Crystallography Open Database
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Searching journal of publication like 'New Journal of Chemistry' volume of publication is 39
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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7054425 | CIF | C30 H38 N3 Ni S8 | C 1 2 1 | 16.624; 7.8685; 28.101 90; 102.325; 90 | 3591.1 | Le Gal, Yann; Vacher, Antoine; Dorcet, Vincent; Fourmigué, Marc; Crassous, Jeanne; Lorcy, Dominique The near infra red (NIR) chiroptical properties of nickel dithiolene complexes New J. Chem., 2015, 39, 122 |
7054426 | CIF | C17 H17 N3 S4 | P 21 21 21 | 8.5565; 11.6085; 37.5518 90; 90; 90 | 3729.95 | Le Gal, Yann; Vacher, Antoine; Dorcet, Vincent; Fourmigué, Marc; Crassous, Jeanne; Lorcy, Dominique The near infra red (NIR) chiroptical properties of nickel dithiolene complexes New J. Chem., 2015, 39, 122 |
7054434 | CIF | C30 H33 N3 | P 1 21/c 1 | 13.508; 24.193; 7.507 90; 94.864; 90 | 2444 | Vishnoi, Pratap; Sen, Saumik; Patwari, G. Naresh; Murugavel, Ramaswamy Charge transfer aided selective sensing and capture of picric acid by triphenylbenzenes New J. Chem., 2015, 39, 886 |
7054435 | CIF | C48 H42 N12 O21 | P -1 | 10.766; 13.96; 17.294 102.357; 98.189; 100.935 | 2447 | Vishnoi, Pratap; Sen, Saumik; Patwari, G. Naresh; Murugavel, Ramaswamy Charge transfer aided selective sensing and capture of picric acid by triphenylbenzenes New J. Chem., 2015, 39, 886 |
7054449 | CIF | C16 H19 Fe N3 O3 | P 1 21/n 1 | 9.8538; 12.9015; 12.7365 90; 97.033; 90 | 1606.99 | Liu, Xuelin; Zhang, Weiqiang; Zhang, Guofang; Gao, Ziwei Low-migratory ionic ferrocene-based burning rate catalysts with high combustion catalytic efficiency New J. Chem., 2015, 39, 155 |
7054450 | CIF | C17 H21 Fe N3 O3 | P 1 21/c 1 | 12.5421; 14.1112; 9.8489 90; 92.506; 90 | 1741.43 | Liu, Xuelin; Zhang, Weiqiang; Zhang, Guofang; Gao, Ziwei Low-migratory ionic ferrocene-based burning rate catalysts with high combustion catalytic efficiency New J. Chem., 2015, 39, 155 |
7054451 | CIF | C17 H23 Fe N3 O4 | P -1 | 7.6098; 9.9244; 12.4142 94.402; 97.669; 107.436 | 879.69 | Liu, Xuelin; Zhang, Weiqiang; Zhang, Guofang; Gao, Ziwei Low-migratory ionic ferrocene-based burning rate catalysts with high combustion catalytic efficiency New J. Chem., 2015, 39, 155 |
7054452 | CIF | C14 H17 Fe N4 O3.5 | P -1 | 6.06; 12.5298; 20.6252 80.833; 87.615; 87.665 | 1543.82 | Liu, Xuelin; Zhang, Weiqiang; Zhang, Guofang; Gao, Ziwei Low-migratory ionic ferrocene-based burning rate catalysts with high combustion catalytic efficiency New J. Chem., 2015, 39, 155 |
7054453 | CIF | C21 H19 Fe N5 O7 | P n a 21 | 43.0383; 5.8461; 8.4347 90; 90; 90 | 2122.22 | Liu, Xuelin; Zhang, Weiqiang; Zhang, Guofang; Gao, Ziwei Low-migratory ionic ferrocene-based burning rate catalysts with high combustion catalytic efficiency New J. Chem., 2015, 39, 155 |
7054454 | CIF | C22 H21 Fe N5 O7 | P -1 | 9.4141; 11.4937; 11.5265 109.571; 96.214; 105.601 | 1104.49 | Liu, Xuelin; Zhang, Weiqiang; Zhang, Guofang; Gao, Ziwei Low-migratory ionic ferrocene-based burning rate catalysts with high combustion catalytic efficiency New J. Chem., 2015, 39, 155 |
7054455 | CIF | C23 H23 Fe N5 O7 | P -1 | 7.4108; 13.2305; 13.7738 63.098; 74.466; 78.581 | 1155.71 | Liu, Xuelin; Zhang, Weiqiang; Zhang, Guofang; Gao, Ziwei Low-migratory ionic ferrocene-based burning rate catalysts with high combustion catalytic efficiency New J. Chem., 2015, 39, 155 |
7054456 | CIF | C23 H23 Fe N5 O7 | P -1 | 11.0568; 11.2915; 11.3242 77.032; 73.612; 62.236 | 1192.99 | Liu, Xuelin; Zhang, Weiqiang; Zhang, Guofang; Gao, Ziwei Low-migratory ionic ferrocene-based burning rate catalysts with high combustion catalytic efficiency New J. Chem., 2015, 39, 155 |
7054457 | CIF | C24 H25 Fe N5 O7 | P n a 21 | 22.3748; 5.7925; 19.342 90; 90; 90 | 2506.8 | Liu, Xuelin; Zhang, Weiqiang; Zhang, Guofang; Gao, Ziwei Low-migratory ionic ferrocene-based burning rate catalysts with high combustion catalytic efficiency New J. Chem., 2015, 39, 155 |
7054458 | CIF | C20 H18 Fe N6 O7 | P -1 | 8.4026; 10.9599; 12.3548 107.976; 102.058; 92.43 | 1051.35 | Liu, Xuelin; Zhang, Weiqiang; Zhang, Guofang; Gao, Ziwei Low-migratory ionic ferrocene-based burning rate catalysts with high combustion catalytic efficiency New J. Chem., 2015, 39, 155 |
7054459 | CIF | C22 H27 Co N2 O9 | P 1 21/c 1 | 15.959; 11.194; 13.281 90; 100.678; 90 | 2331.5 | Mitra, Merry; Raghavaiah, Pallepogu; Ghosh, Rajarshi A mononuclear cobalt(iii) complex and its catecholase activity New J. Chem., 2015, 39, 200 |
7054460 | CIF | C6 H26 As2 N9 Na9 Ni3 O73 W18 | P 63/m | 13.9035; 13.9035; 33.499 90; 90; 120 | 5608 | Liu, Jia-min; Wang, Lu; Yu, Kai; Su, Zhan-hua; Wang, Chun-xiao; Wang, Chun-mei; Zhou, Bai-bin Synthesis, crystal structure and properties of sandwich type compounds based on {AsW9} and a hexa-nuclear unit with three supporting TM‒triazole complexes New J. Chem., 2015, 39, 1139 |
7054461 | CIF | C6 H37 As2 Mn3 N9 Na9 O78.5 W18 | P 63/m | 13.9494; 13.9494; 33.76 90; 90; 120 | 5689.1 | Liu, Jia-min; Wang, Lu; Yu, Kai; Su, Zhan-hua; Wang, Chun-xiao; Wang, Chun-mei; Zhou, Bai-bin Synthesis, crystal structure and properties of sandwich type compounds based on {AsW9} and a hexa-nuclear unit with three supporting TM‒triazole complexes New J. Chem., 2015, 39, 1139 |
7054462 | CIF | C6 H34 As2 Co3 N9 Na9 O77 W18 | P 63/m | 13.9307; 13.9307; 33.554 90; 90; 120 | 5639.2 | Liu, Jia-min; Wang, Lu; Yu, Kai; Su, Zhan-hua; Wang, Chun-xiao; Wang, Chun-mei; Zhou, Bai-bin Synthesis, crystal structure and properties of sandwich type compounds based on {AsW9} and a hexa-nuclear unit with three supporting TM‒triazole complexes New J. Chem., 2015, 39, 1139 |
7054474 | CIF | C4 H6 N6 O4 | P 1 21/n 1 | 6.9708; 14.408; 7.8104 90; 105.99; 90 | 754.1 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054475 | CIF | C4 H8 N12 O4 | P 1 21/n 1 | 7.5509; 7.844; 18.562 90; 94.987; 90 | 1095.3 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054476 | CIF | C4 H10 N12 O7 | P 1 21 1 | 8.0286; 8.0668; 9.6666 90; 90.004; 90 | 626.06 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054477 | CIF | C4 H2 Cl2 N4 O4 | P 21 21 21 | 6.985; 8.4845; 13.8574 90; 90; 90 | 821.25 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054478 | CIF | C4 H2 Cl2 N4 O3 | P 1 21/n 1 | 8.2678; 11.2186; 8.5693 90; 99.912; 90 | 782.97 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054479 | CIF | C4 H6 N6 O3 | C 1 2/c 1 | 12.844; 8.919; 6.988 90; 112.147; 90 | 741.5 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054480 | CIF | C4 K2 N10 O4 | P -1 | 7.1412; 7.2056; 11.498 89.658; 73.514; 64.814 | 508.88 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054481 | CIF | C6 H12 N16 O4 | C 1 2/c 1 | 14.7455; 11.7557; 10.6941 90; 129.904; 90 | 1422.05 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054482 | CIF | C6 H14 N18 O4 | P 1 21/n 1 | 7.0135; 31.347; 7.9795 90; 115.793; 90 | 1579.5 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054483 | CIF | C4 H4 K2 N10 O5 | P 1 21/c 1 | 7.4337; 21.6146; 7.5901 90; 97.741; 90 | 1208.44 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054484 | CIF | C4 H10 N14 O3 | P -1 | 3.7659; 11.0046; 14.3912 97.056; 95.04; 98.978 | 581.14 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054485 | CIF | C4 H8 N12 O3 | P b c a | 14.5573; 7.5523; 19.5093 90; 90; 90 | 2144.9 | Fischer, Dennis; Klapötke, Thomas M.; Reymann, Marius; Stierstorfer, Jörg; Völkl, Maurus B. R. Energetic alliance of tetrazole-1-oxides and 1,2,5-oxadiazoles New J. Chem., 2015, 39, 1619 |
