Crystallography Open Database
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Result: there are 18042 entries in the selection
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Searching year of publication is 2020
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1551255 | CIF | C96 H74 Cd4 N8 O28 P8 Si2 | P -1 | 14.0172; 14.593; 25.8504 105.431; 95.932; 100.167 | 4953.8 | Ai, Jing; Tian, Hong-Rui; Min, Xue; Wang, Zi-Chuan; Sun, Zhong-Ming A fast and highly selective Congo red adsorption material based on a cadmium-phosphonate network. Dalton transactions (Cambridge, England : 2003), 2020, 49, 3700-3705 |
| 1552151 | CIF | C48 H45 B N2 | P 1 21/c 1 | 7.5979; 32.4387; 16.8075 90; 115.761; 90 | 3730.78 | Zhang, Jing; Li, Aisen; Zou, Hang; Peng, Junhui; Guo, Jiali; Wu, Wenjie; Zhang, Haoke; Zhang, Jun; Gu, Xinggui; Xu, Weiqing; Xu, Shuping; Liu, Sheng Hua; Qin, Anjun; Lam, Jacky W. Y.; Tang, Ben Zhong A “simple” donor‒acceptor AIEgen with multi-stimuli responsive behavior Materials Horizons, 2020, 7, 135-142 |
| 1552310 | CIF | C33 H30 N O4 P Pd S2 | P -1 | 10.11; 12.7449; 14.2331 85.456; 75.679; 87.617 | 1770.9 | Tan, Chen; Qasim, Muhammad; Pang, Wenmin; Chen, Changle Ligand‒metal secondary interactions in phosphine‒sulfonate palladium and nickel catalyzed ethylene (co)polymerization Polymer Chemistry, 2020, 11, 411-416 |
| 1552372 | CIF | C64 H52 Br2 P4 Ru S2 | P -1 | 9.3882; 12.9082; 13.5032 117.037; 96.017; 103.315 | 1376.31 | Ho, Po-Yuen; Komber, Hartmut; Horatz, Kilian; Tsuda, Takuya; Mannsfeld, Stefan C. B.; Dmitrieva, Evgenia; Blacque, Olivier; Kraft, Ulrike; Sirringhaus, Henning; Lissel, Franziska Synthesis and characterization of a semiconducting and solution-processable ruthenium-based polymetallayne Polymer Chemistry, 2020, 11, 472-479 |
| 1552456 | CIF | C31 H23 F3 N2 O5 | P 21 21 21 | 8.97942; 10.9358; 27.051 90; 90; 90 | 2656.33 | Shu, Chang; Liu, Honglei; Slawin, Alexandra M. Z.; Carpenter-Warren, Cameron; Smith, Andrew D. Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters Chemical Science, 2020, 11, 241-247 |
| 1552457 | CIF | C28 H26 F3 N3 O2 | P 1 21/c 1 | 19.7387; 13.4237; 9.3356 90; 93.107; 90 | 2469.98 | Shu, Chang; Liu, Honglei; Slawin, Alexandra M. Z.; Carpenter-Warren, Cameron; Smith, Andrew D. Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters Chemical Science, 2020, 11, 241-247 |
| 1552458 | CIF | C28 H26 F3 N3 O2 | P 1 21 1 | 13.5575; 23.9425; 19.8418 90; 93.584; 90 | 6428.06 | Shu, Chang; Liu, Honglei; Slawin, Alexandra M. Z.; Carpenter-Warren, Cameron; Smith, Andrew D. Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters Chemical Science, 2020, 11, 241-247 |
| 1552477 | CIF | C51 H58 O14 | P -1 | 9.6444; 12.2441; 19.4216 93.6475; 99.9526; 92.348 | 2251.2 | Xu, Xiaowen; Jerca, Florica Adriana; Van Hecke, Kristof; Jerca, Valentin Victor; Hoogenboom, Richard High compression strength single network hydrogels with pillar[5]arene junction points Materials Horizons, 2020, 7, 566-573 |
| 1552504 | CIF | C20 H22 B N | F d d 2 | 39.763; 37.788; 8.9491 90; 90; 90 | 13446.6 | Su, Xiaojun; Baker, J. J.; Martin, Caleb D. Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis. Chemical science, 2020, 11, 126-131 |
| 1552505 | CIF | C17 H17 B Cr O3 S | P 1 21/c 1 | 11.605; 9.0305; 15.7985 90; 102.127; 90 | 1618.72 | Su, Xiaojun; Baker, J. J.; Martin, Caleb D. Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis. Chemical science, 2020, 11, 126-131 |
| 1552506 | CIF | C28 H27 B O | P -1 | 8.7781; 10.9283; 12.3004 70.809; 87.538; 79.597 | 1095.91 | Su, Xiaojun; Baker, J. J.; Martin, Caleb D. Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis. Chemical science, 2020, 11, 126-131 |
| 1552507 | CIF | C27 H27 B O | C 1 c 1 | 13.441; 13.1854; 24.0772 90; 94.762; 90 | 4252.4 | Su, Xiaojun; Baker, J. J.; Martin, Caleb D. Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis. Chemical science, 2020, 11, 126-131 |
| 1552508 | CIF | C28 H29 B O | P 1 21/n 1 | 14.454; 7.2349; 21.474 90; 100.708; 90 | 2206.5 | Su, Xiaojun; Baker, J. J.; Martin, Caleb D. Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis. Chemical science, 2020, 11, 126-131 |
| 1552533 | CIF | C88 H76 F24 N14 P4 Ru2 | P -1 | 13.885; 17.841; 22.499 83.99; 73.932; 85.868 | 5320.9 | Smitten, Kirsty L.; Fairbanks, Simon D.; Robertson, Craig C.; Bernardino de la Serna, Jorge; Foster, Simon J.; Thomas, Jim A. Ruthenium based antimicrobial theranostics - using nanoscopy to identify therapeutic targets and resistance mechanisms in <i>Staphylococcus aureus</i>. Chemical science, 2020, 11, 70-79 |
| 1552713 | CIF | C44 H42 F18 N6 P3 S2 | P b a m | 14.8195; 20.8662; 9.5394 90; 90; 90 | 2949.8 | Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes. Chemical science, 2020, 11, 107-112 |
| 1552714 | CIF | C78 H73 F30 N11 P5 | C m c 21 | 19.886; 20.698; 20.515 90; 90; 90 | 8444 | Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes. Chemical science, 2020, 11, 107-112 |
| 1552715 | CIF | C48 H46 F18 N6 P3 | P b a m | 14.1423; 21.9108; 9.5937 90; 90; 90 | 2972.79 | Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes. Chemical science, 2020, 11, 107-112 |
| 1552716 | CIF | C36 H32 F24 N4 P4 | P 1 21/c 1 | 7.4563; 20.125; 13.948 90; 91.831; 90 | 2091.9 | Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes. Chemical science, 2020, 11, 107-112 |
| 1552717 | CIF | C32 H28 F12 N4 P2 S2 | P b a m | 10.3821; 21.5348; 9.6558 90; 90; 90 | 2158.81 | Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes. Chemical science, 2020, 11, 107-112 |
| 1552718 | CIF | C35 H31 F24 N5 P4 | P -1 | 11.2904; 16.9439; 24.966 75.157; 86.061; 86.58 | 4601.4 | Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes. Chemical science, 2020, 11, 107-112 |
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