Crystallography Open Database

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7127113 CIFC116 H144 F24 N16 O30 Pd4 S8P 1 21/c 111.208; 21.44; 29.333
90; 93.016; 90		7038.9O'Connor, Helen M; Coletta, Marco; Etcheverry-Berríos, Alvaro; Nichol, Gary S.; Brechin, Euan K.; Lusby, Paul J.
Kinetic selection of Pd<sub>4</sub>L<sub>2</sub> metallocyclic and Pd<sub>6</sub>L<sub>3</sub> trigonal prismatic assemblies.
Chemical communications (Cambridge, England), 2020, 56, 11799-11802
7127114 CIFC552 H418 F72 N24 O72 P24 Pd12 S24C m c 2118.6651; 51.156; 74.909
90; 90; 90		71525O'Connor, Helen M; Coletta, Marco; Etcheverry-Berríos, Alvaro; Nichol, Gary S.; Brechin, Euan K.; Lusby, Paul J.
Kinetic selection of Pd<sub>4</sub>L<sub>2</sub> metallocyclic and Pd<sub>6</sub>L<sub>3</sub> trigonal prismatic assemblies.
Chemical communications (Cambridge, England), 2020, 56, 11799-11802
7127115 CIFCu3 F N O10 Pb Se2R 3 m :H6.6973; 6.6973; 18.5548
90; 90; 120		720.753Zhang, Mengsi; Zhao, Zhiying; Zhang, Wanwan; Li, Jinyang; Huang, Xiaoying; He, Zhangzhen
Pb(OF)Cu<sub>3</sub>(SeO<sub>3</sub>)<sub>2</sub>(NO<sub>3</sub>): a selenite fluoride nitrate with a breathing kagomé lattice.
Chemical communications (Cambridge, England), 2020, 56, 11965-11968
7127116 CIFC27 H26 Br3 N3P 1 21/c 18.2431; 26.7192; 12.0799
90; 100.315; 90		2617.6B S, Anju; Bhattacharjee, Rameswar; Gupta, Shourya; Ahammad, Soniya; Datta, Ayan; Kundu, Subrata
Deoxygenation of nitrosoarene by N-heterocyclic carbene (NHC): an elusive Breslow-type intermediate bridging carbene and nitrene.
Chemical communications (Cambridge, England), 2020, 56, 12166-12169
7127117 CIFC17 H15 N O3P 21 21 218.5318; 9.341; 18.0021
90; 90; 90		1434.69Li, Yan; Cheng, Xiu-Fen; Fei, Fan; Wu, Tian-Rui; Bian, Kang-Jie; Zhou, Xin; Wang, Xi-Sheng
Palladium(II)-catalyzed asymmetric C-H carbonylation to diverse isoquinoline derivatives bearing all-carbon quaternary stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 11605-11608
7127118 CIFC20 H21 N O2P 1 21 17.8485; 12.7347; 9.0832
90; 90.438; 90		907.82Li, Yan; Cheng, Xiu-Fen; Fei, Fan; Wu, Tian-Rui; Bian, Kang-Jie; Zhou, Xin; Wang, Xi-Sheng
Palladium(II)-catalyzed asymmetric C-H carbonylation to diverse isoquinoline derivatives bearing all-carbon quaternary stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 11605-11608
7127119 CIFC18 H19 N O3P 21 21 217.87176; 12.32287; 16.6389
90; 90; 90		1614.02Li, Yan; Cheng, Xiu-Fen; Fei, Fan; Wu, Tian-Rui; Bian, Kang-Jie; Zhou, Xin; Wang, Xi-Sheng
Palladium(II)-catalyzed asymmetric C-H carbonylation to diverse isoquinoline derivatives bearing all-carbon quaternary stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 11605-11608
7127120 CIFC17 H17 N O3P 1 21 17.3742; 8.5904; 12.0878
90; 101.002; 90		751.656Li, Yan; Cheng, Xiu-Fen; Fei, Fan; Wu, Tian-Rui; Bian, Kang-Jie; Zhou, Xin; Wang, Xi-Sheng
Palladium(II)-catalyzed asymmetric C-H carbonylation to diverse isoquinoline derivatives bearing all-carbon quaternary stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 11605-11608
7127121 CIFC70 H58C 1 2/c 128.3914; 12.6728; 15.826
90; 98.238; 90		5635.4Sharma, Himanshu; Sharma, Priyank Kumar; Das, Soumyajit
Revisiting indeno[2,1-<i>c</i>]fluorene synthesis while exploring the fully conjugated <i>s</i>-indaceno[2,1-<i>c</i>:6,5-<i>c</i>']difluorene.
Chemical communications (Cambridge, England), 2020, 56, 11319-11322
7127122 CIFC23 H26 B10P 1 21/n 112.0902; 10.2573; 17.8407
90; 91.309; 90		2211.9Feuerstein, Wolfram; Breher, Frank
Synthetic access to a phosphorescent non-palindromic pincer complex of palladium by a double oxidative addition - comproportionation sequence.
Chemical communications (Cambridge, England), 2020, 56, 12589-12592
7127123 CIFC22 H16 N2 NiP 1 21/n 19.282; 12.71; 14.038
90; 90.89; 90		1655.9Feuerstein, Wolfram; Breher, Frank
Synthetic access to a phosphorescent non-palindromic pincer complex of palladium by a double oxidative addition - comproportionation sequence.
Chemical communications (Cambridge, England), 2020, 56, 12589-12592
7127124 CIFC58 H42 Co4 N6 O18P 110.298; 10.352; 17.615
105.643; 103.514; 90.658		1753Gao, Yajun; Zhang, Mingxing; Chen, Cong; Zhang, Yong; Gu, Yuming; Wang, Qian; Zhang, Wenwei; Pan, Yi; Ma, Jing; Bai, Junfeng
A low symmetry cluster meets a low symmetry ligand to sharply boost MOF thermal stability.
Chemical communications (Cambridge, England), 2020, 56, 11985-11988
7127125 CIFC26 H14 Co2 N2 O8C 1 c 114.3091; 14.5181; 17.5565
90; 104.706; 90		3527.7Gao, Yajun; Zhang, Mingxing; Chen, Cong; Zhang, Yong; Gu, Yuming; Wang, Qian; Zhang, Wenwei; Pan, Yi; Ma, Jing; Bai, Junfeng
A low symmetry cluster meets a low symmetry ligand to sharply boost MOF thermal stability.
Chemical communications (Cambridge, England), 2020, 56, 11985-11988
7127126 CIFC13 H7 Co N O4P 1 21/c 110.696; 13.078; 12.46
90; 108.79; 90		1650Gao, Yajun; Zhang, Mingxing; Chen, Cong; Zhang, Yong; Gu, Yuming; Wang, Qian; Zhang, Wenwei; Pan, Yi; Ma, Jing; Bai, Junfeng
A low symmetry cluster meets a low symmetry ligand to sharply boost MOF thermal stability.
Chemical communications (Cambridge, England), 2020, 56, 11985-11988
7127127 CIFC28 H56 I6 O7 Sm2C 1 2/c 112.8008; 12.0522; 28.7469
90; 98.444; 90		4386.9Marks, Walker R.; Baumgardner, Douglas F.; Reinheimer, Eric W.; Gilbertson, John D.
Complete denitrification of nitrate and nitrite to N<sub>2</sub> gas by samarium(II) iodide.
Chemical communications (Cambridge, England), 2020, 56, 11441-11444
7127128 CIFH68 I8 O41 Sm6P n n m12.8578; 14.8418; 14.8987
90; 90; 90		2843.16Marks, Walker R.; Baumgardner, Douglas F.; Reinheimer, Eric W.; Gilbertson, John D.
Complete denitrification of nitrate and nitrite to N<sub>2</sub> gas by samarium(II) iodide.
Chemical communications (Cambridge, England), 2020, 56, 11441-11444
7127129 CIFC37.6 H99.4 I8 N2 O29 Sm6P 1 21/n 114.2715; 22.8583; 14.2693
90; 90.739; 90		4654.6Marks, Walker R.; Baumgardner, Douglas F.; Reinheimer, Eric W.; Gilbertson, John D.
Complete denitrification of nitrate and nitrite to N<sub>2</sub> gas by samarium(II) iodide.
Chemical communications (Cambridge, England), 2020, 56, 11441-11444
7127130 CIFC15 H18 N2 OP -110.3988; 11.976; 12.1316
86.151; 70.363; 65.045		1285.2Niu, Kaikai; Song, Lingyun; Hao, Yanke; Liu, Yuxiu; Wang, Qingmin
Electrochemical decarboxylative C3 alkylation of quinoxalin-2(1<i>H</i>)-ones with <i>N</i>-hydroxyphthalimide esters.
Chemical communications (Cambridge, England), 2020, 56, 11673-11676
7127131 CIFC94 H150 N4 Si16P -19.8911; 16.0352; 19.2371
88.17; 76.903; 73.041		2840.61Mateos-Martín, Javier; Carini, Marco; Melle-Franco, Manuel; Mateo-Alonso, Aurelio
Increasing and dispersing strain in pyrene-fused azaacenes.
Chemical communications (Cambridge, England), 2020, 56, 11457-11460
7127132 CIFC52 H34 O4 Si2P 1 21/c 114.4193; 15.3229; 18.272
90; 93.967; 90		4027.4Mateos-Martín, Javier; Carini, Marco; Melle-Franco, Manuel; Mateo-Alonso, Aurelio
Increasing and dispersing strain in pyrene-fused azaacenes.
Chemical communications (Cambridge, England), 2020, 56, 11457-11460
7127133 CIFC90 H158 N4 Si18C 1 2/c 143.6057; 8.5663; 33.257
90; 101.568; 90		12170.5Mateos-Martín, Javier; Carini, Marco; Melle-Franco, Manuel; Mateo-Alonso, Aurelio
Increasing and dispersing strain in pyrene-fused azaacenes.
Chemical communications (Cambridge, England), 2020, 56, 11457-11460
7127134 CIFC230 H308 N8 Si36P -122.1092; 22.318; 29.0414
74.547; 79.773; 71.053		12998.3Mateos-Martín, Javier; Carini, Marco; Melle-Franco, Manuel; Mateo-Alonso, Aurelio
Increasing and dispersing strain in pyrene-fused azaacenes.
Chemical communications (Cambridge, England), 2020, 56, 11457-11460
7127135 CIFC54 H76 I4 O9 Sm2P 21 21 2116.1373; 17.5042; 21.114
90; 90; 90		5964.1Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127136 CIFC38 H30 I2 N5 O SmP 1 21/c 111.6323; 12.3012; 24.5249
90; 91.769; 90		3507.6Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127137 CIFC55 H47 I2 N8 O SmP -115.8733; 16.1883; 19.8595
90; 103.03; 90		4971.74Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127138 CIFC33 H29 I2 N4 O SmP 1 21/c 19.2854; 15.4014; 24.686
90; 100.528; 90		3470.9Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127139 CIFC25 H18 N2 OC 1 2/c 117.8482; 18.0365; 12.5808
90; 117.094; 90		3605.6Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127140 CIFC18 H15 N OP 1 21/c 18.1307; 14.6655; 11.5353
90; 95.749; 90		1368.56Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127141 CIFC41 H31 I2 N6 O SmP -111.4446; 11.9484; 14.6103
78.322; 81.909; 84.338		1931.97Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127142 CIFC14 H14 Br F3 O3P 21 21 218.1811; 17.8856; 21.2028
90; 90; 90		3102.5Murata, Ryuichi; Matsumoto, Akira; Asano, Keisuke; Matsubara, Seijiro
Desymmetrization of gem-diols via water-assisted organocatalytic enantio- and diastereoselective cycloetherification.
Chemical communications (Cambridge, England), 2020, 56, 12335-12338
7127143 CIFC14 H12 Br F3 O2P 21 21 216.382; 14.0024; 15.777
90; 90; 90		1409.9Murata, Ryuichi; Matsumoto, Akira; Asano, Keisuke; Matsubara, Seijiro
Desymmetrization of gem-diols via water-assisted organocatalytic enantio- and diastereoselective cycloetherification.
Chemical communications (Cambridge, England), 2020, 56, 12335-12338
7127144 CIFC20 H21 N OP 1 21/c 110.162; 19.1; 8.941
90; 109.78; 90		1633Zhang, Xiao-Wen; Zhang, Hui; Wang, Hu-Chong; Zhu, Ming-Hui; Cong, Hengjiang; Liu, Wen-Bo
Pd-catalyzed arylation/aza-Michael addition cascade to C2-spiroindolines and azabicyclo[3.2.2]nonanones.
Chemical communications (Cambridge, England), 2020, 56, 12013-12016
7127145 CIFC27 H27 N OC 1 c 113.7872; 16.2182; 9.4765
90; 96.759; 90		2104.25Zhang, Xiao-Wen; Zhang, Hui; Wang, Hu-Chong; Zhu, Ming-Hui; Cong, Hengjiang; Liu, Wen-Bo
Pd-catalyzed arylation/aza-Michael addition cascade to C2-spiroindolines and azabicyclo[3.2.2]nonanones.
Chemical communications (Cambridge, England), 2020, 56, 12013-12016
7127146 CIFC21 H30 Cl O PP -15.7668; 11.743; 28.998
95.169; 90.067; 102.805		1906.7Shintani, Ryo; Ohzono, Ayase; Shirota, Kentaro
Phosphinative cyclopropanation of allyl phosphates with lithium phosphides.
Chemical communications (Cambridge, England), 2020, 56, 11851-11854
7127147 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.4617; 4.2206; 19.5436
90; 90.441; 90		945.4Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127148 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.4724; 4.2238; 19.5467
90; 90.445; 90		947.15Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127149 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.538; 4.2653; 19.7023
90; 90.478; 90		969.58Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127150 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.4918; 4.232; 19.5567
90; 90.451; 90		951.08Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127151 CIFC24 H29 B O4P 21 21 216.48035; 17.3087; 19.7454
90; 90; 90		2214.77Sun, Xiao; Gu, Peiming; Qin, Jiao; Su, Yan
Rhodium-catalysed diastereo- and enantio-selective cyclopropanation of α-boryl styrenes.
Chemical communications (Cambridge, England), 2020, 56, 12379-12382
7127152 CIFC46 H16 Cl16 F12 N2 O4 ZnP -18.9829; 15.1174; 20.8813
97.411; 94.728; 90.909		2801.4Kimura, Shun; Kimura, Shojiro; Nishihara, Hiroshi; Kusamoto, Tetsuro
Excimer emission and magnetoluminescence of radical-based zinc(II) complexes doped in host crystals.
Chemical communications (Cambridge, England), 2020, 56, 11195-11198
7127153 CIFC16 H10 B2 F12P 1 21/n 17.556; 8.4678; 13.593
90; 96.564; 90		864.02Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127154 CIFC32 H50 B2 O2 Si4F d d 218.4614; 34.6525; 11.8617
90; 90; 90		7588.3Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127155 CIFC25 H26 B F9 O Si2P 21 21 2110.9779; 13.7265; 18.8688
90; 90; 90		2843.3Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127156 CIFC34 H28 B2 F12 N2P -18.7742; 9.5777; 11.1573
98.124; 99.074; 113.422		827.78Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127157 CIFC35 H34 B F6 NP 1 21/c 110.311; 14.3855; 21.2243
90; 103.129; 90		3065.89Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127158 CIFC48 H54 B2 F12 Si4P -113.3784; 14.431; 16.3141
65.319; 66.05; 78.62		2614Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127159 CIFC44 H50 B2 F12 S2 Si4P n m a13.3555; 31.172; 11.7335
90; 90; 90		4884.9Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127160 CIFC31 H32 B F6 NP 1 21/c 18.7063; 17.2992; 18.1817
90; 93.565; 90		2733.1Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127161 CIFC23 H13 N SP 1 21/c 121.4278; 4.9469; 15.5164
90; 107.158; 90		1571.56Jana, Arijit; Chakraborty, Papri; Dar, Wakeel Ahmed; Chandra, Sourov; Khatun, Esma; Kannan, M. P.; Ras, Robin H. A.; Pradeep, Thalappil
Dual emitting Ag<sub>35</sub> nanocluster protected by 2-pyrene imine thiol.
Chemical communications (Cambridge, England), 2020, 56, 12550-12553
7127162 CIFC52 H30 Mn N8 O4F d d d :217.6218; 36.0338; 50.356
90; 90; 90		31975Setter, Caitlin J.; Price, Michael B.; Conte, Luke; Schmitt, Wolfgang; Batten, Stuart R.; Richardson, Christopher; Hill, Matthew R.; Babarao, Ravichandar; Macreadie, Lauren K.
Mixed donor, phenanthroline photoactive MOFs with favourable CO<sub>2</sub> selectivity.
Chemical communications (Cambridge, England), 2020, 56, 13377-13380
7127163 CIFC54 H32 N8 O8 Zn2P n a 218.403; 24.858; 33.616
90; 90; 90		7022Setter, Caitlin J.; Price, Michael B.; Conte, Luke; Schmitt, Wolfgang; Batten, Stuart R.; Richardson, Christopher; Hill, Matthew R.; Babarao, Ravichandar; Macreadie, Lauren K.
Mixed donor, phenanthroline photoactive MOFs with favourable CO<sub>2</sub> selectivity.
Chemical communications (Cambridge, England), 2020, 56, 13377-13380
7127164 CIFC78 H79 B Cl2 Dy N5 O2 Si2P -114.3753; 22.1443; 23.4355
100.425; 103.832; 100.857		6911.6Canaj, Angelos B.; Dey, Sourav; Wilson, Claire; Céspedes, Oscar; Rajaraman, Gopalan; Murrie, Mark
Engineering macrocyclic high performance pentagonal bipyramidal Dy(iii) single-ion magnets.
Chemical communications (Cambridge, England), 2020, 56, 12037-12040
7127165 CIFC8 H11 N3 O4P -17.6321; 10.9503; 12.4367
92.39; 95.911; 100.137		1015.8Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127166 CIFC21 H27 N6 O14 YbP -18.8524; 10.434; 15.937
87.131; 87.135; 88.571		1468Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127167 CIFC12 H20 N4 O10P 1 21/c 111.8129; 10.3804; 6.9487
90; 100.27; 90		838.42Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127168 CIFC2.25 H2.25 Ho0.25 N0.5 O2.5P 1 21/n 19.6712; 11.3857; 12.687
90; 96.475; 90		1388.1Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127169 CIFC24 H28 Ho N8 O18C 1 c 112.0981; 17.5518; 18.316
90; 98.538; 90		3846.2Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127170 CIFC24 H28 Lu N8 O18C 1 c 112.038; 17.562; 18.345
90; 98.384; 90		3837Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127171 CIFC27 H48 N4 O19 TmP -111.897; 12.988; 14.598
63.692; 79.555; 74.701		1945Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127172 CIFC8 H7 Er N2 O10.5C 1 2 114.67; 11.5086; 9.198
90; 121.404; 90		1325.4Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127173 CIFC16 H14 Ho2 N4 O20P 1 21/n 110.023; 17.357; 14.354
90; 99.312; 90		2464.2Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127174 CIFC28 H35 Lu N10 O18C 1 c 112.0002; 17.5085; 18.066
90; 98.6189; 90		3752.9Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127175 CIFC24 H28 N8 O18 TmC 1 c 112.0526; 17.5649; 18.317
90; 98.558; 90		3834.6Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127176 CIFC27 H48 N4 O19 YbP -111.6122; 12.8415; 14.4646
64.182; 80.639; 75.308		1874.77Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127177 CIFC5.09 H6.36 N1.82 O3.27 Y0.18C 1 c 112.0684; 17.5403; 18.0493
90; 98.685; 90		3776.93Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127178 CIFC19 H35 Cl2 N2 Ni Rh S2P n a 2122.125; 8.337; 12.839
90; 90; 90		2368.2Ogo, Seiji; Ando, Tatsuya; Minh, Le Tu Thi; Mori, Yuki; Matsumoto, Takahiro; Yatabe, Takeshi; Yoon, Ki-Seok; Sato, Yukio; Hibino, Takashi; Kaneko, Kenji
A NiRhS fuel cell catalyst - lessons from hydrogenase.
Chemical communications (Cambridge, England), 2020, 56, 11787-11790
7127179 CIFC19 H36 Cl N2 Ni Rh S2P b c a15.669; 14.306; 20.014
90; 90; 90		4486Ogo, Seiji; Ando, Tatsuya; Minh, Le Tu Thi; Mori, Yuki; Matsumoto, Takahiro; Yatabe, Takeshi; Yoon, Ki-Seok; Sato, Yukio; Hibino, Takashi; Kaneko, Kenji
A NiRhS fuel cell catalyst - lessons from hydrogenase.
