Christopher Braddock, D.; Mahtey, Areeb; Rzepa, Henry S.; White, Andrew J. P.
Stable bromoallene oxides.
Chemical communications (Cambridge, England), 2016, 52, 11219-11222
7125047 CIFC19 H24 N2 O5P 1 21/c 112.59; 8.3056; 17.163
90; 97.211; 90		1780.5Cheng, Jian; Xu, Pan; Li, Weipeng; Cheng, Yixiang; Zhu, Chengjian
The functionalization of a cascade of C(sp(2))-H/C(sp(3))-H bonds: synthesis of fused dihydropyrazoles via visible-light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 11901-11904
7125048 CIFC48 H64 B4 N4 O8P 1 21/n 16.4277; 10.233; 18.9139
90; 94.954; 90		1239.41Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125049 CIFC40 H26 N2P -13.9995; 9.9251; 17.4542
106.27; 91.672; 92.388		663.92Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125050 CIFC40 H26 N2P 1 21/c 111.0512; 14.4682; 8.5519
90; 91.007; 90		1367.2Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125051 CIFC52 H26 N2P 1 21/c 19.1494; 8.9306; 20.285
90; 92.501; 90		1655.9Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125052 CIFC18 H19 Br O3P 21 21 218.7409; 12.0555; 16.4217
90; 90; 90		1730.45Liu, Yangbin; Hu, Haipeng; Lin, Lili; Hao, Xiaoyu; Liu, Xiaohua; Feng, Xiaoming
Enantioselective construction of branched 1,3-dienyl substituted quaternary carbon stereocenters by asymmetric allenyl Claisen rearrangement.
Chemical communications (Cambridge, England), 2016, 52, 11963-11966
7125053 CIFC16 H13 Br I O3P 21 21 217.5432; 12.7924; 17.2791
90; 90; 90		1667.36Liu, Yangbin; Hu, Haipeng; Lin, Lili; Hao, Xiaoyu; Liu, Xiaohua; Feng, Xiaoming
Enantioselective construction of branched 1,3-dienyl substituted quaternary carbon stereocenters by asymmetric allenyl Claisen rearrangement.
Chemical communications (Cambridge, England), 2016, 52, 11963-11966
7125054 CIFC46 H29.41 Ba3.99 Br0 N2 O20 P6C 1 2/c 143.611; 8.549; 34.589
90; 103.59; 90		12535Fard, Z. H.; Kalinovskyy, Y.; Spasyuk, D. M.; Blight, B. A.; Shimizu, G. K. H.
Alkaline-earth phosphonate MOFs with reversible hydration-dependent fluorescence.
Chemical communications (Cambridge, England), 2016, 52, 12865-12868
7125055 CIFC52 H41 N3C 1 2/c 127.2441; 12.2005; 23.5008
90; 103.574; 90		7593.3Norouzi-Arasi, Hassan; Pal, Amlan K.; Nag, Samik; Chartrand, Daniel; Hanan, Garry S.
Synthesis and photophysical properties of C<sub>3</sub>-symmetric tris(pyridyl)truxene scaffolds of Ru(ii) and Re(i).
Chemical communications (Cambridge, England), 2016, 52, 12159-12162
7125056 CIFC68 H53 Cl60 F6 N3 O3 P ReR -3 :H13.4468; 13.4468; 53.0891
90; 90; 120		8313.3Norouzi-Arasi, Hassan; Pal, Amlan K.; Nag, Samik; Chartrand, Daniel; Hanan, Garry S.
Synthesis and photophysical properties of C<sub>3</sub>-symmetric tris(pyridyl)truxene scaffolds of Ru(ii) and Re(i).
Chemical communications (Cambridge, England), 2016, 52, 12159-12162
7125057 CIFC176 H532 N135 O209 Pd20P -125.125; 25.841; 36.446
71.625; 74.386; 67.204		20408Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125058 CIFC204 H351 N130 O191 Pd20C 1 2/c 148.457; 27.761; 37.941
90; 108.713; 90		48341Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125059 CIFC196 H357 N118.5 O119.5 Pd20 Si3P 1 21/c 146.603; 25.734; 37.303
90; 113.398; 90		41058Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125060 CIFC108 H166 N55 O59.5 Pd8 Si4P 1 21/n 124.8071; 18.2127; 40.556
90; 96.472; 90		18207Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125061 CIFC20 H16 F2 N6 O4P -15.502; 8.865; 10.409
107.757; 97.878; 93.199		476.4Duncan, Andrew J. E.; Dudovitz, Roxanne L.; Dudovitz, Shawna J.; Stojaković, Jelena; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Quantitative and regiocontrolled cross-photocycloaddition of the anticancer drug 5-fluorouracil achieved in a cocrystal.
Chemical communications (Cambridge, England), 2016, 52, 13109-13111
7125062 CIFC16 H13 F N4 O2P -17.8358; 12.4452; 15.629
98.513; 102.02; 101.749		1430.3Duncan, Andrew J. E.; Dudovitz, Roxanne L.; Dudovitz, Shawna J.; Stojaković, Jelena; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Quantitative and regiocontrolled cross-photocycloaddition of the anticancer drug 5-fluorouracil achieved in a cocrystal.
Chemical communications (Cambridge, England), 2016, 52, 13109-13111
7125063 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 113.802; 20.7715; 18.8547
90; 100.48; 90		5315.3El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125064 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 113.869; 20.739; 18.963
90; 100.223; 90		5368El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125065 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 113.935; 20.745; 19.086
90; 100.55; 90		5424El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125066 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 114.023; 20.778; 19.191
90; 100.733; 90		5494El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125067 CIFC4 H4 N2 O2.5 S0.5P 1 21/c 18.533; 13.0141; 9.6918
90; 92.131; 90		1075.5Shemchuk, O.; Braga, D.; Grepioni, F.
Alloying barbituric and thiobarbituric acids: from solid solutions to a highly stable keto co-crystal form.
Chemical communications (Cambridge, England), 2016, 52, 11815-11818
7125068 CIFC8 H8 N4 O5.4 S0.6P 1 21/c 18.4569; 12.94; 9.5593
90; 92.626; 90		1045Shemchuk, O.; Braga, D.; Grepioni, F.
Alloying barbituric and thiobarbituric acids: from solid solutions to a highly stable keto co-crystal form.
Chemical communications (Cambridge, England), 2016, 52, 11815-11818
7125069 CIFC8 H8 N4 O5.2 S0.8P 1 21/c 18.4662; 12.9681; 9.6819
90; 92.49; 90		1062Shemchuk, O.; Braga, D.; Grepioni, F.
Alloying barbituric and thiobarbituric acids: from solid solutions to a highly stable keto co-crystal form.
Chemical communications (Cambridge, England), 2016, 52, 11815-11818
7125070 CIFC5 H12 O P2P n m a18.159; 7.4484; 6.3101
90; 90; 90		853.5Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125071 CIFC18 H39 N7 O2 P2P 1 21/c 111.8762; 15.7545; 13.6079
90; 94.012; 90		2539.8Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125072 CIFC5 H12 N O PP 1 21/m 15.941; 7.4092; 8.8324
90; 99.184; 90		383.8Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125073 CIFC39 H90 P3 Sb11C 1 c 131.443; 11.2133; 21.6617
90; 123.21; 90		6390Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125074 CIFC26 H19 Cl O4P -18.8081; 9.9881; 12.6194
79.9048; 82.4837; 80.2931		1071.49Gao, Wen-Chao; Hu, Fei; Tian, Jun; Li, Xing; Wei, Wen-Long; Chang, Hong-Hong
Hypoiodite-catalysed oxidative cyclisation of Michael adducts of chalcones with 1,3-dicarbonyl compounds: a facile and versatile approach to substituted furans and cyclopropanes.
Chemical communications (Cambridge, England), 2016, 52, 13097-13100
7125075 CIFC26 H22 O4P 1 21/n 18.5852; 15.905; 15.6721
90; 95.176; 90		2131.3Gao, Wen-Chao; Hu, Fei; Tian, Jun; Li, Xing; Wei, Wen-Long; Chang, Hong-Hong
Hypoiodite-catalysed oxidative cyclisation of Michael adducts of chalcones with 1,3-dicarbonyl compounds: a facile and versatile approach to substituted furans and cyclopropanes.
Chemical communications (Cambridge, England), 2016, 52, 13097-13100
7125076 CIFC27 H30 F2 N4 O6P -19.423; 12.742; 12.89
62.717; 70.16; 76.407		1288Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125077 CIFC29 H34 F2 N4 O6P -17.9588; 10.3333; 17.8484
80.749; 87.489; 72.019		1377.99Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125078 CIFC28 H32 F2 N4 O6P -19.5457; 12.8769; 13.338
62.8916; 71.3599; 77.1301		1377.05Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125079 CIFC30 H36 F2 N4 O6P -19.5693; 9.7134; 17.7964
74.767; 76.025; 69.597		1475.24Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125080 CIFC27 H28 Cl2 N6 Ni O8P 1 21/c 19.5286; 17.004; 17.9431
90; 96.744; 90		2887.1Kankanamalage, Pavithra H. A.; Mazumder, Shivnath; Tiwari, Vishwas; Kpogo, Kenneth K.; Bernhard Schlegel, H.; Verani, Cláudio N
Efficient electro/photocatalytic water reduction using a [Ni<sup>II</sup>(N<sub>2</sub>Py<sub>3</sub>)]<sup>2+</sup> complex.
Chemical communications (Cambridge, England), 2016, 52, 13357-13360
7125081 CIFC22 H28 O3P -17.8366; 8.8547; 14.3134
84.725; 88.103; 87.621		987.73Tharra, Prabhakararao; Baire, Beeraiah
The Z-enoate assisted, Meyer-Schuster rearrangement cascade: unconventional synthesis of α-arylenone esters.
Chemical communications (Cambridge, England), 2016, 52, 12147-12150
7125082 CIFC144 H126 Br12 Mn18 N24 Na6 O66R -3 c :H44.3099; 44.3099; 21.2242
90; 90; 120		36088Manoli, Maria; Inglis, Ross; Piligkos, Stergios; Yanhua, Lan; Wernsdorfer, Wolfgang; Brechin, Euan K.; Tasiopoulos, Anastasios J.
A hexameric [MnNa<sub>6</sub>] wheel based on [MnO]<sup>7+</sup> sub-units.
Chemical communications (Cambridge, England), 2016, 52, 12829-12832
7125083 CIFC20 H20 As F6 S12P -16.6588; 8.4075; 15.219
83.79; 77.405; 67.799		769.6Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125084 CIFC20 H20 As F6 S12P 16.6849; 8.3964; 15.203
86.78; 77.306; 68.018		771.63Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125085 CIFC20 H20 F6 S12 SbP -16.6221; 8.485; 15.3114
87.078; 77.556; 68.221		779.75Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125086 CIFC20 H20 F6 S12 SbP 16.6529; 8.4663; 15.2766
87.151; 77.495; 68.478		781.06Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125087 CIFC20 H20 As2 F12 S12P 1 21 18.0663; 16.177; 14.023
90; 100.231; 90		1800.7Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125088 CIFC20 H20 As2 F12 S12P 1 21 18.0746; 16.1837; 14.0446
90; 100.159; 90		1806.53Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125089 CIFC26 H16 N2 O8 Zn2P -110.887; 10.896; 14.07
91.252; 92.588; 104.43		1613.8Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125090 CIFC13 H8 N O4 ZnP -17.9917; 9.4227; 10.5835
65.314; 86.464; 76.513		703.6Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125091 CIFC26.87 H16 N2 O9.73 Zn2P 1 21/c 114.099; 10.997; 21.865
90; 93.971; 90		3382Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125092 CIFC13 H8 N O4 ZnP -17.871; 9.34; 10.629
65.253; 86.362; 77.446		692.3Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125093 CIFC26 H16 N2 O8 Zn2P 1 21/c 114.065; 10.949; 21.771
90; 94.319; 90		3343Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125094 CIFC30 Cu2 N2 O12F m -3 m46.542; 46.542; 46.542
90; 90; 90		100817Zheng, Baishu; Wang, Hang; Wang, Zhaoxu; Ozaki, Noriaki; Hang, Cheng; Luo, Xin; Huang, Lu; Zeng, Wenjiang; Yang, Ming; Duan, Jingui
A highly porous rht-type acylamide-functionalized metal-organic framework exhibiting large CO<sub>2</sub> uptake capabilities.
Chemical communications (Cambridge, England), 2016, 52, 12988-12991
7125095 CIFC20 H26 N O4P 1 21/n 16.1031; 11.4651; 26.396
90; 95.114; 90		1839.6Zhang, Hang; Wang, Bo; Yi, Heng; Sun, Tong; Zhang, Yan; Wang, Jianbo
Transition-metal-free three-component reaction of cyclopropenes, aldehydes and amines.
Chemical communications (Cambridge, England), 2016, 52, 13285-13287
7125096 CIFC144 H232 Sn10P -114.287; 15.4; 16.699
102.618; 97.963; 99.865		3472.7Wiederkehr, J.; Wölper, C; Schulz, S.
Synthesis and solid state structure of a metalloid tin cluster [Sn<sub>10</sub>(trip<sub>8</sub>)].
Chemical communications (Cambridge, England), 2016, 52, 12282-12285
7125097 CIFC44 H64 Mg N2P 21 21 219.0942; 20.5821; 21.2116
90; 90; 90		3970.3Wiederkehr, J.; Wölper, C; Schulz, S.
Synthesis and solid state structure of a metalloid tin cluster [Sn<sub>10</sub>(trip<sub>8</sub>)].
Chemical communications (Cambridge, England), 2016, 52, 12282-12285
7125098 CIFC38 H52 Mg N2P 21 21 2111.2579; 16.4458; 18.2926
90; 90; 90		3386.79Wiederkehr, J.; Wölper, C; Schulz, S.
Synthesis and solid state structure of a metalloid tin cluster [Sn<sub>10</sub>(trip<sub>8</sub>)].
Chemical communications (Cambridge, England), 2016, 52, 12282-12285
7125099 CIFC15 H24 O3P 1 21 19.9792; 6.6848; 10.2099
90; 96.735; 90		676.39Li, Fu-Zhuo; Li, Shuang; Zhang, Peng-Peng; Huang, Zhi-Hui; Zhang, Wei-Bin; Gong, Jianxian; Yang, Zhen
A chiral pool approach for asymmetric syntheses of (-)-antrocin, (+)-asperolide C, and (-)-trans-ozic acid.
Chemical communications (Cambridge, England), 2016, 52, 12426-12429
7125100 CIFC54 H64 B2 Mg O8P 1 21/n 111.3567; 12.2346; 18.4353
90; 108.188; 90		2433.5Mukherjee, Debabrata; Shirase, Satoru; Spaniol, Thomas P.; Mashima, Kazushi; Okuda, Jun
Magnesium hydridotriphenylborate [Mg(thf)<sub>6</sub>][HBPh<sub>3</sub>]<sub>2</sub>: a versatile hydroboration catalyst.
Chemical communications (Cambridge, England), 2016, 52, 13155-13158
7125101 CIFC15 H25 N O3P 1 21/n 111.3879; 10.6012; 12.1055
90; 98.506; 90		1445.37Ho, Guo-Ming; Li, Yu-Jang
Stereoselective synthesis of 2,3,4-highly substituted oxetanes by intramolecular C-C bond forming Michael addition.
Chemical communications (Cambridge, England), 2016, 52, 12108-12111
7125102 CIFC13 H39 N24 O13P -111.1811; 11.6175; 14.5096
70.505; 78.122; 74.189		1695.7Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125103 CIFC19 H13 N O4P 1 21/n 110.7549; 7.0492; 19.1664
90; 102.5; 90		1418.63Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125104 CIFC23 H21 N O3P -18.6755; 10.6916; 11.439
69.968; 73.363; 72.428		930.3Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125105 CIFC20 H16 Br N O3P 1 21/c 14.288; 27.2739; 14.6976
90; 90.213; 90		1718.9Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125106 CIFC31 H55 Co Fe P5 SiP -110.1595; 12.5137; 15.7867
100.375; 100.066; 108.045		1819.16Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125107 CIFC29 H50 Co Fe N P5P 1 21/n 112.73; 15.579; 17.3044
90; 108.258; 90		3259.05Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125108 CIFC29 H50 Fe N Ni P5P 1 21/n 112.7483; 15.4746; 17.3699
90; 107.71; 90		3264.25Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125109 CIFC29 H50 Fe2 N P5P 1 21/c 117.2557; 12.4359; 16.6796
90; 114.972; 90		3244.67Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125110 CIFC31 H55 Cr Fe P5 SiP 1 21/c 119.9256; 11.6275; 16.4157
90; 106.491; 90		3646.82Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125111 CIFC31 H55 Co F6 Fe P6 SiP 1 21/n 114.9545; 16.8539; 15.7381
90; 98.016; 90		3927.9Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125112 CIFC50 H60 B2 N2P b c n12.89; 9.6595; 16.653
90; 90; 90		2073.5Yuan, Ningning; Wang, Wenqing; Wu, Ziye; Chen, Sheng; Tan, Gengwen; Sui, Yunxia; Wang, Xinping; Jiang, Jun; Power, Philip P.
A boron-centered radical: a potassium-crown ether stabilized boryl radical anion.
Chemical communications (Cambridge, England), 2016, 52, 12714-12716
7125113 CIFC41 H62 B K N O7P 1 21 18.243; 20.22; 12.5726
90; 101.097; 90		2056.3Yuan, Ningning; Wang, Wenqing; Wu, Ziye; Chen, Sheng; Tan, Gengwen; Sui, Yunxia; Wang, Xinping; Jiang, Jun; Power, Philip P.
A boron-centered radical: a potassium-crown ether stabilized boryl radical anion.
Chemical communications (Cambridge, England), 2016, 52, 12714-12716
7125114 CIFC60 H93 Cd3 Ce I6 N6 O11 P2P 1 21/c 126.1665; 15.2608; 23.2073
90; 114.863; 90		8408.3Li, Quan-Wen; Wan, Rui-Chen; Chen, Yan-Cong; Liu, Jun-Liang; Wang, Long-Fei; Jia, Jian-Hua; Chilton, Nicholas F.; Tong, Ming-Liang
Unprecedented hexagonal bipyramidal single-ion magnets based on metallacrowns.
Chemical communications (Cambridge, England), 2016, 52, 13365-13368
7125115 CIFC60 H93 Cd3 I6 N6 Nd O11 P2P 1 21/c 126.2751; 15.2788; 23.1448
90; 114.769; 90		8436.7Li, Quan-Wen; Wan, Rui-Chen; Chen, Yan-Cong; Liu, Jun-Liang; Wang, Long-Fei; Jia, Jian-Hua; Chilton, Nicholas F.; Tong, Ming-Liang
Unprecedented hexagonal bipyramidal single-ion magnets based on metallacrowns.
Chemical communications (Cambridge, England), 2016, 52, 13365-13368
7125116 CIFC12 H8 F2 O SP -16.924; 8.665; 8.772
108.778; 94.634; 90.55		496.3Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125117 CIFC37 H12 B F21 O SP n a 2114.6347; 9.785; 23.547
90; 90; 90		3371.9Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125118 CIFC36 H10 B F21 O SP b c a15.099; 18.8792; 23.143
90; 90; 90		6597.1Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125119 CIFC24 H8 B0.5 F11 O SC 1 2/c 125.433; 8.7969; 18.856
90; 97.15; 90		4185.9Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125120 CIFC12 H8 B F5 O SP 1 21/n 16.9113; 10.7857; 16.5078
90; 99.049; 90		1215.2Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125121 CIFC30 H55 Au3 Co2 N6 O18 S6 ZnI 2 2 210.307; 18.544; 27.144
90; 90; 90		5188Surinwong, Sireenart; Yoshinari, Nobuto; Kojima, Tatsuhiro; Konno, Takumi
A drastic change in the superhydrophilic crystal porosities of metallosupramolecular structures via a slight change in pH.
Chemical communications (Cambridge, England), 2016, 52, 12893-12896
7125122 CIFC94 H168 Au9 Co6 N18 Na2 O50 S18 ZnP 61 2 244.2485; 44.2485; 28.4446
90; 90; 120		48231.1Surinwong, Sireenart; Yoshinari, Nobuto; Kojima, Tatsuhiro; Konno, Takumi
A drastic change in the superhydrophilic crystal porosities of metallosupramolecular structures via a slight change in pH.
Chemical communications (Cambridge, England), 2016, 52, 12893-12896
7125123 CIFC29 H80 B20 Cl2 N4 O P2P -111.8867; 12.3732; 16.807
92.305; 91.809; 98.884		2438.5Wong, Yuen Onn; Smith, Mark D.; Peryshkov, Dmitry V.
Reversible water activation driven by contraction and expansion of a 12-vertex-closo-12-vertex-nido biscarborane cluster.
Chemical communications (Cambridge, England), 2016, 52, 12710-12713
7125124 CIFC30 H81 B20 N5 O P2P n a 2144.006; 9.8902; 22.5051
90; 90; 90		9794.9Wong, Yuen Onn; Smith, Mark D.; Peryshkov, Dmitry V.
Reversible water activation driven by contraction and expansion of a 12-vertex-closo-12-vertex-nido biscarborane cluster.
Chemical communications (Cambridge, England), 2016, 52, 12710-12713
7125125 CIFC62 H80 O2 Sn2P 1 21/n 113.542; 13.931; 14.562
90; 97.201; 90		2725.5Erickson, Jeremy D.; Lai, Ting Yi; Liptrot, David J.; Olmstead, Marilyn M.; Power, Philip P.
Catalytic dehydrocoupling of amines and boranes by an incipient tin(ii) hydride.
Chemical communications (Cambridge, England), 2016, 52, 13656-13659
7125126 CIFC59 H69 N Sn2C 1 2/c 125.5341; 22.081; 21.1566
90; 122.336; 90		10078.7Erickson, Jeremy D.; Lai, Ting Yi; Liptrot, David J.; Olmstead, Marilyn M.; Power, Philip P.
Catalytic dehydrocoupling of amines and boranes by an incipient tin(ii) hydride.
Chemical communications (Cambridge, England), 2016, 52, 13656-13659
7125127 CIFC40 H40 B P3 PdP 1 21/c 110.6783; 18.823; 17.516
90; 97.699; 90		3488.9Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125128 CIFC32 H30 Cl2 I2 N P PdP -19.0882; 10.5044; 16.7224
82.47; 80.174; 86.84		1558.56Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125129 CIFC46 H45 B I N P2 PdP 1 21/c 18.8638; 22.432; 19.469
90; 94.012; 90		3861.6Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125130 CIFC36 H28 B I P2 PdF d d 218.47; 31.893; 10.3482
90; 90; 90		6095.7Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125131 CIFC66 H55 B I N O2 P2 PdP 1 21/c 115.188; 20.733; 18.38
90; 109.077; 90		5469.9Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125132 CIFC24 H42 B O6 P Si2 WC 1 2/c 119.042; 9.093; 35.451
90; 94.657; 90		6118Kyri, A. W.; Kunzmann, R.; Schnakenburg, G.; Qu, Z.-W.; Grimme, S.; Streubel, R.
Synthesis of a monomolecular anionic FLP complex.
Chemical communications (Cambridge, England), 2016, 52, 13361-13364
7125133 CIFC14 H23 O6 P Si2 WP 21 21 219.7786; 9.9521; 21.9977
90; 90; 90		2140.76Kyri, A. W.; Kunzmann, R.; Schnakenburg, G.; Qu, Z.-W.; Grimme, S.; Streubel, R.
Synthesis of a monomolecular anionic FLP complex.
Chemical communications (Cambridge, England), 2016, 52, 13361-13364
7125134 CIFC22 H24 B10P -19.52; 13.825; 17.646
88.713; 88.594; 79.932		2285.6Tu, Deshuang; Leong, Pakkin; Li, Zhihong; Hu, Rongrong; Shi, Chao; Zhang, Kenneth Yin; Yan, Hong; Zhao, Qiang
A carborane-triggered metastable charge transfer state leading to spontaneous recovery of mechanochromic luminescence.
Chemical communications (Cambridge, England), 2016, 52, 12494-12497
7125135 CIFC23 H26 B10P 1 21/n 17.684; 23.434; 12.637
90; 94.433; 90		2268.7Tu, Deshuang; Leong, Pakkin; Li, Zhihong; Hu, Rongrong; Shi, Chao; Zhang, Kenneth Yin; Yan, Hong; Zhao, Qiang
A carborane-triggered metastable charge transfer state leading to spontaneous recovery of mechanochromic luminescence.
Chemical communications (Cambridge, England), 2016, 52, 12494-12497
7125136 CIFC H BP 1 21/c 115.683; 13.493; 11.675
90; 108.429; 90		2343.9Tu, Deshuang; Leong, Pakkin; Li, Zhihong; Hu, Rongrong; Shi, Chao; Zhang, Kenneth Yin; Yan, Hong; Zhao, Qiang
A carborane-triggered metastable charge transfer state leading to spontaneous recovery of mechanochromic luminescence.
Chemical communications (Cambridge, England), 2016, 52, 12494-12497
7125137 CIFC25 H15 Cl O4P 21 21 216.3385; 15.072; 20.735
90; 90; 90		1980.9Liu, Yang; Li, Jiangtao; Ye, Xinyi; Zhao, Xiaowei; Jiang, Zhiyong
Organocatalytic asymmetric formal arylation of benzofuran-2(3H)-ones with cooperative visible light photocatalysis.
