Crystallography Open Database
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Searching journal of publication like 'Green Chem.' volume of publication is 18
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1540034 | CIF | C32 H28 F6 N8 O4 Zn | P -1 | 8.8018; 9.2775; 11.3673 82.433; 68.031; 67.635 | 796 | Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand Green Chem., 2016, 18, 1524 |
1540035 | CIF | C40 H44 F6 N8 O4 Zn | P 1 21/n 1 | 14.5768; 8.9341; 15.9047 90; 103.294; 90 | 2015.8 | Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand Green Chem., 2016, 18, 1524 |
1540036 | CIF | C18 H14 F6 N4 O4 Zn | P -1 | 9.7675; 11.262; 11.576 98.815; 107.953; 112.944 | 1059.8 | Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand Green Chem., 2016, 18, 1524 |
7221876 | CIF | C19 H11 N O2 S | P 1 21/c 1 | 12.242; 11.566; 10.526 90; 93.08; 90 | 1488.2 | Wan, Jie-Ping; Zhou, Youyi; Liu, Yunyun; Sheng, Shouri Metal-free oxidative carbonylation on enaminone CC bond for the cascade synthesis of benzothiazole-containing vicinal diketones Green Chem., 2016, 18, 402 |
7221978 | CIF | C4 H6 O4 | P 1 21/c 1 | 10.6016; 9.5305; 10.7702 90; 119.312; 90 | 948.88 | Tryznowski, M.; Żołek-Tryznowska, Z.; Świderska, A.; Parzuchowski, P. G. Synthesis, characterization and reactivity of a six-membered cyclic glycerol carbonate bearing a free hydroxyl group Green Chem., 2016, 18, 802 |
7222111 | CIF | C18 H31 N O4 | P -1 | 9.384; 10.484; 11.281 102.829; 94.191; 113.456 | 976.4 | Maleki, Abbas; Nematollahi, Davood; Rasouli, Fereshteh; Zeinodini-Meimand, Azam Electrode instead of catalyst and enzyme. A greener protocol for the synthesis of new 2-hydroxyacetamide derivatives containing a γ-lactone ring Green Chem., 2016, 18, 672 |
7222916 | CIF | C7 H10 F N O3 | P 1 21 1 | 8.5224; 10.305; 9.1442 90; 90.3404; 90 | 803.06 | Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy Green Chem., 2016, 18, 1313 |
7222917 | CIF | C7 H10 F N O3 | P 1 21 1 | 8.5211; 10.3039; 9.1547 90; 90.365; 90 | 803.77 | Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy Green Chem., 2016, 18, 1313 |
7222918 | CIF | C8 H15 Cl F N O4 | P -1 | 5.821; 6.4875; 15.7485 100.738; 96.625; 94.612 | 577.23 | Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy Green Chem., 2016, 18, 1313 |
7222919 | CIF | C7 H10 F N O3 | P 1 21/c 1 | 12.256; 6.72544; 10.4787 90; 113.193; 90 | 793.92 | Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy Green Chem., 2016, 18, 1313 |
7222920 | CIF | C7 H13 Cl F N O4 | P 1 21/c 1 | 12.235; 11.3068; 7.6415 90; 100.289; 90 | 1040.12 | Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy Green Chem., 2016, 18, 1313 |
7222921 | CIF | C6 H10 F N O4 | P -1 | 6.5648; 6.6759; 9.6206 98.163; 100.929; 101.047 | 399.3 | Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy Green Chem., 2016, 18, 1313 |