7054486 | CIF | C19 H11 F4 N O2 | P 1 21/n 1 | 8.3016; 12.104; 16.4292 90; 98.436; 90 | 1632.99 | Huo, Yanping; Lu, Jiguo; Lu, Tianhua; Fang, Xiaoming; Ouyang, Xinhua; Zhang, Li; Yuan, Guozan Comparative studies on OLED performances of chloro and fluoro substituted Zn(ii) 8-hydroxyquinolinates New J. Chem., 2015, 39, 333 |
7054487 | CIF | C9 H16 N2 O3 | P -1 | 6.9516; 8.1294; 9.6234 74.586; 80.157; 83.657 | 515.35 | Maton, C.; Van Hecke, K.; Stevens, C. V. Peralkylated imidazolium carbonate ionic liquids: synthesis using dimethyl carbonate, reactivity and structure New J. Chem., 2015, 39, 461 |
7054488 | CIF | C8 H15 Cl N2 | P 1 21/c 1 | 6.77997; 14.4971; 9.8785 90; 100.572; 90 | 954.47 | Maton, C.; Van Hecke, K.; Stevens, C. V. Peralkylated imidazolium carbonate ionic liquids: synthesis using dimethyl carbonate, reactivity and structure New J. Chem., 2015, 39, 461 |
7054489 | CIF | C9 H17 Cl N2 | R -3 | 19.8873; 19.8873; 14.4048 90; 90; 120 | 4933.9 | Maton, C.; Van Hecke, K.; Stevens, C. V. Peralkylated imidazolium carbonate ionic liquids: synthesis using dimethyl carbonate, reactivity and structure New J. Chem., 2015, 39, 461 |
7054490 | CIF | C32 H22 N2 O | P 1 21/c 1 | 12.3316; 21.3475; 8.8212 90; 92.34; 90 | 2320.2 | Jayabharathi, Jayaraman; Ramanathan, Periyasamy; Thanikachalam, Venugopal Synthesis and optical properties of phenanthromidazole derivatives for organic electroluminescent devices New J. Chem., 2015, 39, 142 |
7054491 | CIF | C30 H47 F N4 O | P 1 21/c 1 | 9.575; 20.505; 15.88 90; 105.413; 90 | 3006 | Ghosh, Debanjana; Rhodes, Shannon; Hawkins, Karena; Winder, Domonique; Atkinson, Austin; Ming, Weihua; Padgett, Clifford; Orvis, Jeffrey; Aiken, Karelle; Landge, Shainaz A simple and effective 1,2,3-triazole based “turn-on” fluorescence sensor for the detection of anions New J. Chem., 2015, 39, 295 |
7054492 | CIF | C12 H14 O5 Pb | I b a 2 | 16.2354; 19.1181; 8.2268 90; 90; 90 | 2553.5 | Bo, Qi-Bing; Pang, Juan-Juan; Wang, Hong-Yan; Fan, Chun-Hua; Zhang, Zhen-Wei In situ solvent and counteranion-induced synthesis, structural characterization and photoluminescence properties of Pb-based MOFs New J. Chem., 2015, 39, 431 |
7054493 | CIF | C24 H24 O9 Pb3 | P 1 21/c 1 | 18.7933; 17.7755; 8.2471 90; 99.723; 90 | 2715.45 | Bo, Qi-Bing; Pang, Juan-Juan; Wang, Hong-Yan; Fan, Chun-Hua; Zhang, Zhen-Wei In situ solvent and counteranion-induced synthesis, structural characterization and photoluminescence properties of Pb-based MOFs New J. Chem., 2015, 39, 431 |
7054494 | CIF | C36 H36 O13 Pb4 | P n a 21 | 18.4043; 30.9956; 6.9963 90; 90; 90 | 3991.1 | Bo, Qi-Bing; Pang, Juan-Juan; Wang, Hong-Yan; Fan, Chun-Hua; Zhang, Zhen-Wei In situ solvent and counteranion-induced synthesis, structural characterization and photoluminescence properties of Pb-based MOFs New J. Chem., 2015, 39, 431 |
7054495 | CIF | C40 H44 Fe N8 O2 Se2 | P -1 | 10.594; 14.2967; 14.5177 84.866; 68.83; 77.339 | 2000.46 | Nguyen, Luong Lam; Guillot, Régis; Laisney, Jérôme; Rechignat, Lionel; Bedoui, Salma; Molnár, Gabor; Rivière, Eric; Boillot, Marie-Laure Fe(Me2-bpy)2(NCSe)2spin-crossover micro- and nanoparticles showing spin-state switching above 250 K New J. Chem., 2015, 39, 1603 |
7054496 | CIF | C38 H36 Fe N8 O3 Se2 | P 1 21/c 1 | 12.203; 19.513; 15.887 90; 90.858; 90 | 3782.5 | Nguyen, Luong Lam; Guillot, Régis; Laisney, Jérôme; Rechignat, Lionel; Bedoui, Salma; Molnár, Gabor; Rivière, Eric; Boillot, Marie-Laure Fe(Me2-bpy)2(NCSe)2spin-crossover micro- and nanoparticles showing spin-state switching above 250 K New J. Chem., 2015, 39, 1603 |
7054497 | CIF | C27 H41 Au N P S2 | P b c a | 12.3157; 19.6569; 22.945 90; 90; 90 | 5554.7 | Altaf, Muhammad; Monim-ul-Mehboob, M.; Isab, Anvarhusein A.; Dhuna, Vikram; Bhatia, Gaurav; Dhuna, Kshitija; Altuwaijri, Saleh The synthesis, spectroscopic characterization and anticancer activity of new mono and binuclear phosphanegold(i) dithiocarbamate complexes New J. Chem., 2015, 39, 377 |
7054498 | CIF | C29.33 H26 N3 O6.17 | R -3 | 28.3533; 28.3533; 15.9781 90; 90; 120 | 11124.1 | Haddad, Saoussen; Boudriga, Sarra; Akhaja, Tarunkumar Nanjibhai; Raval, Jignesh Priyakant; Porzio, François; Soldera, Armand; Askri, Moheddine; Knorr, Michael; Rousselin, Yoann; Kubicki, Marek M.; Rajani, Dhanji A strategic approach to the synthesis of functionalized spirooxindole pyrrolidine derivatives: in vitro antibacterial, antifungal, antimalarial and antitubercular studies New J. Chem., 2015, 39, 520 |
7054499 | CIF | C17 H19 F I3 N3 O3 | P -1 | 8.1001; 9.6437; 13.9228 87.481; 77.694; 77.279 | 1036.5 | Zou, Wen-Sheng; Lin, Sen; Li, Jia-Yuan; Wei, Hong-Qing; Zhang, Xiao-Qin; Shen, Dong-Xu; Qiao, Jun-Qin; Lian, Hong-Zhen; Xie, Dai-Qian; Ge, Xin Mechanism and application of halogen bond induced fluorescence enhancement and iodine molecule cleavage in solution New J. Chem., 2015, 39, 262 |
7054500 | CIF | C24 H29 Fe N4 O4 S | P 1 21/c 1 | 19.0809; 11.3904; 23.6108 90; 107.42; 90 | 4896.2 | Masárová, Petra; Zoufalý, Pavel; Moncol, Ján; Nemec, Ivan; Pavlik, Ján; Gembický, Milan; Trávníček, Zdeněk; Boča, Roman; Šalitroš, Ivan Spin crossover and high spin electroneutral mononuclear iron(iii) Schiff base complexes involving terminal pseudohalido ligands New J. Chem., 2015, 39, 508 |
7054501 | CIF | C24 H29 Fe N4 O4 S | P 1 21/c 1 | 19.165; 11.6749; 22.449 90; 107.772; 90 | 4783.2 | Masárová, Petra; Zoufalý, Pavel; Moncol, Ján; Nemec, Ivan; Pavlik, Ján; Gembický, Milan; Trávníček, Zdeněk; Boča, Roman; Šalitroš, Ivan Spin crossover and high spin electroneutral mononuclear iron(iii) Schiff base complexes involving terminal pseudohalido ligands New J. Chem., 2015, 39, 508 |
7054502 | CIF | C24 H29 Fe N4 O4 S | P 1 21/c 1 | 19.334; 11.456; 23.831 90; 107.131; 90 | 5044.2 | Masárová, Petra; Zoufalý, Pavel; Moncol, Ján; Nemec, Ivan; Pavlik, Ján; Gembický, Milan; Trávníček, Zdeněk; Boča, Roman; Šalitroš, Ivan Spin crossover and high spin electroneutral mononuclear iron(iii) Schiff base complexes involving terminal pseudohalido ligands New J. Chem., 2015, 39, 508 |
7054503 | CIF | C28 H25 Fe N4 O2 S | P 21 21 21 | 7.5011; 13.0676; 24.704 90; 90; 90 | 2421.5 | Masárová, Petra; Zoufalý, Pavel; Moncol, Ján; Nemec, Ivan; Pavlik, Ján; Gembický, Milan; Trávníček, Zdeněk; Boča, Roman; Šalitroš, Ivan Spin crossover and high spin electroneutral mononuclear iron(iii) Schiff base complexes involving terminal pseudohalido ligands New J. Chem., 2015, 39, 508 |
7054504 | CIF | C28 H25 Fe N4 O2 S | P 21 21 21 | 7.5422; 13.5725; 24.6626 90; 90; 90 | 2524.62 | Masárová, Petra; Zoufalý, Pavel; Moncol, Ján; Nemec, Ivan; Pavlik, Ján; Gembický, Milan; Trávníček, Zdeněk; Boča, Roman; Šalitroš, Ivan Spin crossover and high spin electroneutral mononuclear iron(iii) Schiff base complexes involving terminal pseudohalido ligands New J. Chem., 2015, 39, 508 |
7054505 | CIF | C20 H19 Fe N6 O6 S | P b c n | 15.903; 14.218; 19.6342 90; 90; 90 | 4439.5 | Masárová, Petra; Zoufalý, Pavel; Moncol, Ján; Nemec, Ivan; Pavlik, Ján; Gembický, Milan; Trávníček, Zdeněk; Boča, Roman; Šalitroš, Ivan Spin crossover and high spin electroneutral mononuclear iron(iii) Schiff base complexes involving terminal pseudohalido ligands New J. Chem., 2015, 39, 508 |
7054506 | CIF | C23 H29 Fe N6 O4 | P 1 21/n 1 | 11.0321; 11.3322; 18.9441 90; 96.974; 90 | 2350.8 | Masárová, Petra; Zoufalý, Pavel; Moncol, Ján; Nemec, Ivan; Pavlik, Ján; Gembický, Milan; Trávníček, Zdeněk; Boča, Roman; Šalitroš, Ivan Spin crossover and high spin electroneutral mononuclear iron(iii) Schiff base complexes involving terminal pseudohalido ligands New J. Chem., 2015, 39, 508 |