Chemical communications (Cambridge, England), 2016, 52, 13955-13958
7125138 CIFC26 H18 O5P 1 21 19.903; 6.3446; 16.4435
90; 94.703; 90		1029.68Liu, Yang; Li, Jiangtao; Ye, Xinyi; Zhao, Xiaowei; Jiang, Zhiyong
Organocatalytic asymmetric formal arylation of benzofuran-2(3H)-ones with cooperative visible light photocatalysis.
Chemical communications (Cambridge, England), 2016, 52, 13955-13958
7125139 CIFC31 H20 O4P 1 21 111.1942; 6.6554; 16.7572
90; 108.366; 90		1184.85Liu, Yang; Li, Jiangtao; Ye, Xinyi; Zhao, Xiaowei; Jiang, Zhiyong
Organocatalytic asymmetric formal arylation of benzofuran-2(3H)-ones with cooperative visible light photocatalysis.
Chemical communications (Cambridge, England), 2016, 52, 13955-13958
7125140 CIFC84 H114 Cl3 Ir3 N12 Si3P 1 21/c 120.9974; 14.9781; 31.1032
90; 94.152; 90		9756.3Olaru, Alexandra M.; Burt, Alister; Rayner, Peter J.; Hart, Sam J.; Whitwood, Adrian C.; Green, Gary G. R.; Duckett, Simon B.
Using signal amplification by reversible exchange (SABRE) to hyperpolarise <sup>119</sup>Sn and <sup>29</sup>Si NMR nuclei.
Chemical communications (Cambridge, England), 2016, 52, 14482-14485
7125141 CIFC89.42 H141.68 Cl3 Ir3 N12 O5.42 Si3P a -327.98535; 27.98535; 27.98535
90; 90; 90		21917.6Olaru, Alexandra M.; Burt, Alister; Rayner, Peter J.; Hart, Sam J.; Whitwood, Adrian C.; Green, Gary G. R.; Duckett, Simon B.
Using signal amplification by reversible exchange (SABRE) to hyperpolarise <sup>119</sup>Sn and <sup>29</sup>Si NMR nuclei.
Chemical communications (Cambridge, England), 2016, 52, 14482-14485
7125142 CIFC22 H30 O2 SiP 1 21/c 111.8899; 39.592; 9.1681
90; 94.087; 90		4304.9Akram, Manjur O.; Bera, Saibal; Patil, Nitin T.
A facile strategy for accessing 3-alkynylchromones through gold-catalyzed alkynylation/cyclization of o-hydroxyarylenaminones.
Chemical communications (Cambridge, England), 2016, 52, 12306-12309
7125143 CIFC10.5 H6 Br0.5 Mn0.5 N2 O2C 1 2/m 123.4756; 12.4761; 7.29758
90; 97.067; 90		2121.11Coogan, M. P.; Platts, J. A.
Blue rhenium tricarbonyl DPPZ complexes - low energy charge-transfer absorption at tissue-penetrating wavelengths.
Chemical communications (Cambridge, England), 2016, 52, 12498-12501
7125144 CIFC7 H5 I N3 Se4P -4 21 m16.3764; 16.3764; 4.1533
90; 90; 90		1113.86Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125145 CIFC7 H5 I N3 Se4P -4 21 m16.2024; 16.2024; 4.004
90; 90; 90		1051.1Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125146 CIFC7 H5 I N3 Se4P -4 21 m16.0383; 16.0383; 3.8839
90; 90; 90		999Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125147 CIFC7 H5 I N3 Se4P -4 21 m15.9987; 15.9987; 3.87
90; 90; 90		990.6Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125148 CIFC7 H5 I N3 Se4P -4 21 m15.9908; 15.9908; 3.8382
90; 90; 90		981.4Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125149 CIFC7 H5 I N3 Se4P -4 21 m15.9014; 15.9014; 3.784
90; 90; 90		956.8Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125150 CIFC7 H5 I N3 Se4P -4 21 m15.8651; 15.8651; 3.765
90; 90; 90		947.7Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125151 CIFC7 H5 I N3 Se4P -4 21 m15.7336; 15.7336; 3.7167
90; 90; 90		920.1Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125152 CIFC7 H5 I N3 Se4P -4 21 m15.7128; 15.7128; 3.6914
90; 90; 90		911.4Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125153 CIFC7 H5 I N3 Se4P -4 21 m15.6976; 15.6976; 3.6631
90; 90; 90		902.6Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125154 CIFC7 H5 I N3 Se4P -4 21 m15.6831; 15.6831; 3.6436
90; 90; 90		896.2Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125155 CIFC7 H5 I N3 Se4P -4 21 m16.4704; 16.4704; 4.2345
90; 90; 90		1148.71Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125156 CIFC19 H18 Br N O4P 3115.6261; 15.6261; 6.58142
90; 90; 120		1391.72Donslund, Bjarke S.; Jessen, Nicolaj Inunnguaq; Jakobsen, Joakim Bøgelund; Monleón, Alicia; Nielsen, Rune Pagh; Jørgensen, Karl Anker
Enantioselective formation of cyclopropane spiroindenes from benzofulvenes by phase transfer catalysis.
Chemical communications (Cambridge, England), 2016, 52, 12474-12477
7125157 CIFC44 H60 K2 N2 O3P 1 21/c 121.3422; 9.8659; 19.6135
90; 103.086; 90		4022.57Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125158 CIFC48 H68 Li2 N2 O4P 1 21/n 110.6922; 15.3289; 12.9982
90; 90.058; 90		2130.4Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125159 CIFC44 H60 N2 Na2 O3P 1 21/n 110.30734; 27.6447; 14.8943
90; 105.588; 90		4087.94Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125160 CIFC40 H52 N2 Na2 O2C 1 c 110.2275; 35.0736; 19.991
90; 90.758; 90		7170.4Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125161 CIFC128 H144 N8 Na8P b c n19.8237; 19.6671; 32.4878
90; 90; 90		12666.2Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125162 CIFC72 H88 K4 N4 O2P -110.4694; 16.0165; 20.7659
109.148; 102.765; 92.213		3184.74Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125163 CIFC52 H58 Mn OC c c a :218.67834; 21.44845; 21.13621
90; 90; 90		8467.62Sharpe, Helen R.; Geer, Ana M.; Williams, Huw E. L.; Blundell, Toby J.; Lewis, William; Blake, Alexander J.; Kays, Deborah L.
Cyclotrimerisation of isocyanates catalysed by low-coordinate Mn(ii) and Fe(ii) m-terphenyl complexes.
Chemical communications (Cambridge, England), 2017, 53, 937-940
7125164 CIFC52 H58 Fe OP n n a18.6528; 43.7692; 10.50646
90; 90; 90		8577.66Sharpe, Helen R.; Geer, Ana M.; Williams, Huw E. L.; Blundell, Toby J.; Lewis, William; Blake, Alexander J.; Kays, Deborah L.
Cyclotrimerisation of isocyanates catalysed by low-coordinate Mn(ii) and Fe(ii) m-terphenyl complexes.
Chemical communications (Cambridge, England), 2017, 53, 937-940
7125165 CIFC24 H25 IP n m a5.8071; 27.443; 12.2554
90; 90; 90		1953.1Sharpe, Helen R.; Geer, Ana M.; Williams, Huw E. L.; Blundell, Toby J.; Lewis, William; Blake, Alexander J.; Kays, Deborah L.
Cyclotrimerisation of isocyanates catalysed by low-coordinate Mn(ii) and Fe(ii) m-terphenyl complexes.
Chemical communications (Cambridge, England), 2017, 53, 937-940
7125166 CIFC48 H50 Li2P 43 21 212.4731; 12.4731; 48.7421
90; 90; 90		7583.2Sharpe, Helen R.; Geer, Ana M.; Williams, Huw E. L.; Blundell, Toby J.; Lewis, William; Blake, Alexander J.; Kays, Deborah L.
Cyclotrimerisation of isocyanates catalysed by low-coordinate Mn(ii) and Fe(ii) m-terphenyl complexes.
Chemical communications (Cambridge, England), 2017, 53, 937-940
7125167 CIFC36 H42 N O3C 1 2/c 131.251; 12.6345; 16.0331
90; 99.824; 90		6237.7Sharpe, Helen R.; Geer, Ana M.; Williams, Huw E. L.; Blundell, Toby J.; Lewis, William; Blake, Alexander J.; Kays, Deborah L.
Cyclotrimerisation of isocyanates catalysed by low-coordinate Mn(ii) and Fe(ii) m-terphenyl complexes.
Chemical communications (Cambridge, England), 2017, 53, 937-940
7125168 CIFC9 H8 N2 OP 21 21 215.7785; 9.7172; 14.76
90; 90; 90		828.8Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125169 CIFC9 H7 F N2 OP 21 21 213.7769; 10.7326; 19.387
90; 90; 90		785.87Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125170 CIFC10 H10 N2 O2P 21 21 215.6704; 10.076; 16.296
90; 90; 90		931.1Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125171 CIFC10 H10 N2 OP 1 21/c 17.769; 11.243; 10.244
90; 100.15; 90		880.8Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125172 CIFC14 H24 O P2 S2P 21 21 216.4559; 12.3783; 22.5131
90; 90; 90		1799.09Arisawa, Mieko; Yamada, Tomoki; Tanii, Saori; Kawada, Yuta; Hashimoto, Hisako; Yamaguchi, Masahiko
Rhodium-catalyzed P-P bond exchange reaction of diphosphine disulfides.
Chemical communications (Cambridge, England), 2016, 52, 13580-13583
7125173 CIFC16 H20 P2 S2P 1 21/c 19.3474; 7.1672; 13.3103
90; 101.49; 90		873.85Arisawa, Mieko; Yamada, Tomoki; Tanii, Saori; Kawada, Yuta; Hashimoto, Hisako; Yamaguchi, Masahiko
Rhodium-catalyzed P-P bond exchange reaction of diphosphine disulfides.
Chemical communications (Cambridge, England), 2016, 52, 13580-13583
7125174 CIFC15 H18 P2 S2P b c a9.1542; 16.965; 10.682
90; 90; 90		1658.9Arisawa, Mieko; Yamada, Tomoki; Tanii, Saori; Kawada, Yuta; Hashimoto, Hisako; Yamaguchi, Masahiko
Rhodium-catalyzed P-P bond exchange reaction of diphosphine disulfides.
Chemical communications (Cambridge, England), 2016, 52, 13580-13583
7125175 CIFC17 H24 O2P 1 21/n 112.7728; 8.2427; 14.1842
90; 103.024; 90		1454.93Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125176 CIFC17 H22 O2P -18.9679; 11.9038; 14.801
91.758; 94.311; 110.931		1468.8Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125177 CIFC27 H51 O Si4 SmC m c 2111.6326; 13.777; 21.1559
90; 90; 90		3390.5Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125178 CIFC32 H66 O Si6 SmP 1 21/n 111.287; 22.3415; 16.921
90; 97.974; 90		4225.7Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125179 CIFC44 H50 O2 Si2 SmI -413.1871; 13.1871; 11.4268
90; 90; 90		1987.12Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125180 CIFC54 H54 O2 Si2 SmC 1 c 117.123; 9.6421; 27.6291
90; 99.283; 90		4501.9Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125181 CIFC48 H75 N3 O9P 112.0223; 15.7744; 15.908
61.685; 76.21; 82.022		2578.18Caumes, Xavier; Baldi, Arianna; Gontard, Geoffrey; Brocorens, Patrick; Lazzaroni, Roberto; Vanthuyne, Nicolas; Troufflard, Claire; Raynal, Matthieu; Bouteiller, Laurent
Tuning the structure of 1,3,5-benzene tricarboxamide self-assemblies through stereochemistry.
Chemical communications (Cambridge, England), 2016, 52, 13369-13372
7125182 CIFC45.5 H70.75 N3.25 O9.5P 111.5502; 15.7414; 15.8302
61.491; 83.352; 79.502		2485.47Caumes, Xavier; Baldi, Arianna; Gontard, Geoffrey; Brocorens, Patrick; Lazzaroni, Roberto; Vanthuyne, Nicolas; Troufflard, Claire; Raynal, Matthieu; Bouteiller, Laurent
Tuning the structure of 1,3,5-benzene tricarboxamide self-assemblies through stereochemistry.
Chemical communications (Cambridge, England), 2016, 52, 13369-13372
7125183 CIFC62 H44 Mo4 N22 Ni S2C 1 2/c 117.6253; 13.6069; 24.0534
90; 101.343; 90		5655.9Hung, Wei-Chieh; Sigrist, Marc; Hua, Shao-An; Wu, Lai-Chin; Liu, Tsai-Jung; Jin, Bih-Yaw; Lee, Gene-Hsiang; Peng, Shie-Ming
A heteropentanuclear metal string complex [Mo<sub>2</sub>NiMo<sub>2</sub>(tpda)<sub>4</sub>(NCS)<sub>2</sub>] with two linearly aligned quadruply bonded Mo<sub>2</sub> units connected by a Ni ion and a meso configuration of the complex.
Chemical communications (Cambridge, England), 2016, 52, 12380-12382
7125184 CIFC59 H88 N5 O SmP -112.769; 13.1625; 20.932
76.406; 80.735; 63.678		3058.5Schoo, Christoph; Bestgen, Sebastian; Schmidt, Monika; Konchenko, Sergey N.; Scheer, Manfred; Roesky, Peter W.
Sterically induced reductive linkage of iron polypnictides with bulky lanthanide complexes by ring-opening of THF.
Chemical communications (Cambridge, England), 2016, 52, 13217-13220
7125185 CIFC125 H187 As5 Fe N8 O2 Sm2P -113.1985; 20.5277; 24.6698
108.733; 93.697; 93.654		6291.4Schoo, Christoph; Bestgen, Sebastian; Schmidt, Monika; Konchenko, Sergey N.; Scheer, Manfred; Roesky, Peter W.
Sterically induced reductive linkage of iron polypnictides with bulky lanthanide complexes by ring-opening of THF.
Chemical communications (Cambridge, England), 2016, 52, 13217-13220
7125186 CIFC125 H187 Fe N8 O2 P5 Sm2P -113.12; 20.386; 24.637
109.26; 93.54; 93.97		6181Schoo, Christoph; Bestgen, Sebastian; Schmidt, Monika; Konchenko, Sergey N.; Scheer, Manfred; Roesky, Peter W.
Sterically induced reductive linkage of iron polypnictides with bulky lanthanide complexes by ring-opening of THF.
Chemical communications (Cambridge, England), 2016, 52, 13217-13220
7125187 CIFC30 H16 Br4 N2C 1 2/c 128.8213; 3.9568; 22.0852
90; 101.2; 90		2470.6Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125188 CIFC30 H16 Br4 N2C 1 2/c 128.561; 3.8983; 22.009
90; 100.956; 90		2405.8Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125189 CIFC30 H16 Br4 N2C 1 2/c 128.6436; 3.9085; 22.0408
90; 101.063; 90		2421.7Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125190 CIFC30 H16 Br4 N2C 1 2/c 128.6762; 3.9157; 22.0307
90; 101.079; 90		2427.67Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125191 CIFC30 H16 Br4 N2C 1 2/c 128.708; 3.9259; 22.0256
90; 101.117; 90		2435.8Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125192 CIFC30 H16 Br4 N2C 1 2/c 128.7391; 3.9377; 22.0251
90; 101.118; 90		2445.7Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125193 CIFC25 H18 F3 N3C 1 2/c 121.381; 12.571; 16.69
90; 117.251; 90		3988Yu, Liu-Zhu; Wei, Yin; Shi, Min
Copper-catalyzed cascade cyclization of 1,5-enynes via consecutive trifluoromethylazidation/diazidation and click reaction: self-assembly of triazole fused isoindolines.
Chemical communications (Cambridge, England), 2016, 52, 13163-13166
7125194 CIFC44 H32 N12P -18.1858; 10.1508; 22.15
89.88; 83.44; 78.898		1793.9Yu, Liu-Zhu; Wei, Yin; Shi, Min
Copper-catalyzed cascade cyclization of 1,5-enynes via consecutive trifluoromethylazidation/diazidation and click reaction: self-assembly of triazole fused isoindolines.
Chemical communications (Cambridge, England), 2016, 52, 13163-13166
7125195 CIFC149 H168 Cl16 N6 PdP -112.4144; 17.9604; 33.3206
97.426; 96.076; 105.19		7033.5Wright, James R.; Crowley, James D.; Lucas, Nigel T.
Carbon-rich "Click" 1,2,3-triazoles: hexaphenylbenzene and hexa-peri-hexabenzocoronene-based ligands for Suzuki-Miyaura catalysts.
Chemical communications (Cambridge, England), 2016, 52, 12976-12979
7125196 CIFC142 H130 Cl2 N6 PdP 1 21/c 122.053; 39.391; 14.3467
90; 99.711; 90		12284.3Wright, James R.; Crowley, James D.; Lucas, Nigel T.
Carbon-rich "Click" 1,2,3-triazoles: hexaphenylbenzene and hexa-peri-hexabenzocoronene-based ligands for Suzuki-Miyaura catalysts.
Chemical communications (Cambridge, England), 2016, 52, 12976-12979
7125197 CIFC168 H166 Br4 N10 Pd2P -114.6518; 16.6609; 33.4649
97.604; 92.496; 92.487		8079.7Wright, James R.; Crowley, James D.; Lucas, Nigel T.
Carbon-rich "Click" 1,2,3-triazoles: hexaphenylbenzene and hexa-peri-hexabenzocoronene-based ligands for Suzuki-Miyaura catalysts.
Chemical communications (Cambridge, England), 2016, 52, 12976-12979
7125198 CIFC23 H27 N3P 1 21/c 112.0143; 8.3594; 19.0526
90; 90.316; 90		1913.47Saya, Jordy M.; Oppelaar, Barry; Cioc, Răzvan C; van der Heijden, Gydo; Vande Velde, Christophe M. L.; Orru, Romano V. A.; Ruijter, Eelco
Synthesis of polycyclic spiroindolines by highly diastereoselective interrupted Ugi cascade reactions of 3-(2-isocyanoethyl)indoles.
Chemical communications (Cambridge, England), 2016, 52, 12482-12485
7125199 CIFC9 H16 F3 Li O7 SP 1 21/n 17.0179; 13.5605; 14.8661
90; 96.427; 90		1405.86Reuter, Kirsten; Thiele, Günther; Hafner, Thomas; Uhlig, Frank; von Hänisch, Carsten
Synthesis and coordination ability of a partially silicon based crown ether.
Chemical communications (Cambridge, England), 2016, 52, 13265-13268
7125200 CIFC14 H34 Cl2 F3 Li O7 S Si4P b c a14.6745; 24.0048; 32.5952
90; 90; 90		11481.9Reuter, Kirsten; Thiele, Günther; Hafner, Thomas; Uhlig, Frank; von Hänisch, Carsten
Synthesis and coordination ability of a partially silicon based crown ether.
Chemical communications (Cambridge, England), 2016, 52, 13265-13268
7125201 CIFC25 H32 Cl N5 O4 SP 1 21 16.26161; 25.924; 8.62429
90; 102.226; 90		1368.19Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125202 CIFC12 H11 N3 O3 SP -15.8245; 7.5038; 13.8162
94.785; 94.97; 95.755		595.96Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125203 CIFC23 H28 Cl N5 O4 SP 15.94757; 9.5911; 11.4509
83.8975; 82.015; 71.9997		613.81Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125204 CIFC24 H30 Cl N5 O4 SP 1 21 16.11235; 28.1898; 7.71338
90; 92.9285; 90		1327.33Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125205 CIFC22 H27 Cl N4 O4 S2P 1 21 15.99452; 23.7139; 9.33438
90; 108.528; 90		1258.14Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125206 CIFC24 H31 N5 O4 SP 1 21 16.191; 26.0113; 8.06978
90; 102.689; 90		1267.79Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125207 CIFC24 H30 N4 O5 SP 1 21 16.06973; 23.5497; 9.2011
90; 108.609; 90		1246.45Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125208 CIFC24 H29 Cl N4 O5 SP 1 21 16.00155; 26.1427; 8.40735
90; 105.247; 90		1272.66Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125209 CIFC25 H33 N5 O4 SP 1 21 16.21672; 26.581; 7.98985
90; 99.504; 90		1302.17Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125210 CIFC20 H21 Cl N4 O3 SP 1 21 17.3493; 6.04446; 23.3114
90; 94.695; 90		1032.08Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125211 CIFC16 H26 Cu N4 O9 ZnP 1 2/n 110.95; 6.53; 13.61
90; 92.58; 90		972.2Albalad, Jorge; Aríñez-Soriano, Javier; Vidal-Gancedo, José; Lloveras, Vega; Juanhuix, Jordi; Imaz, Inhar; Aliaga-Alcalde, Núria; Maspoch, Daniel
Hetero-bimetallic paddlewheel clusters in coordination polymers formed by a water-induced single-crystal-to-single-crystal transformation.
Chemical communications (Cambridge, England), 2016, 52, 13397-13400
7125212 CIFC32 H48 Cu3 N8 O26 ZnP 1 21/c 111.56; 16.83; 12.92
90; 110.97; 90		2347.2Albalad, Jorge; Aríñez-Soriano, Javier; Vidal-Gancedo, José; Lloveras, Vega; Juanhuix, Jordi; Imaz, Inhar; Aliaga-Alcalde, Núria; Maspoch, Daniel
Hetero-bimetallic paddlewheel clusters in coordination polymers formed by a water-induced single-crystal-to-single-crystal transformation.
Chemical communications (Cambridge, England), 2016, 52, 13397-13400
7125213 CIFC12 H14 N2 O7P 21 21 215.8274; 9.9168; 23.1227
90; 90; 90		1336.24Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125214 CIFC18 H20 N4 O8P 1 2 18.934; 5.1587; 43.225
90; 93; 90		1989.4Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125215 CIFC24 H28 N4 O14P 15.0886; 7.2518; 17.1681
93.324; 93.952; 97.338		625.42Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125216 CIFC24 H26 N6 O9P 1 21 15.074; 29.696; 8.498
90; 103.16; 90		1246.8Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125217 CIFC13 H18 N2 O8P 15.0892; 7.5329; 19.7851
84.757; 85.752; 81.727		746.03Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125218 CIFC7 H7 N2 O3P b c a7.2149; 12.4451; 15.6775
90; 90; 90		1407.69Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125219 CIFC4 H13 B F3 NP b c m5.577; 11.436; 11.447
90; 90; 90		730.1Duda, Katharina; Himmelspach, Alexander; Landmann, Johannes; Kraus, Florian; Finze, Maik
Synthesis of the fluorohydridoborate anions [BHF<sub>3</sub>]<sup>-</sup> and [1-HF<sub>2</sub>B-9,12-X<sub>2</sub>-closo-1,2-C<sub>2</sub>B<sub>10</sub>H<sub>9</sub>]<sup>-</sup> (X = H, I): deboronation of 1,2- and 1,7-dicarba-closo-dodecaboranes with anhydrous [Me<sub>4</sub>N]F.
Chemical communications (Cambridge, England), 2016, 52, 13241-13244
7125220 CIFC6 H24 B11 F2 NP 1 21 110.452; 13.828; 10.773
90; 90.102; 90		1557Duda, Katharina; Himmelspach, Alexander; Landmann, Johannes; Kraus, Florian; Finze, Maik
Synthesis of the fluorohydridoborate anions [BHF<sub>3</sub>]<sup>-</sup> and [1-HF<sub>2</sub>B-9,12-X<sub>2</sub>-closo-1,2-C<sub>2</sub>B<sub>10</sub>H<sub>9</sub>]<sup>-</sup> (X = H, I): deboronation of 1,2- and 1,7-dicarba-closo-dodecaboranes with anhydrous [Me<sub>4</sub>N]F.
Chemical communications (Cambridge, England), 2016, 52, 13241-13244
7125221 CIFC6 H22 B11 F2 I2 NP -112.4538; 13.5015; 13.544
60.759; 72.3; 86.331		1883.28Duda, Katharina; Himmelspach, Alexander; Landmann, Johannes; Kraus, Florian; Finze, Maik
Synthesis of the fluorohydridoborate anions [BHF<sub>3</sub>]<sup>-</sup> and [1-HF<sub>2</sub>B-9,12-X<sub>2</sub>-closo-1,2-C<sub>2</sub>B<sub>10</sub>H<sub>9</sub>]<sup>-</sup> (X = H, I): deboronation of 1,2- and 1,7-dicarba-closo-dodecaboranes with anhydrous [Me<sub>4</sub>N]F.
Chemical communications (Cambridge, England), 2016, 52, 13241-13244
7125222 CIFC20 H23 N O3 SP 21 21 218.3041; 10.2744; 22.465
90; 90; 90		1916.7Huang, Wei; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Diastereoselective synthesis of 2-methoxyimidoyloxiranes via dimethyl phosphite-mediated coupling of α-keto N-sulfinyl imidates with aldehydes.
Chemical communications (Cambridge, England), 2016, 52, 13592-13595
7125223 CIFC28 H26 O4P 1 2/c 131.22; 10.5893; 13.5925
90; 89.984; 90		4493.7Lu, Danyang; Wan, Yimei; Kong, Lichun; Zhu, Gangguo
Copper-catalyzed cascade annulation between α-bromocarbonyls and biaryl or (Z)-arylvinylacetylenes enabling a direct synthesis of dibenzocycloheptanes and related compounds.
Chemical communications (Cambridge, England), 2016, 52, 13971-13974
7125224 CIFC25 H26 O4P 1 21 18.8392; 12.746; 9.5979
90; 99.664; 90		1066Lu, Danyang; Wan, Yimei; Kong, Lichun; Zhu, Gangguo
Copper-catalyzed cascade annulation between α-bromocarbonyls and biaryl or (Z)-arylvinylacetylenes enabling a direct synthesis of dibenzocycloheptanes and related compounds.