7223202 | CIF | C88 H72 Cd5 N6 O28 | P 1 21/c 1 | 14.6261; 23.2526; 15.7357 90; 107.099; 90 | 5115.1 | Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry Green Chem., 2016, 18, 951 |
7223203 | CIF | C96 H82 Cd5 N8 O28 | P 1 21/c 1 | 14.5196; 23.367; 15.6042 90; 107.475; 90 | 5049.8 | Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry Green Chem., 2016, 18, 951 |
7223204 | CIF | C88 H72 Cd3 Cu2 N6 O27 | P 1 21/c 1 | 14.3997; 23.362; 15.543 90; 106.309; 90 | 5018.4 | Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry Green Chem., 2016, 18, 951 |
7223205 | CIF | C90 H76 Cd5 N6 O28 | P 1 21/c 1 | 14.583; 23.241; 15.6338 90; 106.99; 90 | 5067.4 | Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry Green Chem., 2016, 18, 951 |
7223248 | CIF | C26 H16 N4 O8 Zn | P 1 21/c 1 | 19.13; 26.34; 11.628 90; 90.671; 90 | 5859 | Gong, Le Le; Feng, Xue Feng; Luo, Feng; Yi, Xian Feng; Zheng, An Min Removal and safe reuse of highly toxic allyl alcohol using a highly selective photo-sensitive metal‒organic framework Green Chem., 2016, 18, 2047 |
7223249 | CIF | C36 H28 N4 P2 | P -1 | 8.8542; 12.9976; 14.0901 100.076; 90.969; 92.406 | 1594.63 | Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins Green Chem., 2016, 18, 1798 |
7223250 | CIF | C40 H34 F6 N4 O6 P2 S2 | P -1 | 14.0858; 14.4866; 15.7112 67.615; 78.55; 62.44 | 2627 | Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins Green Chem., 2016, 18, 1798 |
7223251 | CIF | C38 H33 Cl2 I N4 P2 | P 1 21/c 1 | 9.5438; 39.836; 10.6814 90; 116.464; 90 | 3635.4 | Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins Green Chem., 2016, 18, 1798 |
7223441 | CIF | C23 H26 N2 O2 | P 1 21/c 1 | 9.0471; 17.5709; 12.943 90; 109.25; 90 | 1942.5 | Harvey, Benjamin G.; Guenthner, Andrew J.; Koontz, Thomas A.; Storch, Perrin J.; Reams, Josiah T.; Groshens, Thomas J. Sustainable hydrophobic thermosetting resins and polycarbonates from turpentine Green Chem., 2016, 18, 2416 |
7223442 | CIF | C28 H24 N2 O3 S | P -1 | 9.0258; 11.0099; 12.4506 79.449; 76.11; 80.803 | 1172 | Dandia, Anshu; Parewa, Vijay; Kumari, Sukhbeer; Bansal, Sarika; Sharma, Amit Imposed hydrophobic interactions by NaCl: accountable attribute for the synthesis of spiro[acenaphthylene-1,5′-pyrrolo[1,2-c]thiazole] derivatives via 1,3-dipolar cycloaddition reaction in aqueous medium Green Chem., 2016, 18, 2488 |
7223600 | CIF | C38 H48 Cl Cu N4 O S2 | P -1 | 11.443; 12.452; 15.01 71.585; 84.083; 68.386 | 1886.3 | Barman, Milan Kr.; Sinha, Ashish Kumar; Nembenna, Sharanappa An efficient and recyclable thiourea-supported copper(i) chloride catalyst for azide‒alkyne cycloaddition reactions Green Chem., 2016, 18, 2534 |
7223770 | CIF | C75 H47 N5 O9 Zn2 | C 1 2/c 1 | 28.525; 29.966; 14.784 90; 109.02; 90 | 11947.1 | Liu, Yue; Chen, Dashu; Li, Xingyu; Yu, Ziyang; Xia, Qiansu; Liang, Desheng; Xing, Hongzhu Visible-light-induced controlled radical polymerization of methacrylates mediated by a pillared-layer metal‒organic framework Green Chem., 2016, 18, 1475 |