7054507 | CIF | C36 H53 Fe N4 O2 S | P 1 21/c 1 | 18.2879; 11.8974; 17.3763 90; 96.903; 90 | 3753.3 | Masárová, Petra; Zoufalý, Pavel; Moncol, Ján; Nemec, Ivan; Pavlik, Ján; Gembický, Milan; Trávníček, Zdeněk; Boča, Roman; Šalitroš, Ivan Spin crossover and high spin electroneutral mononuclear iron(iii) Schiff base complexes involving terminal pseudohalido ligands New J. Chem., 2015, 39, 508 |
7054508 | CIF | C23 H27 Fe N4 O4 S | P 1 21/n 1 | 11.5785; 11.6541; 18.2132 90; 106.508; 90 | 2356.33 | Masárová, Petra; Zoufalý, Pavel; Moncol, Ján; Nemec, Ivan; Pavlik, Ján; Gembický, Milan; Trávníček, Zdeněk; Boča, Roman; Šalitroš, Ivan Spin crossover and high spin electroneutral mononuclear iron(iii) Schiff base complexes involving terminal pseudohalido ligands New J. Chem., 2015, 39, 508 |
7054509 | CIF | C18 H21 Cl2 N5 Zn | P -1 | 7.927; 10.615; 12.92 78.84; 74.08; 70.62 | 979.9 | Štefane, Bogdan; Perdih, Franc; Višnjevac, Aleksandar; Požgan, Franc Novel triazole-based ligands and their zinc(ii) and nickel(ii) complexes with a nitrogen donor environment as potential structural models for mononuclear active sites New J. Chem., 2015, 39, 566 |
7054510 | CIF | C28 H26 Cl2 N6 Zn | P 1 21/c 1 | 8.8955; 14.5691; 21.5718 90; 91.451; 90 | 2794.8 | Štefane, Bogdan; Perdih, Franc; Višnjevac, Aleksandar; Požgan, Franc Novel triazole-based ligands and their zinc(ii) and nickel(ii) complexes with a nitrogen donor environment as potential structural models for mononuclear active sites New J. Chem., 2015, 39, 566 |
7054511 | CIF | C24 H29 Cl2 N5 Ni O2 | P -1 | 6.4217; 11.6331; 34.4621 89.715; 85.211; 82.58 | 2543.95 | Štefane, Bogdan; Perdih, Franc; Višnjevac, Aleksandar; Požgan, Franc Novel triazole-based ligands and their zinc(ii) and nickel(ii) complexes with a nitrogen donor environment as potential structural models for mononuclear active sites New J. Chem., 2015, 39, 566 |
7054512 | CIF | C27 H23 Cu N3 O4 S | C 1 2/c 1 | 26.919; 8.723; 22.424 90; 107.99; 90 | 5008.1 | Li, Jun-Ling; Jiang, Lin; Wang, Bi-Wei; Tian, Jin-Lei; Gu, Wen; Liu, Xin; Yan, Shi-Ping Significant differences in the biological activity of mononuclear Cu(ii) and Ni(ii) complexes with the polyquinolinyl ligand New J. Chem., 2015, 39, 529 |
7054513 | CIF | C29 H33 N3 Ni O7 S | P 1 21/n 1 | 14.759; 13.805; 14.772 90; 96.14; 90 | 2992.5 | Li, Jun-Ling; Jiang, Lin; Wang, Bi-Wei; Tian, Jin-Lei; Gu, Wen; Liu, Xin; Yan, Shi-Ping Significant differences in the biological activity of mononuclear Cu(ii) and Ni(ii) complexes with the polyquinolinyl ligand New J. Chem., 2015, 39, 529 |
7054514 | CIF | C11 H10 N2 O2 | P 1 21/c 1 | 15.6778; 3.9598; 17.4076 90; 108.928; 90 | 1022.24 | Song, Qingbao; Wang, Yongsheng; Hu, Chenchen; Zhang, Yujian; Sun, Jingwei; Wang, Kunyan; Zhang, Cheng Effect of stacking mode on the mechanofluorochromic properties of 3-aryl-2-cyano acrylamide derivatives New J. Chem., 2015, 39, 659 |
7054515 | CIF | C11 H10 N2 O2 | I 1 2/a 1 | 13.7381; 8.877; 17.564 90; 103.368; 90 | 2083.9 | Song, Qingbao; Wang, Yongsheng; Hu, Chenchen; Zhang, Yujian; Sun, Jingwei; Wang, Kunyan; Zhang, Cheng Effect of stacking mode on the mechanofluorochromic properties of 3-aryl-2-cyano acrylamide derivatives New J. Chem., 2015, 39, 659 |
7054516 | CIF | C11 H10 N2 O2 | P 1 21/c 1 | 3.92; 10.792; 23.124 90; 93.463; 90 | 976.5 | Song, Qingbao; Wang, Yongsheng; Hu, Chenchen; Zhang, Yujian; Sun, Jingwei; Wang, Kunyan; Zhang, Cheng Effect of stacking mode on the mechanofluorochromic properties of 3-aryl-2-cyano acrylamide derivatives New J. Chem., 2015, 39, 659 |
7054517 | CIF | C32 H28 N6 O Ti2 | P 1 21/c 1 | 13.8001; 14.107; 14.966 90; 93.4; 90 | 2908.4 | Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan Titanocene(iii) pseudohalides: an ESR and structural study New J. Chem., 2015, 39, 576 |
7054518 | CIF | C30 H36 N2 O3 S2 Ti2 | P 1 21/c 1 | 9.842; 19.9841; 15.283 90; 99.947; 90 | 2960.7 | Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan Titanocene(iii) pseudohalides: an ESR and structural study New J. Chem., 2015, 39, 576 |
7054519 | CIF | C51 H78 N3 Si6 Ti3 | P -1 | 14.5932; 14.925; 15.54 74.368; 83.551; 61.471 | 2863.2 | Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan Titanocene(iii) pseudohalides: an ESR and structural study New J. Chem., 2015, 39, 576 |
7054520 | CIF | C36 H52 N6 Si4 Ti2 | P -1 | 7.598; 11.523; 25.0561 77.795; 89.851; 84.089 | 2132.3 | Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan Titanocene(iii) pseudohalides: an ESR and structural study New J. Chem., 2015, 39, 576 |
7054521 | CIF | C47 H60 N6 Si4 Ti2 | P -1 | 11.475; 11.6289; 18.8461 92.434; 99.597; 96.7 | 2457.8 | Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan Titanocene(iii) pseudohalides: an ESR and structural study New J. Chem., 2015, 39, 576 |
7054522 | CIF | C32 H52 Cl2 Si4 Ti2 | P -1 | 8.828; 9.427; 12.2471 71.689; 78.624; 89.462 | 947.09 | Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan Titanocene(iii) pseudohalides: an ESR and structural study New J. Chem., 2015, 39, 576 |
7054523 | CIF | C21 H30 N8 O11 V2 | P -1 | 9.616; 12.119; 12.594 90.497; 98.27; 113.05 | 1333 | Ma, Xi Tong; Xing, Na; Yan, Zhi Dan; Zhang, Xiao Xi; Wu, Qiong; Xing, Yong Heng Peroxo- and oxovanadium(iv) complexes with tridentate N-heterocycle ligands: synthesis, structure, and catalytic performance New J. Chem., 2015, 39, 1067 |
7054524 | CIF | C23 H32 N8 O12 S V | P -1 | 9.9813; 12.3482; 13.298 103.22; 93.546; 100.63 | 1558.9 | Ma, Xi Tong; Xing, Na; Yan, Zhi Dan; Zhang, Xiao Xi; Wu, Qiong; Xing, Yong Heng Peroxo- and oxovanadium(iv) complexes with tridentate N-heterocycle ligands: synthesis, structure, and catalytic performance New J. Chem., 2015, 39, 1067 |
7054525 | CIF | C22 H18 N3 O5.5 V | R -3 :H | 21.563; 21.563; 24.14 90; 90; 120 | 9720 | Ma, Xi Tong; Xing, Na; Yan, Zhi Dan; Zhang, Xiao Xi; Wu, Qiong; Xing, Yong Heng Peroxo- and oxovanadium(iv) complexes with tridentate N-heterocycle ligands: synthesis, structure, and catalytic performance New J. Chem., 2015, 39, 1067 |
7054526 | CIF | C42 H33 F10 O3 P3 Pt S2 | P -1 | 11.1223; 13.6579; 16.7386 67.229; 81.64; 71.075 | 2217.22 | Cervantes, Ruy; Tiburcio, Jorge; Torrens, Hugo cis and trans influences on [Pt(SRF)(triphos)]+complexes (SRF= polyfluorobenzothiolate) New J. Chem., 2015, 39, 631 |
7054527 | CIF | C41 H38 F3 O3 P3 Pt S2 | P 1 21/n 1 | 10.2751; 19.9018; 19.3686 90; 93.744; 90 | 3952.3 | Cervantes, Ruy; Tiburcio, Jorge; Torrens, Hugo cis and trans influences on [Pt(SRF)(triphos)]+complexes (SRF= polyfluorobenzothiolate) New J. Chem., 2015, 39, 631 |
7054528 | CIF | C41 H34 F7 O3 P3 Pt S2 | P 1 21/n 1 | 10.188; 19.711; 21.039 90; 96.02; 90 | 4201.7 | Cervantes, Ruy; Tiburcio, Jorge; Torrens, Hugo cis and trans influences on [Pt(SRF)(triphos)]+complexes (SRF= polyfluorobenzothiolate) New J. Chem., 2015, 39, 631 |
7054529 | CIF | C9 H8 N12 O8 | P -1 | 8.0665; 8.3119; 13.9189 90.693; 104.018; 118.084 | 790.11 | Wu, Bo; Wang, Zhixin; Yang, Hongwei; Lin, Qiuhan; Ju, Xuehai; Lu, Chunxu; Cheng, Guangbin Synthesis and characterization of a new family of energetic salts based on a guanidinium cation containing a picryl moiety New J. Chem., 2015, 39, 893 |
7054530 | CIF | C8 H8 N8 O9 | P 1 21/c 1 | 17.582; 10.4936; 15.8405 90; 111.304; 90 | 2722.8 | Wu, Bo; Wang, Zhixin; Yang, Hongwei; Lin, Qiuhan; Ju, Xuehai; Lu, Chunxu; Cheng, Guangbin Synthesis and characterization of a new family of energetic salts based on a guanidinium cation containing a picryl moiety New J. Chem., 2015, 39, 893 |