Chemical communications (Cambridge, England), 2016, 52, 13971-13974
7125225 CIFC24 H24 O5P 1 21/c 112.7888; 15.597; 11.0139
90; 110.204; 90		2061.73Lu, Danyang; Wan, Yimei; Kong, Lichun; Zhu, Gangguo
Copper-catalyzed cascade annulation between α-bromocarbonyls and biaryl or (Z)-arylvinylacetylenes enabling a direct synthesis of dibenzocycloheptanes and related compounds.
Chemical communications (Cambridge, England), 2016, 52, 13971-13974
7125226 CIFC16 H52 B20 Co N2 S4P n a 2136.4636; 9.9056; 9.921
90; 90; 90		3583.4Tu, Deshuang; Shao, Dong; Yan, Hong; Lu, Changsheng
A carborane-incorporated mononuclear Co(ii) complex showing zero-field slow magnetic relaxation.
Chemical communications (Cambridge, England), 2016, 52, 14326-14329
7125227 CIFC26 H46 Cl2 N4 SnC 1 c 110.291; 21.844; 12.742
90; 106.679; 90		2743.8Bertermann, Rüdiger; Braunschweig, Holger; Celik, Mehmet Ali; Dellermann, Theresa; Kelch, Hauke
Cyclisation of biscarbenoids - a novel mode of cyclobutadiene stabilisation.
Chemical communications (Cambridge, England), 2016, 52, 13249-13252
7125228 CIFC92 H56 N8 Zn2P 1 2/c 110.8018; 17.3515; 26.7953
90; 97.145; 90		4983.2Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125229 CIFC53 H38 N4 NiP 1 2/n 110.7748; 11.5828; 35.9716
90; 93.971; 90		4478.6Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125230 CIFC46 H28 N4 NiP c a 2118.03; 11.0785; 16.251
90; 90; 90		3246.1Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125231 CIFC46 H30 N4C 1 2/c 126.2435; 13.5308; 9.407
90; 99.357; 90		3295.9Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125232 CIFC136 H110 Ag4 F12 N16 O15 S4 Zn4P 1 21/n 19.4384; 34.9486; 20.3325
90; 101.347; 90		6575.8Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125233 CIFC63 H40 Ag3 F9 N8 O9 S3 Zn2P 1 21/n 111.3487; 18.6122; 33.9443
90; 95.1; 90		7141.5Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125234 CIFC216 H172 Ag4 F12 N16 O17 S4 Zn4P -115.4217; 16.4469; 22.1055
69.989; 69.909; 73.752		4863.4Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125235 CIFC17 H16 N2 O3P 1 21/n 18.5064; 17.8133; 9.4824
90; 99.126; 90		1418.7Zhou, Tao; Li, Bin; Wang, Baiquan
Rhodium-catalyzed C-H activation of 3-(indolin-1-yl)-3-oxopropanenitriles with diazo compounds and tandem cyclization leading to hydrogenated azepino[3,2,1-hi]indoles.
Chemical communications (Cambridge, England), 2016, 52, 14117-14120
7125236 CIFC21 H20 N2 O4P -19.2814; 10.273; 11.8447
79.305; 79.574; 83.084		1087Zhou, Tao; Li, Bin; Wang, Baiquan
Rhodium-catalyzed C-H activation of 3-(indolin-1-yl)-3-oxopropanenitriles with diazo compounds and tandem cyclization leading to hydrogenated azepino[3,2,1-hi]indoles.
Chemical communications (Cambridge, England), 2016, 52, 14117-14120
7125237 CIFC16 H16 O4 S4P -17.6541; 9.3183; 12.9177
106.268; 100.626; 91.743		865.98Adows, Hadeel; Zhao, Yuming
Redox interactions of Au(iii) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media.
Chemical communications (Cambridge, England), 2016, 52, 13101-13104
7125238 CIFC32 H30 O8 S8C 1 2/c 117.3602; 9.8696; 20.8727
90; 96.315; 90		3554.6Adows, Hadeel; Zhao, Yuming
Redox interactions of Au(iii) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media.
Chemical communications (Cambridge, England), 2016, 52, 13101-13104
7125239 CIFC68 H102 Au2 Cl8 O8 S8P -19.062; 10.7865; 22.897
84.698; 80.375; 70.592		2079.6Adows, Hadeel; Zhao, Yuming
Redox interactions of Au(iii) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media.
Chemical communications (Cambridge, England), 2016, 52, 13101-13104
7125240 CIFC60 H60 Cl2 Cu N12 O14C 1 2/c 136.068; 14.096; 16.023
90; 109.397; 90		7684Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125241 CIFC60 H60 B2 Cu F8 N12 O6C 1 2/c 135.729; 13.9528; 15.8889
90; 109.211; 90		7479.8Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125242 CIFC60 H60 Cu N14 O12C 1 2/c 135.509; 14.304; 15.395
90; 108.369; 90		7421Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125243 CIFC264 H300 Cl6 Cu6 N54 O48P -124.331; 24.388; 24.415
118.745; 91.861; 118.748		10460Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125244 CIFC264 H290 Br12 Cu6 N48 O24C 1 2/c 134.915; 33.412; 34.291
90; 90.352; 90		40002Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125245 CIFC14 H20 F N O2 SP 1 21/c 17.9327; 9.5312; 19.6547
90; 100.885; 90		1459.32Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125246 CIFC16 H18 F N O2 SP 21 21 218.2947; 9.5293; 18.8749
90; 90; 90		1491.92Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125247 CIFC16 H17 N O2 SP 1 21 17.3082; 12.667; 7.9739
90; 102.802; 90		719.82Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125248 CIFC26 H36 F2 N2 O6 S2P -16.3281; 12.8693; 17.8671
105.544; 93.657; 100.435		1368.94Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125249 CIFC12 H7 N O4 ZnP b c a7.1952; 19.7441; 20.4254
90; 90; 90		2901.7Zhang, Ling; Jiang, Ke; Jiang, Mengdie; Yue, Dan; Wan, Yating; Xing, Huabin; Yang, Yu; Cui, Yuanjing; Chen, Banglin; Qian, Guodong
A highly stable amino-coordinated MOF for unprecedented block off N<sub>2</sub> adsorption and extraordinary CO<sub>2</sub>/N<sub>2</sub> separation.
Chemical communications (Cambridge, England), 2016, 52, 13568-13571
7125250 CIFC21 H24 N2 O SiP -110.08; 11.8813; 16.5509
88.653; 86.499; 89.381		1977.86Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu
Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds.
Chemical communications (Cambridge, England), 2016, 52, 13151-13154
7125251 CIFC20 H30 N2 O Si2P 1 21/c 117.5738; 10.3894; 12.0069
90; 100.934; 90		2152.44Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu
Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds.
Chemical communications (Cambridge, England), 2016, 52, 13151-13154
7125252 CIFC26 H29 N3 O3 SiC 1 2 140.8407; 11.72; 10.659
90; 102.731; 90		4976.53Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu
Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds.
Chemical communications (Cambridge, England), 2016, 52, 13151-13154
7125253 CIFC39 H21 Au Cl7 F2 N O4 PP 1 21/n 18.7297; 28.9112; 15.5735
90; 103.822; 90		3816.7Hattori, Yohei; Kusamoto, Tetsuro; Sato, Tohru; Nishihara, Hiroshi
Synergistic luminescence enhancement of a pyridyl-substituted triarylmethyl radical based on fluorine substitution and coordination to gold.
Chemical communications (Cambridge, England), 2016, 52, 13393-13396
7125254 CIFC47 H43 Cl6 F6 Ir N7 O2 PP b c a22.1254; 16.4448; 28.2843
90; 90; 90		10291.2Yellol, Jyoti; Pérez, Sergio A; Yellol, Gorakh; Zajac, Juraj; Donaire, Antonio; Vigueras, Gloria; Novohradsky, Vojtech; Janiak, Christoph; Brabec, Viktor; Ruiz, José
Highly potent extranuclear-targeted luminescent iridium(iii) antitumor agents containing benzimidazole-based ligands with a handle for functionalization.
Chemical communications (Cambridge, England), 2016, 52, 14165-14168
7125255 CIFC35.5 H30.5 Cl F6 Ir N7 O2 PC 1 2/c 124.4157; 16.5559; 23.3462
90; 113.79; 90		8635.2Yellol, Jyoti; Pérez, Sergio A; Yellol, Gorakh; Zajac, Juraj; Donaire, Antonio; Vigueras, Gloria; Novohradsky, Vojtech; Janiak, Christoph; Brabec, Viktor; Ruiz, José
Highly potent extranuclear-targeted luminescent iridium(iii) antitumor agents containing benzimidazole-based ligands with a handle for functionalization.
Chemical communications (Cambridge, England), 2016, 52, 14165-14168
7125256 CIFC15 H18 O2P 1 21/n 16.3004; 8.2192; 25.844
90; 94.486; 90		1334.2Ma, Dengke; Fu, Chunling; Ma, Shengming
Diastereoselective construction of cyclopent-2-enone-4-ols from aldehydes and 1,2-allenones catalyzed by N-heterocyclic carbene.
Chemical communications (Cambridge, England), 2016, 52, 14426-14429
7125257 CIFC36 H28 O2 P2 Pd SP -19.0944; 11.4218; 15.9032
95.9441; 103.474; 102.049		1550.8Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong
Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes.
Chemical communications (Cambridge, England), 2016, 52, 14262-14265
7125258 CIFC24 H36 O2 P2 Pd SP -18.7065; 11.0937; 15.13
73.3056; 80.9582; 74.899		1346.1Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong
Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes.
Chemical communications (Cambridge, England), 2016, 52, 14262-14265
7125259 CIFC28 H44 O2 P2 Pd SP -18.6167; 11.5992; 16.4263
77.1791; 79.8629; 73.9166		1526.6Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong
Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes.
Chemical communications (Cambridge, England), 2016, 52, 14262-14265
7125260 CIFC216 H310 Mn10 N12 O40P -114.9101; 17.9438; 22.3792
69.512; 75.796; 81.501		5424.6Coletta, Marco; McLellan, Ross; Waddington, Amy; Sanz, Sergio; Gagnon, Kevin J.; Teat, Simon J.; Brechin, Euan K.; Dalgarno, Scott J.
Core expansion of bis-calix[4]arene-supported clusters.
Chemical communications (Cambridge, England), 2016, 52, 14246-14249
7125261 CIFC206 H280 Gd2 Mn8 N10 O44P 1 21/n 122.096; 19.157; 27.0764
90; 105.149; 90		11063Coletta, Marco; McLellan, Ross; Waddington, Amy; Sanz, Sergio; Gagnon, Kevin J.; Teat, Simon J.; Brechin, Euan K.; Dalgarno, Scott J.
Core expansion of bis-calix[4]arene-supported clusters.
Chemical communications (Cambridge, England), 2016, 52, 14246-14249
7125262 CIFC20 H24 N2 O5P -18.9003; 9.3364; 11.3581
83.515; 76.869; 82.053		907.1Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125263 CIFC19 H21 N O6P -17.787; 9.08; 12.994
106.14; 91.08; 94.96		878.4Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125264 CIFC19 H21 N O6P c a 2110.2; 12.903; 14.787
90; 90; 90		1946.1Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125265 CIFC18 H19 N O5P 1 21/c 17.3465; 12.3261; 18.1727
90; 95.772; 90		1637.3Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125266 CIFC18 H18 F N O5P 1 21/c 118.99; 5.418; 17.32
90; 113.9; 90		1629.2Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125267 CIFC25 H30 N2 O3 SP 1 21/n 115.6911; 7.8759; 19.8219
90; 106.907; 90		2343.7Kumar, Ravi; Thorat, Shridhar H.; Reddy, Maddi Sridhar
Cu-Catalyzed iminative hydroolefination of unactivated alkynes en route to 4-imino-tetrahydropyridines and 4-aminopyridines.
Chemical communications (Cambridge, England), 2016, 52, 13475-13478
7125268 CIFC72 H110 Cl4 N7 O10P 1 21/n 114.6718; 22.9104; 23.5888
90; 104.564; 90		7674.3Lavendomme, Roy; Marcélis, Lionel; Wouters, Johan; Luhmer, Michel; Jabin, Ivan
A nano-sized container for specific encapsulation of isolated water molecules.
Chemical communications (Cambridge, England), 2016, 52, 14109-14112
7125269 CIFC27 H36 N3 UP 1 21/c 114.318; 11.54; 14.975
90; 93.52; 90		2469.6Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125270 CIFC27 H35 Cl0 N3 ThP -19.59; 11.143; 11.619
88.275; 77.613; 87.316		1211.1Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125271 CIFC111 H116 O S8 ThP 1 21/c 114.983; 25.115; 27.353
90; 92.488; 90		10283Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125272 CIFC118 H124 O S8 UP 1 21/c 115.004; 25.0884; 27.253
90; 92.527; 90		10248.8Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125273 CIFC180 H200 Cl18 N17 O12 PC 1 2/c 130.3787; 19.6365; 32.742
90; 109.719; 90		18386Qiao, Bo; Liu, Yun; Lee, Semin; Pink, Maren; Flood, Amar H.
A high-yield synthesis and acid-base response of phosphate-templated [3]rotaxanes.
Chemical communications (Cambridge, England), 2016, 52, 13675-13678
7125274 CIFC130 H130 N10P 43 3 236.9585; 36.9585; 36.9585
90; 90; 90		50483Qiao, Bo; Liu, Yun; Lee, Semin; Pink, Maren; Flood, Amar H.
A high-yield synthesis and acid-base response of phosphate-templated [3]rotaxanes.
Chemical communications (Cambridge, England), 2016, 52, 13675-13678
7125275 CIFC26 H24 O3P 1 21/n 18.9587; 8.4815; 27.445
90; 92.802; 90		2082.9Tharra, Prabhakararao; Baire, Beeraiah
Regioselective, cascade [3+2] annulation of β-naphthols (resorcinols) with Z-enoate propargylic alcohols: a novel entry for the synthesis of complex naphtho(benzo)furans.
Chemical communications (Cambridge, England), 2016, 52, 14290-14293
7125276 CIFC47 H54 N O2 S2P 1 21/n 116.9652; 13.3015; 18.3142
90; 108.16; 90		3927Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125277 CIFC50 H66 Au2 Cl3 F6 P2 SbP -113.279; 14.462; 15.6401
100.277; 96.426; 115.812		2598.8Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125278 CIFC42.5 H42 Cl F2 N O2P -111.0496; 12.2287; 14.2619
64.774; 82.424; 88.269		1727.4Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125279 CIFC36 H35 N O2P 1 21/n 110.8442; 13.8546; 18.575
90; 92.116; 90		2788.8Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125280 CIFC38 H39 N O4P 1 21/n 112.6921; 17.3656; 14.0302
90; 99.986; 90		3045.5Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125281 CIFC39 H53 Ge N2 OP -110.7269; 11.206; 14.4819
86.134; 88.938; 81.551		1717.93Wu, Yile; Shan, Changkai; Sun, Ying; Chen, Peng; Ying, Jianxi; Zhu, Jun; Liu, Liu Leo; Zhao, Yufen
Main group metal-ligand cooperation of N-heterocyclic germylene: an efficient catalyst for hydroboration of carbonyl compounds.
Chemical communications (Cambridge, England), 2016, 52, 13799-13802
7125282 CIFC28 H24 O4P -15.6126; 8.3452; 12.339
88.55; 78.74; 87.54		566.2Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds.
Chemical communications (Cambridge, England), 2016, 52, 13345-13348
7125283 CIFC28 H24 O6P -110.4453; 10.599; 10.8669
86.506; 84.424; 71.57		1135.4Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds.
Chemical communications (Cambridge, England), 2016, 52, 13345-13348
7125284 CIFC26 H20 O3P 1 21/c 110.2062; 19.416; 10.5696
90; 109.487; 90		1974.5Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds.
Chemical communications (Cambridge, England), 2016, 52, 13345-13348
7125285 CIFC30 H30 O6 Te3P 1 21/n 115.5616; 24.9422; 15.8574
90; 104.681; 90		5954Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng
Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine.
Chemical communications (Cambridge, England), 2016, 52, 14486-14489
7125286 CIFC30 H32 O6 Te2P 1 21/n 18.3225; 15.076; 23.2305
90; 95.2; 90		2902.7Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng
Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine.
Chemical communications (Cambridge, England), 2016, 52, 14486-14489
7125287 CIFC30 H36 Br6 O9 Te3P -110.889; 10.89; 18.299
86.12; 86.29; 71.19		2047.2Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng
Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine.
Chemical communications (Cambridge, England), 2016, 52, 14486-14489
7125288 CIFC23 H27 N3 O2P -18.2014; 10.9469; 12.241
99.951; 94.49; 103.679		1043.58El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent
Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 14490-14493
7125289 CIFC26 H31 N3 O2P -19.3834; 11.8498; 22.2318
87.603; 82.452; 71.9		2329.3El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent
Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 14490-14493
7125290 CIFC25 H27 N4 O5 PC 1 2/c 129.5009; 7.6614; 21.6674
90; 92.924; 90		4890.85El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent
Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 14490-14493
7125291 CIFC24 H24 Cu4 I4 N4 O16 Zr3I 4/m m m17.5411; 17.5411; 34.6975
90; 90; 90		10676.1Tan, Yan-Xi; Yang, Xue; Li, Bei-Bei; Yuan, Daqiang
Rational design of a flu-type heterometallic cluster-based Zr-MOF.
Chemical communications (Cambridge, England), 2016, 52, 13671-13674
7125292 CIFC20 H18 Br N O5 SP -17.88851; 8.9545; 14.9033
92.1745; 99.8465; 107.839		982.77Modak, Atanu; Mondal, Anirban; Watile, Rahul; Mukherjee, Semanti; Maiti, Debabrata
Remote meta C-H bond functionalization of 2-phenethylsulphonic acid and 3-phenylpropanoic acid derivatives.
Chemical communications (Cambridge, England), 2016, 52, 13916-13919
7125293 CIFC25 H26 N2 O6 SP -18.3702; 12.3731; 13.2427
108.688; 105.715; 98.948		1205.6Modak, Atanu; Mondal, Anirban; Watile, Rahul; Mukherjee, Semanti; Maiti, Debabrata
Remote meta C-H bond functionalization of 2-phenethylsulphonic acid and 3-phenylpropanoic acid derivatives.
Chemical communications (Cambridge, England), 2016, 52, 13916-13919
7125294 CIFC21 H23 Br F3 N O6P 21 21 218.6647; 15.3884; 17.0772
90; 90; 90		2277Zhi, Ying; Zhao, Kun; Liu, Qiang; Wang, Ai; Enders, Dieter
Asymmetric synthesis of functionalized trifluoromethyl-substituted pyrrolidines via an organocatalytic domino Michael/Mannich [3+2] cycloaddition.
Chemical communications (Cambridge, England), 2016, 52, 14011-14014
7125295 CIFC26 H19 N OP 1 21/c 127.556; 7.4414; 19.1328
90; 109.435; 90		3699.7Bagle, Pradip N.; Mane, Manoj V.; Vanka, K.; Shinde, Dinesh R.; Shaikh, Samir R.; Gonnade, Rajesh G.; Patil, Nitin T.
Au(i)/Ag(i) co-operative catalysis: interception of Ag-bound carbocations with α-gold(i) enals in the imino-alkyne cyclizations with N-allenamides.
Chemical communications (Cambridge, England), 2016, 52, 14462-14465
7125296 CIFC56 H46 Br Cl2 F4 O3 P3 Pd SP -112.108; 12.5; 18.24
76.07; 74.442; 82.349		2574.3Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W.
A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane.
Chemical communications (Cambridge, England), 2016, 52, 13967-13970
7125297 CIFC63 H53 Br F2 P3 PdP -112.225; 12.671; 19.4112
98.543; 90.489; 118.142		2611.3Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W.
A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane.
Chemical communications (Cambridge, England), 2016, 52, 13967-13970
7125298 CIFC57.5 H47 Br Cl3 F4 O4 P3 Pd SP 1 21/c 114.2329; 20.4798; 19.1729
90; 96.688; 90		5550.6Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W.
A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane.
Chemical communications (Cambridge, England), 2016, 52, 13967-13970
7125299 CIFC22 H54 N8 Ni2 O10.01 P2P -110.3977; 14.1488; 22.4532
90.093; 90.531; 90.097		3303.05Neri, Gaia; Forster, Mark; Walsh, James J.; Robertson, C. M.; Whittles, T. J.; Farràs, Pau; Cowan, Alexander J.
Photochemical CO<sub>2</sub> reduction in water using a co-immobilised nickel catalyst and a visible light sensitiser.
Chemical communications (Cambridge, England), 2016, 52, 14200-14203
7125300 CIFC15 H10 N2P b c a13.936; 7.077; 22.807
90; 90; 90		2249.3Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng
CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates.
Chemical communications (Cambridge, England), 2016, 52, 14404-14407
7125301 CIFC19 H16 N2 O2 SP 1 21/c 19.3811; 20.8484; 8.6963
90; 99.098; 90		1679.43Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng
CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates.
Chemical communications (Cambridge, England), 2016, 52, 14404-14407
7125302 CIFC16 H12 N2 O2 SP 1 21/c 19.0829; 10.2351; 15.664
90; 97.384; 90		1444.1Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng
CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates.
Chemical communications (Cambridge, England), 2016, 52, 14404-14407
7125303 CIFC45 H21 Dy F18 N2 O6P 21 21 2111.111; 17.6697; 22.6965
90; 90; 90		4456Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B.
Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets.
Chemical communications (Cambridge, England), 2016, 52, 14474-14477
7125304 CIFC45 H21 Dy F18 N2 O6P 21 21 2111.1191; 17.6604; 22.693
90; 90; 90		4456.2Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B.
Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets.
Chemical communications (Cambridge, England), 2016, 52, 14474-14477
7125305 CIFC48 H28 Dy F18 N2 O6P -113.216; 13.9132; 14.5959
67.984; 72.454; 84.724		2371.71Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B.
Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets.
Chemical communications (Cambridge, England), 2016, 52, 14474-14477
7125306 CIFC28 H19 N OP 1 21 113.0425; 10.2377; 16.1011
90; 109.601; 90		2025.32Hornillos, Valentín; Ros, Abel; Ramírez-López, Pedro; Iglesias-Sigüenza, Javier; Fernández, Rosario; Lassaletta, José M
Synthesis of axially chiral heterobiaryl alkynes via dynamic kinetic asymmetric alkynylation.
Chemical communications (Cambridge, England), 2016, 52, 14121-14124
7125307 CIFC32 H21 N OP 1 21 17.6244; 7.9489; 18.4283
90; 93.193; 90		1115.12Hornillos, Valentín; Ros, Abel; Ramírez-López, Pedro; Iglesias-Sigüenza, Javier; Fernández, Rosario; Lassaletta, José M
Synthesis of axially chiral heterobiaryl alkynes via dynamic kinetic asymmetric alkynylation.
Chemical communications (Cambridge, England), 2016, 52, 14121-14124
7125308 CIFC22 H25 N O5P 1 21/n 16.2373; 36.3214; 8.6667
90; 94.598; 90		1957.1Fuentes de Arriba, Angel L.; Urbitsch, Felix; Dixon, Darren J.
Umpolung synthesis of branched α-functionalized amines from imines via photocatalytic three-component reductive coupling reactions.
Chemical communications (Cambridge, England), 2016, 52, 14434-14437
7125309 CIFC14 H20 Cl2 N O3 Rh S2P 1 21/n 18.9953; 15.618; 13.4715
90; 103.827; 90		1837.7Zhang, Yun-Liang; Qin, Qi-Pin; Cao, Qian-Qian; Han, Hong-Hua; Liu, Zhu-Ling; Liu, Yan-Cheng; Liang, Hong; Chen, Zhen-Feng
Synthesis, crystal structure, cytotoxicity and action mechanism of a Rh(iii) complex with 8-hydroxy-2-methylquinoline as a ligand.
MedChemComm, 2017, 8, 184-190
7125310 CIFO805 Sr48 U96F m -3 c53.688; 53.688; 53.688
90; 90; 90		154750Falaise, Clément; Hickam, Sarah M.; Burns, Peter C.; Nyman, May
From aqueous speciation to supramolecular assembly in alkaline earth-uranyl polyoxometalates.
Chemical communications (Cambridge, England), 2017, 53, 9550-9553
7125311 CIFCa6 Li8 O172 U24I 4/m18.282; 18.282; 26.436
90; 90; 90		8836Falaise, Clément; Hickam, Sarah M.; Burns, Peter C.; Nyman, May
From aqueous speciation to supramolecular assembly in alkaline earth-uranyl polyoxometalates.
Chemical communications (Cambridge, England), 2017, 53, 9550-9553
7125312 CIFC32 H24 Cu F6 N4 TiC m c m22.924; 20.536; 7.7158
90; 90; 90		3632Bajpai, Alankriti; O'Nolan, Daniel; Madden, David G.; Chen, Kai-Jie; Pham, Tony; Kumar, Amrit; Lusi, Matteo; Perry, John J.; Space, Brian; Zaworotko, Michael J.
The effect of centred versus offset interpenetration on C<sub>2</sub>H<sub>2</sub> sorption in hybrid ultramicroporous materials.
