Crystallography Open Database

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1552456 CIFC31 H23 F3 N2 O5P 21 21 218.97942; 10.9358; 27.051
90; 90; 90		2656.33Shu, Chang; Liu, Honglei; Slawin, Alexandra M. Z.; Carpenter-Warren, Cameron; Smith, Andrew D.
Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters
Chemical Science, 2020, 11, 241-247
1552457 CIFC28 H26 F3 N3 O2P 1 21/c 119.7387; 13.4237; 9.3356
90; 93.107; 90		2469.98Shu, Chang; Liu, Honglei; Slawin, Alexandra M. Z.; Carpenter-Warren, Cameron; Smith, Andrew D.
Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters
Chemical Science, 2020, 11, 241-247
1552458 CIFC28 H26 F3 N3 O2P 1 21 113.5575; 23.9425; 19.8418
90; 93.584; 90		6428.06Shu, Chang; Liu, Honglei; Slawin, Alexandra M. Z.; Carpenter-Warren, Cameron; Smith, Andrew D.
Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters
Chemical Science, 2020, 11, 241-247
1552504 CIFC20 H22 B NF d d 239.763; 37.788; 8.9491
90; 90; 90		13446.6Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1552505 CIFC17 H17 B Cr O3 SP 1 21/c 111.605; 9.0305; 15.7985
90; 102.127; 90		1618.72Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1552506 CIFC28 H27 B OP -18.7781; 10.9283; 12.3004
70.809; 87.538; 79.597		1095.91Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1552507 CIFC27 H27 B OC 1 c 113.441; 13.1854; 24.0772
90; 94.762; 90		4252.4Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1552508 CIFC28 H29 B OP 1 21/n 114.454; 7.2349; 21.474
90; 100.708; 90		2206.5Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1552533 CIFC88 H76 F24 N14 P4 Ru2P -113.885; 17.841; 22.499
83.99; 73.932; 85.868		5320.9Smitten, Kirsty L.; Fairbanks, Simon D.; Robertson, Craig C.; Bernardino de la Serna, Jorge; Foster, Simon J.; Thomas, Jim A.
Ruthenium based antimicrobial theranostics - using nanoscopy to identify therapeutic targets and resistance mechanisms in <i>Staphylococcus aureus</i>.
Chemical science, 2020, 11, 70-79
1552713 CIFC44 H42 F18 N6 P3 S2P b a m14.8195; 20.8662; 9.5394
90; 90; 90		2949.8Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552714 CIFC78 H73 F30 N11 P5C m c 2119.886; 20.698; 20.515
90; 90; 90		8444Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552715 CIFC48 H46 F18 N6 P3P b a m14.1423; 21.9108; 9.5937
90; 90; 90		2972.79Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552716 CIFC36 H32 F24 N4 P4P 1 21/c 17.4563; 20.125; 13.948
90; 91.831; 90		2091.9Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552717 CIFC32 H28 F12 N4 P2 S2P b a m10.3821; 21.5348; 9.6558
90; 90; 90		2158.81Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552718 CIFC35 H31 F24 N5 P4P -111.2904; 16.9439; 24.966
75.157; 86.061; 86.58		4601.4Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552719 CIFC34 H30 F12 N4 P2 SP b a m10.266; 21.7433; 9.8244
90; 90; 90		2193Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552720 CIFC44 H42 F18 N6 P3 SP b a m14.8597; 21.003; 9.5902
90; 90; 90		2993.1Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552721 CIFC18 H16.5 F12 N2.5 P2 S0.5P -113.603; 13.8062; 16.0216
101.314; 111.832; 107.987		2486.3Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552722 CIFC47 H45 F18 N7 P3P b a m14.1183; 21.8905; 9.5412
90; 90; 90		2948.8Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552754 CIFAl B3 Cs F O6P n a 218.064; 11.97; 7.036
90; 90; 90		679.2Liu, Hongkun; Wang, Ying; Zhang, Bingbing; Yang, Zhihua; Pan, Shilie
CsAlB3O6F: a beryllium-free deep-ultraviolet nonlinear optical material with enhanced thermal stability
Chemical Science, 2020, 11, 694-698
1552766 CIFC28 H22 N3 PR 3 :H34.841; 34.841; 5.566
90; 90; 120		5851.3Zhu, Ren-Yi; Chen, Long; Hu, Xiao-Si; Zhou, Feng; Zhou, Jian
Enantioselective synthesis of <i>P</i>-chiral tertiary phosphine oxides with an ethynyl group <i>via</i> Cu(i)-catalyzed azide-alkyne cycloaddition.
Chemical science, 2020, 11, 97-106
1552767 CIFC19 H17 N3 O PP 21 21 219.0625; 10.9721; 18.2236
90; 90; 90		1812.1Zhu, Ren-Yi; Chen, Long; Hu, Xiao-Si; Zhou, Feng; Zhou, Jian
Enantioselective synthesis of <i>P</i>-chiral tertiary phosphine oxides with an ethynyl group <i>via</i> Cu(i)-catalyzed azide-alkyne cycloaddition.
Chemical science, 2020, 11, 97-106
1552768 CIFC19 H23 O3 PP 1 21 18.3114; 10.1411; 10.8128
90; 107.963; 90		866.95Zhu, Ren-Yi; Chen, Long; Hu, Xiao-Si; Zhou, Feng; Zhou, Jian
Enantioselective synthesis of <i>P</i>-chiral tertiary phosphine oxides with an ethynyl group <i>via</i> Cu(i)-catalyzed azide-alkyne cycloaddition.
Chemical science, 2020, 11, 97-106
1552769 CIFC24 H32 N O2 P SP 1 21 16.0745; 19.8094; 9.9683
90; 98.06; 90		1187.66Zhu, Ren-Yi; Chen, Long; Hu, Xiao-Si; Zhou, Feng; Zhou, Jian
Enantioselective synthesis of <i>P</i>-chiral tertiary phosphine oxides with an ethynyl group <i>via</i> Cu(i)-catalyzed azide-alkyne cycloaddition.
Chemical science, 2020, 11, 97-106
1552770 CIFC16 H18 Au Cl3 PP -18.6866; 10.7017; 11.1556
72.428; 86.595; 70.591		931.5Zhu, Ren-Yi; Chen, Long; Hu, Xiao-Si; Zhou, Feng; Zhou, Jian
Enantioselective synthesis of <i>P</i>-chiral tertiary phosphine oxides with an ethynyl group <i>via</i> Cu(i)-catalyzed azide-alkyne cycloaddition.
Chemical science, 2020, 11, 97-106
1552771 CIFC36 H33 Cl N3 O3 PP 1 21 114.421; 7.7894; 16.028
90; 114.539; 90		1637.8Zhu, Ren-Yi; Chen, Long; Hu, Xiao-Si; Zhou, Feng; Zhou, Jian
Enantioselective synthesis of <i>P</i>-chiral tertiary phosphine oxides with an ethynyl group <i>via</i> Cu(i)-catalyzed azide-alkyne cycloaddition.
Chemical science, 2020, 11, 97-106
1552772 CIFC15 H13 O PP 21 21 217.6851; 12.5057; 13.9472
90; 90; 90		1340.43Zhu, Ren-Yi; Chen, Long; Hu, Xiao-Si; Zhou, Feng; Zhou, Jian
Enantioselective synthesis of <i>P</i>-chiral tertiary phosphine oxides with an ethynyl group <i>via</i> Cu(i)-catalyzed azide-alkyne cycloaddition.
Chemical science, 2020, 11, 97-106
1552854 CIFC18 H7 F9P -17.427; 7.782; 13.74
89.382; 89.146; 68.679		739.7Xie, Qiqiang; Zhu, Ziyue; Li, Lingchun; Ni, Chuanfa; Hu, Jinbo
Controllable double CF2-insertion into sp2 C‒Cu bond using TMSCF3: a facile access to tetrafluoroethylene-bridged structures
Chemical Science, 2020, 11, 276-280
1552855 CIFC24 H32 N2 O3 S SiI 1 2/a 114.4384; 16.0496; 20.713
90; 96.573; 90		4768.29Rej, Supriya; Chatani, Naoto
Rh(ii)-catalyzed branch-selective C-H alkylation of aryl sulfonamides with vinylsilanes.
Chemical science, 2020, 11, 389-395
1552856 CIFC38 H36 N4 O12 Rh2 S2I 1 2/a 117.4067; 10.6112; 22.164
90; 98.333; 90		4050.6Rej, Supriya; Chatani, Naoto
Rh(ii)-catalyzed branch-selective C-H alkylation of aryl sulfonamides with vinylsilanes.
Chemical science, 2020, 11, 389-395
1552876 CIFC39 H45 Au N4 O4 SP -110.7063; 13.5187; 13.5554
71.713; 76.289; 70.466		1736.4Romanov, Alexander S.; Jones, Saul T. E.; Gu, Qinying; Conaghan, Patrick J.; Drummond, Bluebell H.; Feng, Jiale; Chotard, Florian; Buizza, Leonardo; Foley, Morgan; Linnolahti, Mikko; Credgington, Dan; Bochmann, Manfred
Carbene metal amide photoemitters: tailoring conformationally flexible amides for full color range emissions including white-emitting OLED.
Chemical science, 2020, 11, 435-446
1552877 CIFC41 H52 Au Cl2 N3P b c a10.4512; 18.0543; 38.7653
90; 90; 90		7314.59Romanov, Alexander S.; Jones, Saul T. E.; Gu, Qinying; Conaghan, Patrick J.; Drummond, Bluebell H.; Feng, Jiale; Chotard, Florian; Buizza, Leonardo; Foley, Morgan; Linnolahti, Mikko; Credgington, Dan; Bochmann, Manfred
Carbene metal amide photoemitters: tailoring conformationally flexible amides for full color range emissions including white-emitting OLED.
Chemical science, 2020, 11, 435-446
1552878 CIFC39 H47 Au N2 SP 1 21/c 112.6173; 13.9286; 19.607
90; 108.245; 90		3272.5Romanov, Alexander S.; Jones, Saul T. E.; Gu, Qinying; Conaghan, Patrick J.; Drummond, Bluebell H.; Feng, Jiale; Chotard, Florian; Buizza, Leonardo; Foley, Morgan; Linnolahti, Mikko; Credgington, Dan; Bochmann, Manfred
Carbene metal amide photoemitters: tailoring conformationally flexible amides for full color range emissions including white-emitting OLED.
Chemical science, 2020, 11, 435-446
1552879 CIFC45 H51 Au N2P 1 21/c 112.6669; 17.4884; 17.3107
90; 108.451; 90		3637.6Romanov, Alexander S.; Jones, Saul T. E.; Gu, Qinying; Conaghan, Patrick J.; Drummond, Bluebell H.; Feng, Jiale; Chotard, Florian; Buizza, Leonardo; Foley, Morgan; Linnolahti, Mikko; Credgington, Dan; Bochmann, Manfred
Carbene metal amide photoemitters: tailoring conformationally flexible amides for full color range emissions including white-emitting OLED.
Chemical science, 2020, 11, 435-446
1552880 CIFC40 H49 Au Cl2 N2 OP b c a10.0502; 17.6546; 39.3833
90; 90; 90		6987.9Romanov, Alexander S.; Jones, Saul T. E.; Gu, Qinying; Conaghan, Patrick J.; Drummond, Bluebell H.; Feng, Jiale; Chotard, Florian; Buizza, Leonardo; Foley, Morgan; Linnolahti, Mikko; Credgington, Dan; Bochmann, Manfred
Carbene metal amide photoemitters: tailoring conformationally flexible amides for full color range emissions including white-emitting OLED.
Chemical science, 2020, 11, 435-446
1552881 CIFC79 H96 Au2 Cl2 N4 O4 S2P 1 21/c 121.965; 16.1816; 20.6249
90; 99.929; 90		7220.9Romanov, Alexander S.; Jones, Saul T. E.; Gu, Qinying; Conaghan, Patrick J.; Drummond, Bluebell H.; Feng, Jiale; Chotard, Florian; Buizza, Leonardo; Foley, Morgan; Linnolahti, Mikko; Credgington, Dan; Bochmann, Manfred
Carbene metal amide photoemitters: tailoring conformationally flexible amides for full color range emissions including white-emitting OLED.
Chemical science, 2020, 11, 435-446
1552882 CIFC42 H53 Au N2P b c n34.2921; 13.9716; 17.0268
90; 90; 90		8157.8Romanov, Alexander S.; Jones, Saul T. E.; Gu, Qinying; Conaghan, Patrick J.; Drummond, Bluebell H.; Feng, Jiale; Chotard, Florian; Buizza, Leonardo; Foley, Morgan; Linnolahti, Mikko; Credgington, Dan; Bochmann, Manfred
Carbene metal amide photoemitters: tailoring conformationally flexible amides for full color range emissions including white-emitting OLED.
Chemical science, 2020, 11, 435-446
1552883 CIFC28 H24 O2P -19.5034; 10.6505; 21.889
96.945; 102.069; 99.44		2109.4Nickerson, Leslie A.; Bergstrom, Benjamin D.; Gao, Mingchun; Shiue, Yuan-Shin; Laconsay, Croix J.; Culberson, Matthew R.; Knauss, Walker A.; Fettinger, James C.; Tantillo, Dean J.; Shaw, Jared T.
Enantioselective synthesis of isochromans and tetrahydroisoquinolines by C-H insertion of donor/donor carbenes.
Chemical science, 2020, 11, 494-498
1552884 CIFC23 H20 OI 1 2 117.3724; 5.5677; 18.8919
90; 111.661; 90		1698.27Nickerson, Leslie A.; Bergstrom, Benjamin D.; Gao, Mingchun; Shiue, Yuan-Shin; Laconsay, Croix J.; Culberson, Matthew R.; Knauss, Walker A.; Fettinger, James C.; Tantillo, Dean J.; Shaw, Jared T.
Enantioselective synthesis of isochromans and tetrahydroisoquinolines by C-H insertion of donor/donor carbenes.
Chemical science, 2020, 11, 494-498
1552885 CIFC18 H17 N O2P 21 21 219.0262; 10.7097; 14.6781
90; 90; 90		1418.9Nickerson, Leslie A.; Bergstrom, Benjamin D.; Gao, Mingchun; Shiue, Yuan-Shin; Laconsay, Croix J.; Culberson, Matthew R.; Knauss, Walker A.; Fettinger, James C.; Tantillo, Dean J.; Shaw, Jared T.
Enantioselective synthesis of isochromans and tetrahydroisoquinolines by C-H insertion of donor/donor carbenes.
Chemical science, 2020, 11, 494-498
1552886 CIFC23 H19 N O2P 21 21 215.5431; 17.2727; 17.7127
90; 90; 90		1695.89Nickerson, Leslie A.; Bergstrom, Benjamin D.; Gao, Mingchun; Shiue, Yuan-Shin; Laconsay, Croix J.; Culberson, Matthew R.; Knauss, Walker A.; Fettinger, James C.; Tantillo, Dean J.; Shaw, Jared T.
Enantioselective synthesis of isochromans and tetrahydroisoquinolines by C-H insertion of donor/donor carbenes.
Chemical science, 2020, 11, 494-498
1552946 CIFC23 H31 N O7 SiP 1 21 110.936; 9.071; 12.562
90; 94.63; 90		1242.1Yu, Haiyong; Zong, Yan; Xu, Tao
Total synthesis of (−)-penicimutanin a and related congeners
Chemical Science, 2020, 11, 656-660
1552947 CIFC45 H47 N4 O9P 1 21 18.7818; 21.1435; 10.5555
90; 92.327; 90		1958.3Yu, Haiyong; Zong, Yan; Xu, Tao
Total synthesis of (−)-penicimutanin a and related congeners
Chemical Science, 2020, 11, 656-660
1552948 CIFC26 H12 Br2 N2 O6P 21 21 217.355; 12.9923; 24.5807
90; 90; 90		2348.9Bao, Xiaoze; Rodriguez, Jean; Bonne, Damien
Bidirectional enantioselective synthesis of bis-benzofuran atropisomeric oligoarenes featuring two distal C-C stereogenic axes.
Chemical science, 2020, 11, 403-408
1552949 CIFC16.05 H12.45 N O5I 1 2 115.0405; 8.4792; 13.8431
90; 106.602; 90		1691.83Bao, Xiaoze; Rodriguez, Jean; Bonne, Damien
Bidirectional enantioselective synthesis of bis-benzofuran atropisomeric oligoarenes featuring two distal C-C stereogenic axes.
Chemical science, 2020, 11, 403-408
1552950 CIFC66 H50 N2 O4P 1 21 115.2114; 15.0318; 22.042
90; 93.831; 90		5028.7Dhbaibi, Kais; Favereau, Ludovic; Srebro-Hooper, Monika; Quinton, Cassandre; Vanthuyne, Nicolas; Arrico, Lorenzo; Roisnel, Thierry; Jamoussi, Bassem; Poriel, Cyril; Cabanetos, Clément; Autschbach, Jochen; Crassous, Jeanne
Modulation of circularly polarized luminescence through excited-state symmetry breaking and interbranched exciton coupling in helical push-pull organic systems.
Chemical science, 2020, 11, 567-576
1552951 CIFC78 H19 N O S2P 1 21/c 114.2115; 13.2334; 26.4184
90; 116.384; 90		4450.9Liu, Kai-Qing; Wang, Jun-Jie; Yan, Xing-Xing; Niu, Chuang; Wang, Guan-Wu
Regioselective electrosynthesis of tetra- and hexa-functionalized [60]fullerene derivatives with unprecedented addition patterns.
Chemical science, 2020, 11, 384-388
1556080 CIFC35 H38 Cl2 F6 Fe N4 O6 S2P 1 21 111.2529; 12.5689; 14.178
90; 101.369; 90		1965.94Wei, Jinhu; Cao, Bei; Tse, Chun-Wai; Chang, Xiao-Yong; Zhou, Cong-Ying; Che, Chi-Ming
Chiral cis-iron(ii) complexes with metal- and ligand-centered chirality for highly regio- and enantioselective alkylation of N-heteroaromatics
Chemical Science, 2020, 11, 684-693
1556081 CIFC38 H44 Cl4 F6 Fe N4 O6 S2P 21 21 2111.265; 16.5488; 23.0009
90; 90; 90		4287.9Wei, Jinhu; Cao, Bei; Tse, Chun-Wai; Chang, Xiao-Yong; Zhou, Cong-Ying; Che, Chi-Ming
Chiral cis-iron(ii) complexes with metal- and ligand-centered chirality for highly regio- and enantioselective alkylation of N-heteroaromatics
Chemical Science, 2020, 11, 684-693
1556082 CIFC24 H26 N3 OC 1 2 121.5973; 5.0981; 17.5377
90; 91.771; 90		1930.07Wei, Jinhu; Cao, Bei; Tse, Chun-Wai; Chang, Xiao-Yong; Zhou, Cong-Ying; Che, Chi-Ming
Chiral cis-iron(ii) complexes with metal- and ligand-centered chirality for highly regio- and enantioselective alkylation of N-heteroaromatics
Chemical Science, 2020, 11, 684-693
1556083 CIFC18 H21 N3 OP 1 21 18.63; 15.205; 12.2
90; 105.42; 90		1543.2Wei, Jinhu; Cao, Bei; Tse, Chun-Wai; Chang, Xiao-Yong; Zhou, Cong-Ying; Che, Chi-Ming
Chiral cis-iron(ii) complexes with metal- and ligand-centered chirality for highly regio- and enantioselective alkylation of N-heteroaromatics
Chemical Science, 2020, 11, 684-693
1556084 CIFC22 H17 N O6 SP 21 21 215.761; 15.9645; 20.7087
90; 90; 90		1904.61Wang, Yunsheng; Yang, Jie; Tian, Yu; Fang, Manman; Liao, Qiuyan; Wang, Liwei; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
Persistent organic room temperature phosphorescence: what is the role of molecular dimers?
Chemical Science, 2020, 11, 833-838
1556085 CIFC22 H17 N O4 SP n m a6.6807; 19.9408; 14.2683
90; 90; 90		1900.8Wang, Yunsheng; Yang, Jie; Tian, Yu; Fang, Manman; Liao, Qiuyan; Wang, Liwei; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
Persistent organic room temperature phosphorescence: what is the role of molecular dimers?
Chemical Science, 2020, 11, 833-838
1556261 CIFC13 H7 F6 N SP 1 21 19.5947; 4.8799; 13.6316
90; 94.414; 90		636.35Zubkov, Mikhail O.; Kosobokov, Mikhail D.; Levin, Vitalij V.; Kokorekin, Vladimir A.; Korlyukov, Alexander A.; Hu, Jinbo; Dilman, Alexander D.
A novel photoredox-active group for the generation of fluorinated radicals from difluorostyrenes
Chemical Science, 2020, 11, 737-741
1556262 CIFC24 H14 F4 N2 SP 1 21/c 18.6198; 7.7249; 29.3919
90; 91.201; 90		1956.69Zubkov, Mikhail O.; Kosobokov, Mikhail D.; Levin, Vitalij V.; Kokorekin, Vladimir A.; Korlyukov, Alexander A.; Hu, Jinbo; Dilman, Alexander D.
