Crystallography Open Database

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Searching year of publication is 2022

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1566398 CIFC46 H38 F12 Fe N14 P2P -110.2078; 11.4083; 21.4035
97.221; 96.811; 93.568
2447.76Birchall, Lee; Truccolo, Giada; Jackson, Lewis; Shepherd, Helena Jane
Co-crystallisation as a Modular Approach to the Discovery of Spin-Crossover Materials
Chemical Science, 2022
1566399 CIFC42 H34 B2 F8 Fe N14P 1 21/n 110.2076; 18.9941; 22.8634
90; 96.403; 90
4405.2Birchall, Lee; Truccolo, Giada; Jackson, Lewis; Shepherd, Helena Jane
Co-crystallisation as a Modular Approach to the Discovery of Spin-Crossover Materials
Chemical Science, 2022
1566400 CIFC46 H42 F12 Fe N14 P2P 1 21 19.45496; 17.9858; 14.95322
90; 101.545; 90
2491.42Birchall, Lee; Truccolo, Giada; Jackson, Lewis; Shepherd, Helena Jane
Co-crystallisation as a Modular Approach to the Discovery of Spin-Crossover Materials
Chemical Science, 2022
1566401 CIFC42 H34 B2 F8 Fe N14P -110.0861; 10.1542; 21.849
96.262; 96.2; 93.852
2204.26Birchall, Lee; Truccolo, Giada; Jackson, Lewis; Shepherd, Helena Jane
Co-crystallisation as a Modular Approach to the Discovery of Spin-Crossover Materials
Chemical Science, 2022
1566402 CIFC46 H38 F12 Fe N14 P2P -19.8294; 22.3967; 22.3209
79.439; 89.335; 89.19
4829.9Birchall, Lee; Truccolo, Giada; Jackson, Lewis; Shepherd, Helena Jane
Co-crystallisation as a Modular Approach to the Discovery of Spin-Crossover Materials
Chemical Science, 2022
1566403 CIF
HKL
Paper
C14 H18 N6 O5 SP 1 21/c 112.1115; 10.6282; 17.4772
90; 127.723; 90
1779.48Peña Hueso, Adrian; Esparza Ruiz, Adriana; Flores Parra, Angelina
Bis(2-aminobenzimidazolium) sulfate monohydrate
IUCrData, 2022, 7, x220172
1566404 CIFC37 H31 F O5P 1 21 110.9625; 9.5991; 14.075
90; 97.804; 90
1467.4Wu, Mingyue; Han, Zhaobin; Ni, Huanzhen; Wang, Nengzhong; Ding, Kuiling; Lu, Yixin
Phosphine-catalyzed divergent domino processes between γ-substituted allenoates and carbonyl-activated alkenes
Chemical Science, 2022
1566405 CIFC38 H34 O8P 21 21 215.0488; 25.2228; 8.6864
90; 90; 90
3297.1Wu, Mingyue; Han, Zhaobin; Ni, Huanzhen; Wang, Nengzhong; Ding, Kuiling; Lu, Yixin
Phosphine-catalyzed divergent domino processes between γ-substituted allenoates and carbonyl-activated alkenes
Chemical Science, 2022
1566406 CIFC10 H11 Cl F N O2P 21 21 215.1224; 8.268; 24.1637
90; 90; 90
1023.38Yamane, Daiki; Onitsuka, Satsuki; Re, Suyong; Isogai, Hikaru; Hamada, Rui; Hiramoto, Tadanari; Kawanishi, Eiji; Mizuguchi, Kenji; Shindo, Naoya; Ojida, Akio
Selective covalent targeting of SARS-CoV-2 main protease by enantiopure chlorofluoroacetamide.
Chemical science, 2022, 13, 3027-3034
1566407 CIFC22 H18 Cl F7 N4 O2 SP 1 21/n 19.4276; 19.5575; 50.822
90; 93.634; 90
9351.7Yamane, Daiki; Onitsuka, Satsuki; Re, Suyong; Isogai, Hikaru; Hamada, Rui; Hiramoto, Tadanari; Kawanishi, Eiji; Mizuguchi, Kenji; Shindo, Naoya; Ojida, Akio
Selective covalent targeting of SARS-CoV-2 main protease by enantiopure chlorofluoroacetamide.
Chemical science, 2022, 13, 3027-3034
1566408 CIFC15 H16 O2C 1 c 18.7883; 12.6773; 10.4803
90; 99.097; 90
1152.94Wu, Wen-Biao; Mu, Bo-Shuai; Yu, Jin-Sheng; Zhou, Jian
Me2(CH2=CH)SiCN: a bifunctional ethylene equivalent for Diels-Alder reaction based controllable tandem synthesis
Chemical Science, 2022
1566409 CIFC17 H18 Br N OP 1 21/c 119.7377; 9.5738; 7.613
90; 99.09; 90
1420.52Wu, Wen-Biao; Mu, Bo-Shuai; Yu, Jin-Sheng; Zhou, Jian
Me2(CH2=CH)SiCN: a bifunctional ethylene equivalent for Diels-Alder reaction based controllable tandem synthesis
Chemical Science, 2022
1566410 CIFC16 H18 OP 1 21/n 17.2763; 13.1879; 12.6095
90; 94.179; 90
1206.78Wu, Wen-Biao; Mu, Bo-Shuai; Yu, Jin-Sheng; Zhou, Jian
Me2(CH2=CH)SiCN: a bifunctional ethylene equivalent for Diels-Alder reaction based controllable tandem synthesis
Chemical Science, 2022
1566411 CIFC18 H21 N O2P -17.2466; 8.3731; 12.6472
95.047; 96.626; 94.254
756.54Wu, Wen-Biao; Mu, Bo-Shuai; Yu, Jin-Sheng; Zhou, Jian
Me2(CH2=CH)SiCN: a bifunctional ethylene equivalent for Diels-Alder reaction based controllable tandem synthesis
Chemical Science, 2022
1566412 CIFC25 H32 O2P 1 21 112.196; 6.2725; 13.2067
90; 97.53; 90
1001.59Wu, Wen-Biao; Mu, Bo-Shuai; Yu, Jin-Sheng; Zhou, Jian
Me2(CH2=CH)SiCN: a bifunctional ethylene equivalent for Diels-Alder reaction based controllable tandem synthesis
Chemical Science, 2022
1566413 CIFC20 H17 N OP 21 21 216.55952; 7.19955; 33.374
90; 90; 90
1576.11Wu, Wen-Biao; Mu, Bo-Shuai; Yu, Jin-Sheng; Zhou, Jian
Me2(CH2=CH)SiCN: a bifunctional ethylene equivalent for Diels-Alder reaction based controllable tandem synthesis
Chemical Science, 2022
1566414 CIFC20 H22 N4 S2 ZnC 1 2 138.805; 6.6795; 16.442
90; 91.833; 90
4259.6Koskela, Kristopher M.; Quiton, Stephen J.; Sharada, Shaama Mallikarjun; Williams, Travis J.; Brutchey, Richard L.
Kinetics and mechanistic details of bulk ZnO dissolution using a thiol–imidazole system
Chemical Science, 2022
1566415 CIFC92 H120 B20 Co2 Cs2 O4 P4P 1 21/n 112.1327; 17.926; 22.865
90; 103.927; 90
4826.7Keener, Megan; Mattejat, Maxwell; Zheng, Shao-Liang; Wu, Guang; Hayton, Trevor W.; Ménard, Gabriel
Selective electrochemical capture and release of uranyl from aqueous alkali, lanthanide, and actinide mixtures using redox-switchable carboranes
Chemical Science, 2022
1566416 CIFC254 H332 B60 Co4 N7 O14 P12 Th2C 1 2/c 170.509; 17.5517; 23.4008
90; 108.146; 90
27519Keener, Megan; Mattejat, Maxwell; Zheng, Shao-Liang; Wu, Guang; Hayton, Trevor W.; Ménard, Gabriel
Selective electrochemical capture and release of uranyl from aqueous alkali, lanthanide, and actinide mixtures using redox-switchable carboranes
Chemical Science, 2022
1566417 CIFC154 H129 B30 Co3 N8 Nd O6 P6P c c n19.004; 23.285; 36.829
90; 90; 90
16297Keener, Megan; Mattejat, Maxwell; Zheng, Shao-Liang; Wu, Guang; Hayton, Trevor W.; Ménard, Gabriel
Selective electrochemical capture and release of uranyl from aqueous alkali, lanthanide, and actinide mixtures using redox-switchable carboranes
Chemical Science, 2022
1566418 CIFC42 H67 B10 N O2 P2P -111.082; 11.112; 37.623
93.075; 96.139; 101.822
4495Keener, Megan; Mattejat, Maxwell; Zheng, Shao-Liang; Wu, Guang; Hayton, Trevor W.; Ménard, Gabriel
Selective electrochemical capture and release of uranyl from aqueous alkali, lanthanide, and actinide mixtures using redox-switchable carboranes
Chemical Science, 2022
1566419 CIFC154 H204 B30 Co3 N8 O6 P6 SmP 1 21/c 119.0168; 23.3163; 36.48
90; 90.563; 90
16174.5Keener, Megan; Mattejat, Maxwell; Zheng, Shao-Liang; Wu, Guang; Hayton, Trevor W.; Ménard, Gabriel
Selective electrochemical capture and release of uranyl from aqueous alkali, lanthanide, and actinide mixtures using redox-switchable carboranes
Chemical Science, 2022
1566420 CIFC25 H33 N O6 S SiP -19.1233; 11.1747; 13.3729
92.8956; 109.796; 90.2891
1280.81Bunyamin, Amanda; Hua, Carol; Polyzos, Anastasios; Priebbenow, Daniel
Intramolecular Photochemical [2+1]-Cycloadditions of Nucleophilic Siloxy Carbenes
Chemical Science, 2022
1566421 CIFC16 H22 O4 SiP 1 21/c 18.6905; 16.3296; 11.4842
90; 98.168; 90
1613.22Bunyamin, Amanda; Hua, Carol; Polyzos, Anastasios; Priebbenow, Daniel
Intramolecular Photochemical [2+1]-Cycloadditions of Nucleophilic Siloxy Carbenes
Chemical Science, 2022
1566422 CIFC23 H29 N O6 S SiC 1 2/c 145.775; 5.703; 18.31
90; 99.58; 90
4713.3Bunyamin, Amanda; Hua, Carol; Polyzos, Anastasios; Priebbenow, Daniel
Intramolecular Photochemical [2+1]-Cycloadditions of Nucleophilic Siloxy Carbenes
Chemical Science, 2022
1566423 CIFC23 H29 N O5 S SiP 1 21 18.92; 18.338; 14.723
90; 99.61; 90
2374.5Bunyamin, Amanda; Hua, Carol; Polyzos, Anastasios; Priebbenow, Daniel
Intramolecular Photochemical [2+1]-Cycloadditions of Nucleophilic Siloxy Carbenes
Chemical Science, 2022
1566424 CIF
HKL
Paper
C23 H19 N O5P 1 21/n 19.7089; 14.351; 14.2749
90; 106.946; 90
1902.6Surya Prakash Rao, H.; M, Prabakaran; Muthukumaran, Jayaraman
Ethyl 10-cyano-7-hydroxy-6-oxo-3-phenyl-8,9,10,10a-tetrahydro-6<i>H</i>-benzo[<i>c</i>]chromene-10-carboxylate
IUCrData, 2022, 7, x220199
1566425 CIF
HKL
Paper
C10 H13 Cl N3 O3 PP 1 21/c 111.5857; 7.0616; 16.6118
90; 108.222; 90
1290.92Chachlaki, Elpiniki; Choquesillo-Lazarte, Duane; Demadis, Konstantinos D.
5-Phenyl-3-(2-phosphonoethyl)-1,2,3-triazol-1-ium chloride
IUCrData, 2022, 7, x220189
1566426 CIFC21 H17 F3 O3 S2P 1 21/n 18.8793; 13.4651; 16.2393
90; 94.659; 90
1935.17Zhang, Qiu-Chi; Xue, Xiaoping; Hong, Biqiong; Gu, Zhenhua
Torsional Strain Inversed Chemoselectivity in Pd-Catalyzed Atroposelective Carboxylation Reaction of Dibenzothiophenium
Chemical Science, 2022
1566427 CIFC30 H29 N O SP 31 2 110.0094; 10.0094; 42.946
90; 90; 120
3726.2Zhang, Qiu-Chi; Xue, Xiaoping; Hong, Biqiong; Gu, Zhenhua
Torsional Strain Inversed Chemoselectivity in Pd-Catalyzed Atroposelective Carboxylation Reaction of Dibenzothiophenium
Chemical Science, 2022
1566428 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566429 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566430 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566431 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566432 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566433 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566434 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566435 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566436 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566437 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566438 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566439 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566440 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566441 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566442 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566443 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566444 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566445 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566446 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566447 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566448 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566449 CIFC3 H7 N O2P 21 21 215.9279; 12.2597; 5.7939
90; 90; 90
421.07Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566450 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566451 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566452 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566453 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566454 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566456 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566457 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566458 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566459 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566460 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566461 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566462 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566463 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566464 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566465 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566466 CIFC13 H11 N O5P 21 21 215.3386; 9.9878; 22.3493
90; 90; 90
1191.68Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566467 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566468 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566469 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566470 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566471 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566472 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566473 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566474 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566475 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566476 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566477 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566478 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566479 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566480 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566481 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566482 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566483 CIFC8 H18 Mg O14P 1 21/c 110.195; 11.759; 6.6206
90; 103.67; 90
771.2Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566484 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566485 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566486 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566487 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566488 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566489 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566490 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566491 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566492 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566493 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566494 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566495 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566496 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566497 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566498 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566499 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566500 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566501 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566502 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566503 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566504 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566505 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566506 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566507 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566508 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566509 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566510 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566511 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566512 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566513 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566514 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566515 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566516 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566517 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566518 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566519 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566520 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566521 CIFC64 H86 Cl2 N6 O6P 3120.2894; 20.2894; 13.6577
90; 90; 120
4869.1Ding, Yanjun; Alimi, Lukman O.; Du, Jing; Hua, Bin; Dey, Avishek; Yu, Pei; Khashab, Niveen M.
Pillar[3]trianglamines: deeper cavity triangular macrocycles for selective hexene isomer separation
Chemical Science, 2022
1566522 CIFC69 H96 N6 O6R 3 :H20.366; 20.366; 13.791
90; 90; 120
4953.79Ding, Yanjun; Alimi, Lukman O.; Du, Jing; Hua, Bin; Dey, Avishek; Yu, Pei; Khashab, Niveen M.
Pillar[3]trianglamines: deeper cavity triangular macrocycles for selective hexene isomer separation
Chemical Science, 2022
1566523 CIFC66 H90 N6 O6R 3 :H20.3338; 20.3338; 13.7372
90; 90; 120
4918.88Ding, Yanjun; Alimi, Lukman O.; Du, Jing; Hua, Bin; Dey, Avishek; Yu, Pei; Khashab, Niveen M.
Pillar[3]trianglamines: deeper cavity triangular macrocycles for selective hexene isomer separation
Chemical Science, 2022
1566524 CIFC74 H104 Ga2 N8 Sb2P -110.4552; 11.9732; 14.9227
93.2189; 97.3354; 107.995
1753.06Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566525 CIFC66 H102 Ga2 N4 O2 Sb2 SiC 1 2/c 159.557; 11.8135; 21.011
90; 108.078; 90
14053Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566526 CIFC78 H116 Ga2 N6 Sb2 SiP -110.919; 14.343; 26.014
83.994; 78.718; 88.053
3973Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566527 CIFC64.5 H98 Cl2 Ga2 N4 Sb2 SiP 1 21/c 119.7547; 10.5843; 33.512
90; 96.97; 90
6955.2Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566528 CIFC71.5 H103 Ga2 N7 Sb2P 1 21/c 119.9634; 12.5667; 29.4717
90; 109.028; 90
6989.7Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566529 CIFC65 H103 Ga2 N7 Sb2 SiP 1 21 110.7967; 21.163; 15.164
90; 96.979; 90
3439.2Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566530 CIFC79 H117 Ga2 N7 Sb2P 1 21/n 110.9672; 45.894; 15.2335
90; 94.502; 90
7643.8Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566531 CIFC72.5 H102 F3 Ga2 N7 Sb2P -110.6581; 12.7136; 27.5744
102.129; 92.993; 98.869
3595.5Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566532 CIFC78 H119 F3 Ga2 N7 Sb2P 1 21/n 112.1758; 27.211; 24.248
90; 99.805; 90
7916.4Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566533 CIFC68 H110 Ga2 N8 Sb2 Si2P 1 21/n 111.889; 18.46; 33.366
90; 96.36; 90
7278Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566534 CIFC81 H112 Ga2 N8 Sb2P -111.6222; 17.8727; 19.5796
108.099; 90.076; 93.817
3856.2Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566535 CIFC77 H110 Ga2 N8 Sb2P 1 21/c 113.6969; 28.763; 20.711
90; 94.587; 90
8133.3Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566536 CIFC84 H108 Ga2 N6 Sb4P -112.0886; 12.3645; 14.1831
86.028; 75.849; 74.786
1983.54Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566537 CIFC44 H45 F6 N6 P Ru2P 1 21/n 112.6141; 12.2041; 27.463
90; 98.846; 90
4177.47Bellini, Marco; Bösken, Jonas; Bartoli, Francesco; Miller, Hamish; Thöny, Debora; Poggini, Lorenzo; Wörle, Michael; Oberhauser, Werner; Gamboa-Carballo, Juan José; Lavacchi, Alessandro; Krumeich, Frank; Grützmacher, Hansjörg; Vizza, Francesco
Remarkable Stability of a Molecular Ruthenium Complex in PEM Water Electrolysis
Chemical Science, 2022
1566538 CIFC36 H35 B F4 N2 O Ru2P -19.5469; 10.1082; 17.4002
78.96; 76.819; 85.773
1603.87Bellini, Marco; Bösken, Jonas; Bartoli, Francesco; Miller, Hamish; Thöny, Debora; Poggini, Lorenzo; Wörle, Michael; Oberhauser, Werner; Gamboa-Carballo, Juan José; Lavacchi, Alessandro; Krumeich, Frank; Grützmacher, Hansjörg; Vizza, Francesco
Remarkable Stability of a Molecular Ruthenium Complex in PEM Water Electrolysis
Chemical Science, 2022
1566539 CIFC37 H33 NC 1 2/c 135.402; 9.1778; 17.961
90; 110.844; 90
5453.8Duan, Shengzu; Zi, Yujin; Wang, Lingling; Cong, Jielun; Chen, Wen; Li, Minyan; Zhang, Hongbin; Yang, Xiaodong; Walsh, Patrick
α-Branched Amines through Radical Coupling with 2-Azaallyl Anions, Redox Active Esters and Alkenes
Chemical Science, 2022
1566540 CIFC21 H15 Cl F3 N3 O2P 1 21/n 115.287; 15.859; 17.629
90; 114.523; 90
3888Yang, Hefei; Wang, Le-Cheng; Zhang, Yu; Zheng, Dongling; Chen, Zhengkai; Wu, Xiao-Feng
Controllable access to trifluoromethyl-containing indoles and indolines: Palladium-catalyzed regioselective functionalization of unactivated alkenes with trifluoroacetimidoyl chlorides
Chemical Science, 2022
1566541 CIFC22 H15 F3 N3 OP 1 21/c 115.6657; 33.014; 7.2436
90; 98.651; 90
3703.7Yang, Hefei; Wang, Le-Cheng; Zhang, Yu; Zheng, Dongling; Chen, Zhengkai; Wu, Xiao-Feng
Controllable access to trifluoromethyl-containing indoles and indolines: Palladium-catalyzed regioselective functionalization of unactivated alkenes with trifluoroacetimidoyl chlorides
Chemical Science, 2022
1566542 CIFC492 H528 N48 O60P 3 c 132.5182; 32.5182; 51.424
90; 90; 120
47092Xu, Ning; Su, Kongzhao; M. El-Sayed, El-Sayed; Ju, Zhanfeng; Yuan, Daqiang
Chiral Proline-Substituted Porous Organic Cages in Asymmetric Organocatalysis
Chemical Science, 2022
1566543 CIFC280 H320 N32 O40P 128.4101; 30.2731; 32.7364
82.444; 81.795; 63.273
24818Xu, Ning; Su, Kongzhao; M. El-Sayed, El-Sayed; Ju, Zhanfeng; Yuan, Daqiang
Chiral Proline-Substituted Porous Organic Cages in Asymmetric Organocatalysis
Chemical Science, 2022
1566544 CIFC28 H28 Br Cl Cu N6 O2P 1 21/c 116.1127; 8.9758; 19.2463
90; 103.825; 90
2702.85Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566545 CIFC28 H28 Cl Cu N6 O1.5P 1 21/c 115.0147; 34.2629; 10.2999
90; 107.565; 90
5051.7Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566546 CIFC32 H39 Cl3 Cu N8 O3P 17.2313; 9.2604; 14.1201
78.16; 77.214; 70.423
859.9Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566547 CIFC60 H63 Br2 Cl N14 Ni O4P -19.7632; 15.6735; 19.622
87.172; 75.925; 85.319
2901.4Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566548 CIFC33 H39 Cl Cu N8 O3C 1 2/c 137.667; 10.5159; 19.22
90; 118.948; 90
6661.9Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566549 CIFC26 H23 Br N6 OP -112.22; 12.7328; 16.424
76.485; 82.598; 67.698
2296.6Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566550 CIFC12 H16 N2 O2P -17.7366; 7.9072; 10.7395
99.872; 102.594; 113.64
562.21Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566551 CIFC17 H29 N OP 1 21 17.18; 4.628; 48.944
90; 92.55; 90
1624.8Wu, Zhen-Long; Zhang, Wei-Yan; Zhong, Jin-Cheng; Huang, Xiao-Jun; Xu, Wei; Chen, Min-Feng; Weng, Shao-Quan; Zhang, Dong-Mei; Che, Chun-Tao; Ye, Wen-Cai; Wang, Ying
Angiogenesis-Inhibitory Piperidine Alkaloids from the Leaves of <i>Microcos paniculata</i>.