Chemical communications (Cambridge, England), 2017, 53, 11592-11595
7125313 CIFC24 H12 N3 Na2.58333 O6F -4 3 c48.1642; 48.1642; 48.1642
90; 90; 90		111731Chen, Di-Ming; Tian, Jia-Yue; Wang, Zhuo-Wei; Liu, Chun-Sen; Chen, Min; Du, Miao
An anionic Na(i)-organic framework platform: separation of organic dyes and post-modification for highly sensitive detection of picric acid.
Chemical communications (Cambridge, England), 2017, 53, 10668-10671
7125314 CIFC54 H66 B2 N4 O4C m c e10.924; 15.753; 27.04
90; 90; 90		4653Böhnke, Julian; Braunschweig, Holger; Deißenberger, Andrea; Dellermann, Theresa; Dewhurst, Rian D.; Jiménez-Halla, J Oscar C; Kachel, Stephanie; Kelch, Hauke; Prieschl, Dominic
Alkylideneborate zwitterions and C-C coupling by atypical diboration of electron-rich alkynes.
Chemical communications (Cambridge, England), 2017, 53, 12132-12135
7125315 CIFC42 H62 B2 F2 N4P 1 21/n 19.595; 24.297; 16.928
90; 106.09; 90		3792Böhnke, Julian; Braunschweig, Holger; Deißenberger, Andrea; Dellermann, Theresa; Dewhurst, Rian D.; Jiménez-Halla, J Oscar C; Kachel, Stephanie; Kelch, Hauke; Prieschl, Dominic
Alkylideneborate zwitterions and C-C coupling by atypical diboration of electron-rich alkynes.
Chemical communications (Cambridge, England), 2017, 53, 12132-12135
7125316 CIFC32 H46 B2 Cl2 N2P -19.198; 10.869; 16.114
97.766; 102.763; 100.085		1521.3Böhnke, Julian; Braunschweig, Holger; Deißenberger, Andrea; Dellermann, Theresa; Dewhurst, Rian D.; Jiménez-Halla, J Oscar C; Kachel, Stephanie; Kelch, Hauke; Prieschl, Dominic
Alkylideneborate zwitterions and C-C coupling by atypical diboration of electron-rich alkynes.
Chemical communications (Cambridge, England), 2017, 53, 12132-12135
7125317 CIFC30 H42 B2 Cl2 N2P 43 21 212.362; 12.362; 38.073
90; 90; 90		5818Böhnke, Julian; Braunschweig, Holger; Deißenberger, Andrea; Dellermann, Theresa; Dewhurst, Rian D.; Jiménez-Halla, J Oscar C; Kachel, Stephanie; Kelch, Hauke; Prieschl, Dominic
Alkylideneborate zwitterions and C-C coupling by atypical diboration of electron-rich alkynes.
Chemical communications (Cambridge, England), 2017, 53, 12132-12135
7125318 CIFC96 H108 N12P 61 2 223.3698; 23.3698; 89.848
90; 90; 120		42496Zhang, Pei; Wang, Xinchang; Xuan, Wei; Peng, Pixian; Li, Zhihao; Lu, Ruqiang; Wu, Shuang; Tian, Zhongqun; Cao, Xiaoyu
Chiral separation and characterization of triazatruxene-based face-rotating polyhedra: the role of non-covalent facial interactions.
Chemical communications (Cambridge, England), 2018, 54, 4685-4688
7125319 CIFC96 H108 N12P 65 2 223.3854; 23.3854; 89.444
90; 90; 120		42362Zhang, Pei; Wang, Xinchang; Xuan, Wei; Peng, Pixian; Li, Zhihao; Lu, Ruqiang; Wu, Shuang; Tian, Zhongqun; Cao, Xiaoyu
Chiral separation and characterization of triazatruxene-based face-rotating polyhedra: the role of non-covalent facial interactions.
Chemical communications (Cambridge, England), 2018, 54, 4685-4688
7125320 CIFC9 H6 Cl0.25 N2 O5 Tb0.5F m -3 c54.8796; 54.8796; 54.8796
90; 90; 90		165285Du, Wei; Zhu, Zhifeng; Bai, Yue-Ling; Yang, Zhen; Zhu, Shourong; Xu, Jiaqiang; Xie, Zhaoxiong; Fang, Jianhui
An anionic sod-type terbium-MOF with extra-large cavities for effective anthocyanin extraction and methyl viologen detection.
Chemical communications (Cambridge, England), 2018, 54, 5972-5975
7125321 CIFC36 H41 B N O PP 1 21/n 110.0854; 17.8383; 16.192
90; 96.009; 90		2897Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125322 CIFC66 H80 B2 N2 P2 PtP b c n16.708; 22.4099; 16.7415
90; 90; 90		6268.4Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125323 CIFC40 H57 B Br3 Co N2 PP 1 21/n 113.563; 16.1347; 18.638
90; 95.679; 90		4058.6Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125324 CIFC32 H33 B N P SeP c a 2117.601; 17.365; 17.358
90; 90; 90		5305.3Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125325 CIFC32 H37 B N PP 1 21/c 118.893; 15.0154; 20.461
90; 114.845; 90		5267.3Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125326 CIFC40 H57 B Br3 Fe N2 PP 1 21/n 113.5457; 16.1351; 18.6839
90; 95.303; 90		4066.1Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125327 CIFC70 H93 B2 Br Co N8 P2C m c e25.9634; 17.706; 29.773
90; 90; 90		13686.9Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125328 CIFC144 H168 B4 Br4 Co3 N6 O6 P4P 1 21/c 122.776; 11.6346; 27.261
90; 113.332; 90		6633.2Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125329 CIFC16 H12 N2 O2P -17.0483; 12.691; 14.4533
103.668; 90.921; 102.65		1222.6Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125330 CIFC19 H21 F N2 O2P -16.3592; 9.7262; 15.058
92.739; 99.147; 106.484		877.5Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125331 CIFC20 H20 N2 O3P 1 21/n 19.8482; 12.1953; 15.5327
90; 106.98; 90		1784.18Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125332 CIFC20 H23 F N2 O2P 1 21/c 111.9347; 13.0246; 12.4263
90; 112.805; 90		1780.61Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125333 CIFC32 H30 N4 O3P -110.711; 11.136; 13.512
100.641; 104.19; 113.52		1358.4Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125334 CIFC16 H16 N2 OP -111.1136; 11.2993; 12.7113
105.175; 101.292; 114.625		1313.2Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125335 CIFC17 H14 N2 O2 SP 1 21/c 17.1819; 12.909; 16.108
90; 99.316; 90		1473.7Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125336 CIFC21 H22 N2 O3I 1 2/a 113.1564; 14.1743; 20.5373
90; 93.892; 90		3821Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125337 CIFC19 H18 N2 O3P 1 21/n 19.0284; 12.6694; 14.298
90; 96.266; 90		1625.7Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125338 CIFC20 H14 N2P 1 21/c 17.0181; 7.9004; 25.5706
90; 92.661; 90		1416.25Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125339 CIFC16 H14 N2 OP 21 21 215.729; 14.295; 15.456
90; 90; 90		1265.8Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125340 CIFC121 H200 N6 O4 Si4 Y2P 1 2/c 123.3487; 12.1983; 21.8684
90; 92.992; 90		6219.9Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125341 CIFC99 H176 N6 O4 Si4 Yb2P -110.9326; 12.067; 21.041
105.472; 96.265; 94.586		2641.9Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125342 CIFC107 H182 N6 O4 Si4 Yb2P 1 2/c 121.5295; 12.1512; 23.1374
90; 93.7523; 90		6040Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125343 CIFC44 H60 N2 O2I 1 2/c 113.5259; 9.785; 29.268
90; 95.506; 90		3855.8Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125344 CIFC44 H72 N2 O2P -19.6188; 9.9837; 12.2473
101.903; 98.362; 113.312		1022.59Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125345 CIFC50 H76 N3 O2 Si2 YP 1 21/c 115.3478; 16.3591; 20.5634
90; 94.045; 90		5150.1Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125346 CIFC46 H84 N3 O2 Si2 YP -110.8751; 12.0478; 20.872
105.371; 96.234; 94.373		2605.5Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125347 CIFC50 H76 N3 O2 Si2 YbP 1 21/c 115.212; 16.174; 20.7742
90; 95.218; 90		5090.1Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125348 CIFC14 H19 Cd Cl N9 PP 21 21 2110.7129; 12.186; 16.3333
90; 90; 90		2132.27Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125349 CIFC14 H18 Cd F N9 PC 1 2/c 118.909; 10.618; 10.507
90; 111.75; 90		1959.4Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125350 CIFC14 H19 Cd Cl N9 PP b c n16.65; 16.667; 15.809
90; 90; 90		4387Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125351 CIFC14 H18 Cd F N9 PC m c e16.172; 15.6943; 16.8867
90; 90; 90		4286Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125352 CIFC24 H20 S4P 1 21/n 17.1311; 8.3942; 17.2693
90; 95.931; 90		1028.2Phan, Ngoc-Minh; Zakharov, Lev N.; Johnson, Darren W.
Copper(ii) serves as an efficient additive for metal-directed self-assembly of over 20 thiacyclophanes.
Chemical communications (Cambridge, England), 2018, 54, 13419-13422
7125353 CIFC24 H20 S4A e a 210.8663; 8.5571; 22.5617
90; 90; 90		2097.88Phan, Ngoc-Minh; Zakharov, Lev N.; Johnson, Darren W.
Copper(ii) serves as an efficient additive for metal-directed self-assembly of over 20 thiacyclophanes.
Chemical communications (Cambridge, England), 2018, 54, 13419-13422
7125354 CIFC224 H306 N16 O74C 1 2/c 134.603; 9.5694; 20.2633
90; 120.599; 90		5775.5Barbas, Rafael; Prohens, Rafel; Bauzá, Antonio; Franconetti, Antonio; Frontera, Antonio
H-Bonded anion-anion complexes in fentanyl citrate polymorphs and solvates.
Chemical communications (Cambridge, England), 2019, 55, 115-118
7125355 CIFC35 H44 N2 O8P 1 21/c 117.904; 9.6858; 19.3593
90; 108.125; 90		3190.6Barbas, Rafael; Prohens, Rafel; Bauzá, Antonio; Franconetti, Antonio; Frontera, Antonio
H-Bonded anion-anion complexes in fentanyl citrate polymorphs and solvates.
Chemical communications (Cambridge, England), 2019, 55, 115-118
7125356 CIFC28 H36 N2 O8P -18.963; 11.2533; 14.874
109.411; 96.728; 107.486		1309.72Barbas, Rafael; Prohens, Rafel; Bauzá, Antonio; Franconetti, Antonio; Frontera, Antonio
H-Bonded anion-anion complexes in fentanyl citrate polymorphs and solvates.
Chemical communications (Cambridge, England), 2019, 55, 115-118
7125357 CIFC12 H11 Cl2 N O2 SP 1 21/c 111.687; 9.657; 11.95
90; 96.8; 90		1339.2Xie, Ming-Sheng; Zhao, Guo-Feng; Qin, Tao; Suo, Yong-Bo; Qu, Gui-Rong; Guo, Hai-Ming
Thiourea participation in [3+2] cycloaddition with donor-acceptor cyclopropanes: a domino process to 2-amino-dihydrothiophenes.
Chemical communications (Cambridge, England), 2019, 55, 1580-1583
7125358 CIFC13 H14 O4P 21 21 217.9156; 9.8147; 15.3289
90; 90; 90		1190.89Xie, Ming-Sheng; Zhao, Guo-Feng; Qin, Tao; Suo, Yong-Bo; Qu, Gui-Rong; Guo, Hai-Ming
Thiourea participation in [3+2] cycloaddition with donor-acceptor cyclopropanes: a domino process to 2-amino-dihydrothiophenes.
Chemical communications (Cambridge, England), 2019, 55, 1580-1583
7125359 CIFC12 H13 N O2 SP 1 21 17.583; 6.1506; 25.4866
90; 95.003; 90		1184.17Xie, Ming-Sheng; Zhao, Guo-Feng; Qin, Tao; Suo, Yong-Bo; Qu, Gui-Rong; Guo, Hai-Ming
Thiourea participation in [3+2] cycloaddition with donor-acceptor cyclopropanes: a domino process to 2-amino-dihydrothiophenes.
Chemical communications (Cambridge, England), 2019, 55, 1580-1583
7125360 CIFC3 H6 N2 O2 SP 1 21/n 17.3625; 9.5369; 16.9216
90; 94.933; 90		1183.76Xie, Ming-Sheng; Zhao, Guo-Feng; Qin, Tao; Suo, Yong-Bo; Qu, Gui-Rong; Guo, Hai-Ming
Thiourea participation in [3+2] cycloaddition with donor-acceptor cyclopropanes: a domino process to 2-amino-dihydrothiophenes.
Chemical communications (Cambridge, England), 2019, 55, 1580-1583
7125361 CIFC16 H20 N2 O6 SP b c a14.0809; 12.1296; 21.4422
90; 90; 90		3662.2Xie, Ming-Sheng; Zhao, Guo-Feng; Qin, Tao; Suo, Yong-Bo; Qu, Gui-Rong; Guo, Hai-Ming
Thiourea participation in [3+2] cycloaddition with donor-acceptor cyclopropanes: a domino process to 2-amino-dihydrothiophenes.
Chemical communications (Cambridge, England), 2019, 55, 1580-1583
7125362 CIFC92 H90 N8 O16P 1 21/a 113.051; 18.73; 19.67
90; 90.889; 90		4808Kawano, Shin-Ichiro; Kawada, Sae; Kitagawa, Yasutaka; Teramoto, Rena; Nakano, Masayoshi; Tanaka, Kentaro
Near-infrared absorption by intramolecular charge-transfer transition in 5,10,15,20-tetra(N-carbazolyl)porphyrin through protonation.
Chemical communications (Cambridge, England), 2019, 55, 2992-2995
7125363 CIFC96 H92 F12 N8 O28 S4P 41 3 233.668; 33.668; 33.668
90; 90; 90		38164Kawano, Shin-Ichiro; Kawada, Sae; Kitagawa, Yasutaka; Teramoto, Rena; Nakano, Masayoshi; Tanaka, Kentaro
Near-infrared absorption by intramolecular charge-transfer transition in 5,10,15,20-tetra(N-carbazolyl)porphyrin through protonation.
Chemical communications (Cambridge, England), 2019, 55, 2992-2995
7125364 CIFC57.5 H48.5 Cl3.5 F24 N4 P4P 1 21/c 128.8044; 13.8129; 17.8677
90; 91.37; 90		7107Cheng, Lin; Zhang, Haiyang; Dong, Yunhong; Zhao, Yanxia; Yu, Yang; Cao, Liping
Tetraphenylethene-based tetracationic cyclophanes and their selective recognition for amino acids and adenosine derivatives in water.
Chemical communications (Cambridge, England), 2019, 55, 2372-2375
7125365 CIFC108 H140 F24 N4 O8 P4C m c e39.9; 9.539; 26.857
90; 90; 90		10222Cheng, Lin; Zhang, Haiyang; Dong, Yunhong; Zhao, Yanxia; Yu, Yang; Cao, Liping
Tetraphenylethene-based tetracationic cyclophanes and their selective recognition for amino acids and adenosine derivatives in water.
Chemical communications (Cambridge, England), 2019, 55, 2372-2375
7125366 CIFC41 H67 Mg N3 OP -19.3179; 12.5656; 18.0807
70.915; 81.783; 85.771		1979.25Bole, Leonie J.; Davin, Laia; Kennedy, Alan R.; McLellan, Ross; Hevia, Eva
Magnesium-mediated arylation of amines via C-F bond activation of fluoroarenes.
Chemical communications (Cambridge, England), 2019, 55, 4339-4342
7125367 CIFC77 H98 Mg2 N10P 1 21/n 113.0738; 14.2398; 19.0456
90; 92.872; 90		3541.2Bole, Leonie J.; Davin, Laia; Kennedy, Alan R.; McLellan, Ross; Hevia, Eva
Magnesium-mediated arylation of amines via C-F bond activation of fluoroarenes.
Chemical communications (Cambridge, England), 2019, 55, 4339-4342
7125368 CIFC41 H51 Mg N3P 1 21/c 118.4812; 18.3287; 10.6762
90; 90.832; 90		3616Bole, Leonie J.; Davin, Laia; Kennedy, Alan R.; McLellan, Ross; Hevia, Eva
Magnesium-mediated arylation of amines via C-F bond activation of fluoroarenes.
Chemical communications (Cambridge, England), 2019, 55, 4339-4342
7125369 CIFC75 H110 Mg2 N6C 1 2/c 119.736; 20.5218; 17.9367
90; 112.105; 90		6730.7Bole, Leonie J.; Davin, Laia; Kennedy, Alan R.; McLellan, Ross; Hevia, Eva
Magnesium-mediated arylation of amines via C-F bond activation of fluoroarenes.
Chemical communications (Cambridge, England), 2019, 55, 4339-4342
7125370 CIFC56 H96 N4 O20 P4 S4 Zn4I b a 221.231; 21.328; 20.064
90; 90; 90		9085Sharma, Kamna; Gupta, Sandeep K.; Borah, Aditya; Murugavel, Ramaswamy
Hitherto unknown eight-connected frameworks formed from A<sub>4</sub>B<sub>4</sub>O<sub>12</sub> metal organophosphate heterocubanes.
Chemical communications (Cambridge, England), 2019, 55, 7994-7997
7125371 CIFC15 H24 N O6 P ZnI -416.942; 16.942; 15.489
90; 90; 90		4446Sharma, Kamna; Gupta, Sandeep K.; Borah, Aditya; Murugavel, Ramaswamy
Hitherto unknown eight-connected frameworks formed from A<sub>4</sub>B<sub>4</sub>O<sub>12</sub> metal organophosphate heterocubanes.
Chemical communications (Cambridge, England), 2019, 55, 7994-7997
7125372 CIFC36 H43 N8 O8 P2 Zn2P 4/n n c :218.2767; 18.2767; 30.7812
90; 90; 90		10282.1Sharma, Kamna; Gupta, Sandeep K.; Borah, Aditya; Murugavel, Ramaswamy
Hitherto unknown eight-connected frameworks formed from A<sub>4</sub>B<sub>4</sub>O<sub>12</sub> metal organophosphate heterocubanes.
Chemical communications (Cambridge, England), 2019, 55, 7994-7997
7125373 CIFC14 H24 N O8 P ZnI -416.7211; 16.7211; 15.5352
90; 90; 90		4343.57Sharma, Kamna; Gupta, Sandeep K.; Borah, Aditya; Murugavel, Ramaswamy
Hitherto unknown eight-connected frameworks formed from A<sub>4</sub>B<sub>4</sub>O<sub>12</sub> metal organophosphate heterocubanes.
Chemical communications (Cambridge, England), 2019, 55, 7994-7997
7125374 CIFC25 H19 Cu2 O12P 4/n m m :218.9546; 18.9546; 13.4969
90; 90; 90		4849.1Hu, Falu; Huang, Pan; Di, Zhengyi; Wu, Mingyan; Jiang, Feilong; Hong, Maochun
A robust cage-based framework for the highly selective purification of natural gas.
Chemical communications (Cambridge, England), 2019, 55, 10257-10260
7125375 CIFC50.04 H35.42 F6 Ir N4 O2 P S2P 1 21 19.0479; 10.7246; 25.204
90; 98.105; 90		2421.2Yan, Zhi-Ping; Liao, Kang; Han, Hua-Bo; Su, Jian; Zheng, You-Xuan; Zuo, Jing-Lin
Chiral iridium(iii) complexes with four-membered Ir-S-P-S chelating rings for high-performance circularly polarized OLEDs.
Chemical communications (Cambridge, England), 2019, 55, 8215-8218
7125376 CIFC50 H28 F6 Ir N4 O2 P S2P 21 21 2111.182; 15.6943; 30.695
90; 90; 90		5386.8Yan, Zhi-Ping; Liao, Kang; Han, Hua-Bo; Su, Jian; Zheng, You-Xuan; Zuo, Jing-Lin
Chiral iridium(iii) complexes with four-membered Ir-S-P-S chelating rings for high-performance circularly polarized OLEDs.
Chemical communications (Cambridge, England), 2019, 55, 8215-8218
7125377 CIFC50 H28 F6 Ir N4 O2 P S2P 21 21 2111.0991; 15.4078; 31.051
90; 90; 90		5310.1Yan, Zhi-Ping; Liao, Kang; Han, Hua-Bo; Su, Jian; Zheng, You-Xuan; Zuo, Jing-Lin
Chiral iridium(iii) complexes with four-membered Ir-S-P-S chelating rings for high-performance circularly polarized OLEDs.
Chemical communications (Cambridge, England), 2019, 55, 8215-8218
7125378 CIFC50 H36 F6 Ir N4 O2 P S2P 1 21 19.0612; 10.7892; 25.3691
90; 97.738; 90		2457.6Yan, Zhi-Ping; Liao, Kang; Han, Hua-Bo; Su, Jian; Zheng, You-Xuan; Zuo, Jing-Lin
Chiral iridium(iii) complexes with four-membered Ir-S-P-S chelating rings for high-performance circularly polarized OLEDs.
Chemical communications (Cambridge, England), 2019, 55, 8215-8218
7125379 CIFC29 H16 Cl4 F6 N3 O8 P S2P -18.7656; 10.8058; 19.768
95.71; 99.202; 112.242		1684.3Waked, Alexander E.; Chitnis, Saurabh S.; Stephan, Douglas W.
P(v) dications: carbon-based Lewis acid initiators for hydrodefluorination.
Chemical communications (Cambridge, England), 2019, 55, 8971-8974
7125380 CIFC43 H37 F6 N4 O9 P S2P 1 21/n 110.6663; 25.7596; 16.1421
90; 100.574; 90		4359.9Waked, Alexander E.; Chitnis, Saurabh S.; Stephan, Douglas W.
P(v) dications: carbon-based Lewis acid initiators for hydrodefluorination.
Chemical communications (Cambridge, England), 2019, 55, 8971-8974
7125381 CIFC14 H16 Cl3 Co N4P -19.1082; 9.8312; 9.9666
93.655; 98.898; 90.006		879.88Sakaguchi, Yuto; Call, Arnau; Cibian, Mihaela; Yamauchi, Kosei; Sakai, Ken
An earth-abundant system for light-driven CO<sub>2</sub> reduction to CO using a pyridinophane iron catalyst.
Chemical communications (Cambridge, England), 2019, 55, 8552-8555
7125382 CIFC14 H16 Cl2 N4 ZnF d d d :28.6064; 28.201; 29.216
90; 90; 90		7091Sakaguchi, Yuto; Call, Arnau; Cibian, Mihaela; Yamauchi, Kosei; Sakai, Ken
An earth-abundant system for light-driven CO<sub>2</sub> reduction to CO using a pyridinophane iron catalyst.
Chemical communications (Cambridge, England), 2019, 55, 8552-8555
7125383 CIFC28 H32 Cl4 Fe2 N8 OP -19.1131; 11.477; 18.784
98.812; 92.127; 91.893		1938.6Sakaguchi, Yuto; Call, Arnau; Cibian, Mihaela; Yamauchi, Kosei; Sakai, Ken
An earth-abundant system for light-driven CO<sub>2</sub> reduction to CO using a pyridinophane iron catalyst.
Chemical communications (Cambridge, England), 2019, 55, 8552-8555
7125384 CIFC28 H32 Cl4 N8 Ni2C 1 2/m 117.178; 8.837; 12.505
90; 112.309; 90		1756.2Sakaguchi, Yuto; Call, Arnau; Cibian, Mihaela; Yamauchi, Kosei; Sakai, Ken
An earth-abundant system for light-driven CO<sub>2</sub> reduction to CO using a pyridinophane iron catalyst.
Chemical communications (Cambridge, England), 2019, 55, 8552-8555
7125385 CIFC53 H31 Cl3 N2 O4 SP -111.9568; 12.3682; 14.6936
109.732; 92.669; 92.147		2039.9Hong, Seong-Jin; Dutta, Ranjan; Kumar, Ravi; He, Qing; Lynch, Vincent M.; Sessler, Jonathan L.; Lee, Chang-Hee
meso-Alkylidenyl dibenzihexaphyrins: synthesis and protonation studies.
Chemical communications (Cambridge, England), 2019, 55, 9693-9696
7125386 CIFC72.89 H33.78 Cl0 F8.89 N3.56 O10.67I 41/a :220.1536; 20.1536; 55.493
90; 90; 90		22539.5Hong, Seong-Jin; Dutta, Ranjan; Kumar, Ravi; He, Qing; Lynch, Vincent M.; Sessler, Jonathan L.; Lee, Chang-Hee
meso-Alkylidenyl dibenzihexaphyrins: synthesis and protonation studies.
Chemical communications (Cambridge, England), 2019, 55, 9693-9696
7125387 CIFC18 H15 Cl0 F0 N4 OP -112.9539; 14.4757; 14.725
70.698; 66.001; 67.022		2273.4Hong, Seong-Jin; Dutta, Ranjan; Kumar, Ravi; He, Qing; Lynch, Vincent M.; Sessler, Jonathan L.; Lee, Chang-Hee
meso-Alkylidenyl dibenzihexaphyrins: synthesis and protonation studies.
Chemical communications (Cambridge, England), 2019, 55, 9693-9696
7125388 CIFC168 H72 Cl12 F20 N8 O16P 1 21/c 119.5016; 35.2797; 23.3317
90; 90.269; 90		16052.3Hong, Seong-Jin; Dutta, Ranjan; Kumar, Ravi; He, Qing; Lynch, Vincent M.; Sessler, Jonathan L.; Lee, Chang-Hee
meso-Alkylidenyl dibenzihexaphyrins: synthesis and protonation studies.