Chemical communications (Cambridge, England), 2020, 56, 11787-11790
7127180 CIFC17 H24 B PP 21 21 216.6359; 7.5137; 34.018
90; 90; 90		1696.1Wang, Cuiying; Yue, Chang-Duo; Yuan, Jia; Zheng, Jia-Lian; Zhang, Ying; Yu, Hong; Chen, Jian; Meng, Sixuan; Yu, Yang; Yu, Guang-Ao; Che, Chi-Ming
Synthesis of P-chiral phosphine compounds by palladium-catalyzed C-P coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 11775-11778
7127181 CIFC20 H28 B PP 21 21 2111.2902; 12.3392; 13.6341
90; 90; 90		1899.4Wang, Cuiying; Yue, Chang-Duo; Yuan, Jia; Zheng, Jia-Lian; Zhang, Ying; Yu, Hong; Chen, Jian; Meng, Sixuan; Yu, Yang; Yu, Guang-Ao; Che, Chi-Ming
Synthesis of P-chiral phosphine compounds by palladium-catalyzed C-P coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 11775-11778
7127182 CIFC17 H14 S2P 1 21/c 114.9903; 5.9477; 16.5251
90; 110.467; 90		1380.34Ielo, Laura; Pillari, Veronica; Gajic, Natalie; Holzer, Wolfgang; Pace, Vittorio
Straightforward chemoselective access to unsymmetrical dithioacetals through a thiosulfonate homologation-nucleophilic substitution sequence.
Chemical communications (Cambridge, England), 2020, 56, 12395-12398
7127183 CIFC14 H11 N O S2P 1 21 19.5155; 4.8412; 13.9736
90; 96.436; 90		639.66Ielo, Laura; Pillari, Veronica; Gajic, Natalie; Holzer, Wolfgang; Pace, Vittorio
Straightforward chemoselective access to unsymmetrical dithioacetals through a thiosulfonate homologation-nucleophilic substitution sequence.
Chemical communications (Cambridge, England), 2020, 56, 12395-12398
7127184 CIFC21 H20 S2P 1 21/n 116.4219; 7.1899; 16.4782
90; 118.374; 90		1711.87Ielo, Laura; Pillari, Veronica; Gajic, Natalie; Holzer, Wolfgang; Pace, Vittorio
Straightforward chemoselective access to unsymmetrical dithioacetals through a thiosulfonate homologation-nucleophilic substitution sequence.
Chemical communications (Cambridge, England), 2020, 56, 12395-12398
7127185 CIFC214 H282 Au10 O22 S2P 21 21 219.6562; 28.6975; 21.2232
90; 90; 90		11971.7Xu, Man-Man; Jia, Tong-Tong; Li, Bingjie; Ma, Wang; Chen, Xiaoyuan; Zhao, Xueli; Zang, Shuang-Quan
Tuning the properties of atomically precise gold nanoclusters for biolabeling and drug delivery.
Chemical communications (Cambridge, England), 2020, 56, 8766-8769
7127186 CIFC53 H59 Cl11 N8 O8 Pd2P 1 21/n 112.18; 15.906; 33.211
90; 93.15; 90		6424Scattolin, Thomas; Bortolamiol, Enrica; Palazzolo, Stefano; Caligiuri, Isabella; Perin, Tiziana; Canzonieri, Vincenzo; Demitri, Nicola; Rizzolio, Flavio; Cavallo, Luigi; Dereli, Busra; Mane, Manoj V.; Nolan, Steven P.; Visentin, Fabiano
The anticancer activity of an air-stable Pd(I)-NHC (NHC = N-heterocyclic carbene) dimer.
Chemical communications (Cambridge, England), 2020, 56, 12238-12241
7127187 CIFC22 H21 N O5 S2P 21 21 218.71695; 13.36161; 17.6913
90; 90; 90		2060.55Yang, Lei; Zhao, Jian-Qiang; You, Yong; Wang, Zhen-Hua; Yuan, Wei-Cheng
Organocatalytic enantioselective tandem sulfa-Michael/aldol reaction to access dihydrothiopyran-fused benzosulfolane skeletons bearing three contiguous stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 12363-12366
7127188 CIFC15 H12 O3 S2P 21 21 217.8266; 13.136; 13.1894
90; 90; 90		1356.01Yang, Lei; Zhao, Jian-Qiang; You, Yong; Wang, Zhen-Hua; Yuan, Wei-Cheng
Organocatalytic enantioselective tandem sulfa-Michael/aldol reaction to access dihydrothiopyran-fused benzosulfolane skeletons bearing three contiguous stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 12363-12366
7127189 CIFC119.5 H108 Cl4 P8 Rh4 S2P -116.3139; 19.5375; 22.4893
71.332; 72.996; 79.948		6468.1Barnett, Harrison J.; Hill, Anthony F.
Dimetalla-heterocyclic carbenes: the interconversion of chalcocarbonyl and carbido ligands.
Chemical communications (Cambridge, England), 2020, 56, 12593-12596
7127190 CIFC15 H10 Br Cl I N O2P 1 21/n 15.0083; 9.7548; 31.964
90; 92.576; 90		1560.02Barnett, Harrison J.; Hill, Anthony F.
Dimetalla-heterocyclic carbenes: the interconversion of chalcocarbonyl and carbido ligands.
Chemical communications (Cambridge, England), 2020, 56, 12593-12596
7127191 CIFC58 H53 Cl5 O5 P4 Rh2 SP 1 21/c 112.7306; 15.6417; 30.6406
90; 92.455; 90		6095.81Barnett, Harrison J.; Hill, Anthony F.
Dimetalla-heterocyclic carbenes: the interconversion of chalcocarbonyl and carbido ligands.
Chemical communications (Cambridge, England), 2020, 56, 12593-12596
7127192 CIFC61.5 H56 Cl2 P4 Rh2 SeP -116.2884; 20.0388; 22.3244
70.671; 75.071; 80.2		6615Barnett, Harrison J.; Hill, Anthony F.
Dimetalla-heterocyclic carbenes: the interconversion of chalcocarbonyl and carbido ligands.
Chemical communications (Cambridge, England), 2020, 56, 12593-12596
7127193 CIFC19 H16 O3P 1 21/c 17.034; 16.0025; 13.2355
90; 100.358; 90		1465.53Gao, Bingjian; Zou, Suchen; Yang, Guoqing; Ding, Yongzheng; Huang, Hanmin
Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons.
Chemical communications (Cambridge, England), 2020, 56, 12198-12201
7127194 CIFC19 H18 O2P 1 21/n 114.4303; 7.16982; 14.45517
90; 90.2129; 90		1495.56Gao, Bingjian; Zou, Suchen; Yang, Guoqing; Ding, Yongzheng; Huang, Hanmin
Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons.
Chemical communications (Cambridge, England), 2020, 56, 12198-12201
7127195 CIFC10.29 H9.14 O1.14P 1 21/n 113.6891; 7.0857; 14.1959
90; 91.491; 90		1376.49Gao, Bingjian; Zou, Suchen; Yang, Guoqing; Ding, Yongzheng; Huang, Hanmin
Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons.
Chemical communications (Cambridge, England), 2020, 56, 12198-12201
7127196 CIFC10.86 H10.29 O1.14P b c a7.2898; 15.8113; 25.4414
90; 90; 90		2932.41Gao, Bingjian; Zou, Suchen; Yang, Guoqing; Ding, Yongzheng; Huang, Hanmin
Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons.
Chemical communications (Cambridge, England), 2020, 56, 12198-12201
7127197 CIFC19 H16 O3P 1 21/c 120.5228; 8.2219; 17.4215
90; 96.111; 90		2922.94Gao, Bingjian; Zou, Suchen; Yang, Guoqing; Ding, Yongzheng; Huang, Hanmin
Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons.
Chemical communications (Cambridge, England), 2020, 56, 12198-12201
7127198 CIFC23 H18 Br Cl3 N2 OP -18.405; 10.003; 15.623
71.488; 78.914; 66.772		1141.2Zhao, Peng; Yu, Xiao-Xiao; Zhou, You; Huang, Chun; Wu, Yan-Dong; Zhu, Yan-Ping; Wu, An-Xin
Arylacetylenes as two-carbon synthons: synthesis of eight-membered rings via C[triple bond, length as m-dash]C bond cleavage.
Chemical communications (Cambridge, England), 2020, 56, 12554-12557
7127199 CIFC22 H18 N2 OC 1 2/c 113.602; 13.685; 19.401
90; 99.361; 90		3563.3Zhao, Peng; Yu, Xiao-Xiao; Zhou, You; Huang, Chun; Wu, Yan-Dong; Zhu, Yan-Ping; Wu, An-Xin
Arylacetylenes as two-carbon synthons: synthesis of eight-membered rings via C[triple bond, length as m-dash]C bond cleavage.
Chemical communications (Cambridge, England), 2020, 56, 12554-12557
7127200 CIFC49 H63 B F6 N3 O P2 RhI 1 2/a 128.3648; 12.213; 32.5843
90; 111.394; 90		10510MacNeil, Connor S.; Hsiang, Shou-Jen; Hayes, Paul G.
Reversible dehydrogenation of a primary aryl borane.
Chemical communications (Cambridge, England), 2020, 56, 12323-12326
7127201 CIFC44 H63 B N3 O P2 RhP -114.5167; 18.5067; 19.7008
65.627; 88.777; 77.349		4689.8MacNeil, Connor S.; Hsiang, Shou-Jen; Hayes, Paul G.
Reversible dehydrogenation of a primary aryl borane.
Chemical communications (Cambridge, England), 2020, 56, 12323-12326
7127202 CIFC27 H24 N2 O2 SP 1 21/n 18.1661; 25.3026; 10.7553
90; 96.512; 90		2207.96Tan, Heng; Khan, Ruhima; Xu, Dandan; Zhou, Yongyun; Zhang, Xuexin; Shi, Guangrui; Fan, Baomin
Cobalt-catalyzed ring-opening addition of azabenzonorbornadienes via C(sp<sup>3</sup>)-H bond activation of 8-methylquinoline.
Chemical communications (Cambridge, England), 2020, 56, 12570-12573
7127203 CIFC279 H381 O48P 1 21/c 121.609; 49.509; 28.125
90; 111.398; 90		28015Shimoyama, Daisuke; Sekiya, Ryo; Haino, Takeharu
Absorption of chemicals in amorphous trisresorcinarene.
Chemical communications (Cambridge, England), 2020, 56, 12582-12585
7127204 CIFC15 H8 Cl F N2 O4P 1 21 14.3265; 13.4831; 12.3293
90; 93.614; 90		717.79Peng, Qiupeng; Guo, Donghui; Zhang, Bei; Liu, Lala; Wang, Jian
Benzotetramisole catalyzed kinetic resolution of 2H-azirines.
Chemical communications (Cambridge, England), 2020, 56, 12427-12430
7127205 CIFC70 H76 N4 O8 S2C 1 2/c 133.803; 13.242; 13.405
90; 108.746; 90		5682Ohtsuka, Nobuhiko; Nakano, Masahiro; Nakagawa, Sae; Shahiduzzaman, Md; Karakawa, Makoto; Taima, Tetsuya; Minoura, Mao
Naphthalene diimide-incorporated helical thienoacene: a helical molecule with high electron mobility, good solubility, and thermally stable solid phase.
Chemical communications (Cambridge, England), 2020, 56, 12343-12346
7127206 CIFC27 H26 Br N OP 21 21 219.6932; 10.7179; 21.842
90; 90; 90		2269.2Zhang, Yu; Li, Yuan; Zhou, Wei; Zhang, Mengru; Zhang, Qian; Jia, Ran; Zhao, Jinbo
Assembly of polysubstituted chiral cyclopropylamines via highly enantioselective Cu-catalyzed three-component cyclopropene alkenylamination.
Chemical communications (Cambridge, England), 2020, 56, 12250-12253
7127207 CIFC51 H33 N3 O13 Zn4P -4 21 m17.2; 17.2; 17.2
90; 90; 90		5088.4Fishburn, Mitchell G.; Skelton, Dayne R.; Telfer, Shane G.; Wagner, Pawel; Richardson, Christopher
Second-order programming the synthesis of metal-organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 12355-12358
7127208 CIFC35 H30 N4 O8P -110.5406; 10.8847; 13.6301
94.515; 101.132; 96.424		1516.65Fishburn, Mitchell G.; Skelton, Dayne R.; Telfer, Shane G.; Wagner, Pawel; Richardson, Christopher
Second-order programming the synthesis of metal-organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 12355-12358
7127209 CIFC10.5 H6 Cl2 N5 O3 ReC 1 2/c 116.06; 13.0072; 13.9753
90; 99.72; 90		2877.5Schnierle, Marc; Blickle, Svenja; Filippou, Vasileios; Ringenberg, Mark R.
Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels-Alder (iEDDA) addition of dienophiles.
Chemical communications (Cambridge, England), 2020, 56, 12033-12036
7127210 CIFC7 H5 N5P 1 21/c 17.2794; 9.3608; 10.4528
90; 96.97; 90		707Schnierle, Marc; Blickle, Svenja; Filippou, Vasileios; Ringenberg, Mark R.
Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels-Alder (iEDDA) addition of dienophiles.
Chemical communications (Cambridge, England), 2020, 56, 12033-12036
7127211 CIFC36 H38 Cl2 N6 O6 Re2C 1 2/c 117.9274; 12.2202; 17.9025
90; 103.284; 90		3817.1Schnierle, Marc; Blickle, Svenja; Filippou, Vasileios; Ringenberg, Mark R.
Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels-Alder (iEDDA) addition of dienophiles.
Chemical communications (Cambridge, England), 2020, 56, 12033-12036
7127212 CIFC22 H17 Cl Fe N3 O3 ReP 1 21/c 112.9074; 12.0184; 14.9765
90; 113.981; 90		2122.71Schnierle, Marc; Blickle, Svenja; Filippou, Vasileios; Ringenberg, Mark R.
Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels-Alder (iEDDA) addition of dienophiles.
Chemical communications (Cambridge, England), 2020, 56, 12033-12036
7127213 CIFC18 H13 Cl N3 O3 ReP 1 21/n 19.0781; 10.9568; 22.08
90; 92.87; 90		2193.5Schnierle, Marc; Blickle, Svenja; Filippou, Vasileios; Ringenberg, Mark R.
Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels-Alder (iEDDA) addition of dienophiles.
Chemical communications (Cambridge, England), 2020, 56, 12033-12036
7127214 CIFC21 H20 O4P c a 2110.5308; 18.5025; 8.737
90; 90; 90		1702.4Dai, Qing-Song; Tao, Ying-Mao; Zhang, Xiang; Leng, Hai-Jun; Huang, Hua; Xiang, Peng; Li, Qing-Zhu; Wang, Qi-Wei; Li, Jun-Long
Palladium-catalysed cyclisation of vinylethylene carbonates and anhydrides: a new approach to diverse medium-sized bislactones.
Chemical communications (Cambridge, England), 2020, 56, 12439-12442
7127215 CIFC19 H17 N O4P 1 21/c 115.6331; 8.0735; 12.5699
90; 92.556; 90		1584.92Dai, Qing-Song; Tao, Ying-Mao; Zhang, Xiang; Leng, Hai-Jun; Huang, Hua; Xiang, Peng; Li, Qing-Zhu; Wang, Qi-Wei; Li, Jun-Long
Palladium-catalysed cyclisation of vinylethylene carbonates and anhydrides: a new approach to diverse medium-sized bislactones.
Chemical communications (Cambridge, England), 2020, 56, 12439-12442
7127216 CIFC22 H16 O4P -14.857; 13.6775; 14.0943
114.792; 97.894; 91.103		838.88Dai, Qing-Song; Tao, Ying-Mao; Zhang, Xiang; Leng, Hai-Jun; Huang, Hua; Xiang, Peng; Li, Qing-Zhu; Wang, Qi-Wei; Li, Jun-Long
Palladium-catalysed cyclisation of vinylethylene carbonates and anhydrides: a new approach to diverse medium-sized bislactones.
Chemical communications (Cambridge, England), 2020, 56, 12439-12442
7127217 CIFC24 H18 O4P 1 21/c 111.2786; 10.8706; 15.3317
90; 97.475; 90		1863.77Dai, Qing-Song; Tao, Ying-Mao; Zhang, Xiang; Leng, Hai-Jun; Huang, Hua; Xiang, Peng; Li, Qing-Zhu; Wang, Qi-Wei; Li, Jun-Long
Palladium-catalysed cyclisation of vinylethylene carbonates and anhydrides: a new approach to diverse medium-sized bislactones.
Chemical communications (Cambridge, England), 2020, 56, 12439-12442
7127218 CIFC6 Cl Cu3 K4 N6 O6P -3 m 111.1833; 11.1833; 3.6304
90; 90; 120		393.21Kang, Kaijin; Liang, Fei; Meng, Xianghe; Tang, Jian; Zeng, Tixian; Xia, Mingjun; Lin, Zheshuai; Yin, Wenlong; Bin, Kang
K<sub>4</sub>Cu<sub>3</sub>(C<sub>3</sub>N<sub>3</sub>O<sub>3</sub>)<sub>2</sub>X (X = Cl, Br): strong anisotropic layered semiconductors containing mixed p-p and d-p conjugated π-bonds.
Chemical communications (Cambridge, England), 2020, 56, 12534-12537
7127219 CIFC6 Br Cu3 K4 N6 O6P -3 m 111.2089; 11.2089; 3.7195
90; 90; 120		404.71Kang, Kaijin; Liang, Fei; Meng, Xianghe; Tang, Jian; Zeng, Tixian; Xia, Mingjun; Lin, Zheshuai; Yin, Wenlong; Bin, Kang
K<sub>4</sub>Cu<sub>3</sub>(C<sub>3</sub>N<sub>3</sub>O<sub>3</sub>)<sub>2</sub>X (X = Cl, Br): strong anisotropic layered semiconductors containing mixed p-p and d-p conjugated π-bonds.
Chemical communications (Cambridge, England), 2020, 56, 12534-12537
7127220 CIFC16 H22 F3 N O2 SnP 1 21 111.7115; 12.6744; 12.5355
90; 103.528; 90		1809.1Delany, Pascal K.; Mortimer, Claire L.; Hodgson, David M.
Electrophile dependent mechanisms in the asymmetric trapping of α-lithio-<i>N</i>-(<i>tert</i>-butoxythiocarbonyl)azetidine.
Chemical communications (Cambridge, England), 2020, 56, 12174-12177
7127221 CIFC19 H21 N3 O2P 1 21/c 18.5708; 17.0112; 12.3358
90; 106.285; 90		1726.4Semenova, Evgeniya; Lahtigui, Ouidad; Scott, Sarah K.; Albritton, Matthew; Abboud, Khalil A.; Ghiviriga, Ion; Roitberg, Adrian E.; Grenning, Alexander J.
Selective ring-rearrangement or ring-closing metathesis of bicyclo[3.2.1]octenes.
Chemical communications (Cambridge, England), 2020, 56, 11779-11782
7127222 CIFC19 H25 N O6P 1 21 110.9242; 7.1718; 12.651
90; 105.167; 90		956.6Pei, Jun-Ping; Lv, Xue-Jiao; Peng, Chen-Jun; Liu, Yan-Kai
Asymmetric organocatalytic multicomponent reactions for efficient construction of bicyclic compounds bearing bisacetal and isoxazolidine moieties.
Chemical communications (Cambridge, England), 2020, 56, 12765-12768
7127223 CIFC17 H21 N O7P 21 21 216.921; 10.91; 24.068
90; 90; 90		1817Zhao, Can; Khan, Ijaz; Zhang, Yong Jian
Enantioselective total synthesis of furofuran lignans <i>via</i> Pd-catalyzed asymmetric allylic cycloadditon of vinylethylene carbonates with 2-nitroacrylates.
Chemical communications (Cambridge, England), 2020, 56, 12431-12434
7127224 CIFC13 H12 O5P 21 21 216.6885; 7.1093; 24.188
90; 90; 90		1150.15Zhao, Can; Khan, Ijaz; Zhang, Yong Jian
Enantioselective total synthesis of furofuran lignans <i>via</i> Pd-catalyzed asymmetric allylic cycloadditon of vinylethylene carbonates with 2-nitroacrylates.
Chemical communications (Cambridge, England), 2020, 56, 12431-12434
7127225 CIFC25 H22 N2 O8P 1 21/n 18.1947; 22.1997; 12.9203
90; 102.07; 90		2298.5Wang, Kai; Jiang, Chenghao; Zhang, Zhenming; Han, Chunyu; Wang, Xuewei; Li, Yaping; Chen, Kaiting; Zhao, Junfeng
Cut and sew: benzofuran-ring-opening enabled cyclopentenone ring formation.
Chemical communications (Cambridge, England), 2020, 56, 12817-12820
7127226 CIFC336 H304 Br82.4 Co8 N48 O34I -4 2 m24.552; 24.552; 17.693
90; 90; 90		10665Rabelo, Renato; Toma, Luminita; Moliner, Nicolás; Julve, Miguel; Lloret, Francesc; Pasán, Jorge; Ruiz-Pérez, Catalina; Ruiz-García, Rafael; Cano, Joan
Electroswitching of the single-molecule magnet behaviour in an octahedral spin crossover cobalt(ii) complex with a redox-active pyridinediimine ligand.
Chemical communications (Cambridge, England), 2020, 56, 12242-12245
7127227 CIFC42 H38 Cl2 Co N6 O12P 4319.3426; 19.3426; 43.5392
90; 90; 90		16289.6Rabelo, Renato; Toma, Luminita; Moliner, Nicolás; Julve, Miguel; Lloret, Francesc; Pasán, Jorge; Ruiz-Pérez, Catalina; Ruiz-García, Rafael; Cano, Joan
Electroswitching of the single-molecule magnet behaviour in an octahedral spin crossover cobalt(ii) complex with a redox-active pyridinediimine ligand.
