Crystallography Open Database

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Searching journal of publication like 'Green Chemistry'

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7250694 CIFC12 H8 N4 Ni O2I m m a22; 6.93; 14.76
90; 90; 90
2250.3Shupletsov, Leonid; Schieck, Alina C.; Senkovska, Irena; Bon, Volodymyr; Kaskel, Stefan
The use of a dynamic solvent system as a novel approach to sustainable MOF crystallization
Green Chemistry, 2025, 27, 10218-10233
7250708 CIFC21 H18 O S2P 1 21/n 111.7103; 9.7878; 15.3735
90; 95.455; 90
1754.1Yuan, Yong; Bai, Chunyan; Tao, Yuyan; Zhang, Ya-Nan; Bao, Xiazhen; Ji, Dongsheng; Wang, Liwei; Qi, Xiaotian; Huo, Congde
Electrochemical ring-opening oxidation of aryl thianthrenium salts
Green Chemistry, 2025, 27, 9777-9786
7250709 CIFC36 H28 O4 S4P n a 2114.712; 9.99449; 21.0468
90; 90; 90
3094.7Yuan, Yong; Bai, Chunyan; Tao, Yuyan; Zhang, Ya-Nan; Bao, Xiazhen; Ji, Dongsheng; Wang, Liwei; Qi, Xiaotian; Huo, Congde
Electrochemical ring-opening oxidation of aryl thianthrenium salts
Green Chemistry, 2025, 27, 9777-9786
7250779 CIFC26 H23 Cl O2 SiP 1 21/c 110.2217; 25.507; 9.3872
90; 110.477; 90
2292.8Gao, Liuzhou; Wen, Yan; Sun, Yan; Sun, Yuxin; Hu, Jingyi; Wang, Shenglong; Li, Zhenxing; Han, Ying; Wang, Yidong
Metal-free C(sp3)–Si activation enables regiocontrolled [4 + 2] cycloaddition to benzosilacycloethers
Green Chemistry, 2025, 27, 10242-10249
7250797 CIFC23 H20 F3 N OP -19.711; 10.465; 11.661
73.798; 73.558; 62.944
996.4Lu, Meiqun; Chen, Kailun; Cai, Hu
Electrochemical intermolecular trifluoromethylimination of alkenes
Green Chemistry, 2025, 27, 10994-10999
7250813 CIFC12 H9 F N4 O2P 1 21/c 14.1879; 19.4145; 13.7194
90; 97.095; 90
1106.93Zhang, Xiaofeng; Nallapati, Sashirekha; Johnson, Shea; Chen, Xian; Lim, Jongwon
A PASE synthesis of tetrazoloquinolines and its applications in the syntheses of bioactive compounds
Green Chemistry, 2025, 27, 10980-10987
7250814 CIFC12 H9 F N4 O2P -14.6263; 12.8003; 20.056
104.633; 95.726; 94.206
1137.41Zhang, Xiaofeng; Nallapati, Sashirekha; Johnson, Shea; Chen, Xian; Lim, Jongwon
A PASE synthesis of tetrazoloquinolines and its applications in the syntheses of bioactive compounds
Green Chemistry, 2025, 27, 10980-10987
7250876 CIFC48 H72 Co2 N18 O51 P V0.5 W11.5P 112.0693; 13.86; 16.1859
111.705; 96.855; 111.816
2229.56Zhu, Yin-Hua; Yang, Jian-Bo; Zhou, Jiu Lin; Ji, Yong-Qi; Mei, Hua; Xu, Yan
Chiral chlorophyll-inspired clusters steering electron transfer for enhanced CO2 photoreduction
Green Chemistry, 2025, 27, 12778-12784
7250918 CIFC12 H15 N O2P 1 21/c 111.6446; 9.385; 10.0559
90; 98.075; 90
1088.1Wang, Zengping; Zhai, Xiaofang; Bai, Pengtao; Fang, Li; Zheng, Shaojun; Zhao, Jiajia; Yang, Fu; Xu, Chen; Song, Heng
An unconventional photochemical amide synthesis from excited-state nitroarenes
Green Chemistry, 2025, 27, 13427-13435
7250919 CIFC11 H13 N O2P b c a11.6455; 9.2112; 18.6069
90; 90; 90
1995.9Wang, Zengping; Zhai, Xiaofang; Bai, Pengtao; Fang, Li; Zheng, Shaojun; Zhao, Jiajia; Yang, Fu; Xu, Chen; Song, Heng
An unconventional photochemical amide synthesis from excited-state nitroarenes
Green Chemistry, 2025, 27, 13427-13435
7250920 CIFC10 H11 N O2P c a 219.9637; 5.741; 15.679
90; 90; 90
896.9Wang, Zengping; Zhai, Xiaofang; Bai, Pengtao; Fang, Li; Zheng, Shaojun; Zhao, Jiajia; Yang, Fu; Xu, Chen; Song, Heng
An unconventional photochemical amide synthesis from excited-state nitroarenes