Chemical communications (Cambridge, England), 2019, 55, 9693-9696
7125389 CIFC36 H28 N4 O2P n n a11.4575; 10.6962; 27.0458
90; 90; 90		3314.51Wang, Yin-Feng; Lu, Hai-Yan; Shen, Yi-Fan; Li, Meng; Chen, Chuan-Feng
Novel oxacalix[2]arene[2]triazines with thermally activated delayed fluorescence and aggregation-induced emission properties.
Chemical communications (Cambridge, England), 2019, 55, 9559-9562
7125390 CIFC60 H44 N8 O4P 1 21/c 19.64598; 27.23322; 18.74004
90; 101.926; 90		4816.59Wang, Yin-Feng; Lu, Hai-Yan; Shen, Yi-Fan; Li, Meng; Chen, Chuan-Feng
Novel oxacalix[2]arene[2]triazines with thermally activated delayed fluorescence and aggregation-induced emission properties.
Chemical communications (Cambridge, England), 2019, 55, 9559-9562
7125391 CIFC80 H48 N8 O4P 1 21/n 114.9786; 9.059; 57.2212
90; 94.208; 90		7743.5Wang, Yin-Feng; Lu, Hai-Yan; Shen, Yi-Fan; Li, Meng; Chen, Chuan-Feng
Novel oxacalix[2]arene[2]triazines with thermally activated delayed fluorescence and aggregation-induced emission properties.
Chemical communications (Cambridge, England), 2019, 55, 9559-9562
7125392 CIFC54 H32 N8 O6P 1 2/c 119.6993; 13.7805; 17.3821
90; 92.071; 90		4715.57Wang, Yin-Feng; Lu, Hai-Yan; Shen, Yi-Fan; Li, Meng; Chen, Chuan-Feng
Novel oxacalix[2]arene[2]triazines with thermally activated delayed fluorescence and aggregation-induced emission properties.
Chemical communications (Cambridge, England), 2019, 55, 9559-9562
7125393 CIFC84 H108 Cl16 Cu0 Fe15 N14 O34P -111.433; 14.879; 25.862
88.484; 84.89; 77.817		4283.1Lin, Li-Dan; Li, Zhong; Zhao, Dan; Liu, Jin-Hua; Li, Xin-Xiong; Zheng, Shou-Tian
Development of a new Lindqvist-like Fe6 cluster secondary building unit for MOFs.
Chemical communications (Cambridge, England), 2019, 55, 10729-10732
7125394 CIFC40 H48 Cl6 Cu Fe7 I N6 O17P 1 21/c 111.4027; 54.461; 18.009
90; 112.514; 90		10331Lin, Li-Dan; Li, Zhong; Zhao, Dan; Liu, Jin-Hua; Li, Xin-Xiong; Zheng, Shou-Tian
Development of a new Lindqvist-like Fe6 cluster secondary building unit for MOFs.
Chemical communications (Cambridge, England), 2019, 55, 10729-10732
7125395 CIFC320 H384 Cl48 Cu0 Fe56 N48 O120C c c a :222.375; 23.965; 27.502
90; 90; 90		14747Lin, Li-Dan; Li, Zhong; Zhao, Dan; Liu, Jin-Hua; Li, Xin-Xiong; Zheng, Shou-Tian
Development of a new Lindqvist-like Fe6 cluster secondary building unit for MOFs.
Chemical communications (Cambridge, England), 2019, 55, 10729-10732
7125396 CIFC25 H21 N7 Ni O5 S2P 21 21 2110.3308; 11.4554; 23.6689
90; 90; 90		2801.06Dey, Mamon; Mudoi, Prashurya Pritam; Choudhury, Anup; Sarma, Bipul; Gogoi, Nayanmoni
Deciphering the influence of structural distortions on the uniaxial magnetic anisotropy of pentagonal bipyramidal Ni(ii) complexes.
Chemical communications (Cambridge, England), 2019, 55, 11547-11550
7125397 CIFC13 H15 N9 Ni O4 S2P -18.758; 11.248; 12.524
65.786; 84.967; 71.813		1067.8Dey, Mamon; Mudoi, Prashurya Pritam; Choudhury, Anup; Sarma, Bipul; Gogoi, Nayanmoni
Deciphering the influence of structural distortions on the uniaxial magnetic anisotropy of pentagonal bipyramidal Ni(ii) complexes.
Chemical communications (Cambridge, England), 2019, 55, 11547-11550
7125398 CIFC17 H23 N11 Ni O2I 41/a :232.1592; 32.1592; 10.0314
90; 90; 90		10374.6Dey, Mamon; Mudoi, Prashurya Pritam; Choudhury, Anup; Sarma, Bipul; Gogoi, Nayanmoni
Deciphering the influence of structural distortions on the uniaxial magnetic anisotropy of pentagonal bipyramidal Ni(ii) complexes.
Chemical communications (Cambridge, England), 2019, 55, 11547-11550
7125399 CIFC24 H28 N4 O S3A m a 232.1098; 13.472; 5.7153
90; 90; 90		2472.34Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Liu, Xiao-Wei; Li, Mian; Zheng, Ji; Ng, Seik Weng; Li, Dan
A luminescent edge-interlocked prismatic heteroleptic metallocage assembled through a ligand replacement reaction.
Chemical communications (Cambridge, England), 2019, 55, 11992-11995
7125400 CIFC58.667 H61.333 Cu6 N12 O0.167 S3C c c a :233.788; 23.8727; 44.3077
90; 90; 90		35739.1Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Liu, Xiao-Wei; Li, Mian; Zheng, Ji; Ng, Seik Weng; Li, Dan
A luminescent edge-interlocked prismatic heteroleptic metallocage assembled through a ligand replacement reaction.
Chemical communications (Cambridge, England), 2019, 55, 11992-11995
7125401 CIFC58.667 H61.333 Cu6 N12 O0.167 S3C c c a :233.7716; 71.5841; 44.3018
90; 90; 90		107100Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Liu, Xiao-Wei; Li, Mian; Zheng, Ji; Ng, Seik Weng; Li, Dan
A luminescent edge-interlocked prismatic heteroleptic metallocage assembled through a ligand replacement reaction.
Chemical communications (Cambridge, England), 2019, 55, 11992-11995
7125402 CIFC128 H156 Cl12 N24 Ni6 O24 Si8P 4/n :222.724; 22.724; 16.435
90; 90; 90		8487Kumar, Kilaparthi Sravan; Mane, Vishwanath S.; Yadav, Ashok; Kumbhar, Avinash S.; Boomishankar, Ramamoorthy
Photochemical hydrogen evolution from water by a 1D-network of octahedral Ni<sub>6</sub>L<sub>8</sub> cages.
Chemical communications (Cambridge, England), 2019, 55, 13156-13159
7125403 CIFC24 H22 Br O3 PP 1 21/n 111.6694; 10.1505; 17.4217
90; 96.448; 90		2050.55Fu, Zhicheng; Sun, Simin; Yang, Anjian; Sun, Fang; Xu, Jiaxi
Transition metal-free access to 3,4-dihydro-1,2-oxaphosphinine-2-oxides from phosphonochloridates and chalcones through tandem Michael addition and nucleophilic substitution.
Chemical communications (Cambridge, England), 2019, 55, 13124-13127
7125404 CIFC25 H22 F3 O3 PR -3 :H17.8304; 17.8304; 36.593
90; 90; 120		10075Fu, Zhicheng; Sun, Simin; Yang, Anjian; Sun, Fang; Xu, Jiaxi
Transition metal-free access to 3,4-dihydro-1,2-oxaphosphinine-2-oxides from phosphonochloridates and chalcones through tandem Michael addition and nucleophilic substitution.
Chemical communications (Cambridge, England), 2019, 55, 13124-13127
7125405 CIFC19 H27 Cl2 N2 O4 P PtP -19.3032; 11.5641; 12.6329
111.392; 106.122; 101.324		1146.41Huang, Ke-Bin; Wang, Feng-Yang; Feng, Hai-Wen; Luo, Hejiang; Long, Yan; Zou, Taotao; Chan, Albert S. C.; Liu, Rong; Zou, Huahong; Chen, Zhen-Feng; Liu, Yan-Cheng; Liu, You-Nian; Liang, Hong
An aminophosphonate ester ligand-containing platinum(ii) complex induces potent immunogenic cell death in vitro and elicits effective anti-tumour immune responses in vivo.
Chemical communications (Cambridge, England), 2019, 55, 13066-13069
7125406 CIFC16 H18 Cl3 N2 O3 P PtP 1 21/c 19.6106; 20.423; 10.6731
90; 96.686; 90		2080.6Huang, Ke-Bin; Wang, Feng-Yang; Feng, Hai-Wen; Luo, Hejiang; Long, Yan; Zou, Taotao; Chan, Albert S. C.; Liu, Rong; Zou, Huahong; Chen, Zhen-Feng; Liu, Yan-Cheng; Liu, You-Nian; Liang, Hong
An aminophosphonate ester ligand-containing platinum(ii) complex induces potent immunogenic cell death in vitro and elicits effective anti-tumour immune responses in vivo.
Chemical communications (Cambridge, England), 2019, 55, 13066-13069
7125407 CIFC18 H25 Cl2 N2 O4 P PtP 1 21/n 19.22386; 13.26158; 18.9212
90; 102.596; 90		2258.79Huang, Ke-Bin; Wang, Feng-Yang; Feng, Hai-Wen; Luo, Hejiang; Long, Yan; Zou, Taotao; Chan, Albert S. C.; Liu, Rong; Zou, Huahong; Chen, Zhen-Feng; Liu, Yan-Cheng; Liu, You-Nian; Liang, Hong
An aminophosphonate ester ligand-containing platinum(ii) complex induces potent immunogenic cell death in vitro and elicits effective anti-tumour immune responses in vivo.
Chemical communications (Cambridge, England), 2019, 55, 13066-13069
7125408 CIFC18 H23 Cl4 N2 O3 P PtP -18.366; 11.425; 14.15
95.168; 106.359; 106.779		1220.7Huang, Ke-Bin; Wang, Feng-Yang; Feng, Hai-Wen; Luo, Hejiang; Long, Yan; Zou, Taotao; Chan, Albert S. C.; Liu, Rong; Zou, Huahong; Chen, Zhen-Feng; Liu, Yan-Cheng; Liu, You-Nian; Liang, Hong
An aminophosphonate ester ligand-containing platinum(ii) complex induces potent immunogenic cell death in vitro and elicits effective anti-tumour immune responses in vivo.
Chemical communications (Cambridge, England), 2019, 55, 13066-13069
7125409 CIFC17 H22 Cl3 N2 O3 P PtP 1 21/c 18.7652; 14.5838; 19.6786
90; 116.45; 90		2252.2Huang, Ke-Bin; Wang, Feng-Yang; Feng, Hai-Wen; Luo, Hejiang; Long, Yan; Zou, Taotao; Chan, Albert S. C.; Liu, Rong; Zou, Huahong; Chen, Zhen-Feng; Liu, Yan-Cheng; Liu, You-Nian; Liang, Hong
An aminophosphonate ester ligand-containing platinum(ii) complex induces potent immunogenic cell death in vitro and elicits effective anti-tumour immune responses in vivo.
Chemical communications (Cambridge, England), 2019, 55, 13066-13069
7125410 CIFC19 H26 Cl3 N2 O4 P PtP -18.5496; 11.5478; 12.5966
83.444; 85.19; 71.014		1166.9Huang, Ke-Bin; Wang, Feng-Yang; Feng, Hai-Wen; Luo, Hejiang; Long, Yan; Zou, Taotao; Chan, Albert S. C.; Liu, Rong; Zou, Huahong; Chen, Zhen-Feng; Liu, Yan-Cheng; Liu, You-Nian; Liang, Hong
An aminophosphonate ester ligand-containing platinum(ii) complex induces potent immunogenic cell death in vitro and elicits effective anti-tumour immune responses in vivo.
Chemical communications (Cambridge, England), 2019, 55, 13066-13069
7125411 CIFC17 H22 Cl3 N2 O4 P PtP b c a12.064; 16.098; 22.941
90; 90; 90		4455.3Huang, Ke-Bin; Wang, Feng-Yang; Feng, Hai-Wen; Luo, Hejiang; Long, Yan; Zou, Taotao; Chan, Albert S. C.; Liu, Rong; Zou, Huahong; Chen, Zhen-Feng; Liu, Yan-Cheng; Liu, You-Nian; Liang, Hong
An aminophosphonate ester ligand-containing platinum(ii) complex induces potent immunogenic cell death in vitro and elicits effective anti-tumour immune responses in vivo.
Chemical communications (Cambridge, England), 2019, 55, 13066-13069
7125412 CIFC16 H19 Cl4 N2 O3 P PtP 1 21/c 18.141; 17.253; 16.187
90; 104.267; 90		2203.5Huang, Ke-Bin; Wang, Feng-Yang; Feng, Hai-Wen; Luo, Hejiang; Long, Yan; Zou, Taotao; Chan, Albert S. C.; Liu, Rong; Zou, Huahong; Chen, Zhen-Feng; Liu, Yan-Cheng; Liu, You-Nian; Liang, Hong
An aminophosphonate ester ligand-containing platinum(ii) complex induces potent immunogenic cell death in vitro and elicits effective anti-tumour immune responses in vivo.
Chemical communications (Cambridge, England), 2019, 55, 13066-13069
7125413 CIFC17 H23 Cl2 N2 O4 P PtP b c a10.0411; 14.3523; 29.091
90; 90; 90		4192.4Huang, Ke-Bin; Wang, Feng-Yang; Feng, Hai-Wen; Luo, Hejiang; Long, Yan; Zou, Taotao; Chan, Albert S. C.; Liu, Rong; Zou, Huahong; Chen, Zhen-Feng; Liu, Yan-Cheng; Liu, You-Nian; Liang, Hong
An aminophosphonate ester ligand-containing platinum(ii) complex induces potent immunogenic cell death in vitro and elicits effective anti-tumour immune responses in vivo.
Chemical communications (Cambridge, England), 2019, 55, 13066-13069
7125414 CIFC33 H44 N8 O4P 42/n :214.5333; 14.5333; 7.83602
90; 90; 90		1655.1Cullen, Duncan A.; Gardiner, Michael G.; White, Nicholas G.
A three dimensional hydrogen bonded organic framework assembled through antielectrostatic hydrogen bonds.
Chemical communications (Cambridge, England), 2019, 55, 12020-12023
7125415 CIFC33 H36 N8 O15P 42/n b c :213.38177; 13.38177; 21.7501
90; 90; 90		3894.83Cullen, Duncan A.; Gardiner, Michael G.; White, Nicholas G.
A three dimensional hydrogen bonded organic framework assembled through antielectrostatic hydrogen bonds.
Chemical communications (Cambridge, England), 2019, 55, 12020-12023
7125416 CIFC78 H42 N4 O16 Zn3P b a n :227.9512; 32.0897; 25.2538
90; 90; 90		22651.3Cao, Li-Hui; Liu, Xin; Tang, Xiao-Han; Liu, Junyi; Xu, Xiao-Qian; Zang, Shuang-Quan; Ma, Yang-Min
A fivefold linker length reduction in an interpenetrated metal-organic framework via sequential solvent-assisted linker exchange.
Chemical communications (Cambridge, England), 2019, 55, 12671-12674
7125417 CIFC66 H40 N2 O12 Zn3P b a n :231.8382; 28.3102; 19.3354
90; 90; 90		17427.9Cao, Li-Hui; Liu, Xin; Tang, Xiao-Han; Liu, Junyi; Xu, Xiao-Qian; Zang, Shuang-Quan; Ma, Yang-Min
A fivefold linker length reduction in an interpenetrated metal-organic framework via sequential solvent-assisted linker exchange.
Chemical communications (Cambridge, England), 2019, 55, 12671-12674
7125418 CIFC30 H38 B10 N2P 49.9221; 9.9221; 16.2619
90; 90; 90		1600.95Liu, Ke; Zhang, Jing; Xu, Ling; Liu, Jing; Ding, Liping; Liu, Taihong; Fang, Yu
Film-based fluorescence sensing: a "chemical nose" for nicotine.
Chemical communications (Cambridge, England), 2019, 55, 12679-12682
7125419 CIFC26 H28 B10P -113.5625; 14.0717; 27.7111
100.471; 99.975; 95.016		5083.2Liu, Ke; Zhang, Jing; Xu, Ling; Liu, Jing; Ding, Liping; Liu, Taihong; Fang, Yu
Film-based fluorescence sensing: a "chemical nose" for nicotine.
Chemical communications (Cambridge, England), 2019, 55, 12679-12682
7125420 CIFC26 H28 B10 O2P 1 21/c 120.3497; 11.0447; 28.6138
90; 110.692; 90		6016.3Liu, Ke; Zhang, Jing; Xu, Ling; Liu, Jing; Ding, Liping; Liu, Taihong; Fang, Yu
Film-based fluorescence sensing: a "chemical nose" for nicotine.
Chemical communications (Cambridge, England), 2019, 55, 12679-12682
7125421 CIFC28 H32 B10 O2P 1 21/n 111.4542; 14.4867; 17.2981
90; 94.005; 90		2863.33Liu, Ke; Zhang, Jing; Xu, Ling; Liu, Jing; Ding, Liping; Liu, Taihong; Fang, Yu
Film-based fluorescence sensing: a "chemical nose" for nicotine.
Chemical communications (Cambridge, England), 2019, 55, 12679-12682
7125422 CIFC24 H23 I N2 O2P 1 21/n 110.7797; 8.0018; 25.0126
90; 94.381; 90		2151.21Leduskrasts, Kaspars; Kinens, Artis; Suna, Edgars
Cation-π interactions secure aggregation induced emission of planar organic luminophores.
Chemical communications (Cambridge, England), 2019, 55, 12663-12666
7125423 CIFC12 H12 Cl N O4P 1 21/c 111.7674; 5.8992; 17.3999
90; 96.609; 90		1199.84Leduskrasts, Kaspars; Kinens, Artis; Suna, Edgars
Cation-π interactions secure aggregation induced emission of planar organic luminophores.
Chemical communications (Cambridge, England), 2019, 55, 12663-12666
7125424 CIFC26 H22 Cl N3 O4P 1 21/n 116.3679; 7.39194; 19.97192
90; 104.187; 90		2342.72Leduskrasts, Kaspars; Kinens, Artis; Suna, Edgars
Cation-π interactions secure aggregation induced emission of planar organic luminophores.
Chemical communications (Cambridge, England), 2019, 55, 12663-12666
7125425 CIFC15 H11 N2 O7 TbP 1 21/c 111.0348; 9.2759; 14.386
90; 97.876; 90		1458.6Wang, Xia; Wang, Yaxing; Wang, Yanlong; Liu, Hanzhou; Zhang, Yugang; Liu, Wei; Wang, Xiangxiang; Wang, Shuao
Color-tunable X-ray scintillation based on a series of isotypic lanthanide-organic frameworks.
Chemical communications (Cambridge, England), 2019, 56, 233-236
7125426 CIFC15 H15 Cl2 N O2 Pt SP 21 21 218.867; 12.232; 15.032
90; 90; 90		1630.4Yuan, Caixia; Wang, Weirong; Wang, Jianwei; Li, Xinhua; Wu, Yan-Bo; Li, Shaodong; Lu, Liping; Zhu, Miaoli; Xing, Shu; Fu, Xueqi
Potent and selective PTP1B inhibition by a platinum(ii) complex: possible implications for a new antitumor strategy.
Chemical communications (Cambridge, England), 2019, 56, 102-105
7125427 CIFC38 H38 N2 O4 S2P 1 21/c 116.4849; 10.3567; 19.7384
90; 98.596; 90		3332.1Chen, Si-Kai; Yang, Ju-Song; Dai, Kun-Long; Zhang, Fu-Min; Zhang, Xiao-Ming; Tu, Yong-Qiang
Exploration of a KI-catalyzed oxidation system for direct construction of bispyrrolidino[2,3-b]indolines and the total synthesis of (+)-WIN 64821.
Chemical communications (Cambridge, England), 2020, 56, 121-124
7125428 CIFC13 H12 B F I N O4I 1 2/a 127.8895; 6.8639; 34.3921
90; 105.296; 90		6350.48Fan, Wen-Xin; Li, Ji-Lin; Lv, Wen-Xin; Yang, Ling; Li, Qingjiang; Wang, Honggen
Synthesis of fluorinated amphoteric organoborons via iodofluorination of alkynyl and alkenyl MIDA boronates.
Chemical communications (Cambridge, England), 2020, 56, 82-85
7125429 CIFC13 H14 B F I N O4P b c a12.6367; 14.4997; 15.6349
90; 90; 90		2864.76Fan, Wen-Xin; Li, Ji-Lin; Lv, Wen-Xin; Yang, Ling; Li, Qingjiang; Wang, Honggen
Synthesis of fluorinated amphoteric organoborons via iodofluorination of alkynyl and alkenyl MIDA boronates.
Chemical communications (Cambridge, England), 2020, 56, 82-85
7125430 CIFC14 H16 B F I N O4P 1 21/c 112.7883; 11.1705; 10.9261
90; 102.02; 90		1526.59Fan, Wen-Xin; Li, Ji-Lin; Lv, Wen-Xin; Yang, Ling; Li, Qingjiang; Wang, Honggen
Synthesis of fluorinated amphoteric organoborons via iodofluorination of alkynyl and alkenyl MIDA boronates.
Chemical communications (Cambridge, England), 2020, 56, 82-85
7125431 CIFC22 H27 N3 O2P 21 21 218.4379; 10.5541; 22.3081
90; 90; 90		1986.64Ye, Xueqian; Pan, Yongkai; Yang, Xiaoyu
Direct enantioselective Mannich reactions of α-azido cyclic ketones: asymmetric construction of chiral azides possessing an α-quaternary stereocenter.
Chemical communications (Cambridge, England), 2019, 56, 98-101
7125432 CIFC19 H28 N4 O4P 1 21 112.1314; 10.4464; 15.7145
90; 95.952; 90		1980.75Ye, Xueqian; Pan, Yongkai; Yang, Xiaoyu
Direct enantioselective Mannich reactions of α-azido cyclic ketones: asymmetric construction of chiral azides possessing an α-quaternary stereocenter.
Chemical communications (Cambridge, England), 2019, 56, 98-101
7125433 CIFC25 H29 B N8 O2 WP 1 21/c 115.3086; 9.8592; 17.7914
90; 96.715; 90		2666.85Hill, Anthony; Frogley, Benjamin
Synthesis of pyridyl carbyne complexes and their conversion to N-heterocyclic vinylidenes
Chemical Communications, 2019
7125434 CIFC43 H54 B3 Cl4 F4 N13 O5 W2P n m a15.8519; 24.1231; 14.0794
90; 90; 90		5383.9Hill, Anthony; Frogley, Benjamin
Synthesis of pyridyl carbyne complexes and their conversion to N-heterocyclic vinylidenes
Chemical Communications, 2019
7125435 CIFC43 H50 Au2 B2 Cl2 N14 O4 W2P 1 21/c 112.7628; 40.553; 11.3383
90; 91.898; 90		5865.14Hill, Anthony; Frogley, Benjamin
Synthesis of pyridyl carbyne complexes and their conversion to N-heterocyclic vinylidenes
Chemical Communications, 2019
7125436 CIFC25 H29 B F3 N7 O5 S WC 1 2/c 133.2746; 13.8436; 14.0874
90; 98.529; 90		6417.46Hill, Anthony; Frogley, Benjamin
Synthesis of pyridyl carbyne complexes and their conversion to N-heterocyclic vinylidenes
Chemical Communications, 2019
7125437 CIFC45.5 H52.5 B2 Cl7.5 F3 N13 O7 S W2P -113.6197; 18.3015; 26.901
88.518; 76.527; 70.518		6137.7Hill, Anthony; Frogley, Benjamin
Synthesis of pyridyl carbyne complexes and their conversion to N-heterocyclic vinylidenes
Chemical Communications, 2019
7125438 CIFC23 H26 Au B Cl N7 O2 WP n a 2115.8904; 9.6054; 17.1964
90; 90; 90		2624.75Hill, Anthony; Frogley, Benjamin
Synthesis of pyridyl carbyne complexes and their conversion to N-heterocyclic vinylidenes
Chemical Communications, 2019
7125439 CIFC25 H30 B Cl2 N7 O2 Pt WP 1 21/n 110.6485; 21.1039; 13.1797
90; 91.758; 90		2960.4Hill, Anthony; Frogley, Benjamin
Synthesis of pyridyl carbyne complexes and their conversion to N-heterocyclic vinylidenes
Chemical Communications, 2019
7125440 CIFC16 H18 OP -19.0268; 12.5394; 12.5931
72.488; 70.192; 87.16		1276.75Lu, Xiao-Yu; Yan, Lu-Yu; Li, Jin-Song; Li, Jia-Mei; Zhou, Hai-Pin; Jiang, Run-Chuang; Liu, Chuang-Chuang; Lu, Ran; Hu, Rong
Base-free Ni-catalyzed Suzuki-type cross-coupling reactions of epoxides with boronic acids.
Chemical communications (Cambridge, England), 2019, 56, 109-112
7125441 CIFC14 H16 O2P 1 21/c 18.8117; 5.8923; 11.6496
90; 101.722; 90		592.25Inaba, Yuya; Yoneda, Tomoki; Kitagawa, Yuichi; Miyata, Kiyoshi; Hasegawa, Yasuchika; Inokuma, Yasuhide
Splitting and reorientation of π-conjugation by an unprecedented photo-rearrangement reaction.