A novel photoredox-active group for the generation of fluorinated radicals from difluorostyrenes
Chemical Science, 2020, 11, 737-741
1556265 CIFC76 H94 Cl6 F6 N6 O10 Pt2 S2P -113.4362; 18.3994; 20.2998
106.666; 108.577; 103.771		4246.8Leung, Sam Ka-Ming; Chan, Alan Kwun-Wa; Leung, Sammual Yu-Lut; Leung, Ming-Yi; Yam, Vivian Wing-Wah
Supramolecular assembly of bent dinuclear amphiphilic alkynylplatinum(ii) terpyridine complexes: diverse nanostructures through subtle tuning of the mode of molecular stacking.
Chemical science, 2020, 11, 499-507
1556406 CIFC54 H54 N18 O12P 1 21/c 116.615; 27.205; 13.426
90; 112.678; 90		5600Nakashima, Kensuke; Shimizu, Takeshi; Kamakura, Yoshinobu; Hinokimoto, Akira; Kitagawa, Yasutaka; Yoshikawa, Hirofumi; Tanaka, Daisuke
A new design strategy for redox-active molecular assemblies with crystalline porous structures for lithium-ion batteries.
Chemical science, 2020, 11, 37-43
1556409 CIFC37 H47 B N3 O PP 1 21/n 110.6925; 19.6374; 17.0321
90; 101.118; 90		3509.16Wilson, Daniel W. N.; Franco, Mauricio P.; Myers, William K.; McGrady, John E.; Goicoechea, Jose M.
Base induced isomerisation of a phosphaethynolato-borane: mechanistic insights into boryl migration and decarbonylation to afford a triplet phosphinidene
Chemical Science, 2020, 11, 862-869
1556410 CIFC46 H58 B N4 PP -110.6744; 13.4621; 14.8146
82.534; 88.654; 84.679		2101.57Wilson, Daniel W. N.; Franco, Mauricio P.; Myers, William K.; McGrady, John E.; Goicoechea, Jose M.
Base induced isomerisation of a phosphaethynolato-borane: mechanistic insights into boryl migration and decarbonylation to afford a triplet phosphinidene
Chemical Science, 2020, 11, 862-869
1556411 CIFC31 H45 B N3 PP 1 21/n 117.2385; 10.9928; 33.0859
90; 96.506; 90		6229.38Wilson, Daniel W. N.; Franco, Mauricio P.; Myers, William K.; McGrady, John E.; Goicoechea, Jose M.
Base induced isomerisation of a phosphaethynolato-borane: mechanistic insights into boryl migration and decarbonylation to afford a triplet phosphinidene
Chemical Science, 2020, 11, 862-869
1556412 CIFC52 H72 B2 N4 P2P 1 21/n 113.0269; 14.1779; 14.8915
90; 112.746; 90		2536.47Wilson, Daniel W. N.; Franco, Mauricio P.; Myers, William K.; McGrady, John E.; Goicoechea, Jose M.
Base induced isomerisation of a phosphaethynolato-borane: mechanistic insights into boryl migration and decarbonylation to afford a triplet phosphinidene
Chemical Science, 2020, 11, 862-869
1556413 CIFC36 H47 B N3 PP 1 21/c 118.9679; 7.4054; 25.1568
90; 107.29; 90		3373.97Wilson, Daniel W. N.; Franco, Mauricio P.; Myers, William K.; McGrady, John E.; Goicoechea, Jose M.
Base induced isomerisation of a phosphaethynolato-borane: mechanistic insights into boryl migration and decarbonylation to afford a triplet phosphinidene
Chemical Science, 2020, 11, 862-869
1556414 CIFC74 H113 B2 N6 O2 P2P -114.0563; 14.7947; 20.1864
73.781; 76.257; 67.558		3684.82Wilson, Daniel W. N.; Franco, Mauricio P.; Myers, William K.; McGrady, John E.; Goicoechea, Jose M.
Base induced isomerisation of a phosphaethynolato-borane: mechanistic insights into boryl migration and decarbonylation to afford a triplet phosphinidene
Chemical Science, 2020, 11, 862-869
1556415 CIFC27 H36 B N2 O PP 1 21/n 19.3904; 14.2038; 20.3914
90; 99.177; 90		2684.98Wilson, Daniel W. N.; Franco, Mauricio P.; Myers, William K.; McGrady, John E.; Goicoechea, Jose M.
Base induced isomerisation of a phosphaethynolato-borane: mechanistic insights into boryl migration and decarbonylation to afford a triplet phosphinidene
Chemical Science, 2020, 11, 862-869
1556534 CIFC34.5 H29 Cl F6 N PP 1 21/n 111.2525; 9.2194; 59.1397
90; 93.8053; 90		6121.7Khorloo, Michidmaa; Cheng, Yanhua; Zhang, Haoke; Chen, Ming; Sung, Herman H. Y.; Williams, Ian D.; Lam, Jacky W. Y.; Tang, Ben Zhong
Polymorph selectivity of an AIE luminogen under nano-confinement to visualize polymer microstructures
Chemical Science, 2020, 11, 997-1005
1556535 CIFC34 H28 F6 N PP 1 21/c 124.8939; 9.1783; 12.5794
90; 98.168; 90		2845.03Khorloo, Michidmaa; Cheng, Yanhua; Zhang, Haoke; Chen, Ming; Sung, Herman H. Y.; Williams, Ian D.; Lam, Jacky W. Y.; Tang, Ben Zhong
Polymorph selectivity of an AIE luminogen under nano-confinement to visualize polymer microstructures
Chemical Science, 2020, 11, 997-1005
1556536 CIFC15 H13 N2 O5 ReP 21 21 216.345; 14.5492; 16.7909
90; 90; 90		1550.05Morrison, Christine N.; Prosser, Kathleen E.; Stokes, Ryjul W.; Cordes, Anna; Metzler-Nolte, Nils; Cohen, Seth M.
Expanding medicinal chemistry into 3D space: metallofragments as 3D scaffolds for fragment-based drug discovery
Chemical Science, 2020, 11, 1216-1225
1556537 CIFC13 H9 N2 O5 ReP 1 21/c 19.1929; 13.3161; 11.3352
90; 106.8; 90		1328.36Morrison, Christine N.; Prosser, Kathleen E.; Stokes, Ryjul W.; Cordes, Anna; Metzler-Nolte, Nils; Cohen, Seth M.
Expanding medicinal chemistry into 3D space: metallofragments as 3D scaffolds for fragment-based drug discovery
Chemical Science, 2020, 11, 1216-1225
1556538 CIFC15 H12 N O4 Re SP 1 21/n 18.5304; 8.156; 22.7941
90; 96.365; 90		1576.1Morrison, Christine N.; Prosser, Kathleen E.; Stokes, Ryjul W.; Cordes, Anna; Metzler-Nolte, Nils; Cohen, Seth M.
Expanding medicinal chemistry into 3D space: metallofragments as 3D scaffolds for fragment-based drug discovery
Chemical Science, 2020, 11, 1216-1225
1556539 CIFC20.5 H15 Cl N O5 ReP 1 21/c 120.753; 7.0352; 13.7941
90; 105.388; 90		1941.8Morrison, Christine N.; Prosser, Kathleen E.; Stokes, Ryjul W.; Cordes, Anna; Metzler-Nolte, Nils; Cohen, Seth M.
Expanding medicinal chemistry into 3D space: metallofragments as 3D scaffolds for fragment-based drug discovery
Chemical Science, 2020, 11, 1216-1225
1556540 CIFC13 H11 N2 O6 ReP -19.108; 9.5099; 9.7673
70.669; 80.012; 61.781		703.28Morrison, Christine N.; Prosser, Kathleen E.; Stokes, Ryjul W.; Cordes, Anna; Metzler-Nolte, Nils; Cohen, Seth M.
Expanding medicinal chemistry into 3D space: metallofragments as 3D scaffolds for fragment-based drug discovery
Chemical Science, 2020, 11, 1216-1225
1556629 CIFC15 H13 FP 1 21/n 113.5004; 5.6062; 15.1666
90; 104.738; 90		1110.13Fu, Wai Chung; Kwong, Fuk Yee
A denitrogenative palladium-catalyzed cascade for regioselective synthesis of fluorenes
Chemical Science, 2020, 11, 1411-1417
1556630 CIFC40 H50 Br N5 O5P 1 21/c 111.9227; 17.3502; 17.7857
90; 90.611; 90		3678.96Miao, Hong-Jie; Wang, Le-Le; Han, Hua-Bin; Zhao, Yong-De; Wang, Qi-Lin; Bu, Zhan-Wei
Regio- and diastereoselective dearomatizations of N-alkyl activated azaarenes: the maximization of the reactive sites
Chemical Science, 2020, 11, 1418-1424
1556631 CIFC29 H27 Cl N2 OP 1 21/c 110.8554; 18.2505; 12.2873
90; 105.01; 90		2351.26Miao, Hong-Jie; Wang, Le-Le; Han, Hua-Bin; Zhao, Yong-De; Wang, Qi-Lin; Bu, Zhan-Wei
Regio- and diastereoselective dearomatizations of N-alkyl activated azaarenes: the maximization of the reactive sites
Chemical Science, 2020, 11, 1418-1424
1556632 CIFC46 H42 Br N3 OP 1 21/n 110.2078; 19.152; 18.9514
90; 94.804; 90		3691.98Miao, Hong-Jie; Wang, Le-Le; Han, Hua-Bin; Zhao, Yong-De; Wang, Qi-Lin; Bu, Zhan-Wei
Regio- and diastereoselective dearomatizations of N-alkyl activated azaarenes: the maximization of the reactive sites
Chemical Science, 2020, 11, 1418-1424
1556633 CIFC28 H29 N3 OP 1 21/c 19.0448; 14.0503; 18.8685
90; 102.053; 90		2344.99Miao, Hong-Jie; Wang, Le-Le; Han, Hua-Bin; Zhao, Yong-De; Wang, Qi-Lin; Bu, Zhan-Wei
Regio- and diastereoselective dearomatizations of N-alkyl activated azaarenes: the maximization of the reactive sites
Chemical Science, 2020, 11, 1418-1424
1556634 CIFC31 H31 Br N2 OP 1 21/n 114.485; 10.8239; 16.4134
90; 90.869; 90		2573.07Miao, Hong-Jie; Wang, Le-Le; Han, Hua-Bin; Zhao, Yong-De; Wang, Qi-Lin; Bu, Zhan-Wei
Regio- and diastereoselective dearomatizations of N-alkyl activated azaarenes: the maximization of the reactive sites
Chemical Science, 2020, 11, 1418-1424
1556635 CIFC39 H39 N5 O5P 1 21/c 111.80408; 18.74504; 31.2581
90; 79.1361; 90		6792.46Miao, Hong-Jie; Wang, Le-Le; Han, Hua-Bin; Zhao, Yong-De; Wang, Qi-Lin; Bu, Zhan-Wei
Regio- and diastereoselective dearomatizations of N-alkyl activated azaarenes: the maximization of the reactive sites
Chemical Science, 2020, 11, 1418-1424
1556636 CIFC45 H39 Cl2 N3 OP 1 21/n 113.58053; 20.7753; 29.2921
90; 102.897; 90		8055.96Miao, Hong-Jie; Wang, Le-Le; Han, Hua-Bin; Zhao, Yong-De; Wang, Qi-Lin; Bu, Zhan-Wei
Regio- and diastereoselective dearomatizations of N-alkyl activated azaarenes: the maximization of the reactive sites
Chemical Science, 2020, 11, 1418-1424
1556642 CIFC50 H67 B2 P3P -110.6022; 10.6218; 20.1023
94.418; 99.288; 100.371		2184.47Stennett, Tom E.; Jayaraman, Arumugam; Brückner, Tobias; Schneider, Lea; Braunschweig, Holger
Hydrophosphination of boron‒boron multiple bonds
Chemical Science, 2020, 11, 1335-1341
1556643 CIFC34 H48 B2 Br P3P b c a10.5062; 17.5469; 36.649
90; 90; 90		6756.3Stennett, Tom E.; Jayaraman, Arumugam; Brückner, Tobias; Schneider, Lea; Braunschweig, Holger
Hydrophosphination of boron‒boron multiple bonds
Chemical Science, 2020, 11, 1335-1341
1556644 CIFC34 H48 B2 Br P3P 1 21/n 111.8091; 16.5734; 17.4767
90; 107.828; 90		3256.2Stennett, Tom E.; Jayaraman, Arumugam; Brückner, Tobias; Schneider, Lea; Braunschweig, Holger
Hydrophosphination of boron‒boron multiple bonds
Chemical Science, 2020, 11, 1335-1341
1556645 CIFC40 H55 B2 Br N2 P2F d d 228.3736; 57.198; 10.0055
90; 90; 90		16238.1Stennett, Tom E.; Jayaraman, Arumugam; Brückner, Tobias; Schneider, Lea; Braunschweig, Holger
Hydrophosphination of boron‒boron multiple bonds
Chemical Science, 2020, 11, 1335-1341
1556646 CIFC58 H71 B2 N4 PP -111.3635; 13.09; 19.2394
89.968; 76.353; 70.181		2606.41Stennett, Tom E.; Jayaraman, Arumugam; Brückner, Tobias; Schneider, Lea; Braunschweig, Holger
Hydrophosphination of boron‒boron multiple bonds
Chemical Science, 2020, 11, 1335-1341
1556647 CIFC26 H18 B F10 NP 1 21/c 116.8585; 9.6751; 15.4623
90; 111.832; 90		2341.14Tao, Xin; Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Borane-induced ring closure reaction of oligomethylene-linked bis-allenes
Chemical Science, 2020, 11, 1542-1548
1556648 CIFC44 H30 B F10 PP -18.3209; 11.319; 19.7803
99.399; 98.04; 104.051		1751.34Tao, Xin; Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Borane-induced ring closure reaction of oligomethylene-linked bis-allenes
Chemical Science, 2020, 11, 1542-1548
1556649 CIFC27 H20 B F10 NP 21 21 219.724; 14.9525; 16.4897
90; 90; 90		2397.57Tao, Xin; Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Borane-induced ring closure reaction of oligomethylene-linked bis-allenes
Chemical Science, 2020, 11, 1542-1548
1556650 CIFC46 H38 B Cl2 F10 PP 1 21/c 111.605; 20.1373; 17.8823
90; 102.818; 90		4074.83Tao, Xin; Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Borane-induced ring closure reaction of oligomethylene-linked bis-allenes
Chemical Science, 2020, 11, 1542-1548
1556651 CIFC46 H38 B Cl2 F10 PP -111.1982; 11.5411; 16.5533
96.789; 96.943; 106.576		2009Tao, Xin; Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Borane-induced ring closure reaction of oligomethylene-linked bis-allenes
Chemical Science, 2020, 11, 1542-1548
1556652 CIFC39 H28 B F10 PP 1 21/c 112.2953; 14.3056; 20.8746
90; 100.3; 90		3612.5Tao, Xin; Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Borane-induced ring closure reaction of oligomethylene-linked bis-allenes
Chemical Science, 2020, 11, 1542-1548
1556653 CIFC27 H21 B F10P 1 21/c 16.4255; 17.461; 21.2763
90; 95.037; 90		2377.9Tao, Xin; Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Borane-induced ring closure reaction of oligomethylene-linked bis-allenes
Chemical Science, 2020, 11, 1542-1548
1556654 CIFC40 H30 B F10 PP -112.4783; 15.7635; 20.7617
102.312; 93.184; 112.263		3650.3Tao, Xin; Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Borane-induced ring closure reaction of oligomethylene-linked bis-allenes
Chemical Science, 2020, 11, 1542-1548
1556655 CIFC43 H24 B2 F20 N2P -19.0564; 10.3497; 21.915
91.873; 96.63; 96.996		2022.9Tao, Xin; Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Borane-induced ring closure reaction of oligomethylene-linked bis-allenes
Chemical Science, 2020, 11, 1542-1548
1556673 CIFC36 H23 Cu2 F14 N8 O8 P S4P 1 21/c 119.7106; 9.9489; 22.7748
90; 99.808; 90		4400.83Nicolay, Amélie; Ziegler, Micah S.; Small, David W.; Grünbauer, Rebecca; Scheer, Manfred; Tilley, T. Don
Isomerism and dynamic behavior of bridging phosphaalkynes bound to a dicopper complex.
Chemical science, 2020, 11, 1607-1616
1556674 CIFC42 H34 Cu2 F14 N8 O9 S4P -112.5211; 14.8116; 15.6245
76.518; 67.701; 76.651		2574.23Nicolay, Amélie; Ziegler, Micah S.; Small, David W.; Grünbauer, Rebecca; Scheer, Manfred; Tilley, T. Don
Isomerism and dynamic behavior of bridging phosphaalkynes bound to a dicopper complex.
Chemical science, 2020, 11, 1607-1616
1556675 CIFC43 H39 Cu2 F14 N8 O9 P S4P -112.4499; 12.637; 18.5946
89.354; 84.84; 72.243		2774.4Nicolay, Amélie; Ziegler, Micah S.; Small, David W.; Grünbauer, Rebecca; Scheer, Manfred; Tilley, T. Don
Isomerism and dynamic behavior of bridging phosphaalkynes bound to a dicopper complex.
Chemical science, 2020, 11, 1607-1616
1556676 CIFC45 H35 Cu2 F14 N9 O8 S4P 21 21 2110.918; 20.4455; 23.1939
90; 90; 90		5177.4Nicolay, Amélie; Ziegler, Micah S.; Small, David W.; Grünbauer, Rebecca; Scheer, Manfred; Tilley, T. Don
Isomerism and dynamic behavior of bridging phosphaalkynes bound to a dicopper complex.
Chemical science, 2020, 11, 1607-1616
1556677 CIFC45 H35 Cu2 F14 N8 O8 P S4P 1 21/n 118.6915; 16.5896; 18.8035
90; 96.346; 90		5794.9Nicolay, Amélie; Ziegler, Micah S.; Small, David W.; Grünbauer, Rebecca; Scheer, Manfred; Tilley, T. Don
Isomerism and dynamic behavior of bridging phosphaalkynes bound to a dicopper complex.
Chemical science, 2020, 11, 1607-1616
1556703 CIFC65.25 N4 O8 S2P -122.2613; 26.916; 28.2117
83.387; 73.393; 69.33		15154.3Su, Feng; Chen, Shuqi; Mo, Xiaogang; Wu, Kongchuan; Wu, Jiajun; Lin, Weidong; Lin, Zhiwei; Lin, Jianbin; Zhang, Hui-Jun; Wen, Ting-Bin
Trisulfur radical anion-triggered stitching thienannulation: rapid access to largely π-extended thienoacenes
Chemical Science, 2020, 11, 1503-1509
1556704 CIFC37 N4 O8 S3P 1 21 122.0328; 21.2168; 33.589
90; 102.198; 90		15347.2Su, Feng; Chen, Shuqi; Mo, Xiaogang; Wu, Kongchuan; Wu, Jiajun; Lin, Weidong; Lin, Zhiwei; Lin, Jianbin; Zhang, Hui-Jun; Wen, Ting-Bin
Trisulfur radical anion-triggered stitching thienannulation: rapid access to largely π-extended thienoacenes
Chemical Science, 2020, 11, 1503-1509
1556719 CIFC21 H19 N O SP -17.2702; 8.7819; 13.6782
98.564; 100.026; 104.633		814.84Ho, Hon Eong; Pagano, Angela; Rossi-Ashton, James A.; Donald, James R.; Epton, Ryan G.; Churchill, Jonathan C.; James, Michael J.; O'Brien, Peter; Taylor, Richard J. K.; Unsworth, William P.
Visible-light-induced intramolecular charge transfer in the radical spirocyclisation of indole-tethered ynones
Chemical Science, 2020, 11, 1353-1360
1556720 CIFC18 H13 N OP 1 21/c 111.42288; 8.41061; 28.0872
90; 100.454; 90		2653.64Ho, Hon Eong; Pagano, Angela; Rossi-Ashton, James A.; Donald, James R.; Epton, Ryan G.; Churchill, Jonathan C.; James, Michael J.; O'Brien, Peter; Taylor, Richard J. K.; Unsworth, William P.
Visible-light-induced intramolecular charge transfer in the radical spirocyclisation of indole-tethered ynones
Chemical Science, 2020, 11, 1353-1360
1556721 CIFC24 H19 N O SP 21 21 215.81156; 17.547; 18.1227
90; 90; 90		1848.07Ho, Hon Eong; Pagano, Angela; Rossi-Ashton, James A.; Donald, James R.; Epton, Ryan G.; Churchill, Jonathan C.; James, Michael J.; O'Brien, Peter; Taylor, Richard J. K.; Unsworth, William P.
Visible-light-induced intramolecular charge transfer in the radical spirocyclisation of indole-tethered ynones
Chemical Science, 2020, 11, 1353-1360
1556722 CIFC19 H15 N OP 21 21 217.4225; 9.90594; 19.5109
90; 90; 90		1434.57Ho, Hon Eong; Pagano, Angela; Rossi-Ashton, James A.; Donald, James R.; Epton, Ryan G.; Churchill, Jonathan C.; James, Michael J.; O'Brien, Peter; Taylor, Richard J. K.; Unsworth, William P.