Journal of natural products, 2022, 85, 375-383
1566552 CIFC17 H31 N O3P 1 21 112.37896; 5.01515; 13.9105
90; 99.1891; 90
852.51Wu, Zhen-Long; Zhang, Wei-Yan; Zhong, Jin-Cheng; Huang, Xiao-Jun; Xu, Wei; Chen, Min-Feng; Weng, Shao-Quan; Zhang, Dong-Mei; Che, Chun-Tao; Ye, Wen-Cai; Wang, Ying
Angiogenesis-Inhibitory Piperidine Alkaloids from the Leaves of <i>Microcos paniculata</i>.
Journal of natural products, 2022, 85, 375-383
1566553 CIFC16 H27 N OP 21 21 215.1556; 9.493; 31.8376
90; 90; 90
1558.2Wu, Zhen-Long; Zhang, Wei-Yan; Zhong, Jin-Cheng; Huang, Xiao-Jun; Xu, Wei; Chen, Min-Feng; Weng, Shao-Quan; Zhang, Dong-Mei; Che, Chun-Tao; Ye, Wen-Cai; Wang, Ying
Angiogenesis-Inhibitory Piperidine Alkaloids from the Leaves of <i>Microcos paniculata</i>.
Journal of natural products, 2022, 85, 375-383
1566554 CIFC16 H25 N OP 21 21 215.0809; 9.5095; 31.1268
90; 90; 90
1503.95Wu, Zhen-Long; Zhang, Wei-Yan; Zhong, Jin-Cheng; Huang, Xiao-Jun; Xu, Wei; Chen, Min-Feng; Weng, Shao-Quan; Zhang, Dong-Mei; Che, Chun-Tao; Ye, Wen-Cai; Wang, Ying
Angiogenesis-Inhibitory Piperidine Alkaloids from the Leaves of <i>Microcos paniculata</i>.
Journal of natural products, 2022, 85, 375-383
1566555 CIFC21 H22 O8 SP 1 21/c 19.3577; 25.184; 9.0558
90; 96.873; 90
2118.8Xu, Yanchao; Liu, Wen; Wu, Dan; He, Wenwen; Zuo, Mingxing; Wang, Dongyang; Fu, Peng; Wang, Liping; Zhu, Weiming
Sulfur-Containing Phenolic Compounds from the Cave Soil-Derived <i>Aspergillus fumigatus</i> GZWMJZ-152.
Journal of natural products, 2022, 85, 433-440
1566556 CIFC9 H9 N O3 SP 21 21 218.2204; 8.5993; 13.4964
90; 90; 90
954.06Xu, Yanchao; Liu, Wen; Wu, Dan; He, Wenwen; Zuo, Mingxing; Wang, Dongyang; Fu, Peng; Wang, Liping; Zhu, Weiming
Sulfur-Containing Phenolic Compounds from the Cave Soil-Derived <i>Aspergillus fumigatus</i> GZWMJZ-152.
Journal of natural products, 2022, 85, 433-440
1566557 CIFC19 H20 O8 SP -18.1509; 10.0095; 12.0777
106.945; 90.36; 90.567
942.51Xu, Yanchao; Liu, Wen; Wu, Dan; He, Wenwen; Zuo, Mingxing; Wang, Dongyang; Fu, Peng; Wang, Liping; Zhu, Weiming
Sulfur-Containing Phenolic Compounds from the Cave Soil-Derived <i>Aspergillus fumigatus</i> GZWMJZ-152.
Journal of natural products, 2022, 85, 433-440
1566558 CIFC21 H22 O9 SP -18.1167; 9.0623; 15.8947
86.54; 87.286; 65.417
1060.92Xu, Yanchao; Liu, Wen; Wu, Dan; He, Wenwen; Zuo, Mingxing; Wang, Dongyang; Fu, Peng; Wang, Liping; Zhu, Weiming
Sulfur-Containing Phenolic Compounds from the Cave Soil-Derived <i>Aspergillus fumigatus</i> GZWMJZ-152.
Journal of natural products, 2022, 85, 433-440
1566559 CIFBi O2P 1 21/m 111.6212; 3.4067; 7.3247
90; 99.9889; 90
285.589Feng, Xuezhen; Zou, Haiyuan; Zheng, Renji; Wei, Wenfei; Wang, Ranhao; Zou, Wensong; Lim, Gukhyun; Hong, Jihyun; Duan, Lele; Chen, Hong
Bi<sub>2</sub>O<sub>3</sub>/BiO<sub>2</sub> Nanoheterojunction for Highly Efficient Electrocatalytic CO<sub>2</sub> Reduction to Formate.
Nano letters, 2022, 22, 1656-1664
1566560 CIF
HKL
Paper
C6 H13 Cl6 N3 O2 SnP -17.4224; 7.4518; 8.4986
105.726; 97.426; 112.383
403.85Ghallab, Rochdi; Bougueria, Hassiba; Merazig, Hocine
4-Amidinopyridinium hexachloridostannate(IV) dihydrate
IUCrData, 2022, 7, x220195
1566561 CIF
HKL
Paper
C10 H14 Cl10 N4 O2 SnP -17.4624; 8.4715; 10.1324
101.434; 90.043; 107.554
597.34Ghallab, Rochdi; Bougueria, Hassiba; Merazig, Hocine
Bis(2-amino-3,5-dichloropyridinium) hexachloridostannate(IV) dihydrate
IUCrData, 2022, 7, x220191
1566562 CIFC34 H38 Au2 O4 P2 S2P 1 21/n 111.7462; 39.197; 15.6529
90; 107.882; 90
6858.7Duminy, Welni; Pillay, Michael N.; van Zyl, Werner E.
Silver(I) and Gold(I) Monothiocarbonate Complexes: Synthesis, Structure, Luminescence
Inorganics, 2022, 10, 19
1566563 CIFC17 H22 O10P 21 21 217.776; 8.6993; 26.8196
90; 90; 90
1814.23Chen, Jianwei; Chen, Jun; Wang, Siqi; Bao, Xiaoze; Li, Songwei; Wei, Bin; Zhang, Huawei; Wang, Hong
Amycolachromones A–F, Isolated from a Streptomycin-Resistant Strain of the Deep-Sea Marine Actinomycete Amycolatopsis sp. WP1
Marine Drugs, 2022, 20, 162
1566564 CIFC1.21 H1.21 O0.6P 21 21 217.776; 8.6993; 26.8196
90; 90; 90
1814.23Chen, Jianwei; Chen, Jun; Wang, Siqi; Bao, Xiaoze; Li, Songwei; Wei, Bin; Zhang, Huawei; Wang, Hong
Amycolachromones A–F, Isolated from a Streptomycin-Resistant Strain of the Deep-Sea Marine Actinomycete Amycolatopsis sp. WP1
Marine Drugs, 2022, 20, 162
1566565 CIFC13.25 H13.25 O13.25P 21 21 217.776; 8.6993; 26.8196
90; 90; 90
1814.23Chen, Jianwei; Chen, Jun; Wang, Siqi; Bao, Xiaoze; Li, Songwei; Wei, Bin; Zhang, Huawei; Wang, Hong
Amycolachromones A–F, Isolated from a Streptomycin-Resistant Strain of the Deep-Sea Marine Actinomycete Amycolatopsis sp. WP1
Marine Drugs, 2022, 20, 162
1566566 CIFC17 H22 O10P 21 21 217.776; 8.6993; 26.8196
90; 90; 90
1814.23Chen, Jianwei; Chen, Jun; Wang, Siqi; Bao, Xiaoze; Li, Songwei; Wei, Bin; Zhang, Huawei; Wang, Hong
Amycolachromones A–F, Isolated from a Streptomycin-Resistant Strain of the Deep-Sea Marine Actinomycete Amycolatopsis sp. WP1
Marine Drugs, 2022, 20, 162
1566567 CIFC36 H31 N5 OP -17.8563; 9.2517; 21.803
95.923; 98.136; 96.538
1547.1Guillon, Jean; Savrimoutou, Solène; Albenque-Rubio, Sandra; Pinaud, Noël; Moreau, Stéphane; Desplat, Vanessa
Synthesis, Crystal Structure and Anti-Leukemic Activity of 1,3-Dihydro-1-{1-[4-(4-phenylpyrrolo[1,2-a]quinoxalin-3-yl)benzyl]piperidin-4-yl}-2H-benzimidazol-2-one
Molbank, 2022, 2022, M1333
1566568 CIFC80 H110 Cu4 O2 P6P 1 21/n 117.127; 19.946; 23.841
90; 105.715; 90
7840Dannenberg, Steven G.; Waterman, Rory
Cyclo-Tetrakis(μ-diphenylphosphido)-1,5-bis(tri-tert-butylphosphine)-Tetracopper
Molbank, 2022, 2022, M1334
1566569 CIFC28 H37 Cl4 I N2 SP 1 21/n 110.5912; 18.7089; 16.071
90; 102.093; 90
3113.8Saab, Marina; Nahra, Fady; Van Hecke, Kristof
Charge-Transfer Adducts of Chalcogenourea Derivatives of N-Heterocyclic Carbenes with Iodine Monochloride
Molbank, 2022, 2022, M1344
1566570 CIFC30 H42 Cl3 I N2 SeP 1 21/n 19.741; 16.9218; 19.8068
90; 97.399; 90
3237.67Saab, Marina; Nahra, Fady; Van Hecke, Kristof
Charge-Transfer Adducts of Chalcogenourea Derivatives of N-Heterocyclic Carbenes with Iodine Monochloride
Molbank, 2022, 2022, M1344
1566571 CIFC20 H24 N6 O4P -19.6243; 9.859; 12.5952
68.645; 72.467; 75.23
1047.06Lopes, Susana M. M.; Lemos, Américo; Paixão, José A.; Pinho e Melo, Teresa M. V. D.
Ethyl 7-Acetyl-8a-methyl-3-(1-phenyl-1H-tetrazol-5-yl)-1,4,4a,5,6,8a-hexahydro-7H-pyrano[2,3-c]pyridazine-1-carboxylate
Molbank, 2022, 2022, M1338
1566572 CIFC26 H31 N O12P 1 21 110.1989; 8.7455; 15.8721
90; 99.068; 90
1398.01Fitzgerald, Liam S.; O’Malley, Ciaran; Murphy, Paul V.
(1R,2R,3S,4R)-1-(Acetylamino)-2,4,5-tris(acetyloxy)-1-((2S)-4-(benzyloxy)-5-oxo-2,5-dihydrofuran-2-yl)pentan-3-yl Acetate
Molbank, 2022, 2022, M1337
1566573 CIFC13 H13 Cl N2P 1 21/c 19.4547; 16.2237; 7.9004
90; 104.169; 90
1174.98Adeleke, Adesola A.; Omondi, Bernard
Crystal Structure of a Chiral Sec-Amine, 4-Chloro-N-(1-(pyridin-2-yl)ethyl)aniline
Molbank, 2022, 2022, M1335
1566574 CIFC11 H10 N4 O3C 1 c 123.794; 5.347; 8.9367
90; 96.216; 90
1130.3Pokhodylo, Nazariy T.; Slyvka, Yuriy I.; Goreshnik, Evgeny A.; Obushak, Mykola D.
Ethyl 5-Formyl-1-(pyridin-3-yl)-1H-1,2,3-triazole-4-carboxylate: Synthesis, Crystal Structure, Hirshfeld Surface Analysis, and DFT Calculation
Molbank, 2022, 2022, M1340
1566575 CIFC14 H16 Co N2 O12P 1 21/n 16.9863; 23.7443; 10.6564
90; 100.456; 90
1738.38Xia, Zhengyao; Li, Yan; Ji, Cheng; Jiang, Yucheng; Ma, Chunlan; Gao, Ju; Zhang, Jinlei
Slow-Relaxation Behavior of a Mononuclear Co(II) Complex Featuring Long Axial Co-O Bond.
Nanomaterials (Basel, Switzerland), 2022, 12, 707
1566576 CIFC70 H81 B N2 O4P 1 21/c 125.398; 21.296; 11.522
90; 96.49; 90
6192Han, Jianmei; Huang, Zhongyan; Miao, Jingsheng; Qiu, Yuntao; Xie, Ziyang; Yang, Chuluo
Narrowband blue emission with insensitivity to the doping concentration from an oxygen-bridged triarylboron-based TADF emitter: nondoped OLEDs with a high external quantum efficiency up to 21.4%
Chemical Science, 2022
1566577 CIFC20 H46 Cl N2 P2 ReP 1 21/n 18.5852; 23.581; 12.2292
90; 92.515; 90
2473.39Connor, Gannon P.; Delony, Daniel; Weber, Jeremy E.; Mercado, Brandon Q.; Curley, Julia B.; Schneider, Sven; Mayer, James M.; Holland, Patrick L.
Facile conversion of ammonia to a nitride in a rhenium system that cleaves dinitrogen
Chemical Science, 2022
1566578 CIFC54 H67 B Cl F24 N3 O0.5 P2 ReP -112.2681; 15.3208; 17.9247
92.777; 109.357; 97.022
3140.5Connor, Gannon P.; Delony, Daniel; Weber, Jeremy E.; Mercado, Brandon Q.; Curley, Julia B.; Schneider, Sven; Mayer, James M.; Holland, Patrick L.
Facile conversion of ammonia to a nitride in a rhenium system that cleaves dinitrogen
Chemical Science, 2022
1566579 CIFC14 H22 OP 4110.0087; 10.0087; 12.7456
90; 90; 90
1276.78Pan, Aaron; Chojnacka, Maja; Crowley, Robert; Göttemann, Lucas; Haines, Brandon E.; Kou, Kevin G. M.