Chemical communications (Cambridge, England), 2020, 56, 348-351
7125442 CIFC28 H34 O4P 1 21/c 18.6894; 5.8144; 23.4264
90; 99.837; 90		1166.19Inaba, Yuya; Yoneda, Tomoki; Kitagawa, Yuichi; Miyata, Kiyoshi; Hasegawa, Yasuchika; Inokuma, Yasuhide
Splitting and reorientation of π-conjugation by an unprecedented photo-rearrangement reaction.
Chemical communications (Cambridge, England), 2020, 56, 348-351
7125443 CIFC28 H30 O4P 1 21/c 18.7961; 5.8385; 22.8947
90; 99.317; 90		1160.27Inaba, Yuya; Yoneda, Tomoki; Kitagawa, Yuichi; Miyata, Kiyoshi; Hasegawa, Yasuchika; Inokuma, Yasuhide
Splitting and reorientation of π-conjugation by an unprecedented photo-rearrangement reaction.
Chemical communications (Cambridge, England), 2020, 56, 348-351
7125444 CIFC28 H30 O4P 1 21/c 112.6447; 17.9325; 10.8014
90; 103.228; 90		2384.24Inaba, Yuya; Yoneda, Tomoki; Kitagawa, Yuichi; Miyata, Kiyoshi; Hasegawa, Yasuchika; Inokuma, Yasuhide
Splitting and reorientation of π-conjugation by an unprecedented photo-rearrangement reaction.
Chemical communications (Cambridge, England), 2020, 56, 348-351
7125445 CIFC36 H32 I14 N4P -110.3325; 12.4358; 21.5144
95.149; 99.946; 98.812		2671.52Savastano, Matteo; Bazzicalupi, Carla; Gellini, Cristina; Bianchi, Antonio
Infinite supramolecular pseudo-polyrotaxane with poly[3]catenane axle: assembling nanosized rings from mono- and diatomic I<sup>-</sup> and I<sub>2</sub> tectons.
Chemical communications (Cambridge, England), 2020, 56, 551-554
7125446 CIFC36 H32 I16 N4P -110.1476; 13.0508; 21.8164
94.315; 100.436; 97.64		2801.6Savastano, Matteo; Bazzicalupi, Carla; Gellini, Cristina; Bianchi, Antonio
Infinite supramolecular pseudo-polyrotaxane with poly[3]catenane axle: assembling nanosized rings from mono- and diatomic I<sup>-</sup> and I<sub>2</sub> tectons.
Chemical communications (Cambridge, England), 2020, 56, 551-554
7125447 CIFC78 H62 B2 Fe N6 O8C 1 2 131.9544; 16.4618; 17.8159
90; 104.814; 90		9060.1Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125448 CIFC78 H62 B2 Fe N6 O8C 1 2 132.761; 16.907; 18.032
90; 106.009; 90		9600Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125449 CIFC78 H62 B2 Fe N6 O8C 1 2 132.45; 16.983; 18.105
90; 106.85; 90		9549Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125450 CIFC78 H62 B2 Fe N6 O8C 1 2 132.027; 16.64; 17.903
90; 105.183; 90		9208Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125451 CIFC78 H62 B2 Fe N6 O8C 1 2 131.8352; 16.6477; 17.9355
90; 105.495; 90		9160Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125452 CIFC156 H124 B4 Fe2 N12 O16P 1 21 118.08; 16.715; 32.015
90; 106.028; 90		9299Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125453 CIFCu3 Li O6 Ru2C 1 2/m 15.208536; 9.023652; 6.027403
90; 106.64; 90		271.424Huang, Bin; Liu, Ziyi; Han, Yifeng; Zhao, Shuang; Wu, Meixia; Frank, Corey E.; Greenblatt, Martha; Croft, Mark; Quackenbush, Nicholas F.; Liu, Sizhan; Tyson, Trevor A.; Zhang, Lei; Sun, Junliang; Shan, Pengfei; Dai, Jianhong; Yu, Xiaohui; Cheng, Jinguang; Li, Man-Rong
Nonmetallic metal toward a pressure-induced bad-metal state in two-dimensional Cu<sub>3</sub>LiRu<sub>2</sub>O<sub>6</sub>.
Chemical communications (Cambridge, England), 2019, 56, 265-268
7125454 CIFC57 H55 N5 P2P 1 21/c 115.7507; 17.1271; 18.3836
90; 104.119; 90		4809.42Groß, C; Sun, Y.; Jost, T.; Grimm, T.; Klein, M. P.; Niedner-Schatteburg, G; Becker, S.; Thiel, W. R.
Generation of a zinc and rhodium containing metallomacrocycle by rearrangement of a six-coordinate precursor complex.
Chemical communications (Cambridge, England), 2020, 56, 368-371
7125455 CIFC123 H124 B Cl6 F7 N10 O6 P4 Rh2 S ZnP -115.3537; 19.4633; 22.6951
90.78; 106.494; 109.253		6096Groß, C; Sun, Y.; Jost, T.; Grimm, T.; Klein, M. P.; Niedner-Schatteburg, G; Becker, S.; Thiel, W. R.
Generation of a zinc and rhodium containing metallomacrocycle by rearrangement of a six-coordinate precursor complex.
Chemical communications (Cambridge, England), 2020, 56, 368-371
7125456 CIFC24 H18 Cl N O2P 1 21/n 110.9587; 7.7456; 22.4121
90; 100.151; 90		1872.6Trofimov, B. A.; Belyaeva, K. V.; Nikitina, L. P.; Mal'kina, A. G.; Afonin, A. V.; Ushakov, I. A.; Vashchenko, A. V.
Transition metal-free one-pot double C-H functionalization of quinolines with disubstituted electron-deficient acetylenes.
Chemical communications (Cambridge, England), 2018, 54, 5863-5866
7125457 CIFC21 H15 N O2 SP n a 2110.0386; 16.6863; 10.3764
90; 90; 90		1738.1Trofimov, B. A.; Belyaeva, K. V.; Nikitina, L. P.; Mal'kina, A. G.; Afonin, A. V.; Ushakov, I. A.; Vashchenko, A. V.
Transition metal-free one-pot double C-H functionalization of quinolines with disubstituted electron-deficient acetylenes.
Chemical communications (Cambridge, England), 2018, 54, 5863-5866
7125458 CIFC20 H13 N O2P 1 21/c 112.115; 16.3598; 7.7826
90; 108.183; 90		1465.5Trofimov, B. A.; Belyaeva, K. V.; Nikitina, L. P.; Mal'kina, A. G.; Afonin, A. V.; Ushakov, I. A.; Vashchenko, A. V.
Transition metal-free one-pot double C-H functionalization of quinolines with disubstituted electron-deficient acetylenes.
Chemical communications (Cambridge, England), 2018, 54, 5863-5866
7125459 CIFC15 H12 Br F N2 O3P 1 21/c 115.548; 24.427; 8.266
90; 91.708; 90		3138Zaheer, Mohd Khalid; Gupta, Ekta; Kant, Ruchir; Mohanan, Kishor
Metal-free α-arylation of α-fluoro-α-nitroacetamides employing diaryliodonium salts.
Chemical communications (Cambridge, England), 2019, 56, 153-156
7125460 CIFC32 H56P -19.5552; 9.5131; 17.1505
88.553; 83.021; 87.903		1546.05Takahashi, Tamotsu; Sun, Wen-Hua; Nakajima, Kiyohiko
Formation of cyclooctatetraenes from zirconacyclopentadienes
Chemical Communications, 1999, 1595
7125461 CIFC20 H32 N2 O3P 21 21 2110.861; 20.595; 8.948
90; 90; 90		2001.5Pérollier, Céline; Pécaut, Jacques; Ramasseul, René; Marchon, Jean-Claude; Bau, Robert
High-yield synthesis of a chiroporphyrin by hydrogen bond-directed cyclisation
Chemical Communications, 1999, 1597
7125462 CIFC106 H168 N12 Ni O16 S5P 43 21 215.091; 15.091; 63.545
90; 90; 90		14472Pérollier, Céline; Pécaut, Jacques; Ramasseul, René; Marchon, Jean-Claude; Bau, Robert
High-yield synthesis of a chiroporphyrin by hydrogen bond-directed cyclisation
Chemical Communications, 1999, 1597
7125463 CIFC41 H28 O4C 1 2/c 115.359; 19.181; 10.616
90; 101.12; 90		3068.8Yang, Xiao-Ping; Du, Da-Ming; Li, Qi; Mak, Thomas C. W.; Wong, Henry N. C.
Synthesis, structure and inclusion properties of 1,4,15,18-tetrahydro-1,4,15,18-tetraoxodibenzo[b,h]tetraphenylene†
Chemical Communications, 1999, 1607
7125464 CIFC38 H30 O4C 1 2/c 115.807; 18.59; 10.59
90; 100.55; 90		3059.3Yang, Xiao-Ping; Du, Da-Ming; Li, Qi; Mak, Thomas C. W.; Wong, Henry N. C.
Synthesis, structure and inclusion properties of 1,4,15,18-tetrahydro-1,4,15,18-tetraoxodibenzo[b,h]tetraphenylene†
Chemical Communications, 1999, 1607
7125465 CIFC34 H20 O6P -19.345; 10.121; 14.498
98.648; 101.23; 101.23		1293.7Yang, Xiao-Ping; Du, Da-Ming; Li, Qi; Mak, Thomas C. W.; Wong, Henry N. C.
Synthesis, structure and inclusion properties of 1,4,15,18-tetrahydro-1,4,15,18-tetraoxodibenzo[b,h]tetraphenylene†
Chemical Communications, 1999, 1607
7125466 CIFC38 H28 O4P 1 2/n 110.498; 9.646; 14.687
90; 101.08; 90		1459.5Yang, Xiao-Ping; Du, Da-Ming; Li, Qi; Mak, Thomas C. W.; Wong, Henry N. C.
Synthesis, structure and inclusion properties of 1,4,15,18-tetrahydro-1,4,15,18-tetraoxodibenzo[b,h]tetraphenylene†
Chemical Communications, 1999, 1607
7125467 CIFC23 H38 N2 O4 S2P -19.891; 10.419; 13.574
67.91; 74.89; 87.88		1248.4Coldham, Iain; Crapnell, Katherine M.; Fernàndez, Joan-Carles; Haxell, Thomas F. N.; Treacy, Alan B.; Coles, Simon J.; Hursthouse, Michael B.; Moseley, Jonathan D.
A new stereoselective approach to the manzamine alkaloids
Chemical Communications, 1999, 1757
7125468 CIFN4 S4P 1 21/n 18.7286; 7.0783; 8.6377
90; 93.7219; 90		532.54Scherer, Wolfgang; Spiegler, Michael; Pedersen, Bjørn; Tafipolsky, Maxim; Hieringer, Wolfgang; Reinhard, Björn; Downs, Anthony J.; McGrady, G. Sean
Molecular recognition in the solid state: topology of experimental and theoretical charge densities for tetrasulfur tetranitride
Chemical Communications, 2000, 635
7125469 CIFC66 H753 Mo154 N22 Na3 O804 S22C 1 2/m 136.243; 42.788; 31.541
90; 107.886; 90		46549Müller, Achim; Das, Samar K.; Kuhlmann, Christoph; Bögge, Hartmut; Schmidtmann, Marc; Diemann, Ekkehard; Krickemeyer, Erich; Hormes, Josef; Modrow, Hartwig; Schindler, Matthias
On the option of generating novel type surfaces with multiphilic ligands within the cavity of a giant metal‒oxide based wheel type cluster: chemical reactions with well-defined nanoobjects
Chemical Communications, 2001, 655
7125470 CIFC26 H61 N4 Si2 YP -19.815; 9.859; 17.291
95.6; 90.68; 98.63		1645.7Bambirra, Sergio; van Leusen, Daan; Meetsma, Auke; Hessen, Bart; H. Teuben, Jan
Neutral and cationic yttrium alkyl complexes with linked 1,4,7-triazacyclononane-amide monoanionic ancillary ligands: synthesis and catalytic ethene polymerisation
Chemical Communications, 2001, 637
7125471 CIFC31 H38 Fe N11 O14 PrP -18.3607; 15.4388; 15.4924
84.78; 80.671; 85.655		1961.32Tanase, Stefania; Andruh, Marius; Müller, Achim; Schmidtmann, Marc; Mathonière, Corine; Rombaut, Guillaume
Construction of 3d‒4f heterometallic coordination polymers by simultaneous use of hexacyanometalate building-blocks and exo-bidentate ligands
Chemical Communications, 2001, 1084
7125472 CIFC21 H22 N2 O3P -112.191; 12.434; 12.916
101.743; 104.914; 90.647		1848.09Godsi, O.; Peskin, U.; Kapon, M.; Natan, E.; Eichen, Y.
Site effects in controlling the chemical reactivity in crystals: solid-state photochromism of N-(n-propyl)nitrospiropyrane.
Chemical communications (Cambridge, England), 2001, 2132-2133
7125473 CIFC64 H90 F9 N15 O24.5 Rh3 S3P 21 21 2121.0185; 21.366; 19.4924
90; 90; 90		8753.7Yamanari, Kazuaki; Ito, Rie; Yamamoto, Shiori; Fuyuhiro, Akira
Diastereomeric separation of [{M(Cp*)(ado)}3]3+ (M = RhIII, IrIII; ado = adenosinato): crystal structure of an inclusion compound [{Rh(Cp*)(ado)}3](CF3SO3)3·MeOH
Chemical Communications, 2001, 1414
7125474 CIFC79 H119 Al4 B4 O8P -114.0027; 14.2483; 22.7478
79.888; 86.886; 65.389		4061.2Richter, Bodo; Meetsma, Auke; Hessen, Bart; Teuben, Jan H.
Synthesis and structural characterisation of a boralumoxane capable of activating a zirconocene ethene polymerisation catalyst
Chemical Communications, 2001, 1286
7125475 CIFC31 H39 N3 O4P 1 21/n 114.049; 9.982; 20.886
90; 97.64; 90		2903González-Zamora, E; Fayol, A.; Bois-Choussy, M; Chiaroni, A.; Zhu, J.
Three component synthesis of oxa-bridged tetracyclic tetrahydroquinolines.
Chemical communications (Cambridge, England), 2001, 1684-1685
7125476 CIFC29 H20 Mn2 O4P 1 21/c 112.8434; 8.3575; 22.265
90; 97.62; 90		2368.8Ortin, Y.; Copple, Y.; Lugan, N.; Mathieu, R.; McGlinchey, M. J.
Dynamic equilibration of eta 1-carbene and eta 2-alkyne moieties within an alkynylcarbene dimanganese complex.
Chemical communications (Cambridge, England), 2001, 1690-1691
7125477 CIFC18 H16 Cd N3 O5C 1 2/m 112.6442; 14.7052; 11.158
90; 112.773; 90		1912.94Fu, Z. Y.; Wu, X. T.; Dai, J. C.; Wu, L. M.; Cui, C. P.; Hu, S. M.
Interpenetration in [Cd(isonicotinate)2(1,2-bis(4-pyridyl)-ethane)0.5(H2O)]n, a novel octahedral polymer containing an unusual two-dimensional bilayer motif generated by self-assembly of rectangle building blocks.
Chemical communications (Cambridge, England), 2001, 1856-1857
7125478 CIFC31 H50 B9 Co0.5 N O9 Sr0.25P 42/n :217.7771; 17.7771; 23.6753
90; 90; 90		7481.99Hardie, M. J.; Raston, C. L.; Salinas, A.
A 3,12-connected vertice sharing adamantoid hydrogen bonded network featuring tetrameric clusters of cyclotriveratrylene.
Chemical communications (Cambridge, England), 2001, 1850-1851
7125479 CIFC31 H50 B9 Co0.5 La0.13 N Na0.13 O9P 42/n :217.6914; 17.6914; 23.6592
90; 90; 90		7405Hardie, M. J.; Raston, C. L.; Salinas, A.
A 3,12-connected vertice sharing adamantoid hydrogen bonded network featuring tetrameric clusters of cyclotriveratrylene.
Chemical communications (Cambridge, England), 2001, 1850-1851
7125480 CIFC31 H50 B9 Co0.5 N Na0.125 O9 Y0.125P 42/n :217.6918; 17.6918; 23.7339
90; 90; 90		7428.7Hardie, M. J.; Raston, C. L.; Salinas, A.
A 3,12-connected vertice sharing adamantoid hydrogen bonded network featuring tetrameric clusters of cyclotriveratrylene.
Chemical communications (Cambridge, England), 2001, 1850-1851
7125481 CIFC40 H63 N5 Nb PP -110.584; 12.626; 17.968
106.92; 90.52; 114.37		2069Brask, J. K.; Fickes, M. G.; Sangtrirutnugul, P.; Durà-Vilà, V; Odom, A. L.; Cummins, C. C.
Niobium and vanadium iminophosphinimide complexes.
Chemical communications (Cambridge, England), 2001, 1676-1677
7125482 CIFC4 H12 Au NP 4/n m m :27.599; 7.599; 5.433
90; 90; 90		313.7Dietzel, P. D.; Jansen, M.
Synthesis and crystal structure determination of tetramethylammonium auride.
Chemical communications (Cambridge, England), 2001, 2208-2209
7125483 CIFC12 H20 B2 F8 N4 Ni S4F d d d :216.646; 18.189; 14.887
90; 90; 90		4507Bigoli, F.; Chen, C. T.; Wu, W. C.; Deplano, P.; Mercuri, M. L.; Pellinghelli, M. A.; Pilia, L.; Pintus, G.; Serpe, A.; Trogu, E. F.
[Ni(R2pipdt)2](BF4)2 (R2pipdt = 1,4-disubstituted-piperazine-3,2-dithione) as useful precursors of mixed-ligand dithiolenes of interest for non-linear optics.
Chemical communications (Cambridge, England), 2001, 2246-2247
7125484 CIFC10 H10 N4 Ni S4C 1 2/c 115.381; 13.623; 7.464
90; 106.16; 90		1502.2Bigoli, F.; Chen, C. T.; Wu, W. C.; Deplano, P.; Mercuri, M. L.; Pellinghelli, M. A.; Pilia, L.; Pintus, G.; Serpe, A.; Trogu, E. F.
[Ni(R2pipdt)2](BF4)2 (R2pipdt = 1,4-disubstituted-piperazine-3,2-dithione) as useful precursors of mixed-ligand dithiolenes of interest for non-linear optics.
Chemical communications (Cambridge, England), 2001, 2246-2247
7125485 CIFC20 H24 Co N6 O14I 41/a :219.3309; 19.3309; 13.4691
90; 90; 90		5033.2Blake, A. J.; Brett, M. T.; Champness, N. R.; Khlobystov, A. N.; Long, D. L.; Wilson, C.; Schröder, M
Inorganic-organic interpenetrating frameworks: 4,4'-bipyridine N,N'-dioxide as a bridging hydrogen-bond acceptor.
Chemical communications (Cambridge, England), 2001, 2258-2259
7125486 CIFC10 H12 N3 Ni0.5 O7I 41 c d19.3091; 19.3091; 13.4271
90; 90; 90		5006.2Blake, A. J.; Brett, M. T.; Champness, N. R.; Khlobystov, A. N.; Long, D. L.; Wilson, C.; Schröder, M
Inorganic-organic interpenetrating frameworks: 4,4'-bipyridine N,N'-dioxide as a bridging hydrogen-bond acceptor.
Chemical communications (Cambridge, England), 2001, 2258-2259
7125487 CIFC60 H48 Co N14 O18P -18.9447; 11.716; 14.0734
104.712; 96.797; 98.233		1393.2Blake, A. J.; Brett, M. T.; Champness, N. R.; Khlobystov, A. N.; Long, D. L.; Wilson, C.; Schröder, M
Inorganic-organic interpenetrating frameworks: 4,4'-bipyridine N,N'-dioxide as a bridging hydrogen-bond acceptor.
Chemical communications (Cambridge, England), 2001, 2258-2259
7125488 CIFC47 H41 B F15 Ga N2P 1 21/c 118.1799; 23.84; 21.5818
90; 111.279; 90		8716Hardman, N. J.; Power, P. P.; Gorden, J. D.; Macdonald, C. L.; Cowley, A. H.
Gallium-boron donor-acceptor bonds.
Chemical communications (Cambridge, England), 2001, 1866-1867
7125489 CIFC28 H15 B F15 GaP 1 21/c 19.222; 24; 12.063
90; 93.67; 90		2664.4Hardman, N. J.; Power, P. P.; Gorden, J. D.; Macdonald, C. L.; Cowley, A. H.
Gallium-boron donor-acceptor bonds.
Chemical communications (Cambridge, England), 2001, 1866-1867
7125490 CIFC36 H28 B N6 NaC 1 2/c 117.2064; 12.4777; 15.3058
90; 115.529; 90		2965.27Constable, E. C.; Housecroft, C. E.; Kariuki, B. M.; Kelly, N.; Smith, C. B.
A polymeric sodium complex of 3,6-bis(2-pyridyl)-1,2,4,5-tetrazine.
Chemical communications (Cambridge, England), 2001, 2134-2135
7125491 CIFC46 H59 N3 O17P -111.4558; 11.6273; 18.6627
102.785; 90.042; 102.881		2360Shivanyuk, A.; Rebek, Jr, J
Hydrogen-bonded capsules in polar, protic solvents.
Chemical communications (Cambridge, England), 2001, 2374-2375
7125492 CIFC16 H36 N4 Sn2 Te2P 1 21/n 110.2669; 16.4668; 14.9671
90; 94.6721; 90		2521.97Chivers, T.; Schatte, G.
Synthesis and characterization of [ButNSn(mu-NBut)2TeNBut](mu3-SnTe), a stannanetellurone with four-coordinate tin.
Chemical communications (Cambridge, England), 2001, 2264-2265
7125493 CIFC12 H18 Co N O7P -16.442; 7.007; 9.12
68.79; 89.06; 69.72		357.2Braga, D.; Cojazzi, G.; Emiliani, D.; Maini, L.; Grepioni, F.
Reversible trapping of acid and base vapours into an amphoteric crystalline material.
Chemical communications (Cambridge, England), 2001, 2272-2273
7125494 CIFC17 Cl N6 O3P 1 21/c 115.2023; 7.151; 17.6577
90; 111.213; 90		1789.53Shankland, N.; David, W. I.; Shankland, K.; Kennedy, A. R.; Frampton, C. S.; Florence, A. J.
Structural transformations in zopiclone.
Chemical communications (Cambridge, England), 2001, 2204-2205
7125495 CIFC17 Cl N6 O5P 1 21/c 116.4834; 7.1465; 17.4026
90; 109.807; 90		1928.73Shankland, N.; David, W. I.; Shankland, K.; Kennedy, A. R.; Frampton, C. S.; Florence, A. J.
Structural transformations in zopiclone.
Chemical communications (Cambridge, England), 2001, 2204-2205
7125496 CIFC17 Cl N6 O3P 21 21 215.5813; 8.8467; 35.6588
90; 90; 90		1760.69Shankland, N.; David, W. I.; Shankland, K.; Kennedy, A. R.; Frampton, C. S.; Florence, A. J.
Structural transformations in zopiclone.
Chemical communications (Cambridge, England), 2001, 2204-2205
7125497 CIFC17 H17 Cl N6 O3P 21 21 215.5054; 8.7686; 35.5277
90; 90; 90		1715.09Shankland, N.; David, W. I.; Shankland, K.; Kennedy, A. R.; Frampton, C. S.; Florence, A. J.
Structural transformations in zopiclone.
Chemical communications (Cambridge, England), 2001, 2204-2205
7125498 CIFC17 H17 Cl N6 O3P 21 21 215.5023; 8.7676; 35.5314
90; 90; 90		1714.1Shankland, N.; David, W. I.; Shankland, K.; Kennedy, A. R.; Frampton, C. S.; Florence, A. J.
Structural transformations in zopiclone.
Chemical communications (Cambridge, England), 2001, 2204-2205
7125499 CIFC17 H21 Cl N6 O5P 1 21/c 116.374; 7.03; 17.185
90; 108.62; 90		1874.6Shankland, N.; David, W. I.; Shankland, K.; Kennedy, A. R.; Frampton, C. S.; Florence, A. J.
Structural transformations in zopiclone.
Chemical communications (Cambridge, England), 2001, 2204-2205
7125500 CIFC32 H53 B Co N8 OP 1 21/c 119.9942; 9.8211; 18.7466
90; 109.131; 90		3477.9Thyagarajan, S.; Incarvito, C. D.; Rheingold, A. L.; Theopold, K. H.
Formation and reactivity of a cobalt (II) hydroperoxide intermediate.
Chemical communications (Cambridge, England), 2001, 2198-2199
7125501 CIFC13 H12 P2 S4P 1 21/c 19.8833; 8.837; 18.375
90; 94.948; 90		1598.87Kilian, P.; Slawin, A. M.; Woollins, J. D.
Novel small organo-P-S/Se heterocycles.
Chemical communications (Cambridge, England), 2001, 2288-2289
7125502 CIFC13 H12 P2 Se4P 1 21/c 110.0165; 8.9836; 18.677
90; 93.687; 90		1677.2Kilian, P.; Slawin, A. M.; Woollins, J. D.
Novel small organo-P-S/Se heterocycles.
Chemical communications (Cambridge, England), 2001, 2288-2289
7125503 CIFC15 H16 P2 Se3P n a 2117.7582; 27.4561; 7.1512
90; 90; 90		3486.72Kilian, P.; Slawin, A. M.; Woollins, J. D.