Visible-light-induced intramolecular charge transfer in the radical spirocyclisation of indole-tethered ynones
Chemical Science, 2020, 11, 1353-1360
1556723 CIFC25 H21 N O SP -18.7543; 9.971; 11.6327
81.846; 74.281; 81.076		960.27Ho, Hon Eong; Pagano, Angela; Rossi-Ashton, James A.; Donald, James R.; Epton, Ryan G.; Churchill, Jonathan C.; James, Michael J.; O'Brien, Peter; Taylor, Richard J. K.; Unsworth, William P.
Visible-light-induced intramolecular charge transfer in the radical spirocyclisation of indole-tethered ynones
Chemical Science, 2020, 11, 1353-1360
1556844 CIFC45 H57 B N2 O2P -19.6381; 11.485; 19.0369
85.238; 75.946; 75.838		1981.44Bhunia, Mrinal; Sahoo, Sumeet Ranjan; Das, Arpan; Ahmed, Jasimuddin; P., Sreejyothi; Mandal, Swadhin K.
Transition metal-free catalytic reduction of primary amides using an abnormal NHC based potassium complex: integrating nucleophilicity with Lewis acidic activation
Chemical Science, 2020, 11, 1848-1854
1556845 CIFC244 H327 Ag31 Cl5 F24 O2 P6 Pt S16 Sb4P -121.515; 24.1156; 35.321
81.037; 78.006; 68.595		16625Kang, Xi; Jin, Shan; Xiong, Lin; Wei, Xiao; Zhou, Manman; Qin, Chenwanli; Pei, Yong; Wang, Shuxin; Zhu, Manzhou
Nanocluster growth <i>via</i> "graft-onto": effects on geometric structures and optical properties.
Chemical science, 2020, 11, 1691-1697
1556846 CIFC11 H13 F9 O2P 21 21 215.6044; 9.5819; 26.472
90; 90; 90		1421.57Sperandio, Céline; Rodriguez, Jean; Quintard, Adrien
Development of copper-catalyzed enantioselective decarboxylative aldolization for the preparation of perfluorinated 1,3,5-triols featuring supramolecular recognition properties.
Chemical science, 2020, 11, 1629-1635
1556847 CIFC7 H10 F6 O3P 1 21 14.9029; 9.8824; 10.7838
90; 100.543; 90		513.68Sperandio, Céline; Rodriguez, Jean; Quintard, Adrien
Development of copper-catalyzed enantioselective decarboxylative aldolization for the preparation of perfluorinated 1,3,5-triols featuring supramolecular recognition properties.
Chemical science, 2020, 11, 1629-1635
1556860 CIFC45 H44 Cl F5 N4 NiP 1 21/c 119.2423; 10.9261; 21.5899
90; 106.046; 90		4362.3Dong, Yuyang; Lukens, James T.; Clarke, Ryan M.; Zheng, Shao-Liang; Lancaster, Kyle M.; Betley, Theodore A.
Synthesis, characterization and C‒H amination reactivity of nickel iminyl complexes
Chemical Science, 2020, 11, 1260-1268
1556861 CIFC45 H50 F5 N3 NiP 1 21/c 112.0799; 14.6404; 24.1769
90; 91.408; 90		4274.5Dong, Yuyang; Lukens, James T.; Clarke, Ryan M.; Zheng, Shao-Liang; Lancaster, Kyle M.; Betley, Theodore A.
Synthesis, characterization and C‒H amination reactivity of nickel iminyl complexes
Chemical Science, 2020, 11, 1260-1268
1556862 CIFC44 H45 F5 N3 NiP -19.5949; 11.8426; 18.3253
92.953; 104.293; 100.626		1972.9Dong, Yuyang; Lukens, James T.; Clarke, Ryan M.; Zheng, Shao-Liang; Lancaster, Kyle M.; Betley, Theodore A.
Synthesis, characterization and C‒H amination reactivity of nickel iminyl complexes
Chemical Science, 2020, 11, 1260-1268
1556863 CIFC45 H49 F5 N3 NiP n a 2114.1294; 16.6197; 15.8282
90; 90; 90		3716.9Dong, Yuyang; Lukens, James T.; Clarke, Ryan M.; Zheng, Shao-Liang; Lancaster, Kyle M.; Betley, Theodore A.
Synthesis, characterization and C‒H amination reactivity of nickel iminyl complexes
Chemical Science, 2020, 11, 1260-1268
1556864 CIFC40 H39 F5 N3 NiP 1 21/c 117.7017; 15.1269; 13.141
90; 109.571; 90		3315.5Dong, Yuyang; Lukens, James T.; Clarke, Ryan M.; Zheng, Shao-Liang; Lancaster, Kyle M.; Betley, Theodore A.
Synthesis, characterization and C‒H amination reactivity of nickel iminyl complexes
Chemical Science, 2020, 11, 1260-1268
1556865 CIFC12 H8 I2 N2 O7P n a 218.2007; 7.7793; 24.6164
90; 90; 90		1570.42Zhang, Guangtao; Wang, Yuanxun; Xu, Jun; Sun, Jiyun; Sun, Fengxia; Zhang, Yilin; Zhang, Chenglin; Du, Yunfei
A new hypervalent iodine(iii/v) oxidant and its application to the synthesis of 2H-azirines
Chemical Science, 2020, 11, 947-953
1556866 CIFC36 H50 B2P -19.035; 12.0924; 14.7514
92.899; 103.022; 103.134		1520.32Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1556867 CIFC32 H35 B OP 1 21/c 110.6036; 17.5824; 17.446
90; 125.621; 90		2643.98Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1556868 CIFC34 H31 B OP b c a10.0358; 12.1076; 43.226
90; 90; 90		5252.4Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1556869 CIFC61 H60 Cl2 N4 O2 RuP 1 21/c 111.5545; 17.3432; 25.028
90; 95.757; 90		4990.1Wang, Hai-Xu; Wan, Qingyun; Low, Kam-Hung; Zhou, Cong-Ying; Huang, Jie-Sheng; Zhang, Jun-Long; Che, Chi-Ming
Stable group 8 metal porphyrin mono- and bis(dialkylcarbene) complexes: synthesis, characterization, and catalytic activity.
Chemical science, 2020, 11, 2243-2259
1556870 CIFC64 H52 F4 N4 OsP -111.0536; 11.1353; 11.8926
97.46; 108.927; 107.647		1276.53Wang, Hai-Xu; Wan, Qingyun; Low, Kam-Hung; Zhou, Cong-Ying; Huang, Jie-Sheng; Zhang, Jun-Long; Che, Chi-Ming
Stable group 8 metal porphyrin mono- and bis(dialkylcarbene) complexes: synthesis, characterization, and catalytic activity.
Chemical science, 2020, 11, 2243-2259
1556871 CIFC59 H27 F20 Fe N5P 110.5317; 14.347; 17.434
76.71; 80.147; 84.826		2522.3Wang, Hai-Xu; Wan, Qingyun; Low, Kam-Hung; Zhou, Cong-Ying; Huang, Jie-Sheng; Zhang, Jun-Long; Che, Chi-Ming
Stable group 8 metal porphyrin mono- and bis(dialkylcarbene) complexes: synthesis, characterization, and catalytic activity.
Chemical science, 2020, 11, 2243-2259
1556872 CIFC59 H50 Cl3 D Fe N4P -111.3588; 13.5043; 16.5422
85.786; 84.24; 70.986		2384.6Wang, Hai-Xu; Wan, Qingyun; Low, Kam-Hung; Zhou, Cong-Ying; Huang, Jie-Sheng; Zhang, Jun-Long; Che, Chi-Ming
Stable group 8 metal porphyrin mono- and bis(dialkylcarbene) complexes: synthesis, characterization, and catalytic activity.
Chemical science, 2020, 11, 2243-2259
1556873 CIFC65.5 H39.5 F20 N8 RuC 1 2/c 124.815; 20.891; 24.043
90; 100.174; 90		12268Wang, Hai-Xu; Wan, Qingyun; Low, Kam-Hung; Zhou, Cong-Ying; Huang, Jie-Sheng; Zhang, Jun-Long; Che, Chi-Ming
Stable group 8 metal porphyrin mono- and bis(dialkylcarbene) complexes: synthesis, characterization, and catalytic activity.
Chemical science, 2020, 11, 2243-2259
1556874 CIFC48 H54 Cu F12 N6 O2 P2P 1 21/n 121.313; 9.951; 24.687
90; 107.778; 90		4986Ryan, Michael C.; Kim, Yeon Jung; Gerken, James B.; Wang, Fei; Aristov, Michael M.; Martinelli, Joseph R.; Stahl, Shannon S.
Mechanistic insights into copper-catalyzed aerobic oxidative coupling of N‒N bonds
Chemical Science, 2020, 11, 1170-1175
1556875 CIFC311.2 H387.9 B90.2 F18 Fe4 N55.5 O36 S6C 1 c 133.357; 32.3478; 45.8124
90; 102.32; 90		48294.4Lu, Zhenpin; Ronson, Tanya K.; Nitschke, Jonathan R.
Reversible reduction drives anion ejection and C60 binding within an FeII4L6 cage
Chemical Science, 2020, 11, 1097-1101
1556876 CIFC26 H42 N2 S8 Sn2P -17.7711; 10.3961; 12.6341
113.062; 96.284; 98.114		914.39Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S.
Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds
Chemical Science, 2020, 11, 1066-1078
1556877 CIFC120 H88 B2 F48 Fe2 O2 S8 Sn2P 1 21/c 112.734; 31.568; 18.543
90; 107.358; 90		7115Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S.
Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds
Chemical Science, 2020, 11, 1066-1078
1556878 CIFC57 H53.5 B F24 N0.5 O0.5 S8 Sn2P 1 21/c 19.5804; 23.505; 30.294
90; 97.92; 90		6756.8Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S.
Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds
Chemical Science, 2020, 11, 1066-1078
1556879 CIFC122 H72 B2 F48 Ni2 P4 S8C 1 2/c 140.752; 18.985; 17.7197
90; 107.903; 90		13045.5Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S.
Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds
Chemical Science, 2020, 11, 1066-1078
1556880 CIFC90 H60 B F24 Ni2 P4 S8P -114.1624; 18.3974; 20.189
94.073; 103.397; 106.515		4852.9Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S.
Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds
Chemical Science, 2020, 11, 1066-1078
1556881 CIFC102 H92 B2 F48 O4 S8 Sn2P -112.9111; 15.863; 16.368
88.537; 88.979; 69.195		3132.6Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S.
Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds
Chemical Science, 2020, 11, 1066-1078
1556882 CIFC106 H68 B F24 Fe2 P4 Pd2 S8P -113.503; 19.054; 28.239
105.082; 91.975; 90.73		7009Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S.
Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds
Chemical Science, 2020, 11, 1066-1078
1556883 CIFC540 H360 B6 F144 P24 Pd12 S48P -129.421; 31.324; 35.123
92.011; 91.984; 99.304		31897Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S.
Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds
Chemical Science, 2020, 11, 1066-1078
1556884 CIFC40 H36 F6 N3 O3 PP 1 21 18.20579; 29.4208; 16.5731
90; 93.223; 90		3994.76Duwald, Romain; Bosson, Johann; Pascal, Simon; Grass, Stéphane; Zinna, Francesco; Besnard, Céline; Di Bari, Lorenzo; Jacquemin, Denis; Lacour, Jérôme
Merging polyacenes and cationic helicenes: from weak to intense chiroptical properties in the far red region
Chemical Science, 2020, 11, 1165-1169
1556885 CIFC61 H46 F6 N5 O2 PC 1 2/c 127.6234; 16.7146; 21.7661
90; 106.545; 90		9633.6Duwald, Romain; Bosson, Johann; Pascal, Simon; Grass, Stéphane; Zinna, Francesco; Besnard, Céline; Di Bari, Lorenzo; Jacquemin, Denis; Lacour, Jérôme
Merging polyacenes and cationic helicenes: from weak to intense chiroptical properties in the far red region
Chemical Science, 2020, 11, 1165-1169
1556886 CIFC95 H78 Cl6 F12 N6 O2 P2P 1 21/c 111.678; 12.9347; 27.785
90; 90.912; 90		4196.4Duwald, Romain; Bosson, Johann; Pascal, Simon; Grass, Stéphane; Zinna, Francesco; Besnard, Céline; Di Bari, Lorenzo; Jacquemin, Denis; Lacour, Jérôme
Merging polyacenes and cationic helicenes: from weak to intense chiroptical properties in the far red region
Chemical Science, 2020, 11, 1165-1169
1556900 CIFC62 H79 Cl2 N5 O6 Pt SI 1 2/a 126.7934; 12.4321; 39.1414
90; 106.494; 90		12501.4Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M.
Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour
Chemical Science, 2020, 11, 1839-1847
1556901 CIFC67 H79 B2 F8 N7 O6 PtP -110.1982; 18.2063; 19.7708
105.665; 99.693; 96.105		3439.2Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M.
Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour
Chemical Science, 2020, 11, 1839-1847
1556902 CIFC65 H76 F6 N6 O6 Pt SbP -111.78747; 15.5279; 22.4447
101.252; 102.144; 103.723		3769.49Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M.
Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour
Chemical Science, 2020, 11, 1839-1847
1556903 CIFC66 H77 B F4 N8 O5 PtP 1 21/n 121.738; 14.9289; 21.8888
90; 107.531; 90		6773.5Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M.
Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour
Chemical Science, 2020, 11, 1839-1847
1556904 CIFC69 H85 Ag F12 N6 O6 Pt Sb2P 1 21/n 118.7462; 15.4022; 27.6759
90; 104.791; 90		7726.1Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M.
Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour
Chemical Science, 2020, 11, 1839-1847
1556905 CIFC60 H72 B F4 N5 O5 PtP -112.2375; 14.6363; 18.2789
81.118; 76.017; 74.098		3041.7Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M.
Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour
Chemical Science, 2020, 11, 1839-1847
1556906 CIFC67 H77 Ag F15 N7 O5 Pt Sb2.5P -113.0371; 18.3984; 18.4639
88.81; 89.789; 83.438		4398.8Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M.
Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour
Chemical Science, 2020, 11, 1839-1847
1556907 CIFC23 H24 N2 O5 SP 21 21 230.4605; 11.6596; 6.1159
90; 90; 90		2172.11Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556908 CIFC20 H23 N3 O3P 21 21 217.191; 13.5045; 18.6644
90; 90; 90		1812.52Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556909 CIFC20 H25 N3 O2P 1 21/n 16.8118; 17.5495; 15.1113
90; 91.427; 90		1805.9Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556910 CIFC22 H21.25 N3 O2.125P 1 21 110.18405; 9.71457; 18.82762
90; 93.0169; 90		1860.1Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556911 CIFC24 H21 F3 N2 O4 SP 21 21 2132.8358; 11.60538; 5.85758
90; 90; 90		2232.16Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556912 CIFC22 H25 N3 O2P 1 21 112.4713; 9.02632; 17.84198
90; 92.8702; 90		2005.95Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556913 CIFC20 H19 N3 OP 1 21 110.10659; 5.94958; 13.62038
90; 99.5974; 90		807.53Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556914 CIFC28 H30 N2 O2P 21 21 218.33247; 15.71709; 17.93381
90; 90; 90		2348.65Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556915 CIFC24 H24 N2 O4 SP 21 21 216.0985; 11.5023; 30.8387
90; 90; 90		2163.2Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556992 CIFC18 H16 O4P b c n9.7263; 11.8883; 24.935
90; 90; 90		2883.2Liang, Kangjiang; Li, Tao; Li, Na; Zhang, Yang; Shen, Lei; Ma, Zhixian; Xia, Chengfeng
Redox-neutral photochemical Heck-type arylation of vinylphenols activated by visible light
Chemical Science, 2020, 11, 2130-2135
1556993 CIFC26 H24 N2 O2 SP -110.6565; 11.1408; 12.3
69.374; 76.912; 65.303		1236.26Lee, Jiyoun; Ko, Donguk; Park, Hyunju; Yoo, Eun Jeong
Direct cyclopropanation of activated N-heteroarenes <i>via</i> site- and stereoselective dearomative reactions.
Chemical science, 2020, 11, 1672-1676
1556994 CIFC28 H26 N2P 21 21 219.072; 9.846; 23.918
90; 90; 90		2136.4Lee, Jiyoun; Ko, Donguk; Park, Hyunju; Yoo, Eun Jeong
Direct cyclopropanation of activated N-heteroarenes <i>via</i> site- and stereoselective dearomative reactions.
Chemical science, 2020, 11, 1672-1676
1556995 CIFC54 H31.2 F0.8 O8 Zn2C 1 2/c 137.1066; 31.0733; 11.8903
90; 99.208; 90		13533.1Lustig, William P.; Shen, Zeqing; Teat, Simon J.; Javed, Nasir; Velasco, Ever; O'Carroll, Deirdre M.; Li, Jing
Rational design of a high-efficiency, multivariate metal‒organic framework phosphor for white LED bulbs
Chemical Science, 2020, 11, 1814-1824
1557024 CIFC38 H34 S4C 1 2/c 141.708; 5.7563; 12.67
90; 98.46; 90		3008.8Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko
Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents
Chemical Science, 2020, 11, 1825-1831
1557025 CIFC42 H42 S4P 1 21/c 123.82; 5.837; 12.5
90; 104.133; 90		1685Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko
Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents
Chemical Science, 2020, 11, 1825-1831
1557026 CIFC42 H42 S4P 1 21/c 122.15; 5.7413; 13.1188
90; 95.85; 90		1659.6Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko
Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents
Chemical Science, 2020, 11, 1825-1831
1557027 CIFC66 H30 Al3 Ba F89 O9P 1 c 128.173; 16.4313; 20.453
90; 90.107; 90		9468.1Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557028 CIFC52 H26 Al2 Ca F68 O7P 1 21 117.765; 20.654; 20.031
90; 93.018; 90		7340Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557029 CIFC36 H18 Al2 F55 In O6P -110.6319; 22.3961; 24.4869
79.144; 79.696; 77.759		5537.2Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557030 CIFC50 H22 Al2 F74 Mg N6 O8P 114.3953; 18.2606; 25.8315
73.784; 74.37; 66.821		5895.1Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557031 CIFC84 H34 Al4 F118 O12 SrP -113.8661; 20.2883; 23.0336
80.031; 85.985; 79.942		6278.6Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557032 CIFC84 H34 Al4 Ca F118 O12P -113.9542; 20.3286; 22.9128
80.085; 84.743; 80.239		6296.8Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557033 CIFC60 H26 Al3 Ca F87 O9P 1 21/c 123.429; 18.9075; 22.4874
90; 118.27; 90		8773.4Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557034 CIFC66 H30 Al3 F89 O9 SrP -113.5412; 25.3825; 27.3385
90.017; 90.111; 92.474		9387.7Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557045 CIFC17 H14 Cl N O2P 21 21 215.3182; 10.94; 23.9705
90; 90; 90		1394.63Burg, Finn; Breitenlechner, Stefan; Jandl, Christian; Bach, Thorsten
Enantioselective oxygenation of exocyclic methylene groups by a manganese porphyrin catalyst with a chiral recognition site
Chemical Science, 2020, 11, 2121-2129
1557052 CIFC22 H28 NP -15.899; 7.547; 20.535
83.465; 84.681; 82.512		897.7Mongin, Cédric; Ardoy, Alejandro Mendez; Méreau, Raphaël; Bassani, Dario M.; Bibal, Brigitte
Singlet oxygen stimulus for switchable functional organic cages
Chemical Science, 2020, 11, 1478-1484
1557053 CIFC28 H18 O2P 1 21/c 113.0175; 9.329; 8.3512
90; 106.37; 90		973.06Mongin, Cédric; Ardoy, Alejandro Mendez; Méreau, Raphaël; Bassani, Dario M.; Bibal, Brigitte
Singlet oxygen stimulus for switchable functional organic cages
Chemical Science, 2020, 11, 1478-1484
1557060 CIFC18 H19 N S SiP -18.52831; 10.39109; 11.21545
117.584; 92.3119; 95.1854		873.5Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557061 CIFC17 H13 N O SC 1 2/c 120.6204; 9.4103; 16.7239
90; 120.205; 90		2804.6Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557062 CIFC18 H15 N O SP b c a13.1964; 13.3812; 16.7048
90; 90; 90		2949.79Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557063 CIFC11 H9 N O SP 1 21/c 110.9143; 7.26579; 12.4737
90; 104.425; 90		957.99Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557064 CIFC16 H21 N S Se SiP 1 21/c 110.6588; 8.0663; 20.1272
90; 95.886; 90		1721.35Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557065 CIFC22 H23 N SP 1 21/c 113.9373; 7.7203; 17.0136
90; 105.984; 90		1759.89Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557066 CIFC21 H20 SP 1 21/n 17.5133; 25.6215; 8.2645
90; 100.591; 90		1563.83Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557067 CIFC10 H7 N SP -16.9027; 7.3743; 9.3503
68.861; 73.292; 84.246		425.18Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557068 CIFC16 H11 N O SP b c a12.2557; 9.5626; 21.5616
90; 90; 90		2526.94Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557069 CIFC17 H17 N SP 1 21/c 111.1885; 11.263; 12.1884
90; 116.756; 90		1371.48Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557075 CIFC55 H67 N3 O6 P2 RuP 1 21/n 117.5623; 13.934; 20.8795
90; 92.113; 90		5106Artús Suàrez, Lluís; Jayarathne, Upul; Balcells, David; Bernskoetter, Wesley H.; Hazari, Nilay; Jaraiz, Martín; Nova, Ainara
Rational selection of co-catalysts for the deaminative hydrogenation of amides.