7054531 | CIF | C16 H28 N2 O S | P 1 21/c 1 | 20.6963; 4.89894; 16.9658 90; 97.371; 90 | 1705.95 | Yadav, Priyanka; Ballabh, Amar Odd‒even effect in a thiazole based organogelator: understanding the interplay of non-covalent interactions on property and applications New J. Chem., 2015, 39, 721 |
7054532 | CIF | C17 H30 N2 O S | P 1 21/c 1 | 23.237; 4.9497; 15.6429 90; 90.966; 90 | 1798.9 | Yadav, Priyanka; Ballabh, Amar Odd‒even effect in a thiazole based organogelator: understanding the interplay of non-covalent interactions on property and applications New J. Chem., 2015, 39, 721 |
7054533 | CIF | C18 H32 N2 O S | P 1 21/c 1 | 22.1166; 19.4545; 9.42062 90; 101.186; 90 | 3976.38 | Yadav, Priyanka; Ballabh, Amar Odd‒even effect in a thiazole based organogelator: understanding the interplay of non-covalent interactions on property and applications New J. Chem., 2015, 39, 721 |
7054534 | CIF | C17 H30 N2 O S | P -1 | 4.9139; 8.2041; 23.1603 84.043; 87.033; 78.743 | 910.3 | Yadav, Priyanka; Ballabh, Amar Odd‒even effect in a thiazole based organogelator: understanding the interplay of non-covalent interactions on property and applications New J. Chem., 2015, 39, 721 |
7054535 | CIF | C15 H26 N2 O5 | P 1 | 10.036; 11.838; 15.884 79.36; 78.98; 74.71 | 1768.7 | Shi, Ming W.; Sobolev, Alexandre N.; Schirmeister, Tanja; Engels, Bernd; Schmidt, Thomas C.; Luger, Peter; Mebs, Stefan; Dittrich, Birger; Chen, Yu-Sheng; Bąk, Joanna M.; Jayatilaka, Dylan; Bond, Charles S.; Turner, Michael J.; Stewart, Scott G.; Spackman, Mark A.; Grabowsky, Simon Electrostatic complementarity in pseudoreceptor modeling based on drug molecule crystal structures: the case of loxistatin acid (E64c) New J. Chem., 2015, 39, 1628 |
7054536 | CIF | C20 H24 N2 O6 | C 1 2/c 1 | 29.7753; 4.8973; 13.9889 90; 103.74; 90 | 1981.47 | Parveen, Mehtab; Azaz, Shaista; Malla, Ali Mohammed; Ahmad, Faheem; Pereira da Silva, Pedro Sidonio; Ramos Silva, Manuela Solvent-free, [Et3NH][HSO4] catalyzed facile synthesis of hydrazone derivatives New J. Chem., 2015, 39, 469 |
7054537 | CIF | C23 H8 Br N O9 Ru3 | P -1 | 10.13; 10.886; 11.806 95.962; 105.519; 93.803 | 1241.6 | Ma, Zhihong; Fan, Dong; Li, Suzhen; Han, Zhangang; Li, Xiaoyan; Zheng, Xuezhong; Lin, Jin Reactivity of a trinuclear ruthenium complex involving C‒H activation and insertion of alkene New J. Chem., 2015, 39, 1075 |
7054538 | CIF | C32 H17 Br N2 O4 Ru2 | C 1 2/c 1 | 24.724; 10.628; 23.593 90; 115.263; 90 | 5607 | Ma, Zhihong; Fan, Dong; Li, Suzhen; Han, Zhangang; Li, Xiaoyan; Zheng, Xuezhong; Lin, Jin Reactivity of a trinuclear ruthenium complex involving C‒H activation and insertion of alkene New J. Chem., 2015, 39, 1075 |
7054539 | CIF | C28 H16 Br2 N2 | C 1 2/c 1 | 23.277; 6.251; 14.611 90; 92.423; 90 | 2124 | Ma, Zhihong; Fan, Dong; Li, Suzhen; Han, Zhangang; Li, Xiaoyan; Zheng, Xuezhong; Lin, Jin Reactivity of a trinuclear ruthenium complex involving C‒H activation and insertion of alkene New J. Chem., 2015, 39, 1075 |
7054540 | CIF | C21 H8 Br N O7 Ru3 | P -1 | 7.181; 9.6498; 16.7441 95.889; 98.26; 104.031 | 1102.52 | Ma, Zhihong; Fan, Dong; Li, Suzhen; Han, Zhangang; Li, Xiaoyan; Zheng, Xuezhong; Lin, Jin Reactivity of a trinuclear ruthenium complex involving C‒H activation and insertion of alkene New J. Chem., 2015, 39, 1075 |
7054541 | CIF | C22 H14 O4 Ru2 | P 1 21/c 1 | 9.241; 13.168; 8.138 90; 112.245; 90 | 916.6 | Ma, Zhihong; Fan, Dong; Li, Suzhen; Han, Zhangang; Li, Xiaoyan; Zheng, Xuezhong; Lin, Jin Reactivity of a trinuclear ruthenium complex involving C‒H activation and insertion of alkene New J. Chem., 2015, 39, 1075 |
7054542 | CIF | C27 H16 Br N O5 Ru2 | P 1 21/c 1 | 13.5255; 12.8602; 15.6149 90; 114.691; 90 | 2467.7 | Ma, Zhihong; Fan, Dong; Li, Suzhen; Han, Zhangang; Li, Xiaoyan; Zheng, Xuezhong; Lin, Jin Reactivity of a trinuclear ruthenium complex involving C‒H activation and insertion of alkene New J. Chem., 2015, 39, 1075 |
7054543 | CIF | C69 H59.33 Eu2 N12 O11.67 | C 1 2/c 1 | 46.333; 17.299; 32.343 90; 123.542; 90 | 21607 | Das, Kuheli; Nandi, Soumendra; Mondal, Sudipa; Askun, Tulin; Cantürk, Zerrin; Celikboyun, Pinar; Massera, Chiara; Garribba, Eugenio; Datta, Amitabha; Sinha, Chittaranjan; Akitsu, Takashiro Triply phenoxo bridged Eu(iii) and Sm(iii) complexes with 2,6-diformyl-4-methylphenol-di(benzoylhydrazone): structure, spectra and biological study in human cell lines New J. Chem., 2015, 39, 1101 |
7054544 | CIF | C80 H104 Li N8 Nd O3 | P -1 | 12.6452; 15.0817; 20.7038 101.662; 97.13; 106.03 | 3648 | Yakovenko, Marina V.; Udilova, Natalia Yu.; Glukhova, Tatyana A.; Cherkasov, Anton V.; Fukin, Georgy K.; Trifonov, Alexander A. Amido rare-earth complexes supported by an ansa bis(amidinate) ligand with a rigid 1,8-naphthalene linker: synthesis, structures and catalytic activity in rac-lactide polymerization and hydrophosphonylation of carbonyl compounds New J. Chem., 2015, 39, 1083 |
7054545 | CIF | C46 H68 N5 Nd O Si2 | P 1 21/c 1 | 23.9499; 19.4258; 21.8709 90; 116.878; 90 | 9076.1 | Yakovenko, Marina V.; Udilova, Natalia Yu.; Glukhova, Tatyana A.; Cherkasov, Anton V.; Fukin, Georgy K.; Trifonov, Alexander A. Amido rare-earth complexes supported by an ansa bis(amidinate) ligand with a rigid 1,8-naphthalene linker: synthesis, structures and catalytic activity in rac-lactide polymerization and hydrophosphonylation of carbonyl compounds New J. Chem., 2015, 39, 1083 |
7054546 | CIF | C26 H28 Br2 F8 N4 | C 1 2 1 | 13.0391; 6.8246; 15.9891 90; 92.828; 90 | 1421.08 | Yi, Hai; Albrecht, Markus; Valkonen, Arto; Rissanen, Kari Perfluoro-1,1′-biphenyl and perfluoronaphthalene and their derivatives as π-acceptors for anions New J. Chem., 2015, 39, 746 |
7054547 | CIF | C18 H18 Br F7 N2 O | P b c a | 13.647; 12.4533; 22.0643 90; 90; 90 | 3749.83 | Yi, Hai; Albrecht, Markus; Valkonen, Arto; Rissanen, Kari Perfluoro-1,1′-biphenyl and perfluoronaphthalene and their derivatives as π-acceptors for anions New J. Chem., 2015, 39, 746 |
7054548 | CIF | C18 H33 B10 N5 O5 | P 21 21 21 | 7.32285; 13.0124; 26.9145 90; 90; 90 | 2564.62 | Matuszewski, Michał; Kiliszek, Agnieszka; Rypniewski, Wojciech; Lesnikowski, Zbigniew J.; Olejniczak, Agnieszka B. Nucleoside bearing boron clusters and their phosphoramidites ‒ building blocks for modified oligonucleotide synthesis New J. Chem., 2015, 39, 1202 |
7054549 | CIF | C4 H16.86 Fe2 N12 O8.43 S5 | P b c a | 12.6104; 10.35013; 37.1231 90; 90; 90 | 4845.28 | Sanina, Nataliya A.; Aldoshin, Sergey M.; Shmatko, Natal'ya Yu.; Korchagin, Denis V.; Shilov, Gennadii V.; Knyazkina, Ekaterine V.; Ovanesyan, Nikolay S.; Kulikov, Alexander V. Nitrosyl iron complexes with enhanced NO donating ability: synthesis, structure and properties of a new type of salt with the DNIC cations [Fe(SC(NH2)2)2(NO)2]+ New J. Chem., 2015, 39, 1022 |
7054550 | CIF | C4 H16 Fe4 N16 O14 S8 | P -1 | 6.2712; 10.4132; 12.1912 86.462; 88.363; 87.613 | 793.65 | Sanina, Nataliya A.; Aldoshin, Sergey M.; Shmatko, Natal'ya Yu.; Korchagin, Denis V.; Shilov, Gennadii V.; Knyazkina, Ekaterine V.; Ovanesyan, Nikolay S.; Kulikov, Alexander V. Nitrosyl iron complexes with enhanced NO donating ability: synthesis, structure and properties of a new type of salt with the DNIC cations [Fe(SC(NH2)2)2(NO)2]+ New J. Chem., 2015, 39, 1022 |
7054551 | CIF | C13.4 H24.5 Cl0 Cu N1.5 O5.92 Y0.5 | P -1 | 9.4934; 13.2045; 14.699 76.486; 85.811; 83.394 | 1777.66 | Ahmed, Sohail; Mansoor, Muhammad Adil; Basirun, Wan Jefrey; Sookhakian, Mehran; Huang, Nay Ming; Mun, Lo Kong; Söhnel, Tilo; Arifin, Zainudin; Mazhar, Muhammad The synthesis and characterization of a hexanuclear copper‒yttrium complex for deposition of semiconducting CuYO2‒0.5Cu2O composite thin films New J. Chem., 2015, 39, 1031 |