Chemical communications (Cambridge, England), 2020, 56, 12242-12245
7127228 CIFC27 H19 N3 O2P 1 21/n 110.329; 19.409; 10.902
90; 98.698; 90		2160.4Singh, Sangh Priya; Tripathi, Shashank; Yadav, Anamika; Kant, Ruchir; Srivastava, Hemant Kumar; Srivastava, Ajay Kumar
Synthesis of β- and γ-lactam fused dihydropyrazinones from Ugi adducts <i>via</i> a sequential ring construction strategy.
Chemical communications (Cambridge, England), 2020, 56, 12789-12792
7127229 CIFC26 H19 F N2 O2P 21 21 219.0888; 10.564; 21.463
90; 90; 90		2060.8Singh, Sangh Priya; Tripathi, Shashank; Yadav, Anamika; Kant, Ruchir; Srivastava, Hemant Kumar; Srivastava, Ajay Kumar
Synthesis of β- and γ-lactam fused dihydropyrazinones from Ugi adducts <i>via</i> a sequential ring construction strategy.
Chemical communications (Cambridge, England), 2020, 56, 12789-12792
7127230 CIFC66 H35 N6 O0.5 Tb0.5C 1 2/m 122.7366; 17.3024; 22.0606
90; 90.923; 90		8677.5Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127231 CIFC69 H62 Cl8 N12 Sb TbP -113.1037; 15.3447; 18.9271
108.883; 104.223; 91.574		3466.69Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127232 CIFC72 H36 N6 Tb0.5C 1 2/c 124.8514; 15.5073; 27.2445
90; 118.812; 90		9199.7Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127233 CIFC67 H37 N6 Tb0.5C 1 2/m 122.811; 17.4164; 22.0814
90; 90.987; 90		8771.32Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127234 CIFC84 H96 N13 TbP 1 21/n 114.9131; 23.0259; 21.9427
90; 104.777; 90		7285.6Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127235 CIFC64 H30 B0.5 F2 N6 Tb0.5P 1 21/m 115.1885; 21.4887; 19.099
90; 104.999; 90		6021.2Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127236 CIFC162 H90 F6 N18 P Tb1.5C m c 2126.9958; 42.7901; 23.1133
90; 90; 90		26699.4Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127237 CIFC19 H13 F6 N3 O4P 1 21/n 110.5749; 11.9556; 15.5244
90; 94.202; 90		1957.46Su, Hai-Yan; Zhu, Xiao-Lei; Huang, Yangen; Xu, Xiu-Hua; Qing, Feng-Ling
Copper-catalyzed chemoselective C-H functionalization of quinoxalin-2(1<i>H</i>)-ones with hexafluoroisopropanol.
Chemical communications (Cambridge, England), 2020, 56, 12805-12808
7127238 CIFC16 H20 B10P -17.2684; 10.407; 12.7741
74.227; 81.33; 86.111		918.89Lee, Sunhee; Shin, Jisu; Ko, Doo-Hyun; Han, Won-Sik
A new type of carborane-based electron-accepting material.
Chemical communications (Cambridge, England), 2020, 56, 12741-12744
7127239 CIFC9 H15 B10P 1 21/n 110.7957; 9.7951; 13.7818
90; 112.281; 90		1348.5Lee, Sunhee; Shin, Jisu; Ko, Doo-Hyun; Han, Won-Sik
A new type of carborane-based electron-accepting material.
Chemical communications (Cambridge, England), 2020, 56, 12741-12744
7127240 CIFC23 H17 Br Cl0 N2 O3P 21 21 217.7448; 15.656; 18.122
90; 90; 90		2197.3Zhang, Dong; Dong, Shunxi; He, Qianwen; Luo, Yao; Liu, Yun; Liu, Xiaohua; Feng, Xiaoming
Enantioselective dicarbofunctionalization of (<i>E</i>)-alkenyloxindoles with pyridinium salts by chiral Lewis acid/photo relay catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12757-12760
7127241 CIFC27 H25 Br N2 O4P 1 21/n 19.4091; 11.5174; 22.8668
90; 91.996; 90		2476.53Zhang, Dong; Dong, Shunxi; He, Qianwen; Luo, Yao; Liu, Yun; Liu, Xiaohua; Feng, Xiaoming
Enantioselective dicarbofunctionalization of (<i>E</i>)-alkenyloxindoles with pyridinium salts by chiral Lewis acid/photo relay catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12757-12760
7127242 CIFC27 H25 Br N2 O4P 1 21/c 113.2371; 16.5924; 11.5023
90; 106.316; 90		2424.57Zhang, Dong; Dong, Shunxi; He, Qianwen; Luo, Yao; Liu, Yun; Liu, Xiaohua; Feng, Xiaoming
Enantioselective dicarbofunctionalization of (<i>E</i>)-alkenyloxindoles with pyridinium salts by chiral Lewis acid/photo relay catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12757-12760
7127243 CIFC27 H27 Br N2 O4C 1 2/c 121.8518; 10.5122; 22.7425
90; 108.208; 90		4962.6Zhang, Dong; Dong, Shunxi; He, Qianwen; Luo, Yao; Liu, Yun; Liu, Xiaohua; Feng, Xiaoming
Enantioselective dicarbofunctionalization of (<i>E</i>)-alkenyloxindoles with pyridinium salts by chiral Lewis acid/photo relay catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12757-12760
7127244 CIFC28 H27 Br N2 O4P 1 21/c 110.957; 22.742; 11.167
90; 110.062; 90		2613.8Zhang, Dong; Dong, Shunxi; He, Qianwen; Luo, Yao; Liu, Yun; Liu, Xiaohua; Feng, Xiaoming
Enantioselective dicarbofunctionalization of (<i>E</i>)-alkenyloxindoles with pyridinium salts by chiral Lewis acid/photo relay catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12757-12760
7127245 CIFC43 H53 N O6P 1 21/n 112.9369; 17.1825; 17.9062
90; 102.098; 90		3891.9Tlustý, Martin; Spálovská, Dita; Kohout, Michal; Eigner, Václav; Lhoták, Pavel
Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes.
Chemical communications (Cambridge, England), 2020, 56, 12773-12776
7127246 CIFC43 H53 N O6P 1 21/n 113.1917; 16.8403; 18.4369
90; 106.313; 90		3930.9Tlustý, Martin; Spálovská, Dita; Kohout, Michal; Eigner, Václav; Lhoták, Pavel
Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes.
Chemical communications (Cambridge, England), 2020, 56, 12773-12776
7127247 CIFC41 H46 O6P 1 21/c 118.1214; 12.6174; 16.0888
90; 103.99; 90		3569.5Tlustý, Martin; Spálovská, Dita; Kohout, Michal; Eigner, Václav; Lhoták, Pavel
Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes.
Chemical communications (Cambridge, England), 2020, 56, 12773-12776
7127248 CIFC41 H47 N O5P n a 219.4753; 19.0877; 39.5036
90; 90; 90		7144.7Tlustý, Martin; Spálovská, Dita; Kohout, Michal; Eigner, Václav; Lhoták, Pavel
Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes.
Chemical communications (Cambridge, England), 2020, 56, 12773-12776
7127249 CIFC94 H64 F10 N4C 1 2/c 124.2592; 14.9349; 21.0144
90; 90.863; 90		7612.8Murugavel, M.; Adinarayana, B.; Das, Mainak; Peruncheralathan, S.; Palepu, Narasinga Rao; Srinivasan, A.
PtCl<sub>2</sub> mediated peripheral transformation of carbatriphyrin(3.1.1) into a <i>meso</i>-fused β-β' dimer and its monomer analogue.
Chemical communications (Cambridge, England), 2020, 56, 12809-12812
7127250 CIFC3.36 H2.21 F0.36 N0.14 O0.07P -110.4374; 13.2672; 16.3284
71.893; 73.259; 69.076		1967.1Murugavel, M.; Adinarayana, B.; Das, Mainak; Peruncheralathan, S.; Palepu, Narasinga Rao; Srinivasan, A.
PtCl<sub>2</sub> mediated peripheral transformation of carbatriphyrin(3.1.1) into a <i>meso</i>-fused β-β' dimer and its monomer analogue.
Chemical communications (Cambridge, England), 2020, 56, 12809-12812
7127251 CIFC16 H9 F4 N OP 1 21/c 126.225; 5.008; 10.261
90; 93.42; 90		1345.2Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127252 CIFC16 H9 F4 N OP 1 21/c 126.224; 5.008; 10.26
90; 93.41; 90		1345.1Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127253 CIFC16 H9 F4 N OP 1 21/c 126.225; 5.007; 10.259
90; 93.37; 90		1344.8Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127254 CIFC16 H9 F4 N OP 1 21/c 126.232; 5.008; 10.264
90; 93.43; 90		1346Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127255 CIFC16 H9 F4 N OP 1 21/c 126.2128; 5.0027; 10.2514
90; 93.435; 90		1341.9Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127256 CIFC16 H9 F4 N OP 1 21/c 126.233; 5.007; 10.266
90; 93.36; 90		1346.1Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127257 CIFC16 H9 F4 N OP 1 21/c 126.219; 5.009; 10.26
90; 93.4; 90		1345.1Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127258 CIFC16 H9 F4 N OP 1 21/c 126.23; 5.008; 10.263
90; 93.46; 90		1345.7Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127259 CIFC16 H9 F4 N OP 1 21/c 126.226; 5.007; 10.264
90; 93.46; 90		1345.3Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127260 CIFC16 H9 F4 N OP 1 21/c 126.229; 5.008; 10.259
90; 93.39; 90		1345.2Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127261 CIFC16 H9 F4 N OP 1 21/c 126.223; 5.007; 10.266
90; 93.45; 90		1345.5Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127262 CIFC16 H9 F4 N OP 1 21/c 126.23; 5.008; 10.263
90; 93.49; 90		1345.6Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127263 CIFC16 H9 F4 N OP 1 21/c 126.231; 5.008; 10.259
90; 93.42; 90		1345.3Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127264 CIFC16 H9 F4 N OP 1 21/c 126.231; 5.008; 10.262
90; 93.44; 90		1345.6Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127265 CIFC104 H106 N4 O77 Zn14P 1 21/n 122.1643; 16.4288; 23.8287
90; 93.08; 90		8664.3Li, Chuan-Ping; Long, Wei-Wei; Lei, Zhen; Guo, Ling; Xie, Ming-Jun; Lü, Jian; Zhu, Xian-Dong
Anionic metal-organic framework as a unique turn-on fluorescent chemical sensor for ultra-sensitive detection of antibiotics.
Chemical communications (Cambridge, England), 2020, 56, 12403-12406
7127266 CIFC34 H64 N4 Si4 YbP 1 21/c 115.5992; 11.4432; 23.1873
90; 94.693; 90		4125.2Lapshin, Ivan V.; Cherkasov, Anton V.; Asachenko, Andrey F.; Trifonov, Alexander A.
Ln(II) amido complexes coordinated by ring-expanded N-heterocyclic carbenes - promising catalysts for olefin hydrophosphination.
Chemical communications (Cambridge, England), 2020, 56, 12913-12916
7127267 CIFC34 H64 N4 Si4 SmP 1 21/c 115.5699; 11.47; 23.5397
90; 94.58; 90		4190.45Lapshin, Ivan V.; Cherkasov, Anton V.; Asachenko, Andrey F.; Trifonov, Alexander A.
Ln(II) amido complexes coordinated by ring-expanded N-heterocyclic carbenes - promising catalysts for olefin hydrophosphination.
Chemical communications (Cambridge, England), 2020, 56, 12913-12916
7127268 CIFC33 H28 F2 N2 O4P c a 2126.9151; 13.9396; 7.31714
90; 90; 90		2745.29Shi, Wei-Yu; Ding, Ya-Nan; Liu, Ce; Zheng, Nian; Gou, Xue-Ya; Li, Ming; Zhang, Zhe; Liu, Hong-Chao; Niu, Zhi-Jie; Liang, Yong-Min
Three-component ruthenium-catalyzed remote C-H functionalization of 8-aminoquinoline amides.
Chemical communications (Cambridge, England), 2020, 56, 12729-12732
7127269 CIFC6 N12 O16P 1 21/c 19.6672; 9.6302; 9.0564
90; 101.776; 90		825.38Mohammad, Khaja; Thaltiri, Vikranth; Kommu, Nagarjuna; Vargeese, Anuj A.
Octanitropyrazolopyrazole: a gem-trinitromethyl based green high-density energetic oxidizer.
Chemical communications (Cambridge, England), 2020, 56, 12945-12948
7127270 CIFC21 H16 O3P b c a8.8744; 11.4021; 60.208
90; 90; 90		6092.3Yasui, Takeshi; Kikuchi, Tomohiro; Yamamoto, Yoshihiko
Rhodium-catalyzed cycloisomerization of ester-tethered 1,6-diynes with cyclopropanol moiety leading to tetralone/exocyclic diene hybrid molecules.
Chemical communications (Cambridge, England), 2020, 56, 12865-12868
7127271 CIFC24 H20 O3P 1 21/n 113.017; 10.8103; 13.8173
90; 110.376; 90		1822.68Yasui, Takeshi; Kikuchi, Tomohiro; Yamamoto, Yoshihiko
Rhodium-catalyzed cycloisomerization of ester-tethered 1,6-diynes with cyclopropanol moiety leading to tetralone/exocyclic diene hybrid molecules.
Chemical communications (Cambridge, England), 2020, 56, 12865-12868
7127272 CIFC19 H20 O3P 1 21 18.6683; 8.386; 11.3586
90; 110.379; 90		774Yasui, Takeshi; Kikuchi, Tomohiro; Yamamoto, Yoshihiko
Rhodium-catalyzed cycloisomerization of ester-tethered 1,6-diynes with cyclopropanol moiety leading to tetralone/exocyclic diene hybrid molecules.
Chemical communications (Cambridge, England), 2020, 56, 12865-12868
7127273 CIFC21 H16 O3P 1 21 19.6092; 8.1201; 10.9799
90; 116.426; 90		767.22Yasui, Takeshi; Kikuchi, Tomohiro; Yamamoto, Yoshihiko
Rhodium-catalyzed cycloisomerization of ester-tethered 1,6-diynes with cyclopropanol moiety leading to tetralone/exocyclic diene hybrid molecules.
Chemical communications (Cambridge, England), 2020, 56, 12865-12868
7127274 CIFC22 H18 O3P 1 21/c 115.8736; 9.6592; 10.7426
90; 93.45; 90		1644.14Yasui, Takeshi; Kikuchi, Tomohiro; Yamamoto, Yoshihiko
Rhodium-catalyzed cycloisomerization of ester-tethered 1,6-diynes with cyclopropanol moiety leading to tetralone/exocyclic diene hybrid molecules.
Chemical communications (Cambridge, England), 2020, 56, 12865-12868
7127275 CIFC9.75 H7.75C m c e20.155; 4.7512; 26.999
90; 90; 90		2585.4Jiménez, Vicente G; Mayorga-Burrezo, Paula; Blanco, Victor; Lloveras, Vega; Gómez-García, Carlos J; Šolomek, Tomáš; Cuerva, Juan M.; Veciana, Jaume; Campaña, Araceli G
Dibenzocycloheptatriene as end-group of Thiele and tetrabenzo-Chichibabin hydrocarbons.
Chemical communications (Cambridge, England), 2020, 56, 12813-12816
7127276 CIFC59 H40 Cl2 O2P -110.9191; 14.2474; 15.1184
87.56; 70.753; 71.905		2106Jiménez, Vicente G; Mayorga-Burrezo, Paula; Blanco, Victor; Lloveras, Vega; Gómez-García, Carlos J; Šolomek, Tomáš; Cuerva, Juan M.; Veciana, Jaume; Campaña, Araceli G
Dibenzocycloheptatriene as end-group of Thiele and tetrabenzo-Chichibabin hydrocarbons.
Chemical communications (Cambridge, England), 2020, 56, 12813-12816
7127277 CIFC48 H42 Cl2 O4 P4 Pd2P -111.8642; 13.1675; 17.343
68.772; 78.937; 63.277		2254.4Oka, Sayaka; Shigehiro, Yuma; Kataoka, Yasutaka; Ura, Yasuyuki
Secondary phosphine oxide-triggered selective oxygenation of a benzyl ligand on palladium.
Chemical communications (Cambridge, England), 2020, 56, 12977-12980
7127278 CIFC42 H44 Cl2 O2.67 P2 Pd2P -110.05; 13.715; 23.78
78.415; 81.104; 86.079		3170Oka, Sayaka; Shigehiro, Yuma; Kataoka, Yasutaka; Ura, Yasuyuki
Secondary phosphine oxide-triggered selective oxygenation of a benzyl ligand on palladium.
Chemical communications (Cambridge, England), 2020, 56, 12977-12980
7127279 CIFC28 H37 Cl2 Mn N7 O9P 1 21 18.8444; 14.0029; 13.7453
90; 99.99; 90		1676.5Xu, Daqian; Sun, Qiangsheng; Lin, Jin; Sun, Wei
Ligand regulation for manganese-catalyzed enantioselective epoxidation of olefins without acid.
Chemical communications (Cambridge, England), 2020, 56, 13101-13104
7127280 CIFC103 H63 Cl9 O2P -115.3787; 16.0584; 16.3664
85.569; 82.256; 71.671		3799.1Pozo, Iago; Peña, Diego; Guitián, Enrique; Pérez, Dolores
2,6,10-Triphenylenotriyne: a star-shaped trisaryne.
Chemical communications (Cambridge, England), 2020, 56, 12853-12856
7127281 CIFC15 H22 B10 S2C m c 2120.2845; 11.9988; 8.454
90; 90; 90		2057.62Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127282 CIFC15 H20 B10 F2 S2C m c 2119.7267; 12.6094; 8.409
90; 90; 90		2091.67Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127283 CIFC5 H18 B10 S2P n m a8.4713; 13.2354; 12.3156
90; 90; 90		1380.84Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127284 CIFC15 H20 B10 Cl2 S2C m c 2121.136; 12.146; 8.5666
90; 90; 90		2199.2Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127285 CIFC20 H24 B10 S2C 1 2/c 125.878; 11.6738; 20.3229
90; 128.273; 90		4819.9Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127286 CIFC15 H22 B10 Se2C m c 2119.6577; 12.2928; 8.5569
90; 90; 90		2067.8Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127287 CIFC15 H20 B10 Br2 S2P b c a17.4444; 11.2142; 23.4319
90; 90; 90		4583.9Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127288 CIFC15 H22 B10 O2 S2C m c 2119.5554; 12.2522; 8.6766
90; 90; 90		2078.9Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127289 CIFC79 H39 B2 F40 SbP 1 21/c 116.5682; 15.2566; 28.2917
90; 90.006; 90		7151.4Zhou, Jiliang; Kim, Hyehwang; Liu, Liu Leo; Cao, Levy L.; Stephan, Douglas W.
An arene-stabilized η<sup>5</sup>-pentamethylcyclopentadienyl antimony dication acts as a source of Sb<sup>+</sup> or Sb<sup>3+</sup> cations.
Chemical communications (Cambridge, England), 2020, 56, 12953-12956
7127290 CIFC25 H21 F9 N4 O9.5 S3 SbP -19.101; 13.275; 13.8328
81.615; 86.39; 84.352		1643.32Zhou, Jiliang; Kim, Hyehwang; Liu, Liu Leo; Cao, Levy L.; Stephan, Douglas W.
An arene-stabilized η<sup>5</sup>-pentamethylcyclopentadienyl antimony dication acts as a source of Sb<sup>+</sup> or Sb<sup>3+</sup> cations.
Chemical communications (Cambridge, England), 2020, 56, 12953-12956
7127291 CIFC61 H64 B F20 N4 SbP 1 2/n 119.218; 8.3161; 20.922
90; 111.897; 90		3102.5Zhou, Jiliang; Kim, Hyehwang; Liu, Liu Leo; Cao, Levy L.; Stephan, Douglas W.
An arene-stabilized η<sup>5</sup>-pentamethylcyclopentadienyl antimony dication acts as a source of Sb<sup>+</sup> or Sb<sup>3+</sup> cations.
Chemical communications (Cambridge, England), 2020, 56, 12953-12956
7127292 CIFC20 H21 N O2 SP 16.0451; 8.3029; 9.2867
107.436; 107.421; 90.517		421.8Tao, Mengna; Li, Wenbo; Zhang, Junliang
Pd/Xiang-Phos-catalyzed enantioselective intermolecular carboheterofunctionalization of norbornene and norbornadiene.
Chemical communications (Cambridge, England), 2020, 56, 13125-13128
7127293 CIFC15 H16 O3P 21 21 216.0733; 11.523; 17.1932
90; 90; 90		1203.23Tao, Mengna; Li, Wenbo; Zhang, Junliang
Pd/Xiang-Phos-catalyzed enantioselective intermolecular carboheterofunctionalization of norbornene and norbornadiene.