Synergistic Brønsted/Lewis acid catalyzed aromatic alkylation with unactivated tertiary alcohols or di-tert-butylperoxide to synthesize quaternary carbon centers
Chemical Science, 2022
1566580 CIFC261 H476 Ag55 Cu3 F3 Mo8 O38 S43P -123.3674; 23.7497; 38.3998
73.33; 75.236; 73.633
19233.6Gao, Jin-Ping; Qi, Zhikai; Zhang, Fu-Qiang; Zhang, Xian-Ming
In situ insertion of copper to form heteroanionic D3h-symmetric [Cu3Mo8O32]10− for a templated Ag55 nanocluster
Nanoscale, 2022
1566581 CIF
Paper
C68.39 H67.65 Cl6 N12 O4 Zn3C 1 2/c 133.3132; 14.4948; 31.7714
90; 102.245; 90
14992.4Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566582 CIFC68.62 H68.92 Cl6 N12 O4 Zn3C 1 2/c 133.306; 14.488; 31.8026
90; 102.247; 90
14996.7Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566583 CIFC54.5 H43 I6 N12 O4 Zn3C 1 2/c 134.4866; 14.9746; 31.0009
90; 101.933; 90
15663.6Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566584 CIFC55 H42 I6 N12 O4 Zn3C 1 2/c 134.4862; 15.0052; 31.125
90; 101.958; 90
15756.8Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566585 CIFC63 H78 I6 N12 Zn3C 1 2/c 134.5713; 15.1587; 29.5198
90; 100.649; 90
15203.6Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566586 CIFC64.69 H81.39 I6 N12 Zn3C 1 2/c 134.595; 15.1725; 29.535
90; 100.647; 90
15235.8Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566587 CIFC25 H21 F3 N2 O3 SP 1 21/c 115.2479; 19.58181; 16.7407
90; 116.095; 90
4488.95Dai, Yating; Liang, Shuangshuang; Zeng, Guangkuo; Huang, Hongchun; Zhao, Xiaowei; Cao, Shanshan; Jiang, Zhiyong
Asymmetric [3 + 2] photocycloadditions of cyclopropylamines with electron-rich and electron-neutral olefins
Chemical Science, 2022
1566588 CIFC36 H32 F3 N O5 SC 1 2 129.3277; 7.49483; 18.2663
90; 124.382; 90
3313.6Dai, Yating; Liang, Shuangshuang; Zeng, Guangkuo; Huang, Hongchun; Zhao, Xiaowei; Cao, Shanshan; Jiang, Zhiyong
Asymmetric [3 + 2] photocycloadditions of cyclopropylamines with electron-rich and electron-neutral olefins
Chemical Science, 2022
1566589 CIFC33 H34 Cl N O2P 1 21 111.1324; 7.5493; 16.7445
90; 90.526; 90
1407.18Dai, Yating; Liang, Shuangshuang; Zeng, Guangkuo; Huang, Hongchun; Zhao, Xiaowei; Cao, Shanshan; Jiang, Zhiyong
Asymmetric [3 + 2] photocycloadditions of cyclopropylamines with electron-rich and electron-neutral olefins
Chemical Science, 2022
1566590 CIFC30 H29 Cl N2 O3P 21 21 2112.3663; 16.7129; 25.3786
90; 90; 90
5245.17Dai, Yating; Liang, Shuangshuang; Zeng, Guangkuo; Huang, Hongchun; Zhao, Xiaowei; Cao, Shanshan; Jiang, Zhiyong
Asymmetric [3 + 2] photocycloadditions of cyclopropylamines with electron-rich and electron-neutral olefins
Chemical Science, 2022
1566591 CIFC25 H25 O2 PP 21 21 215.89107; 16.00327; 22.3169
90; 90; 90
2103.96Zhang, Ya-Qian; Zhang, Qingwei; Han, Xue-Yu; Wu, Yue; Qi, Peng-Jia; Zhang, Qing
Ni-Catalyzed Asymmetric Hydrophosphinylation of Conjugated Enynes and Mechanistic Studies
Chemical Science, 2022
1566592 CIFC23 H22 O3 SP 17.2748; 12.2905; 12.5063
63.599; 79.446; 75.302
965.6Li, Yanjun; Liou, Yan-Cheng; Chen, Xinran; Ackermann, Lutz
Thioether-enabled palladium-catalyzed atroposelective C–H olefination for N−C and C−C axial chirality
Chemical Science, 2022
1566593 CIFC20 H20 N2 O SP 1 21 111.0831; 6.8389; 12.0729
90; 109.142; 90
864.48Li, Yanjun; Liou, Yan-Cheng; Chen, Xinran; Ackermann, Lutz
Thioether-enabled palladium-catalyzed atroposelective C–H olefination for N−C and C−C axial chirality
Chemical Science, 2022
1566594 CIF
HKL
Paper
C15 H26 I N3 O6P 1 21 110.816; 7.0106; 13.169
90; 106.833; 90
955.8Lambrecht, Sina; Villinger, Alexander; Jopp, Stefan
1-(Methyl-α-<small>D</small>-glucopyranosid-6-yl)-3-vinylimidazolium iodide dimethylformamide monosolvate
IUCrData, 2022, 7, x220265
1566595 CIF
HKL
Paper
C77 H83 Cl4 K Mn N6 O8 SP b c a19.5585; 24.7224; 29.8538
90; 90; 90
14435.3Yuan, Yiwen; Li, Jianfeng
([2.2.2]Cryptand)potassium (4-methylbenzenethiolato)[5,10,15,20-tetrakis(4-chlorophenyl)porphyrinato]manganate(II) tetrahydrofuran disolvate
IUCrData, 2022, 7, x220241
1566596 CIF
HKL
Paper
C17 H15 B F4 N2P 1 21/n 111.426; 9.0735; 15.5434
90; 102.118; 90
1575.54Welton, Claire E.; Nesterov, Vladimir N.; Smucker, Bradley W.
1-(2-Methylphenyl)-4,4'-bipyridin-1-ium tetrafluoridoborate
IUCrData, 2022, 7, x220248
1566597 CIFC28 H24 O6 S2P 21 21 219.2608; 14.3014; 18.9339
90; 90; 90
2507.65Hu, Linfeng; Li, Jinzhao; Zhang, Yongyan; Feng, Xiaoming; Liu, Xiaohua
Enantioselective [1,2]-Stevens Rearrangement of Thiosulfonates to Construct Dithio-Substituted Quaternary Carbon Centers
Chemical Science, 2022
1566598 CIFC33 H43 Cl2 Cr N2 O2P -116.326; 16.389; 16.464
70.953; 89.935; 71.859
3932.2Tian, Jiliang; Zhang, Xingwang; Liu, Shaofeng; Li, Zhibo
Chromium complexes supported by NNO-tridentate ligands: an unprecedented activity with the requirement of a small amount of MAO
Polymer Chemistry, 2022, 13, 1852-1860
1566599 CIFC31 H37 Cl2 Cr F2 N2 O2P 1 21/c 114.4764; 14.5398; 15.5208
90; 109.539; 90
3078.75Tian, Jiliang; Zhang, Xingwang; Liu, Shaofeng; Li, Zhibo
Chromium complexes supported by NNO-tridentate ligands: an unprecedented activity with the requirement of a small amount of MAO
Polymer Chemistry, 2022, 13, 1852-1860
1566600 CIFC36 H48 Ca Gd K O3P 1 21/c 19.2772; 13.9703; 26.2056
90; 90.079; 90
3396.4Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566601 CIFC36 H48 Ca Er K O3P 1 21/c 19.2555; 13.9514; 26.113
90; 90.709; 90
3371.6Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566602 CIFC36 H48 Ca Dy K O3P 1 21/c 19.2628; 13.9533; 26.1417
90; 90.377; 90
3378.7Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566603 CIFC36 H48 Ca Ho K O3P 1 21/c 19.2613; 13.9568; 26.1226
90; 90.566; 90
3376.4Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566604 CIFC36 H48 Ca K O3 TmP 1 21/c 19.2649; 13.9648; 26.111
90; 90.8583; 90
3377.9Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566605 CIFC36 H48 Ca K O3 TbP 1 21/c 19.2738; 13.9561; 26.155
90; 90.302; 90
3385.1Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566606 CIFC36 H48 Ca K O3 YbP 1 21/c 19.2602; 13.9561; 26.1046
90; 90.935; 90
3373.2Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566607 CIFC92 H166 Fe N4 O28 Si16P 21 21 2116.2474; 17.2899; 46.6858
90; 90; 90
13114.8Zong, Zhaohui; Hao, Aiyou; Xing, Pengyao; Zhao, Yanli
Chiral Molecular Nanosilicas
Chemical Science, 2022
1566608 CIFC92 H182 Fe N4 O32 Si16P 1 21 116.9205; 17.5657; 21.7093
90; 90.98; 90
6451.5Zong, Zhaohui; Hao, Aiyou; Xing, Pengyao; Zhao, Yanli
Chiral Molecular Nanosilicas
Chemical Science, 2022
1566609 CIFC76.5 Fe N4 O27.5 S2 Si16I 1 2 137.4731; 17.2234; 42.6209
90; 103.053; 90
26797.4Zong, Zhaohui; Hao, Aiyou; Xing, Pengyao; Zhao, Yanli
Chiral Molecular Nanosilicas
Chemical Science, 2022
1566610 CIFCl Ga6 K3 Mn2 S12P 3 1 c10.9208; 10.9208; 6.1774
90; 90; 120
638.04Liu, Bin-Wen; Pei, Shao-Min; Jiang, Xiao-Ming; Guo, Guo-Cong
Broad transparency and wide band gap achieved in a magnetic infrared nonlinear optical chalcogenide by suppressing d-d transitions.
Materials horizons, 2022, 9, 1513-1517
1566611 CIFC28 H41 F O4P 1 21 110.3779; 7.2974; 33.47
90; 98.797; 90
2504.9Jiang, Liyin; Sarró, Pau; Teo, Wei Jie; Llop, Jordi; Suero, Marcos
Catalytic alkene skeletal modification for the construction of fluorinated tertiary stereocenters
Chemical Science, 2022
1566612 CIFC26 H39 F O4C 1 2 114.7648; 6.0876; 26.974
90; 96.281; 90
2409.9Jiang, Liyin; Sarró, Pau; Teo, Wei Jie; Llop, Jordi; Suero, Marcos
Catalytic alkene skeletal modification for the construction of fluorinated tertiary stereocenters
Chemical Science, 2022
1566613 CIFC227 H209 Ag6 Au19 B2 F8 O17 P6 S17P -120.4536; 20.7898; 33.6586
72.945; 82.104; 63.917
12289Shi, Wan-Qi; Guan, Zong-Jie; Li, Jiao-Jiao; Han, Xu-Shuang; Wang, Quan-Ming
Site-Specified Doping of Silver Atoms into Au25 Nanocluster as Directed by Ligand Binding Preference
Chemical Science, 2022
1566614 CIFC66 H72 N4 Ni Si4P -111.7807; 11.8079; 22.9033
80.502; 78.053; 71.215
2934.25Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566615 CIFC34 H29 N2 Si2P -110.31; 12.326; 12.941
77.219; 79.312; 79.801
1560Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566616 CIFC83 H103 N7 Ni5 Si4P -113.9645; 14.7686; 24.4091
89.5959; 79.412; 63.052
4394.3Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566617 CIFC73 H85 N5 Ni2 Si4P -114.392; 22.272; 22.51
97.75; 95.438; 102.855
6912Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566618 CIFC35 H48 N PP -110.677; 11.8045; 12.4452
96.831; 101.037; 111.157
1405.1Chen, Zicong; Gu, Changxue; Yuen, On Ying; So, Chau Ming
Palladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates at the C–Cl site
Chemical Science, 2022
1566619 CIFC42 H34 B F3 P2 SeP -19.6724; 12.8821; 14.5407
84.961; 77.687; 74.085
1701.43Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566620 CIFC43 H39 B F3 O3 P2 RhP -19.1533; 13.0253; 33.273
83.172; 88.634; 79.181
3868.8Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566621 CIFC36.96 H31.91 B0.95 F2.87 I0.05 P2 Se0.95P n a 2114.5444; 19.8328; 11.0256
90; 90; 90
3180.4Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566622 CIFC15 H16 B F3 K O0.5 PP -15.6907; 21.5917; 26.847
78.455; 89.976; 89.948
3232Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566623 CIFC91 H144 O10P -111.9787; 17.3956; 22.0177
110.06; 90.8994; 101.377
4207.6Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566624 CIFC16 H16 F10 O2P 1 21/a 111.164; 5.0419; 15.9267
90; 91.317; 90
896.2Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566625 CIFC108 H108 F60 O12C 1 2/c 169.979; 13.9205; 24.2019
90; 96.4154; 90
23428.5Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566626 CIFC81 H94 F30 O10P 1 21/a 123.6441; 22.5243; 31.147
90; 95.0726; 90
16522.9Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566627 CIFC91 H94 F50 O10P -120.9282; 22.7403; 24.2682
98.976; 98.951; 114.017
10108.6Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566628 CIFC90.65 H93.56 F50 O10P 1 21/n 122.9793; 21.8597; 40.474
90; 102.22; 90
19870Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566629 CIFC18 H26 Cd N4 O6 P2 S4P -17.2387; 9.6411; 10.4545
81.448; 75.399; 70.165
662.56Tan, Yee Seng; Yeo, Chien Ing; Kwong, Huey Chong; Tiekink, Edward R. T.
Unusual {⋯HNC <sub>2</sub> O⋯HC <sub> <i>n</i> </sub> O}, <i>n</i> = 1 or 2, synthons predominate in the molecular packing of one-dimensional coordination polymers, {Cd[S <sub>2</sub> P(OR) <sub>2</sub> ] <sub>2</sub> ( <sup>3</sup> LH <sub>2</sub> )} <sub> <i>n</i> </sub> , for R = Me and Et, but are precluded when R = i-Pr; <sup>3</sup> LH <sub>2</sub> = <i>N</i> , <i>N</i> ′-bis(3-pyridylmethyl)oxalamide
CrystEngComm, 2022, 24, 2992-3004
1566630 CIFC26 H42 Cd N4 O6 P2 S4P -19.9154; 12.3655; 15.4749
106.08; 99.172; 91.827
1794.03Tan, Yee Seng; Yeo, Chien Ing; Kwong, Huey Chong; Tiekink, Edward R. T.
Unusual {⋯HNC <sub>2</sub> O⋯HC <sub> <i>n</i> </sub> O}, <i>n</i> = 1 or 2, synthons predominate in the molecular packing of one-dimensional coordination polymers, {Cd[S <sub>2</sub> P(OR) <sub>2</sub> ] <sub>2</sub> ( <sup>3</sup> LH <sub>2</sub> )} <sub> <i>n</i> </sub> , for R = Me and Et, but are precluded when R = i-Pr; <sup>3</sup> LH <sub>2</sub> = <i>N</i> , <i>N</i> ′-bis(3-pyridylmethyl)oxalamide
CrystEngComm, 2022, 24, 2992-3004
1566631 CIFC22 H34 Cd N4 O6 P2 S4P -19.0611; 9.2065; 10.5703
82.436; 77.672; 64.113
774.27Tan, Yee Seng; Yeo, Chien Ing; Kwong, Huey Chong; Tiekink, Edward R. T.
Unusual {⋯HNC <sub>2</sub> O⋯HC <sub> <i>n</i> </sub> O}, <i>n</i> = 1 or 2, synthons predominate in the molecular packing of one-dimensional coordination polymers, {Cd[S <sub>2</sub> P(OR) <sub>2</sub> ] <sub>2</sub> ( <sup>3</sup> LH <sub>2</sub> )} <sub> <i>n</i> </sub> , for R = Me and Et, but are precluded when R = i-Pr; <sup>3</sup> LH <sub>2</sub> = <i>N</i> , <i>N</i> ′-bis(3-pyridylmethyl)oxalamide
CrystEngComm, 2022, 24, 2992-3004
1566632 CIFC78 H78 N6 O3P -114.2538; 17.1903; 17.3592
79.038; 72.546; 68.828
3767.7Fang, Lingyi; Zhang, Yuyan; Ren, Ming; Xie, Xinrui; Li, Tianyu; Yuan, Yi; Zhang, Jing; Wang, Peng
A triple helicene based molecular semiconductor characteristic of a fully fused conjugated backbone for perovskite solar cells
Energy & Environmental Science, 2022, 15, 1630-1637
1566633 CIFC15 H15 N3 O SP 1 21/n 16.6492; 13.731; 15.329
90; 101.032; 90
1373.7Kshtriya, Vivekshinh; Koshti, Bharti; Mehmood, Tahir; Singh, Ramesh; Joshi, Khashti Ballabh; Bandyopadhyay, Sujoy; Boukhvalov, Danil W.; Reddy, J. Prakasha; Gour, Nidhi
A new aggregation induced emission enhancement (AIEE) dye which self-assembles to panchromatic fluorescent flowers and has application in sensing dichromate ions.