Chemical science, 2020, 11, 2225-2230
1557079 CIFC25 H23 N O3P 1 21 112.77764; 5.95718; 12.86001
90; 100.546; 90		962.352Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones
Chemical Science, 2020, 11, 2401-2406
1557080 CIFC23 H29 N O2P 21 21 2110.3193; 10.5258; 18.2046
90; 90; 90		1977.36Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones
Chemical Science, 2020, 11, 2401-2406
1557081 CIFC25 H25 N O3 SP 21 21 215.909; 12.8175; 27.4929
90; 90; 90		2082.27Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones
Chemical Science, 2020, 11, 2401-2406
1557082 CIFC24 H18 O3C 1 2/c 121.613; 12.1859; 13.5922
90; 104.043; 90		3472.8He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557083 CIFC26 H24 O6P 1 21/c 114.145; 7.441; 24.56
90; 96.17; 90		2570He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557084 CIFC22 H15 Cl O3P 1 21/n 116.2589; 6.7715; 16.4568
90; 106.511; 90		1737.14He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557085 CIFC25 H24 O7P 1 21/n 112.5579; 5.2167; 35.021
90; 94.917; 90		2285.8He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557086 CIFC25 H28 O8C 1 2/c 129.9022; 11.0935; 13.4816
90; 99.73; 90		4407.8He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557087 CIFC39 H34 F6 N3 O PP 1 21/c 19.3923; 29.4208; 11.9664
90; 102.511; 90		3228.14Zheng, Zheng; Liu, Haixiang; Zhai, Shaodong; Zhang, Haoke; Shan, Guogang; Kwok, Ryan T. K.; Ma, Chao; Sung, Herman H. Y.; Williams, Ian D.; Lam, Jacky W. Y.; Wong, Kam Sing; Hu, Xianglong; Tang, Ben Zhong
Highly efficient singlet oxygen generation, two-photon photodynamic therapy and melanoma ablation by rationally designed mitochondria-specific near-infrared AIEgens
Chemical Science, 2020, 11, 2494-2503
1557088 CIFC27 H22 N2 OP 1 21/n 19.53897; 23.141; 9.5721
90; 107.33; 90		2017.04Zheng, Zheng; Liu, Haixiang; Zhai, Shaodong; Zhang, Haoke; Shan, Guogang; Kwok, Ryan T. K.; Ma, Chao; Sung, Herman H. Y.; Williams, Ian D.; Lam, Jacky W. Y.; Wong, Kam Sing; Hu, Xianglong; Tang, Ben Zhong
Highly efficient singlet oxygen generation, two-photon photodynamic therapy and melanoma ablation by rationally designed mitochondria-specific near-infrared AIEgens
Chemical Science, 2020, 11, 2494-2503
1557089 CIFC78 H190 Dy2 K2 N6 O21 Si12C 1 2/c 125.4899; 18.8304; 25.7453
90; 103.128; 90		12034.4Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557090 CIFC42 H102 Dy K N3 O12 Si6P 1 21/n 111.0616; 27.199; 21.7721
90; 103.885; 90		6359Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557091 CIFC78 H190 K2 N6 O21 Si12 Tm2C 1 2/c 125.453; 18.757; 25.744
90; 103.142; 90		11969Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557092 CIFC42 H102 K N3 O12 Si6 TmP 21 21 2121.956; 22.554; 25.737
90; 90; 90		12745Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557093 CIFC52 H124 Gd2 K2 N4 O16 Si8P -112.6614; 15.5498; 21.205
94.4758; 94.0831; 105.746		3987.4Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557094 CIFC36 H90 Gd K N5 O6 Si6R 3 2 :H18.564; 18.564; 18.05
90; 90; 120		5387Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557095 CIFC42 H102 Er K N3 O12 Si6P 1 21/n 111.064; 27.08; 21.797
90; 103.991; 90		6337Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557096 CIFC42 H102 Ho K N3 O12 Si6P 1 21/n 111.0476; 27.157; 21.797
90; 103.905; 90		6347.9Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557097 CIFC42 H102 Gd K N3 O12 Si6P 1 21/n 111.1493; 27.059; 21.755
90; 104.007; 90		6368.1Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557098 CIFC42 H102 K N3 O12 Si6 TbP 1 21/n 111.1324; 27.081; 21.775
90; 103.924; 90		6371.8Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557099 CIFC78 H190 Gd2 K2 N6 O21 Si12C 1 2/c 125.507; 18.806; 25.726
90; 103.21; 90		12014Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557100 CIFC42 H102 K N3 O12 Si6 YP 1 21/n 111.0774; 27.0905; 21.7959
90; 104; 90		6346.5Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557101 CIFC78 H190 Ho2 K2 N6 O21 Si12C 1 2/c 125.514; 18.8; 25.712
90; 103.167; 90		12009Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557105 CIFC104 H96 B4 F16 N8 O4 Pd2I 1 2/a 128.36; 12.35285; 27.666
90; 94.6541; 90		9660.2Lewis, James E. M.; Tarzia, Andrew; White, Andrew J. P.; Jelfs, Kim E.
Conformational control of Pd2L4 assemblies with unsymmetrical ligands
Chemical Science, 2020, 11, 677-683
1557106 CIFC123 H119 B4 F16 N17 O9 Pd2C 1 2/c 123.2193; 15.8896; 38.7298
90; 112.281; 90		13222.3Lewis, James E. M.; Tarzia, Andrew; White, Andrew J. P.; Jelfs, Kim E.
Conformational control of Pd2L4 assemblies with unsymmetrical ligands
Chemical Science, 2020, 11, 677-683
1557107 CIFC16 H19 I N2P 1 21/c 16.29025; 7.62301; 32.0065
90; 90.1584; 90		1534.73Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang
A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells
Chemical Science, 2020, 11, 661-670
1557108 CIFC64 H87 I3 N5 O2P -114.6729; 15.6807; 16.4518
85.945; 73.88; 62.636		3222.3Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang
A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells
Chemical Science, 2020, 11, 661-670
1557109 CIFC17 H18 I N2P 21 21 216.9063; 7.9318; 30.157
90; 90; 90		1651.98Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang
A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells
Chemical Science, 2020, 11, 661-670
1557110 CIFC73 H92 N5 O2 UP -113.2857; 13.9411; 20.5686
103.573; 95.666; 116.252		3230.4Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557111 CIFC75 H88 N8 UP -113.1219; 13.5561; 20.3099
78.109; 76.264; 68.201		3230.5Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557112 CIFC76 H99 N6 O P UP 1 21/c 125.884; 13.889; 21.315
90; 110.09; 90		7197Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557113 CIFC75 H96 N6 UP 1 21/n 114.7113; 12.979; 36.748
90; 94.521; 90		6994.8Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557114 CIFC82 H101 N7 O UP -113.1812; 15.8571; 19.6743
110.71; 90.48; 105.002		3692.6Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557115 CIFC33 H26 O2P 21 21 2111.3659; 11.9259; 17.9314
90; 90; 90		2430.58Liu, Xihong; Zhang, Jingying; Bai, Lutao; Wang, Linqing; Yang, Dongxu; Wang, Rui
Catalytic asymmetric multiple dearomatizations of phenols enabled by a cascade 1,8-addition and Diels‒Alder reaction
Chemical Science, 2020, 11, 671-676
1557116 CIFC64 H88P -114.635; 18.1373; 22.0161
79.631; 75.201; 74.12		5396.2Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557117 CIFC61 H39 B F24 N7 RhP -112.9083; 14.2464; 20.148
74.898; 79.351; 89.459		3512.7Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557118 CIFC67 H62 B F24 N5 RhP -111.7452; 16.7896; 18.5777
84.062; 73.668; 70.038		3304.3Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557119 CIFC32 H16 F8P -110.7497; 11.175; 11.5688
96.962; 96.945; 116.711		1207.93Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557120 CIFC60 H51 B Cl2 F24 N5 RhC 1 c 119.4406; 17.1714; 19.516
90; 103.079; 90		6345.86Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557121 CIFC54 H37 B F24 N5 RhC 1 2/c 116.95902; 18.45666; 34.7576
90; 98.7133; 90		10753.8Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557122 CIFC68 H45 B F25 N5 O RhP -113.01044; 20.05043; 26.99316
90.7652; 97.9088; 106.636		6672.31Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557123 CIFC21 H20 O6P 21 21 218.6977; 9.9164; 20.6241
90; 90; 90		1778.83Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557124 CIFC37 H32 Br2 O9P 1 21/c 115.4799; 12.7561; 17.7032
90; 110.471; 90		3275Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557125 CIFC20 H20 O6P 1 21/c 111.1979; 12.5205; 24.904
90; 93.401; 90		3485.5Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557126 CIFC18 H16 O5P 1 21 111.2987; 10.6941; 11.9582
90; 90.723; 90		1444.79Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557127 CIFC18 H18 O7P 1 21/n 113.6526; 9.772; 24.8831
90; 101.015; 90		3258.6Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557128 CIFC27 H29 N O8P 1 21 110.1038; 12.0566; 10.4153
90; 97.827; 90		1256.95Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557129 CIFC17 H20 O6P 1 21 17.091; 16.2621; 13.2704
90; 92.494; 90		1528.82Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557130 CIFC27 H29 N O8C 1 2 126.9187; 7.6682; 12.9814
90; 108.271; 90		2544.5Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557131 CIFC6 H5 D N2P b c a6.0431; 13.3857; 14.3592
90; 90; 90		1161.53Yang, Huan; Zhang, Li; Zhou, Fei-Yu; Jiao, Lei
An umpolung approach to the hydroboration of pyridines: a novel and efficient synthesis of N-H 1,4-dihydropyridines
Chemical Science, 2020, 11, 742-747
1557132 CIFIn8 Ir1.5 S5.25P 3 1 m13.9378; 13.9378; 8.2316
90; 90; 120		1384.9Khoury, Jason F.; He, Jiangang; Pfluger, Jonathan E.; Hadar, Ido; Balasubramanian, Mahalingam; Stoumpos, Constantinos C.; Zu, Rui; Gopalan, Venkatraman; Wolverton, Chris; Kanatzidis, Mercouri G.
Ir6In32S21, a polar, metal-rich semiconducting subchalcogenide
Chemical Science, 2020, 11, 870-878
1557142 CIFC18 H20 Cl N3 O PdP -17.5074; 11.2005; 11.2581
70.42; 78.131; 84.462		872.46Czyz, Milena L.; Weragoda, Geethika K.; Horngren, Tyra H.; Connell, Timothy U.; Gomez, Daniel; O'Hair, Richard A. J.; Polyzos, Anastasios
Photoexcited Pd(ii) auxiliaries enable light-induced control in C(sp3)‒H bond functionalisation
Chemical Science, 2020, 11, 2455-2463
1557165 CIFC100 H102 Au4 P2 Ru2 S8P 1 21/c 113.9904; 14.295; 48.384
90; 94.664; 90		9644.4Sun, Yongnan; Pei, Wei; Xie, Mingcai; Xu, Shun; Zhou, Si; Zhao, Jijun; Xiao, Kang; Zhu, Yan
Excitonic Au4Ru2(PPh3)2(SC2H4Ph)8 cluster for light-driven dinitrogen fixation
Chemical Science, 2020, 11, 2440-2447
1557189 CIFC22 H12 F6 N2 O3P 1 21/n 110.7749; 15.2475; 12.314
90; 108.515; 90		1918.4Malla, Javid Ahmad; Umesh, Rintu M.; Vijay, Amal; Mukherjee, Arnab; Lahiri, Mayurika; Talukdar, Pinaki
Apoptosis-inducing activity of a fluorescent barrel-rosette M+/Cl− channel
Chemical Science, 2020, 11, 2420-2428
1557197 CIFC58 H62 N6 O13 Zn2P 1 21/c 115.21; 16.731; 23.716
90; 104.529; 90		5842Fu, Guorui; He, Yani; Li, Wentao; Miao, Tiezheng; Lü, Xingqiang; He, Hongshan; Liu, Li; Wong, Wai-Yeung
Efficient white polymer light-emitting diodes (WPLEDs) based on covalent-grafting of [Zn2(MP)3(OAc)] into PVK
Chemical Science, 2020, 11, 2640-2646
1557206 CIFC20 H30 N2 O2P 1 21/c 111.012; 16.138; 11.225
90; 96.899; 90		1980Chen, Hang; Ye, Hebo; Hai, Yu; Zhang, Ling; You, Lei
n →π* interactions as a versatile tool for controlling dynamic imine chemistry in both organic and aqueous media
Chemical Science, 2020, 11, 2707-2715
1557207 CIFC19 H29 N3 O2I 1 2/a 117.03; 10.58; 22.26
90; 103.23; 90		3904Chen, Hang; Ye, Hebo; Hai, Yu; Zhang, Ling; You, Lei
n →π* interactions as a versatile tool for controlling dynamic imine chemistry in both organic and aqueous media
Chemical Science, 2020, 11, 2707-2715
1557228 CIFC101 H48 F40 N12 Ni O7P n a 2127.571; 19.7599; 19.1951
90; 90; 90		10457.5Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion
Chemical Science, 2020, 11, 2790-2795
1557229 CIFC89.5 H19 Cl Cu F40 N8 Ni O3C 1 2/c 147.886; 13.8742; 28.061
90; 119.602; 90		16210Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion
Chemical Science, 2020, 11, 2790-2795
1557230 CIFC89 H22 F40 N8 O3P -111.6188; 14.403; 26.7956
82.937; 77.65; 70.954		4133.7Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion
Chemical Science, 2020, 11, 2790-2795
1557231 CIFC97 H32 F40 N12 Ni O3P -114.057; 14.08; 24.646
92.257; 101.581; 108.23		4511.4Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion
Chemical Science, 2020, 11, 2790-2795
1557232 CIFC89 H18 Cu F40 N8 Ni O3P -114.0363; 14.1385; 24.8547
91.904; 101.174; 107.743		4586.3Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion
Chemical Science, 2020, 11, 2790-2795
1557234 CIFC61 H90 Au2 Cl2 F12 N2 P2 Sb2P 1 21/n 110.4398; 18.5854; 16.9617
90; 94.354; 90		3281.5Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557235 CIFC34 H50 Au Cl2 F6 N O P SbP 1 21/c 110.9121; 17.7644; 19.509
90; 104.904; 90		3654.5Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557236 CIFC33 H48 Au Cl2 F6 N O2 P SbP 1 21 114.8546; 12.2517; 20.5946
90; 99.848; 90		3692.9Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557237 CIFC21 H20 N4 O5P 1 21/c 115.4212; 13.4652; 9.4134
90; 102.515; 90		1908.2Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557238 CIFC29 H36 Au B10 Cl2 F6 P2 SbP 1 n 110.0221; 13.3021; 14.7578
90; 95.633; 90		1957.94Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557239 CIFC38 H47 Au F6 N2 O2 P SbP 1 21/c 110.7728; 11.143; 30.591
90; 98.974; 90		3627.2Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557253 CIFC54 H99 Am Br3 O3 P3P c a 2128.768; 11.456; 18.185
90; 90; 90		5993Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E.
Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes
Chemical Science, 2020, 11, 2770-2782
1557254 CIFC54 H99 Br3 Nd O3 P3P c a 2128.7058; 11.4228; 18.1359
90; 90; 90		5946.8Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E.
Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes
Chemical Science, 2020, 11, 2770-2782
1557255 CIFC54 H99 Br3 Ce O3 P3P c a 2128.92; 11.434; 18.209
90; 90; 90		6021.2Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E.
Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes
Chemical Science, 2020, 11, 2770-2782
1557256 CIFC54 H99 Br3 La O3 P3P c a 2128.879; 11.4223; 18.2083
90; 90; 90		6006.3Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E.
Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes
Chemical Science, 2020, 11, 2770-2782
1557257 CIFC54 H99 Br3 O3 P3 PrP c a 2128.7155; 11.4126; 18.1299
90; 90; 90		5941.5Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E.
Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes
Chemical Science, 2020, 11, 2770-2782
1557262 CIFC21 H21 F O2P 1 21 16.512; 15.336; 8.7541
90; 111.502; 90		813.41Groves, Alistair; Sun, Jinwei; Parke, Hal R. I.; Callingham, Michael; Argent, Stephen P.; Taylor, Laurence J.; Lam, Hon Wai
Catalytic enantioselective arylative cyclizations of alkynyl 1,3-diketones by 1,4-rhodium(i) migration
Chemical Science, 2020, 11, 2759-2764
1557263 CIFC22 H22 O2P 21 21 219.5439; 10.5734; 17.3218
90; 90; 90		1747.97Groves, Alistair; Sun, Jinwei; Parke, Hal R. I.; Callingham, Michael; Argent, Stephen P.; Taylor, Laurence J.; Lam, Hon Wai
Catalytic enantioselective arylative cyclizations of alkynyl 1,3-diketones by 1,4-rhodium(i) migration
Chemical Science, 2020, 11, 2759-2764
1557283 CIFC25 H30 N4 O3P -16.6601; 7.4588; 23.5097
94.931; 90.774; 105.499		1120.43Shi, Xiujuan; Yan, Neng; Niu, Guangle; Sung, Simon H. P.; Liu, Zhiyang; Liu, Junkai; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wang, Wen-Xiong; Sung, Herman H.-Y.; Williams, Ian D.; Tang, Ben Zhong
In vivo monitoring of tissue regeneration using a ratiometric lysosomal AIE probe
Chemical Science, 2020, 11, 3152-3163
1557284 CIFC60 H44 Mn4 N12 O52 Si W12C 1 2/c 124.8686; 23.1581; 17.7369
90; 98.907; 90		10091.7Du, Jing; Lang, Zhong-Ling; Ma, Yuan-Yuan; Tan, Hua-Qiao; Liu, Bai-Ling; Wang, Yong-Hui; Kang, Zhen-Hui; Li, Yang-Guang
Polyoxometalate-based electron transfer modulation for efficient electrocatalytic carbon dioxide reduction
Chemical Science, 2020, 11, 3007-3015
1557285 CIFC49 H39 Mn3 Mo12 N11 O49 PP -113.034; 15.6737; 20.2719
79.875; 88.908; 87.011		4071.1Du, Jing; Lang, Zhong-Ling; Ma, Yuan-Yuan; Tan, Hua-Qiao; Liu, Bai-Ling; Wang, Yong-Hui; Kang, Zhen-Hui; Li, Yang-Guang
Polyoxometalate-based electron transfer modulation for efficient electrocatalytic carbon dioxide reduction
Chemical Science, 2020, 11, 3007-3015
1557286 CIFC49 H39 Mn3 N11 O49 P W12P -113.0328; 15.6142; 20.1424
79.88; 89.029; 86.775		4028.6Du, Jing; Lang, Zhong-Ling; Ma, Yuan-Yuan; Tan, Hua-Qiao; Liu, Bai-Ling; Wang, Yong-Hui; Kang, Zhen-Hui; Li, Yang-Guang
Polyoxometalate-based electron transfer modulation for efficient electrocatalytic carbon dioxide reduction
Chemical Science, 2020, 11, 3007-3015
1557287 CIFC25 H22 N2 O3P 1 21 19.0919; 9.9836; 11.7719
90; 95.822; 90		1063.02Zhang, Xiang; Li, Xiang; Li, Jun-Long; Wang, Qi-Wei; Zou, Wen-Lin; Liu, Yan-Qing; Jia, Zhi-Qiang; Peng, Fu; Han, Bo
Regiodivergent construction of medium-sized heterocycles from vinylethylene carbonates and allylidenemalononitriles
Chemical Science, 2020, 11, 2888-2894
1557288 CIFC25 H22 N2 O3P 1 21/n 19.6576; 13.2796; 17.3578
90; 99.745; 90		2194Zhang, Xiang; Li, Xiang; Li, Jun-Long; Wang, Qi-Wei; Zou, Wen-Lin; Liu, Yan-Qing; Jia, Zhi-Qiang; Peng, Fu; Han, Bo
Regiodivergent construction of medium-sized heterocycles from vinylethylene carbonates and allylidenemalononitriles
Chemical Science, 2020, 11, 2888-2894
1557289 CIFC25 H22 N2 O3P -17.8691; 9.8641; 13.184
87.285; 85.531; 74.852		984.41Zhang, Xiang; Li, Xiang; Li, Jun-Long; Wang, Qi-Wei; Zou, Wen-Lin; Liu, Yan-Qing; Jia, Zhi-Qiang; Peng, Fu; Han, Bo
Regiodivergent construction of medium-sized heterocycles from vinylethylene carbonates and allylidenemalononitriles
Chemical Science, 2020, 11, 2888-2894
1557290 CIFC2 H Cl N4P b c a11.2724; 6.279; 12.5272
90; 90; 90		886.67Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl
3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines
Chemical Science, 2020, 11, 3042-3047
1557291 CIFC8 H6 N4 OP 1 21/c 110.7358; 5.14454; 14.9437
90; 105.056; 90		797.02Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl
3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines
Chemical Science, 2020, 11, 3042-3047
1557292 CIFC10 H7 N5F d d 238.7645; 11.93147; 7.70847
90; 90; 90		3565.3Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl
3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines
Chemical Science, 2020, 11, 3042-3047
1557293 CIFC9 H9 N7 O2 S2C 1 2/c 117.7417; 6.22991; 23.2377
90; 93.9389; 90		2562.38Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl
3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines
Chemical Science, 2020, 11, 3042-3047
1557294 CIFC2 H Br N4P b c a12.7468; 5.60166; 12.9507
90; 90; 90		924.72Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl
3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines
Chemical Science, 2020, 11, 3042-3047
1557295 CIFC17 H21 N5 O5C 1 2 132.663; 5.161; 11.0162
90; 94.704; 90		1850.79Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl
3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines
Chemical Science, 2020, 11, 3042-3047
1557296 CIFC22 H39 Al Ge Si2P 1 21/n 19.6414; 13.3432; 19.6279
90; 95.4683; 90		2513.6Albers, Lena; Tholen, Patrik; Schmidtmann, Marc; Müller, Thomas
A germaaluminocene
Chemical Science, 2020, 11, 2982-2986
1557298 CIFC6 H12 O6P 21 21 217.7012; 7.7746; 12.6751
90; 90; 90		758.91Zhou, Qing; Yang, Tianjia; Zhong, Zihao; Kausar, Fahmeeda; Wang, Ziyi; Zhang, Yongming; Yuan, Wang Zhang
A clustering-triggered emission strategy for tunable multicolor persistent phosphorescence
Chemical Science, 2020, 11, 2926-2933
1557299 CIFC5 H12 O4I -46.0826; 6.0826; 8.792
90; 90; 90		325.29Zhou, Qing; Yang, Tianjia; Zhong, Zihao; Kausar, Fahmeeda; Wang, Ziyi; Zhang, Yongming; Yuan, Wang Zhang
A clustering-triggered emission strategy for tunable multicolor persistent phosphorescence
Chemical Science, 2020, 11, 2926-2933
1557300 CIFC5 H10 O5P 21 21 215.6107; 9.1858; 12.5998
90; 90; 90		649.38Zhou, Qing; Yang, Tianjia; Zhong, Zihao; Kausar, Fahmeeda; Wang, Ziyi; Zhang, Yongming; Yuan, Wang Zhang
A clustering-triggered emission strategy for tunable multicolor persistent phosphorescence
Chemical Science, 2020, 11, 2926-2933
1557301 CIFC6 H12 O6P 21 21 218.091; 9.212; 10.056
90; 90; 90		749.5Zhou, Qing; Yang, Tianjia; Zhong, Zihao; Kausar, Fahmeeda; Wang, Ziyi; Zhang, Yongming; Yuan, Wang Zhang
A clustering-triggered emission strategy for tunable multicolor persistent phosphorescence
Chemical Science, 2020, 11, 2926-2933
1557331 CIFC203.82 H244.63 Cl7.63 N0 O40P -111.5721; 16.6408; 26.1539
84.725; 81.758; 89.936		4962.9Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P.
Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes.
Chemical science, 2020, 11, 2614-2620
1557332 CIFC112.95 H130.95 Cl15.56 O28P 114.334; 15.534; 16.891
69.752; 70.947; 76.995		3308.6Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P.
Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes.
Chemical science, 2020, 11, 2614-2620
1557333 CIFC106 H124 Cl6 O20P 1 21/n 119.6983; 20.2034; 26.3162
90; 97.77; 90		10377Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P.
Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes.
Chemical science, 2020, 11, 2614-2620
1557334 CIFC108.36 H122.64 Cl2.26 O20P 1 21/c 121.532; 19.643; 25.299
90; 90.699; 90		10699Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P.
Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes.
Chemical science, 2020, 11, 2614-2620
1557335 CIFC116.82 H140.82 Cl8.45 O28P -114.4911; 17.0462; 27.359
72.867; 86.978; 77.872		6313.8Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P.
Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes.
Chemical science, 2020, 11, 2614-2620
1557336 CIFC76 H74 O11P -113.0381; 16.6752; 17.4483
61.711; 79.037; 74.295		3207.14Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P.
Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes.
Chemical science, 2020, 11, 2614-2620
1557337 CIFC226.36 H257.54 O43.98P 1 21/c 121.154; 19.669; 25.429
90; 90.27; 90		10580Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P.
Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes.
Chemical science, 2020, 11, 2614-2620
1557338 CIFC31 H53 B Eu N5 O17P 1 21/n 113.2696; 15.8873; 18.2435
90; 93.3; 90		3839.7Breen, Colum; Pal, Robert; Elsegood, Mark R. J.; Teat, Simon J.; Iza, Felipe; Wende, Kristian; Buckley, Benjamin R.; Butler, Stephen J.
Time-resolved luminescence detection of peroxynitrite using a reactivity-based lanthanide probe
Chemical Science, 2020, 11, 3164-3170
1557341 CIFC15 H21 Cl0 N O2P 21 21 218.5161; 10.575; 15.9557
90; 90; 90		1436.93Lin, Qianchi; Hu, Bowen; Xu, Xi; Dong, Shunxi; Liu, Xiaohua; Feng, Xiaoming
Chiral N,N′-dioxide/Mg(OTf)2 complex-catalyzed asymmetric [2,3]-rearrangement of in situ generated ammonium salts
Chemical Science, 2020, 11, 3068-3073
1557360 CIFC8 H14 N2 O4P 1 21/c 15.6483; 9.0345; 9.1851
90; 103.599; 90		455.57Blake, Timothy R.; Ho, Wilson C.; Turlington, Christopher R.; Zang, Xiaoyu; Huttner, Melanie A.; Wender, Paul A.; Waymouth, Robert M.
Synthesis and mechanistic investigations of pH-responsive cationic poly(aminoester)s
Chemical Science, 2020, 11, 2951-2966
1557371 CIFC27 H19 N O3P 17.1378; 9.8466; 14.7942
88.9786; 79.0044; 74.6213		983.56Sasaki, Yui; Kojima, Soya; Hamedpour, Vahid; Kubota, Riku; Takizawa, Shin-ya; Yoshikawa, Isao; Houjou, Hirohiko; Kubo, Yuji; Minami, Tsuyoshi
Accurate chiral pattern recognition for amines from just a single chemosensor
Chemical Science, 2020, 11, 3790-3796
1557372 CIFC20 H12 SP b c n21.4461; 8.4399; 7.3436
90; 90; 90		1329.21Xu, Niansheng; Zheng, Aibin; Wei, Yuefang; Yuan, Yi; Zhang, Jing; Lei, Ming; Wang, Peng
D‒π‒D molecular semiconductors for perovskite solar cells: the superior role of helical versus planar π-linkers
Chemical Science, 2020, 11, 3418-3426
1557373 CIFC48 H36 N2 O4 SP -19.2973; 11.5371; 17.8524
99.629; 101.049; 97.562		1826.25Xu, Niansheng; Zheng, Aibin; Wei, Yuefang; Yuan, Yi; Zhang, Jing; Lei, Ming; Wang, Peng
D‒π‒D molecular semiconductors for perovskite solar cells: the superior role of helical versus planar π-linkers
Chemical Science, 2020, 11, 3418-3426
1557374 CIFC97 H78 Cl2 N4 O8 S2P -110.5796; 13.7266; 14.368
85.956; 83.941; 82.064		2051.7Xu, Niansheng; Zheng, Aibin; Wei, Yuefang; Yuan, Yi; Zhang, Jing; Lei, Ming; Wang, Peng
D‒π‒D molecular semiconductors for perovskite solar cells: the superior role of helical versus planar π-linkers
Chemical Science, 2020, 11, 3418-3426
1557376 CIFC22 H14 Au2 Fe N6P 1 21/c 110.8116; 14.4381; 14.9803
90; 96.596; 90		2322.93Chen, Yan-Cong; Meng, Yan; Dong, Yan-Jie; Song, Xiao-Wei; Huang, Guo-Zhang; Zhang, Chuan-Lei; Ni, Zhao-Ping; Navařík, Jakub; Malina, Ondřej; Zbořil, Radek; Tong, Ming-Liang
Light- and temperature-assisted spin state annealing: accessing the hidden multistability
Chemical Science, 2020, 11, 3281-3289
1557377 CIFC22 H14 Au2 Fe N6P 1 21/c 110.7397; 14.1109; 14.679
90; 95.98; 90		2212.5Chen, Yan-Cong; Meng, Yan; Dong, Yan-Jie; Song, Xiao-Wei; Huang, Guo-Zhang; Zhang, Chuan-Lei; Ni, Zhao-Ping; Navařík, Jakub; Malina, Ondřej; Zbořil, Radek; Tong, Ming-Liang
Light- and temperature-assisted spin state annealing: accessing the hidden multistability
Chemical Science, 2020, 11, 3281-3289
1557378 CIFC22 H14 Au2 Fe N6P 1 21/c 110.7739; 13.9861; 14.5762
90; 95.77; 90		2185.28Chen, Yan-Cong; Meng, Yan; Dong, Yan-Jie; Song, Xiao-Wei; Huang, Guo-Zhang; Zhang, Chuan-Lei; Ni, Zhao-Ping; Navařík, Jakub; Malina, Ondřej; Zbořil, Radek; Tong, Ming-Liang
Light- and temperature-assisted spin state annealing: accessing the hidden multistability
Chemical Science, 2020, 11, 3281-3289
1557379 CIFC22 H14 Au2 Fe N6P -110.7701; 14.1621; 14.7425
90.082; 96.077; 90.471		2235.9Chen, Yan-Cong; Meng, Yan; Dong, Yan-Jie; Song, Xiao-Wei; Huang, Guo-Zhang; Zhang, Chuan-Lei; Ni, Zhao-Ping; Navařík, Jakub; Malina, Ondřej; Zbořil, Radek; Tong, Ming-Liang
Light- and temperature-assisted spin state annealing: accessing the hidden multistability
Chemical Science, 2020, 11, 3281-3289
1557380 CIFC60 H56 B2 F8 N2 O8P 1 n 112.5252; 16.8071; 12.9207
90; 90.786; 90		2719.7Kim, Inwon; Im, Honggu; Lee, Hyeonyeong; Hong, Sungwoo
N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts
Chemical Science, 2020, 11, 3192-3197
1557381 CIFC23 H23 N O2P 1 21/c 19.3351; 20.6304; 9.7275
90; 105.289; 90		1807.1Kim, Inwon; Im, Honggu; Lee, Hyeonyeong; Hong, Sungwoo
N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts
Chemical Science, 2020, 11, 3192-3197
1557382 CIFC33 H28 B F4 N O2P 1 21/n 111.0604; 16.678; 15.1704
90; 100.639; 90		2750.3Kim, Inwon; Im, Honggu; Lee, Hyeonyeong; Hong, Sungwoo
N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts
Chemical Science, 2020, 11, 3192-3197
1557383 CIFC20 H21 N O4P 1 21/c 19.2314; 19.6394; 19.9121
90; 93.605; 90		3602.9Kim, Inwon; Im, Honggu; Lee, Hyeonyeong; Hong, Sungwoo
N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts
Chemical Science, 2020, 11, 3192-3197
1557384 CIFC17 H18 F2 O2 SP 1 21/c 18.497; 13.357; 13.775
90; 85.689; 90		1559Huang, Xin; Zhang, Yage; Liang, Weijian; Zhang, Qifeng; Zhan, Yaling; Kong, Lichun; Peng, Bo
Dearomatization of aryl sulfoxides: a switch between mono- and dual-difluoroalkylation
Chemical Science, 2020, 11, 3048-3053
1557385 CIFC33 H29 Cl F4 O4 S2P -110.2309; 13.2445; 13.5012
66.799; 70.33; 75.627		1569.19Huang, Xin; Zhang, Yage; Liang, Weijian; Zhang, Qifeng; Zhan, Yaling; Kong, Lichun; Peng, Bo
Dearomatization of aryl sulfoxides: a switch between mono- and dual-difluoroalkylation
Chemical Science, 2020, 11, 3048-3053
1557394 CIFC16 H14 O2P 1 21 16.2309; 7.4169; 13.0054
90; 90.1686; 90		601.03Liu, Lei; Lee, Wes; Yuan, Mingbin; Acha, Chris; Geherty, Michael B.; Williams, Brandon; Gutierrez, Osvaldo
Intra- and intermolecular Fe-catalyzed dicarbofunctionalization of vinyl cyclopropanes
Chemical Science, 2020, 11, 3146-3151
1557395 CIFC102 H68 N18 O27 Zn8R -3 :H22.979; 22.979; 15.496
90; 90; 120		7086Chen, Sheng-Chun; Zhang, Fei-Hang; Huang, Kun-Lin; Tian, Feng; Zhang, Zhi-Hui; Zhou, Renxian; Feng, Xue-Jun; Zhou, Xiaoying; He, Ming-Yang; Gu, Jiande; Chen, Qun; Wu, Chuan-De
The crucial roles of guest water in a biocompatible coordination network in the catalytic ring-opening polymerization of cyclic esters: a new mechanistic perspective
Chemical Science, 2020, 11, 3345-3354
1557396 CIFC30 H26 B BrP 1 21/c 116.2062; 8.1904; 17.137
90; 91.218; 90		2274.2Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557397 CIFC36 H36 B BrP -18.4803; 9.1672; 19.9099
80.254; 85.195; 68.593		1419.82Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557398 CIFC22 H26 B Br O2P 1 21/n 16.4265; 15.8695; 20.617
90; 97.511; 90		2084.6Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557399 CIFC62 H78 B2 Br2P -19.4752; 9.8107; 15.1088
93.579; 100.145; 90.47		1379.57Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557400 CIFC22 H26 B Br O2P c a 2120.7096; 6.4384; 15.5735
90; 90; 90		2076.52Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557401 CIFC14 H10 B Br3P 1 21/n 113.2781; 5.936; 18.4485
90; 100.58; 90		1429.37Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557402 CIFC44 H42 B2 Br2 O2P c c n42.071; 29.3977; 6.6541
90; 90; 90		8229.7Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557403 CIFC28 H22 B Br OP 1 21/c 116.0697; 19.1015; 7.184
90; 99.697; 90		2173.7Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557404 CIFC100 H108 B4 Br4P -18.0182; 16.5443; 17.4491
64.933; 86.117; 77.027		2042.2Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557405 CIFC62 H56 B2 Br2P -19.836; 10.894; 14.514
82.02; 73.02; 71.06		1405.2Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557406 CIFC64 H68 B2 Br2P -113.45; 14.624; 15.214
91.36; 92.15; 116.43		2675.1Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557428 CIFC33 H27 N2 O2 PP -110.6898; 11.775; 11.9913
71.708; 65.4407; 89.239		1291.4Zhuang, Zeyan; Dai, Jun; Yu, Maoxing; Li, Jianqing; Shen, Pingchuan; Hu, Rong; Lou, Xiaoding; Zhao, Zujin; Tang, Ben Zhong
Type I photosensitizers based on phosphindole oxide for photodynamic therapy: apoptosis and autophagy induced by endoplasmic reticulum stress
Chemical Science, 2020, 11, 3405-3417
1557429 CIFC33 H27 N2 O2 PP -19.1957; 10.841; 13.3381
100.85; 100.343; 93.057		1279.46Zhuang, Zeyan; Dai, Jun; Yu, Maoxing; Li, Jianqing; Shen, Pingchuan; Hu, Rong; Lou, Xiaoding; Zhao, Zujin; Tang, Ben Zhong
Type I photosensitizers based on phosphindole oxide for photodynamic therapy: apoptosis and autophagy induced by endoplasmic reticulum stress
Chemical Science, 2020, 11, 3405-3417
1557430 CIFC228 H104 B4 Cl4 F96 N12 O2 Pd2C 1 2/c 140.6116; 14.3027; 43.1791
90; 108.163; 90		23831.1Martí-Centelles, Vicente; Spicer, Rebecca L.; Lusby, Paul J.
Non-covalent allosteric regulation of capsule catalysis
Chemical Science, 2020, 11, 3236-3240
1557435 CIFC20 H19 B N2 O5P 1 21/c 19.8085; 8.9262; 21.7277
90; 99.222; 90		1877.73Williams, Alexander F.; White, Andrew J. P.; Spivey, Alan C.; Cordier, Christopher J.
meta-Selective C‒H functionalisation of aryl boronic acids directed by a MIDA-derived boronate ester
Chemical Science, 2020, 11, 3301-3306
1557437 CIFC172 H168 Ca F21 N24 O30 Rh6 S7P 6323.302; 23.302; 21.347
90; 90; 120		10038Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
s-Block metal ions induce structural transformations between figure-eight and double trefoil knots
Chemical Science, 2020, 11, 1226-1232
1557438 CIFC333 H250 F35 K2 N99 O100 Rh12 S7P -122.5096; 25.221; 39.36
72.977; 89.886; 76.76		20747Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
s-Block metal ions induce structural transformations between figure-eight and double trefoil knots
Chemical Science, 2020, 11, 1226-1232
1557439 CIFC170 H185 F24 N24 O34.5 Rh6 S8 SrP 6322.673; 22.673; 20.482
90; 90; 120		9118Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
s-Block metal ions induce structural transformations between figure-eight and double trefoil knots
Chemical Science, 2020, 11, 1226-1232
1557440 CIFC173 H189 F24 N24 O37.5 Rh6 S8 SrP 6322.564; 22.564; 20.375
90; 90; 120		8984Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
s-Block metal ions induce structural transformations between figure-eight and double trefoil knots
Chemical Science, 2020, 11, 1226-1232
1557441 CIFC190 H252 Ba2 F30 N24 O60 Rh6 S14C 1 2/c 172.911; 20.9282; 33.246
90; 106.419; 90		48661Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
s-Block metal ions induce structural transformations between figure-eight and double trefoil knots
Chemical Science, 2020, 11, 1226-1232
1557442 CIFC16 H20 N2 Ni O2P 1 21/n 114.557; 10.2366; 8.2137
90; 141.27; 90		765.8Fisher, Katherine J.; Feuer, Margalit L.; Lant, Hannah M. C.; Mercado, Brandon Q.; Crabtree, Robert H.; Brudvig, Gary W.
Concerted proton-electron transfer oxidation of phenols and hydrocarbons by a high-valent nickel complex.
Chemical science, 2020, 11, 1683-1690
1557443 CIFC20 H28 N2 Ni O6P 1 21/n 18.3939; 14.9329; 8.7611
90; 108.791; 90		1039.63Fisher, Katherine J.; Feuer, Margalit L.; Lant, Hannah M. C.; Mercado, Brandon Q.; Crabtree, Robert H.; Brudvig, Gary W.
Concerted proton-electron transfer oxidation of phenols and hydrocarbons by a high-valent nickel complex.
Chemical science, 2020, 11, 1683-1690
1557444 CIFC31 H35 F6 N5 Ni O2 PI 1 2/a 122.4997; 8.4913; 17.7726
90; 111.646; 90		3156Fisher, Katherine J.; Feuer, Margalit L.; Lant, Hannah M. C.; Mercado, Brandon Q.; Crabtree, Robert H.; Brudvig, Gary W.
Concerted proton-electron transfer oxidation of phenols and hydrocarbons by a high-valent nickel complex.
Chemical science, 2020, 11, 1683-1690
1557445 CIFC14 H8 S2P -15.8903; 7.8065; 11.6922
90.458; 101.223; 93.037		526.52Wang, Chengyuan; Hashizume, Daisuke; Nakano, Masahiro; Ogaki, Takuya; Takenaka, Hiroyuki; Kawabata, Kohsuke; Takimiya, Kazuo
“Disrupt and induce” intermolecular interactions to rationally design organic semiconductor crystals: from herringbone to rubrene-like pitched π-stacking
Chemical Science, 2020, 11, 1573-1580
1557446 CIFC20 H14 S4P 1 21/c 17.45474; 16.2651; 6.76866
90; 90.98; 90		820.59Wang, Chengyuan; Hashizume, Daisuke; Nakano, Masahiro; Ogaki, Takuya; Takenaka, Hiroyuki; Kawabata, Kohsuke; Takimiya, Kazuo
“Disrupt and induce” intermolecular interactions to rationally design organic semiconductor crystals: from herringbone to rubrene-like pitched π-stacking
Chemical Science, 2020, 11, 1573-1580
1557447 CIFC16 H12 S4P 1 21/c 17.6311; 17.4783; 5.2771
90; 91.18; 90		703.7Wang, Chengyuan; Hashizume, Daisuke; Nakano, Masahiro; Ogaki, Takuya; Takenaka, Hiroyuki; Kawabata, Kohsuke; Takimiya, Kazuo
“Disrupt and induce” intermolecular interactions to rationally design organic semiconductor crystals: from herringbone to rubrene-like pitched π-stacking
Chemical Science, 2020, 11, 1573-1580
1557448 CIFC26 H26P 1 21 19.423; 10.032; 11.391
90; 104.61; 90		1042Lei, Guangyue; Zhang, Hanwen; Chen, Bin; Xu, Meichen; Zhang, Guozhu
Copper-catalyzed enantioselective arylalkynylation of alkenes.