Novel small organo-P-S/Se heterocycles.
Chemical communications (Cambridge, England), 2001, 2288-2289
7125504 CIFC38 H51 Cl2 Mn2 N6 O14P n a 2122.331; 18.351; 10.9217
90; 90; 90		4475.7Boisen, A.; Hazell, A.; McKenzie, C. J.
Structural characterisation of the H-bonded [MnII(OH2)2...(OCH3)2MnIII] motif: a model for resting state hydroxylic solvent coordination in M(II)-M(III) enzymes.
Chemical communications (Cambridge, England), 2001, 2136-2137
7125505 CIFC33 H43 Cl Co N3P 1 21/n 18.8194; 23.121; 15.744
90; 101.076; 90		3150.6Gibson, V. C.; Humphries, M. J.; Tellmann, K. P.; Wass, D. F.; White, A. J.; Williams, D. J.
The nature of the active species in bis(imino)pyridyl cobalt ethylene polymerisation catalysts.
Chemical communications (Cambridge, England), 2001, 2252-2253
7125506 CIFC52 H46 B Co F15 N5P -110.7639; 15.7966; 15.8811
100.546; 102.862; 98.797		2534.7Gibson, V. C.; Humphries, M. J.; Tellmann, K. P.; Wass, D. F.; White, A. J.; Williams, D. J.
The nature of the active species in bis(imino)pyridyl cobalt ethylene polymerisation catalysts.
Chemical communications (Cambridge, England), 2001, 2252-2253
7125507 CIFC56 H104 Si16C 1 2/c 110.317; 48.495; 15.523
90; 105.28; 90		7492Kyushin, Soichiro; Kitahara, Tsukasa; Tanaka, Ryoji; Takeda, Masanori; Matsumoto, Takeshi; Matsumoto, Hideyuki
1,2,9,10,17,18,25,26,27,28,35,36,37,38,39,40-Hexadecasila[28](1,2,4,5)-cyclophane and its open-chain homologs
Chemical Communications, 2001, 2714
7125508 CIFC20 H18 F3 N O4 PdP 1 21/c 112.8622; 17.3734; 8.6466
90; 95.13; 90		1924.4Omnès, L; Timimi, B. A.; Gelbrich, T.; Hursthouse, M. B.; Luckhurst, G. R.; Bruce, D. W.
Specific molecular interactions in Pd(II) complexes identify a new approach to the biaxial nematic phase.
Chemical communications (Cambridge, England), 2001, 2248-2249
7125509 CIFC23 H40 Cl2 N4 O4C 1 c 120.527; 11.3091; 13.0364
90; 110.933; 90		2826.56Arnold, P. L.; Scarisbrick, A. C.; Blake, A. J.; Wilson, C.
Chelating alkoxy-N-heterocyclic carbene complexes of silver and copper.
Chemical communications (Cambridge, England), 2001, 2340-2341
7125510 CIFC23 H31 Cu N4 OC 1 2/c 121.33; 12.2341; 25.177
90; 112.377; 90		6075.3Arnold, P. L.; Scarisbrick, A. C.; Blake, A. J.; Wilson, C.
Chelating alkoxy-N-heterocyclic carbene complexes of silver and copper.
Chemical communications (Cambridge, England), 2001, 2340-2341
7125511 CIFC43 H90 O7 P Re Si3P -113.2908; 13.4716; 17.7266
96.464; 104.696; 116.971		2639.1Veige, Adam S.; Wolczanski, Peter T.; Lobkovsky, Emil B.
(silox)3RePMe3 (silox = tBu3SiO) is carbonylated to the double insertion product (silox)(Me3P){cis-(CO)2}Re{ trans-(CO2SitBu3)2 }
Chemical Communications, 2001, 2734
7125512 CIFC37 H81 O4 Re Si3P 1 21/n 18.701; 21.072; 24.334
90; 93.89; 90		4451.3Veige, Adam S.; Wolczanski, Peter T.; Lobkovsky, Emil B.
(silox)3RePMe3 (silox = tBu3SiO) is carbonylated to the double insertion product (silox)(Me3P){cis-(CO)2}Re{ trans-(CO2SitBu3)2 }
Chemical Communications, 2001, 2734
7125513 CIFC5 H21 N3 O16 P4 Zn3P -18.4408; 9.263; 13.843
81.119; 83.643; 72.647		1018.3Neeraj, S.; Forster, P. M.; Rao, C. N. R.; Cheetham, A. K.
A new route for the synthesis of open-framework metal phosphates using organophosphates
Chemical Communications, 2001, 2716
7125514 CIFC6 H4.5 N2 O18.25 P4 Zn5P 1 21/n 15.1601; 25.075; 14.986
90; 92.61; 90		1937Neeraj, S.; Forster, P. M.; Rao, C. N. R.; Cheetham, A. K.
A new route for the synthesis of open-framework metal phosphates using organophosphates
Chemical Communications, 2001, 2716
7125515 CIFC2 H7 Co N O6 P1.5C 1 2/c 113.444; 12.874; 8.224
90; 94.64; 90		1418.7Neeraj, S.; Forster, P. M.; Rao, C. N. R.; Cheetham, A. K.
A new route for the synthesis of open-framework metal phosphates using organophosphates
Chemical Communications, 2001, 2716
7125516 CIFC4 H12 Co2 N2 O8 P2P -15.1534; 10.7578; 10.8329
66.381; 89.058; 81.674		543.89Neeraj, S.; Forster, P. M.; Rao, C. N. R.; Cheetham, A. K.
A new route for the synthesis of open-framework metal phosphates using organophosphates
Chemical Communications, 2001, 2716
7125517 CIFC1.71 H0 Co N0.71 O3.43 P0.86R -3 :H13.4892; 13.4892; 14.984
90; 90; 120		2361.2Neeraj, S.; Forster, P. M.; Rao, C. N. R.; Cheetham, A. K.
A new route for the synthesis of open-framework metal phosphates using organophosphates
Chemical Communications, 2001, 2716
7125518 CIFC24 H26 B2 N12 TiC 1 2/c 121.175; 16.6805; 7.568
90; 90.261; 90		2673.1Kayal, A.; Kuncheria, J.; Lee, S. C.
Bis[hydrotris(pyrazol-1-yl)borato]titanium(II): a stable Tp2M complex of singular reactivity.
Chemical communications (Cambridge, England), 2001, 2482-2483
7125519 CIFC18 H20 B2 F6 N12 P TiI 4/m13.4375; 13.4375; 14.2741
90; 90; 90		2577.4Kayal, A.; Kuncheria, J.; Lee, S. C.
Bis[hydrotris(pyrazol-1-yl)borato]titanium(II): a stable Tp2M complex of singular reactivity.
Chemical communications (Cambridge, England), 2001, 2482-2483
7125520 CIFC60 H64 B4 N24 O Ti2P n a 2120.5983; 15.627; 20.2307
90; 90; 90		6512.1Kayal, A.; Kuncheria, J.; Lee, S. C.
Bis[hydrotris(pyrazol-1-yl)borato]titanium(II): a stable Tp2M complex of singular reactivity.
Chemical communications (Cambridge, England), 2001, 2482-2483
7125521 CIFC18 H20 B2 N12 Se TiP b c a17.2584; 17.2192; 31.9869
90; 90; 90		9505.7Kayal, A.; Kuncheria, J.; Lee, S. C.
Bis[hydrotris(pyrazol-1-yl)borato]titanium(II): a stable Tp2M complex of singular reactivity.
Chemical communications (Cambridge, England), 2001, 2482-2483
7125522 CIFC18 H20 B2 N12 S2 TiP b c a17.0677; 17.2213; 32.9623
90; 90; 90		9688.5Kayal, A.; Kuncheria, J.; Lee, S. C.
Bis[hydrotris(pyrazol-1-yl)borato]titanium(II): a stable Tp2M complex of singular reactivity.
Chemical communications (Cambridge, England), 2001, 2482-2483
7125523 CIFC31 H47 Co P6P 1 21/c 19.634; 32.706; 10.51
90; 98.16; 90		3278.1Hitchcock, Peter B.; Nixon, John F.; Büyükkidan, Nurgün Sakarya
Remarkable organophosphorus cage compounds from the reaction of cobaltocene and the triphosphole P3C2But2CH(SiMe3) 2: crystal and molecular structures of [Co(η5-C5H5)(η4-C 4H4CHCHP6C4But 4)] and P6C4But4CH(SiMe3)
Chemical Communications, 2001, 2720
7125524 CIFC24 H46 P6 SiP -110.2274; 12.3429; 12.7112
100.21; 97.134; 102		1522.92Hitchcock, Peter B.; Nixon, John F.; Büyükkidan, Nurgün Sakarya
Remarkable organophosphorus cage compounds from the reaction of cobaltocene and the triphosphole P3C2But2CH(SiMe3) 2: crystal and molecular structures of [Co(η5-C5H5)(η4-C 4H4CHCHP6C4But 4)] and P6C4But4CH(SiMe3)
Chemical Communications, 2001, 2720
7125525 CIFC14 H20 Mo0.5 O2.5P 4/n n c :222.5679; 22.5679; 13.0099
90; 90; 90		6626.1Liu, Cai-Ming; Restorp, Per; Nordlander, Ebbe; Pierpont, Cortlandt G.
Oxo-deficient dioxylene complexes of Mo(vi) containing 3,6-di-tert-butylcatechol
Chemical Communications, 2001, 2686
7125526 CIFC30 H46 Mo O6 SP -112.2701; 16.7146; 18.4327
92.217; 90.072; 93.114		3771.9Liu, Cai-Ming; Restorp, Per; Nordlander, Ebbe; Pierpont, Cortlandt G.
Oxo-deficient dioxylene complexes of Mo(vi) containing 3,6-di-tert-butylcatechol
Chemical Communications, 2001, 2686
7125527 CIFC34 H54 Mo O6C 1 2/c 111.1595; 29.0306; 11.8944
90; 116.703; 90		3442.42Liu, Cai-Ming; Restorp, Per; Nordlander, Ebbe; Pierpont, Cortlandt G.
Oxo-deficient dioxylene complexes of Mo(vi) containing 3,6-di-tert-butylcatechol
Chemical Communications, 2001, 2686
7125528 CIFC8 H12 Ag F3 N2 O2C m c e12.5745; 12.3972; 14.2861
90; 90; 90		2227.04Brammer, L.; Burgard, M. D.; Rodger, C. S.; Swearingen, J. K.; Rath, N. P.
Silver(I) carboxylates: versatile inorganic analogs of carboxylic acids for supramolecular network formation.
Chemical communications (Cambridge, England), 2001, 2468-2469
7125529 CIFC10 H12 Ag F3 N2 O2P -19.0587; 9.1231; 9.6097
117.553; 116.433; 91.471		603.07Brammer, L.; Burgard, M. D.; Rodger, C. S.; Swearingen, J. K.; Rath, N. P.
Silver(I) carboxylates: versatile inorganic analogs of carboxylic acids for supramolecular network formation.
Chemical communications (Cambridge, England), 2001, 2468-2469
7125530 CIFC6 H4 Ag F3 N2 O2C 1 2/c 112.766; 10.141; 7.0078
90; 102.03; 90		887.3Brammer, L.; Burgard, M. D.; Rodger, C. S.; Swearingen, J. K.; Rath, N. P.
Silver(I) carboxylates: versatile inorganic analogs of carboxylic acids for supramolecular network formation.
Chemical communications (Cambridge, England), 2001, 2468-2469
7125531 CIFC24 H35 N O10 SP 21 21 219.7493; 15.794; 17.251
90; 90; 90		2656.3Enders, D.; Berner, O. M.; Vignola, N.; Bats, J. W.
Diastereo- and enantioselective synthesis of alpha,beta-disubstituted gamma-nitro methyl sulfonates.
Chemical communications (Cambridge, England), 2001, 2498-2499
7125532 CIFC14 H20 As Li N2 O2P n a 2111.83; 8.6933; 14.914
90; 90; 90		1533.8Paver, M. A.; Joy, J. S.; Hursthouse, M. B.
The first example of a diazaarsolyl anion: structure and coordination polymerisation of the aromatic metallacycle benzo[1,3,2]diazaarsolyl lithium.2THF.
Chemical communications (Cambridge, England), 2001, 2480-2481
7125533 CIFC15 H24 O Si2P n a 2112.4355; 13.6661; 9.8989
90; 90; 90		1682.27Blake, Alexander J.; Giblin, Gerard M. P.; Kirk, Douglas T.; Simpkins, Nigel S.; Wilson, Claire
The enantioselective generation of bridgehead enolates
Chemical Communications, 2001, 2668
7125534 CIFC12 H16 O SiP 1 21 16.1568; 7.4191; 12.9873
90; 101.996; 90		580.28Blake, Alexander J.; Giblin, Gerard M. P.; Kirk, Douglas T.; Simpkins, Nigel S.; Wilson, Claire
The enantioselective generation of bridgehead enolates
Chemical Communications, 2001, 2668
7125535 CIFC10 H7 N O2P -15.539; 7.2645; 10.4291
83.673; 83.789; 80.624		409.77Ramtohul, Yeeman K.; Martin, Nathaniel I.; Silkin, Lara; James, Michael N. G.; Vederas, John C.
Pseudoxazolones, a new class of inhibitors for cysteine proteinases: inhibition of hepatitis A virus and human rhinovirus 3C proteinases
Chemical Communications, 2001, 2740
7125536 CIFC11 H9 N O2P -16.0008; 7.237; 10.9282
95.403; 101.029; 102.046		451.1Ramtohul, Yeeman K.; Martin, Nathaniel I.; Silkin, Lara; James, Michael N. G.; Vederas, John C.
Pseudoxazolones, a new class of inhibitors for cysteine proteinases: inhibition of hepatitis A virus and human rhinovirus 3C proteinases
Chemical Communications, 2001, 2740
7125537 CIFC24 H32 N4P 1 21/a 116.123; 8.683; 16.789
90; 118.319; 90		2069.1Tripier, Raphaël; Lagrange, Jean-Marie; Espinosa, Enrique; Denat, Franck; Guilard, Roger
From new tricyclic bisaminal derivatives to trans-N,N′-disubstituted cyclams
Chemical Communications, 2001, 2728
7125538 CIFC22 H30 N6P 1 21/c 112.399; 12.813; 12.525
90; 96.354; 90		1977.6Tripier, Raphaël; Lagrange, Jean-Marie; Espinosa, Enrique; Denat, Franck; Guilard, Roger
From new tricyclic bisaminal derivatives to trans-N,N′-disubstituted cyclams
Chemical Communications, 2001, 2728
7125539 CIFC26 H50 Cl2 N6 O4 Pd S4P 1 21/c 115.283; 11.365; 10.302
90; 95.31; 90		1781.7Love, Jason B.; Vere, Joanna M.; Glenny, Mark W.; Blake, Alexander J.; Schröder, Martin
Ditopic azathioether macrocycles as hosts for transition metal saltsElectronic supplementary information (ESI) available: full experimental details. See http://www.rsc.org/suppdata/cc/b1/b109486f/
Chemical Communications, 2001, 2678
7125540 CIFC34 H66 Cl6 Cu3 N8 O5 S6P 1 21/n 19.419; 17.06; 33.09
90; 93.2; 90		5309Love, Jason B.; Vere, Joanna M.; Glenny, Mark W.; Blake, Alexander J.; Schröder, Martin
Ditopic azathioether macrocycles as hosts for transition metal saltsElectronic supplementary information (ESI) available: full experimental details. See http://www.rsc.org/suppdata/cc/b1/b109486f/
Chemical Communications, 2001, 2678
7125541 CIFC17 H27 Ag N5 O5 S3I b a 234.987; 8.892; 16.046
90; 90; 90		4992Love, Jason B.; Vere, Joanna M.; Glenny, Mark W.; Blake, Alexander J.; Schröder, Martin
Ditopic azathioether macrocycles as hosts for transition metal saltsElectronic supplementary information (ESI) available: full experimental details. See http://www.rsc.org/suppdata/cc/b1/b109486f/
Chemical Communications, 2001, 2678
7125542 CIFC13 H13 Br O2P 1 21 115.468; 5.6049; 15.501
90; 98.61; 90		1328.7Ma, Shengming; Shi, Zhangjie
Mechanistic switch leading to highly efficient chirality transfer in Pd(0)-catalyzed coupling-cyclization of aryl iodides with 1:1 acid-base salts of 2,3-allenoic acids and L-(-)-cinchonidine or D-(+)-/L-(-)-alpha-methylbenzylamine. Enantioselective synthesis of highly optically active 3-aryl polysubstituted butenolides.
Chemical communications (Cambridge, England), 2002, 540-541
7125543 CIFC19 H17 Br O2P 1 21 15.7446; 8.535; 16.9094
90; 95.02; 90		825.9Ma, Shengming; Shi, Zhangjie
Mechanistic switch leading to highly efficient chirality transfer in Pd(0)-catalyzed coupling-cyclization of aryl iodides with 1:1 acid-base salts of 2,3-allenoic acids and L-(-)-cinchonidine or D-(+)-/L-(-)-alpha-methylbenzylamine. Enantioselective synthesis of highly optically active 3-aryl polysubstituted butenolides.
Chemical communications (Cambridge, England), 2002, 540-541
7125544 CIFC96 H105 F18 N15 O25 Pt3 S6P -115.2398; 18.154; 23.4615
79.115; 84.232; 77.554		6212.2Qin, Zengquan; Jennings, Michael C.; Puddephatt, Richard J.
Stacked molecular triangles: self-assembly using coordination chemistry and hydrogen bonding
Chemical Communications, 2001, 2676
7125545 CIFC44 H32 Cl4 Co2 N4 O4P 1 21/n 18.5272; 18.3653; 13.3493
90; 103.574; 90		2032.2Fiscus, Jeffrey E.; Shotwell, Sandra; Layland, Ralph C.; Smith, Mark D.; zur Loye, Hans-Conrad; Bunz, Uwe H. F.
Three unique coordination geometries involving 1,2-dimethoxy-4,5-bis(2-pyridylethynyl)benzene
Chemical Communications, 2001, 2674
7125546 CIFC27 H26 Cu N2 O7P -18.2357; 12.5088; 13.3128
78.3; 72.117; 76.681		1257.12Fiscus, Jeffrey E.; Shotwell, Sandra; Layland, Ralph C.; Smith, Mark D.; zur Loye, Hans-Conrad; Bunz, Uwe H. F.
Three unique coordination geometries involving 1,2-dimethoxy-4,5-bis(2-pyridylethynyl)benzene
Chemical Communications, 2001, 2674
7125547 CIFC31 H30 Cl2 N2 O10 Rh2C 1 2/c 121.5985; 20.248; 8.0207
90; 103.265; 90		3414.1Fiscus, Jeffrey E.; Shotwell, Sandra; Layland, Ralph C.; Smith, Mark D.; zur Loye, Hans-Conrad; Bunz, Uwe H. F.
Three unique coordination geometries involving 1,2-dimethoxy-4,5-bis(2-pyridylethynyl)benzene
Chemical Communications, 2001, 2674
7125548 CIFC6 H16.5 Fe0.5 O9 S1.5R -3 :H13.979; 13.979; 23.869
90; 90; 120		4039.4Dalrymple, Sean A.; Parvez, Masood; Shimizu, George K. H.
Supramolecular encapsulation of hexaaquo metal ions by second sphere coordination
Chemical Communications, 2001, 2672
7125549 CIFC23 H15 B F4 O6 Ru3P -114.292; 10.397; 9.281
93.04; 103.04; 107.29		1272.1Griffith, Christopher S.; Koutsantonis, George A.; Skelton, Brian W.; White, Allan H.
Reactions of metalloalkynes. New C2 bonding mode in a trimetallic complex.
Chemical communications (Cambridge, England), 2002, 2174-2175
7125550 CIFC20 H19 Cl2 N3 TiP 21 21 219.868; 10.32; 18.84
90; 90; 90		1918.6Kretschmer, Winfried P.; Dijkhuis, Chris; Meetsma, Auke; Hessen, Bart; Teuben, Jan H.
A highly efficient titanium-based olefin polymerisation catalyst with a monoanionic iminoimidazolidide pi-donor ancillary ligand.
Chemical communications (Cambridge, England), 2002, 608-609
7125551 CIFC38 H39 Cl4 O4 RhP 1 21/n 110.705; 20.317; 16.187
90; 93.46; 90		3514.1Ishii, Youichi; Onaka, Ken-ichi; Hirakawa, Hidehiko; Shiramizu, Kohei
Site-selective and stepwise complexation of two M(cod)+ (M = Rh, Ir) fragments with calix[4]arene.
Chemical communications (Cambridge, England), 2002, 1150-1151
7125552 CIFC45 H48 Cl2 O4 Rh2P 1 21/c 18.8; 19.972; 22.563
90; 100.86; 90		3894.5Ishii, Youichi; Onaka, Ken-ichi; Hirakawa, Hidehiko; Shiramizu, Kohei
Site-selective and stepwise complexation of two M(cod)+ (M = Rh, Ir) fragments with calix[4]arene.
Chemical communications (Cambridge, England), 2002, 1150-1151
7125553 CIFC44 H46 Ir O4 RhP -113.593; 13.72; 19.038
93.94; 98.81; 90.4		3499.8Ishii, Youichi; Onaka, Ken-ichi; Hirakawa, Hidehiko; Shiramizu, Kohei
Site-selective and stepwise complexation of two M(cod)+ (M = Rh, Ir) fragments with calix[4]arene.
Chemical communications (Cambridge, England), 2002, 1150-1151
7125554 CIFC48 H36 N4 O4P 1 21/n 110.168; 33.916; 11.277
90; 98.58; 90		3845.4Varshney, Dushyant B.; Papaefstathiou, Giannis S.; MacGillivray, Leonard R.
Site-directed regiocontrolled synthesis of a 'head-to-head' photodimer via a single-crystal-to-single-crystal transformation involving a linear template.
Chemical communications (Cambridge, England), 2002, 1964-1965
7125555 CIFC48 H36 N4 O8P 1 21/n 110.169; 34.357; 11.181
90; 100.32; 90		3843.2Varshney, Dushyant B.; Papaefstathiou, Giannis S.; MacGillivray, Leonard R.
Site-directed regiocontrolled synthesis of a 'head-to-head' photodimer via a single-crystal-to-single-crystal transformation involving a linear template.
Chemical communications (Cambridge, England), 2002, 1964-1965
7125556 CIFC14 H11 N3 O3P b c a10.8897; 14.2214; 15.2607
90; 90; 90		2363.4Henderson, Alistair P.; Mutlu, Esra; Leclercq, Amélie; Bleasdale, Christine; Clegg, William; Henderson, Richard A.; Golding, Bernard T.
Trapping of benzene oxide-oxepin and methyl-substituted derivatives with 4-phenyl- and 4-pentafluorophenyl-1,2,4-triazoline-3,5-dione.
Chemical communications (Cambridge, England), 2002, 1956-1957
7125557 CIFC16 H15 N3 O3P n a 2113.5339; 11.3119; 9.3316
90; 90; 90		1428.61Henderson, Alistair P.; Mutlu, Esra; Leclercq, Amélie; Bleasdale, Christine; Clegg, William; Henderson, Richard A.; Golding, Bernard T.
Trapping of benzene oxide-oxepin and methyl-substituted derivatives with 4-phenyl- and 4-pentafluorophenyl-1,2,4-triazoline-3,5-dione.
Chemical communications (Cambridge, England), 2002, 1956-1957
7125558 CIFC26 H24 Cl4 N6 O5P -19.1142; 9.5955; 17.0216
85.792; 78.365; 74.561		1405.1Henderson, Alistair P.; Mutlu, Esra; Leclercq, Amélie; Bleasdale, Christine; Clegg, William; Henderson, Richard A.; Golding, Bernard T.
Trapping of benzene oxide-oxepin and methyl-substituted derivatives with 4-phenyl- and 4-pentafluorophenyl-1,2,4-triazoline-3,5-dione.
Chemical communications (Cambridge, England), 2002, 1956-1957
7125559 CIFC301 H618.8 O237.4P 1 21 132.537; 19.013; 33.136
90; 98.428; 90		20277Harata, Kazuaki; Akasaka, Hiroaki; Endo, Tomohiro; Nagase, Hiromasa; Ueda, Haruhisa
X-ray structure of the delta-cyclodextrin complex with cycloundecanone.
Chemical communications (Cambridge, England), 2002, 1968-1969
7125560 CIFC93 H108 F9 N6 Na3 O21 S3P 1 21/c 134.5427; 23.4946; 27.6861
90; 96.908; 90		22306Capó, Magdalena; Saá, José M; Alvarez, Angel
Self-assembly of a stereoselective trinuclear sodium/lithium triple helix.
Chemical communications (Cambridge, England), 2002, 1982-1983
7125561 CIFC93 H108 F9 Li3 N6 O21 S3P 1 21/n 115.331; 27.404; 23.137
90; 98.033; 90		9625Capó, Magdalena; Saá, José M; Alvarez, Angel
Self-assembly of a stereoselective trinuclear sodium/lithium triple helix.
Chemical communications (Cambridge, England), 2002, 1982-1983
7125562 CIFC11 H19 I7 N3 Pb2 S2A e a 28.838; 41.52; 8.769
90; 90; 90		3218Zhu, Xu-Hui; Mercier, Nicolas; Riou, Amédée; Blanchard, Philippe; Frère, Pierre
(C4H3SCH2NH3)2(CH3NH3)Pb2I7: non-centrosymmetrical crystal structure of a bilayer hybrid perovskite.