Green Chemistry, 2025, 27, 13427-13435
7250921 CIFC10 H11 N O2P 1 21/n 17.314; 12.846; 10.041
90; 92.34; 90
942.6Wang, Zengping; Zhai, Xiaofang; Bai, Pengtao; Fang, Li; Zheng, Shaojun; Zhao, Jiajia; Yang, Fu; Xu, Chen; Song, Heng
An unconventional photochemical amide synthesis from excited-state nitroarenes
Green Chemistry, 2025, 27, 13427-13435
7250922 CIFC10 H7 N O3P 1 21/c 15.158; 16.263; 11.109
90; 99.35; 90
919.5Wang, Zengping; Zhai, Xiaofang; Bai, Pengtao; Fang, Li; Zheng, Shaojun; Zhao, Jiajia; Yang, Fu; Xu, Chen; Song, Heng
An unconventional photochemical amide synthesis from excited-state nitroarenes
Green Chemistry, 2025, 27, 13427-13435
7250923 CIFC10 H10 F N O2P n m a7.4227; 6.7898; 18.749
90; 90; 90
944.9Wang, Zengping; Zhai, Xiaofang; Bai, Pengtao; Fang, Li; Zheng, Shaojun; Zhao, Jiajia; Yang, Fu; Xu, Chen; Song, Heng
An unconventional photochemical amide synthesis from excited-state nitroarenes
Green Chemistry, 2025, 27, 13427-13435
7250924 CIFC14 H13 N O2P 1 21/c 17.4116; 12.5682; 12.6455
90; 92.181; 90
1177.08Wang, Zengping; Zhai, Xiaofang; Bai, Pengtao; Fang, Li; Zheng, Shaojun; Zhao, Jiajia; Yang, Fu; Xu, Chen; Song, Heng
An unconventional photochemical amide synthesis from excited-state nitroarenes
Green Chemistry, 2025, 27, 13427-13435
7251018 CIFC13 H13 Br2 N O2P 1 21/c 110.5935; 14.8164; 9.1423
90; 114.945; 90
1301.09Jia, Longxia; Liu, Hongling; Shi, Weiwei; Xu, Yingru; Sun, Ruihan; Zuo, Jia; Wang, Bin; Huang, Jianjian; Zhong, Fangrui; Wang, Dangui
A bifunctional recyclable Gemini surfactant catalyst for oxidative nitroso Diels–Alder reactions in water
Green Chemistry, 2025, 27, 13885-13892
7251019 CIFC27 H21 N3 OC 1 2/c 117.309; 12.0431; 20.6182
90; 105.402; 90
4143.59Zou, Pei-Sen; Geng, Yi-Fan; Liu, Xiao-Qing; Su, Jun-Cheng; Pan, Cheng-Xue; Mo, Dong-Liang; Su, Gui-Fa
An unexpected transition-metal free regioselective cyclization of alkynyl-tethered indoles to prepare indole-fused azepino[2,1-b]quinazolinones and spiroindole-pyrrolo[2,1-b]quinazolinones
Green Chemistry, 2025, 27, 14556-14563
7251020 CIFC25 H17 N3 OP 1 21/n 111.4831; 11.2094; 15.2029
90; 92.885; 90
1954.42Zou, Pei-Sen; Geng, Yi-Fan; Liu, Xiao-Qing; Su, Jun-Cheng; Pan, Cheng-Xue; Mo, Dong-Liang; Su, Gui-Fa
An unexpected transition-metal free regioselective cyclization of alkynyl-tethered indoles to prepare indole-fused azepino[2,1-b]quinazolinones and spiroindole-pyrrolo[2,1-b]quinazolinones
Green Chemistry, 2025, 27, 14556-14563
7251021 CIFC18 H21 F3 N2C 1 2/c 127.2009; 8.2531; 14.6469
90; 91.613; 90
3286.81Wu, Ziyan; Fang, Guodong; Li, Xindi; Wu, Yuhao; Li, Jinshan; Feng, Yan; Xie, Jialin; Zhou, Xueqing; Wen, Zhenchang; Jia, Chunman
Different paths lead to the same destination: a highly efficient TMSOTf/HFIP catalytic system for large-scale synthesis of fluoroalkyl-containing 4,4′-methylenedianiline (MDA) monomers
Green Chemistry, 2025, 27, 13751-13761
7251022 CIFC16 H18 F2 N2P 1 21/c 112.3495; 7.3054; 15.1869
90; 93.228; 90
1367.96Wu, Ziyan; Fang, Guodong; Li, Xindi; Wu, Yuhao; Li, Jinshan; Feng, Yan; Xie, Jialin; Zhou, Xueqing; Wen, Zhenchang; Jia, Chunman
Different paths lead to the same destination: a highly efficient TMSOTf/HFIP catalytic system for large-scale synthesis of fluoroalkyl-containing 4,4′-methylenedianiline (MDA) monomers
Green Chemistry, 2025, 27, 13751-13761

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