Chemical science, 2020, 11, 1623-1628
1557449 CIFC55 H72 Cl F3 N3 O3 P SP -111.0592; 12.9006; 18.7834
98.063; 91.131; 103.315		2578.25Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557450 CIFC59 H80 Cl15 Ga3 N3 PP 1 21/c 119.16275; 13.46701; 28.2924
90; 94.584; 90		7277.92Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557451 CIFC57 H76 N3 PP 1 21/c 118.56527; 11.96597; 22.85445
90; 101.614; 90		4973.19Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557452 CIFC54 H72 Cl8 Ga2 N3 PP b c a24.13916; 18.9021; 26.08922
90; 90; 90		11904Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557453 CIFC54 H72 Cl4 Ga N3 PP 1 21/c 111.5123; 12.8811; 37.2397
90; 97.724; 90		5472.21Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557454 CIFC54 H72 N3 PP 1 21/n 112.5627; 15.9337; 23.6169
90; 93.554; 90		4718.31Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557455 CIFC115 H154 Cl10 Ga2 N6 P2C 1 2/c 140.7612; 12.3237; 23.4798
90; 101.398; 90		11562Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557456 CIFC46 H88 Ag2 Li4 N6 O2P -18.3861; 11.5994; 14.05
86.881; 79.282; 83.876		1334.35Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu
Lipshutz-type bis(amido)argentates for directed ortho argentation
Chemical Science, 2020, 11, 1855-1861
1557457 CIFC36 H72 Ag2 Li2 N4C 1 2/c 122.1326; 8.3936; 22.8868
90; 109.561; 90		4006.34Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu
Lipshutz-type bis(amido)argentates for directed ortho argentation
Chemical Science, 2020, 11, 1855-1861
1557458 CIFC42 H56 Ag Li N2 O3P 1 21/n 112.4986; 14.8962; 21.7554
90; 93.742; 90		4041.82Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu
Lipshutz-type bis(amido)argentates for directed ortho argentation
Chemical Science, 2020, 11, 1855-1861
1557459 CIFC56 H84 Ag2 Li2 N4 O2P 1 21/c 113.3743; 18.2477; 22.9463
90; 103.316; 90		5449.49Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu
Lipshutz-type bis(amido)argentates for directed ortho argentation
Chemical Science, 2020, 11, 1855-1861
1557502 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.7583; 20.7341; 12.2345
90; 101.16; 90		2677.47Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi
Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules
Chemical Science, 2020, 11, 3610-3618
1557503 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.866; 21.1945; 12.2707
90; 101.413; 90		2770.1Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi
Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules
Chemical Science, 2020, 11, 3610-3618
1557504 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.874; 20.9284; 12.2372
90; 101.859; 90		2725.4Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi
Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules
Chemical Science, 2020, 11, 3610-3618
1557505 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.9375; 21.278; 12.2835
90; 100.818; 90		2807.9Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi
Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules
Chemical Science, 2020, 11, 3610-3618
1557506 CIFC140 H104 Cu4 N8 O20P -114.987; 16.858; 17.478
116.53; 107.31; 93.21		3679Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557507 CIFC218 H138 Cu8 N6 O48P -113.914; 20.891; 21.446
71.94; 87.87; 81.2		5857Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557508 CIFC116 H84 Cu4 N4 O24P 1 21/c 114.0177; 28.7314; 17.0738
90; 110.611; 90		6436.3Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557509 CIFC53 H31 Cu2 N O12I 1 2/m 125.8186; 22.6806; 27.2079
90; 109.69; 90		15000.9Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557510 CIFC106 H60 Cu4 O24C 1 2/m 119.687; 28.163; 10.475
90; 97.91; 90		5753Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557511 CIFC108 H72 Cu4 O24 S4C 1 2/c 114.151; 32.563; 26.766
90; 102.26; 90		12052Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557512 CIFC168 H124 Cu4 N12 O20P 1 21/n 120.979; 21.168; 23.76
90; 108.37; 90		10014Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557513 CIFC16 H21 N2 O0.1 PP n m a8.613; 17.7; 9.511
90; 90; 90		1450Zhang, Jingjing; Yang, Jin-Dong; Cheng, Jin-Pei
Diazaphosphinanes as hydride, hydrogen atom, proton or electron donors under transition-metal-free conditions: thermodynamics, kinetics, and synthetic applications
Chemical Science, 2020, 11, 3672-3679
1557531 CIFC21 Al F36 N O10 WP 4/n :213.699; 13.699; 9.5293
90; 90; 90		1788.29Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557532 CIFC30 Al2 F55 Mo O12P a -317.285; 17.285; 17.285
90; 90; 90		5164.3Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557533 CIFC22 Al F36 Mo O10P 4/n :213.759; 13.759; 9.5821
90; 90; 90		1813.99Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557534 CIFC30 Al2 F55 O12 WP a -317.3168; 17.3168; 17.3168
90; 90; 90		5192.82Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557535 CIFC21 Al F36 Mo N O10P 4/n :213.7152; 13.7152; 9.5418
90; 90; 90		1794.88Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557536 CIFC36 Al2 F73 O12 WP -111.5888; 11.5986; 12.7755
82.965; 67.136; 87.863		1570.27Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557537 CIFC32 Al2 Cl3 F55 O14 W2P -111.3269; 12.2795; 23.4349
76.883; 86.161; 66.485		2909.8Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557538 CIFC46 Al2 F72 I3 Mo3 O22P 1 21/n 113.9703; 28.8124; 20.6169
90; 90.443; 90		8298.4Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557539 CIFC30 Al2 F55 I O12 WP -110.5119; 12.5617; 21.1226
85.595; 76.545; 78.485		2656.7Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557540 CIFC68 Al4 F128 O26 W2P -115.848; 17.229; 22.395
94.072; 102.24; 101.653		5811.1Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557541 CIFC22 Al F36 I O10 WP 1 21/c 116.438; 28.3511; 17.5878
90; 110.764; 90		7664.2Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557542 CIFC96 Al6 F165 I6 Mo6 O42P -113.385; 21.4285; 31.305
85.822; 81.782; 83.84		8820.3Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557543 CIFC57 H88 N2 OP 1 21/n 116.2198; 10.77; 28.9971
90; 96.1; 90		5036.7Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557544 CIFC71 H94 Mg2 N8P 1 21/c 112.8246; 21.5786; 24.2161
90; 103.493; 90		6516.52Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557545 CIFC49 H60 Mg2 N6P 1 21/c 112.4858; 12.0704; 31.1338
90; 92.762; 90		4686.68Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557546 CIFC137.5 H189.63 I0.04 Mg2 N4 O0.13P 1 21/n 118.2067; 26.3297; 25.8355
90; 105.806; 90		11916.7Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557547 CIFC117 H144 Mg4 N12 O4P -115.1058; 19.0783; 20.0582
85.762; 88.909; 66.998		5306.17Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557548 CIFC70 H86 Mg2 N8C 1 2/c 118.7699; 15.7829; 22.8274
90; 109.172; 90		6387.4Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557549 CIFC57 H76 Mg2 N6P 1 21/c 118.7194; 11.3129; 26.0645
90; 103.791; 90		5360.57Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557550 CIFC57 H87 I Mg N2 OP -110.437; 14.8235; 18.7188
84.547; 75.886; 71.426		2661.85Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557551 CIFC151 H208 Mg4 N12 O6P -117.919; 19.6004; 20.9467
79.292; 75.685; 86.86		7004Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557552 CIFC134 H184 Mg4 N12 O12P 1 21/c 115.48; 15.114; 27.505
90; 103.08; 90		6268Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557570 CIFC20 H18 N2 O5P -18.27; 9.1848; 12.4194
71.619; 82.065; 79.191		876.19Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R.
Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction
Chemical Science, 2020, 11, 3569-3573
1557571 CIFC44 H44 N4 O11P 21 21 2110.9162; 11.3807; 31.809
90; 90; 90		3951.8Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R.
Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction
Chemical Science, 2020, 11, 3569-3573
1557572 CIFC8 H8 O5P 1 21 19.2321; 18.768; 18.876
90; 93.72; 90		3263.7Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R.
Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction
Chemical Science, 2020, 11, 3569-3573
1557580 CIFC15 H12 N4 O3 SP 21 21 216.4901; 13.5853; 17.2054
90; 90; 90		1517Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian
H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins
Chemical Science, 2020, 11, 3852-3861
1557581 CIFC25 H21 Cl N2 O3P 21 21 216.2023; 15.1707; 23.3424
90; 90; 90		2196.36Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian
H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins
Chemical Science, 2020, 11, 3852-3861
1557582 CIFC18 H14 Br2 N4 O3P 1 21 17.6364; 11.6851; 11.5473
90; 104.259; 90		998.65Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian
H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins
Chemical Science, 2020, 11, 3852-3861
1557583 CIFC19 H15 F N4 O3P 21 21 2110.3148; 11.9114; 14.6673
90; 90; 90		1802.08Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian
H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins
Chemical Science, 2020, 11, 3852-3861
1557584 CIFC25 H21 Cl N2 O3P 21 21 216.6447; 14.3101; 22.5008
90; 90; 90		2139.5Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian
H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins
Chemical Science, 2020, 11, 3852-3861
1557585 CIFC37 H61 Eu N8 O15F d d d :218.1194; 20.3557; 43.9834
90; 90; 90		16222.5Hewitt, Sarah H.; Macey, Georgina; Mailhot, Romain; Elsegood, Mark R. J.; Duarte, Fernanda; Kenwright, Alan M.; Butler, Stephen J.
Tuning the anion binding properties of lanthanide receptors to discriminate nucleoside phosphates in a sensing array
Chemical Science, 2020, 11, 3619-3628
1557586 CIFC22 H18 Br Cl0 N O2P 21 21 215.8675; 12.4208; 24.4967
90; 90; 90		1785.3Shen, Bin; He, Qianwen; Dong, Shunxi; Liu, Xiaohua; Feng, Xiaoming
A chiral cobalt(ii) complex catalyzed enantioselective aza-Piancatelli rearrangement/Diels‒Alder cascade reaction
Chemical Science, 2020, 11, 3862-3867
1557587 CIFC11 H10 Br N OP -16.732; 7.228; 12.0162
80.831; 86.517; 62.902		513.81Ikeda, Hideaki; Nishi, Kohei; Tsurugi, Hayato; Mashima, Kazushi
Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine
Chemical Science, 2020, 11, 3604-3609
1557598 CIFC18 H18 F3 N O4P 21 21 2110.186; 11.3558; 15.5296
90; 90; 90		1796.31Zhang, Shuyue; Greenhalgh, Mark D.; Slawin, Alexandra M. Z.; Smith, Andrew D.
Tandem sequential catalytic enantioselective synthesis of highly-functionalised tetrahydroindolizine derivatives
Chemical Science, 2020, 11, 3885-3892
1557603 CIFC21 H18 N2 O2 SC 1 2/c 117.4822; 9.78677; 20.9912
90; 103.576; 90		3491.13Li, Guofeng; Zhao, Man; Xie, Junqiu; Yao, Ying; Mou, Lingyun; Zhang, Xiaowei; Guo, Xiaomin; Sun, Wangsheng; Wang, Zheng; Xu, Jiecheng; Xue, Jianzhong; Hu, Tao; Zhang, Ming; Li, Min; Hong, Liang
Efficient synthesis of cyclic amidine-based fluorophores via 6π-electrocyclic ring closure
Chemical Science, 2020, 11, 3586-3591
1557604 CIFC20 H44 Cl2 N2 O2 P2 UP 1 21/c 112.7105; 28.115; 8.1727
90; 105.391; 90		2815.8Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557605 CIFC18 H40 Cl2 N2 O2 P2 UP 1 21/c 114.48; 14.59; 12.5668
90; 102.29; 90		2594.1Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557606 CIFC40 H88 Cl4 N4 O4 P4 Pd2 U2P c c n16.3226; 22.813; 14.7718
90; 90; 90		5500.5Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557607 CIFC44 H96 Cl4 N4 O6 P4 Pt3 U2C 1 2/c 112.663; 21.4809; 23.0838
90; 99.354; 90		6195.6Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557608 CIFC22 H48 Cl2 N2 Ni O3 P2 UP 1 21/n 111.3508; 12.914; 20.597
90; 95.165; 90		3006.9Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557609 CIFC44 H96 Cl4 N4 Ni2 O5 P4 U2P 1 21/n 114.5223; 15.8953; 27.339
90; 103.728; 90		6130.6Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557610 CIFC40 H63 Cl2 N2 O3 P3 Pd UP -112.208; 12.209; 17.048
108.557; 90.701; 108.839		2261Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557613 CIFC22 H28 O5 SP -17.3975; 10.7485; 13.1441
92.571; 96.25; 97.449		1028.29Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557614 CIFC15 H22 O3P 1 21/n 17.6688; 22.4305; 15.4747
90; 101.329; 90		2610.02Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro–Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557615 CIFC12 H20 O2P 1 21/c 17.1285; 11.9273; 13.4833
90; 104.629; 90		1109.24Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557616 CIFC15 H20 O3P -17.2165; 8.3504; 11.317
82.649; 76.258; 68.964		617.61Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557617 CIFC23 H28 N2 O3 SP 1 21/c 110.3539; 19.9619; 11.8443
90; 113.384; 90		2246.95Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557618 CIFC22 H30 N2 O4 SP 1 21/n 19.961; 17.5295; 13.2899
90; 101.667; 90		2272.62Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557625 CIFC48 H55 Au F6 N4 O11 S2P 21 21 219.1199; 23.4191; 23.6083
90; 90; 90		5042.3Reid, Jolene P.; Hu, Mingyou; Ito, Susumu; Huang, Banruo; Hong, Cynthia M.; Xiang, Hengye; Sigman, Matthew S.; Toste, F. Dean
Strategies for remote enantiocontrol in chiral gold(iii) complexes applied to catalytic enantioselective γ,δ-Diels‒Alder reactions
Chemical Science, 2020, 11, 6450-6456
1557626 CIFC21 H9 N3 O6 TiP a -320.9953; 20.9953; 20.9953
90; 90; 90		9254.8Cao, Jing; Ma, Wenjie; Lyu, Kangjie; Zhuang, Lin; Cong, Hengjiang; Deng, Hexiang
Twist and sliding dynamics between interpenetrated frames in Ti-MOF revealing high proton conductivity
Chemical Science, 2020, 11, 3978-3985
1557627 CIFC3.5 H1.5 N0.5 O Ti0.17P a -321.1222; 21.1222; 21.1222
90; 90; 90		9423.6Cao, Jing; Ma, Wenjie; Lyu, Kangjie; Zhuang, Lin; Cong, Hengjiang; Deng, Hexiang
Twist and sliding dynamics between interpenetrated frames in Ti-MOF revealing high proton conductivity
Chemical Science, 2020, 11, 3978-3985
1557628 CIFC H N O TiP a -321.1205; 21.1205; 21.1205
90; 90; 90		9421.3Cao, Jing; Ma, Wenjie; Lyu, Kangjie; Zhuang, Lin; Cong, Hengjiang; Deng, Hexiang
Twist and sliding dynamics between interpenetrated frames in Ti-MOF revealing high proton conductivity
Chemical Science, 2020, 11, 3978-3985
1557633 CIFC26 H10 B Br F15 NP -17.3; 11.867; 15.598
78.16; 80.45; 88.78		1304.1Aramaki, Yoshitaka; Imaizumi, Naoki; Hotta, Mao; Kumagai, Jun; Ooi, Takashi
Exploiting single-electron transfer in Lewis pairs for catalytic bond-forming reactions
Chemical Science, 2020, 11, 4305-4311
1557634 CIFC26 H37 N3 OP 1 21/n 19.6311; 19.6619; 13.541
90; 106.977; 90		2452.5Odella, Emmanuel; Mora, S. Jimena; Wadsworth, Brian L.; Goings, Joshua J.; Gervaldo, Miguel A.; Sereno, Leonides E.; Groy, Thomas L.; Gust, Devens; Moore, Thomas A.; Moore, Gary F.; Hammes-Schiffer, Sharon; Moore, Ana L.
Proton-coupled electron transfer across benzimidazole bridges in bioinspired proton wires
Chemical Science, 2020, 11, 3820-3828
1557635 CIFC73 H76 Cl2 N10 O4C 1 2/c 133.136; 6.8671; 30.967
90; 100.031; 90		6938.8Odella, Emmanuel; Mora, S. Jimena; Wadsworth, Brian L.; Goings, Joshua J.; Gervaldo, Miguel A.; Sereno, Leonides E.; Groy, Thomas L.; Gust, Devens; Moore, Thomas A.; Moore, Gary F.; Hammes-Schiffer, Sharon; Moore, Ana L.