7223872 | CIF | C26 H34 O3 S | P 21 21 2 | 9.7748; 36.406; 6.5704 90; 90; 90 | 2338.2 | Huang, Mingming; Hu, Liangzhen; Shen, Hang; Liu, Qing; Hussain, Muhammad Ijaz; Pan, Jing; Xiong, Yan Sulfination of alcohols with sodium sulfinates promoted by BF3·OEt2: an unexpected access Green Chem., 2016, 18, 1874 |
7224061 | CIF | C20 H22 O | P -1 | 8.4061; 8.6026; 12.582 91.647; 102.618; 112.149 | 816.1 | Wang, Kuai; Meng, Ling-Guo; Zhang, Qi; Wang, Lei Direct construction of 4-aryl tetralones via visible-light-induced cyclization of styrenes with molecular oxygen Green Chem., 2016, 18, 2864 |
7224113 | CIF | C14 H14 N2 O2 | P 1 21 1 | 7.5292; 5.7936; 13.9668 90; 93.766; 90 | 607.93 | Chaudhary, Priyanka; Gupta, Surabhi; Muniyappan, Nalluchamy; Sabiah, Shahulhameed; Kandasamy, Jeyakumar An efficient synthesis of N-nitrosamines under solvent, metal and acid free conditions using tert-butyl nitrite Green Chem., 2016, 18, 2323 |
7224294 | CIF | C18 H13 Cl N4 O Pd | P 1 21/c 1 | 13.0361; 12.7404; 20.0773 90; 94.398; 90 | 3324.7 | Arumugam, Vignesh; Kaminsky, Werner; Nallasamy, Dharmaraj Pd(ii) pincer type complex catalyzed tandem C‒H and N‒H activation of acetanilide in aqueous media: a concise access to functionalized carbazoles in a single step Green Chem., 2016, 18, 3295 |
7224295 | CIF | C17 H12 Cl N3 O2 Pd | P n a 21 | 18.2644; 9.0854; 19.045 90; 90; 90 | 3160.3 | Arumugam, Vignesh; Kaminsky, Werner; Nallasamy, Dharmaraj Pd(ii) pincer type complex catalyzed tandem C‒H and N‒H activation of acetanilide in aqueous media: a concise access to functionalized carbazoles in a single step Green Chem., 2016, 18, 3295 |
7224493 | CIF | C17 H12 N2 S | P 1 21/c 1 | 12.247; 13.34; 8.315 90; 77.29; 90 | 1325 | Đud, Mateja; Magdysyuk, Oxana V.; Margetić, Davor; Štrukil, Vjekoslav Synthesis of monosubstituted thioureas by vapour digestion and mechanochemical amination of thiocarbamoyl benzotriazoles Green Chem., 2016, 18, 2666 |
7224494 | CIF | C15 H12 N2 S | P 21/c 1 1 | 5.873; 9.367; 22.93 91.31; 90; 90 | 1261.1 | Đud, Mateja; Magdysyuk, Oxana V.; Margetić, Davor; Štrukil, Vjekoslav Synthesis of monosubstituted thioureas by vapour digestion and mechanochemical amination of thiocarbamoyl benzotriazoles Green Chem., 2016, 18, 2666 |
7224566 | CIF | C20 H21 N5 O4 | P 1 21/n 1 | 9.9263; 15.4568; 12.4445 90; 96.737; 90 | 1896.16 | Zhang, Xiaofeng; Zhi, Sanjun; Wang, Wei; Liu, Shuai; Jasinski, Jerry P.; Zhang, Wei A pot-economical and diastereoselective synthesis involving catalyst-free click reaction for fused-triazolobenzodiazepines Green Chem., 2016, 18, 2642 |
7224593 | CIF | C19 H16 F N O4 | P -1 | 8.747; 11.406; 16.58 80.72; 85.21; 85.46 | 1623.2 | Ahankar, Hamideh; Ramazani, Ali; Ślepokura, Katarzyna; Lis, Tadeusz; Joo, Sang Woo Synthesis of pyrrolidinone derivatives from aniline, an aldehyde and diethyl acetylenedicarboxylate in an ethanolic citric acid solution under ultrasound irradiation Green Chem., 2016, 18, 3582 |