Soft matter, 2022, 18, 3019-3030
1566663 CIFC36 H37 K N3 O3 P2 Ru SP c a 2112.6529; 18.7504; 15.5836
90; 90; 90
3697.2Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566664 CIFC100 H83 N6 O3 P6 Ru2P 1 21/c 114.8971; 22.753; 28.6172
90; 100.332; 90
9542.6Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566665 CIFC51 H48 Cl N4 O2 P3 RuP b c n25.849; 19.5041; 21.0152
90; 90; 90
10595Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566666 CIFC23 H27 B O3P n a 2112.912; 10.1397; 15.597
90; 90; 90
2042Wei, Yu-Bai; Luo, Dong; Xiong, Xiao; Huang, Yong-Liang; Xie, Mo; Lu, Weigang; Li, Dan
Biomimetic Mimicry of Formaldehyde-Induced DNA–Protein Crosslinks in the Confined Space of Metal–Organic Framework
Chemical Science, 2022
1566667 CIFC23 H27 B O3P 1 21/n 112.4943; 9.9586; 16.762
90; 95.6616; 90
2075.5Wei, Yu-Bai; Luo, Dong; Xiong, Xiao; Huang, Yong-Liang; Xie, Mo; Lu, Weigang; Li, Dan
Biomimetic Mimicry of Formaldehyde-Induced DNA–Protein Crosslinks in the Confined Space of Metal–Organic Framework
Chemical Science, 2022
1566668 CIFC16 H29 N O6 SP 21 21 215.46991; 10.15896; 34.3303
90; 90; 90
1907.69Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566669 CIFC18 H22 O2 SP n a 219.3374; 6.0661; 28.5106
90; 90; 90
1614.89Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566670 CIFC15 H20 Cl N O3 SP -15.0188; 9.6241; 16.1198
89.487; 85.132; 82.136
768.5Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566671 CIFC10 H18 O4 S2P 1 21/n 16.4691; 11.4368; 8.7387
90; 102.114; 90
632.143Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566672 CIFC11 H14 O3 SP -15.72076; 8.13039; 11.8424
91.8184; 91.4466; 103.412
535.219Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566673 CIFC10 H11 F O3 SP 1 c 15.7165; 12.1828; 14.7356
90; 91.722; 90
1025.77Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566674 CIFC15 H27 N O6 SP 1 21/c 111.1742; 16.6182; 10.3665
90; 116.394; 90
1724.34Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566675 CIFC10 H18 O4 S2P 1 21/c 16.09765; 8.92648; 22.0926
90; 91.4743; 90
1202.11Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566676 CIFC15 H17 N O2 SP 1 21/c 19.0612; 15.82137; 10.2622
90; 114.837; 90
1335.12Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566677 CIFC25 H30 O8 SP 1 21 110.04584; 19.87397; 12.32816
90; 95.9688; 90
2447.98Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566678 CIFC23 H27 B O3P n a 2112.912; 10.1397; 15.597
90; 90; 90
2042wu, Fu-Peng; Wu, Xiao-Feng
Catalyst-Controlled Selective Borocarbonylation of Benzylidenecyclopropanes: Regiodivergent Synthesis of γ-Vinylboryl Ketones and β-Cyclopropylboryl Ketones
Chemical Science, 2022
1566679 CIFC23 H27 B O3P 1 21/n 112.4943; 9.9586; 16.762
90; 95.6616; 90
2075.5wu, Fu-Peng; Wu, Xiao-Feng
Catalyst-Controlled Selective Borocarbonylation of Benzylidenecyclopropanes: Regiodivergent Synthesis of γ-Vinylboryl Ketones and β-Cyclopropylboryl Ketones
Chemical Science, 2022
1566680 CIFC50.5 H47 Co O3 P2P 1 21/n 19.9652; 18.349; 23.3602
90; 96.462; 90
4244.3Martínez-Carrión, Alicia; Romero-Navarro, Andrés; Núñez-Rico, José Luis; Gutiérrez, Albert; Grabulosa, Arnald; Vidal-Ferran, Anton
Valorisation of mixtures of linear alkenes using cobalt-mediated isomerisation and hydroformylation chemistries
Catalysis Science & Technology, 2022, 12, 3219-3227
1566681 CIFC45 H32 Co2 O7 P2P -110.8578; 11.6947; 17.4282
106.744; 95.84; 112.496
1900.9Martínez-Carrión, Alicia; Romero-Navarro, Andrés; Núñez-Rico, José Luis; Gutiérrez, Albert; Grabulosa, Arnald; Vidal-Ferran, Anton
Valorisation of mixtures of linear alkenes using cobalt-mediated isomerisation and hydroformylation chemistries
Catalysis Science & Technology, 2022, 12, 3219-3227
1566682 CIFC16 H19 N O6 SP 21 21 218.0346; 12.621; 16.5455
90; 90; 90
1677.79Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566683 CIFC16 H19 N O6 SP 1 21 110.1269; 8.043; 10.8756
90; 114.408; 90
806.66Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566684 CIFC17 H26 F6 N3 O7 S2P 1 21 111.0402; 9.5966; 12.5085
90; 115.079; 90
1200.32Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566685 CIFC16 H20 N2 O6 SP 21 21 218.1051; 14.1921; 15.2659
90; 90; 90
1756.01Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566686 CIFC160 H218 N8 O49 S8P 1 21 113.5261; 12.674; 25.4683
90; 99.78; 90
4302.6Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566687 CIFC1220 H968 B11.95 Cu24 F47.82 N52 O104P 1 21/n 118.838; 32.458; 64.439
90; 94.55; 90
39277Domoto, Yuya; Yamamoto, Kidai; Horie, Shumpei; Yu, Zhengsu; Fujita, Makoto
Multiplication of weak chiral inductions for excellent control over the helical orientation of discrete topologically chiral (M3L2)n polyhedra
Chemical Science, 2022
1566688 CIFC29.4 H40.8 Cl8.8 N2 P2 PdP 1 21/n 115.262; 12.8154; 20.9917
90; 108.535; 90
3892.8Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566689 CIFC26 H40 B2 N2 P2P -19.1591; 11.3142; 15.1394
103.273; 102.525; 105.201
1408Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566690 CIFC28 H34 F6 N2 O6 P2 Pd S2P -111.2734; 12.1729; 13.5903
73.9005; 72.8892; 73.6404
1671.4Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566691 CIFC17 H21 B F2 N4 OP 21 21 218.9883; 11.1112; 17.485
90; 90; 90
1746.2Zeng, Lintao; Chen, Tianhong; Zhu, Beitong; Koo, Seyoung; Tang, Yonghe; Lin, Weiying; James, Tony D.; Kim, Jong Seung
A molecular recognition platform for the simultaneous sensing of diverse chemical weapons
Chemical Science, 2022
1566692 CIFC15 H19 B F2 N4P 4110.5675; 10.5675; 13.404
90; 90; 90
1496.9Zeng, Lintao; Chen, Tianhong; Zhu, Beitong; Koo, Seyoung; Tang, Yonghe; Lin, Weiying; James, Tony D.; Kim, Jong Seung
A molecular recognition platform for the simultaneous sensing of diverse chemical weapons
Chemical Science, 2022
1566693 CIFC16 H17 B F2 N4 OP -16.9141; 9.2485; 12.7582
93.651; 101.649; 97.353
789.08Zeng, Lintao; Chen, Tianhong; Zhu, Beitong; Koo, Seyoung; Tang, Yonghe; Lin, Weiying; James, Tony D.; Kim, Jong Seung
A molecular recognition platform for the simultaneous sensing of diverse chemical weapons
Chemical Science, 2022
1566694 CIFC83 H135 As7 K La2 O6 Si8P -115.7346; 18.2731; 19.7473
106.435; 102.572; 100.222
5139Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566695 CIFC96 H164 As14 Ce2 K2 O12 Si8P -111.223; 16.579; 18.693
72.888; 89.816; 73.008
3166Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566696 CIFC80 H132 As7 K Nd2 O6 Si8P -115.6899; 18.4469; 20.1223
111.299; 104.839; 100.119
5006.3Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566697 CIFC77 H129 As3 K Nd2 O6 Si8P -111.7764; 17.4676; 26.292
84.855; 79.39; 71.581
5040.7Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566698 CIFC58 H102 As7 K2 Nd O12 Si4P 1 21/n 114.2709; 31.995; 17.4941
90; 98.678; 90
7896.3Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566699 CIFC77 H132 As7 Ce2 K O6 Si8P 1 21/n 120.0117; 18.0444; 27.5019
90; 96.273; 90
9871.5Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566700 CIFC74 H138 As14 K2 Nd2 O12 Si8C 1 2/c 141.591; 13.2497; 19.5306
90; 95.516; 90
10712.9Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566701 CIFC43 H40 Au N O6P 21 21 219.9306; 13.2468; 27.4297
90; 90; 90
3608.3Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566702 CIFC38 H24 N O2 PP 21 21 2111.8935; 12.6595; 18.8734
90; 90; 90
2841.7Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566703 CIFC41.17 H29.17 Au Cl3.5 N O3P 21 21 2112.999; 13.954; 22.15
90; 90; 90
4018Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566704 CIFC42 H32 Au Cl4 N O3P 21 21 2112.578; 13.7123; 21.0398
90; 90; 90
3628.8Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566705 CIFC42 H36 Au N O5P 21 21 219.9266; 13.1669; 27.3976
90; 90; 90
3580.9Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566706 CIFH66 Mo60 Na8 O187I 41/a c d :223.5571; 23.5571; 61.035
90; 90; 90
33870.6Li, xuexin; Ji, Tuo; Gao, Jun-Yang; Chen, Wei-Chao; Yuan, Ye; Sha, Haoyan; Faller, Roland; Shan, Guo-Gang; Shao, Kui-Zhan; Wang, Xinlong; Su, Zhong-Min
An Unprecedented Fully Reduced {MoV60} Polyoxometalate: From All-Inorganic Molecular Light-Absorber Model to Improved Photoelectronic Performance
Chemical Science, 2022
1566707 CIFC54.5 H53 B Cl P2 SP -18.8424; 11.4067; 24.8662
81.957; 80.897; 69.046
2303.2Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566708 CIFC29.25 H31.5 B Cl0.5 F4 P2 Pt SP b a m20.9374; 10.9959; 14.9555
90; 90; 90
3443.14Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566709 CIFC28 H28 Cl O P2 Rh SP 21 21 2110.4581; 14.2792; 17.4031
90; 90; 90
2598.86Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566710 CIFC54 H53 B Cl P2 Rh SP 1 21/n 110.9915; 34.1432; 12.5533
90; 99.76; 90
4642.9Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566711 CIFC45.5 H36 Cl F7 P3 Rh SP -19.1404; 12.3384; 19.4965
102.063; 92.077; 103.656
2080.95Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566712 CIFC43 H32 F4 O3 P2 S2P 1 21/n 112.4956; 28.031; 12.6611
90; 119.324; 90
3866.48Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566713 CIFC56 H59 B P2 Pt SP 1 21/c 116.6775; 15.3273; 19.3126
90; 102.496; 90
4819.76Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566714 CIFC47 H35 F13 N2 O8 P2 Pt S5P 1 21/c 123.6369; 12.7303; 18.9449
90; 98.297; 90
5640.95Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566715 CIFC32 H39 B2 F8 N O2 P2 Pt SP -110.727; 13.1882; 15.143
65.687; 75.111; 75.546
1861.41Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566718 CIF
HKL
Paper
C21 H18 N2 OC 1 2/c 130.3989; 8.7177; 14.0581
90; 115.367; 90
3366.3Meenatchi, C. Selva; Athimoolam, S.; Suresh, J.; Priya, R. Vishnu; Rubina, S. Raja; Bhandari, S. R.
(<i>E</i>)-5-(4-Methylbenzylidene)-1-phenyl-4,5,6,7-tetrahydro-1<i>H</i>-indazol-4-one
IUCrData, 2022, 7, x220283
1566719 CIFC20 H56 Bi2 Br10 N4P -112.4378; 13.2166; 14.021
97.835; 93.139; 90.289
2279.7Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566720 CIFC20 H56 Ag Bi Br8 N4P -18.4797; 8.7683; 13.9411
73.253; 88.908; 87.415
991.56Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566721 CIFC20 Ag Bi Br8 N8C m m m8.774; 27.47; 8.771
90; 90; 90
2114Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566722 CIFC25 H69 Br9 N5 Pb2P -111.996; 13.422; 17.477
72.658; 70.158; 77.179
2503.7Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566723 CIFC25 H70 Br9 N5 Pb2P -111.975; 13.366; 17.472
72.618; 70.213; 77.258
2488.9Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566724 CIFC23 H23 Cl N2 O2P 1 21 19.6064; 7.9331; 13.748
90; 101.106; 90
1028.09Xiao, Lu; Li, Bo; Xiao, Fan; Fu, Cong; Wei, Liang; Dang, Yanfeng; Dong, Xiu-Qin; Wang, Chun-Jiang
Stereodivergent Synthesis of Enantioenriched Azepino[3,4,5-cd]-Indoles via Cooperative Cu/Ir-Catalyzed Asymmetric Allylic Alkylation and Intramolecular Friedel-Crafts Reaction
Chemical Science, 2022
1566725 CIFC23 H23 Cl N2 O2P 21 21 219.2992; 18.0846; 24.744
90; 90; 90
4161.26Xiao, Lu; Li, Bo; Xiao, Fan; Fu, Cong; Wei, Liang; Dang, Yanfeng; Dong, Xiu-Qin; Wang, Chun-Jiang
Stereodivergent Synthesis of Enantioenriched Azepino[3,4,5-cd]-Indoles via Cooperative Cu/Ir-Catalyzed Asymmetric Allylic Alkylation and Intramolecular Friedel-Crafts Reaction
Chemical Science, 2022
1566726 CIFC23 H23 Cl N2 O2P 21 21 219.11893; 17.37833; 50.2087
90; 90; 90
7956.66Xiao, Lu; Li, Bo; Xiao, Fan; Fu, Cong; Wei, Liang; Dang, Yanfeng; Dong, Xiu-Qin; Wang, Chun-Jiang
Stereodivergent Synthesis of Enantioenriched Azepino[3,4,5-cd]-Indoles via Cooperative Cu/Ir-Catalyzed Asymmetric Allylic Alkylation and Intramolecular Friedel-Crafts Reaction
Chemical Science, 2022
1566727 CIFC23 H30 N4 O2P 1 21/c 116.0767; 12.9097; 10.9767
90; 99.712; 90
2245.51Zhan, Yi-Zhou; Meng, Huan; Shu, Wei
Rapid Access to t-Butylalkylated Olefins Enabled by Ni-Catalyzed Intermolecular Regio- and trans-Selective Cross-Electrophile t-Butylalkylation of Alkynes
Chemical Science, 2022
1566728 CIF
HKL
Paper
C15 H14 Cl N5 O2P 1 21 17.1533; 11.936; 9.004
90; 98.128; 90
761.1Song, Jingjing; Jiang, Xinyu; Wang, Ziyi; Pei, Jingyao; Li, Hongsen
4-Chloro-5-(dimethylamino)-2-[(5-phenyl-1,3,4-oxadiazol-2-yl)methyl]pyridazin-3(2<i>H</i>)-one
IUCrData, 2022, 7, x220342
1566729 CIF
HKL
Paper
C16 H9 N O2 SP 1 21/c 14.60717; 20.7275; 12.6444
90; 91.911; 90
1206.81Abdallah, Amira E. M.; Elgemeie, Galal H.; Jones, Peter G.
3-(Benzo[<i>d</i>]thiazol-2-yl)-2<i>H</i>-chromen-2-one
IUCrData, 2022, 7, x220332
1566730 CIFC61 H45 Cl3P -113.1323; 14.2033; 14.7079
94.606; 111.041; 97.973
2510.43Bergman, Harrison; Beattie, D. Dawson; Kiel, Gavin R.; Handford, Rex; Liu, Yi; Tilley, T. Don
A sequential cyclization/π-extension strategy for modular construction of nanographenes enabled by stannole cycloadditions
Chemical Science, 2022
1566731 CIFC22 H9 Br N4 SP -17.5508; 8.0138; 8.139
85.38; 77.75; 75.07
464.86Liu, Kun; Li, Shuai; Fu, Liyuan; Lei, Yilong; Liao, Qing; Fu, Hongbing
Cocrystallization Tailoring Radiative Decay Pathways for Thermally Activated Delayed Fluorescence and Room Temperature Phosphorescence Emission
Nanoscale, 2022
1566732 CIFC22 H9 Br N4 SP 1 21/c 17.4921; 8.1212; 30.277
90; 92.33; 90
1840.7Liu, Kun; Li, Shuai; Fu, Liyuan; Lei, Yilong; Liao, Qing; Fu, Hongbing
Cocrystallization Tailoring Radiative Decay Pathways for Thermally Activated Delayed Fluorescence and Room Temperature Phosphorescence Emission
Nanoscale, 2022
1566733 CIFC32 H28 N2 O5 SP -17.2319; 11.7336; 16.6396
102.141; 94.257; 104.092
1327.08Dong, Jingyue; Gao, Wei; Li, Kun; Hong, Zeyu; Tang, Liangfu; Han, Lijun; Wang, Zhihong; Fan, Zhijin
Design, Synthesis, and Biological Evaluation of Novel Psoralen-Based 1,3,4-Oxadiazoles as Potent Fungicide Candidates Targeting Pyruvate Kinase.
Journal of agricultural and food chemistry, 2022, 70, 3435-3446
1566734 CIFC29 H22 N2 O4 SP b c a9.6146; 15.9025; 29.7245
90; 90; 90
4544.8Dong, Jingyue; Gao, Wei; Li, Kun; Hong, Zeyu; Tang, Liangfu; Han, Lijun; Wang, Zhihong; Fan, Zhijin
Design, Synthesis, and Biological Evaluation of Novel Psoralen-Based 1,3,4-Oxadiazoles as Potent Fungicide Candidates Targeting Pyruvate Kinase.
Journal of agricultural and food chemistry, 2022, 70, 3435-3446
1566735 CIFC22 H22 Cl F3 N4 OC 1 2/c 119.4942; 8.0752; 27.7657
90; 102.868; 90
4261.09Sun, Susu; Chen, Lai; Huo, Jingqian; Wang, Ying; Kou, Song; Yuan, Shitao; Fu, Yining; Zhang, Jinlin
Discovery of Novel Pyrazole Amides as Potent Fungicide Candidates and Evaluation of Their Mode of Action.
Journal of agricultural and food chemistry, 2022, 70, 3447-3457
1566736 CIFC15 H14 O3P 21 21 215.5437; 8.4551; 52.42
90; 90; 90
2457.06Müller, Christoph; Gleixner, Jakob; Tahk, Maris-Johanna; Kopanchuk, Sergei; Laasfeld, Tõnis; Weinhart, Michael; Schollmeyer, Dieter; Betschart, Martin U.; Lüdeke, Steffen; Koch, Pierre; Rinken, Ago; Keller, Max
Structure-Based Design of High-Affinity Fluorescent Probes for the Neuropeptide Y Y<sub>1</sub> Receptor.
Journal of medicinal chemistry, 2022, 65, 4832-4853
1566737 CIFC108.96 H78.42 Cl1.5 N5 O12P -110.4997; 15.5071; 35.5889
83.392; 82.236; 71.57
5430.8Loong, Hao; Zhou, Jiadong; Jiang, Nianqiang; Feng, Yi; Xie, Guojing; Liu, Linlin; Xie, Zengqi
Photoinduced Cascading Charge Transfer in Perylene Bisimide-Based Triads.
The journal of physical chemistry. B, 2022, 126, 2441-2448
1566738 CIFC46 H31 N3 O2P 1 21/c 112.1514; 26.995; 10.64
90; 99.479; 90
3442.6Dey, Suvendu; Hasan, Monirul; Shukla, Atul; Acharya, Nirmalya; Upadhyay, Manoj; Lo, Shih-Chun; Namdas, Ebinazar B.; Ray, Debdas
Thermally Activated Delayed Fluorescence and Room-Temperature Phosphorescence in Asymmetric Phenoxazine-Quinoline (D2–A) Conjugates and Dual Electroluminescence
The Journal of Physical Chemistry C, 2022, 126, 5649-5657
1566739 CIFC17 H15 N O2P 21 21 216.562; 14.232; 14.4563
90; 90; 90
1350.1Kim, Alexia N.; Ngamnithiporn, Aurapat; Bartberger, Michael D.; Stoltz, Brian M.