Chemical communications (Cambridge, England), 2002, 2160-2161
7125563 CIFC10 H16 I4 N2 Pb S2P b c a8.842; 8.693; 28.995
90; 90; 90		2228.7Zhu, Xu-Hui; Mercier, Nicolas; Riou, Amédée; Blanchard, Philippe; Frère, Pierre
(C4H3SCH2NH3)2(CH3NH3)Pb2I7: non-centrosymmetrical crystal structure of a bilayer hybrid perovskite.
Chemical communications (Cambridge, England), 2002, 2160-2161
7125564 CIFC32 H72 Br16 Cl2 N2 PtP 1 21/c 111.604; 15.53; 17.764
90; 108.671; 90		3033Berkei, Michael; Bickley, Jamie F.; Heaton, Brian T.; Steiner, Alexander
Polymeric anionic networks using dibromine as a crosslinker; the preparation and crystal structure of [(C4H9)4N]2[Pt2Br10].(Br2)7 and [(C4H9)4N]2[PtBr4Cl2].(Br2)6.
Chemical communications (Cambridge, England), 2002, 2180-2181
7125565 CIFC32 H72 Br24 N2 Pt2P -111.3186; 17.1659; 18.743
103.257; 101.864; 93.605		3445.7Berkei, Michael; Bickley, Jamie F.; Heaton, Brian T.; Steiner, Alexander
Polymeric anionic networks using dibromine as a crosslinker; the preparation and crystal structure of [(C4H9)4N]2[Pt2Br10].(Br2)7 and [(C4H9)4N]2[PtBr4Cl2].(Br2)6.
Chemical communications (Cambridge, England), 2002, 2180-2181
7125566 CIFC7 H7 N O3 S ZnP 1 21 19.099; 5.098; 10.075
90; 108.445; 90		443.3Kondo, Mitsuru; Miyazawa, Makoto; Irie, Yasuhiko; Shinagawa, Reiko; Horiba, Tomonori; Nakamura, Akira; Naito, Tetsuyoshi; Maeda, Kenji; Utsuno, Shunji; Uchida, Fumio
A new Zn(II) coordination polymer with 4-pyridylthioacetate: assemblies of homo-chiral helices with sulfide sites.
Chemical communications (Cambridge, England), 2002, 2156-2157
7125567 CIFC24 H20 N5 O7 ZnP -110.0919; 11.3865; 12.1526
88.182; 68.57; 69.239		1207.82Wagner, Brian D.; McManus, Gregory J.; Moulton, Brian; Zaworotko, Michael J.
Exciplex fluorescence of ([Zn(bipy)1.5(NO3)2)].CH3OH.0.5pyrene)n: a coordination polymer containing intercalated pyrene molecules (bipy = 4,4'-bipyridine).
Chemical communications (Cambridge, England), 2002, 2176-2177
7125568 CIFC27 H31 Cl Cu F3 N4 O4.5 SC 1 2 129.723; 8.506; 11.882
90; 94.335; 90		2995Pallavicini, Piersandro; Amendola, Valeria; Massera, Chiara; Mundum, Etienne; Taglietti, Angelo
'On-off-on' fluorescent indicators of pH windows based on three separated components.
Chemical communications (Cambridge, England), 2002, 2452-2453
7125569 CIFC2.5 H0.5 Fe0.5 O2C 1 2/m 16.2378; 17.589; 4.6039
90; 115.863; 90		454.53Sanselme, M.; Grenèche, J M; Riou-Cavellec, M; Férey, G
[Fe2(C10O8H2)]: an antiferromagnetic 3D iron(II) carboxylate built from ferromagnetic edge-sharing octahedral chains (MIL-62).
Chemical communications (Cambridge, England), 2002, 2172-2173
7125570 CIFC132 H168 Na6 O36 Sb6P -115.7605; 16.6786; 17.2709
103.943; 100.057; 98.356		4254.2Paver, Michael A.; Joy, Jonathan S.; Hursthouse, Michael B.
A twenty-four membered mixed-metal macrocycle; synthesis and structure of cyclo-[(3-Me-1,2-C6H3O2)2SbNa(THF)2]6.
Chemical communications (Cambridge, England), 2002, 2150-2151
7125571 CIFC19 H11 Mn3 O10.5 S0.5P 41 21 216.798; 16.798; 16.2379
90; 90; 90		4581.9Oh, Moonhyun; Carpenter, Gene B.; Sweigart, Dwight A.
A coordination network containing metal-organometallic secondary building units based on pi-bonded benzoquinone complexes.
Chemical communications (Cambridge, England), 2002, 2168-2169
7125572 CIFC18 H28 Cr N2 Si2P b c a9.504; 20.006; 22.638
90; 90; 90		4304.3Gallant, Amanda J.; Smith, Kevin M.; Patrick, Brian O.
Cyclopentadienyl benzamidinato chromium complexes as models for alkyl halide activation by chromium reagents.
Chemical communications (Cambridge, England), 2002, 2914-2915
7125573 CIFC25 H35 Cr N2 Si2P 1 21/n 111.3146; 21.332; 11.9997
90; 113.493; 90		2656.21Gallant, Amanda J.; Smith, Kevin M.; Patrick, Brian O.
Cyclopentadienyl benzamidinato chromium complexes as models for alkyl halide activation by chromium reagents.
Chemical communications (Cambridge, England), 2002, 2914-2915
7125574 CIFC18 H28 Cl Cr N2 Si2P 1 21/n 110.1145; 12.0381; 18.5467
90; 104.055; 90		2190.63Gallant, Amanda J.; Smith, Kevin M.; Patrick, Brian O.
Cyclopentadienyl benzamidinato chromium complexes as models for alkyl halide activation by chromium reagents.
Chemical communications (Cambridge, England), 2002, 2914-2915
7125575 CIFC26 H34 Cr F3 N2 Si2C 1 2/c 116.205; 9.982; 35.488
90; 97.757; 90		5688Gallant, Amanda J.; Smith, Kevin M.; Patrick, Brian O.
Cyclopentadienyl benzamidinato chromium complexes as models for alkyl halide activation by chromium reagents.
Chemical communications (Cambridge, England), 2002, 2914-2915
7125576 CIFC67 H121 N13 O17P 1 21 117.179; 13.686; 19.053
90; 108.845; 90		4239Aravinda, Subrayashastry; Shamala, Narayanaswamy; Desiraju, Shrilakshmi; Balaram, Padmanabhan
A right handed peptide helix containing a central double D-amino acid segment.
Chemical communications (Cambridge, England), 2002, 2454-2455
7125577 CIFC26 H22P 1 21/c 17.4391; 26.165; 9.2788
90; 92.125; 90		1804.8Geertsema, Edzard M.; Koumura, Nagatoshi; ter Wiel, Matthijs K. J.; Meetsma, Auke; Feringa, Ben L.
In control of the speed of rotation in molecular motors. Unexpected retardation of rotary motion.
Chemical communications (Cambridge, England), 2002, 2962-2963
7125578 CIFC23 H48 Cl N P2 RuP 21 21 218.439; 14.581; 21.989
90; 90; 90		2705.73Kuznetsov, Vladimir F.; Lough, Alan J.; Gusev, Dmitry G.
Triple C-H activation of 1,5-bis(di-tert-butylphosphino)-2-(S)-dimethylaminopentane on ruthenium gives a chiral carbene complex.
Chemical communications (Cambridge, England), 2002, 2432-2433
7125579 CIFC16 H65 N4 Na2 O47 P W11C 1 c 118.494; 18.102; 19.214
90; 106.206; 90		6176.8Honma, Noritaka; Kusaka, Katsuhiro; Ozeki, Tomoji
Self-assembly of a lacunary alpha-Keggin undecatungstophosphate into a three-dimensional network linked by s-block cations.
Chemical communications (Cambridge, England), 2002, 2896-2897
7125580 CIFC22 H18 B2 F8 Fe N10P 1 21 18.4615; 8.3695; 18.759
90; 97.15; 90		1318.2Money, Victoria A.; Evans, Ivana Radosavljevic; Halcrow, Malcolm A.; Goeta, Andrés E; Howard, Judith A. K.
Light induced excited high spin-state trapping in [FeL2](BF4)2 (L = 2,6-di(pyrazol-1-yl)pyridine).
Chemical communications (Cambridge, England), 2003, 158-159
7125581 CIFC22 H18 B2 F8 Fe N10P 1 21 18.4098; 8.4731; 18.2909
90; 98.575; 90		1288.79Money, Victoria A.; Evans, Ivana Radosavljevic; Halcrow, Malcolm A.; Goeta, Andrés E; Howard, Judith A. K.
Light induced excited high spin-state trapping in [FeL2](BF4)2 (L = 2,6-di(pyrazol-1-yl)pyridine).
Chemical communications (Cambridge, England), 2003, 158-159
7125582 CIFC39 H47 N2 P2 Si2 SmP 1 21/n 112.305; 19.623; 15.65
90; 99.364; 90		3728.5Zulys, Agustino; Panda, Tarun K.; Gamer, Michael T.; Roesky, Peter W.
A samarium cyclooctatetraene complex as catalyst for hydroamination/cyclisation catalysis.
Chemical communications (Cambridge, England), 2004, 2584-2585
7125583 CIFC48 H64 Mg N8 Na2P 1 21/a 115.83; 16.8625; 17.9095
90; 91.237; 90		4779.53Conway, Ben; Hevia, Eva; Kennedy, Alan R.; Mulvey, Robert E.
Structurally-defined direct C-magnesiation and C-zincation of N-heterocyclic aromatic compounds using alkali-metal-mediated metallation.
Chemical communications (Cambridge, England), 2007, 2864-2866
7125584 CIFC24 H32 N4 ZnP 21 21 2112.2666; 13.1709; 14.3918
90; 90; 90		2325.17Conway, Ben; Hevia, Eva; Kennedy, Alan R.; Mulvey, Robert E.
Structurally-defined direct C-magnesiation and C-zincation of N-heterocyclic aromatic compounds using alkali-metal-mediated metallation.
Chemical communications (Cambridge, England), 2007, 2864-2866
7125585 CIFC24 H49 N4 Na ZnP 21 21 2110.9318; 14.4362; 17.5664
90; 90; 90		2772.22Conway, Ben; Hevia, Eva; Kennedy, Alan R.; Mulvey, Robert E.
Structurally-defined direct C-magnesiation and C-zincation of N-heterocyclic aromatic compounds using alkali-metal-mediated metallation.
Chemical communications (Cambridge, England), 2007, 2864-2866
7125586 CIFC38 H50 N2 O4 SP -111.464; 12.033; 14.111
83.464; 81.891; 69.071		1795.7Kuhlmann, Jan-Carlos; de Bruyn, Paul; Bouwer, Ricardo K. M.; Meetsma, Auke; Blom, Paul W. M.; Hummelen, Jan C.
Improving the compatibility of fullerene acceptors with fluorene-containing donor-polymers in organic photovoltaic devices.
Chemical communications (Cambridge, England), 2010, 46, 7232-7234
7125587 CIFC6 H6 Eu N4C 1 2/c 19.436; 10.408; 7.177
90; 90.05; 90		704.9Zurawski, Alexander; Mai, Marit; Baumann, Dominik; Feldmann, Claus; Müller-Buschbaum, Klaus
Homoleptic imidazolate frameworks [Sr(1-x)Eu(x)(Im)2]‒hybrid materials with efficient and tuneable luminescence.
Chemical communications (Cambridge, England), 2011, 47, 496-498
7125588 CIFC6 H6 N4 SrC 1 2/c 19.4371; 10.4565; 7.2353
90; 89.96; 90		713.97Zurawski, Alexander; Mai, Marit; Baumann, Dominik; Feldmann, Claus; Müller-Buschbaum, Klaus
Homoleptic imidazolate frameworks [Sr(1-x)Eu(x)(Im)2]–hybrid materials with efficient and tuneable luminescence.
Chemical communications (Cambridge, England), 2011, 47, 496-498
7125589 CIFC12 H14 Eu N8P 1 21/n 110.55; 10.559; 13.782
90; 95.16; 90		1529.1Zurawski, Alexander; Mai, Marit; Baumann, Dominik; Feldmann, Claus; Müller-Buschbaum, Klaus
Homoleptic imidazolate frameworks [Sr(1-x)Eu(x)(Im)2]‒hybrid materials with efficient and tuneable luminescence.
Chemical communications (Cambridge, England), 2011, 47, 496-498
7125590 CIFC64 H100 Cu2 N12 O20P 1 21/c 111.847; 19.317; 37.831
90; 93.95; 90		8637Wenzel, Marco; Knapp, Quintin W.; Plieger, Paul G.
A bis-salicylaldoximato-copper(II) receptor for selective sulfate uptake.
Chemical communications (Cambridge, England), 2011, 47, 499-501
7125591 CIFC66 H108 Cl2 Cu2 N8 O14 SP 1 21/c 119.805; 20.32; 21.84
90; 109.52; 90		8284Wenzel, Marco; Knapp, Quintin W.; Plieger, Paul G.
A bis-salicylaldoximato-copper(II) receptor for selective sulfate uptake.
Chemical communications (Cambridge, England), 2011, 47, 499-501
7125592 CIFC64 H100 Cu2 N8 O20 P2 SP b c a20.2187; 21.9011; 38.781
90; 90; 90		17172.7Wenzel, Marco; Knapp, Quintin W.; Plieger, Paul G.
A bis-salicylaldoximato-copper(II) receptor for selective sulfate uptake.
Chemical communications (Cambridge, England), 2011, 47, 499-501
7125593 CIFC72 H121 Cu2 N11 O22 SP -110.464; 18.668; 21.678
78.77; 85.67; 85.96		4135Wenzel, Marco; Knapp, Quintin W.; Plieger, Paul G.
A bis-salicylaldoximato-copper(II) receptor for selective sulfate uptake.
Chemical communications (Cambridge, England), 2011, 47, 499-501
7125594 CIFC48 H58P -18.4918; 9.8418; 12.6119
101.641; 109.323; 96.475		955.64Kulisic, Niksa; More, Sandeep; Mateo-Alonso, Aurelio
A tetraalkylated pyrene building block for the synthesis of pyrene-fused azaacenes with enhanced solubility.
Chemical communications (Cambridge, England), 2011, 47, 514-516
7125595 CIFC160 H174 F3 Fe4 N28 O51 S12.5P -3 c 133.788; 33.788; 39.938
90; 90; 120		39486Riddell, Imogen A.; Smulders, Maarten M. J.; Clegg, Jack K.; Nitschke, Jonathan R.
Encapsulation, storage and controlled release of sulfur hexafluoride from a metal-organic capsule.
Chemical communications (Cambridge, England), 2011, 47, 457-459
7125596 CIFC6.5 H15.5 Cl N2 O Pt0.5 SC 1 2/c 118.1852; 11.5308; 12.079
90; 100.628; 90		2489.39Alves, Georges; Morel, Laurent; El-Ghozzi, Malika; Avignant, Daniel; Legeret, Bertrand; Nauton, Lionel; Cisnetti, Federico; Gautier, Arnaud
A platinum Chugaev carbene complex as a potent anticancer agent.
Chemical communications (Cambridge, England), 2011, 47, 7830-7832
7125597 CIFC97 H78 Cl4 F9 Ir3 N16 O9 S3P -113.693; 16.735; 26.001
88.665; 86.297; 85.269		5924.5Chandrasekhar, Vadapalli; Rahaman, S. M. Wahidur; Hajra, Tanima; Das, Dipak; Ghatak, Tapas; Rafiq, Shahnawaz; Sen, Pratik; Bera, Jitendra K.
A trinuclear bright red luminophore containing cyclometallated Ir(III) motifs.
Chemical communications (Cambridge, England), 2011, 47, 10836-10838
7125598 CIFC35 H24 F3 Ir N6 O3 SP 1 21/n 18.6494; 31.08; 12.1964
90; 94.251; 90		3269.7Chandrasekhar, Vadapalli; Rahaman, S. M. Wahidur; Hajra, Tanima; Das, Dipak; Ghatak, Tapas; Rafiq, Shahnawaz; Sen, Pratik; Bera, Jitendra K.
A trinuclear bright red luminophore containing cyclometallated Ir(III) motifs.
Chemical communications (Cambridge, England), 2011, 47, 10836-10838
7125599 CIFC17 H29 N3 O3P 21 21 2110.1; 10.997; 16.768
90; 90; 90		1862.4Reddy, Damodara N.; Thirupathi, Ravula; Prabhakaran, Erode N.
Accessing the disallowed conformations of peptides employing amide-to-imidate modification.
Chemical communications (Cambridge, England), 2011, 47, 9417-9419
7125600 CIFC17 H31 N3 O4P 1 21 16.031; 8.634; 18.78
90; 94.933; 90		974.3Reddy, Damodara N.; Thirupathi, Ravula; Prabhakaran, Erode N.
Accessing the disallowed conformations of peptides employing amide-to-imidate modification.
Chemical communications (Cambridge, England), 2011, 47, 9417-9419
7125601 CIFC72 H92 Cu4 Dy4 N12 O46P b c a24.7894; 14.3443; 25.929
90; 90; 90		9220Kühne, Irina A; Magnani, Nicola; Mereacre, Valeriu; Wernsdorfer, Wolfgang; Anson, Christopher E.; Powell, Annie K.
An octanuclear {Cu(II)4Dy(III)4} coordination cluster showing single molecule magnet behaviour from field accessible states.
Chemical communications (Cambridge, England), 2014, 50, 1882-1885
7125602 CIFC70.4 H88.8 Cu4 N12 O46 Y4P b c a24.8476; 14.0945; 25.6548
90; 90; 90		8984.7Kühne, Irina A; Magnani, Nicola; Mereacre, Valeriu; Wernsdorfer, Wolfgang; Anson, Christopher E.; Powell, Annie K.
An octanuclear {Cu(II)4Dy(III)4} coordination cluster showing single molecule magnet behaviour from field accessible states.
Chemical communications (Cambridge, England), 2014, 50, 1882-1885
7125603 CIFC50 H44 Cd Cl8 N6 O26P 1 21/c 110.4535; 18.918; 17.278
90; 100.905; 90		3355.2Mukherjee, Gargi; Biradha, Kumar
Modulation of breathing behavior of layered coordination polymers via a solid solution approach: the influence of metal ions on sorption behavior.
Chemical communications (Cambridge, England), 2014, 50, 670-672
7125604 CIFC52 H52 Cd Cl6 F12 N6 O20 P2P 1 21/c 110.3591; 19.0085; 16.9399
90; 101.516; 90		3268.5Mukherjee, Gargi; Biradha, Kumar
Modulation of breathing behavior of layered coordination polymers via a solid solution approach: the influence of metal ions on sorption behavior.
Chemical communications (Cambridge, England), 2014, 50, 670-672
7125605 CIFC50 H44 Cl8 N6 O26 ZnP 1 21/c 110.321; 18.735; 17.405
90; 99.987; 90		3314.5Mukherjee, Gargi; Biradha, Kumar
Modulation of breathing behavior of layered coordination polymers via a solid solution approach: the influence of metal ions on sorption behavior.
Chemical communications (Cambridge, England), 2014, 50, 670-672
7125606 CIFC50 H44 Cd0.6 Cl8 N6 O26 Zn0.4P 1 21/c 110.391; 18.819; 17.351
90; 100.537; 90		3335.7Mukherjee, Gargi; Biradha, Kumar
Modulation of breathing behavior of layered coordination polymers via a solid solution approach: the influence of metal ions on sorption behavior.
Chemical communications (Cambridge, England), 2014, 50, 670-672
7125607 CIFC117 H110 Cu2 F60 N8 O32 Tb2P 1 21/c 121.853; 23.682; 28.76
90; 100.782; 90		14621Zhu, Mei; Mei, Xuelan; Ma, Yue; Li, Licun; Liao, Daizheng; Sutter, Jean-Pascal
Nitronyl nitroxide-metal complexes as metallo-ligands for the construction of hetero-tri-spin (2p-3d-4f) chains.
Chemical communications (Cambridge, England), 2014, 50, 1906-1908
7125608 CIFC115 H97 Cu F66 N8 O35 Tb3P -119.973; 19.983; 21.679
90.959; 107.219; 114.941		7393Zhu, Mei; Mei, Xuelan; Ma, Yue; Li, Licun; Liao, Daizheng; Sutter, Jean-Pascal
Nitronyl nitroxide-metal complexes as metallo-ligands for the construction of hetero-tri-spin (2p-3d-4f) chains.
Chemical communications (Cambridge, England), 2014, 50, 1906-1908
7125609 CIFC12 H13 Mn N O5P n a 217.491; 15.386; 11.226
90; 90; 90		1293.9Tian, Chong-Bin; Chen, Rui-Ping; He, Chao; Li, Wei-Jin; Wei, Qi; Zhang, Xu-Dong; Du, Shao-Wu
Reversible crystal-to-amorphous-to-crystal phase transition and a large magnetocaloric effect in a spongelike metal organic framework material.
Chemical communications (Cambridge, England), 2014, 50, 1915-1917
7125610 CIFC78 H96 O18 PbP n -3 n :228.3035; 28.3035; 28.3035
90; 90; 90		22673.6Adhikari, Birendra Babu; Ohto, Keisuke; Schramm, Michael P.
p-tert-Butylcalix[6]arene hexacarboxylic acid conformational switching and octahedral coordination with Pb(II) and Sr(II).
Chemical communications (Cambridge, England), 2014, 50, 1903-1905
7125611 CIFC75 H112 N8 Ni2 O3C 1 2/c 132.632; 8.9933; 24.821
90; 94.39; 90		7263Leconte, N.; Ciccione, J.; Gellon, G.; Philouze, C.; Thomas, F.
Unprecedented redox-driven ligand ejection in nickel(II)-diiminosemiquinonate radical complexes.
Chemical communications (Cambridge, England), 2014, 50, 1918-1920
7125612 CIFC78 H110 N8 NiP 1 21/n 113.686; 23.219; 23.157
90; 96.26; 90		7315Leconte, N.; Ciccione, J.; Gellon, G.; Philouze, C.; Thomas, F.
Unprecedented redox-driven ligand ejection in nickel(II)-diiminosemiquinonate radical complexes.
Chemical communications (Cambridge, England), 2014, 50, 1918-1920
7125613 CIFC28 H25 Eu N2 O17P 1 21/n 115.535; 12.555; 15.636
90; 104.005; 90		2959Zhu, Min; Hao, Zhao-Min; Song, Xue-Zhi; Meng, Xing; Zhao, Shu-Na; Song, Shu-Yan; Zhang, Hong-Jie
A new type of double-chain based 3D lanthanide(III) metal-organic framework demonstrating proton conduction and tunable emission.
Chemical communications (Cambridge, England), 2014, 50, 1912-1914
7125614 CIFC72 H90 K N7P -114.4327; 14.6585; 17.8114
82.841; 74.731; 68.234		3374.5Bezuidenhout, Daniela I.; Kleinhans, George; Guisado-Barrios, Gregorio; Liles, David C.; Ung, Gaël; Bertrand, Guy
Isolation of a potassium bis(1,2,3-triazol-5-ylidene)carbazolide: a stabilizing pincer ligand for reactive late transition metal complexes.
Chemical communications (Cambridge, England), 2014, 50, 2431-2433
7125615 CIFC35 H46 Cu F6 N2 SbP b c a18.355; 18.334; 42.496
90; 90; 90		14301Parvin, Nasrina; Hossain, Jabed; George, Anjana; Parameswaran, Pattiyil; Khan, Shabana
N-heterocyclic silylene stabilized monocordinated copper(i)-arene cationic complexes and their application in click chemistry.
Chemical communications (Cambridge, England), 2019, 56, 273-276
7125616 CIFC34 H44 Cu F6 N2 SbC 1 c 124.087; 9.1915; 19.165
90; 124.966; 90		3477.1Parvin, Nasrina; Hossain, Jabed; George, Anjana; Parameswaran, Pattiyil; Khan, Shabana
N-heterocyclic silylene stabilized monocordinated copper(i)-arene cationic complexes and their application in click chemistry.
Chemical communications (Cambridge, England), 2019, 56, 273-276
7125617 CIFC28 H49 Cu F6 N3 Sb Si3P 21 21 2111.762; 14.725; 21.3
90; 90; 90		3689Parvin, Nasrina; Hossain, Jabed; George, Anjana; Parameswaran, Pattiyil; Khan, Shabana
N-heterocyclic silylene stabilized monocordinated copper(i)-arene cationic complexes and their application in click chemistry.
Chemical communications (Cambridge, England), 2019, 56, 273-276
7125618 CIFC38 H50 Cu F6 N4 SbP n m a13.623; 14.768; 20.118
90; 90; 90		4047Parvin, Nasrina; Hossain, Jabed; George, Anjana; Parameswaran, Pattiyil; Khan, Shabana
N-heterocyclic silylene stabilized monocordinated copper(i)-arene cationic complexes and their application in click chemistry.
Chemical communications (Cambridge, England), 2019, 56, 273-276
7125619 CIFC29 H51 Cu F6 N3 Sb Si3P 1 n 19.226; 11.541; 18.052
90; 98.414; 90		1901Parvin, Nasrina; Hossain, Jabed; George, Anjana; Parameswaran, Pattiyil; Khan, Shabana
N-heterocyclic silylene stabilized monocordinated copper(i)-arene cationic complexes and their application in click chemistry.
Chemical communications (Cambridge, England), 2019, 56, 273-276

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