7054552 | CIF | C12 H12 Cu4 N10 | P 1 21/c 1 | 15.368; 8.37; 13.71 90; 101.697; 90 | 1727 | Xu, Hui; Zhou, Bo-Yu; Yu, Kai; Su, Zhan-Hua; Zhao, Zhi-Feng; Sun, Wen-Long; Zhou, Bai-Bin Two novel topological structures of [Cu(CN)] coordination polymers modified by flexible triazole ligands New J. Chem., 2015, 39, 1301 |
7054553 | CIF | C6 H8 Cu N4 | F d d 2 | 15.836; 24.736; 7.948 90; 90; 90 | 3113.4 | Xu, Hui; Zhou, Bo-Yu; Yu, Kai; Su, Zhan-Hua; Zhao, Zhi-Feng; Sun, Wen-Long; Zhou, Bai-Bin Two novel topological structures of [Cu(CN)] coordination polymers modified by flexible triazole ligands New J. Chem., 2015, 39, 1301 |
7054554 | CIF | C12 H18 Cl O4 P | C 1 2/c 1 | 33.1; 11.236; 8.061 90; 97.58; 90 | 2971.8 | Dar, Aijaz A.; Mallick, Abhijit; Murugavel, Ramaswamy Synthetic strategies to achieve further-functionalised monoaryl phosphate primary building units: crystal structures and solid-state aggregation behavior New J. Chem., 2015, 39, 1186 |
7054555 | CIF | C12 H18 Br O4 P | C 1 2/c 1 | 33.434; 11.241; 7.946 90; 97.374; 90 | 2962 | Dar, Aijaz A.; Mallick, Abhijit; Murugavel, Ramaswamy Synthetic strategies to achieve further-functionalised monoaryl phosphate primary building units: crystal structures and solid-state aggregation behavior New J. Chem., 2015, 39, 1186 |
7054556 | CIF | C12 H18 I O4 P | C 1 2/c 1 | 34.091; 11.245; 8.001 90; 97.511; 90 | 3041 | Dar, Aijaz A.; Mallick, Abhijit; Murugavel, Ramaswamy Synthetic strategies to achieve further-functionalised monoaryl phosphate primary building units: crystal structures and solid-state aggregation behavior New J. Chem., 2015, 39, 1186 |
7054557 | CIF | C20 H27 O4 P | C 1 2/c 1 | 33.71; 6.824; 17.253 90; 90.834; 90 | 3968 | Dar, Aijaz A.; Mallick, Abhijit; Murugavel, Ramaswamy Synthetic strategies to achieve further-functionalised monoaryl phosphate primary building units: crystal structures and solid-state aggregation behavior New J. Chem., 2015, 39, 1186 |
7054558 | CIF | C39 H48 N O4 P | P 1 21/c 1 | 13.664; 10.956; 23.642 90; 98.563; 90 | 3500 | Dar, Aijaz A.; Mallick, Abhijit; Murugavel, Ramaswamy Synthetic strategies to achieve further-functionalised monoaryl phosphate primary building units: crystal structures and solid-state aggregation behavior New J. Chem., 2015, 39, 1186 |
7054559 | CIF | C21 H27 O5 P | P -1 | 6.69; 9.064; 17.502 79.175; 89.61; 82.167 | 1032.5 | Dar, Aijaz A.; Mallick, Abhijit; Murugavel, Ramaswamy Synthetic strategies to achieve further-functionalised monoaryl phosphate primary building units: crystal structures and solid-state aggregation behavior New J. Chem., 2015, 39, 1186 |
7054560 | CIF | C19 H23 O5 P | C 1 2/c 1 | 41.181; 11.01; 8.186 90; 92.162; 90 | 3709 | Dar, Aijaz A.; Mallick, Abhijit; Murugavel, Ramaswamy Synthetic strategies to achieve further-functionalised monoaryl phosphate primary building units: crystal structures and solid-state aggregation behavior New J. Chem., 2015, 39, 1186 |
7054561 | CIF | C8 H6.5 N5 O1.75 | C 1 2/c 1 | 26.008; 6.836; 22.709 90; 123.384; 90 | 3371.3 | Chen, Wen-Bin; Li, Zhi-Xin; Yu, Xin-Wei; Yang, Meng; Qiu, Yan-Xuan; Dong, Wen M2+and Ln3±catalyzed synthesis of a [1,2,4]triazine core via intramolecular C‒H/N‒H functionalization and C‒N bond formation (M = Mn, Zn, Cd; Ln = Dy, Tb) New J. Chem., 2015, 39, 1222 |
7054562 | CIF | C16 H16 Mn N10 O6 | C 1 2/c 1 | 19.315; 8.088; 11.97 90; 94.203; 90 | 1864.9 | Chen, Wen-Bin; Li, Zhi-Xin; Yu, Xin-Wei; Yang, Meng; Qiu, Yan-Xuan; Dong, Wen M2+and Ln3±catalyzed synthesis of a [1,2,4]triazine core via intramolecular C‒H/N‒H functionalization and C‒N bond formation (M = Mn, Zn, Cd; Ln = Dy, Tb) New J. Chem., 2015, 39, 1222 |
7054563 | CIF | C16 H16 N10 O6 Zn | C 1 2/c 1 | 19.02; 8.0801; 11.953 90; 94.235; 90 | 1832 | Chen, Wen-Bin; Li, Zhi-Xin; Yu, Xin-Wei; Yang, Meng; Qiu, Yan-Xuan; Dong, Wen M2+and Ln3±catalyzed synthesis of a [1,2,4]triazine core via intramolecular C‒H/N‒H functionalization and C‒N bond formation (M = Mn, Zn, Cd; Ln = Dy, Tb) New J. Chem., 2015, 39, 1222 |
7054564 | CIF | C16 H16 Cd N10 O6 | C 1 2/c 1 | 19.4542; 8.1626; 12.0696 90; 94.203; 90 | 1911.46 | Chen, Wen-Bin; Li, Zhi-Xin; Yu, Xin-Wei; Yang, Meng; Qiu, Yan-Xuan; Dong, Wen M2+and Ln3±catalyzed synthesis of a [1,2,4]triazine core via intramolecular C‒H/N‒H functionalization and C‒N bond formation (M = Mn, Zn, Cd; Ln = Dy, Tb) New J. Chem., 2015, 39, 1222 |
7054565 | CIF | C9 H8 N5 O1.5 | P 1 21/n 1 | 6.8792; 20.841; 13.359 90; 103.471; 90 | 1862.6 | Chen, Wen-Bin; Li, Zhi-Xin; Yu, Xin-Wei; Yang, Meng; Qiu, Yan-Xuan; Dong, Wen M2+and Ln3±catalyzed synthesis of a [1,2,4]triazine core via intramolecular C‒H/N‒H functionalization and C‒N bond formation (M = Mn, Zn, Cd; Ln = Dy, Tb) New J. Chem., 2015, 39, 1222 |
7054566 | CIF | C30 H32 Br Cl2 Cu N6 | P 1 21/c 1 | 13.3142; 15.6092; 14.3394 90; 98.779; 90 | 2945.16 | Chou, Chang-Chuan; Liu, Hsueh-Ju; Chao, Lucas Hung-Chieh; Yang, Chia-Chi Halide-modulated bistate and tristate fluorescence switching for Cu(i) and Ag(i) complexes New J. Chem., 2015, 39, 1260 |
7054567 | CIF | C30 H32 Cl4 Cu2 N6 | P 1 21/c 1 | 25.9994; 15.1102; 17.1561 90; 107.436; 90 | 6430.2 | Chou, Chang-Chuan; Liu, Hsueh-Ju; Chao, Lucas Hung-Chieh; Yang, Chia-Chi Halide-modulated bistate and tristate fluorescence switching for Cu(i) and Ag(i) complexes New J. Chem., 2015, 39, 1260 |
7054568 | CIF | C29 H30 Ag Cl N6 O4 | P -1 | 10.2448; 12.581; 13.3336 71.022; 86.393; 66.479 | 1485.7 | Chou, Chang-Chuan; Liu, Hsueh-Ju; Chao, Lucas Hung-Chieh; Yang, Chia-Chi Halide-modulated bistate and tristate fluorescence switching for Cu(i) and Ag(i) complexes New J. Chem., 2015, 39, 1260 |
7054569 | CIF | C43 H53 B Co F4 N6 O6 P2 S2 | P 1 21/c 1 | 13.3203; 25.2381; 15.0807 90; 109.346; 90 | 4783.5 | Jing, Xu; Wu, Pengyan; Liu, Xin; Yang, Linlin; He, Cheng; Duan, Chunying Light-driven hydrogen evolution with a nickel thiosemicarbazone redox catalyst featuring Ni⋯H interactions under basic conditions New J. Chem., 2015, 39, 1051 |
7054570 | CIF | C42 H47 B F4 N6 Ni O5 P2 S2 | P -1 | 9.43; 12.8553; 21.7668 93.409; 91.482; 111.218 | 2452.3 | Jing, Xu; Wu, Pengyan; Liu, Xin; Yang, Linlin; He, Cheng; Duan, Chunying Light-driven hydrogen evolution with a nickel thiosemicarbazone redox catalyst featuring Ni⋯H interactions under basic conditions New J. Chem., 2015, 39, 1051 |
7054571 | CIF | C24 H34 O4 S4 | P -1 | 4.919; 7.285; 18.574 84.19; 86.42; 84.08 | 657.7 | Turbiez, Mathieu; Faye, Djibril; Leriche, Philippe; Frère, Pierre Bis-EDOT end capped by n-hexyl or n-hexylsulfanyl groups: the effect of the substituents on the stability of the oxidized states New J. Chem., 2015, 39, 1678 |
7054572 | CIF | C19 H27 F N2 O4 | P 43 | 10.1585; 10.1585; 19.0174 90; 90; 90 | 1962.5 | Hassoun, Ammar; Grison, Claire M.; Guillot, Régis; Boddaert, Thomas; Aitken, David J. Conformational preferences in the β-peptide oligomers of cis-2-amino-1-fluorocyclobutane-1-carboxylic acid New J. Chem., 2015, 39, 3270 |
7054573 | CIF | C32 H40 F4 N4 O7 | P 21 21 21 | 5.35; 20.2; 29.927 90; 90; 90 | 3234.2 | Hassoun, Ammar; Grison, Claire M.; Guillot, Régis; Boddaert, Thomas; Aitken, David J. Conformational preferences in the β-peptide oligomers of cis-2-amino-1-fluorocyclobutane-1-carboxylic acid New J. Chem., 2015, 39, 3270 |
7054574 | CIF | C17 H15 Cu N7 O8 | P 1 21/n 1 | 12.4021; 12.3286; 13.1324 90; 105.544; 90 | 1934.5 | Ma, Lu-Fang; Shi, Zhen-Zhen; Li, Fei-Fei; Zhang, Jian; Wang, Li-Ya Coordination polymers with free Brønsted acid sites for selective catalysis New J. Chem., 2015, 39, 810 |