Chemical communications (Cambridge, England), 2020, 56, 13125-13128
7127294 CIFC35 H35 F6 N5 O11 Ru S2P 110.011; 13.646; 16.369
66.564; 72.663; 78.969		1951.7Hirahara, Masanari; Goto, Hiroki; Yagi, Masayuki; Umemura, Yasushi
A multi-stimuli responsive ruthenium complex for catalytic water oxidation.
Chemical communications (Cambridge, England), 2020, 56, 12825-12828
7127295 CIFC35 H35 F6 N5 O11 Ru S2P -111.5955; 13.3944; 13.4286
94.6542; 108.322; 99.0418		1936.28Hirahara, Masanari; Goto, Hiroki; Yagi, Masayuki; Umemura, Yasushi
A multi-stimuli responsive ruthenium complex for catalytic water oxidation.
Chemical communications (Cambridge, England), 2020, 56, 12825-12828
7127296 CIFC58 H50 N7 O3 P2 ReP -113.556; 13.655; 16.754
71.32; 88.136; 61.543		2556Sasaki, Kenta; Yamate, Hitomi; Yoshino, Haruka; Miura, Hiroki; Shimoda, Yuushi; Miyata, Kiyoshi; Onda, Ken; Ohtani, Ryo; Ohba, Masaaki
Vapor switching of the luminescence mechanism in a Re(V) complex.
Chemical communications (Cambridge, England), 2020, 56, 12961-12964
7127297 CIFC55 H43 N5 O5 P2 ReP -113.437; 13.848; 16.639
71.036; 89.469; 61.39		2530.3Sasaki, Kenta; Yamate, Hitomi; Yoshino, Haruka; Miura, Hiroki; Shimoda, Yuushi; Miyata, Kiyoshi; Onda, Ken; Ohtani, Ryo; Ohba, Masaaki
Vapor switching of the luminescence mechanism in a Re(V) complex.
Chemical communications (Cambridge, England), 2020, 56, 12961-12964
7127298 CIFC62 H56 N7 O2 P2 ReP -113.6167; 14.0119; 15.9593
109.223; 90.428; 106.99		2731.5Sasaki, Kenta; Yamate, Hitomi; Yoshino, Haruka; Miura, Hiroki; Shimoda, Yuushi; Miyata, Kiyoshi; Onda, Ken; Ohtani, Ryo; Ohba, Masaaki
Vapor switching of the luminescence mechanism in a Re(V) complex.
Chemical communications (Cambridge, England), 2020, 56, 12961-12964
7127299 CIFC19 H13 N3 O2 PtP 1 21/c 111.0034; 12.6502; 23.9841
90; 98.435; 90		3302.36Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127300 CIFC21 H17 N3 O2 PtR -3 :H30.2541; 30.2541; 10.0134
90; 90; 120		7937.4Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127301 CIFC19 H14.33 N3 O2.67 PtR -3 :H30.4714; 30.4714; 10.0419
90; 90; 120		8074.79Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127302 CIFC19 H13 N3 O2 PtR -3 :H30.402; 30.402; 10.0404
90; 90; 120		8036.9Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127303 CIFC21 H17 N3 O2 PtR -3 :H30.2896; 30.2896; 10.057
90; 90; 120		7990.72Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127304 CIFC39 H52 Cl0.33 Co N2.33 P3P -19.4001; 10.1799; 19.692
96.945; 98.651; 92.505		1845.6Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127305 CIFC37 H48 Cl Co N P3P b c a11.1139; 17.2203; 36.7506
90; 90; 90		7033.5Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127306 CIFC39 H52 Cl Co N P3P b c a18.5652; 15.3844; 25.5535
90; 90; 90		7298.4Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127307 CIFC37 H48 Cl2 Co N P3P 1 21/c 118.0756; 12.9004; 16.8278
90; 112.241; 90		3632Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127308 CIFC25 H39 Cl Co P3P 1 21/n 110.5437; 16.2502; 15.7679
90; 98.878; 90		2669.26Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127309 CIFC71 H63 B Co F24 N2 P3P 1 21/n 112.5472; 41.432; 13.4271
90; 92.586; 90		6973Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127310 CIFC74 H98 Co2 N4 P6P -111.285; 15.184; 21.077
89.329; 89.127; 75.629		3498Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127311 CIFC39 H52 Cl2 Co N P3P 4115.4027; 15.4027; 32.0302
90; 90; 90		7598.9Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127312 CIFC39 H52 Cl Co N P3P -19.751; 12.142; 17.953
72.006; 76.941; 71.219		1895Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127313 CIFC25 H24 O9P b c a22.085; 9.856; 22.387
90; 90; 90		4873Manna, Sabyasachi; Someswara Ashwathappa, Puneeth Kumar; Prabhu, Kandikere Ramaiah
Visible light-mediated ipso-annulation of activated alkynes: access to 3-alkylated spiro[4,5]-trienones, thiaspiro[4,5]-trienones and azaspiro[4,5]-trienones.
Chemical communications (Cambridge, England), 2020, 56, 13165-13168
7127314 CIFC19 H13 N3 O2 PtP 1 21/c 111.0034; 12.6502; 23.9841
90; 98.435; 90		3302.36Kimura, Mari; Yoshida, Masaki; Fujii, Sho; Miura, Atsushi; Ueno, Kosei; Shigeta, Yasuhiro; Kobayashi, Atsushi; Kato, Masako
Liquid-liquid interface-promoted formation of a porous molecular crystal based on a luminescent platinum(II) complex.
Chemical communications (Cambridge, England), 2020, 56, 12989-12992
7127315 CIFC21 H17 N3 O2 PtR -3 :H30.2541; 30.2541; 10.0134
90; 90; 120		7937.4Kimura, Mari; Yoshida, Masaki; Fujii, Sho; Miura, Atsushi; Ueno, Kosei; Shigeta, Yasuhiro; Kobayashi, Atsushi; Kato, Masako
Liquid-liquid interface-promoted formation of a porous molecular crystal based on a luminescent platinum(II) complex.
Chemical communications (Cambridge, England), 2020, 56, 12989-12992
7127316 CIFC19 H14.33 N3 O2.67 PtR -3 :H30.4714; 30.4714; 10.0419
90; 90; 120		8074.79Kimura, Mari; Yoshida, Masaki; Fujii, Sho; Miura, Atsushi; Ueno, Kosei; Shigeta, Yasuhiro; Kobayashi, Atsushi; Kato, Masako
Liquid-liquid interface-promoted formation of a porous molecular crystal based on a luminescent platinum(II) complex.
Chemical communications (Cambridge, England), 2020, 56, 12989-12992
7127317 CIFC19 H13 N3 O2 PtR -3 :H30.402; 30.402; 10.0404
90; 90; 120		8036.9Kimura, Mari; Yoshida, Masaki; Fujii, Sho; Miura, Atsushi; Ueno, Kosei; Shigeta, Yasuhiro; Kobayashi, Atsushi; Kato, Masako
Liquid-liquid interface-promoted formation of a porous molecular crystal based on a luminescent platinum(II) complex.
Chemical communications (Cambridge, England), 2020, 56, 12989-12992
7127318 CIFC21 H17 N3 O2 PtR -3 :H30.2896; 30.2896; 10.057
90; 90; 120		7990.72Kimura, Mari; Yoshida, Masaki; Fujii, Sho; Miura, Atsushi; Ueno, Kosei; Shigeta, Yasuhiro; Kobayashi, Atsushi; Kato, Masako
Liquid-liquid interface-promoted formation of a porous molecular crystal based on a luminescent platinum(II) complex.
Chemical communications (Cambridge, England), 2020, 56, 12989-12992
7127319 CIFC34 H34 Cl4 O10P b c a10.519; 14.5588; 22.7509
90; 90; 90		3484.2Joshi, Saurabh; Yip, Yong Jie; Türel, Tankut; Verma, Sandeep; Valiyaveettil, Suresh
Cu-tetracatechol metallopolymer catalyst for three component click reactions and β-borylation of α,β-unsaturated carbonyl compounds.
Chemical communications (Cambridge, England), 2020, 56, 13044-13047
7127320 CIFC30 H25 F N2 O5P -110.0079; 11.0103; 13.8154
68.117; 74.662; 67.141		1288.86Lv, Yunhe; Pu, Weiya; Wang, Xiaoxing
Ligand-free copper-catalyzed regio- and stereoselective 1,1-alkylmonofluoroalkylation of terminal alkynes.
Chemical communications (Cambridge, England), 2020, 56, 12933-12936
7127321 CIFC30 H22 N2 O5P 1 21 18.8477; 14.2309; 9.6371
90; 95.549; 90		1207.73Yuan, Xi; Wu, Xudong; Peng, Fei; Yang, Haijun; Zhu, Changjin; Fu, Hua
Organocatalytic asymmetric synthesis of arylindolyl indolin-3-ones with both axial and central chirality.
Chemical communications (Cambridge, England), 2020, 56, 12648-12651
7127322 CIFC20 H20 F6 Fe N2 O7 S5C 1 2/c 124.4848; 11.4726; 20.4806
90; 108.738; 90		5448.2Chan, Siu-Chung; Yeung, Chi-Fung; Shek, Hau-Lam; Ng, Sze-Wing; Tse, Sheung-Ying; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Iron(ii)-induced cycloisomerization of alkynes via"non-vinylidene" pathways for iron(ii)-indolizine and -indolizinone complexes.
Chemical communications (Cambridge, England), 2020, 56, 12644-12647
7127323 CIFC40 H42 F6 Fe N3 O8.5 S5P -110.277; 14.2819; 15.9309
88; 71.475; 89.017		2215.7Chan, Siu-Chung; Yeung, Chi-Fung; Shek, Hau-Lam; Ng, Sze-Wing; Tse, Sheung-Ying; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Iron(ii)-induced cycloisomerization of alkynes via"non-vinylidene" pathways for iron(ii)-indolizine and -indolizinone complexes.
Chemical communications (Cambridge, England), 2020, 56, 12644-12647
7127324 CIFC33 H29 F6 Fe N3 O7 S5P -113.0248; 13.4754; 21.3868
86.09; 76.878; 81.685		3614.8Chan, Siu-Chung; Yeung, Chi-Fung; Shek, Hau-Lam; Ng, Sze-Wing; Tse, Sheung-Ying; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Iron(ii)-induced cycloisomerization of alkynes via"non-vinylidene" pathways for iron(ii)-indolizine and -indolizinone complexes.
Chemical communications (Cambridge, England), 2020, 56, 12644-12647
7127325 CIFC35 H31 F6 Fe N3 O7 S5P b c a14.2635; 17.4695; 30.1975
90; 90; 90		7524.5Chan, Siu-Chung; Yeung, Chi-Fung; Shek, Hau-Lam; Ng, Sze-Wing; Tse, Sheung-Ying; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Iron(ii)-induced cycloisomerization of alkynes via"non-vinylidene" pathways for iron(ii)-indolizine and -indolizinone complexes.
Chemical communications (Cambridge, England), 2020, 56, 12644-12647
7127326 CIFC42 H44 Co N6 O10P 1 21/n 110.2874; 19.8376; 11.0367
90; 111.416; 90		2096.8Koyama, Shohei; Tanabe, Tappei; Takaishi, Shinya; Yamashita, Masahiro; Iguchi, Hiroaki
Preliminary chemical reduction for synthesizing a stable porous molecular conductor with neutral metal nodes.
Chemical communications (Cambridge, England), 2020, 56, 13109-13112
7127327 CIFC42 H44 Co N6 O10 Rb0.5P 64 2 219.8453; 19.8453; 9.5591
90; 90; 120		3260.3Koyama, Shohei; Tanabe, Tappei; Takaishi, Shinya; Yamashita, Masahiro; Iguchi, Hiroaki
Preliminary chemical reduction for synthesizing a stable porous molecular conductor with neutral metal nodes.
Chemical communications (Cambridge, England), 2020, 56, 13109-13112
7127328 CIFC74 H75 Au5 Cl2 P3 Ru2 S0P -113.98; 16.129; 17.64
112.192; 90.973; 92.718		3676.1Sun, Yongnan; Yang, Dan; Zhang, Yuying; Hu, Weigang; Cheng, Xinglian; Liu, Xu; Chen, Mingyang; Zhu, Yan
Ligand-protected Au<sub>4</sub>Ru<sub>2</sub> and Au<sub>5</sub>Ru<sub>2</sub> nanoclusters: distinct structures and implications for site-cooperation catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12833-12836
7127329 CIFC23 H34 OP 1 21 16.689; 10.95; 13.04
90; 94.67; 90		951.9Bettoni, Léo; Gaillard, Sylvain; Renaud, Jean-Luc
A phosphine-free iron complex-catalyzed synthesis of cycloalkanes <i>via</i> the borrowing hydrogen strategy.
Chemical communications (Cambridge, England), 2020, 56, 12909-12912
7127330 CIFC25 H26 O2 SP 1 21/c 110.361; 22.362; 10.254
90; 113.65; 90		2176.2Parameshwar, Matam; Singam, Maneesh Kumar Reddy; Nagireddy, Attunuri; Nanubolu, Jagadeesh Babu; Reddy, Maddi Sridhar
Regioselective benzannulation of allylic sulfur ylides with ynones: a rapid access to substituted thioanisoles.
Chemical communications (Cambridge, England), 2020, 56, 13457-13460
7127331 CIFC6 F1.87 La0.09 O0.8 S0.36P -115.184; 15.6113; 47.3346
99.304; 91.333; 110.381		10341Zhang, Yuan; Zhou, Yanyan; Gao, Ting; Yan, Pengfei; Li, Hongfeng
Metal-directed synthesis of quadruple-stranded helical Eu(III) molecular switch: a significant improvement in photocyclization quantum yield.
Chemical communications (Cambridge, England), 2020, 56, 13213-13216
7127332 CIFC54 H54 N4 O15 Zn4C 1 2/m 122.3686; 25.4298; 17.1469
90; 101.016; 90		9573.9Xi, Fu-Gui; Sun, Wei; Dong, Zhi-Yun; Yang, Ning-Ning; Gong, Teng; Gao, En-Qing
An in situ approach to functionalize metal-organic frameworks with tertiary aliphatic amino groups.
Chemical communications (Cambridge, England), 2020, 56, 13177-13180
7127333 CIFC9.6 H21.12 Eu O18 S3P 1 21/n 18.9194; 8.8509; 25.242
90; 90.154; 90		1992.7Ruaysap, Makabodee; Kennedy, Stuart R.; Mayhan, Collin M.; Kelley, Steven P.; Kumari, Harshita; Deakyne, Carol A.; Atwood, Jerry L.
Novel keto-enol tautomerism in 1,3,5-trihydroxybenzene systems.
Chemical communications (Cambridge, England), 2020, 56, 12985-12988
7127334 CIFC9.6 H19.5 O18 S3 SmP 1 21/n 18.9342; 8.8762; 25.291
90; 90.34; 90		2005.6Ruaysap, Makabodee; Kennedy, Stuart R.; Mayhan, Collin M.; Kelley, Steven P.; Kumari, Harshita; Deakyne, Carol A.; Atwood, Jerry L.
Novel keto-enol tautomerism in 1,3,5-trihydroxybenzene systems.
Chemical communications (Cambridge, England), 2020, 56, 12985-12988
7127335 CIFC16 H18 Br N O4P 1 21 110.42782; 7.6985; 11.51764
90; 106.53; 90		886.41Mato, Raquel; Reyes, Efraim; Carrillo, Luisa; Uria, Uxue; Prieto, Liher; Manzano, Ruben; Vicario, Jose L.
Catalytic enantioselective domino Michael/transannular aldol reaction under bifunctional catalysis.
Chemical communications (Cambridge, England), 2020, 56, 13149-13152
7127336 CIFC18 H21 N O4P 21 21 219.19139; 11.21187; 15.13619
90; 90; 90		1559.82Mato, Raquel; Reyes, Efraim; Carrillo, Luisa; Uria, Uxue; Prieto, Liher; Manzano, Ruben; Vicario, Jose L.
Catalytic enantioselective domino Michael/transannular aldol reaction under bifunctional catalysis.
Chemical communications (Cambridge, England), 2020, 56, 13149-13152
7127337 CIFC29 H22 Br N O SP 1 21 110.663; 9.0225; 12.3447
90; 90.216; 90		1187.6Chang, Fenzhen; Shen, Bin; Wang, Sijing; Lin, Lili; Feng, Xiaoming
Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles.
Chemical communications (Cambridge, England), 2020, 56, 13429-13432
7127338 CIFC29 H23 N O2P 21 21 217.1433; 16.4271; 18.919
90; 90; 90		2220.03Chang, Fenzhen; Shen, Bin; Wang, Sijing; Lin, Lili; Feng, Xiaoming
Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles.
Chemical communications (Cambridge, England), 2020, 56, 13429-13432
7127339 CIFC29 H23 N O SP 1 21 19.7976; 8.723; 14.089
90; 110.142; 90		1130.5Chang, Fenzhen; Shen, Bin; Wang, Sijing; Lin, Lili; Feng, Xiaoming
Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles.
Chemical communications (Cambridge, England), 2020, 56, 13429-13432
7127340 CIFC29 H23 N O SP 21 21 2110.0966; 16.0127; 27.6462
90; 90; 90		4469.7Chang, Fenzhen; Shen, Bin; Wang, Sijing; Lin, Lili; Feng, Xiaoming
Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles.
Chemical communications (Cambridge, England), 2020, 56, 13429-13432
7127341 CIFC22 H23 Eu N4 O14P 1 21/c 116.3413; 10.2541; 15.7957
90; 91.96; 90		2645.26Fu, Ting; Wei, Yong-Li; Zhang, Chong; Li, Lin-Ke; Liu, Xiao-Fei; Li, Hai-Yang; Zang, Shuang-Quan
A viologen-based multifunctional Eu-MOF: photo/electro-modulated chromism and luminescence.
Chemical communications (Cambridge, England), 2020, 56, 13093-13096
7127342 CIFC34.5 H38 Cl Ir N2 O5.5P -17.7989; 9.4618; 24.171
95.058; 94.646; 112.464		1629.1Nguyen, Huong T. H.; Do, Loi H.
Organoiridium-quinone conjugates for facile hydrogen peroxide generation.
Chemical communications (Cambridge, England), 2020, 56, 13381-13384
7127343 CIFC54 H74 As4 Fe2 N4P -113.2431; 13.9354; 16.0383
89.203; 87.031; 67.239		2725.6Spitzer, Fabian; Balázs, Gábor; Graßl, Christian; Scheer, Manfred
Iron β-diiminate complexes with As<sub>2</sub>-, As<sub>4</sub>- and As<sub>8</sub>-ligands.
Chemical communications (Cambridge, England), 2020, 56, 13209-13212
7127344 CIFC54 H74 As4 Fe2 N4P -113.2706; 14.0867; 15.8705
89.309; 86.365; 67.8		2741.13Spitzer, Fabian; Balázs, Gábor; Graßl, Christian; Scheer, Manfred
Iron β-diiminate complexes with As<sub>2</sub>-, As<sub>4</sub>- and As<sub>8</sub>-ligands.
Chemical communications (Cambridge, England), 2020, 56, 13209-13212
7127345 CIFC101.5 H120 As8 Fe4 N8P -113.60288; 14.75365; 26.0325
82.1763; 76.4461; 78.1144		4948.88Spitzer, Fabian; Balázs, Gábor; Graßl, Christian; Scheer, Manfred
Iron β-diiminate complexes with As<sub>2</sub>-, As<sub>4</sub>- and As<sub>8</sub>-ligands.
Chemical communications (Cambridge, England), 2020, 56, 13209-13212
7127346 CIFC83 H92 As8 Fe4 N8C 1 2/c 124.8828; 12.9874; 26.3513
90; 103.716; 90		8272.9Spitzer, Fabian; Balázs, Gábor; Graßl, Christian; Scheer, Manfred
Iron β-diiminate complexes with As<sub>2</sub>-, As<sub>4</sub>- and As<sub>8</sub>-ligands.
Chemical communications (Cambridge, England), 2020, 56, 13209-13212
7127347 CIFC58 H82 As3.78 Fe2 N4P 1 21/n 114.2884; 13.6019; 15.3559
90; 103.879; 90		2897.28Spitzer, Fabian; Balázs, Gábor; Graßl, Christian; Scheer, Manfred
Iron β-diiminate complexes with As<sub>2</sub>-, As<sub>4</sub>- and As<sub>8</sub>-ligands.
Chemical communications (Cambridge, England), 2020, 56, 13209-13212
7127348 CIFC19 H14 N2 OP -16.1633; 10.2878; 11.0233
88.901; 81.769; 81.501		684.15Chakraborty, Soumi; Das, Arpan; Ahmed, Jasimuddin; Barman, Sayani; Mandal, Swadhin K.
Designing a Cr-catalyst bearing redox non-innocent phenalenyl-based ligand towards hydrosilylative CO<sub>2</sub> functionalization.
Chemical communications (Cambridge, England), 2020, 56, 13788-13791
7127349 CIFC40 H36 Cl Cr N4 O5P -19.8879; 16.9397; 20.5976
83.383; 76.246; 89.429		3328.3Chakraborty, Soumi; Das, Arpan; Ahmed, Jasimuddin; Barman, Sayani; Mandal, Swadhin K.
Designing a Cr-catalyst bearing redox non-innocent phenalenyl-based ligand towards hydrosilylative CO<sub>2</sub> functionalization.