Iridium-catalyzed asymmetric trans-selective hydrogenation of 1,3-disubstituted isoquinolines
Chemical Science, 2022, 13, 3227-3232
1566740 CIFC20 H10 B11 Cl11 F6C 1 2 121.8423; 11.6968; 19.7476
90; 98.58; 90
4988.8Gunther, S. Olivia; Lee, Chun-I; Song, Ellen; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Isolable Fluorinated Triphenymethyl Cation Salts of [HCB11Cl11]-: Demonstration of Remarkable Hydride Affinity
Chemical Science, 2022
1566741 CIFC24.5 H17 B11 Cl12.5 F2P -112.5709; 13.3424; 23.0855
83.592; 88.189; 73.431
3688.1Gunther, S. Olivia; Lee, Chun-I; Song, Ellen; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Isolable Fluorinated Triphenymethyl Cation Salts of [HCB11Cl11]-: Demonstration of Remarkable Hydride Affinity
Chemical Science, 2022
1566742 CIFC23 H16 OP -110.9971; 21.3867; 28.861
76.152; 85.884; 86.204
6565.14Kodama, Takuya; Saito, Kanako; Tobisu, Mamoru
Nickel-Catalyzed Skeletal Transformation of Tropone Derivatives via C–C Bond Activation: Catalyst-Controlled Access to Diverse Ring Systems
Chemical Science, 2022
1566743 CIFC45 H34 O2P -110.26982; 12.9; 13.4161
101.787; 98.9295; 108.913
1598.21Kodama, Takuya; Saito, Kanako; Tobisu, Mamoru
Nickel-Catalyzed Skeletal Transformation of Tropone Derivatives via C–C Bond Activation: Catalyst-Controlled Access to Diverse Ring Systems
Chemical Science, 2022
1566744 CIFC41 H26 OP -110.4122; 11.1627; 14.3485
103.578; 103.147; 112.391
1402.62Kodama, Takuya; Saito, Kanako; Tobisu, Mamoru
Nickel-Catalyzed Skeletal Transformation of Tropone Derivatives via C–C Bond Activation: Catalyst-Controlled Access to Diverse Ring Systems
Chemical Science, 2022
1566745 CIFC77 H89 Ni O3 P2P -110.9952; 14.137; 21.6909
104.76; 97.213; 100.584
3151.76Kodama, Takuya; Saito, Kanako; Tobisu, Mamoru
Nickel-Catalyzed Skeletal Transformation of Tropone Derivatives via C–C Bond Activation: Catalyst-Controlled Access to Diverse Ring Systems
Chemical Science, 2022
1566746 CIFC69 H76 Ni O P2P 1 21/c 133.7405; 13.5307; 24.6084
90; 105.039; 90
10849.8Kodama, Takuya; Saito, Kanako; Tobisu, Mamoru
Nickel-Catalyzed Skeletal Transformation of Tropone Derivatives via C–C Bond Activation: Catalyst-Controlled Access to Diverse Ring Systems
Chemical Science, 2022
1566747 CIFC43 H30 OP 1 21/n 113.0907; 10.1466; 22.1188
90; 94.055; 90
2930.6Kodama, Takuya; Saito, Kanako; Tobisu, Mamoru
Nickel-Catalyzed Skeletal Transformation of Tropone Derivatives via C–C Bond Activation: Catalyst-Controlled Access to Diverse Ring Systems
Chemical Science, 2022
1566748 CIFC29.5 H32 N2 Ni O3P 1 21/c 119.0889; 15.9034; 18.9504
90; 106.854; 90
5505.8Kodama, Takuya; Saito, Kanako; Tobisu, Mamoru
Nickel-Catalyzed Skeletal Transformation of Tropone Derivatives via C–C Bond Activation: Catalyst-Controlled Access to Diverse Ring Systems
Chemical Science, 2022
1566749 CIFC12 H4 F6 N2P 1 21/n 14.487; 9.3652; 13.1716
90; 97.27; 90
549.04Peng, Hang; Qi, Jun-Chao; Song, Xian-Jiang; Xiong, Ren-Gen; Liao, Wei-Qiang
An Unprecedented Azobenzene-Based Organic Single-Component Ferroelectric
Chemical Science, 2022
1566750 CIFC12 H6 F5 N3P 1 21 13.76719; 6.2632; 24.1516
90; 92.008; 90
569.5Peng, Hang; Qi, Jun-Chao; Song, Xian-Jiang; Xiong, Ren-Gen; Liao, Wei-Qiang
An Unprecedented Azobenzene-Based Organic Single-Component Ferroelectric
Chemical Science, 2022
1566751 CIFC123 H116 F21 N12 O21 Rh4 S7P 1 21/c 124.6083; 12.7106; 23.5913
90; 114.206; 90
6730.2Dang, Li-Long; Li, Ting-Ting; Zhang, Ting-Ting; Zhao, Ying; Chen, Tian; Gao, Xiang; Ma, Lufang; Jin, Guo-Xin
Highly selective synthesis and near-infrared photothermal conversion of metalla-Borromean ring and [2]catenane assemblies
Chemical Science, 2022
1566752 CIFC211.76 H184 F35.28 Ir8 N8 O51.28 S11.76P 1 21/c 121.3182; 15.4343; 19.1459
90; 99.14; 90
6219.6Dang, Li-Long; Li, Ting-Ting; Zhang, Ting-Ting; Zhao, Ying; Chen, Tian; Gao, Xiang; Ma, Lufang; Jin, Guo-Xin
Highly selective synthesis and near-infrared photothermal conversion of metalla-Borromean ring and [2]catenane assemblies
Chemical Science, 2022
1566753 CIFC113.5 H132 F12 N4 O24.5 Rh4 S4P 1 21 115.5383; 19.2201; 41.5739
90; 94.273; 90
12381.4Dang, Li-Long; Li, Ting-Ting; Zhang, Ting-Ting; Zhao, Ying; Chen, Tian; Gao, Xiang; Ma, Lufang; Jin, Guo-Xin
Highly selective synthesis and near-infrared photothermal conversion of metalla-Borromean ring and [2]catenane assemblies
Chemical Science, 2022
1566754 CIFC134 H116 F30 N4 O38 Rh4 S10P n a 2129.3957; 27.2297; 40.625
90; 90; 90
32518Dang, Li-Long; Li, Ting-Ting; Zhang, Ting-Ting; Zhao, Ying; Chen, Tian; Gao, Xiang; Ma, Lufang; Jin, Guo-Xin
Highly selective synthesis and near-infrared photothermal conversion of metalla-Borromean ring and [2]catenane assemblies
Chemical Science, 2022
1566755 CIFC366 H318 F54 N24 O94 Rh14 S18P 1 21/c 120.474; 34.09; 38.801
90; 105.086; 90
26148Dang, Li-Long; Li, Ting-Ting; Zhang, Ting-Ting; Zhao, Ying; Chen, Tian; Gao, Xiang; Ma, Lufang; Jin, Guo-Xin
Highly selective synthesis and near-infrared photothermal conversion of metalla-Borromean ring and [2]catenane assemblies
Chemical Science, 2022
1566756 CIFC122 H100 F18 N4 O26 Rh4 S6P 1 21/n 123.67; 36.843; 25.731
90; 112.251; 90
20768Dang, Li-Long; Li, Ting-Ting; Zhang, Ting-Ting; Zhao, Ying; Chen, Tian; Gao, Xiang; Ma, Lufang; Jin, Guo-Xin
Highly selective synthesis and near-infrared photothermal conversion of metalla-Borromean ring and [2]catenane assemblies
Chemical Science, 2022
1566757 CIF
HKL
Al0.067 Fe0.067 Mg1.94 O6 Si1.93P b c a5.1815; 18.2321; 8.8085
90; 90; 90
832.14Glazyrin, K.; Khandarkhaeva, S.; Fedotenko, T.; Dong, W.; Laniel, D.; Seiboth, F.; Schropp, A.; Garrevoet, J.; Brückner, D.; Falkenberg, G.; Kubec, A.; David, C.; Wendt, M.; Wenz, S.; Dubrovinsky, L.; Dubrovinskaia, N.; Liermann, H.-P.
Sub-micrometer focusing setup for high-pressure crystallography at the Extreme Conditions beamline at PETRAIII
Journal of Synchrotron Radiation, 2022, 29, 654-663
1566758 CIFFe0.091 Mg0.909 O3 SiP b n m4.194; 4.525; 6.191
90; 90; 90
117.49Glazyrin, K.; Khandarkhaeva, S.; Fedotenko, T.; Dong, W.; Laniel, D.; Seiboth, F.; Schropp, A.; Garrevoet, J.; Brückner, D.; Falkenberg, G.; Kubec, A.; David, C.; Wendt, M.; Wenz, S.; Dubrovinsky, L.; Dubrovinskaia, N.; Liermann, H.-P.
Sub-micrometer focusing setup for high-pressure crystallography at the Extreme Conditions beamline at PETRAIII
Journal of Synchrotron Radiation, 2022, 29, 654-663
1566759 CIFCo Sb3I m -39.036; 9.036; 9.036
90; 90; 90
737.783Glazyrin, K.; Khandarkhaeva, S.; Fedotenko, T.; Dong, W.; Laniel, D.; Seiboth, F.; Schropp, A.; Garrevoet, J.; Brückner, D.; Falkenberg, G.; Kubec, A.; David, C.; Wendt, M.; Wenz, S.; Dubrovinsky, L.; Dubrovinskaia, N.; Liermann, H.-P.
Sub-micrometer focusing setup for high-pressure crystallography at the Extreme Conditions beamline at PETRAIII
Journal of Synchrotron Radiation, 2022, 29, 654-663
1566760 CIFC151 H250 Al4 K4 N8 O4 S4 Si8P 1 21/c 125.01159; 19.41543; 33.7313
90; 100.884; 90
16085.6Evans, Matthew J.; Anker, Mathew D.; McMullin, Claire L.; Neale, Samuel E.; Rajabi, Nasir A.; Coles, Martyn P.
Carbon–chalcogen bond formation initiated by [Al(NONDipp)(E)]− anions containing Al–E{16} (E{16} = S, Se) multiple bonds
Chemical Science, 2022
1566761 CIFC82 H140 Al2 K2 N4 O12 Se2 Si4P 1 21/n 115.4374; 13.47603; 22.5971
90; 93.2318; 90
4693.51Evans, Matthew J.; Anker, Mathew D.; McMullin, Claire L.; Neale, Samuel E.; Rajabi, Nasir A.; Coles, Martyn P.
Carbon–chalcogen bond formation initiated by [Al(NONDipp)(E)]− anions containing Al–E{16} (E{16} = S, Se) multiple bonds
Chemical Science, 2022
1566762 CIFC49 H66 Al K N2 O3 S Si2P 1 21/n 114.78551; 13.04163; 25.96015
90; 104.132; 90
4854.33Evans, Matthew J.; Anker, Mathew D.; McMullin, Claire L.; Neale, Samuel E.; Rajabi, Nasir A.; Coles, Martyn P.
Carbon–chalcogen bond formation initiated by [Al(NONDipp)(E)]− anions containing Al–E{16} (E{16} = S, Se) multiple bonds
Chemical Science, 2022
1566763 CIFC53 H80 Al K N2 O5 Se Si2P 1 21/n 19.75833; 31.8983; 17.54162
90; 92.6949; 90
5454.21Evans, Matthew J.; Anker, Mathew D.; McMullin, Claire L.; Neale, Samuel E.; Rajabi, Nasir A.; Coles, Martyn P.
Carbon–chalcogen bond formation initiated by [Al(NONDipp)(E)]− anions containing Al–E{16} (E{16} = S, Se) multiple bonds
Chemical Science, 2022
1566764 CIFC50 H90 Al K N4 O8 S Si2P -110.0626; 17.1004; 17.2361
88.851; 83.037; 84.293
2929.33Evans, Matthew J.; Anker, Mathew D.; McMullin, Claire L.; Neale, Samuel E.; Rajabi, Nasir A.; Coles, Martyn P.
Carbon–chalcogen bond formation initiated by [Al(NONDipp)(E)]− anions containing Al–E{16} (E{16} = S, Se) multiple bonds
Chemical Science, 2022
1566765 CIFC45 H66 Al K N2 O3 S Si2P 1 21/c 115.45971; 12.3875; 24.7548
90; 90.4615; 90
4740.57Evans, Matthew J.; Anker, Mathew D.; McMullin, Claire L.; Neale, Samuel E.; Rajabi, Nasir A.; Coles, Martyn P.
Carbon–chalcogen bond formation initiated by [Al(NONDipp)(E)]− anions containing Al–E{16} (E{16} = S, Se) multiple bonds
Chemical Science, 2022
1566766 CIFC74 H132 Al2 K2 N4 O10 S2 Si4P 1 21 112.27766; 24.87997; 14.9006
90; 94.3187; 90
4538.73Evans, Matthew J.; Anker, Mathew D.; McMullin, Claire L.; Neale, Samuel E.; Rajabi, Nasir A.; Coles, Martyn P.
Carbon–chalcogen bond formation initiated by [Al(NONDipp)(E)]− anions containing Al–E{16} (E{16} = S, Se) multiple bonds
Chemical Science, 2022
1566767 CIFC49 H66 Al K N2 O3 Se Si2P 1 21/n 114.84213; 13.02613; 26.0062
90; 103.725; 90
4884.35Evans, Matthew J.; Anker, Mathew D.; McMullin, Claire L.; Neale, Samuel E.; Rajabi, Nasir A.; Coles, Martyn P.
Carbon–chalcogen bond formation initiated by [Al(NONDipp)(E)]− anions containing Al–E{16} (E{16} = S, Se) multiple bonds
Chemical Science, 2022
1566768 CIF
HKL
Paper
C36 H48 N4 O14P -16.0921; 8.5778; 18.726
94.922; 90.428; 98.945
962.88Naeem, Marilyn; Chadeayne, Andrew R.; Golen, James A.; Manke, David R.
Bis(oxotremorine) fumarate bis(fumaric acid)
IUCrData, 2022, 7, x220364
1566769 CIFC48 H28 Bi N4 O9P 21 21 2117.3; 17.4; 18.975
90; 90; 90
5711.9Xie, Dale; Wang, Sheng; Li, Shihao; Yang, Wenqing; Feng, Yi-Si
A two-dimensional Bi-based porphyrin metal–organic framework photocatalyst for white light-driven selective oxidation of sulfides
Catalysis Science & Technology, 2022, 12, 3254-3260
1566770 CIFC54 H78 Cl2 N10 O4C 1 2 120.799; 14.2717; 20.0159
90; 114.881; 90
5390Li, Hongfei; Kou, Lei; Liang, Lin; Li, Boyang; Zhao, Wei; Yang, Xiao-Juan; Wu, Biao
Anion-coordination-driven single-double helix switching and chiroptical molecular switch based on oligoureas
Chemical Science, 2022
1566771 CIFC99 H134 N20 O15.5 PP 113.8456; 13.8504; 26.594
98.63; 90.112; 101.91
4930.7Li, Hongfei; Kou, Lei; Liang, Lin; Li, Boyang; Zhao, Wei; Yang, Xiao-Juan; Wu, Biao
Anion-coordination-driven single-double helix switching and chiroptical molecular switch based on oligoureas
Chemical Science, 2022
1566772 CIFC67 H96 N15 O13 PP 1 21 113.007; 20.8259; 13.9625
90; 106.566; 90
3625.2Li, Hongfei; Kou, Lei; Liang, Lin; Li, Boyang; Zhao, Wei; Yang, Xiao-Juan; Wu, Biao
Anion-coordination-driven single-double helix switching and chiroptical molecular switch based on oligoureas
Chemical Science, 2022
1566773 CIFC77 H44 Cl2 N12 O5P 1 21 111.9428; 25.5121; 12.5127
90; 92.975; 90
3807.3Li, Hongfei; Kou, Lei; Liang, Lin; Li, Boyang; Zhao, Wei; Yang, Xiao-Juan; Wu, Biao
Anion-coordination-driven single-double helix switching and chiroptical molecular switch based on oligoureas
Chemical Science, 2022
1566774 CIFC29 H18 NP -18.4867; 12.972; 18.128
105.478; 90.206; 96.312
1910.5Wei, Xiao; Xu, Chao; Li, Hao; Kang, Xi; Zhu, Manzhou
Fabrication of a Family of Atomically Precise Silver Nanoclusters via Dual-Level Kinetical Control
Chemical Science, 2022
1566775 CIFC30 H38 B2 N2 O4P 1 21/n 115.0763; 9.9694; 19.4363
90; 103.775; 90
2837.29Li, Manhong; Liu, Siqi; Bao, Haoshi; Li, Qini; Deng, Yi-Hui; Sun, Tian-Yu; Wang, Leifeng
Photoinduced metal-free borylation of aryl halides catalysed by an in situ formed donor–acceptor complex
Chemical Science, 2022
1566776 CIFC56 H71.75 Li5 Ni2 O5P 1 21/c 116.24036; 14.66026; 22.76116
90; 101.713; 90
5306.3Somerville, Rosie J.; Campos, Jesús; Carmona, Ernesto; Grabowsky, Simon; Malaspina, Lorraine A.; Balcells, David; Hevia, Eva; Nova, Ainara; Pérez-Jiménez, Marina; Borys, Andryj M.
Unmasking the constitution and bonding of the proposed lithium nickelate “Li3NiPh3(solv)3”: Revealing the hidden C6H4 ligand
Chemical Science, 2022
1566777 CIFC64 H112 Br2 Li6 Ni2 O8P 1 21/c 118.677; 19.8681; 39.575
90; 91.001; 90
14683.1Somerville, Rosie J.; Campos, Jesús; Carmona, Ernesto; Grabowsky, Simon; Malaspina, Lorraine A.; Balcells, David; Hevia, Eva; Nova, Ainara; Pérez-Jiménez, Marina; Borys, Andryj M.
Unmasking the constitution and bonding of the proposed lithium nickelate “Li3NiPh3(solv)3”: Revealing the hidden C6H4 ligand
Chemical Science, 2022
1566778 CIFC58 H73 Li6 Ni2 O4P -113.176; 14.1453; 15.9321
101.573; 103.502; 101.439
2733.3Somerville, Rosie J.; Campos, Jesús; Carmona, Ernesto; Grabowsky, Simon; Malaspina, Lorraine A.; Balcells, David; Hevia, Eva; Nova, Ainara; Pérez-Jiménez, Marina; Borys, Andryj M.
Unmasking the constitution and bonding of the proposed lithium nickelate “Li3NiPh3(solv)3”: Revealing the hidden C6H4 ligand
Chemical Science, 2022
1566779 CIFC88 H124 Li12 N4 Ni4 O12P 1 21/c 119.0297; 12.2915; 21.1653
90; 110.588; 90
4634.5Somerville, Rosie J.; Campos, Jesús; Carmona, Ernesto; Grabowsky, Simon; Malaspina, Lorraine A.; Balcells, David; Hevia, Eva; Nova, Ainara; Pérez-Jiménez, Marina; Borys, Andryj M.
Unmasking the constitution and bonding of the proposed lithium nickelate “Li3NiPh3(solv)3”: Revealing the hidden C6H4 ligand
Chemical Science, 2022
1566780 CIFC64 H92 Na4 Ni2 O6P -111.6655; 12.7905; 22.787
104.121; 90.47; 109.712
3088.75Somerville, Rosie J.; Campos, Jesús; Carmona, Ernesto; Grabowsky, Simon; Malaspina, Lorraine A.; Balcells, David; Hevia, Eva; Nova, Ainara; Pérez-Jiménez, Marina; Borys, Andryj M.
Unmasking the constitution and bonding of the proposed lithium nickelate “Li3NiPh3(solv)3”: Revealing the hidden C6H4 ligand
Chemical Science, 2022
1566781 CIFC80 H126 Na6 Ni2 O6C 1 2/c 121.45144; 17.82545; 22.25202
90; 109.731; 90
8009.22Somerville, Rosie J.; Campos, Jesús; Carmona, Ernesto; Grabowsky, Simon; Malaspina, Lorraine A.; Balcells, David; Hevia, Eva; Nova, Ainara; Pérez-Jiménez, Marina; Borys, Andryj M.