7054575 | CIF | C42 H34 Cu2 N14 O18 | P -1 | 10.272; 15.184; 16.2 100.009; 99.61; 108.045 | 2299.2 | Ma, Lu-Fang; Shi, Zhen-Zhen; Li, Fei-Fei; Zhang, Jian; Wang, Li-Ya Coordination polymers with free Brønsted acid sites for selective catalysis New J. Chem., 2015, 39, 810 |
7054576 | CIF | C36 H36 N4 O12 S4 | P 1 21/c 1 | 13.0584; 17.2823; 17.4795 90; 94.228; 90 | 3934.02 | Mačková, Michaela; Mikšátko, Jiří; Budka, Jan; Eigner, Václav; Cuřínová, Petra; Lhoták, Pavel Chiral anion recognition by a ureido-thiacalix[4]arene ligand immobilized in the 1,3-alternate conformation New J. Chem., 2015, 39, 1382 |
7054577 | CIF | C44 H52 N4 O12 S4 | P -1 | 11.0672; 12.3077; 18.3099 101.125; 95.076; 102.421 | 2367.8 | Mačková, Michaela; Mikšátko, Jiří; Budka, Jan; Eigner, Václav; Cuřínová, Petra; Lhoták, Pavel Chiral anion recognition by a ureido-thiacalix[4]arene ligand immobilized in the 1,3-alternate conformation New J. Chem., 2015, 39, 1382 |
7054578 | CIF | C48 H58 N6 O12 S4 | P 42/n :2 | 13.2452; 13.2452; 14.9787 90; 90; 90 | 2627.79 | Mačková, Michaela; Mikšátko, Jiří; Budka, Jan; Eigner, Václav; Cuřínová, Petra; Lhoták, Pavel Chiral anion recognition by a ureido-thiacalix[4]arene ligand immobilized in the 1,3-alternate conformation New J. Chem., 2015, 39, 1382 |
7054579 | CIF | C52 H36 N4 O12 S4 | P 41 21 2 | 12.73537; 12.73537; 28.8831 90; 90; 90 | 4684.54 | Mačková, Michaela; Mikšátko, Jiří; Budka, Jan; Eigner, Václav; Cuřínová, Petra; Lhoták, Pavel Chiral anion recognition by a ureido-thiacalix[4]arene ligand immobilized in the 1,3-alternate conformation New J. Chem., 2015, 39, 1382 |
7054580 | CIF | C48 H60 N4 O12 S4 | P 1 21/c 1 | 27.261; 16.3468; 17.9466 90; 139.366; 90 | 5208.2 | Mačková, Michaela; Mikšátko, Jiří; Budka, Jan; Eigner, Václav; Cuřínová, Petra; Lhoták, Pavel Chiral anion recognition by a ureido-thiacalix[4]arene ligand immobilized in the 1,3-alternate conformation New J. Chem., 2015, 39, 1382 |
7054581 | CIF | C36 H20 N4 O12 S4 | C 1 2/c 1 | 11.2845; 18.1827; 18.8706 90; 105.953; 90 | 3722.8 | Mačková, Michaela; Mikšátko, Jiří; Budka, Jan; Eigner, Václav; Cuřínová, Petra; Lhoták, Pavel Chiral anion recognition by a ureido-thiacalix[4]arene ligand immobilized in the 1,3-alternate conformation New J. Chem., 2015, 39, 1382 |
7054582 | CIF | C44 H52 N4 O12 S4 | P 1 21 1 | 12.64786; 14.04823; 13.3958 90; 101.233; 90 | 2334.57 | Mačková, Michaela; Mikšátko, Jiří; Budka, Jan; Eigner, Václav; Cuřínová, Petra; Lhoták, Pavel Chiral anion recognition by a ureido-thiacalix[4]arene ligand immobilized in the 1,3-alternate conformation New J. Chem., 2015, 39, 1382 |
7054583 | CIF | C48 H56 N8 O12 S4 | C 1 2/m 1 | 28.7209; 19.3593; 13.9154 90; 136.11; 90 | 5364 | Mačková, Michaela; Mikšátko, Jiří; Budka, Jan; Eigner, Václav; Cuřínová, Petra; Lhoták, Pavel Chiral anion recognition by a ureido-thiacalix[4]arene ligand immobilized in the 1,3-alternate conformation New J. Chem., 2015, 39, 1382 |
7054585 | CIF | C150.6 H206.4 N8 O14.6 | P -1 | 15.65; 17.82; 26.44 70.56; 86.08; 87.57 | 6936 | Gattuso, Giuseppe; Notti, Anna; Parisi, Melchiorre F.; Pisagatti, Ilenia; Marcos, Paula Maria; Ascenso, José Rosário; Brancatelli, Giovanna; Geremia, Silvano Selective recognition of biogenic amine hydrochlorides by heteroditopic dihomooxacalix[4]arenes New J. Chem., 2015, 39, 817 |
7054586 | CIF | C26 H25 N3 O2 S | P 1 21/c 1 | 15.6352; 16.2677; 8.8947 90; 103.891; 90 | 2196.2 | Sharma, Shilpa; Pradeep, Chullikkattill. P.; Dhir, Abhimanew Dansyl-carbazole AIEE material for selective recognition of thiourea derivatives New J. Chem., 2015, 39, 1822 |
7054587 | CIF | C55 H41 Er N2 O6 | P 1 21/c 1 | 14.9946; 17.0429; 22.7907 90; 128.291; 90 | 4571.3 | Martín-Ramos, Pablo; Coutinho, Joana T.; Ramos Silva, Manuela; Pereira, Laura C. J.; Lahoz, Fernando; da Silva, Pedro S. Pereira; Lavín, Víctor; Martín-Gil, Jesús Slow magnetic relaxation and photoluminescent properties of a highly coordinated erbium(iii) complex with dibenzoylmethane and 2,2′-bipyridine New J. Chem., 2015, 39, 1703 |
7054588 | CIF | C55 H41 Er N2 O6 | P -1 | 15.2886; 17.7424; 20.7735 73.91; 70.046; 68.647 | 4857.3 | Martín-Ramos, Pablo; Coutinho, Joana T.; Ramos Silva, Manuela; Pereira, Laura C. J.; Lahoz, Fernando; da Silva, Pedro S. Pereira; Lavín, Víctor; Martín-Gil, Jesús Slow magnetic relaxation and photoluminescent properties of a highly coordinated erbium(iii) complex with dibenzoylmethane and 2,2′-bipyridine New J. Chem., 2015, 39, 1703 |
7054589 | CIF | C50 H44 B Cu N7 S2 | P 1 21/c 1 | 13.9619; 25.3276; 12.567 90; 104.037; 90 | 4311.3 | Harding, David J.; Phonsri, Wasinee; Harding, Phimphaka; Sirirak, Jitnapa; Tangtirungrotechai, Yuthana; Webster, Richard D.; Adams, Harry Copper hydrotris(3,5-diphenylpyrazolyl)borate dithiocarbamates: mimicking green copper proteins New J. Chem., 2015, 39, 1498 |
7054590 | CIF | C60 H48 B Cu N7 S2 | P 1 21/c 1 | 17.804; 18.099; 17.81 90; 119.686; 90 | 4986 | Harding, David J.; Phonsri, Wasinee; Harding, Phimphaka; Sirirak, Jitnapa; Tangtirungrotechai, Yuthana; Webster, Richard D.; Adams, Harry Copper hydrotris(3,5-diphenylpyrazolyl)borate dithiocarbamates: mimicking green copper proteins New J. Chem., 2015, 39, 1498 |
7054591 | CIF | C50 H42 B Cu N7 S2 | P 1 21/c 1 | 13.9204; 25.042; 12.6285 90; 102.523; 90 | 4297.5 | Harding, David J.; Phonsri, Wasinee; Harding, Phimphaka; Sirirak, Jitnapa; Tangtirungrotechai, Yuthana; Webster, Richard D.; Adams, Harry Copper hydrotris(3,5-diphenylpyrazolyl)borate dithiocarbamates: mimicking green copper proteins New J. Chem., 2015, 39, 1498 |
7054592 | CIF | C16 H17 N O4 S | P 1 21/c 1 | 15.7805; 5.0908; 21.06 90; 110.851; 90 | 1581.06 | Ragab, Sherif Shaban; Swaminathan, Subramani; Garcia-Amorós, Jaume; Captain, Burjor; Raymo, Françisco M. Bimolecular photoactivation of NBD fluorescence New J. Chem., 2015, 39, 1570 |
7054593 | CIF | C26 H25 Cl2 N5 Ni O9 | P 1 21/c 1 | 15.5059; 11.4074; 16.1421 90; 100.036; 90 | 2811.56 | Song, Xiaowei; Wen, Huimin; Ma, Chengbing; Chen, Hui; Chen, Changneng Hydrogen photogeneration catalyzed by a cobalt complex of a pentadentate aminopyridine-based ligand New J. Chem., 2015, 39, 1734 |
7054594 | CIF | C26 H25 Cl2 Co N5 O9 | P 1 21/c 1 | 15.5452; 11.45475; 16.1105 90; 99.8494; 90 | 2826.46 | Song, Xiaowei; Wen, Huimin; Ma, Chengbing; Chen, Hui; Chen, Changneng Hydrogen photogeneration catalyzed by a cobalt complex of a pentadentate aminopyridine-based ligand New J. Chem., 2015, 39, 1734 |
7054595 | CIF | C39 H55 Cl6 N5 O8 | P -1 | 11.307; 13.8002; 17.341 70.683; 73.734; 71.237 | 2371.71 | Pike, Sarah J.; Boddaert, Thomas; Raftery, James; Webb, Simon J.; Clayden, Jonathan Participation of non-aminoisobutyric acid (Aib) residues in the 310helical conformation of Aib-rich foldamers: a solid state study New J. Chem., 2015, 39, 3288 |
7054596 | CIF | C54 H82 Cl4 P2 Ru | P 1 21/c 1 | 19.2677; 14.6496; 22.219 90; 122.706; 90 | 5277.3 | Yu, Baoyi; Xie, Yu; Hamad, Fatma B.; Leus, Karen; Lyapkov, Alex A.; Van Hecke, Kristof; Verpoort, Francis Synthesis and characterization of non-chelating ruthenium‒indenylidene olefin metathesis catalysts derived from substituted 1,1-diphenyl-2-propyn-1-ols New J. Chem., 2015, 39, 1858 |
7054597 | CIF | C51 H76 Cl2 P2 Ru | R -3 | 46.1591; 46.1591; 13.9447 90; 90; 120 | 25730.9 | Yu, Baoyi; Xie, Yu; Hamad, Fatma B.; Leus, Karen; Lyapkov, Alex A.; Van Hecke, Kristof; Verpoort, Francis Synthesis and characterization of non-chelating ruthenium‒indenylidene olefin metathesis catalysts derived from substituted 1,1-diphenyl-2-propyn-1-ols New J. Chem., 2015, 39, 1858 |