Chemical communications (Cambridge, England), 2020, 56, 13788-13791
7127350 CIFC48 H84 Co Li N3 O6P 1 21 110.8897; 21.2774; 11.9691
90; 113.656; 90		2540.26Das, Chinmoy; Rasamsetty, Amaleswari; Tripathi, Shalini; Shanmugam, Maheswaran
Magnetization relaxation dynamics of a rare coordinatively unsaturated Co(II) complex: experimental and theoretical insights.
Chemical communications (Cambridge, England), 2020, 56, 13397-13400
7127351 CIFC39 H46 Cu N2 PP -110.0805; 10.9216; 16.5042
73.491; 88.101; 84.877		1735.11Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127352 CIFC106 H122 Cu2 N6 P2 S2P -116.7653; 16.7976; 17.4582
99.123; 103.295; 92.374		4708.68Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127353 CIFC68 H76 Cu2 N4 P2P -111.3727; 11.3954; 22.6857
90.164; 91.091; 101.25		2882.91Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127354 CIFC40 H50 Cu N2 PP -112.8035; 16.6298; 17.6961
104.81; 90.293; 95.555		3623.82Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127355 CIFC33 H36 Cu N2 PP 1 21/c 112.9476; 19.6806; 13.1443
90; 119.072; 90		2927.4Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127356 CIFC47 H56 Cu N2 P S2P 1 21/c 110.7063; 12.6577; 32.3409
90; 98.799; 90		4331.17Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127357 CIFC44 H57 Cu N3 O PP 1 21/n 112.5486; 18.9533; 17.66
90; 106.233; 90		4032.76Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127358 CIFC22 H36 Ca Cl2 N6 O6P -17.968; 12.17; 15.304
87.17; 86.3; 74.76		1428.1Song, Lixing; Robeyns, Koen; Tumanov, Nikolay; Wouters, Johan; Leyssens, Tom
Combining API in a dual-drug ternary cocrystal approach.
Chemical communications (Cambridge, England), 2020, 56, 13229-13232
7127359 CIFC22 H36 Ca Cl2 N6 O6P 1 21 111.9243; 8.0669; 15.4348
90; 92.338; 90		1483.47Song, Lixing; Robeyns, Koen; Tumanov, Nikolay; Wouters, Johan; Leyssens, Tom
Combining API in a dual-drug ternary cocrystal approach.
Chemical communications (Cambridge, England), 2020, 56, 13229-13232
7127360 CIFC22 H36 Ca Cl2 N6 O6P 21 21 217.9303; 15.1768; 23.7226
90; 90; 90		2855.17Song, Lixing; Robeyns, Koen; Tumanov, Nikolay; Wouters, Johan; Leyssens, Tom
Combining API in a dual-drug ternary cocrystal approach.
Chemical communications (Cambridge, England), 2020, 56, 13229-13232
7127361 CIFC23 H22 O4 S2P -18.8162; 9.9355; 12.7903
88.965; 85.831; 70.437		1052.86Wang, Yu; Tang, Kongshuang; Liu, Zhaohong; Ning, Yongquan
Disulfonation of terminal alkynes for 1,2-bisulfonylethenes.
Chemical communications (Cambridge, England), 2020, 56, 13141-13144
7127362 CIFC26 H23 Br F3 N O5P 1 21 18.78349; 25.2447; 11.5445
90; 92.4781; 90		2557.44Zhang, Xia-Yan; You, Yong; Wang, Zhen-Hua; Zhao, Jian-Qiang; Yuan, Wei-Cheng
Organocatalytic asymmetric tandem α-functionalization/1,3-proton shift reaction of benzylidene succinimides with β-trifluoromethyl enones.
Chemical communications (Cambridge, England), 2020, 56, 13449-13452
7127363 CIFC91 H10 Br O4 S4 YP 1 21/c 111.2309; 22.0675; 20.7788
90; 98.817; 90		5088.9Shen, Wangqiang; Yang, Le; Li, Bo; Jin, Peng; Yu, Bing; Cong, Hailin; Akasaka, Takeshi; Lu, Xing
Metal-encapsulation induces a highly regioselective Bingel-Hirsch reaction of the labile Y@<i>C</i><sub>s</sub>(6)-C<sub>82</sub>.
Chemical communications (Cambridge, England), 2020, 56, 14357-14360
7127364 CIFC24 H22 Br2 N2 O2P 1 21/n 16.0728; 24.305; 15.0006
90; 98.929; 90		2187.2Silvestri, A. P.; Oakdale, J. S.
Intermolecular cyclotrimerization of haloketoalkynes and internal alkynes: facile access to arenes and phthalides.
Chemical communications (Cambridge, England), 2020, 56, 13417-13420
7127365 CIFC12 H11 Br2 N O4P -18.5662; 8.5847; 9.5341
96.065; 102.093; 95.978		675.95Silvestri, A. P.; Oakdale, J. S.
Intermolecular cyclotrimerization of haloketoalkynes and internal alkynes: facile access to arenes and phthalides.
Chemical communications (Cambridge, England), 2020, 56, 13417-13420
7127366 CIFC47 H46 Cl N5 O5 P2 PtP 1 21 114.809; 9.7032; 18.6573
90; 113.307; 90		2462.2Leitão, Maria Inês P S; Gonzalez, Carmen; Francescato, Giulia; Filipiak, Zuzanna; Petronilho, Ana
On the reactivity of mRNA Cap0: C-H oxidative addition of 7-methylguanosine to Pt<sup>0</sup> and base pairing studies.
Chemical communications (Cambridge, England), 2020, 56, 13365-13368
7127367 CIFC46 H40 Co F18 N10 P3C 1 2/c 115.05; 15.46; 22.031
90; 108.853; 90		4851Mansoor, Iram F.; Wozniak, Derek I.; Wu, Yilei; Lipke, Mark C.
A delocalized cobaltoviologen with seven reversibly accessible redox states and highly tunable electrochromic behaviour.
Chemical communications (Cambridge, England), 2020, 56, 13864-13867
7127368 CIFC44 H37 Co F24 N9 P4P 1 21/c 112.9089; 31.053; 25.429
90; 90.106; 90		10193.5Mansoor, Iram F.; Wozniak, Derek I.; Wu, Yilei; Lipke, Mark C.
A delocalized cobaltoviologen with seven reversibly accessible redox states and highly tunable electrochromic behaviour.
Chemical communications (Cambridge, England), 2020, 56, 13864-13867
7127369 CIFC15 H19 Br2 N3 ZnP 1 21/n 113.6806; 9.1444; 14.0282
90; 100.311; 90		1726.6Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127370 CIFC17 H25 Br2 N3 ZnP 1 21/n 112.8681; 11.5859; 14.3384
90; 103.984; 90		2074.34Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127371 CIFC24 H39 B Br N5 ZnP -110.8931; 11.4206; 12.3188
83.305; 63.943; 73.559		1320.41Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127372 CIFC25 H38 B Br2 N3 ZnP 1 21/c 115.0468; 11.2801; 16.7588
90; 103.198; 90		2769.3Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127373 CIFC23 H34 B Br2 N3 ZnP -113.0034; 13.5104; 15.0119
86.957; 87.514; 73.838		2528.4Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127374 CIFC25 H40 B Br F3 N5 O3 S ZnP -111.9524; 11.9577; 12.1827
107.294; 93.865; 110.961		1522.69Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127375 CIFC29 H44 B Br2 N5 ZnP -110.661; 11.8149; 13.2704
105.494; 99.734; 101.5		1534.07Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127376 CIFC24 H60 F12 O4 P6 ZnP -112.419; 12.4357; 30.319
89.995; 90.007; 119.911		4058.7Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127377 CIFC28 H45 B Br2 N5 ZnC 1 2/c 112.0353; 24.2453; 21.535
90; 92.423; 90		6278.3Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127378 CIFC26 H44 B Br Cl2 F6 N5 P ZnC 1 2/c 127.6433; 15.2931; 18.2871
90; 119.684; 90		6716.4Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127379 CIFC55.41 H91.23 B2 Br4 N8 O2.04 Zn2P -115.0988; 20.3399; 21.5241
87.7923; 84.8814; 71.6768		6249.7Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127380 CIFC17 H23 Br2 N3 ZnP 1 21/n 117.2348; 11.4411; 20.0805
90; 92.729; 90		3955.1Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127381 CIFC28 H46 B Br F3 N5 O4 S ZnP -111.5579; 12.4732; 14.2722
106.92; 101.436; 113.029		1693.95Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127382 CIFC19 H16 N2P b c a17.2098; 7.3662; 22.672
90; 90; 90		2874.1Jiang, Bo; Jia, Jingwen; Sun, Yufei; Wang, Yichun; Zeng, Jing; Bu, Xiubin; Shi, Liangliang; Sun, Xiaoying; Yang, Xiaobo
γ-Carboline synthesis enabled by Rh(iii)-catalysed regioselective C-H annulation.
Chemical communications (Cambridge, England), 2020, 56, 13389-13392
7127383 CIFC22 H28 Cl N2 O RhP 1 21/c 118.1856; 7.4674; 16.226
90; 111.448; 90		2050.89Jiang, Bo; Jia, Jingwen; Sun, Yufei; Wang, Yichun; Zeng, Jing; Bu, Xiubin; Shi, Liangliang; Sun, Xiaoying; Yang, Xiaobo
γ-Carboline synthesis enabled by Rh(iii)-catalysed regioselective C-H annulation.
Chemical communications (Cambridge, England), 2020, 56, 13389-13392
7127384 CIFC27.72 H73.15 Cl0.28 Li6 N6 OC 1 2/c 137.719; 9.9975; 27.5561
90; 129.915; 90		7970.1Knauer, Lena; Strohmann, Carsten
The structure-defining incorporation of chloride in methyllithium dimers.
Chemical communications (Cambridge, England), 2020, 56, 13543-13546
7127385 CIFC11.89 H31.67 Cl0.11 Li3 N3C 1 2/c 119.9942; 11.0399; 17.1245
90; 110.506; 90		3540.44Knauer, Lena; Strohmann, Carsten
The structure-defining incorporation of chloride in methyllithium dimers.
Chemical communications (Cambridge, England), 2020, 56, 13543-13546
7127386 CIFC16 H32 Cl2 Li2 O4P 1 21/n 19.4887; 11.075; 9.7615
90; 95.203; 90		1021.6Knauer, Lena; Strohmann, Carsten
The structure-defining incorporation of chloride in methyllithium dimers.
Chemical communications (Cambridge, England), 2020, 56, 13543-13546
7127387 CIFC54 H32 O8P n n n :23.7618; 24.323; 41.416
90; 90; 90		3789.5Suzuki, Yuto; Tohnai, Norimitsu; Saeki, Akinori; Hisaki, Ichiro
Hydrogen-bonded organic frameworks of twisted polycyclic aromatic hydrocarbon.
Chemical communications (Cambridge, England), 2020, 56, 13369-13372
7127388 CIFC54 H32 O8I 41/a c d :247.5006; 47.5006; 7.417
90; 90; 90		16735Suzuki, Yuto; Tohnai, Norimitsu; Saeki, Akinori; Hisaki, Ichiro
Hydrogen-bonded organic frameworks of twisted polycyclic aromatic hydrocarbon.
Chemical communications (Cambridge, England), 2020, 56, 13369-13372
7127389 CIFC23 H20 O2P 1 21/n 15.97592; 22.3752; 13.3264
90; 97.3628; 90		1767.21Gu, Jia-Yi; Zhang, Wei; Jackson, Seth R.; He, Yan-Hong; Guan, Zhi
Photoinduced umpolung addition of carbonyl compounds with α,β-unsaturated esters enables the polysubstituted γ-lactone formation.
Chemical communications (Cambridge, England), 2020, 56, 13441-13444
7127390 CIFC23 H20 O2P 1 21/n 16.11677; 21.9208; 13.21139
90; 96.7434; 90		1759.19Gu, Jia-Yi; Zhang, Wei; Jackson, Seth R.; He, Yan-Hong; Guan, Zhi
Photoinduced umpolung addition of carbonyl compounds with α,β-unsaturated esters enables the polysubstituted γ-lactone formation.
Chemical communications (Cambridge, England), 2020, 56, 13441-13444
7127391 CIFC17 H40 Cu N3 Si2P -18.858; 9.6854; 14.7645
104.257; 103.276; 101.697		1148.85Boysen, Nils; Misimi, Bujamin; Muriqi, Arbresha; Wree, Jan-Lucas; Hasselmann, Tim; Rogalla, Detlef; Haeger, Tobias; Theirich, Detlef; Nolan, Michael; Riedl, Thomas; Devi, Anjana
A carbene stabilized precursor for the spatial atomic layer deposition of copper thin films.
Chemical communications (Cambridge, England), 2020, 56, 13752-13755
7127392 CIFCs4 H62 K7 Na5 Nb23 O108 V5P 1 21/c 114.9822; 25.2721; 31.619
90; 93.655; 90		11947.6Zhen, Ni; Dong, Jing; Lin, Zhengguo; Li, Xiaoxia; Chi, Yingnan; Hu, Changwen
Self-assembly of polyoxovanadate-capped polyoxoniobates and their catalytic decontamination of sulfur mustard simulants.
Chemical communications (Cambridge, England), 2020, 56, 13967-13970
7127393 CIFCs4 H74 K8 Na5 Nb23 O115 V6P 1 21/m 115.9678; 23.5105; 16.2976
90; 104.33; 90		5927.9Zhen, Ni; Dong, Jing; Lin, Zhengguo; Li, Xiaoxia; Chi, Yingnan; Hu, Changwen
Self-assembly of polyoxovanadate-capped polyoxoniobates and their catalytic decontamination of sulfur mustard simulants.
Chemical communications (Cambridge, England), 2020, 56, 13967-13970
7127394 CIFC26 H27 Al Cl2 F6 N2 O3P 21 21 219.0833; 13.9679; 20.8666
90; 90; 90		2647.4Hador, Rami; Lipstman, Sophia; Rescigno, Raffaella; Venditto, Vincenzo; Kol, Moshe
Aluminium complexes of salanol ligands: coordination chemistry and stereoselective lactide polymerization.
Chemical communications (Cambridge, England), 2020, 56, 13528-13531
7127395 CIFC56 H59 Al N2 O3P 110.2589; 10.8028; 11.3273
100.728; 97.616; 109.85		1133.8Hador, Rami; Lipstman, Sophia; Rescigno, Raffaella; Venditto, Vincenzo; Kol, Moshe
Aluminium complexes of salanol ligands: coordination chemistry and stereoselective lactide polymerization.
Chemical communications (Cambridge, England), 2020, 56, 13528-13531
7127396 CIFC45 H56 Au B2 O2 P2P -111.1923; 13.0857; 15.6457
84.3144; 74.4558; 68.8762		2059.29Taylor, Jordan W.; Harman, W. Hill
H<sub>2</sub> evolution from H<sub>2</sub>O via O-H oxidative addition across a 9,10-diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 13804-13807
7127397 CIFC53 H81 Au B2 K O8.5 P2P 1 21/n 112.4601; 27.1704; 16.4408
90; 94.0898; 90		5551.8Taylor, Jordan W.; Harman, W. Hill
H<sub>2</sub> evolution from H<sub>2</sub>O via O-H oxidative addition across a 9,10-diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 13804-13807
7127398 CIFC48 H69.47 Au B2 K O7.53 P2P -111.5721; 13.3494; 17.4347
77.4593; 77.1738; 68.9764		2423.17Taylor, Jordan W.; Harman, W. Hill
H<sub>2</sub> evolution from H<sub>2</sub>O via O-H oxidative addition across a 9,10-diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 13804-13807
7127399 CIFC36 H45 Au B2 O P2P b c a19.5549; 17.1275; 19.6848
90; 90; 90		6592.96Taylor, Jordan W.; Harman, W. Hill
H<sub>2</sub> evolution from H<sub>2</sub>O via O-H oxidative addition across a 9,10-diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 13804-13807
7127400 CIFC5 H20 N10 S5P 1 21/c 110.5332; 21.0945; 8.1916
90; 94.7245; 90		1813.93Liu, Ziwei; Wu, Long-Fei; Bond, Andrew D.; Sutherland, John D.
Photoredox chemistry in the synthesis of 2-aminoazoles implicated in prebiotic nucleic acid synthesis.
Chemical communications (Cambridge, England), 2020, 56, 13563-13566
7127401 CIFC6 H16 Bi Cl5 N2 S2P 1 21/c 112.1998; 7.4008; 21.8754
90; 123.518; 90		1646.66Liu, Yu-Ting; He, Lei; Shi, Ping-Ping; Ye, Qiong; Fu, Da-Wei
A one-dimensional switchable dielectric material with Pd uptake function: [(CH<sub>2</sub>)<sub>3</sub>NH<sub>2</sub>S]<sub>2</sub>BiCl<sub>5</sub>.
Chemical communications (Cambridge, England), 2020, 56, 13764-13767
7127402 CIFC6 H16 Bi Cl5 N2 S2P 1 21/c 112.232; 7.5245; 22.0936
90; 123.339; 90		1698.84Liu, Yu-Ting; He, Lei; Shi, Ping-Ping; Ye, Qiong; Fu, Da-Wei
A one-dimensional switchable dielectric material with Pd uptake function: [(CH<sub>2</sub>)<sub>3</sub>NH<sub>2</sub>S]<sub>2</sub>BiCl<sub>5</sub>.
Chemical communications (Cambridge, England), 2020, 56, 13764-13767
7127403 CIFC15 H12 O3 SP -110.049; 10.24; 13.391
76.934; 77.667; 71.574		1258.3Chen, Xiang-Long; Tang, Bo-Cheng; He, Cai; Ma, Jin-Tian; Zhuang, Shi-Yi; Wu, Yan-Dong; Wu, An-Xin
Rongalite as a sulfone source: a novel copper-catalyzed sulfur dioxide anion incorporation process.
Chemical communications (Cambridge, England), 2020, 56, 13653-13656
7127404 CIFC68 H57 N9 O4 SP -18.9409; 16.6725; 20.1342
100.612; 93.221; 90.152		2945.1Feng, Xin; Chen, Yating; Lei, Yunxiang; Zhou, Yunbing; Gao, Wenxia; Liu, Miaochang; Huang, Xiaobo; Wu, Huayue
Multifunctional properties of a star-shaped triphenylamine-benzene-1,3,5-tricarbohydrazide fluorescent molecule containing multiple flexible chains.
Chemical communications (Cambridge, England), 2020, 56, 13638-13641
7127405 CIFC68 H57 N9 O4 SP -18.967; 16.6; 20.124
79.369; 86.581; 89.896		2938.7Feng, Xin; Chen, Yating; Lei, Yunxiang; Zhou, Yunbing; Gao, Wenxia; Liu, Miaochang; Huang, Xiaobo; Wu, Huayue
Multifunctional properties of a star-shaped triphenylamine-benzene-1,3,5-tricarbohydrazide fluorescent molecule containing multiple flexible chains.
Chemical communications (Cambridge, England), 2020, 56, 13638-13641
7127406 CIFC18 H54 Cl Ge N3 Si6R 3 c :H17.85648; 17.85648; 16.97342
90; 90; 120		4686.96Barrett, A. N.; Sanderson, H. J.; Mahon, M. F.; Webster, R. L.
Hydrophosphination using [GeCl{N(SiMe<sub>3</sub>)<sub>2</sub>}<sub>3</sub>] as a pre-catalyst.
Chemical communications (Cambridge, England), 2020, 56, 13623-13626
7127407 CIFC31 H19 N3 O2P -15.1443; 14.4148; 14.9692
92.88; 93.257; 90.232		1106.8Tang, Lele; Zan, Jie; Peng, Hao; Yan, Xi; Tao, Ye; Tian, Dan; Yang, Qingqing; Li, Huanhuan; Chen, Qiushui; Huang, Wei; Chen, Runfeng
X-ray excited ultralong room-temperature phosphorescence for organic afterglow scintillators.
Chemical communications (Cambridge, England), 2020, 56, 13559-13562
7127408 CIFC60 H72 K3 Mo6 O16.5 P3C 1 2 143.5147; 7.94643; 20.3986
90; 100.944; 90		6925.3Riedlberger, Felix; Seidl, Michael; Scheer, Manfred
The reaction behavior of [Cp<sub>2</sub>Mo<sub>2</sub>(CO)<sub>4</sub>(μ,η<sup>2:2</sup>-P<sub>2</sub>)] and [Cp''Ta(CO)<sub>2</sub>(η<sup>4</sup>-P<sub>4</sub>)] towards hydroxide and tert-butyl nucleophiles.
Chemical communications (Cambridge, England), 2020, 56, 13836-13839
7127409 CIFC35 H61 Li O6 P4 TaP 1 21/n 111.8625; 21.7618; 16.0909
90; 94.017; 90		4143.65Riedlberger, Felix; Seidl, Michael; Scheer, Manfred
The reaction behavior of [Cp<sub>2</sub>Mo<sub>2</sub>(CO)<sub>4</sub>(μ,η<sup>2:2</sup>-P<sub>2</sub>)] and [Cp''Ta(CO)<sub>2</sub>(η<sup>4</sup>-P<sub>4</sub>)] towards hydroxide and tert-butyl nucleophiles.