Proton-coupled electron transfer across benzimidazole bridges in bioinspired proton wires
Chemical Science, 2020, 11, 3820-3828
1557636 CIFC21 H27 N3 O12 TbP -110.4608; 10.9006; 12.5293
104.61; 107.84; 97.204		1283.78Anderson, Samantha L.; Tiana, Davide; Ireland, Christopher P.; Capano, Gloria; Fumanal, Maria; Gładysiak, Andrzej; Kampouri, Stavroula; Rahmanudin, Aiman; Guijarro, Néstor; Sivula, Kevin; Stylianou, Kyriakos C.; Smit, Berend
Taking lanthanides out of isolation: tuning the optical properties of metal‒organic frameworks
Chemical Science, 2020, 11, 4164-4170
1557637 CIFC11 H10 N O7 TbP 1 21/n 113.388; 6.6366; 15.567
90; 98.599; 90		1367.6Anderson, Samantha L.; Tiana, Davide; Ireland, Christopher P.; Capano, Gloria; Fumanal, Maria; Gładysiak, Andrzej; Kampouri, Stavroula; Rahmanudin, Aiman; Guijarro, Néstor; Sivula, Kevin; Stylianou, Kyriakos C.; Smit, Berend
Taking lanthanides out of isolation: tuning the optical properties of metal‒organic frameworks
Chemical Science, 2020, 11, 4164-4170
1557638 CIFC15 H11 N O2 S2P 1 21/c 15.9915; 29.952; 7.8574
90; 95.092; 90		1404.5Gao, Wen-Chao; Tian, Jun; Shang, Yu-Zhu; Jiang, Xuefeng
Steric and stereoscopic disulfide construction for cross-linkage via N-dithiophthalimides
Chemical Science, 2020, 11, 3903-3908
1557639 CIFC18 H15 O3 S2P -19.234; 9.723; 10.6174
99.463; 113.869; 105.929		796.06Gao, Wen-Chao; Tian, Jun; Shang, Yu-Zhu; Jiang, Xuefeng
Steric and stereoscopic disulfide construction for cross-linkage via N-dithiophthalimides
Chemical Science, 2020, 11, 3903-3908
1557640 CIFC30 H27 Br O3 S2P 1 21 123.8898; 6.7617; 24.8099
90; 102.215; 90		3916.95Gao, Wen-Chao; Tian, Jun; Shang, Yu-Zhu; Jiang, Xuefeng
Steric and stereoscopic disulfide construction for cross-linkage via N-dithiophthalimides
Chemical Science, 2020, 11, 3903-3908
1557644 CIFC112 H192 In26 Mn4 N32 S51I 41/a :222.436; 22.436; 38.165
90; 90; 90		19211Xue, Chaozhuang; Fan, Xing; Zhang, Jiaxu; Hu, Dandan; Wang, Xiao-Li; Wang, Xiang; Zhou, Rui; Lin, Haiping; Li, Youyong; Li, Dong-Sheng; Wei, Xiao; Zheng, Daoyuan; Yang, Yang; Han, Keli; Wu, Tao
Direct observation of charge transfer between molecular heterojunctions based on inorganic semiconductor clusters
Chemical Science, 2020, 11, 4085-4096
1557645 CIFC112 H192 Fe4 In26 N32 O0 S51I 41/a :222.329; 22.329; 38.059
90; 90; 90		18976Xue, Chaozhuang; Fan, Xing; Zhang, Jiaxu; Hu, Dandan; Wang, Xiao-Li; Wang, Xiang; Zhou, Rui; Lin, Haiping; Li, Youyong; Li, Dong-Sheng; Wei, Xiao; Zheng, Daoyuan; Yang, Yang; Han, Keli; Wu, Tao
Direct observation of charge transfer between molecular heterojunctions based on inorganic semiconductor clusters
Chemical Science, 2020, 11, 4085-4096
1557646 CIFC19 H19 Br O5P -18.9606; 9.9217; 11.8105
72.29; 88.75; 63.972		891.12Zhao, Qiang; Jin, Ji-Kang; Wang, Jie; Zhang, Feng-Lian; Wang, Yi-Feng
Radical α-addition involved electrooxidative [3 + 2] annulation of phenols and electron-deficient alkenes
Chemical Science, 2020, 11, 3909-3913
1557647 CIFC54 H72 Fe3 Ho Li3 O6P 1 21/c 111.3991; 63.596; 13.7285
90; 92.383; 90		9943.7Latendresse, Trevor P.; Vieru, Veacheslav; Upadhyay, Apoorva; Bhuvanesh, Nattamai S.; Chibotaru, Liviu F.; Nippe, Michael
Trends in trigonal prismatic Ln-[1]ferrocenophane complexes and discovery of a Ho3+ single-molecule magnet
Chemical Science, 2020, 11, 3936-3951
1557648 CIFC54 H72 Fe3 Gd Li3 O6P 1 21/c 111.3774; 63.872; 13.7293
90; 92.491; 90		9967.6Latendresse, Trevor P.; Vieru, Veacheslav; Upadhyay, Apoorva; Bhuvanesh, Nattamai S.; Chibotaru, Liviu F.; Nippe, Michael
Trends in trigonal prismatic Ln-[1]ferrocenophane complexes and discovery of a Ho3+ single-molecule magnet
Chemical Science, 2020, 11, 3936-3951
1557649 CIFC54 H72 Fe3 Li3 O6 YbP 1 21/c 111.4155; 63.489; 13.73
90; 92.17; 90		9943.8Latendresse, Trevor P.; Vieru, Veacheslav; Upadhyay, Apoorva; Bhuvanesh, Nattamai S.; Chibotaru, Liviu F.; Nippe, Michael
Trends in trigonal prismatic Ln-[1]ferrocenophane complexes and discovery of a Ho3+ single-molecule magnet
Chemical Science, 2020, 11, 3936-3951
1557650 CIFC60 H84 Fe3 Ho Li3 O6P 1 21/n 111.3389; 13.7172; 36.2329
90; 95.344; 90		5611.1Latendresse, Trevor P.; Vieru, Veacheslav; Upadhyay, Apoorva; Bhuvanesh, Nattamai S.; Chibotaru, Liviu F.; Nippe, Michael
Trends in trigonal prismatic Ln-[1]ferrocenophane complexes and discovery of a Ho3+ single-molecule magnet
Chemical Science, 2020, 11, 3936-3951
1557651 CIFC64.38 H58.38 Fe3 Ho Li3 N6.88P 21 21 2121.206; 22.6446; 23.1321
90; 90; 90		11108.1Latendresse, Trevor P.; Vieru, Veacheslav; Upadhyay, Apoorva; Bhuvanesh, Nattamai S.; Chibotaru, Liviu F.; Nippe, Michael
Trends in trigonal prismatic Ln-[1]ferrocenophane complexes and discovery of a Ho3+ single-molecule magnet
Chemical Science, 2020, 11, 3936-3951
1557652 CIFC54 H72 Fe3 Li3 Lu O6P 1 21/c 111.4149; 63.246; 13.743
90; 92.282; 90		9914Latendresse, Trevor P.; Vieru, Veacheslav; Upadhyay, Apoorva; Bhuvanesh, Nattamai S.; Chibotaru, Liviu F.; Nippe, Michael
Trends in trigonal prismatic Ln-[1]ferrocenophane complexes and discovery of a Ho3+ single-molecule magnet
Chemical Science, 2020, 11, 3936-3951
1557653 CIFC54 H72 Fe3 Li3 O6 TmP 1 21/c 111.4199; 63.606; 13.7467
90; 92.28; 90		9977Latendresse, Trevor P.; Vieru, Veacheslav; Upadhyay, Apoorva; Bhuvanesh, Nattamai S.; Chibotaru, Liviu F.; Nippe, Michael
Trends in trigonal prismatic Ln-[1]ferrocenophane complexes and discovery of a Ho3+ single-molecule magnet
Chemical Science, 2020, 11, 3936-3951
1557654 CIFC54 H72 Er Fe3 Li3 O6P 1 21/c 111.4007; 63.598; 13.7293
90; 92.262; 90		9946.8Latendresse, Trevor P.; Vieru, Veacheslav; Upadhyay, Apoorva; Bhuvanesh, Nattamai S.; Chibotaru, Liviu F.; Nippe, Michael
Trends in trigonal prismatic Ln-[1]ferrocenophane complexes and discovery of a Ho3+ single-molecule magnet
Chemical Science, 2020, 11, 3936-3951
1557655 CIFC58 H80 Fe3 Li3 Lu O7I 1 a 120.62; 32.856; 25.081
90; 104.923; 90		16419Latendresse, Trevor P.; Vieru, Veacheslav; Upadhyay, Apoorva; Bhuvanesh, Nattamai S.; Chibotaru, Liviu F.; Nippe, Michael
Trends in trigonal prismatic Ln-[1]ferrocenophane complexes and discovery of a Ho3+ single-molecule magnet
Chemical Science, 2020, 11, 3936-3951
1557656 CIFC58 H80 Fe3 Li3 O7 YbC 1 c 128.077; 32.756; 20.619
90; 120.475; 90		16343Latendresse, Trevor P.; Vieru, Veacheslav; Upadhyay, Apoorva; Bhuvanesh, Nattamai S.; Chibotaru, Liviu F.; Nippe, Michael
Trends in trigonal prismatic Ln-[1]ferrocenophane complexes and discovery of a Ho3+ single-molecule magnet
Chemical Science, 2020, 11, 3936-3951
1557674 CIFC12 H18 OP -16.2162; 12.5583; 20.7881
92.381; 98.293; 100.115		1577.16Nelson, Ronald; Calvelo, Martín; García-Fandiño, Rebeca; Lledós, Agustí; Ujaque, Gregori; Mascareñas, José L.; López, Fernando
Skeletal diversity in Pt- and Au-catalyzed annulations of allenedienes: dissecting unconventional mechanistic pathways
Chemical Science, 2020, 11, 4209-4220
1557675 CIFC19 H24 N2 O6P 1 21/c 119.54; 8.3364; 11.3992
90; 95.016; 90		1849.7Nelson, Ronald; Calvelo, Martín; García-Fandiño, Rebeca; Lledós, Agustí; Ujaque, Gregori; Mascareñas, José L.; López, Fernando
Skeletal diversity in Pt- and Au-catalyzed annulations of allenedienes: dissecting unconventional mechanistic pathways
Chemical Science, 2020, 11, 4209-4220
1557676 CIFC19 H34 O SiP 1 21/c 123.4244; 6.2336; 13.0105
90; 90.557; 90		1899.68Nelson, Ronald; Calvelo, Martín; García-Fandiño, Rebeca; Lledós, Agustí; Ujaque, Gregori; Mascareñas, José L.; López, Fernando
Skeletal diversity in Pt- and Au-catalyzed annulations of allenedienes: dissecting unconventional mechanistic pathways
Chemical Science, 2020, 11, 4209-4220
1557677 CIFC12 H18 OI 41/a :222.3413; 22.3413; 8.6532
90; 90; 90		4319.1Nelson, Ronald; Calvelo, Martín; García-Fandiño, Rebeca; Lledós, Agustí; Ujaque, Gregori; Mascareñas, José L.; López, Fernando
Skeletal diversity in Pt- and Au-catalyzed annulations of allenedienes: dissecting unconventional mechanistic pathways
Chemical Science, 2020, 11, 4209-4220
1557678 CIFC20 H23 Br O2P n a 2111.4263; 19.625; 15.7208
90; 90; 90		3525.25Nelson, Ronald; Calvelo, Martín; García-Fandiño, Rebeca; Lledós, Agustí; Ujaque, Gregori; Mascareñas, José L.; López, Fernando
Skeletal diversity in Pt- and Au-catalyzed annulations of allenedienes: dissecting unconventional mechanistic pathways
Chemical Science, 2020, 11, 4209-4220
1557679 CIFC62 H114 Fe N4 Na4 Zn4C 1 2/c 127.395; 44.055; 14.5103
90; 100.575; 90		17215Honeyman, Gordon W.; Armstrong, David R.; Clegg, William; Hevia, Eva; Kennedy, Alan R.; McLellan, Ross; Orr, Samantha A.; Parkinson, John A.; Ramsay, Donna L.; Robertson, Stuart D.; Towie, Stephen; Mulvey, Robert E.
A regioselectively 1,1′,3,3′-tetrazincated ferrocene complex displaying core and peripheral reactivity
Chemical Science, 2020, 11, 6510-6520
1557680 CIFC39 H42 N7 Na ZnP 21 21 218.8556; 17.4144; 23.9796
90; 90; 90		3698.01Honeyman, Gordon W.; Armstrong, David R.; Clegg, William; Hevia, Eva; Kennedy, Alan R.; McLellan, Ross; Orr, Samantha A.; Parkinson, John A.; Ramsay, Donna L.; Robertson, Stuart D.; Towie, Stephen; Mulvey, Robert E.
A regioselectively 1,1′,3,3′-tetrazincated ferrocene complex displaying core and peripheral reactivity
Chemical Science, 2020, 11, 6510-6520
1557681 CIFC68 H110 Fe N4 Na4 Zn4P 1 21/c 114.895; 26.966; 18.622
90; 111.871; 90		6941.3Honeyman, Gordon W.; Armstrong, David R.; Clegg, William; Hevia, Eva; Kennedy, Alan R.; McLellan, Ross; Orr, Samantha A.; Parkinson, John A.; Ramsay, Donna L.; Robertson, Stuart D.; Towie, Stephen; Mulvey, Robert E.
A regioselectively 1,1′,3,3′-tetrazincated ferrocene complex displaying core and peripheral reactivity
Chemical Science, 2020, 11, 6510-6520
1557682 CIFC55 H102 Fe N6 Na2 Zn2P -112.9797; 15.0261; 15.9756
99.482; 90.798; 99.459		3028.7Honeyman, Gordon W.; Armstrong, David R.; Clegg, William; Hevia, Eva; Kennedy, Alan R.; McLellan, Ross; Orr, Samantha A.; Parkinson, John A.; Ramsay, Donna L.; Robertson, Stuart D.; Towie, Stephen; Mulvey, Robert E.
A regioselectively 1,1′,3,3′-tetrazincated ferrocene complex displaying core and peripheral reactivity
Chemical Science, 2020, 11, 6510-6520
1557687 CIFC26 H39 F3 N3 O3 SP 1 21/c 111.3959; 8.8582; 26.7626
90; 91.58; 90		2700.58Messelberger, Julian; Grünwald, Annette; Goodner, Stephen J.; Zeilinger, Florian; Pinter, Piermaria; Miehlich, Matthias E.; Heinemann, Frank W.; Hansmann, Max M.; Munz, Dominik
Aromaticity and sterics control whether a cationic olefin radical is resistant to disproportionation
Chemical Science, 2020, 11, 4138-4149
1557688 CIFC26 H39 F3 N3 O3 SP 1 21/n 114.9305; 11.67; 16.4062
90; 109.508; 90		2694.5Messelberger, Julian; Grünwald, Annette; Goodner, Stephen J.; Zeilinger, Florian; Pinter, Piermaria; Miehlich, Matthias E.; Heinemann, Frank W.; Hansmann, Max M.; Munz, Dominik
Aromaticity and sterics control whether a cationic olefin radical is resistant to disproportionation
Chemical Science, 2020, 11, 4138-4149
1557695 CIFC24 H23 N OP 1 21/c 111.129; 9.485; 18.178
90; 90.821; 90		1918.6Liu, Zhengfen; Li, Minyan; Deng, Guogang; Wei, Wanshi; Feng, Ping; Zi, Quanxing; Li, Tiantian; Zhang, Hongbin; Yang, Xiaodong; Walsh, Patrick J.
Transition-metal-free C(sp3)‒H/C(sp3)‒H dehydrogenative coupling of saturated heterocycles with N-benzyl imines
Chemical Science, 2020, 11, 7619-7625
1557696 CIFC25 H26 N2 OP 1 21/c 110.9067; 9.988; 18.4338
90; 94.55; 90		2001.78Liu, Zhengfen; Li, Minyan; Deng, Guogang; Wei, Wanshi; Feng, Ping; Zi, Quanxing; Li, Tiantian; Zhang, Hongbin; Yang, Xiaodong; Walsh, Patrick J.
Transition-metal-free C(sp3)‒H/C(sp3)‒H dehydrogenative coupling of saturated heterocycles with N-benzyl imines
Chemical Science, 2020, 11, 7619-7625
1557708 CIFC19 H19 N O2P 1 21/c 110.8161; 8.4185; 16.7407
90; 97.266; 90		1512.09Zheng, Shuai; Zhang, Shuo-Qing; Saeednia, Borna; Zhou, Jiawang; Anna, Jessica M.; Hong, Xin; Molander, Gary A.
Diastereoselective olefin amidoacylation via photoredox PCET/nickel-dual catalysis: reaction scope and mechanistic insights
Chemical Science, 2020, 11, 4131-4137
1557732 CIFC53 H39 N5 O2 SP -110.3043; 10.5271; 21.1147
88.634; 86.866; 70.331		2153.5Lv, Chunyan; Liu, Wangwang; Luo, Qing; Yi, Haiyan; Yu, Huakang; Yang, Zhongmin; Zou, Bo; Zhang, Yujian
A highly emissive AIE-active luminophore exhibiting deep-red to near-infrared piezochromism and high-quality lasing
Chemical Science, 2020, 11, 4007-4015
1557737 CIFC114 H810 Mo132 N46 O708 S2R -3 :H32.6262; 32.6262; 73.225
90; 90; 120		67503Pow, Robert W.; Xuan, Weimin; Long, De-Liang; Bell, Nicola L.; Cronin, Leroy
Embedding alkenes within an icosahedral inorganic fullerene {(NH4)42[Mo132O372(L)30(H2O)72]} for trapping volatile organics
Chemical Science, 2020, 11, 2388-2393
1557738 CIFC120 H806 Mo132 N48 O676 S3R -3 :H32.3898; 32.3898; 72.8225
90; 90; 120		66162.6Pow, Robert W.; Xuan, Weimin; Long, De-Liang; Bell, Nicola L.; Cronin, Leroy
Embedding alkenes within an icosahedral inorganic fullerene {(NH4)42[Mo132O372(L)30(H2O)72]} for trapping volatile organics
Chemical Science, 2020, 11, 2388-2393
1557739 CIFC120 H926 Mo132 N48 O736 S3R -3 :H32.4465; 32.4465; 72.887
90; 90; 120		66453.3Pow, Robert W.; Xuan, Weimin; Long, De-Liang; Bell, Nicola L.; Cronin, Leroy
Embedding alkenes within an icosahedral inorganic fullerene {(NH4)42[Mo132O372(L)30(H2O)72]} for trapping volatile organics
Chemical Science, 2020, 11, 2388-2393
1557747 CIFC44 H96 Ca2 Cl N6 O36 V12P 1 21/c 110.6954; 29.2218; 28.2691
90; 95.3952; 90		8796.1Greiner, Simon; Schwarz, Benjamin; Ringenberg, Mark; Dürr, Maximilian; Ivanovic-Burmazovic, Ivana; Fichtner, Maximilian; Anjass, Montaha; Streb, Carsten
Redox-inactive ions control the redox-activity of molecular vanadium oxides
Chemical Science, 2020, 11, 4450-4455
1557749 CIFC27 H27 Cl4 F3 N2 PdP 21 21 217.3222; 16.3645; 22.9119
90; 90; 90		2745.4Baek, Doohyun; Ryu, Huijeong; Ryu, Ji Yeon; Lee, Junseong; Stoltz, Brian M.; Hong, Sukwon
Catalytic enantioselective synthesis of tetrasubstituted chromanones via palladium-catalyzed asymmetric conjugate arylation using chiral pyridine-dihydroisoquinoline ligands
Chemical Science, 2020, 11, 4602-4607
1557750 CIFC20 H22 O2C 1 2 123.2747; 6.7781; 10.2443
90; 91.9349; 90		1615.2Baek, Doohyun; Ryu, Huijeong; Ryu, Ji Yeon; Lee, Junseong; Stoltz, Brian M.; Hong, Sukwon
Catalytic enantioselective synthesis of tetrasubstituted chromanones via palladium-catalyzed asymmetric conjugate arylation using chiral pyridine-dihydroisoquinoline ligands
Chemical Science, 2020, 11, 4602-4607
1557760 CIFC6 H11 S3 SbP 1 21/n 17.5797; 9.1057; 27.371
90; 95.218; 90		1881.3Moaven, Shiva; Watson, Brandon T.; Thompson, Shelby B.; Lyons, Veronica J.; Unruh, Daniel K.; Casadonte, Dominick J.; Pappas, Dimitri; Cozzolino, Anthony F.
Self-assembly of reversed bilayer vesicles through pnictogen bonding: water-stable supramolecular nanocontainers for organic solvents
Chemical Science, 2020, 11, 4374-4380
1557761 CIFC71 H53 B Cl2 F20 N2P -113.2446; 13.7731; 20.2266
94.923; 102.959; 114.918		3192.4Dong, Zhaowen; Pezzato, Cristian; Sienkiewicz, Andrzej; Scopelliti, Rosario; Fadaei-Tirani, Farzaneh; Severin, Kay
SET processes in Lewis acid‒base reactions: the tritylation of N-heterocyclic carbenes
Chemical Science, 2020, 11, 7615-7618
1557762 CIFC35 H21 B F20 N2P 1 21 18.40488; 18.0272; 11.0843
90; 91.4773; 90		1678.9Dong, Zhaowen; Pezzato, Cristian; Sienkiewicz, Andrzej; Scopelliti, Rosario; Fadaei-Tirani, Farzaneh; Severin, Kay
SET processes in Lewis acid‒base reactions: the tritylation of N-heterocyclic carbenes
Chemical Science, 2020, 11, 7615-7618
1557763 CIFC52 H39 B Cl2 F20 N2P -112.4784; 12.6328; 17.6483
69.366; 84.7909; 78.9069		2554.12Dong, Zhaowen; Pezzato, Cristian; Sienkiewicz, Andrzej; Scopelliti, Rosario; Fadaei-Tirani, Farzaneh; Severin, Kay
SET processes in Lewis acid‒base reactions: the tritylation of N-heterocyclic carbenes
Chemical Science, 2020, 11, 7615-7618
1557764 CIFC64 H39 B F20 N2P b c a18.0482; 18.05071; 34.8012
90; 90; 90		11337.6Dong, Zhaowen; Pezzato, Cristian; Sienkiewicz, Andrzej; Scopelliti, Rosario; Fadaei-Tirani, Farzaneh; Severin, Kay
SET processes in Lewis acid‒base reactions: the tritylation of N-heterocyclic carbenes
Chemical Science, 2020, 11, 7615-7618
1557765 CIFC12 Bi2 N12 S12 Zn3C 1 2/c 126.3104; 8.4587; 15.7403
90; 93.63; 90		3496Cliffe, Matthew J.; Keyzer, Evan N.; Bond, Andrew D.; Astle, Maxwell A.; Grey, Clare P.
The structures of ordered defects in thiocyanate analogues of Prussian Blue
Chemical Science, 2020, 11, 4430-4438
1557766 CIFC12 Bi2 N12 S12 Zn3P 1 21/c 117.7331; 13.6501; 16.4375
90; 114.397; 90		3623.55Cliffe, Matthew J.; Keyzer, Evan N.; Bond, Andrew D.; Astle, Maxwell A.; Grey, Clare P.
The structures of ordered defects in thiocyanate analogues of Prussian Blue
Chemical Science, 2020, 11, 4430-4438
1557767 CIFC7 H14 Bi Mn2 N7 O7 S7P 1 21/n 18.3065; 25.8428; 12.2664
90; 90.2358; 90		2633.12Cliffe, Matthew J.; Keyzer, Evan N.; Bond, Andrew D.; Astle, Maxwell A.; Grey, Clare P.
The structures of ordered defects in thiocyanate analogues of Prussian Blue
Chemical Science, 2020, 11, 4430-4438
1557768 CIFC36 H76 Bi6 Co9 N36 O38 S36P -112.0209; 12.1613; 23.8319
94.2; 94.003; 91.452		3464.52Cliffe, Matthew J.; Keyzer, Evan N.; Bond, Andrew D.; Astle, Maxwell A.; Grey, Clare P.
The structures of ordered defects in thiocyanate analogues of Prussian Blue
Chemical Science, 2020, 11, 4430-4438
1557769 CIFC30 H74 Bi5 N33 Ni6 O16 S30P -111.8567; 11.8653; 18.3824
84.0731; 76.714; 85.1942		2498.6Cliffe, Matthew J.; Keyzer, Evan N.; Bond, Andrew D.; Astle, Maxwell A.; Grey, Clare P.
The structures of ordered defects in thiocyanate analogues of Prussian Blue
Chemical Science, 2020, 11, 4430-4438
1557770 CIFC7 H14 Bi Mn2 N7 O7 S7P 1 21/n 18.3698; 26.0037; 12.2466
90; 91.208; 90		2664.83Cliffe, Matthew J.; Keyzer, Evan N.; Bond, Andrew D.; Astle, Maxwell A.; Grey, Clare P.