7054598 | CIF | C28 H45 Cl2 O P Ru | P 1 21/c 1 | 11.4775; 19.2194; 25.7969 90; 96.478; 90 | 5654.2 | Yu, Baoyi; Xie, Yu; Hamad, Fatma B.; Leus, Karen; Lyapkov, Alex A.; Van Hecke, Kristof; Verpoort, Francis Synthesis and characterization of non-chelating ruthenium‒indenylidene olefin metathesis catalysts derived from substituted 1,1-diphenyl-2-propyn-1-ols New J. Chem., 2015, 39, 1858 |
7054599 | CIF | C53 H44 Cl2 P2 Ru | P -1 | 10.2241; 12.7121; 20.0557 72.94; 76.718; 81.407 | 2415.8 | Yu, Baoyi; Xie, Yu; Hamad, Fatma B.; Leus, Karen; Lyapkov, Alex A.; Van Hecke, Kristof; Verpoort, Francis Synthesis and characterization of non-chelating ruthenium‒indenylidene olefin metathesis catalysts derived from substituted 1,1-diphenyl-2-propyn-1-ols New J. Chem., 2015, 39, 1858 |
7054600 | CIF | C17 H16 O | P 1 21/c 1 | 6.6764; 16.5673; 11.6107 90; 92.308; 90 | 1283.22 | Yu, Baoyi; Xie, Yu; Hamad, Fatma B.; Leus, Karen; Lyapkov, Alex A.; Van Hecke, Kristof; Verpoort, Francis Synthesis and characterization of non-chelating ruthenium‒indenylidene olefin metathesis catalysts derived from substituted 1,1-diphenyl-2-propyn-1-ols New J. Chem., 2015, 39, 1858 |
7054601 | CIF | C53 H80 Cl2 P2 Ru | R -3 | 47.1514; 47.1514; 13.6692 90; 90; 120 | 26318.6 | Yu, Baoyi; Xie, Yu; Hamad, Fatma B.; Leus, Karen; Lyapkov, Alex A.; Van Hecke, Kristof; Verpoort, Francis Synthesis and characterization of non-chelating ruthenium‒indenylidene olefin metathesis catalysts derived from substituted 1,1-diphenyl-2-propyn-1-ols New J. Chem., 2015, 39, 1858 |
7054602 | CIF | C55 H78 Cl2 P2 Ru | R -3 | 46.042; 46.042; 14.0313 90; 90; 120 | 25759.5 | Yu, Baoyi; Xie, Yu; Hamad, Fatma B.; Leus, Karen; Lyapkov, Alex A.; Van Hecke, Kristof; Verpoort, Francis Synthesis and characterization of non-chelating ruthenium‒indenylidene olefin metathesis catalysts derived from substituted 1,1-diphenyl-2-propyn-1-ols New J. Chem., 2015, 39, 1858 |
7054603 | CIF | C51 H75 Cl2 F P2 Ru | R -3 | 45.479; 45.479; 14.179 90; 90; 120 | 25398 | Yu, Baoyi; Xie, Yu; Hamad, Fatma B.; Leus, Karen; Lyapkov, Alex A.; Van Hecke, Kristof; Verpoort, Francis Synthesis and characterization of non-chelating ruthenium‒indenylidene olefin metathesis catalysts derived from substituted 1,1-diphenyl-2-propyn-1-ols New J. Chem., 2015, 39, 1858 |
7054604 | CIF | C26 H25 N3 O4 | P -1 | 10.1589; 11.3338; 11.6688 68.322; 67.396; 82.841 | 1152.4 | Yan, Xingchen; Xu, Jiakun; Wu, Xiaojing; Zhang, Zhongyu; Zhang, Xia; Fan, Yuhua; Bi, Caifeng Proteasome inhibition and cytostatic effects on human cancer cells by pyrazolone-enamines: a combined crystallographic, structural and computational study New J. Chem., 2015, 39, 2168 |
7054605 | CIF | C25 H24 N4 O3 | P -1 | 7.3752; 10.9275; 14.5614 101.707; 92.769; 98.544 | 1132.64 | Yan, Xingchen; Xu, Jiakun; Wu, Xiaojing; Zhang, Zhongyu; Zhang, Xia; Fan, Yuhua; Bi, Caifeng Proteasome inhibition and cytostatic effects on human cancer cells by pyrazolone-enamines: a combined crystallographic, structural and computational study New J. Chem., 2015, 39, 2168 |
7054606 | CIF | C24 H21 N3 O2 | P -1 | 7.7356; 10.8256; 13.5508 112.683; 90.907; 107.741 | 985.67 | Yan, Xingchen; Xu, Jiakun; Wu, Xiaojing; Zhang, Zhongyu; Zhang, Xia; Fan, Yuhua; Bi, Caifeng Proteasome inhibition and cytostatic effects on human cancer cells by pyrazolone-enamines: a combined crystallographic, structural and computational study New J. Chem., 2015, 39, 2168 |
7054607 | CIF | C32 H34 N4 O3 | P -1 | 9.5274; 10.4205; 14.7518 77.254; 82.096; 84.377 | 1411.4 | Yan, Xingchen; Xu, Jiakun; Wu, Xiaojing; Zhang, Zhongyu; Zhang, Xia; Fan, Yuhua; Bi, Caifeng Proteasome inhibition and cytostatic effects on human cancer cells by pyrazolone-enamines: a combined crystallographic, structural and computational study New J. Chem., 2015, 39, 2168 |
7054608 | CIF | C24 H21 N3 O2 | P -1 | 7.2287; 11.0934; 14.0509 107.981; 99.534; 105.146 | 996.58 | Yan, Xingchen; Xu, Jiakun; Wu, Xiaojing; Zhang, Zhongyu; Zhang, Xia; Fan, Yuhua; Bi, Caifeng Proteasome inhibition and cytostatic effects on human cancer cells by pyrazolone-enamines: a combined crystallographic, structural and computational study New J. Chem., 2015, 39, 2168 |
7054609 | CIF | C27 H25 N3 O6 | P -1 | 8.4482; 10.4238; 13.9303 86.458; 77.239; 86.317 | 1192.54 | Yan, Xingchen; Xu, Jiakun; Wu, Xiaojing; Zhang, Zhongyu; Zhang, Xia; Fan, Yuhua; Bi, Caifeng Proteasome inhibition and cytostatic effects on human cancer cells by pyrazolone-enamines: a combined crystallographic, structural and computational study New J. Chem., 2015, 39, 2168 |
7054610 | CIF | C34 H36 Al2 N2 O4 | P 1 21/c 1 | 11.552; 12.366; 22.149 90; 97.83; 90 | 3134.53 | Forder, Thomas R.; Jones, Matthew D. Synthesis and characterisation of aluminium(iii) imine bis(phenolate) complexes with application for the polymerisation of rac-LA New J. Chem., 2015, 39, 1974 |
7054611 | CIF | C102 H95 Al4 Cl8 N4 O8 | P b n 21 | 12.0601; 22.5938; 35.5013 90; 90; 90 | 9673.5 | Forder, Thomas R.; Jones, Matthew D. Synthesis and characterisation of aluminium(iii) imine bis(phenolate) complexes with application for the polymerisation of rac-LA New J. Chem., 2015, 39, 1974 |
7054612 | CIF | C69 H100 Al2 N2 O4 | P 1 21/n 1 | 13.632; 19.128; 25.491 90; 99.037; 90 | 6564.3 | Forder, Thomas R.; Jones, Matthew D. Synthesis and characterisation of aluminium(iii) imine bis(phenolate) complexes with application for the polymerisation of rac-LA New J. Chem., 2015, 39, 1974 |
7054613 | CIF | C14 H13 N O2 | C 1 2/c 1 | 22.383; 5.781; 17.844 90; 99.915; 90 | 2274.5 | Forder, Thomas R.; Jones, Matthew D. Synthesis and characterisation of aluminium(iii) imine bis(phenolate) complexes with application for the polymerisation of rac-LA New J. Chem., 2015, 39, 1974 |
7054614 | CIF | C16 H17 N O2 | P 1 21/a 1 | 9.505; 11.258; 13.533 90; 109.058; 90 | 1368.76 | Forder, Thomas R.; Jones, Matthew D. Synthesis and characterisation of aluminium(iii) imine bis(phenolate) complexes with application for the polymerisation of rac-LA New J. Chem., 2015, 39, 1974 |
7054615 | CIF | C14 H11 Cl2 N O2 | P 1 21/n 1 | 8.041; 8.647; 18.742 90; 95.121; 90 | 1297.94 | Forder, Thomas R.; Jones, Matthew D. Synthesis and characterisation of aluminium(iii) imine bis(phenolate) complexes with application for the polymerisation of rac-LA New J. Chem., 2015, 39, 1974 |
7054616 | CIF | C30 H45 N O2 | P 1 21/c 1 | 9.96; 24.276; 12.226 90; 104.981; 90 | 2855.64 | Forder, Thomas R.; Jones, Matthew D. Synthesis and characterisation of aluminium(iii) imine bis(phenolate) complexes with application for the polymerisation of rac-LA New J. Chem., 2015, 39, 1974 |
7054617 | CIF | C48 H42 Eu2 I6 N2 O16 | P 1 21/c 1 | 8.3983; 25.31; 14.1228 90; 105.357; 90 | 2894.8 | Monteiro, Jorge H. S. K.; de Bettencourt-Dias, Ana; Mazali, Italo O.; Sigoli, Fernando A. The effect of 4-halogenobenzoate ligands on luminescent and structural properties of lanthanide complexes: experimental and theoretical approaches New J. Chem., 2015, 39, 1883 |
7054618 | CIF | C25 H26 Mo N4 O7 S | P -1 | 8.782; 11.521; 14.083 106.769; 98.537; 91.636 | 1345.3 | Maurya, Mannar R.; Dhaka, Sarita; Avecilla, Fernando Oxidation of secondary alcohols by conventional and microwave-assisted methods using molybdenum complexes of ONO donor ligands New J. Chem., 2015, 39, 2130 |
7054619 | CIF | C24 H26 Mo N6 O7 S | P -1 | 7.3114; 13.174; 13.6623 98.512; 91.457; 90.513 | 1300.9 | Maurya, Mannar R.; Dhaka, Sarita; Avecilla, Fernando Oxidation of secondary alcohols by conventional and microwave-assisted methods using molybdenum complexes of ONO donor ligands New J. Chem., 2015, 39, 2130 |