Chemical communications (Cambridge, England), 2020, 56, 13836-13839
7127410 CIFC46 H69 N2 O4 P4 TaP b c a19.8677; 17.9409; 27.8048
90; 90; 90		9910.9Riedlberger, Felix; Seidl, Michael; Scheer, Manfred
The reaction behavior of [Cp<sub>2</sub>Mo<sub>2</sub>(CO)<sub>4</sub>(μ,η<sup>2:2</sup>-P<sub>2</sub>)] and [Cp''Ta(CO)<sub>2</sub>(η<sup>4</sup>-P<sub>4</sub>)] towards hydroxide and tert-butyl nucleophiles.
Chemical communications (Cambridge, England), 2020, 56, 13836-13839
7127411 CIFC23 H23 Cl2 N O6P 3112.3959; 12.3959; 13.34104
90; 90; 120		1775.32Xu, Huacheng; Nazli, Adila; Zou, Cheng; Wang, Zhi-Peng; He, Yun
Bench-stable imine surrogates for the one-pot and catalytic asymmetric synthesis of α-amino esters/ketones.
Chemical communications (Cambridge, England), 2020, 56, 14243-14246
7127412 CIFC28 H16 N2 S2P 1 21 13.9035; 44.025; 6.0394
90; 95.692; 90		1032.8Deng, Jian; Wan, Yuejuan; Cai, Chang; Gu, Cheng; Ma, Yuguang
Organic single crystals of cyano-substituted <i>p</i>-phenylene vinylene derivatives as transistors with low surface trap density.
Chemical communications (Cambridge, England), 2020, 56, 13776-13779
7127413 CIFC10 H6 N SP -13.938; 5.87; 18.06
80.84; 87.25; 86.08		410.9Deng, Jian; Wan, Yuejuan; Cai, Chang; Gu, Cheng; Ma, Yuguang
Organic single crystals of cyano-substituted <i>p</i>-phenylene vinylene derivatives as transistors with low surface trap density.
Chemical communications (Cambridge, England), 2020, 56, 13776-13779
7127414 CIFC23 H20 Br N3 O4 SC 1 2 118.6217; 9.3855; 14.7978
90; 101.185; 90		2537.1Liu, Hui; Yan, Yingkun; Zhang, Jiayan; Liu, Min; Cheng, Shaobing; Wang, Zhouyu; Zhang, Xiaomei
Enantioselective dearomative [3+2] annulation of 5-amino-isoxazoles with quinone monoimines.
Chemical communications (Cambridge, England), 2020, 56, 13591-13594
7127415 CIFC22 H25 N3 O6 SP 1 21 111.6772; 6.3645; 15.4108
90; 93.913; 90		1142.65Liu, Hui; Yan, Yingkun; Zhang, Jiayan; Liu, Min; Cheng, Shaobing; Wang, Zhouyu; Zhang, Xiaomei
Enantioselective dearomative [3+2] annulation of 5-amino-isoxazoles with quinone monoimines.
Chemical communications (Cambridge, England), 2020, 56, 13591-13594
7127416 CIFC22 H25 N3 O6 SP 1 21 111.6772; 6.3645; 15.4108
90; 93.913; 90		1142.65Liu, Hui; Yan, Yingkun; Zhang, Jiayan; Liu, Min; Cheng, Shaobing; Wang, Zhouyu; Zhang, Xiaomei
Enantioselective dearomative [3+2] annulation of 5-amino-isoxazoles with quinone monoimines.
Chemical communications (Cambridge, England), 2020, 56, 13591-13594
7127417 CIFC23 H20 Br N3 O4 SC 1 2 118.6217; 9.3855; 14.7978
90; 101.185; 90		2537.1Liu, Hui; Yan, Yingkun; Zhang, Jiayan; Liu, Min; Cheng, Shaobing; Wang, Zhouyu; Zhang, Xiaomei
Enantioselective dearomative [3+2] annulation of 5-amino-isoxazoles with quinone monoimines.
Chemical communications (Cambridge, England), 2020, 56, 13591-13594
7127418 CIFC18 H13 N5P n a 2118.6944; 5.0904; 15.1667
90; 90; 90		1443.29Zhang, Chunyan; Liang, Zuyu; Jia, Xiaofei; Wang, Maorong; Zhang, Guoying; Hu, Mao-Lin
A practical base mediated synthesis of 1,2,4-triazoles enabled by a deamination annulation strategy.
Chemical communications (Cambridge, England), 2020, 56, 14215-14218
7127419 CIFC6 H18 Br7 Cs N2 Pb2P c a 218.2772; 8.0905; 35.589
90; 90; 90		2383.3Fu, Dongying; Wu, Shichao; Xin, Jianli; Zhang, Xinyuan; Han, Gaoyi; Zhang, Xian-Ming
Polar CsPbBr<sub>3</sub>-based Dion-Jacobson hybrid for promising UV photodetection.
Chemical communications (Cambridge, England), 2020, 56, 14381-14384
7127420 CIFC75 H49 Gd3 N8 O37P -114.3007; 17.1091; 18.9641
88.689; 83.151; 70.462		4340.9Li, Pei-Xin; Xie, Zhi-Xin; Jin, Ai-Ping; Li, Jing; Guo, Guo-Cong
A new photochromic Gd-MOF with photoswitchable bluish-white to greenish-yellow emission based on electron transfer.
Chemical communications (Cambridge, England), 2020, 56, 14689-14692
7127421 CIFC18 H16 N2 O6P 1 21/n 18.0723; 17.6758; 11.6674
90; 93.046; 90		1662.4Li, Pei-Xin; Xie, Zhi-Xin; Jin, Ai-Ping; Li, Jing; Guo, Guo-Cong
A new photochromic Gd-MOF with photoswitchable bluish-white to greenish-yellow emission based on electron transfer.
Chemical communications (Cambridge, England), 2020, 56, 14689-14692
7127422 CIFC25 H42 Cl2 Ge N2 P2 PdP 1 21/c 111.496; 18.413; 14.671
90; 106.665; 90		2975.06Cabeza, Javier A.; García-Álvarez, Pablo; Laglera-Gándara, Carlos J; Pérez-Carreño, Enrique
A Z-type PGeP pincer germylene ligand in a T-shaped palladium(0) complex.
Chemical communications (Cambridge, England), 2020, 56, 14095-14097
7127423 CIFC37 H52 Ge N2 P2 Pd S2P 1 21/n 117.5001; 12.1142; 18.945
90; 114.67; 90		3649.75Cabeza, Javier A.; García-Álvarez, Pablo; Laglera-Gándara, Carlos J; Pérez-Carreño, Enrique
A Z-type PGeP pincer germylene ligand in a T-shaped palladium(0) complex.
Chemical communications (Cambridge, England), 2020, 56, 14095-14097
7127424 CIFC41.5 H37 Cl15 K N O6P -111.603; 13.398; 19.749
90.788; 105.517; 113.557		2686.3Mayorga-Burrezo, Paula; Sporer, Christian; de Sousa, J. Alejandro; Capra, Nicola; Wurst, Klaus; Crivillers, Núria; Veciana, Jaume; Rovira, Concepció
Electrocatalytic oxidative Z/E isomerization of a stilbene favoured by the presence of an electroactive persistent radical.
Chemical communications (Cambridge, England), 2020, 56, 14211-14214
7127425 CIFC32 H20 F2 N OP -19.0495; 11.3463; 13.2051
84.652; 76.728; 75.775		1278.2Gao, Yuan; Zhang, Mengfan; Wang, Chaoyu; Yang, Zhen; Huang, Xianqiang; Feng, Ruokun; Qi, Chenze
Cobalt(ii)-catalyzed hydroarylation of 1,3-diynes and internal alkynes with picolinamides promoted by alcohol.
Chemical communications (Cambridge, England), 2020, 56, 14231-14234
7127426 CIFC27 H21 Cl N2 O3P 1 21/n 113.51; 9.6529; 17.2677
90; 95.515; 90		2241.5Gao, Yuan; Zhang, Mengfan; Wang, Chaoyu; Yang, Zhen; Huang, Xianqiang; Feng, Ruokun; Qi, Chenze
Cobalt(ii)-catalyzed hydroarylation of 1,3-diynes and internal alkynes with picolinamides promoted by alcohol.
Chemical communications (Cambridge, England), 2020, 56, 14231-14234
7127427 CIFC32 H23 N2 OP 1 21/n 110.6041; 18.1154; 13.0961
90; 104.601; 90		2434.5Gao, Yuan; Zhang, Mengfan; Wang, Chaoyu; Yang, Zhen; Huang, Xianqiang; Feng, Ruokun; Qi, Chenze
Cobalt(ii)-catalyzed hydroarylation of 1,3-diynes and internal alkynes with picolinamides promoted by alcohol.
Chemical communications (Cambridge, England), 2020, 56, 14231-14234
7127428 CIFC31 H26 N2 O5 SP -19.9502; 11.9913; 14.0968
113.915; 96.434; 93.254		1518.19Fang, Qing-Yun; Zhao, Li-Ming
A [4+3] annulation of benzofuran-derived azadienes and α-bromohydroxamates for the synthesis of benzofuran-fused 1,4-diazepinones.
Chemical communications (Cambridge, England), 2020, 56, 14079-14082
7127429 CIFC22 H36 Cl2 Co2 N10 O8P 6520.399; 20.399; 14.7613
90; 90; 120		5319.5Dolui, Dependu; Mir, Ab Qayoom; Dutta, Arnab
Probing the peripheral role of amines in photo- and electrocatalytic H<sub>2</sub> production by molecular cobalt complexes.
Chemical communications (Cambridge, England), 2020, 56, 14841-14844
7127430 CIFC36 H30 Li2 N5 O13C 1 2/c 123.699; 16.6746; 10.1581
90; 101.153; 90		3938.4Nath, Karabi; Bin Rahaman, Abdulla; Moi, Rajib; Maity, Kartik; Biradha, Kumar
Porous Li-MOF as a solid-state electrolyte: exploration of lithium ion conductivity through bio-inspired ionic channels.
Chemical communications (Cambridge, England), 2020, 56, 14873-14876
7127431 CIFC34 H38 Li2 N2 O12C 1 2/c 121.9; 16.99; 9.436
90; 109.177; 90		3316Nath, Karabi; Bin Rahaman, Abdulla; Moi, Rajib; Maity, Kartik; Biradha, Kumar
Porous Li-MOF as a solid-state electrolyte: exploration of lithium ion conductivity through bio-inspired ionic channels.
Chemical communications (Cambridge, England), 2020, 56, 14873-14876
7127434 CIFC53 H47 B Ir N3 O0.25P 1 21/c 122.2922; 13.8681; 14.6786
90; 107.043; 90		4338.6Pham, Pierce; Hilty, Christian
Tunable iridium catalyst designs with bidentate N-heterocyclic carbene ligands for SABRE hyperpolarization of sterically hindered substrates.
Chemical communications (Cambridge, England), 2020, 56, 15466-15469
7127451 CIFAl12 O67.44 P12P 21 21 215.0698; 17.9944; 5.03671
90; 90; 90		1365.81Komura, Kenichi; Aoki, Hisakazu; Tanaka, Kentaro; Ikeda, Takuji
GAM-3: a zeolite formed from AlPO<sub>4</sub>-5 <i>via</i> multistep structural changes.
Chemical communications (Cambridge, England), 2020, 56, 14901-14904
7127452 CIFC4 H9 Al3 N O12.75 P3P 21 21 216.7631; 17.4946; 4.97975
90; 90; 90		1460.38Komura, Kenichi; Aoki, Hisakazu; Tanaka, Kentaro; Ikeda, Takuji
GAM-3: a zeolite formed from AlPO<sub>4</sub>-5 <i>via</i> multistep structural changes.
Chemical communications (Cambridge, England), 2020, 56, 14901-14904
7127455 CIFC19 H14 N2 O3P -17.5891; 10.1094; 20.3877
95.642; 97.677; 104.552		1486.17Marques, Carolina S.; Cruz, Hugo; Lawrence, Simon E.; Gago, Sandra; Prates Ramalho, João P; Morgado, Jorge; Branco, Luís C; Burke, Anthony J.
Ambipolar pentacyclic diamides with interesting electrochemical and optoelectronic properties.
Chemical communications (Cambridge, England), 2020, 56, 14893-14896
7127456 CIFC30 H35 B O3 SeP -110.574; 10.8402; 12.7623
70.58; 82.1; 86.46		1366.3Mizoguchi, Haruki; Seriu, Masaya; Sakakura, Akira
Synthesis of functionalized cyclopropylboronic esters based on a 1,2-metallate rearrangement of cyclopropenylboronate.
Chemical communications (Cambridge, England), 2020, 56, 15545-15548
7127461 CIFC80 H86 N4 O4 Pt2P 1 21 121.7528; 51.3282; 22.4375
90; 113.392; 90		22993.2Inoue, Ryo; Kondo, Riki; Morisaki, Yasuhiro
Experimental and theoretical studies on circularly polarized phosphorescence of a [2.2]paracyclophane-based platinum(ii) complex.
Chemical communications (Cambridge, England), 2020, 56, 15438-15441
7127462 CIFC33 H37 N O5P 1 21 110.2748; 14.2248; 10.9525
90; 115.5; 90		1444.84Xiang, Min; Li, Chen-Yi; Song, Xiang-Jia; Zou, Ying; Huang, Zhi-Cheng; Li, Xia; Tian, Fang; Wang, Li-Xin
Organocatalytic and enantioselective [4+2] cyclization between hydroxymaleimides and <i>ortho</i>-hydroxyphenyl <i>para</i>-quinone methide-selective preparation of chiral hemiketals.
Chemical communications (Cambridge, England), 2020, 56, 14825-14828
7127463 CIFC34 H38 Cl3 N O5P -110.538; 12.9179; 13.0658
98.879; 105.364; 95.484		1677Xiang, Min; Li, Chen-Yi; Song, Xiang-Jia; Zou, Ying; Huang, Zhi-Cheng; Li, Xia; Tian, Fang; Wang, Li-Xin
Organocatalytic and enantioselective [4+2] cyclization between hydroxymaleimides and <i>ortho</i>-hydroxyphenyl <i>para</i>-quinone methide-selective preparation of chiral hemiketals.
Chemical communications (Cambridge, England), 2020, 56, 14825-14828
7127464 CIFC16 H11 N O2P -16.0435; 7.958; 13.3572
75.36; 83.114; 77.584		605.55Wang, Ali; Xie, Xin; Zhang, Chunli; Liu, Yuanhong
Gold/Lewis acid catalyzed oxidative cyclization involving activation of nitriles.
Chemical communications (Cambridge, England), 2020, 56, 15581-15584
7127465 CIFC17 H13 N O2P 1 21/c 115.5206; 10.7027; 7.9095
90; 90.741; 90		1313.76Wang, Ali; Xie, Xin; Zhang, Chunli; Liu, Yuanhong
Gold/Lewis acid catalyzed oxidative cyclization involving activation of nitriles.
Chemical communications (Cambridge, England), 2020, 56, 15581-15584
7127466 CIFC15 H11 N O3 SP c a 2116.21; 5.463; 30.5412
90; 90; 90		2704.6Wang, Ali; Xie, Xin; Zhang, Chunli; Liu, Yuanhong
Gold/Lewis acid catalyzed oxidative cyclization involving activation of nitriles.
Chemical communications (Cambridge, England), 2020, 56, 15581-15584
7127467 CIFC24 H132 Cs7.5 Dy4 K0.5 O180 P8 W32P -112.757; 14.616; 24.915
73.84; 86.54; 79.7		4389.8Wang, Wenyan; Izarova, Natalya V.; van Leusen, Jan; Kögerler, Paul
Polyoxometalates with separate lacuna sites.
Chemical communications (Cambridge, England), 2020, 56, 14857-14860
7127468 CIFC24 H128 Cs7.5 K0.5 O178 P8 W32 Y4P -112.902; 14.649; 24.956
73.56; 86.69; 79.61		4449.6Wang, Wenyan; Izarova, Natalya V.; van Leusen, Jan; Kögerler, Paul
Polyoxometalates with separate lacuna sites.
Chemical communications (Cambridge, England), 2020, 56, 14857-14860
7127469 CIFC30 H51 Al N3 Ni P3P 1 21/n 111.29; 17.502; 16.876
90; 96.935; 90		3310Lai, Qingheng; Cosio, Mario N.; Ozerov, Oleg V.
Ni complexes of an alane/tris(phosphine) ligand built around a strongly Lewis acidic tris(<i>N</i>-pyrrolyl)aluminum.
Chemical communications (Cambridge, England), 2020, 56, 14845-14848
7127470 CIFC24 H21 B F2 N2 O2 SP 21 21 218.7927; 13.0246; 19.6787
90; 90; 90		2253.63Lv, Fan; Guo, Xing; Wu, Hao; Li, Heng; Tang, Bing; Yu, Changjiang; Hao, Erhong; Jiao, Lijuan
Direct sulfonylation of BODIPY dyes with sodium sulfinates through oxidative radical hydrogen substitution at the α-position.
Chemical communications (Cambridge, England), 2020, 56, 15577-15580
7127472 CIFC17 H19 N O3P 1 21/n 110.7764; 8.4814; 15.9946
90; 97.431; 90		1449.61Mayakrishnan, Sivakalai; Tamizmani, Masilamani; Maheswari, Naryanan Uma
Harnessing hypervalent iodonium ylides as carbene precursors: C-H activation of N-methoxybenzamides with a Rh(iii)-catalyst.
Chemical communications (Cambridge, England), 2020, 56, 15462-15465
7127473 CIFC31 H27 N O4P -19.9039; 11.0962; 11.7769
87.0152; 68.9253; 88.648		1206.01Mayakrishnan, Sivakalai; Tamizmani, Masilamani; Maheswari, Naryanan Uma
Harnessing hypervalent iodonium ylides as carbene precursors: C-H activation of N-methoxybenzamides with a Rh(iii)-catalyst.
Chemical communications (Cambridge, England), 2020, 56, 15462-15465
7127475 CIFC88.19 H116.39 La Na3 O13.05P 21 21 228.4265; 27.2114; 10.4341
90; 90; 90		8071Deng, Min; Schley, Nathan D.; Ung, Gaël
High circularly polarized luminescence brightness from analogues of Shibasaki's lanthanide complexes.
Chemical communications (Cambridge, England), 2020, 56, 14813-14816
7127476 CIFC80 H120 K La N4 O6 P4P -114.168; 18.79; 19.86
105.16; 97.23; 104.28		4842Watt, Fabian A.; McCabe, Karl N.; Schoch, Roland; Maron, Laurent; Hohloch, Stephan
A transient lanthanum phosphinidene complex.
Chemical communications (Cambridge, England), 2020, 56, 15410-15413
7127477 CIFC65 H96 K La N2 O7 P2P -113.3178; 25.2864; 25.5213
116.117; 98.326; 99.911		7361.7Watt, Fabian A.; McCabe, Karl N.; Schoch, Roland; Maron, Laurent; Hohloch, Stephan
A transient lanthanum phosphinidene complex.
Chemical communications (Cambridge, England), 2020, 56, 15410-15413
7127478 CIFC71 H109 K La N4 O6 P3P -112.75; 15.9812; 21.2031
105.285; 94.133; 109.532		3866.2Watt, Fabian A.; McCabe, Karl N.; Schoch, Roland; Maron, Laurent; Hohloch, Stephan
A transient lanthanum phosphinidene complex.
Chemical communications (Cambridge, England), 2020, 56, 15410-15413
7127479 CIFC134 H204 K2 La2 N4 O13 P6P -114.0506; 14.3744; 18.1614
99.417; 90.617; 91.294		3617.3Watt, Fabian A.; McCabe, Karl N.; Schoch, Roland; Maron, Laurent; Hohloch, Stephan
A transient lanthanum phosphinidene complex.
Chemical communications (Cambridge, England), 2020, 56, 15410-15413
7127480 CIFC112 H72.53 Cd3 Cl1.47 N24 O0.53C m c e47.491; 18.5114; 27.2738
90; 90; 90		23977Huang, Qing; Niu, Qian; Ma, Na-Na; Dong, Long-Zhang; Li, Shun-Li; Li, Dong-Sheng; Cai, Yue-Peng; Lan, Ya-Qian
Axial Cl/Br atom-mediated CO<sub>2</sub> electroreduction performance in a stable porphyrin-based metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 14817-14820
7127481 CIFC112 H74.8 Br1.2 Cd3 N24 O0.8C m c e47.7736; 18.5513; 27.2877
90; 90; 90		24184.1Huang, Qing; Niu, Qian; Ma, Na-Na; Dong, Long-Zhang; Li, Shun-Li; Li, Dong-Sheng; Cai, Yue-Peng; Lan, Ya-Qian
Axial Cl/Br atom-mediated CO<sub>2</sub> electroreduction performance in a stable porphyrin-based metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 14817-14820
7127482 CIFC17 H18 F6 N3 PP 1 21/c 16.352; 8.2274; 33.0348
90; 91.298; 90		1725.97OwYong, Tze Cin; Ding, Siyang; Wu, Na; Fellowes, Thomas; Chen, Sijie; White, Jonathan M.; Wong, Wallace W. H.; Hong, Yuning
Optimising molecular rotors to AIE fluorophores for mitochondria uptake and retention.