The structures of ordered defects in thiocyanate analogues of Prussian Blue
Chemical Science, 2020, 11, 4430-4438
1557790 CIFC43 H39 B F4 N2 O2P 1 21/c 114.502; 12.866; 20.32
90; 106.828; 90		3629Zhou, Chengcheng; Jiang, Meijuan; Du, Jian; Bai, Haotian; Shan, Guogang; Kwok, Ryan T. K.; Chau, Joe H. C.; Zhang, Jun; Lam, Jacky W. Y.; Huang, Peng; Tang, Ben Zhong
One stone, three birds: one AIEgen with three colors for fast differentiation of three pathogens
Chemical Science, 2020, 11, 4730-4740
1557811 CIFC35 H33 N O4F 2 d d8.4764; 33.008; 40.934
90; 90; 90		11453Mateos, Javier; Vega-Peñaloza, Alberto; Franceschi, Pietro; Rigodanza, Francesco; Andreetta, Philip; Companyó, Xavier; Pelosi, Giorgio; Bonchio, Marcella; Dell’Amico, Luca
A visible-light Paternò–Büchi dearomatisation process towards the construction of oxeto-indolinic polycycles
Chemical Science, 2020, 11, 6532-6538
1557826 CIFC120 H56 Dy2 N4 Ni OP -114.3857; 14.7255; 19.1301
84.837; 88.064; 61.889		3559.7Velkos, Georgios; Yang, Wei; Yao, Yang-Rong; Sudarkova, Svetlana M.; Liu, XinYe; Büchner, Bernd; Avdoshenko, Stanislav M.; Chen, Ning; Popov, Alexey A.
Shape-adaptive single-molecule magnetism and hysteresis up to 14 K in oxide clusterfullerenes Dy2O@C72 and Dy2O@C74 with fused pentagon pairs and flexible Dy‒(μ2-O)‒Dy angle
Chemical Science, 2020, 11, 4766-4772
1557827 CIFC117 H50 Dy2 N4 Ni O S2P 1 21/c 117.914; 16.589; 25.753
90; 106.775; 90		7327.5Velkos, Georgios; Yang, Wei; Yao, Yang-Rong; Sudarkova, Svetlana M.; Liu, XinYe; Büchner, Bernd; Avdoshenko, Stanislav M.; Chen, Ning; Popov, Alexey A.
Shape-adaptive single-molecule magnetism and hysteresis up to 14 K in oxide clusterfullerenes Dy2O@C72 and Dy2O@C74 with fused pentagon pairs and flexible Dy‒(μ2-O)‒Dy angle
Chemical Science, 2020, 11, 4766-4772
1557828 CIFC82 H88 N14 O12P -110.5727; 12.998; 15.4783
104.398; 102.401; 109.792		1831.32Guo, Chenxing; Wang, Hu; Lynch, Vincent M.; Ji, Xiaofan; Page, Zachariah A.; Sessler, Jonathan L.
Molecular recognition of pyrazine N,N′-dioxide using aryl extended calix[4]pyrroles
Chemical Science, 2020, 11, 5650-5657
1557829 CIFC86 H88 N14 O4P 1 21/n 116.711; 12.6971; 18.2586
90; 99.327; 90		3822.9Guo, Chenxing; Wang, Hu; Lynch, Vincent M.; Ji, Xiaofan; Page, Zachariah A.; Sessler, Jonathan L.
Molecular recognition of pyrazine N,N′-dioxide using aryl extended calix[4]pyrroles
Chemical Science, 2020, 11, 5650-5657
1557830 CIFC78 H92 N14 O6C 1 2/c 112.761; 17.133; 31.684
90; 93.976; 90		6911Guo, Chenxing; Wang, Hu; Lynch, Vincent M.; Ji, Xiaofan; Page, Zachariah A.; Sessler, Jonathan L.
Molecular recognition of pyrazine N,N′-dioxide using aryl extended calix[4]pyrroles
Chemical Science, 2020, 11, 5650-5657
1557831 CIFC4 H4 N2 O2P n m a11.866; 11.883; 6.3933
90; 90; 90		901.5Guo, Chenxing; Wang, Hu; Lynch, Vincent M.; Ji, Xiaofan; Page, Zachariah A.; Sessler, Jonathan L.
Molecular recognition of pyrazine N,N′-dioxide using aryl extended calix[4]pyrroles
Chemical Science, 2020, 11, 5650-5657
1557832 CIFC82 H92 N10 O8R -3 :H43.6284; 43.6284; 10.7942
90; 90; 120		17793.4Guo, Chenxing; Wang, Hu; Lynch, Vincent M.; Ji, Xiaofan; Page, Zachariah A.; Sessler, Jonathan L.
Molecular recognition of pyrazine N,N′-dioxide using aryl extended calix[4]pyrroles
Chemical Science, 2020, 11, 5650-5657
1557833 CIFC53 H52 N6 O7P 1 21/c 110.9587; 59.0761; 22.009
90; 101.952; 90		13939.7Guo, Chenxing; Wang, Hu; Lynch, Vincent M.; Ji, Xiaofan; Page, Zachariah A.; Sessler, Jonathan L.
Molecular recognition of pyrazine N,N′-dioxide using aryl extended calix[4]pyrroles
Chemical Science, 2020, 11, 5650-5657
1557834 CIFC208.5 H180 Fe8 N12P -119.2992; 19.3512; 27.206
105.998; 90.079; 119.907		8348.1Cook, Andrew W.; Bocarsly, Joshua D.; Lewis, Richard A.; Touchton, Alexander J.; Morochnik, Simona; Hayton, Trevor W.
An iron ketimide single-molecule magnet [Fe4(NCPh2)6] with suppressed through-barrier relaxation
Chemical Science, 2020, 11, 4753-4757
1557836 CIFC26 H43 Al I2 N2P 1 21/n 110.145; 17.053; 17.044
90; 102.029; 90		2883.9Weetman, Catherine; Porzelt, Amelie; Bag, Prasenjit; Hanusch, Franziska; Inoue, Shigeyoshi
Dialumenes ‒ aryl vs. silyl stabilisation for small molecule activation and catalysis
Chemical Science, 2020, 11, 4817-4827
1557837 CIFC58 H100 Al2 N4 O1.79C 1 2/c 136.035; 15.3951; 21.8876
90; 104.19; 90		11771.9Weetman, Catherine; Porzelt, Amelie; Bag, Prasenjit; Hanusch, Franziska; Inoue, Shigeyoshi
Dialumenes ‒ aryl vs. silyl stabilisation for small molecule activation and catalysis
Chemical Science, 2020, 11, 4817-4827
1557838 CIFC72 H102 Al2 N4P 1 2/c 113.5339; 13.5131; 18.1559
90; 100.481; 90		3265Weetman, Catherine; Porzelt, Amelie; Bag, Prasenjit; Hanusch, Franziska; Inoue, Shigeyoshi
Dialumenes ‒ aryl vs. silyl stabilisation for small molecule activation and catalysis
Chemical Science, 2020, 11, 4817-4827
1557839 CIFC70 H104 Al2 N6C 1 2/c 121.6994; 15.8898; 20.777
90; 90.177; 90		7163.9Weetman, Catherine; Porzelt, Amelie; Bag, Prasenjit; Hanusch, Franziska; Inoue, Shigeyoshi
Dialumenes ‒ aryl vs. silyl stabilisation for small molecule activation and catalysis
Chemical Science, 2020, 11, 4817-4827
1557840 CIFC54 H90 Al2 N4P 1 21/c 112.4062; 18.1378; 24.62
90; 101.846; 90		5422Weetman, Catherine; Porzelt, Amelie; Bag, Prasenjit; Hanusch, Franziska; Inoue, Shigeyoshi
Dialumenes ‒ aryl vs. silyl stabilisation for small molecule activation and catalysis
Chemical Science, 2020, 11, 4817-4827
1557841 CIFC55 H93 Al2 N4C 1 2/c 135.126; 15.4352; 21.8147
90; 109.512; 90		11148.2Weetman, Catherine; Porzelt, Amelie; Bag, Prasenjit; Hanusch, Franziska; Inoue, Shigeyoshi
Dialumenes ‒ aryl vs. silyl stabilisation for small molecule activation and catalysis
Chemical Science, 2020, 11, 4817-4827
1557864 CIFC44 H59 In N2 O SP 1 21/c 118.3672; 14.0583; 17.9736
90; 118.814; 90		4066.4Goonesinghe, Chatura; Roshandel, Hootan; Diaz, Carlos; Jung, Hyuk-Joon; Nyamayaro, Kudzanai; Ezhova, Maria; Mehrkhodavandi, Parisa
Cationic indium catalysts for ring opening polymerization: tuning reactivity with hemilabile ligands
Chemical Science, 2020, 11, 6485-6491
1557865 CIFC44 H59 In N2 O2P 1 21/c 117.5732; 13.8493; 18.4226
90; 117.891; 90		3962.8Goonesinghe, Chatura; Roshandel, Hootan; Diaz, Carlos; Jung, Hyuk-Joon; Nyamayaro, Kudzanai; Ezhova, Maria; Mehrkhodavandi, Parisa
Cationic indium catalysts for ring opening polymerization: tuning reactivity with hemilabile ligands
Chemical Science, 2020, 11, 6485-6491
1557866 CIFC46 H61 In N2 OP 1 21/n 118.402; 13.9008; 18.4542
90; 119.051; 90		4126.7Goonesinghe, Chatura; Roshandel, Hootan; Diaz, Carlos; Jung, Hyuk-Joon; Nyamayaro, Kudzanai; Ezhova, Maria; Mehrkhodavandi, Parisa
Cationic indium catalysts for ring opening polymerization: tuning reactivity with hemilabile ligands
Chemical Science, 2020, 11, 6485-6491
1557867 CIFC45 H60 In N3 OP 1 21/c 118.3804; 13.9887; 18.328
90; 119.839; 90		4087.7Goonesinghe, Chatura; Roshandel, Hootan; Diaz, Carlos; Jung, Hyuk-Joon; Nyamayaro, Kudzanai; Ezhova, Maria; Mehrkhodavandi, Parisa
Cationic indium catalysts for ring opening polymerization: tuning reactivity with hemilabile ligands
Chemical Science, 2020, 11, 6485-6491
1557868 CIFC88 H92 B F24 In N2 O6P -112.616; 13.343; 26.255
80.163; 76.369; 85.869		4229.7Goonesinghe, Chatura; Roshandel, Hootan; Diaz, Carlos; Jung, Hyuk-Joon; Nyamayaro, Kudzanai; Ezhova, Maria; Mehrkhodavandi, Parisa
Cationic indium catalysts for ring opening polymerization: tuning reactivity with hemilabile ligands
Chemical Science, 2020, 11, 6485-6491
1557869 CIFC14 H17 Br O4P b c n21.874; 15.366; 8.915
90; 90; 90		2996.5Yan, Chenting; Takeshita, Masato; Nakatsuji, Jun-ya; Kurosaki, Akihiro; Sato, Kaoko; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke; Adachi, Yohei; Furukawa, Ko; Kishi, Ryohei; Nakano, Masayoshi
Synthesis and properties of hypervalent electron-rich pentacoordinate nitrogen compounds
Chemical Science, 2020, 11, 5082-5088
1557870 CIFC26 H25 Cl8 N O4 SbP 1 21/n 111.6398; 18.4868; 16.2027
90; 109.07; 90		3295.2Yan, Chenting; Takeshita, Masato; Nakatsuji, Jun-ya; Kurosaki, Akihiro; Sato, Kaoko; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke; Adachi, Yohei; Furukawa, Ko; Kishi, Ryohei; Nakano, Masayoshi
Synthesis and properties of hypervalent electron-rich pentacoordinate nitrogen compounds
Chemical Science, 2020, 11, 5082-5088
1557871 CIFC26 H25 Cl2 N O4P b c a18.383; 13.3271; 20.1022
90; 90; 90		4924.9Yan, Chenting; Takeshita, Masato; Nakatsuji, Jun-ya; Kurosaki, Akihiro; Sato, Kaoko; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke; Adachi, Yohei; Furukawa, Ko; Kishi, Ryohei; Nakano, Masayoshi
Synthesis and properties of hypervalent electron-rich pentacoordinate nitrogen compounds
Chemical Science, 2020, 11, 5082-5088
1557872 CIFC32 H33 F6 N O4P -110.089; 11.8293; 13.7884
97.567; 107.754; 95.274		1538.29Yan, Chenting; Takeshita, Masato; Nakatsuji, Jun-ya; Kurosaki, Akihiro; Sato, Kaoko; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke; Adachi, Yohei; Furukawa, Ko; Kishi, Ryohei; Nakano, Masayoshi
Synthesis and properties of hypervalent electron-rich pentacoordinate nitrogen compounds
Chemical Science, 2020, 11, 5082-5088
1557873 CIFC28 H31 N O6P 1 21/c 110.3036; 18.9257; 13.0352
90; 94.843; 90		2532.8Yan, Chenting; Takeshita, Masato; Nakatsuji, Jun-ya; Kurosaki, Akihiro; Sato, Kaoko; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke; Adachi, Yohei; Furukawa, Ko; Kishi, Ryohei; Nakano, Masayoshi
Synthesis and properties of hypervalent electron-rich pentacoordinate nitrogen compounds
Chemical Science, 2020, 11, 5082-5088
1557874 CIFC28 H25 F6 N O4P 1 21/n 111.7241; 12.3047; 18.3432
90; 100.077; 90		2605.4Yan, Chenting; Takeshita, Masato; Nakatsuji, Jun-ya; Kurosaki, Akihiro; Sato, Kaoko; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke; Adachi, Yohei; Furukawa, Ko; Kishi, Ryohei; Nakano, Masayoshi
Synthesis and properties of hypervalent electron-rich pentacoordinate nitrogen compounds
Chemical Science, 2020, 11, 5082-5088
1557875 CIFC30 H33 Cl2 N O4P -111.84; 14.543; 18.231
97.047; 105.059; 102.364		2907.7Yan, Chenting; Takeshita, Masato; Nakatsuji, Jun-ya; Kurosaki, Akihiro; Sato, Kaoko; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke; Adachi, Yohei; Furukawa, Ko; Kishi, Ryohei; Nakano, Masayoshi
Synthesis and properties of hypervalent electron-rich pentacoordinate nitrogen compounds
Chemical Science, 2020, 11, 5082-5088
1557876 CIFC30 H33 Cl8 N O4 SbP 1 21/n 112.156; 15.548; 19.482
90; 90.77; 90		3681.8Yan, Chenting; Takeshita, Masato; Nakatsuji, Jun-ya; Kurosaki, Akihiro; Sato, Kaoko; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke; Adachi, Yohei; Furukawa, Ko; Kishi, Ryohei; Nakano, Masayoshi
Synthesis and properties of hypervalent electron-rich pentacoordinate nitrogen compounds
Chemical Science, 2020, 11, 5082-5088
1557898 CIFC12 H28 B Co F4 N5 O2P b c a13.0883; 14.8329; 19.5325
90; 90; 90		3791.99Das, Sandip; Kulbir,; Ghosh, Somnath; Chandra Sahoo, Subash; Kumar, Pankaj
Nitric oxide monooxygenation (NOM) reaction of cobalt-nitrosyl {Co(NO)}8 to CoII-nitrito {CoII(NO2−)}: base induced hydrogen gas (H2) evolution
Chemical Science, 2020, 11, 5037-5042
1557899 CIFC76 H76 Cl2 F14 N4 Ni2 O2 P2 Sb2P -110.5566; 14.6779; 14.7391
109.074; 108.271; 97.907		1974.9Yang, Jian; Postils, Verònica; Lipschutz, Michael I.; Fasulo, Meg; Raynaud, Christophe; Clot, Eric; Eisenstein, Odile; Tilley, T. Don
Efficient alkene hydrosilation with bis(8-quinolyl)phosphine (NPN) nickel catalysts. The dominant role of silyl-over hydrido-nickel catalytic intermediates
Chemical Science, 2020, 11, 5043-5051
1557900 CIFC30 H26 F3 N3 OP 1 21/n 114.0809; 10.9917; 17.1659
90; 108.846; 90		2514.4Okude, Ryo; Mori, Genki; Yagi, Akiko; Itami, Kenichiro
Programmable synthesis of multiply arylated cubanes through C‒H metalation and arylation
Chemical Science, 2020, 11, 7672-7675
1557901 CIFC42 H34 F9 N OP c c n37.632; 14.8891; 13.0219
90; 90; 90		7296.3Okude, Ryo; Mori, Genki; Yagi, Akiko; Itami, Kenichiro
Programmable synthesis of multiply arylated cubanes through C‒H metalation and arylation
Chemical Science, 2020, 11, 7672-7675
1557902 CIFC34 H42 N2 O2P -113.5226; 14.169; 17.1029
103.45; 107.34; 103.234		2881Okude, Ryo; Mori, Genki; Yagi, Akiko; Itami, Kenichiro
Programmable synthesis of multiply arylated cubanes through C–H metalation and arylation
Chemical Science, 2020, 11, 7672-7675
1557903 CIFC43 H35 F9 N2 OP -19.7571; 10.1037; 19.23
86.6; 88.612; 81.412		1870.97Okude, Ryo; Mori, Genki; Yagi, Akiko; Itami, Kenichiro
Programmable synthesis of multiply arylated cubanes through C‒H metalation and arylation
Chemical Science, 2020, 11, 7672-7675
1557904 CIFC31 H42 N2 O4P 1 21/n 112.9747; 12.3749; 17.7595
90; 101.948; 90		2789.71Okude, Ryo; Mori, Genki; Yagi, Akiko; Itami, Kenichiro
Programmable synthesis of multiply arylated cubanes through C‒H metalation and arylation
Chemical Science, 2020, 11, 7672-7675
1557905 CIFC32 H40 N2 O2P 1 21/n 110.4974; 24.3; 11.3737
90; 109.196; 90		2739.97Okude, Ryo; Mori, Genki; Yagi, Akiko; Itami, Kenichiro
Programmable synthesis of multiply arylated cubanes through C‒H metalation and arylation
Chemical Science, 2020, 11, 7672-7675
1557906 CIFC31 H39 N3 O2P -18.974; 11.737; 14.0121
113.955; 97.7538; 91.349		1331.4Okude, Ryo; Mori, Genki; Yagi, Akiko; Itami, Kenichiro
Programmable synthesis of multiply arylated cubanes through C‒H metalation and arylation
Chemical Science, 2020, 11, 7672-7675
1557907 CIFC29 H37 N3 O2P b c a16.4161; 12.4001; 25.3104
90; 90; 90		5152.2Okude, Ryo; Mori, Genki; Yagi, Akiko; Itami, Kenichiro
Programmable synthesis of multiply arylated cubanes through C‒H metalation and arylation
Chemical Science, 2020, 11, 7672-7675
1557908 CIFC38 H32 Cd N6 O6 S3P c c a19.0673; 26.1197; 15.5005
90; 90; 90		7719.7Doheny, Patrick W.; Clegg, Jack K.; Tuna, Floriana; Collison, David; Kepert, Cameron J.; D'Alessandro, Deanna M.
Quantification of the mixed-valence and intervalence charge transfer properties of a cofacial metal‒organic framework via single crystal electronic absorption spectroscopy
Chemical Science, 2020, 11, 5213-5220
1557909 CIFC26 H16 N4 S2P -15.665; 7.55; 22.845
80.52; 86.53; 88.94		962Doheny, Patrick W.; Clegg, Jack K.; Tuna, Floriana; Collison, David; Kepert, Cameron J.; D'Alessandro, Deanna M.
Quantification of the mixed-valence and intervalence charge transfer properties of a cofacial metal‒organic framework via single crystal electronic absorption spectroscopy
Chemical Science, 2020, 11, 5213-5220
1557923 CIFC44 H30P -19.9378; 9.9882; 17.7699
93.791; 94.905; 98.931		1730.4Curbet, Idriss; Colombel-Rouen, Sophie; Manguin, Romane; Clermont, Anthony; Quelhas, Alexandre; Müller, Daniel S.; Roisnel, Thierry; Baslé, Olivier; Trolez, Yann; Mauduit, Marc
Expedient synthesis of conjugated triynes via alkyne metathesis
Chemical Science, 2020, 11, 4934-4938
1557924 CIFC43 H31 Cl3 Si2P 1 21/n 110.4193; 21.2154; 17.2115
90; 99.801; 90		3749.1Curbet, Idriss; Colombel-Rouen, Sophie; Manguin, Romane; Clermont, Anthony; Quelhas, Alexandre; Müller, Daniel S.; Roisnel, Thierry; Baslé, Olivier; Trolez, Yann; Mauduit, Marc
Expedient synthesis of conjugated triynes via alkyne metathesis
Chemical Science, 2020, 11, 4934-4938
1557925 CIFC34 H36 SiP -18.5423; 10.4335; 16.821
76.313; 77.803; 83.761		1421Curbet, Idriss; Colombel-Rouen, Sophie; Manguin, Romane; Clermont, Anthony; Quelhas, Alexandre; Müller, Daniel S.; Roisnel, Thierry; Baslé, Olivier; Trolez, Yann; Mauduit, Marc
Expedient synthesis of conjugated triynes via alkyne metathesis
Chemical Science, 2020, 11, 4934-4938

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