Unmasking the constitution and bonding of the proposed lithium nickelate “Li3NiPh3(solv)3”: Revealing the hidden C6H4 ligand
Chemical Science, 2022
1566782 CIFC188.19 H213.43 N59.05 Ni6 O59.05R -3 :H45.98; 45.98; 9.5196
90; 90; 120
17429.6Cui, Mengxing; Murase, Ryuichi; Shen, Yongbing; Sato, Tetsu; Koyama, Shohei; Uchida, Kaiji; Tanabe, Tappei; Takaishi, Shinya; Yamashita, Masahiro; Iguchi, Hiroaki
An electrically conductive metallocycle: densely packed molecular hexagons with π-stacked radicals
Chemical Science, 2022
1566783 CIFC26 H35 N5 O2P 1 21/c 110.3083; 24.752; 10.4153
90; 108.265; 90
2523.58Liu, Hong-Chao; Kong, Xiangtao; Gong, Xiao-Ping; Li, Yuke; Niu, Zhi-Jie; Gou, Xue-Ya; Li, Xue-Song; Wang, Yu-Zhao; Shi, Wei-Yu; Huang, Yan-Chong; Liu, Xue-Yuan; Liang, Yong-Min
Site-Selective Coupling of Remote C(sp3)−H/meta-C(sp2)−H Bonds Enabled by Ru/Photoredox Dual Catalysis and Mechanistic Studies
Chemical Science, 2022
1566784 CIFC20 H26 Br N3 OP 1 21/c 16.36816; 31.0073; 10.01092
90; 97.3165; 90
1960.66Liu, Hong-Chao; Kong, Xiangtao; Gong, Xiao-Ping; Li, Yuke; Niu, Zhi-Jie; Gou, Xue-Ya; Li, Xue-Song; Wang, Yu-Zhao; Shi, Wei-Yu; Huang, Yan-Chong; Liu, Xue-Yuan; Liang, Yong-Min
Site-Selective Coupling of Remote C(sp3)−H/meta-C(sp2)−H Bonds Enabled by Ru/Photoredox Dual Catalysis and Mechanistic Studies
Chemical Science, 2022
1566785 CIFC22 H30 N2 O2P 1 21/c 119.4831; 10.88; 9.8987
90; 99.028; 90
2072.29Liu, Hong-Chao; Kong, Xiangtao; Gong, Xiao-Ping; Li, Yuke; Niu, Zhi-Jie; Gou, Xue-Ya; Li, Xue-Song; Wang, Yu-Zhao; Shi, Wei-Yu; Huang, Yan-Chong; Liu, Xue-Yuan; Liang, Yong-Min
Site-Selective Coupling of Remote C(sp3)−H/meta-C(sp2)−H Bonds Enabled by Ru/Photoredox Dual Catalysis and Mechanistic Studies
Chemical Science, 2022
1566786 CIFO S6 Sn2 Sr2 ZnP -4 21 m9.664; 9.664; 6.33
90; 90; 90
591.177Cheng, Yansong; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng
Rational Design of a Promising Oxychalcogenide Infrared Nonlinear Optical Crystal
Chemical Science, 2022
1566787 CIFC82 H82 Si2C 1 2/c 139.1632; 5.9464; 27.7746
90; 96.8606; 90
6421.8Ringström, Rasmus; Edhborg, Fredrik; Schroeder, Zachary W.; Chen, Lan; Ferguson, Michael J.; Tykwinski, Rik R.; Albinsson, Bo
Molecular rotational conformation controls the rate of singlet fission and triplet decay in pentacene dimers
Chemical Science, 2022
1566788 CIFC106 H126 Cl4 Si4P 1 21/c 18.3982; 34.669; 16.6828
90; 90.028; 90
4857.3Ringström, Rasmus; Edhborg, Fredrik; Schroeder, Zachary W.; Chen, Lan; Ferguson, Michael J.; Tykwinski, Rik R.; Albinsson, Bo
Molecular rotational conformation controls the rate of singlet fission and triplet decay in pentacene dimers
Chemical Science, 2022
1566789 CIFC106.65 H135.3 Cl1.3 Si4P 1 21/c 18.0655; 14.6582; 41.104
90; 91.616; 90
4857.6Ringström, Rasmus; Edhborg, Fredrik; Schroeder, Zachary W.; Chen, Lan; Ferguson, Michael J.; Tykwinski, Rik R.; Albinsson, Bo
Molecular rotational conformation controls the rate of singlet fission and triplet decay in pentacene dimers
Chemical Science, 2022
1566790 CIF
HKL
Paper
C26 H13 F8 I4 N3P -19.1574; 12.0339; 14.0667
91.989; 96.924; 102.996
1496.35Bosch, Eric; Bowling, Nathan P.
5-{[4-(Dimethylamino)phenyl]ethynyl}pyrimidine–1,2,3,5-tetrafluoro-4,6-diiodobenzene (1/2)
IUCrData, 2022, 7, x220380
1566791 CIFC38 H63 In N2 O3P -111.4082; 13.035; 14.939
66.497; 68.941; 83.213
1900.3Bruckmoser, Jonas; Henschel, Daniel; Vagin, Sergei; Rieger, Bernhard
Combining high activity with broad monomer scope: indium salan catalysts in the ring-opening polymerization of various cyclic esters
Catalysis Science & Technology, 2022, 12, 3295-3302
1566792 CIFC20 H17 N SP 18.3698; 8.6024; 11.6963
103.438; 103.111; 102.977
762.79Yan, Qiaolin; Duan, Meng; Chen, Cien; Deng, Zhiqin; Wu, Mandi; Yu, Peiyuan; He, Ming-Liang; Zhu, Guangyu; Houk, Kendall N.; Sun, Jianwei
Organocatalytic Discrimination of Non-Directing Aryl and Heteroaryl Groups: Enantioselective Synthesis of Bioactive Indole-Containing Triarylmethanes
Chemical Science, 2022
1566793 CIFC20 H17 N SP 18.4366; 8.5299; 11.8199
103.482; 103.756; 102.858
767.86Yan, Qiaolin; Duan, Meng; Chen, Cien; Deng, Zhiqin; Wu, Mandi; Yu, Peiyuan; He, Ming-Liang; Zhu, Guangyu; Houk, Kendall N.; Sun, Jianwei
Organocatalytic Discrimination of Non-Directing Aryl and Heteroaryl Groups: Enantioselective Synthesis of Bioactive Indole-Containing Triarylmethanes
Chemical Science, 2022
1566794 CIFC14 H12 F6 OP 21 21 215.8199; 11.7062; 18.082
90; 90; 90
1231.9Sathe, Devavrat; Zhou, Junfeng; Chen, Hanlin; Schrage, Briana R.; Yoon, Seiyoung; Wang, Zeyu; Ziegler, Christopher J.; Wang, Junpeng
Depolymerizable semi-fluorinated polymers for sustainable functional materials
Polymer Chemistry, 2022, 13, 2608-2614
1566795 CIFC155 H119 Er2 N16 O21 PrP -116.3636; 19.5224; 23.3873
108.669; 108.321; 92.112
6640.37Aromi, Guillem; Maniaki, Diamantoula; Garay-Ruiz, Diego; Barrios, Leoní A.; Aguilà, David; Reta, Daniel; Roubeau, Olivier; Bo, Carles; Tuna, Floriana; Martins, Daniel O. T. A.
Unparalleled selectivity and electronic structure of heterometallic [LnLn’Ln] molecules as 3-qubit quantum gates
Chemical Science, 2022
1566796 CIFC463 H730 N26 O239 P8 V52P -126.268; 27.835; 30.643
87.768; 71.483; 69.654
19855Guo, Ji; Liu, Junrui; Cui, Yingcui; Liu, Chuanhong; Wang, Yangming; Wang, Mou; Huang, Danmeng; Chen, Guanying; Wang, Wei; Xia, Debin; Fang, Xikui
Timing matters: pre-assembly versus post-assembly functionalization of a polyoxovanadate–organic cuboid
Chemical Science, 2022
1566797 CIFC423 H697 N33 O273 S8 V54P -120.5891; 28.609; 33.168
113.872; 92.142; 103.627
17168Guo, Ji; Liu, Junrui; Cui, Yingcui; Liu, Chuanhong; Wang, Yangming; Wang, Mou; Huang, Danmeng; Chen, Guanying; Wang, Wei; Xia, Debin; Fang, Xikui
Timing matters: pre-assembly versus post-assembly functionalization of a polyoxovanadate–organic cuboid
Chemical Science, 2022
1566798 CIFC462 H719 N29 O236 P8 S0 V48C 1 2/c 145.21; 27.4006; 55.215
90; 113.919; 90
62525Guo, Ji; Liu, Junrui; Cui, Yingcui; Liu, Chuanhong; Wang, Yangming; Wang, Mou; Huang, Danmeng; Chen, Guanying; Wang, Wei; Xia, Debin; Fang, Xikui
Timing matters: pre-assembly versus post-assembly functionalization of a polyoxovanadate–organic cuboid
Chemical Science, 2022
1566799 CIFC61 H75 N4 Y2P -110.5717; 11.0365; 12.4271
67.8112; 87.4492; 79.2874
1318.6Benner, Florian; Demir, Selvan
Isolation of the elusive bisbenzimidazole Bbim3−Ë™ radical anion and its employment in a metal complex
Chemical Science, 2022
1566800 CIFC84 H128 K N6 O9 Y2P -113.03; 18.0681; 18.371
86.907; 78.05; 76.349
4111.72Benner, Florian; Demir, Selvan
Isolation of the elusive bisbenzimidazole Bbim3−Ë™ radical anion and its employment in a metal complex
Chemical Science, 2022
1566801 CIFC21 H19 N3P 1 21/c 115.2933; 5.6759; 18.003
90; 99.217; 90
1542.5Begam, Hasina Mamataj; Nandi, Shantanu; Jana, Ranjan
Directing group switch in copper-catalyzed electrophilic C–H amination/migratory annulation cascade: divergent access to benzimidazolone/benzimidazole
Chemical Science, 2022
1566802 CIFC16 H12 N2 SP 1 21/c 16.1282; 14.1422; 14.4603
90; 95.255; 90
1247.95Begam, Hasina Mamataj; Nandi, Shantanu; Jana, Ranjan
Directing group switch in copper-catalyzed electrophilic C–H amination/migratory annulation cascade: divergent access to benzimidazolone/benzimidazole
Chemical Science, 2022
1566803 CIFC2.44 H2.44 N0.44 O0.11P -17.9957; 10.4307; 12.5078
67.727; 89.073; 71.4
908.36Begam, Hasina Mamataj; Nandi, Shantanu; Jana, Ranjan
Directing group switch in copper-catalyzed electrophilic C–H amination/migratory annulation cascade: divergent access to benzimidazolone/benzimidazole
Chemical Science, 2022
1566804 CIFC17 H13 N3P 1 21/n 110.9333; 7.34; 16.2518
90; 98.655; 90
1289.36Begam, Hasina Mamataj; Nandi, Shantanu; Jana, Ranjan
Directing group switch in copper-catalyzed electrophilic C–H amination/migratory annulation cascade: divergent access to benzimidazolone/benzimidazole
Chemical Science, 2022
1566805 CIFC23 H17 N3P 1 21/n 111.8246; 8.7668; 16.2183
90; 90.457; 90
1681.2Begam, Hasina Mamataj; Nandi, Shantanu; Jana, Ranjan
Directing group switch in copper-catalyzed electrophilic C–H amination/migratory annulation cascade: divergent access to benzimidazolone/benzimidazole
Chemical Science, 2022
1566806 CIFC19 H19 N O6P 21 21 218.7619; 9.0395; 21.2088
90; 90; 90
1679.8Zhang, Fangqing; Ren, Bing-Tao; Zhou, Yuqiao; Liu, Yangbin; Feng, Xiaoming
Enantioselective Construction of cis-Hydroindole Scaffolds via Asymmetric Inverse-Electron-Demand Diels–Alder Reaction: Application to the Formal Total Synthesis of (+)-Minovincine
Chemical Science, 2022
1566807 CIFC10 H9 B N2P 1 21/c 18.8712; 11.4894; 9.7181
90; 114.973; 90
897.91Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566808 CIFC21 H15 B N4P -19.6002; 9.8523; 10.4405
112.05; 100.947; 100.116
864.9Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566809 CIFC22 H17 B Cl2 N4P -17.6707; 8.6999; 15.3408
95.995; 100.572; 91.45
999.84Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566810 CIFC22 H17 B N4 OP -19.6949; 9.9989; 10.3454
74.22; 68.3124; 89.2819
892.41Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566811 CIFC15 H11 B N4P c a 2115.4138; 5.2751; 15.4456
90; 90; 90
1255.87Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566812 CIFC22 H17 B N4P 1 21/n 17.1974; 14.8004; 16.7357
90; 100.303; 90
1754.01Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566813 CIFC23 H19 B N4 O2P 1 21/n 111.0625; 11.3405; 15.4611
90; 94.428; 90
1933.87Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566814 CIFC24 H14 B F6 N3 O4P 1 21/c 111.8628; 19.2303; 11.1122
90; 114.593; 90
2305.02Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566815 CIFC20 H14 B Cl3 N4 SP -19.5849; 9.6966; 12.5042
102.614; 92.073; 115.981
1007.91Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566816 CIFC20 H16 B N3P 1 21/c 16.7975; 8.0452; 29.5872
90; 95.797; 90
1609.77Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566817 CIFC22 H14 B F3 N4P -18.8691; 9.7159; 11.5592
87.751; 85.002; 66.221
908.04Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566818 CIFC34 H30 B2 N8 O2P b c a15.0807; 9.7071; 19.4956
90; 90; 90
2853.96Tang, Qi; Shi, Xiaodong; Richardson, David; Wojtas, Lukasz; Shan, Chuan; He, Ying; Lan, Yu; Yuan, Teng; Ye, Xiaohan; Li, Shi-Jun; Zhao, Kai
Design and Synthesis of Stable Four-Coordinated Benzotriazole-Borane with Tunable Fluorescence Emission
Chemical Science, 2022
1566819 CIFC30 H25 F6 N S SbC 1 2/c 115.8665; 24.95; 16.2233
90; 99.104; 90
6341.4Zhou, Jun; Mao, Lijun; Wu, Meng-Xiang; Peng, Zhiyong; Yang, Yiming; Zhou, Manfei; Zhao, Xiao-Li; Shi, Xueliang; Yang, Hai-Bo
Extended phenothiazines: synthesis, photophysical and redox properties, and efficient photocatalytic oxidative coupling of amines
Chemical Science, 2022
1566820 CIFC48 H45 N SP 1 21/n 116.8923; 13.2924; 17.9856
90; 113.172; 90
3712.68Zhou, Jun; Mao, Lijun; Wu, Meng-Xiang; Peng, Zhiyong; Yang, Yiming; Zhou, Manfei; Zhao, Xiao-Li; Shi, Xueliang; Yang, Hai-Bo
Extended phenothiazines: synthesis, photophysical and redox properties, and efficient photocatalytic oxidative coupling of amines
Chemical Science, 2022
1566821 CIFC31 H27 Cl2 N SP 1 21/n 111.1803; 7.7394; 30.7513
90; 99.961; 90
2620.76Zhou, Jun; Mao, Lijun; Wu, Meng-Xiang; Peng, Zhiyong; Yang, Yiming; Zhou, Manfei; Zhao, Xiao-Li; Shi, Xueliang; Yang, Hai-Bo
Extended phenothiazines: synthesis, photophysical and redox properties, and efficient photocatalytic oxidative coupling of amines
Chemical Science, 2022
1566822 CIFC52 H47 N SR -3 :H36.5917; 36.5917; 17.7385
90; 90; 120
20569Zhou, Jun; Mao, Lijun; Wu, Meng-Xiang; Peng, Zhiyong; Yang, Yiming; Zhou, Manfei; Zhao, Xiao-Li; Shi, Xueliang; Yang, Hai-Bo
Extended phenothiazines: synthesis, photophysical and redox properties, and efficient photocatalytic oxidative coupling of amines
Chemical Science, 2022
1566823 CIFC74 H69 N SP -17.169; 17.2492; 25.1684
106.66; 90.552; 96.116
2962.06Zhou, Jun; Mao, Lijun; Wu, Meng-Xiang; Peng, Zhiyong; Yang, Yiming; Zhou, Manfei; Zhao, Xiao-Li; Shi, Xueliang; Yang, Hai-Bo
Extended phenothiazines: synthesis, photophysical and redox properties, and efficient photocatalytic oxidative coupling of amines
Chemical Science, 2022
1566824 CIFC11 H10 O SP 17.0221; 7.9102; 9.5017
106.659; 105.234; 101.17
466.74Zhou, Jun; Mao, Lijun; Wu, Meng-Xiang; Peng, Zhiyong; Yang, Yiming; Zhou, Manfei; Zhao, Xiao-Li; Shi, Xueliang; Yang, Hai-Bo
Extended phenothiazines: synthesis, photophysical and redox properties, and efficient photocatalytic oxidative coupling of amines
Chemical Science, 2022
1566825 CIFC26 H23 N SP c c n23.8497; 21.8615; 7.9142
90; 90; 90
4126.4Zhou, Jun; Mao, Lijun; Wu, Meng-Xiang; Peng, Zhiyong; Yang, Yiming; Zhou, Manfei; Zhao, Xiao-Li; Shi, Xueliang; Yang, Hai-Bo
Extended phenothiazines: synthesis, photophysical and redox properties, and efficient photocatalytic oxidative coupling of amines
Chemical Science, 2022
1566826 CIFC18 H16 O2 SP b c n19.5758; 8.4512; 18.7056
90; 90; 90
3094.64Zhou, Jun; Mao, Lijun; Wu, Meng-Xiang; Peng, Zhiyong; Yang, Yiming; Zhou, Manfei; Zhao, Xiao-Li; Shi, Xueliang; Yang, Hai-Bo
Extended phenothiazines: synthesis, photophysical and redox properties, and efficient photocatalytic oxidative coupling of amines
Chemical Science, 2022
1566827 CIFC18 H10 F6 O6 S3P -18.4229; 10.6178; 12.2594
100.265; 102.985; 94.205
1043.88Zhou, Jun; Mao, Lijun; Wu, Meng-Xiang; Peng, Zhiyong; Yang, Yiming; Zhou, Manfei; Zhao, Xiao-Li; Shi, Xueliang; Yang, Hai-Bo
Extended phenothiazines: synthesis, photophysical and redox properties, and efficient photocatalytic oxidative coupling of amines
Chemical Science, 2022
1566828 CIFC13 H11.5 F3 N0.5 S0.5 Sb0.5C 1 2/m 127.184; 6.8384; 19.415
90; 133.036; 90
2638Zhou, Jun; Mao, Lijun; Wu, Meng-Xiang; Peng, Zhiyong; Yang, Yiming; Zhou, Manfei; Zhao, Xiao-Li; Shi, Xueliang; Yang, Hai-Bo
Extended phenothiazines: synthesis, photophysical and redox properties, and efficient photocatalytic oxidative coupling of amines
Chemical Science, 2022
1566829 CIFC18 H20 B10P -17.1379; 19.799; 27.542
110.801; 90.566; 90.757
3637.9Ji, Lei; Riese, Stefan; Schmiedel, Alexander; Holzapfel, Marco; Fest, Maximillian; Nitsch, Jörn; Curchod, Basile F. E.; Friedrich, Alexandra; Wu, Lin; Al Mamari, Hamad H.; Hammer, Sebastian; Pflaum, Jens; Fox, Mark A.; Tozer, David J.; Finze, Maik; Lambert, Christoph; Marder, Todd B.
Thermodynamic equilibrium between locally excited and charge-transfer states through thermally activated charge transfer in 1-(pyren-2′-yl)-o-carborane
Chemical Science, 2022
1566830 CIFC24 H37 F6 N2 O P RuP -19.637; 9.944; 27.528
95.325; 97.691; 96.476
2582Sumitani, Ryo; Yamanaka, Masamichi; Mochida, Tomoyuki
On-demand gelation of ionic liquids using photoresponsive organometallic gelators.
Soft matter, 2022, 18, 3479-3486
1566831 CIFC36 H24 N3 P S4P 1 21 19.351; 14.475; 12.042
90; 111.149; 90
1520.2Jena, Satyam; Jusaina, Jusaina; Behera, Santosh Kumar; Kitahara, Maho; Imai, Yoshitane; Thilagar, P.
Crystallization Induced Room-Temperature Phosphorescence and Chiral Photoluminescence Properties of Phosphoramides
Chemical Science, 2022
1566832 CIFC36 H24 N3 O P S3C 1 2/c 127.1703; 14.9942; 17.8873
90; 111.203; 90
6793.9Jena, Satyam; Jusaina, Jusaina; Behera, Santosh Kumar; Kitahara, Maho; Imai, Yoshitane; Thilagar, P.
