Crystallography Open Database

Result: there are 688 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)

Searching journal of publication like 'Chemical science' volume of publication is 11

Left arrow Left arrow First | Left arrow Previous 500 | of 2 | Next 500 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
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

Left arrow Left arrow First | Left arrow Previous 500 | of 2 | Next 500 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!
Top of the page
All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.