7224743 | CIF | C25 H25 N O9 | P 1 21/c 1 | 23.7419; 8.0217; 31.6881 90; 127.152; 90 | 4810.1 | Samai, Subhasis; Ghosh, Debasish; Das, Uttam K.; Atta, Sanghamitra; Manna, Saikat K.; Maiti, Dilip K. Water ‒ the best solvent for DMAP-mediated dual cyclization towards metal-free first synthesis of fully substituted phthalimides Green Chem., 2016, 18, 2961 |
7224744 | CIF | C21 H17 N O8 | P -1 | 8.133; 11.671; 11.708 63.061; 84.432; 75.914 | 960.8 | Samai, Subhasis; Ghosh, Debasish; Das, Uttam K.; Atta, Sanghamitra; Manna, Saikat K.; Maiti, Dilip K. Water ‒ the best solvent for DMAP-mediated dual cyclization towards metal-free first synthesis of fully substituted phthalimides Green Chem., 2016, 18, 2961 |
7225073 | CIF | C20 H22 N2 | P 1 21/c 1 | 10.815; 19.201; 7.858 90; 104.8; 90 | 1577.6 | Cai, Jinhui; Li, Feifei; Deng, Guo-Jun; Ji, Xiaochen; Huang, Huawen The cyclopropylimine rearrangement/Povarov reaction cascade for the assembly of pyrrolo[3,2-c]quinoline derivatives Green Chem., 2016, 18, 3503 |
7225077 | CIF | C20 H21 N4 O2.5 | P b c n | 15.4558; 18.7716; 26.327 90; 90; 90 | 7638.3 | Singh, Nongthombam Geetmani; Lily, Makroni; Devi, Shougaijam Premila; Rahman, Noimur; Ahmed, Aziz; Chandra, Asit K.; Nongkhlaw, Rishanlang Synthetic, mechanistic and kinetic studies on the organo-nanocatalyzed synthesis of oxygen and nitrogen containing spiro compounds under ultrasonic conditions Green Chem., 2016, 18, 4216 |
7225078 | CIF | C20 H11 N3 O4 | P -1 | 10.3603; 13.054; 14.655 75.239; 84.652; 69.915 | 1800 | Singh, Nongthombam Geetmani; Lily, Makroni; Devi, Shougaijam Premila; Rahman, Noimur; Ahmed, Aziz; Chandra, Asit K.; Nongkhlaw, Rishanlang Synthetic, mechanistic and kinetic studies on the organo-nanocatalyzed synthesis of oxygen and nitrogen containing spiro compounds under ultrasonic conditions Green Chem., 2016, 18, 4216 |
7225170 | CIF | C50 H68 N14 O16 Zn2 | I m -3 | 28.6573; 28.6573; 28.6573 90; 90; 90 | 23534.5 | Han, Yun-Hu; Zhou, Zhong-Yuan; Tian, Chong-Bin; Du, Shao-Wu A dual-walled cage MOF as an efficient heterogeneous catalyst for the conversion of CO2under mild and co-catalyst free conditions Green Chem., 2016, 18, 4086 |
7225274 | CIF | C19 H21 N3 O | C 1 2/c 1 | 11.725; 17.259; 16.041 90; 90.789; 90 | 3245.8 | Lezana, Nicolás; Matus-Pérez, Massiel; Galdámez, Antonio; Lühr, Susan; Vilches-Herrera, Marcelo Highly stereoselective and catalyst-free synthesis of annulated tetrahydropyridines by intramolecular imino-Diels‒Alder reaction under microwave irradiation in water Green Chem., 2016, 18, 3712 |
7225275 | CIF | C55 H81 N2 Nd O5 | P -1 | 13.61; 15.446; 15.506 98.661; 107.06; 112.68 | 2743.8 | Qin, Jie; Xu, Bin; Zhang, Yong; Yuan, Dan; Yao, Yingming Cooperative rare earth metal‒zinc based heterometallic catalysts for copolymerization of CO2and cyclohexene oxide Green Chem., 2016, 18, 4270 |