Chemical communications (Cambridge, England), 2020, 56, 14853-14856
7127483 CIFC23 H22 F6 N3 PC 1 2/c 130.1428; 6.1951; 23.4009
90; 93.329; 90		4362.46OwYong, Tze Cin; Ding, Siyang; Wu, Na; Fellowes, Thomas; Chen, Sijie; White, Jonathan M.; Wong, Wallace W. H.; Hong, Yuning
Optimising molecular rotors to AIE fluorophores for mitochondria uptake and retention.
Chemical communications (Cambridge, England), 2020, 56, 14853-14856
7127484 CIFC70 H56P 1 21/n 18.80384; 9.18711; 30.3074
90; 96.5951; 90		2435.1Kitamura, Kei; Kudo, Ryoji; Sugiyama, Haruki; Uekusa, Hidehiro; Hamura, Toshiyuki
Isoacenofuran: a novel quinoidal building block for efficient access to high-ordered polyacene derivatives.
Chemical communications (Cambridge, England), 2020, 56, 14988-14991
7127485 CIFC25 H16 O2P 1 21/c 18.30435; 23.1463; 9.755
90; 108.672; 90		1776.37Chen, Xingyu; Yan, Lipeng; Liu, Yanhong; Yang, Yudong; You, Jingsong
Switchable cascade C-H annulation to polycyclic pyryliums and pyridiniums: discovering mitochondria-targeting fluorescent probes.
Chemical communications (Cambridge, England), 2020, 56, 15080-15083
7127486 CIFC53 H34 B F4 N OP 1 21/n 116.353; 13.2053; 20.2472
90; 100.35; 90		4301.2Chen, Xingyu; Yan, Lipeng; Liu, Yanhong; Yang, Yudong; You, Jingsong
Switchable cascade C-H annulation to polycyclic pyryliums and pyridiniums: discovering mitochondria-targeting fluorescent probes.
Chemical communications (Cambridge, England), 2020, 56, 15080-15083
7127487 CIFC53.5 H34 B0.5 Cl F2 O2P 42/n :219.1081; 19.1081; 24.3996
90; 90; 90		8908.8Chen, Xingyu; Yan, Lipeng; Liu, Yanhong; Yang, Yudong; You, Jingsong
Switchable cascade C-H annulation to polycyclic pyryliums and pyridiniums: discovering mitochondria-targeting fluorescent probes.
Chemical communications (Cambridge, England), 2020, 56, 15080-15083
7127488 CIFC23 H18 Cl N3 OP b c a18.3148; 7.58; 27.7096
90; 90; 90		3846.82Cui, Yixin; Bai, Dachang; Liu, Bingxian; Chang, Junbiao; Li, Xingwei
Rh(iii)-Catalyzed acylation of heteroarenes with cyclobutenones via C-H/C-C bond activation.
Chemical communications (Cambridge, England), 2020, 56, 15631-15634
7127489 CIFC34 H64 Si6C 1 2/c 113.861; 13.3307; 20.858
90; 98.406; 90		3812.7Ishida, Shintaro; Sugawara, Shohei; Honda, Shunya; Iwamoto, Takeaki
Naphtho- and anthra-disilacyclobutadienes.
Chemical communications (Cambridge, England), 2020, 56, 15072-15075
7127490 CIFC45 H74 Si6P -112.95; 13.4087; 14.2041
92.261; 101.164; 100.116		2375.2Ishida, Shintaro; Sugawara, Shohei; Honda, Shunya; Iwamoto, Takeaki
Naphtho- and anthra-disilacyclobutadienes.
Chemical communications (Cambridge, England), 2020, 56, 15072-15075
7127494 CIFCl Mn7 Rb6 Se44 Yb23R -3 m :H19.844; 19.844; 19.496
90; 90; 120		6649Chen, Hong; Liu, Peng-Fei; Lin, Hua; Wu, Xin-Tao
A new type of novel salt-inclusion chalcogenide with ultralow thermal conductivity.
Chemical communications (Cambridge, England), 2020, 56, 15149-15152
7127495 CIFCl Er23 Mn7 Rb6 Se44R -3 m :H19.948; 19.948; 19.5948
90; 90; 120		6752.6Chen, Hong; Liu, Peng-Fei; Lin, Hua; Wu, Xin-Tao
A new type of novel salt-inclusion chalcogenide with ultralow thermal conductivity.
Chemical communications (Cambridge, England), 2020, 56, 15149-15152
7127496 CIFCl Ho23 Mn7 Rb6 Se44R -3 m :H20.0423; 20.0423; 19.6668
90; 90; 120		6841.6Chen, Hong; Liu, Peng-Fei; Lin, Hua; Wu, Xin-Tao
A new type of novel salt-inclusion chalcogenide with ultralow thermal conductivity.
Chemical communications (Cambridge, England), 2020, 56, 15149-15152
7127497 CIFCl Mn7 Rb6 Se44 Tm23R -3 m :H19.9137; 19.9137; 19.547
90; 90; 120		6713Chen, Hong; Liu, Peng-Fei; Lin, Hua; Wu, Xin-Tao
A new type of novel salt-inclusion chalcogenide with ultralow thermal conductivity.
Chemical communications (Cambridge, England), 2020, 56, 15149-15152
7127498 CIFC38 H35 N O5P -110.5434; 12.209; 12.9764
89.428; 77.02; 75.639		1574.99Kumar, Krishna; Singh, Bhuvnesh; Singh, Ravi P.
A silver-catalyzed stereoselective domino cycloisomerization-vinylogous aldol reaction of <i>ortho</i>-alkynylbenzaldehydes with 3-alkylidene oxindoles: an entry to functionalized isochromenes.
Chemical communications (Cambridge, England), 2020, 56, 15153-15156
7127499 CIFC37 H33 N O4P 1 21/n 115.1432; 12.4911; 16.2178
90; 104.238; 90		2973.4Kumar, Krishna; Singh, Bhuvnesh; Singh, Ravi P.
A silver-catalyzed stereoselective domino cycloisomerization-vinylogous aldol reaction of <i>ortho</i>-alkynylbenzaldehydes with 3-alkylidene oxindoles: an entry to functionalized isochromenes.
Chemical communications (Cambridge, England), 2020, 56, 15153-15156
7127500 CIFC36 H56 Bi N P2 PtP 1 21/c 118.0184; 12.0638; 19.2753
90; 115.96; 90		3767.1Shimada, Shigeru; Wang, Xiang-Bo; Tanaka, Masato
Oxidative addition of Bi-C bonds to Pt(0): reaction of Pt(PEt<sub>3</sub>)<sub>3</sub> with cyclic organobismuth compounds.
Chemical communications (Cambridge, England), 2020, 56, 15216-15219
7127501 CIFC30 H51 Bi Cl N P2 PtP 1 21/n 112.278; 14.7178; 18.1372
90; 91.378; 90		3276.5Shimada, Shigeru; Wang, Xiang-Bo; Tanaka, Masato
Oxidative addition of Bi-C bonds to Pt(0): reaction of Pt(PEt<sub>3</sub>)<sub>3</sub> with cyclic organobismuth compounds.
Chemical communications (Cambridge, England), 2020, 56, 15216-15219
7127502 CIFC31 H53 Bi Cl3 N P2 PtP 1 21/c 112.8505; 13.1916; 21.3892
90; 94.966; 90		3612.3Shimada, Shigeru; Wang, Xiang-Bo; Tanaka, Masato
Oxidative addition of Bi-C bonds to Pt(0): reaction of Pt(PEt<sub>3</sub>)<sub>3</sub> with cyclic organobismuth compounds.
Chemical communications (Cambridge, England), 2020, 56, 15216-15219
7127504 CIFC38 H16 F12 I6P -15.9321; 11.9878; 14.8586
73.9545; 80.1893; 84.8797		999.63Vainauskas, Jogirdas; Topić, Filip; Bushuyev, Oleksandr S.; Barrett, Christoper J.; Friščić, Tomislav
Halogen bonding to the azulene π-system: cocrystal design of pleochroism.
Chemical communications (Cambridge, England), 2020, 56, 15145-15148
7127505 CIFC34 H8 F16 I4 N4P -16.0619; 11.9613; 12.6449
88.7995; 79.8911; 88.7903		902.3Vainauskas, Jogirdas; Topić, Filip; Bushuyev, Oleksandr S.; Barrett, Christoper J.; Friščić, Tomislav
Halogen bonding to the azulene π-system: cocrystal design of pleochroism.
Chemical communications (Cambridge, England), 2020, 56, 15145-15148
7127506 CIFC38 H16 F12 I6P -15.9617; 12.0425; 14.9758
73.9375; 80.8173; 85.0271		1018.93Vainauskas, Jogirdas; Topić, Filip; Bushuyev, Oleksandr S.; Barrett, Christoper J.; Friščić, Tomislav
Halogen bonding to the azulene π-system: cocrystal design of pleochroism.
Chemical communications (Cambridge, England), 2020, 56, 15145-15148
7127507 CIFC54 H24 F16 I4 N4P -16.0053; 11.9473; 18.8788
71.556; 89.199; 83.434		1276.14Vainauskas, Jogirdas; Topić, Filip; Bushuyev, Oleksandr S.; Barrett, Christoper J.; Friščić, Tomislav
Halogen bonding to the azulene π-system: cocrystal design of pleochroism.
Chemical communications (Cambridge, England), 2020, 56, 15145-15148
7127508 CIFC22 H8 F8 I4P -15.9541; 9.6644; 11.8639
67.331; 85.205; 80.816		621.68Vainauskas, Jogirdas; Topić, Filip; Bushuyev, Oleksandr S.; Barrett, Christoper J.; Friščić, Tomislav
Halogen bonding to the azulene π-system: cocrystal design of pleochroism.
Chemical communications (Cambridge, England), 2020, 56, 15145-15148
7127509 CIFC30 H36 Co N1.5 O1.5 Se1.5P -116.0226; 17.1096; 23.7566
93.645; 98.841; 94.484		6396.6Sarkar, Prasenjit; Konch, Tukhar Jyoti; Kamilya, Tapas; Raidongia, Kalyan; Acharya, Somobrata; Mukherjee, Chandan
The range of antiferromagnetic coupling governs the conductivity: semiconducting behavior and ammonia gas sensing property of diamagnetic hexaradical-containing tetranuclear Co<sup>III</sup><sub>4</sub> cluster and its nonradical congener.
Chemical communications (Cambridge, England), 2020, 56, 15220-15223
7127510 CIFC126 H150 Co4 N6 O6 Se6P -117.1932; 19.1994; 21.9119
98.522; 101.989; 110.296		6442Sarkar, Prasenjit; Konch, Tukhar Jyoti; Kamilya, Tapas; Raidongia, Kalyan; Acharya, Somobrata; Mukherjee, Chandan
The range of antiferromagnetic coupling governs the conductivity: semiconducting behavior and ammonia gas sensing property of diamagnetic hexaradical-containing tetranuclear Co<sup>III</sup><sub>4</sub> cluster and its nonradical congener.
Chemical communications (Cambridge, England), 2020, 56, 15220-15223
7127511 CIFC58 H38 O4P -111.14; 13.27; 16.669
98.91; 90.453; 99.668		2398.4Chang, Hao; Liu, Haoliang; Dmitrieva, Evgenia; Chen, Qiang; Ma, Ji; He, Piao; Liu, Pengcai; Popov, Alexey A.; Cao, Xiao-Yu; Wang, Xiao-Ye; Zou, Yingping; Narita, Akimitsu; Müllen, Klaus; Peng, Hongjian; Hu, Yunbin
Furan-containing double tetraoxa[7]helicene and its radical cation.
Chemical communications (Cambridge, England), 2020, 56, 15181-15184
7127515 CIFC47 H48 O6P -18.5959; 18.7821; 27.0537
108.997; 95.076; 94.172		4089.7Yao, Liangliang; Fang, Bo; Hu, Qiong; Lei, Yu; Bao, Li; Hu, Yimin
Phenanthrenes/dihydrophenanthrenes: the selectivity controlled by different benzynes and allenes.
Chemical communications (Cambridge, England), 2020, 56, 15185-15188
7127516 CIFC41 H36 O6P -18.662; 11.8573; 17.3792
96.695; 99.325; 108.28		1645.59Yao, Liangliang; Fang, Bo; Hu, Qiong; Lei, Yu; Bao, Li; Hu, Yimin
Phenanthrenes/dihydrophenanthrenes: the selectivity controlled by different benzynes and allenes.
Chemical communications (Cambridge, England), 2020, 56, 15185-15188
7127517 CIFC19 H18 O3P 1 21/n 19.1429; 10.3536; 16.2762
90; 105.372; 90		1485.6Yao, Liangliang; Fang, Bo; Hu, Qiong; Lei, Yu; Bao, Li; Hu, Yimin
Phenanthrenes/dihydrophenanthrenes: the selectivity controlled by different benzynes and allenes.
Chemical communications (Cambridge, England), 2020, 56, 15185-15188
7127520 CIFC60 H57 Cu4 Mo12 N16 O50 P3C 1 2/m 124.841; 18.316; 10.897
90; 105.586; 90		4776Li, Shaobin; Tan, Xiaoguo; Yue, Ming; Zhang, Li; Chai, Dongfeng; Wang, Wendi; Pan, Hong; Fan, Linlin; Zhao, Chunyan
A polyoxometalate-encapsulated nanocage cluster organic framework built from {Cu<sub>4</sub>P<sub>2</sub>} units and its efficient bifunctional electrochemical performance.
Chemical communications (Cambridge, England), 2020, 56, 15177-15180
7127535 CIFC29.5 H24 Cl N O3 SP 1 21/n 18.3459; 31.8448; 18.0413
90; 92.018; 90		4791.9De, Sukanya; Jash, Moumita; Chowdhury, Chinmay
Palladium(ii) catalysed cascade strategy for the synthesis of dibenzo[5,6:7,8]cycloocta[1,2-b]indol-10-ols/-10(15H)-ones: easy access to 1,3,5,7-cyclooctatetraenes (COTs).
Chemical communications (Cambridge, England), 2020, 56, 15659-15662
7127536 CIFC29 H21 N O3 SC 1 2/c 117.1953; 11.2998; 23.4679
90; 99.631; 90		4495.63De, Sukanya; Jash, Moumita; Chowdhury, Chinmay
Palladium(ii) catalysed cascade strategy for the synthesis of dibenzo[5,6:7,8]cycloocta[1,2-b]indol-10-ols/-10(15H)-ones: easy access to 1,3,5,7-cyclooctatetraenes (COTs).
Chemical communications (Cambridge, England), 2020, 56, 15659-15662
7127537 CIFC29 H21 N O2 SP -18.5406; 10.0271; 13.9349
89.172; 79.068; 66.547		1072.43De, Sukanya; Jash, Moumita; Chowdhury, Chinmay
Palladium(ii) catalysed cascade strategy for the synthesis of dibenzo[5,6:7,8]cycloocta[1,2-b]indol-10-ols/-10(15H)-ones: easy access to 1,3,5,7-cyclooctatetraenes (COTs).
Chemical communications (Cambridge, England), 2020, 56, 15659-15662
7127538 CIFC30 H23 N O4 SP 1 21/c 112.6739; 16.317; 12.1213
90; 109.725; 90		2359.6De, Sukanya; Jash, Moumita; Chowdhury, Chinmay
Palladium(ii) catalysed cascade strategy for the synthesis of dibenzo[5,6:7,8]cycloocta[1,2-b]indol-10-ols/-10(15H)-ones: easy access to 1,3,5,7-cyclooctatetraenes (COTs).
Chemical communications (Cambridge, England), 2020, 56, 15659-15662
7127539 CIFC32 H29 N O5 SP -18.748; 14.05; 22.585
97.243; 100.218; 97.968		2673De, Sukanya; Jash, Moumita; Chowdhury, Chinmay
Palladium(ii) catalysed cascade strategy for the synthesis of dibenzo[5,6:7,8]cycloocta[1,2-b]indol-10-ols/-10(15H)-ones: easy access to 1,3,5,7-cyclooctatetraenes (COTs).
Chemical communications (Cambridge, England), 2020, 56, 15659-15662
7127590 CIFC17 H17 B Cl F N2 O2P 1 21/c 18.4212; 14.1413; 13.5406
90; 101.611; 90		1579.5Ohtani, Shunsuke; Takeda, Yusuke; Gon, Masayuki; Tanaka, Kazuo; Chujo, Yoshiki
Facile strategy for obtaining luminescent polymorphs based on the chirality of a boron-fused azomethine complex.
Chemical communications (Cambridge, England), 2020, 56, 15305-15308
7127591 CIFC17 H17 B Cl F N2 O2P 3212.8397; 12.8397; 8.5551
90; 90; 120		1221.4Ohtani, Shunsuke; Takeda, Yusuke; Gon, Masayuki; Tanaka, Kazuo; Chujo, Yoshiki
Facile strategy for obtaining luminescent polymorphs based on the chirality of a boron-fused azomethine complex.
Chemical communications (Cambridge, England), 2020, 56, 15305-15308
7127599 CIFC33 H24P -16.9996; 10.3778; 17.063
91.762; 99.022; 105.266		1177.6Wu, Li-Jun; Yang, Liang-Feng; Lv, Gui-Fen; Li, Jin-Heng
Divergent functionalization of terminal alkynes enabled alkynylative [5+1] benzannulation of 3-acetoxy-1,4-enynes.
Chemical communications (Cambridge, England), 2020, 56, 15329-15332
7127600 CIFC90.88 H116.1 Cl0.6 Ir0.6 Mn3 N12 O20.02P 1 21/m 112.364; 33.5; 12.912
90; 97.29; 90		5305Perlata, Ricardo A.; Huxley, Michael T.; Shi, Zhaolin; Zhang, Yue-Biao; Sumby, Christopher J.; Doonan, Christian J.
A metal-organic framework supported iridium catalyst for the gas phase hydrogenation of ethylene.
Chemical communications (Cambridge, England), 2020, 56, 15313-15316
7127601 CIFC22 H17 N O SeP 21 21 215.5032; 14.7847; 21.373
90; 90; 90		1739Liu, Xiang; Wang, Yajun; Song, Dan; Wang, Yuhan; Cao, Hua
Electrochemical regioselective selenylation/oxidation of N-alkylisoquinolinium salts via double C(sp<sup>2</sup>)-H bond functionalization.
Chemical communications (Cambridge, England), 2020, 56, 15325-15328
7127602 CIFB3 F2 O4 RbP 1 21/c 14.698; 17.77; 7.328
90; 118.95; 90		535.3Lu, Zixiu; Zhang, Fangfang; Tudi, Abudukadi; Yang, Zhihua; Pan, Shilie
RbB<sub>3</sub>O<sub>4</sub>F<sub>2</sub>: a rubidium fluorooxoborate with an unprecedented [B<sub>3</sub>O<sub>5</sub>F<sub>2</sub>]<sup>3-</sup> functionalized unit and a large birefringence.
Chemical communications (Cambridge, England), 2020, 56, 15333-15336
7127604 CIFC34 H20 SP 1 21/c 110.7856; 24.1392; 9.3144
90; 94.959; 90		2416Manikandan, Palani; Karunakaran, Jayachandran; Varathan, Elumalai; Schreckenbach, Georg; Mohanakrishnan, Arasambattu K.
Diels-Alder reaction of tetraarylcyclopentadienones with benzo[b]thiophene S,S-dioxides: an unprecedented de-oxygenation vs. sulfur dioxide extrusion.
Chemical communications (Cambridge, England), 2020, 56, 15317-15320
7127605 CIFC36 H26 O2P -110.417; 11.3442; 12.577
108.867; 105.293; 99.814		1302.26Manikandan, Palani; Karunakaran, Jayachandran; Varathan, Elumalai; Schreckenbach, Georg; Mohanakrishnan, Arasambattu K.
Diels-Alder reaction of tetraarylcyclopentadienones with benzo[b]thiophene S,S-dioxides: an unprecedented de-oxygenation vs. sulfur dioxide extrusion.
Chemical communications (Cambridge, England), 2020, 56, 15317-15320
7127606 CIFC30 H18 S2P 1 21/c 111.7855; 9.5702; 19.7443
90; 96.996; 90		2210.4Manikandan, Palani; Karunakaran, Jayachandran; Varathan, Elumalai; Schreckenbach, Georg; Mohanakrishnan, Arasambattu K.
Diels-Alder reaction of tetraarylcyclopentadienones with benzo[b]thiophene S,S-dioxides: an unprecedented de-oxygenation vs. sulfur dioxide extrusion.