Crystallization Induced Room-Temperature Phosphorescence and Chiral Photoluminescence Properties of Phosphoramides
Chemical Science, 2022
1566833 CIFC36 H24 N3 P0.5 S4 SeP 1 21 19.3508; 14.3508; 11.9256
90; 111.396; 90
1490.02Jena, Satyam; Jusaina, Jusaina; Behera, Santosh Kumar; Kitahara, Maho; Imai, Yoshitane; Thilagar, P.
Crystallization Induced Room-Temperature Phosphorescence and Chiral Photoluminescence Properties of Phosphoramides
Chemical Science, 2022
1566834 CIFC9 H11 N O3P 1 21 17.6764; 5.887; 9.6143
90; 94.575; 90
433.1Smalley, Christopher J. H.; Hoskyns, Harriet E.; Hughes, Colan E.; Johnstone, Duncan N.; Willhammar, Tom; Young, Mark T.; Pickard, Christopher J.; Logsdail, Andrew J.; Midgley, Paul A.; Harris, Kenneth D. M.
A structure determination protocol based on combined analysis of 3D-ED data, powder XRD data, solid-state NMR data and DFT-D calculations reveals the structure of a new polymorph of l-tyrosine
Chemical Science, 2022
1566835 CIFC18 H15 N3P 1 21/c 113.5606; 14.1429; 7.6056
90; 93.62; 90
1455.7Li, Taian; Chiou, Mong-Feng; Li, Yajun; Ye, Changqing; Su, Min; Xue, Mengyu; Yuan, Xiaobin; Wang, Chuanchuan; Wan, Wen-Ming; Li, Daliang; Bao, Hongli
Synthesis of Unsymmetrically Tetrasubstituted Pyrroles and Studies of AIEE in Pyrrolo[1,2-a]pyrimidine Derivatives
Chemical Science, 2022
1566836 CIFC23 H19 N3P -17.4368; 11.5205; 11.7843
107.748; 101.471; 103.216
895.98Li, Taian; Chiou, Mong-Feng; Li, Yajun; Ye, Changqing; Su, Min; Xue, Mengyu; Yuan, Xiaobin; Wang, Chuanchuan; Wan, Wen-Ming; Li, Daliang; Bao, Hongli
Synthesis of Unsymmetrically Tetrasubstituted Pyrroles and Studies of AIEE in Pyrrolo[1,2-a]pyrimidine Derivatives
Chemical Science, 2022
1566837 CIFC22 H17 N3P -17.5636; 10.607; 11.488
104.037; 99.019; 104.02
844.45Li, Taian; Chiou, Mong-Feng; Li, Yajun; Ye, Changqing; Su, Min; Xue, Mengyu; Yuan, Xiaobin; Wang, Chuanchuan; Wan, Wen-Ming; Li, Daliang; Bao, Hongli
Synthesis of Unsymmetrically Tetrasubstituted Pyrroles and Studies of AIEE in Pyrrolo[1,2-a]pyrimidine Derivatives
Chemical Science, 2022
1566838 CIFC24 H21 N3P 1 21/c 110.9544; 15.459; 12.2647
90; 113.683; 90
1902Li, Taian; Chiou, Mong-Feng; Li, Yajun; Ye, Changqing; Su, Min; Xue, Mengyu; Yuan, Xiaobin; Wang, Chuanchuan; Wan, Wen-Ming; Li, Daliang; Bao, Hongli
Synthesis of Unsymmetrically Tetrasubstituted Pyrroles and Studies of AIEE in Pyrrolo[1,2-a]pyrimidine Derivatives
Chemical Science, 2022
1566839 CIFC27 H19 N3P 1 21/n 17.4603; 14.026; 19.2722
90; 98.736; 90
1993.2Li, Taian; Chiou, Mong-Feng; Li, Yajun; Ye, Changqing; Su, Min; Xue, Mengyu; Yuan, Xiaobin; Wang, Chuanchuan; Wan, Wen-Ming; Li, Daliang; Bao, Hongli
Synthesis of Unsymmetrically Tetrasubstituted Pyrroles and Studies of AIEE in Pyrrolo[1,2-a]pyrimidine Derivatives
Chemical Science, 2022
1566840 CIFC35 H23 N3P 1 21/c 19.7978; 27.007; 10.7502
90; 116.236; 90
2551.6Li, Taian; Chiou, Mong-Feng; Li, Yajun; Ye, Changqing; Su, Min; Xue, Mengyu; Yuan, Xiaobin; Wang, Chuanchuan; Wan, Wen-Ming; Li, Daliang; Bao, Hongli
Synthesis of Unsymmetrically Tetrasubstituted Pyrroles and Studies of AIEE in Pyrrolo[1,2-a]pyrimidine Derivatives
Chemical Science, 2022
1566841 CIFC38 H25 Cl2 N3P 1 21/c 111.6662; 23.9537; 12.582
90; 115.611; 90
3170.6Li, Taian; Chiou, Mong-Feng; Li, Yajun; Ye, Changqing; Su, Min; Xue, Mengyu; Yuan, Xiaobin; Wang, Chuanchuan; Wan, Wen-Ming; Li, Daliang; Bao, Hongli
Synthesis of Unsymmetrically Tetrasubstituted Pyrroles and Studies of AIEE in Pyrrolo[1,2-a]pyrimidine Derivatives
Chemical Science, 2022
1566842 CIFC26 H25 N3P b c n19.753; 10.6344; 20.535
90; 90; 90
4313.6Li, Taian; Chiou, Mong-Feng; Li, Yajun; Ye, Changqing; Su, Min; Xue, Mengyu; Yuan, Xiaobin; Wang, Chuanchuan; Wan, Wen-Ming; Li, Daliang; Bao, Hongli
Synthesis of Unsymmetrically Tetrasubstituted Pyrroles and Studies of AIEE in Pyrrolo[1,2-a]pyrimidine Derivatives
Chemical Science, 2022
1566843 CIFC29 H23 N3 S2P 1 21/n 117.7692; 7.587; 17.8377
90; 91.248; 90
2404.2Li, Taian; Chiou, Mong-Feng; Li, Yajun; Ye, Changqing; Su, Min; Xue, Mengyu; Yuan, Xiaobin; Wang, Chuanchuan; Wan, Wen-Ming; Li, Daliang; Bao, Hongli
Synthesis of Unsymmetrically Tetrasubstituted Pyrroles and Studies of AIEE in Pyrrolo[1,2-a]pyrimidine Derivatives
Chemical Science, 2022
1566844 CIFC16 H11 N O2C m c 2114.732; 10.702; 7.661
90; 90; 90
1207.8Owatari, Yoshihiro; Iseki, Shuta; Ogata, Daiji; Yuasa, Junpei
Catalytic electron drives host–guest recognition
Chemical Science, 2022
1566845 CIFC117 H190 Br6 Mg6 N8 O6P 1 21 119.2717; 16.1154; 19.692
90; 93.454; 90
6104.66Monasterolo, Claudio; O'Gara, Ryan; Kavanagh, Saranna; Byrne, Sadbh Elise; Bieszczad, Bartosz; Murray, Orla; Wiesinger, Michael; Lynch, Rebecca; Nikitin, Kirill; Gilheany, Declan Gerard
Asymmetric addition of Grignard reagents to ketones: culmination of the ligand-mediated methodology allows modular construction of chiral tertiary alcohols
Chemical Science, 2022
1566846 CIFC20 H23 Br2 N O2P 1 21 115.0842; 18.1183; 15.8577
90; 109.235; 90
4091.96Monasterolo, Claudio; O'Gara, Ryan; Kavanagh, Saranna; Byrne, Sadbh Elise; Bieszczad, Bartosz; Murray, Orla; Wiesinger, Michael; Lynch, Rebecca; Nikitin, Kirill; Gilheany, Declan Gerard
Asymmetric addition of Grignard reagents to ketones: culmination of the ligand-mediated methodology allows modular construction of chiral tertiary alcohols
Chemical Science, 2022
1566847 CIFC15 H21 N O2P 1 21/n 19.7766; 13.914; 21.1903
90; 97.758; 90
2856.17Guan, Zhipeng; Zhong, Xingxing; Ye, Yayu; Li, Xiangwei; Cong, Hengjiang; Yi, Hong; Zhang, Heng; Huang, Zhiliang; Lei, Aiwen
Selective Radical Cascade (4+2) Annulation with Olefins towards the Synthesis of Chroman Derivatives via Organo-Photoredox Catalysis
Chemical Science, 2022
1566848 CIF
HKL
Paper
C15 H11 N O3 SP 1 21/c 112.6886; 9.2655; 11.6024
90; 105.374; 90
1315.24Pineda, Leslie W.; Ferllini, Natasha; Cabezas, Jorge A.
1-(Phenylsulfonyl)-1<i>H</i>-indole-2-carbaldehyde
IUCrData, 2022, 7, x220401
1566849 CIF
HKL
Paper
C50 H38 Mn N5 O3P c c n20.1021; 21.5505; 17.9807
90; 90; 90
7789.4Cao, Hongli; Wang, Junwen; Li, Jianfeng
Nitrato(5,10,15,20-tetraphenylporphinato)manganese(III)–benzene–<i>n</i>-hexane (2/1/1)
IUCrData, 2022, 7, x220386
1566850 CIFC3 H18 Al F9 O18 S3P 21 21 216.4503; 15.415; 22.904
90; 90; 90
2277.38Pastel, Glenn R.; Chen, Ying; Pollard, Travis P.; Schroeder, Marshall A.; Bowden, Mark E.; Zheng, Allen; Hahn, Nathan T.; Ma, Lin; Murugesan, Vijayakumar; Ho, Janet; Garaga, Mounesha; Borodin, Oleg; Mueller, Karl; Greenbaum, Steven; Xu, Kang
A sobering examination of the feasibility of aqueous aluminum batteries
Energy & Environmental Science, 2022, 15, 2460-2469
1566851 CIFC14 H17 N2 O PP 21 21 217.2488; 10.7508; 17.638
90; 90; 90
1374.5Zhang, Ying; Yuan, Jia; Huang, Guanglong; Yu, Hong; Liu, Jinpeng; Chen, Jian; Meng, Sixuan; Zhong, Jian-Ji; Dang, Li; Yu, Guang-Ao; Che, Chi-Ming
Direct visible-light-induced synthesis of P-stereogenic phosphine oxides under air conditions.
Chemical science, 2022, 13, 6519-6524
1566852 CIFC18 H35 Cl N2 O P2P 1 21 110.2116; 22.6532; 10.5288
90; 114.869; 90
2209.74Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566853 CIFC27 H48 I N3 O P2P 21 21 2111.3375; 16.044; 17.0248
90; 90; 90
3096.79Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566854 CIFC28 H50 I N3 O P2P 21 21 2111.2847; 16.6693; 16.9948
90; 90; 90
3196.86Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566855 CIFC18 H36 N2 O2 P2P 110.1507; 10.483; 12.0198
71.0631; 77.4831; 65.8533
1098.71Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566856 CIFC28 H52 N2 O2 P2P 21 21 219.9457; 13.5082; 22.3174
90; 90; 90
2998.31Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566857 CIFC27 H47 N3 O P2P 19.5345; 11.9909; 13.3121
104.379; 90.136; 94.2154
1469.93Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566858 CIFC26 H45 N3 O P2P 1 21 115.1934; 13.5842; 20.878
90; 101.6; 90
4221.01Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566859 CIFC28 H50 I N3 O P2P 1 21 110.0206; 28.85; 11.9155
90; 110.382; 90
3229.03Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566860 CIFC28 H50 I N3 O P2P 21 21 2111.3691; 16.4031; 17.294
90; 90; 90
3225.13Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566861 CIFC27 H47 N3 O P2P 19.5482; 12.0125; 13.2604
103.899; 90.8396; 94.8447
1470.17Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566862 CIFC26 H45 N3 O P2P 21 21 219.3035; 15.6398; 19.0287
90; 90; 90
2768.77Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566863 CIFC27 H47 N3 O P2P 19.5547; 11.9843; 13.3167
103.719; 90.305; 94.423
1476.49Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566864 CIFC28.5 H56 I N3 O P2C 1 2 114.361; 11.6776; 20.98
90; 92.239; 90
3515.7Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566865 CIFC27 H54 I N3 O P2P 21 21 2111.0895; 16.8933; 17.0952
90; 90; 90
3202.6Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566866 CIFC27 H48 I N3 O P2P 21 21 2111.7716; 15.9064; 16.4323
90; 90; 90
3076.85Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566867 CIFC23 H48 I N3 O P2C 1 2 114.3333; 11.7334; 18.0008
90; 97.111; 90
3004.1Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566868 CIFC28.5 H56 I N3 O P2C 1 2 114.3801; 11.8816; 20.9273
90; 100.971; 90
3510.3Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566869 CIFC28 H50 I N3 O P2P 1 21 19.9808; 28.802; 11.8786
90; 109.431; 90
3220.21Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566870 CIFC23 H48 I N3 O P2P 1 21 114.2761; 11.8123; 18.2335
90; 97.663; 90
3047.3Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566871 CIFC28 H50 I N3 O P2P 1 21 19.9968; 28.7847; 11.8857
90; 109.645; 90
3221.1Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566872 CIFC27 H54 I N3 O P2P 1 21 19.6161; 35.768; 9.7814
90; 98.955; 90
3323.3Peel, Andrew J.; Terzopoulos, Alexandros; Jethwa, Rajesh B.; Choudhury, Dipanjana; Niu, Hao-Che; Bond, Andrew D.; Slaughter, Jonathan; Wright, Dominic S.
A chiral phosphazane reagent strategy for the determination of enantiomeric excess of amines
Chemical Science, 2022
1566873 CIFC11 H10 F N O2P 1 21/c 113.2434; 3.8259; 19.122
90; 92.63; 90
967.85Xing, Yi; Li, Zhongyu; Baryshnikov, Glib; Shen, Shen; Ye, Danfeng; Ågren, Hans; Zhu, Liangliang
Water Molecular Bridge-Induced Selective Dual Polarization in Crystals for Stable Multi-Emitter
Chemical Science, 2022
1566874 CIFC16 H14 N2 O2P 1 2/c 19.948; 5.7541; 23.8405
90; 100.984; 90
1339.67Xing, Yi; Li, Zhongyu; Baryshnikov, Glib; Shen, Shen; Ye, Danfeng; Ågren, Hans; Zhu, Liangliang
Water Molecular Bridge-Induced Selective Dual Polarization in Crystals for Stable Multi-Emitter
Chemical Science, 2022
1566875 CIFC16 H13 F N2 O2P -110.5395; 10.6712; 13.2594
76.844; 85.075; 72.914
1387.8Xing, Yi; Li, Zhongyu; Baryshnikov, Glib; Shen, Shen; Ye, Danfeng; Ågren, Hans; Zhu, Liangliang
Water Molecular Bridge-Induced Selective Dual Polarization in Crystals for Stable Multi-Emitter
Chemical Science, 2022
1566876 CIFC15 H15 I O3 SR -3 :H20.7704; 20.7704; 21.5736
90; 90; 120
8060.1Soldatova, Natalia S.; Postnikov, Pavel S.; Ivanov, Daniil M.; Semyonov, Oleg V.; Kukurina, Olga S.; Guselnikova, Olga; Yamauchi, Yusuke; Wirth, Thomas; Zhdankin, Viktor V.; Yusubov, Mekhman S.; Gomila, Rosa M.; Frontera, Antonio; Resnati, Giuseppe; Kukushkin, Vadim Yu.
Zwitterionic iodonium species afford halogen bond-based porous organic frameworks
Chemical Science, 2022
1566877 CIFC14 H13 I O3 SP 1 21/c 17.0964; 23.1449; 8.145
90; 97.033; 90
1327.71Soldatova, Natalia S.; Postnikov, Pavel S.; Ivanov, Daniil M.; Semyonov, Oleg V.; Kukurina, Olga S.; Guselnikova, Olga; Yamauchi, Yusuke; Wirth, Thomas; Zhdankin, Viktor V.; Yusubov, Mekhman S.; Gomila, Rosa M.; Frontera, Antonio; Resnati, Giuseppe; Kukushkin, Vadim Yu.
Zwitterionic iodonium species afford halogen bond-based porous organic frameworks
Chemical Science, 2022
1566878 CIFC12 H8 Cl I O3 SP -16.0981; 8.1137; 25.8853
94.961; 93.997; 91.858
1271.9Soldatova, Natalia S.; Postnikov, Pavel S.; Ivanov, Daniil M.; Semyonov, Oleg V.; Kukurina, Olga S.; Guselnikova, Olga; Yamauchi, Yusuke; Wirth, Thomas; Zhdankin, Viktor V.; Yusubov, Mekhman S.; Gomila, Rosa M.; Frontera, Antonio; Resnati, Giuseppe; Kukushkin, Vadim Yu.
Zwitterionic iodonium species afford halogen bond-based porous organic frameworks
Chemical Science, 2022
1566879 CIFC15 H15 I O3 SP -110.1666; 14.3384; 20.5652
84.479; 82.633; 74.902
2864.29Soldatova, Natalia S.; Postnikov, Pavel S.; Ivanov, Daniil M.; Semyonov, Oleg V.; Kukurina, Olga S.; Guselnikova, Olga; Yamauchi, Yusuke; Wirth, Thomas; Zhdankin, Viktor V.; Yusubov, Mekhman S.; Gomila, Rosa M.; Frontera, Antonio; Resnati, Giuseppe; Kukushkin, Vadim Yu.