7225276 | CIF | C55 H79 N2 O4 Y | P 1 21/n 1 | 15.2272; 14.1936; 24.434 90; 99.252; 90 | 5212.2 | Qin, Jie; Xu, Bin; Zhang, Yong; Yuan, Dan; Yao, Yingming Cooperative rare earth metal‒zinc based heterometallic catalysts for copolymerization of CO2and cyclohexene oxide Green Chem., 2016, 18, 4270 |
7225277 | CIF | C142 H214 N4 Nd2 O10 Zn | C 1 2/c 1 | 25.713; 25.211; 25.54 90; 115.838; 90 | 14901 | Qin, Jie; Xu, Bin; Zhang, Yong; Yuan, Dan; Yao, Yingming Cooperative rare earth metal‒zinc based heterometallic catalysts for copolymerization of CO2and cyclohexene oxide Green Chem., 2016, 18, 4270 |
7225288 | CIF | C18 H33 B2 F8 Ir N4 O2 | P -1 | 8.6729; 11.3034; 13.751 85.039; 74.421; 78.507 | 1271.7 | Lu, Sheng-Mei; Wang, Zhijun; Li, Jun; Xiao, Jianliang; Li, Can Base-free hydrogenation of CO2to formic acid in water with an iridium complex bearing a N,N′-diimine ligand Green Chem., 2016, 18, 4553 |
7225401 | CIF | C10 H10 O5 | P 1 21/c 1 | 10.6927; 7.81215; 10.6458 90; 95.5149; 90 | 885.16 | Bai, Yinjuan; De bruyn, Mario; Clark, James H.; Dodson, Jennifer R.; Farmer, Thomas J.; Honoré, Mathilde; Ingram, Ian D. V.; Naguib, Mohamed; Whitwood, Adrian C.; North, Michael Ring opening metathesis polymerisation of a new bio-derived monomer from itaconic anhydride and furfuryl alcohol Green Chem., 2016, 18, 3945 |
7225495 | CIF | C15 H11 N O | P 1 21/n 1 | 13.2486; 7.0891; 13.5496 90; 114.155; 90 | 1161.2 | Shi, Qing; Li, Pinhua; Zhu, Xianjin; Wang, Lei Decarboxylative/decarbonylative C3-acylation of indoles via photocatalysis: a simple and efficient route to 3-acylindoles Green Chem., 2016, 18, 4916 |
7225644 | CIF | C17 H17 Br O2 | P -1 | 9.5598; 9.6393; 18.0624 75.207; 81.884; 72.871 | 1533.97 | Chen, Dao-Qian; Guo, Chun-Huan; Zhang, Heng-Rui; Jin, Dong-Po; Li, Xue-Song; Gao, Pin; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min A metal-free transformation of alkynes to carbonyls directed by remote OH group Green Chem., 2016, 18, 4176 |
7225655 | CIF | C16 H8 F3 I N0 O2 | P 1 21/c 1 | 10.392; 15.7128; 9.0091 90; 102.556; 90 | 1435.9 | Ni, Shengyang; Cao, Jia; Mei, Haibo; Han, Jianlin; Li, Shuhua; Pan, Yi Sunlight-promoted cyclization versus decarboxylation in the reaction of alkynoates with N-iodosuccinimide: easy access to 3-iodocoumarins Green Chem., 2016, 18, 3935 |
7225779 | CIF | C17 H12 O2 | P -1 | 7.1649; 7.1976; 25.276 92.384; 92.571; 90.05 | 1301 | Zhang, Wen-Zhen; Yang, Ming-Wang; Lu, Xiao-Bing Carboxylative cyclization of substituted propenyl ketones using CO2: transition-metal-free synthesis of α-pyrones Green Chem., 2016, 18, 4181 |
7225883 | CIF | C32 H27 Br Cl3 O P | P 1 21/c 1 | 12.9435; 13.19; 17.35 90; 96.085; 90 | 2945.4 | Liu, Shiyao; Suematsu, Naoki; Maruoka, Keiji; Shirakawa, Seiji Design of bifunctional quaternary phosphonium salt catalysts for CO2fixation reaction with epoxides under mild conditions Green Chem., 2016, 18, 4611 |
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