Chemical communications (Cambridge, England), 2020, 56, 15317-15320
7127647 CIFC20 H20 Br N O2P -19.6343; 19.0413; 19.4763
83.018; 89.376; 82.19		3513.47Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127648 CIFC27 H19 Br Cl3 N O2P 1 21/m 112.6799; 6.6733; 15.0742
90; 109.16; 90		1204.87Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127649 CIFC25 H28 N2 O3P n a 2110.1266; 21.0008; 10.2483
90; 90; 90		2179.47Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127650 CIFC22 H16 Br N O SP 1 21/m 18.5848; 6.8902; 15.8079
90; 98.98; 90		923.59Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127651 CIFC22 H16 Br N O SeP c c n30.762; 10.8014; 11.0953
90; 90; 90		3686.7Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127652 CIFC23 H18 Br Cl2 N O2P -18.7249; 9.7643; 13.4767
90.141; 106.286; 112.456		1010.68Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127653 CIFC31 H40 N2 O4P c c n20.58; 24.0995; 11.4414
90; 90; 90		5674.6Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127688 CIFC22 H36 N4 O6 S2P 1 21/n 19.7754; 12.5427; 22.3714
90; 96.082; 90		2727.52Wang, Yijie; Zhang, Minghui; Yang, Qianqian; Yin, Jianbo; Liu, Di; Shang, Yanxue; Kang, Zixi; Wang, Rongming; Sun, Daofeng; Jiang, Jianzhuang
Single-crystal-to-single-crystal transformation and proton conductivity of three hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 15529-15532
7127689 CIFC16 H0 N11 O6 S2P 1 21/n 19.6616; 12.3127; 22.5851
90; 97.458; 90		2664Wang, Yijie; Zhang, Minghui; Yang, Qianqian; Yin, Jianbo; Liu, Di; Shang, Yanxue; Kang, Zixi; Wang, Rongming; Sun, Daofeng; Jiang, Jianzhuang
Single-crystal-to-single-crystal transformation and proton conductivity of three hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 15529-15532
7127690 CIFC22 H44 N4 O10 S2P 1 21/c 111.2723; 18.109; 14.821
90; 110.51; 90		2833.6Wang, Yijie; Zhang, Minghui; Yang, Qianqian; Yin, Jianbo; Liu, Di; Shang, Yanxue; Kang, Zixi; Wang, Rongming; Sun, Daofeng; Jiang, Jianzhuang
Single-crystal-to-single-crystal transformation and proton conductivity of three hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 15529-15532
7127718 CIFC24 H28 Cl O PP 1 21/c 111.7689; 15.1355; 13.096
90; 111.37; 90		2172.38Niu, Yuan; Qi, Zhichao; Lou, Qinxin; Bai, Pengbo; Yang, Shangdong
Copper-catalyzed arylation of polycyclic aromatic hydrocarbons by the P[double bond, length as m-dash]O group.
Chemical communications (Cambridge, England), 2020, 56, 14721-14724
7127719 CIFC6 H16 Cl2 N12 OC m c 2116.7812; 12.2467; 6.9816
90; 90; 90		1434.82Liu, Lehui; Hu, Chun-Li; Bai, Zhiyong; Yuan, Feifei; Huang, Yisheng; Zhang, Lizhen; Lin, Zhoubin
2(C<sub>3</sub>H<sub>7</sub>N<sub>6</sub>)<sup>+</sup>·2Cl<sup>-</sup>·H<sub>2</sub>O: an ultraviolet nonlinear optical crystal with large birefrigence and strong second-harmonic generation.
Chemical communications (Cambridge, England), 2020, 56, 14657-14660
7127720 CIFC23 H18 Au O P S3P -112.027; 12.23; 33.79
83.652; 86.895; 62.035		4362.9Roesch, Saskia; Fermi, Valentina; Rominger, Frank; Herold-Mende, Christel; Romero-Nieto, Carlos
Gold(i) complexes based on six-membered phosphorus heterocycles as bio-active molecules against brain cancer.
Chemical communications (Cambridge, England), 2020, 56, 14593-14596
7127721 CIFC21 H13 Au N P S2P 1 21/c 112.7527; 18.7996; 16.53
90; 108.271; 90		3763.2Roesch, Saskia; Fermi, Valentina; Rominger, Frank; Herold-Mende, Christel; Romero-Nieto, Carlos
Gold(i) complexes based on six-membered phosphorus heterocycles as bio-active molecules against brain cancer.
Chemical communications (Cambridge, England), 2020, 56, 14593-14596
7127722 CIFC122 H118 Ag3 B2 N13 O7 P6 W2P 1 21/n 115.377; 30.6356; 28.8107
90; 98.31; 90		13429.7Manzano, Richard A.; Hill, Anthony F.; Georgelin, Rosemary L.
Tetrel and pnictogen functionalised propargylidynes.
Chemical communications (Cambridge, England), 2020, 56, 14597-14600
7127723 CIFC33 H37 B2 Cl2 N6 O2 P WP 1 21/c 114.6458; 13.04801; 19.07
90; 102.382; 90		3559.48Manzano, Richard A.; Hill, Anthony F.; Georgelin, Rosemary L.
Tetrel and pnictogen functionalised propargylidynes.
Chemical communications (Cambridge, England), 2020, 56, 14597-14600
7127724 CIFC16 H21 N O5 SC 1 2/c 119.9401; 5.3894; 32.9348
90; 101.506; 90		3468.2Zhang, Chun; Huang, Jiapian; Ye, Shengqing; Tang, Jie; Wu, Jie
A metal-free reaction of sulfur dioxide, cyclopropanols and electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 13852-13855
7127725 CIFC106 H146 O20 Ti4P 1 21/c 114.6214; 28.2561; 14.335
90; 93.955; 90		5908.3Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127726 CIFC104 H136 N4 O22 Ti4P -114.2318; 14.6532; 18.081
103.02; 102.821; 107.509		3328.9Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127727 CIFC136 H174 N6 O26 Ti6P 1 21/n 118.742; 15.6878; 24.515
90; 106.32; 90		6917.5Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127728 CIFC137 H169 O26 Ti6P 1 21/n 118.124; 15.607; 25.066
90; 105.645; 90		6827.5Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127729 CIFC128 H188 N8 O26 Ti4P -114.4277; 14.608; 17.6599
82.875; 72.447; 75.012		3423.7Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127730 CIFC144 H172 Br4 N8 O20 Ti4C 1 2/c 126.9642; 24.087; 23.819
90; 94.28; 90		15427Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127731 CIFC95 H150 O27.52 Ti6P -115.419; 19.356; 20.165
84.214; 70.821; 86.94		5654Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127732 CIFC128 H164 O30 Ti6P 1 21/n 117.654; 15.3326; 24.8024
90; 105.996; 90		6453.6Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127733 CIFC151 H225 O34 Ti6P 1 21/n 121.3911; 25.7936; 33.0748
90; 99.423; 90		18002.9Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127734 CIFC130 H164 Br12 O46 Ti10P -114.966; 15.4941; 20.8678
98.6889; 110.598; 100.033		4340.33Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127735 CIFC196 H158 F60 O46 Ti10P -117.6619; 18.0164; 21.2467
68.017; 69.349; 61.753		5393.7Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127736 CIFC91 H130 N6 Ni P8 Si2P 1 21/c 123.6231; 13.3113; 30.4842
90; 105.741; 90		9226.4Ziegler, Christoph G. P.; Taube, Clemens; Kelly, John A.; Hierlmeier, Gabriele; Uttendorfer, Maria; Weigand, Jan J.; Wolf, Robert
An unusual Ni<sub>2</sub>Si<sub>2</sub>P<sub>8</sub> cluster formed by complexation and thermolysis.
Chemical communications (Cambridge, England), 2020, 56, 14071-14074
7127737 CIFC85 H118 N6 Ni P8 Si2P 1 21/c 117.4813; 22.9979; 22.0196
90; 97.889; 90		8768.8Ziegler, Christoph G. P.; Taube, Clemens; Kelly, John A.; Hierlmeier, Gabriele; Uttendorfer, Maria; Weigand, Jan J.; Wolf, Robert
An unusual Ni<sub>2</sub>Si<sub>2</sub>P<sub>8</sub> cluster formed by complexation and thermolysis.
Chemical communications (Cambridge, England), 2020, 56, 14071-14074
7127738 CIFC56 H76 N4 Ni P4 SiP b c a17.4645; 15.4359; 42.649
90; 90; 90		11497.3Ziegler, Christoph G. P.; Taube, Clemens; Kelly, John A.; Hierlmeier, Gabriele; Uttendorfer, Maria; Weigand, Jan J.; Wolf, Robert
An unusual Ni<sub>2</sub>Si<sub>2</sub>P<sub>8</sub> cluster formed by complexation and thermolysis.
Chemical communications (Cambridge, England), 2020, 56, 14071-14074
7127739 CIFC85 H116 N6 Ni2 P8 Si2P 1 21/c 123.3638; 16.0951; 27.7549
90; 107.229; 90		9968.7Ziegler, Christoph G. P.; Taube, Clemens; Kelly, John A.; Hierlmeier, Gabriele; Uttendorfer, Maria; Weigand, Jan J.; Wolf, Robert
An unusual Ni<sub>2</sub>Si<sub>2</sub>P<sub>8</sub> cluster formed by complexation and thermolysis.
Chemical communications (Cambridge, England), 2020, 56, 14071-14074
7127740 CIFC39.5 H49 Al Cl4 N2 O2P -19.1488; 17.223; 25.5541
74.736; 86.924; 89.597		3878.81Popowski, Yanay; Moreno, Juan J.; Nichols, Asa W.; Hooe, Shelby L.; Bouchey, Caitlin J.; Rath, Nigam P.; Machan, Charles W.; Tolman, William B.
Mechanistic insight into initiation and regioselectivity in the copolymerization of epoxides and anhydrides by Al complexes.
Chemical communications (Cambridge, England), 2020, 56, 14027-14030
7127741 CIFC52 H63 Al Cl6 N2 O6P -113.562; 13.8874; 15.489
99.761; 94.142; 108.246		2705.8Popowski, Yanay; Moreno, Juan J.; Nichols, Asa W.; Hooe, Shelby L.; Bouchey, Caitlin J.; Rath, Nigam P.; Machan, Charles W.; Tolman, William B.
Mechanistic insight into initiation and regioselectivity in the copolymerization of epoxides and anhydrides by Al complexes.
Chemical communications (Cambridge, England), 2020, 56, 14027-14030
7127742 CIFC135 H175 Al3 N6 O15C 2 2 2122.6444; 30.8757; 21.0423
90; 90; 90		14712Popowski, Yanay; Moreno, Juan J.; Nichols, Asa W.; Hooe, Shelby L.; Bouchey, Caitlin J.; Rath, Nigam P.; Machan, Charles W.; Tolman, William B.
Mechanistic insight into initiation and regioselectivity in the copolymerization of epoxides and anhydrides by Al complexes.
Chemical communications (Cambridge, England), 2020, 56, 14027-14030
7127743 CIFC137 H179 Al3 N6 O15C 2 2 2122.7869; 30.5983; 21.2437
90; 90; 90		14812Popowski, Yanay; Moreno, Juan J.; Nichols, Asa W.; Hooe, Shelby L.; Bouchey, Caitlin J.; Rath, Nigam P.; Machan, Charles W.; Tolman, William B.
Mechanistic insight into initiation and regioselectivity in the copolymerization of epoxides and anhydrides by Al complexes.
Chemical communications (Cambridge, England), 2020, 56, 14027-14030
7127744 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.5103; 4.2412; 19.5894
90; 90.446; 90		956.28Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127745 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.5218; 4.2497; 19.6222
90; 90.458; 90		960.75Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127746 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.5363; 4.2584; 19.6624
90; 90.49; 90		965.9Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127747 CIFC120 H100 Cu4 N8 O28P -119.294; 19.413; 23.421
72.2; 86.15; 65.93		7610Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127748 CIFC168 H124 Cu4 N12 O28P -116.005; 17.777; 20.441
104.91; 109.45; 104.86		4912Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127749 CIFC18 H14 K2 N2 O11 S2P -15.6244; 6.1097; 15.9088
89.883; 81.215; 76.999		526.121Ke, Hua; Hu, Fen; Meng, Lingyi; Chen, Qi-Hua; Lai, Qian-Sheng; Li, Ze-Chen; Huang, Ze-Long; Liao, Jian-Zhen; Qiu, Jian-Ding; Lu, Can-Zhong
Ultrastable radical-doped coordination compounds with antimicrobial activity against antibiotic-resistant bacteria.
Chemical communications (Cambridge, England), 2020, 56, 14353-14356
7127750 CIFC18 H16 Ca N2 O12 S2P 1 21/n 18.8177; 28.7454; 8.9688
90; 108.766; 90		2152.46Ke, Hua; Hu, Fen; Meng, Lingyi; Chen, Qi-Hua; Lai, Qian-Sheng; Li, Ze-Chen; Huang, Ze-Long; Liao, Jian-Zhen; Qiu, Jian-Ding; Lu, Can-Zhong
Ultrastable radical-doped coordination compounds with antimicrobial activity against antibiotic-resistant bacteria.
Chemical communications (Cambridge, England), 2020, 56, 14353-14356
7127751 CIFC160 H184 B4 Cl4 N24 O8 Pt4 ZnP -112.1513; 17.9898; 19.21888
77.5748; 80.99; 89.3233		4051.17Rubbiani, Riccardo; Wu, Wenyu; Naik, Anu; Larocca, Michele; Schneider, Lukas; Padrutt, Roxane; Babu, Vipin; König, Christiane; Hinger, Doris; Maake, Caroline; Ferrari, Stefano; Gasser, Gilles; Spingler, Bernhard
Studying the cellular distribution of highly phototoxic platinated metalloporphyrins using isotope labelling.
Chemical communications (Cambridge, England), 2020, 56, 14373-14376
7127752 CIFC64 H92 F12 K2 N16 O16 P2P 1 21/n 114.5377; 16.9875; 31.4097
90; 92.689; 90		7748.4Xiao, Tangxin; Zhong, Weiwei; Yang, Weiwei; Qi, Lijie; Gao, Yan; Sue, Andrew C.-H.; Li, Zheng-Yi; Sun, Xiao-Qiang; Lin, Chen; Wang, Leyong
Reversible hydrogen-bonded polymerization regulated by allosteric metal templation.
Chemical communications (Cambridge, England), 2020, 56, 14385-14388
7127753 CIFC24 H19 ClP c a 2110.8825; 21.5798; 8.2395
90; 90; 90		1935Xue, Ze-Jian; Li, Meng-Yao; Zhu, Bin-Bin; He, Zhi-Tao; Feng, Chen-Guo; Lin, Guo-Qiang
Stereoselective synthesis of conjugated trienes <i>via</i> 1,4-palladium migration/Heck sequence.
Chemical communications (Cambridge, England), 2020, 56, 14420-14422
7127754 CIFC24 H38 F3 Fe N3 O6 SP -19.1103; 9.944; 15.5023
77.338; 89.422; 88.622		1369.8Sánchez-Eguía, Brenda N; Serrano-Plana, Joan; Company, Anna; Costas, Miquel
Catalytic O<sub>2</sub> activation with synthetic models of α-ketoglutarate dependent oxygenases.
Chemical communications (Cambridge, England), 2020, 56, 14369-14372
7127755 CIFC27 H44 F3 Fe N5 O5 SP -110.8333; 12.2736; 13.012
79.726; 74.064; 81.746		1628.8Sánchez-Eguía, Brenda N; Serrano-Plana, Joan; Company, Anna; Costas, Miquel
Catalytic O<sub>2</sub> activation with synthetic models of α-ketoglutarate dependent oxygenases.
Chemical communications (Cambridge, England), 2020, 56, 14369-14372
7127756 CIFC52 H88 Cl2 Fe2 N6 O10P 1 21/n 112.832; 15.977; 30.509
90; 98.773; 90		6182Sánchez-Eguía, Brenda N; Serrano-Plana, Joan; Company, Anna; Costas, Miquel
Catalytic O<sub>2</sub> activation with synthetic models of α-ketoglutarate dependent oxygenases.
Chemical communications (Cambridge, England), 2020, 56, 14369-14372
7127757 CIFC25.5 H17 F6 N5 O0.5 P PtP 1 21/c 16.8545; 39.3855; 17.3529
90; 98.991; 90		4627.2He, Lei; Meng, Zhenyu; Guo, Qianqian; Wu, Xiangyang; Teulade-Fichou, Marie-Paule; Yeow, Edwin Kok Lee; Shao, Fangwei
Fluorogenic Pt complexes distinguish the quantity and folding behavior of RNA G-quadruplexes between live cancerous and healthy cells.
Chemical communications (Cambridge, England), 2020, 56, 14459-14462
7127758 CIFC25 H25 B F2 O4P -17.813; 9.3837; 16.3462
101.355; 97.002; 104.391		1119.53Yan, Cai-Xin; Lin, Qian-Qian; Li, Sha; Wu, Cheng-Juan; Li, Yan-An; Fan, Jian-Zhong; Ma, Jian-Ping; Geng, Yan; Dong, Yu-Bin
Synthesis of fulvene-containing boron complexes with aggregation-induced emission and mechanochromic luminescence.
Chemical communications (Cambridge, England), 2020, 56, 14435-14438
7127759 CIFC31 H26 O2P -19.6358; 10.2626; 12.5875
75.48; 73.81; 83.749		1156.19Yan, Cai-Xin; Lin, Qian-Qian; Li, Sha; Wu, Cheng-Juan; Li, Yan-An; Fan, Jian-Zhong; Ma, Jian-Ping; Geng, Yan; Dong, Yu-Bin
Synthesis of fulvene-containing boron complexes with aggregation-induced emission and mechanochromic luminescence.
Chemical communications (Cambridge, England), 2020, 56, 14435-14438
7127760 CIFC31 H25 B F2 O2C 1 2/c 124.5441; 12.1699; 20.6663
90; 123.726; 90		5134.1Yan, Cai-Xin; Lin, Qian-Qian; Li, Sha; Wu, Cheng-Juan; Li, Yan-An; Fan, Jian-Zhong; Ma, Jian-Ping; Geng, Yan; Dong, Yu-Bin
Synthesis of fulvene-containing boron complexes with aggregation-induced emission and mechanochromic luminescence.
Chemical communications (Cambridge, England), 2020, 56, 14435-14438
7127761 CIFC316 H437 Ag51 Cl7 F12 P2 Pt2 S28 Sb2P -125.6867; 30.3229; 37.02
107.289; 99.777; 110.352		24582Liu, Ying; Wang, Shuxin; Kang, Xi; Yin, Bing; Jin, Shan; Chen, Shuang; Zhu, Manzhou
Heterogeneous metal alloy engineering: embryonic growth of M<sub>13</sub> icosahedra in Ag-based alloy superatomic nanoclusters.
Chemical communications (Cambridge, England), 2020, 56, 14203-14206
7127762 CIFC280 H406 Ag48 Au3 Cl7 F12 S28 Sb2C 1 2/c 141.694; 29.9362; 62.1774
90; 108.961; 90		73396.4Liu, Ying; Wang, Shuxin; Kang, Xi; Yin, Bing; Jin, Shan; Chen, Shuang; Zhu, Manzhou
Heterogeneous metal alloy engineering: embryonic growth of M<sub>13</sub> icosahedra in Ag-based alloy superatomic nanoclusters.
Chemical communications (Cambridge, England), 2020, 56, 14203-14206
7127763 CIFC52 H52 N4 Si2P -110.2134; 14.0734; 16.2616
100.776; 93.428; 109.092		2151.38Espinosa-Jalapa, Noel Angel; Berg, Nele; Seidl, Michael; Shenderovich, Ilya G.; Gschwind, Ruth M.; Bauer, Jonathan O.
Complexation behaviour of LiCl and LiPF<sub>6</sub>- model studies in the solid-state and in solution using a bidentate picolyl-based ligand.
Chemical communications (Cambridge, England), 2020, 56, 13335-13338
7127764 CIFC24 H22 N2 SiP -19.8911; 10.3035; 10.8066
82.034; 64.483; 87.683		984.09Espinosa-Jalapa, Noel Angel; Berg, Nele; Seidl, Michael; Shenderovich, Ilya G.; Gschwind, Ruth M.; Bauer, Jonathan O.
Complexation behaviour of LiCl and LiPF<sub>6</sub>- model studies in the solid-state and in solution using a bidentate picolyl-based ligand.
Chemical communications (Cambridge, England), 2020, 56, 13335-13338
7127765 CIFC52 H50 Cl2 Li2 N6 Si2P 18.9867; 11.6858; 12.4491
77.799; 74.843; 78.754		1219.77Espinosa-Jalapa, Noel Angel; Berg, Nele; Seidl, Michael; Shenderovich, Ilya G.; Gschwind, Ruth M.; Bauer, Jonathan O.
Complexation behaviour of LiCl and LiPF<sub>6</sub>- model studies in the solid-state and in solution using a bidentate picolyl-based ligand.
Chemical communications (Cambridge, England), 2020, 56, 13335-13338
7127766 CIFC48.7 H45.4 Cl1.4 F12 Li2 N4 P2 Si2P 1 21/n 110.5712; 18.1992; 27.2894
90; 100.784; 90		5157.42Espinosa-Jalapa, Noel Angel; Berg, Nele; Seidl, Michael; Shenderovich, Ilya G.; Gschwind, Ruth M.; Bauer, Jonathan O.
Complexation behaviour of LiCl and LiPF<sub>6</sub>- model studies in the solid-state and in solution using a bidentate picolyl-based ligand.
Chemical communications (Cambridge, England), 2020, 56, 13335-13338

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