Zwitterionic iodonium species afford halogen bond-based porous organic frameworks
Chemical Science, 2022
1566880 CIFC50 H32 O4P 1 21 16.9528; 13.3069; 37.0562
90; 91.951; 90
3426.46Han, Jianlei; Shi, Yonghong; Jin, Xue; Yang, Xuefeng; Duan, Pengfei
Regulating the Excited State Chirality to Fabricate High-Performance-Solid-State Circularly Polarized Luminescence Materials
Chemical Science, 2022
1566881 CIFC52 H36 O5P 21 21 217.2123; 17.9092; 27.4926
90; 90; 90
3551.12Han, Jianlei; Shi, Yonghong; Jin, Xue; Yang, Xuefeng; Duan, Pengfei
Regulating the Excited State Chirality to Fabricate High-Performance-Solid-State Circularly Polarized Luminescence Materials
Chemical Science, 2022
1566882 CIFC54 H38 O4P 21 21 2125.8331; 10.6809; 13.7334
90; 90; 90
3789.3Han, Jianlei; Shi, Yonghong; Jin, Xue; Yang, Xuefeng; Duan, Pengfei
Regulating the Excited State Chirality to Fabricate High-Performance-Solid-State Circularly Polarized Luminescence Materials
Chemical Science, 2022
1566883 CIFC54 H30 O4P 21 21 2110.2762; 13.1669; 26.875
90; 90; 90
3636.3Han, Jianlei; Shi, Yonghong; Jin, Xue; Yang, Xuefeng; Duan, Pengfei
Regulating the Excited State Chirality to Fabricate High-Performance-Solid-State Circularly Polarized Luminescence Materials
Chemical Science, 2022
1566884 CIFC39 H34 O3P 1 21 110.9647; 18.7819; 14.2842
90; 98.404; 90
2910.07Han, Jianlei; Shi, Yonghong; Jin, Xue; Yang, Xuefeng; Duan, Pengfei
Regulating the Excited State Chirality to Fabricate High-Performance-Solid-State Circularly Polarized Luminescence Materials
Chemical Science, 2022
1566885 CIFC H N O SC 1 m 19.1813; 32.2736; 40.651
90; 96.354; 90
11971.5Zhang, Zhe; Bai, Qixia; Manandhar, Erendra; Zeng, Yunting; Wu, Tun; Wang, Ming; Yao, Liao-Yuan; Newkome, George R.; Wang, Pingshan; Xie, Tingzheng
Supramolecular Cuboctahedra with Aggregation-Induced Emission Enhancement and External Binding Ability
Chemical Science, 2022
1566886 CIFC98 H61 N12 S2P -113.8636; 15.9137; 20.4987
83.865; 73.294; 85.019
4299.28Zhang, Zhe; Bai, Qixia; Manandhar, Erendra; Zeng, Yunting; Wu, Tun; Wang, Ming; Yao, Liao-Yuan; Newkome, George R.; Wang, Pingshan; Xie, Tingzheng
Supramolecular Cuboctahedra with Aggregation-Induced Emission Enhancement and External Binding Ability
Chemical Science, 2022
1566887 CIFC29 H18 NP -18.4867; 12.972; 18.128
105.478; 90.206; 96.312
1910.5Meng, Guoyun; Zhang, Dongdong; Wei, Jinbei; Zhang, Yuewei; Huang, Tianyu; Liu, Ziyang; Yin, Chen; Hong, Xiangchen; Wang, Xiang; Zeng, Xuan; Yang, Dezhi; Ma, Dongge; Li, Guomeng; Duan, Lian
Highly efficient and stable deep-blue OLEDs based on narrowband emitters featuring an orthogonal spiro-configured indolo[3,2,1-de]acridine structure
Chemical Science, 2022
1566888 CIFC28 H31 Cl N2 O2 SiP -18.2938; 10.0055; 17.6368
74.549; 88.4; 68.207
1305.72Miller, Stephen; Rao, Desaboini Nageswara; Ji, Xincai
Silicon functionalization expands the repertoire of Si-rhodamine fluorescent probes
Chemical Science, 2022
1566889 CIFC31 H39 Al N2P 1 21/n 18.6731; 13.6845; 22.6164
90; 95.026; 90
2673.95Dhara, Debabrata; Jayaraman, Arumugam; Härterich, Marcel; Dewhurst, Rian; Braunschweig, Holger
Generation of a transient base-stabilised arylalumylene for the facile deconstruction of aromatic molecules
Chemical Science, 2022
1566890 CIFC68 H80 Al2 N4I 1 2/a 116.9198; 22.2833; 17.4576
90; 117.934; 90
5815.14Dhara, Debabrata; Jayaraman, Arumugam; Härterich, Marcel; Dewhurst, Rian; Braunschweig, Holger
Generation of a transient base-stabilised arylalumylene for the facile deconstruction of aromatic molecules
Chemical Science, 2022
1566891 CIFC159 H188 Al4 I8 N8P -115.879; 16.076; 16.533
92.956; 109.505; 102.27
3853Dhara, Debabrata; Jayaraman, Arumugam; Härterich, Marcel; Dewhurst, Rian; Braunschweig, Holger
Generation of a transient base-stabilised arylalumylene for the facile deconstruction of aromatic molecules
Chemical Science, 2022
1566892 CIFC78 H91 Al2 N4P 1 21/c 115.4528; 15.2329; 28.0296
90; 96.742; 90
6552.29Dhara, Debabrata; Jayaraman, Arumugam; Härterich, Marcel; Dewhurst, Rian; Braunschweig, Holger
Generation of a transient base-stabilised arylalumylene for the facile deconstruction of aromatic molecules
Chemical Science, 2022
1566893 CIFC71 H83 Al2 N4P -113.438; 15.123; 15.478
75.326; 80.106; 84.764
2993.9Dhara, Debabrata; Jayaraman, Arumugam; Härterich, Marcel; Dewhurst, Rian; Braunschweig, Holger
Generation of a transient base-stabilised arylalumylene for the facile deconstruction of aromatic molecules
Chemical Science, 2022
1566894 CIFC68 H88 Al2 N4P -111.884; 15.4141; 18.4138
112.49; 90.87; 105.49
2977.13Dhara, Debabrata; Jayaraman, Arumugam; Härterich, Marcel; Dewhurst, Rian; Braunschweig, Holger
Generation of a transient base-stabilised arylalumylene for the facile deconstruction of aromatic molecules
Chemical Science, 2022
1566895 CIFC33 H34 F3 O12 P SP 1 21 110.5045; 16.82; 11.0991
90; 112.514; 90
1811.6Liu, Fen; Huang, Haiyang; Sun, Longgen; Yan, Zeen; Tan, Xiao; Li, Jing; Luo, Xinyue; Ding, Haixin; Xiao, Qiang
P(v) intermediate-mediated E1cB elimination for the synthesis of glycals
Chemical Science, 2022
1566896 CIFC51 H54 B N3C 1 2/c 115.582; 33.295; 18.241
90; 90.452; 90
9463Jiang, Long; Wang, Yu; Tan, Dehui; Chen, Xiaobin; Ma, Tinghao; Zhang, Baoliang; Yang, Deng-Tao
Access to tetracoordinate boron-doped polycyclic aromatic hydrocarbons with delayed fluorescence and aggregation-induced emission under mild conditions
Chemical Science, 2022
1566897 CIFC59.42 H70.28 B N3I 1 2/a 121.747; 19.582; 23.834
90; 90.748; 90
10148.8Jiang, Long; Wang, Yu; Tan, Dehui; Chen, Xiaobin; Ma, Tinghao; Zhang, Baoliang; Yang, Deng-Tao
Access to tetracoordinate boron-doped polycyclic aromatic hydrocarbons with delayed fluorescence and aggregation-induced emission under mild conditions
Chemical Science, 2022
1566898 CIFC56 H62 B N3P -111.0795; 14.238; 15.3074
83.621; 78.486; 77.897
2307.5Jiang, Long; Wang, Yu; Tan, Dehui; Chen, Xiaobin; Ma, Tinghao; Zhang, Baoliang; Yang, Deng-Tao
Access to tetracoordinate boron-doped polycyclic aromatic hydrocarbons with delayed fluorescence and aggregation-induced emission under mild conditions
Chemical Science, 2022
1566899 CIFC22 H17 F3 O3P 1 21/c 111.6118; 9.7486; 17.4474
90; 102.403; 90
1928.9Zhang, Qi; Chiou, Mong-Feng; Ye, Changqing; Yuan, Xiaobin; Li, Yajun; Bao, Hongli
Radical 1,2,3-Tricarbofunctionalization of α-Vinyl-β-Ketoesters Enabled by Carbon Shift from All-carbon Quaternary Center
Chemical Science, 2022
1566900 CIFC23 H18 Cl F3 O4P 1 21/n 18.9925; 15.5533; 16.006
90; 105.451; 90
2157.7Zhang, Qi; Chiou, Mong-Feng; Ye, Changqing; Yuan, Xiaobin; Li, Yajun; Bao, Hongli
Radical 1,2,3-Tricarbofunctionalization of α-Vinyl-β-Ketoesters Enabled by Carbon Shift from All-carbon Quaternary Center
Chemical Science, 2022
1566901 CIFC23 H18 Cl F3 O3P 1 21/c 112.5234; 9.7432; 17.5168
90; 97.018; 90
2121.35Zhang, Qi; Chiou, Mong-Feng; Ye, Changqing; Yuan, Xiaobin; Li, Yajun; Bao, Hongli
Radical 1,2,3-Tricarbofunctionalization of α-Vinyl-β-Ketoesters Enabled by Carbon Shift from All-carbon Quaternary Center
Chemical Science, 2022
1566902 CIFC22 H19 F3 O3P 1 21/c 115.1282; 11.8989; 11.623
90; 111.112; 90
1951.8Zhang, Qi; Chiou, Mong-Feng; Ye, Changqing; Yuan, Xiaobin; Li, Yajun; Bao, Hongli
Radical 1,2,3-Tricarbofunctionalization of α-Vinyl-β-Ketoesters Enabled by Carbon Shift from All-carbon Quaternary Center
Chemical Science, 2022
1566903 CIF
HKL
Paper
C32 H29 Br N2 O10 S3P 1 21 116.99261; 6.02635; 17.4076
90; 107.831; 90
1696.97Azzam, Rasha A.; Elgemeie, Galal H.; Gad, Nagwa M.; Jones, Peter G.
4-Amino-5-(4-bromobenzoyl)-3-(benzo[<i>d</i>]thiazol-2-yl)-2-[(2',3',4',6'-tetra-<i>O</i>-acetyl-β-<small>D</small>-galactopyranosyl)sulfanyl]thiophene
IUCrData, 2022, 7, x220412
1566904 CIF
HKL
Paper
C16 H20 Cl2 N2 O4P 1 21/c 119.1257; 9.3864; 10.0502
90; 103.546; 90
1754.04Obidova, Nodira; Ashurov, Jamshid; Izotova, Lidiya; Ibragimov, Bakhtiyar
2-Hydroxyethylammonium [2-(2,6-dichloroanilino)phenyl]acetate monohydrate
IUCrData, 2022, 7, x220441
1566905 CIFC64 H50 N30 O15 Zn6P 1 2/c 120.5713; 15.332; 21.6572
90; 96.891; 90
6781.3Wei, Yu-Bai; Luo, Dong; Xiong, Xiao; Huang, Yong-Liang; Xie, Mo; Lu, Weigang; Li, Dan
Biomimetic mimicry of formaldehyde-induced DNA–protein crosslinks in the confined space of a metal–organic framework
Chemical Science, 2022, 13, 4813-4820
1566906 CIFC66 H50 N30 O15 Zn6P 1 2/c 120.7927; 15.218; 21.7299
90; 93.52; 90
6862.9Wei, Yu-Bai; Luo, Dong; Xiong, Xiao; Huang, Yong-Liang; Xie, Mo; Lu, Weigang; Li, Dan
Biomimetic mimicry of formaldehyde-induced DNA–protein crosslinks in the confined space of a metal–organic framework
Chemical Science, 2022, 13, 4813-4820
1566907 CIFC67 H50 N30 O15 Zn6P 1 2/c 120.6916; 15.2813; 21.6745
90; 92.481; 90
6846.93Wei, Yu-Bai; Luo, Dong; Xiong, Xiao; Huang, Yong-Liang; Xie, Mo; Lu, Weigang; Li, Dan
Biomimetic mimicry of formaldehyde-induced DNA–protein crosslinks in the confined space of a metal–organic framework
Chemical Science, 2022, 13, 4813-4820
1566908 CIFC66 H50 N30 O15 Zn6P 1 2/c 120.5389; 15.2128; 21.6422
90; 94.526; 90
6741.1Wei, Yu-Bai; Luo, Dong; Xiong, Xiao; Huang, Yong-Liang; Xie, Mo; Lu, Weigang; Li, Dan
Biomimetic mimicry of formaldehyde-induced DNA–protein crosslinks in the confined space of a metal–organic framework
Chemical Science, 2022, 13, 4813-4820
1566909 CIFC66 H50 N30 O15 Zn6P 1 2/c 120.7798; 15.2345; 21.6564
90; 93.144; 90
6845.4Wei, Yu-Bai; Luo, Dong; Xiong, Xiao; Huang, Yong-Liang; Xie, Mo; Lu, Weigang; Li, Dan
Biomimetic mimicry of formaldehyde-induced DNA–protein crosslinks in the confined space of a metal–organic framework
Chemical Science, 2022, 13, 4813-4820
1566910 CIFC30 H20 As Co O2P -19.0514; 10.5907; 12.8357
76.116; 84.418; 78.076
1167.24Kirk, Ryan M.; Hill, Anthony
Arsolyl-Supported Intermetallic Dative Bonding
Chemical Science, 2022
1566911 CIFC18 H12 As Co O2P n a 2111.2347; 17.2771; 7.8356
90; 90; 90
1520.91Kirk, Ryan M.; Hill, Anthony
Arsolyl-Supported Intermetallic Dative Bonding
Chemical Science, 2022
1566912 CIFC10 H12 As Cl2 Co Hg O2C 1 2/c 114.1928; 14.4745; 14.7169
90; 99.34; 90
2983.27Kirk, Ryan M.; Hill, Anthony
Arsolyl-Supported Intermetallic Dative Bonding
Chemical Science, 2022
1566913 CIFC23 H12 As Co F10 O3 PtP 21 21 219.1891; 12.7559; 21.0227
90; 90; 90
2464.18Kirk, Ryan M.; Hill, Anthony
Arsolyl-Supported Intermetallic Dative Bonding
Chemical Science, 2022
1566914 CIFC10 H12 As Cl2 Co Hg O2P 1 21/n 18.8304; 14.2969; 11.846
90; 94.222; 90
1491.47Kirk, Ryan M.; Hill, Anthony
Arsolyl-Supported Intermetallic Dative Bonding
Chemical Science, 2022
1566915 CIFC16 H33 As Co O4 P Si2C 1 c 17.9385; 19.9045; 15.3637
90; 90.3; 90
2427.61Kirk, Ryan M.; Hill, Anthony
Arsolyl-Supported Intermetallic Dative Bonding
Chemical Science, 2022
1566916 CIFC32 H24 As2 Au2 Co2 F10 O4P -115.1208; 21.7675; 23.8537
100.283; 104.78; 91.078
7452.43Kirk, Ryan M.; Hill, Anthony
Arsolyl-Supported Intermetallic Dative Bonding
Chemical Science, 2022
1566917 CIFC12 H21 As Co O4 PP 1 21/n 18.198; 14.8986; 26.2475
90; 97.071; 90
3181.45Kirk, Ryan M.; Hill, Anthony
Arsolyl-Supported Intermetallic Dative Bonding
Chemical Science, 2022
1566918 CIFC22 H38 N2 O7P 21 21 219.608; 13.2461; 20.0321
90; 90; 90
2549.46Chen, Wei-An; Chen, Yu-Hsin; Hsieh, Chiao-Yun; Hung, Pi-Fang; Chen, Chiao-Wen; Chen, Chien-Hung; Lin, Jung-Lee; Cheng, Ting-Jen R.; Hsu, Tsui-Ling; Wu, Ying-Ta; Shen, Chia-Ning; Cheng, Wei-Chieh
Harnessing natural-product-inspired combinatorial chemistry and computation-guided synthesis to develop N-glycan modulators as anticancer agents
Chemical Science, 2022
1566920 CIFC30 H28 O4P -110.891; 11.4276; 11.5284
116.793; 90.271; 101.247
1249.11Zhang, Qiao; Wang, Wenbo; Cai, Changyong; Wu, Shuanggen; Li, Jialing; Li, Fenfang; Dong, Shengyi
Underwater luminescent labeling materials constructed from a supramolecular approach.
Materials horizons, 2022, 9, 1984-1991
1566921 CIFC30 H28 O4P -17.8756; 11.8787; 13.8525
84.512; 84.625; 71.646
1221.59Zhang, Qiao; Wang, Wenbo; Cai, Changyong; Wu, Shuanggen; Li, Jialing; Li, Fenfang; Dong, Shengyi
Underwater luminescent labeling materials constructed from a supramolecular approach.
Materials horizons, 2022, 9, 1984-1991
1566922 CIFC108 H99 Cl9 O12P -114.9569; 17.9039; 22.5745
69.1; 74.702; 88.173
5434.3Fang, Shuai; Wang, Mengbin; Wu, Yating; Guo, Qing-Hui; Li, Errui; Li, Hao; Huang, Feihe
Cagearenes: synthesis, characterization, and application for programmed vapor release
Chemical Science, 2022
1566923 CIFC123 H114 O12C 1 2/c 125.7782; 18.2534; 27.4389
90; 117.813; 90
11419.5Fang, Shuai; Wang, Mengbin; Wu, Yating; Guo, Qing-Hui; Li, Errui; Li, Hao; Huang, Feihe
Cagearenes: synthesis, characterization, and application for programmed vapor release
Chemical Science, 2022
1566924 CIFC145 H148 O12P -114.166; 18.6824; 23.8099
82.321; 87.364; 74.141
6006.9Fang, Shuai; Wang, Mengbin; Wu, Yating; Guo, Qing-Hui; Li, Errui; Li, Hao; Huang, Feihe
Cagearenes: synthesis, characterization, and application for programmed vapor release
Chemical Science, 2022
1566925 CIFC114 H108 O12P -113.898; 19.031; 24.191
112.073; 103.948; 93.107
5680Fang, Shuai; Wang, Mengbin; Wu, Yating; Guo, Qing-Hui; Li, Errui; Li, Hao; Huang, Feihe
Cagearenes: synthesis, characterization, and application for programmed vapor release
Chemical Science, 2022
1566926 CIFC40 H58 Li2 O10 S2P 1 21/n 111.2936; 21.8827; 17.1083
90; 94.544; 90
4214.8Plajer, Alex Johannes; Pröhm, Patrick; Rupf, Susanne M.
Lithium achieves sequence selective ring-opening terpolymerisation (ROTERP) of ternary monomer mixtures
Chemical Science, 2022
1566927 CIFC12 H13 Na O3 SP -15.9833; 9.3642; 11.7461
90.127; 101.89; 97.726
637.85Plajer, Alex Johannes; Pröhm, Patrick; Rupf, Susanne M.
Lithium achieves sequence selective ring-opening terpolymerisation (ROTERP) of ternary monomer mixtures
Chemical Science, 2022
1566928 CIFC12 H13 K O3 SP 1 2/n 115.1783; 6.6961; 30.176
90; 104.412; 90
2970.4Plajer, Alex Johannes; Pröhm, Patrick; Rupf, Susanne M.
Lithium achieves sequence selective ring-opening terpolymerisation (ROTERP) of ternary monomer mixtures
Chemical Science, 2022
1566929 CIFC8 H8 Cr N4 Ni O5P 1 21 16.6931; 8.4975; 9.8328
90; 102.711; 90
545.53Tang, Hsu-Yen; Lee, Gene-Hsiang; Ng, Kwai-Kong; Yang, Chen-I
A Three-Dimensional Coordination Framework with a Ferromagnetic Coupled Ni(II)-CrO4 Layer: Synthesis, Structure, and Magnetic Studies
Polymers, 2022, 14, 1735
1566930 CIFC27 H27 N O2P 1 21 19.6464; 23.7748; 10.1622
90; 112.225; 90
2157.46Wei, Wan-Xu; Kong, Xiangtao; Jiao, Rui-Qiang; Li, Xue-Song; Wang, Cui-Tian; Li, Yuke; Liang, Yong-Min
Regioselective Synthesis of Spirocyclic Pyrrolines via a Palladium-Catalyzed Narasaka-Heck/C-H Activation/[4+2] Annulation Cascade Reaction
Chemical Science, 2022

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