7054620 | CIF | C10 H13 N4 O3 Zn | P 4/n c c :2 | 13.4761; 13.4761; 27.254 90; 90; 90 | 4949.5 | Zhu, Yu; Wang, Yan-Mei; Liu, Pan; Wu, Yun-Long; Wei, Wei; Xia, Chang-Kun; Xie, Ji-Min Cage-like pores of a metal‒organic framework for separations and encapsulation of Pd nanoparticles for efficient catalysis New J. Chem., 2015, 39, 2669 |
7054621 | CIF | C19 H33 N3 O7 | P 1 21 1 | 9.4237; 11.6936; 9.8675 90; 95.103; 90 | 1083.06 | Kwon, Sunmi; Kang, Philjae; Choi, Moon-Gun; Choi, Soo Hyuk cis-2-Aminocyclohex-4-enecarboxylic acid as a new building block of helical foldamers New J. Chem., 2015, 39, 3221 |
7054622 | CIF | C29 H47 N5 O9 | P 1 21 1 | 9.4408; 11.5247; 15.054 90; 91.567; 90 | 1637.3 | Kwon, Sunmi; Kang, Philjae; Choi, Moon-Gun; Choi, Soo Hyuk cis-2-Aminocyclohex-4-enecarboxylic acid as a new building block of helical foldamers New J. Chem., 2015, 39, 3221 |
7054623 | CIF | C39 H59 N7 O10 | C 1 2 1 | 31.232; 8.842; 18.831 90; 95.848; 90 | 5173 | Kwon, Sunmi; Kang, Philjae; Choi, Moon-Gun; Choi, Soo Hyuk cis-2-Aminocyclohex-4-enecarboxylic acid as a new building block of helical foldamers New J. Chem., 2015, 39, 3221 |
7054624 | CIF | C29 H45 N5 O8 | P 21 21 21 | 9.2829; 17.955; 23.143 90; 90; 90 | 3857.3 | Kwon, Sunmi; Kang, Philjae; Choi, Moon-Gun; Choi, Soo Hyuk cis-2-Aminocyclohex-4-enecarboxylic acid as a new building block of helical foldamers New J. Chem., 2015, 39, 3221 |
7054625 | CIF | C2 H8 O8 Zn | P 31 2 1 | 7.42; 7.42; 12.11 90; 90; 120 | 577.41 | Mei, Hong-Xin; Zhang, Ting; Wang, Dan-Feng; Huang, Rong-Bin; Zheng, Lan-Sun A Zn-oxalate helix linked by a water helix: spontaneous chiral resolution of a Zn helical coordination polymer New J. Chem., 2015, 39, 2075 |
7054626 | CIF | C2 H8 O8 Zn | P 32 2 1 | 7.42; 7.42; 12.11 90; 90; 120 | 577.41 | Mei, Hong-Xin; Zhang, Ting; Wang, Dan-Feng; Huang, Rong-Bin; Zheng, Lan-Sun A Zn-oxalate helix linked by a water helix: spontaneous chiral resolution of a Zn helical coordination polymer New J. Chem., 2015, 39, 2075 |
7054627 | CIF | C15 H18 Cl2 N4 O2 Pd | P -1 | 9.8262; 9.8965; 9.9887 104.009; 99.865; 110.767 | 845.09 | Kumar, Sushil; Jha, Rajeev Ranjan; Yadav, Sunil; Gupta, Rajeev Pd(ii) complexes with amide-based macrocycles: syntheses, properties and applications in cross-coupling reactions New J. Chem., 2015, 39, 2042 |
7054628 | CIF | C15 H20 N4 O2 Pd | P 1 21/c 1 | 9.606; 15.616; 10.6058 90; 104.624; 90 | 1539.4 | Kumar, Sushil; Jha, Rajeev Ranjan; Yadav, Sunil; Gupta, Rajeev Pd(ii) complexes with amide-based macrocycles: syntheses, properties and applications in cross-coupling reactions New J. Chem., 2015, 39, 2042 |
7054629 | CIF | C17 H24 N4 O4 Pd | P 1 21/n 1 | 10.4774; 10.9664; 16.1533 90; 99.73; 90 | 1829.31 | Kumar, Sushil; Jha, Rajeev Ranjan; Yadav, Sunil; Gupta, Rajeev Pd(ii) complexes with amide-based macrocycles: syntheses, properties and applications in cross-coupling reactions New J. Chem., 2015, 39, 2042 |
7054630 | CIF | C17 H24 N4 O2 Pd | P 1 21/c 1 | 9.864; 10.537; 17.033 90; 106.046; 90 | 1701.4 | Kumar, Sushil; Jha, Rajeev Ranjan; Yadav, Sunil; Gupta, Rajeev Pd(ii) complexes with amide-based macrocycles: syntheses, properties and applications in cross-coupling reactions New J. Chem., 2015, 39, 2042 |
7054631 | CIF | C41 H66 N2 O4 Ti | C 1 2/c 1 | 16.43; 26.165; 21.2458 90; 105.579; 90 | 8797.8 | Gao, Bo; Li, Xiang; Duan, Ranlong; Pang, Xuan Titanium complexes with octahedral geometry chelated by salen ligands adopting β-cis configuration for the ring-opening polymerisation of lactide New J. Chem., 2015, 39, 2404 |
7054632 | CIF | C80 H92 Eu3 N11 O38 | P 1 21/n 1 | 15.4724; 14.1459; 24.04 90; 90.188; 90 | 5261.6 | Li, Ao; Li, Liang; Lin, Zhi; Song, Lin; Wang, Zi-Hao; Chen, Qiang; Yang, Tao; Zhou, Xin-Hui; Xiao, Hong-Ping; Yin, Xiu-Ju Guest-induced reversible structural transitions and concomitant on/off luminescence switching of an Eu(iii) metal‒organic framework and its application in detecting picric acid New J. Chem., 2015, 39, 2289 |
7054634 | CIF | Dy0.5 Mn O3 Yb0.5 | P n m a | 5.8352; 7.3473; 5.2561 90; 90; 90 | 225.34 | Zhang, Yingnan; Liu, Fuyang; Zheng, Tong; Zhang, Ziqing; Liu, Wei; Zhao, Xudong; Liu, Xiaoyang Synthesis of perovskite-type manganites Yb1−xDyxMnO3(0.1 ≤ x ≤ 0.5) via solid-state reaction and high-pressure flux methods followed by structural characterization and magnetic property studies New J. Chem., 2015, 39, 2596 |
7054635 | CIF | C28 H25 F6 N5 O2 S | P 1 21/c 1 | 8.2512; 30.1101; 11.634 90; 102.212; 90 | 2825 | Guo, Jixi; Liu, Li; Jia, Dianzeng; Guo, Mingxi; Zhang, Yucai; Song, Xianli Photochromism and fluorescence modulation of pyrazolone derivatives in the solid state New J. Chem., 2015, 39, 3059 |
7054636 | CIF | C23 H23 Cl N2 O2 | P -1 | 9.2721; 10.3272; 10.7817 81.614; 81.335; 89.456 | 1009.62 | Sutariya, Tushar R.; Labana, Balvantsingh M.; Parmar, Narsidas J.; Kant, Rajni; Gupta, Vivek K.; Plata, Gabriela B.; Padrón, José M. Efficient synthesis of some new antiproliferative N-fused indoles and isoquinolines via 1,3-dipolar cycloaddition reaction in an ionic liquid New J. Chem., 2015, 39, 2657 |
7054637 | CIF | C23 H23 Cl N2 O2 | P 1 21/n 1 | 13.9521; 6.6102; 21.977 90; 106.352; 90 | 1944.9 | Sutariya, Tushar R.; Labana, Balvantsingh M.; Parmar, Narsidas J.; Kant, Rajni; Gupta, Vivek K.; Plata, Gabriela B.; Padrón, José M. Efficient synthesis of some new antiproliferative N-fused indoles and isoquinolines via 1,3-dipolar cycloaddition reaction in an ionic liquid New J. Chem., 2015, 39, 2657 |
7054638 | CIF | C14 H34 Co N4 O18 S2 | P -1 | 6.7203; 8.2504; 12.3358 84.469; 79.593; 85.31 | 668.13 | Kammoun, Omar; Rekik, Walid; Naïli, Houcine; Bataille, Thierry Inorganic layered structures in hybrid double sulfates: related phases and thermal reactivity New J. Chem., 2015, 39, 2682 |
7054639 | CIF | C14 H34 Cu N4 O18 S2 | P -1 | 6.8292; 8.1314; 12.3445 85.429; 81.437; 85.436 | 674.11 | Kammoun, Omar; Rekik, Walid; Naïli, Houcine; Bataille, Thierry Inorganic layered structures in hybrid double sulfates: related phases and thermal reactivity New J. Chem., 2015, 39, 2682 |
7054640 | CIF | C14 H32 Fe N4 O17 S2 | P 1 21/n 1 | 6.6706; 26.5804; 15.2009 90; 92.254; 90 | 2693.14 | Kammoun, Omar; Rekik, Walid; Naïli, Houcine; Bataille, Thierry Inorganic layered structures in hybrid double sulfates: related phases and thermal reactivity New J. Chem., 2015, 39, 2682 |
7054641 | CIF | C14 H34 N4 Ni O18 S2 | P -1 | 6.6415; 8.2264; 12.2601 84.337; 79.491; 85.886 | 654.4 | Kammoun, Omar; Rekik, Walid; Naïli, Houcine; Bataille, Thierry Inorganic layered structures in hybrid double sulfates: related phases and thermal reactivity New J. Chem., 2015, 39, 2682 |
7054642 | CIF | C22 H33 Co2 I3 N4 O | P 1 21/n 1 | 11.6864; 17.6541; 14.7499 90; 113.152; 90 | 2798.02 | Khandar, Ali Akbar; Kirschbaum, Kristin; Abedi, Marjan; Mock, Kristi; Tracy, Greg; Spasojevic, Vojislav; Hosseini-Yazdi, Seyed Abolfazl Synthesis, characterization and crystal structures of mono and dinuclear macrocyclic cobalt(ii) complexes with a new tetraaza m-xylyl-based macrocyclic ligand New J. Chem., 2015, 39, 2822 |
7054643 | CIF | C22 H34 Cl4 Co N4 | P 21 21 21 | 8.8736; 13.6929; 21.0647 90; 90; 90 | 2559.47 | Khandar, Ali Akbar; Kirschbaum, Kristin; Abedi, Marjan; Mock, Kristi; Tracy, Greg; Spasojevic, Vojislav; Hosseini-Yazdi, Seyed Abolfazl Synthesis, characterization and crystal structures of mono and dinuclear macrocyclic cobalt(ii) complexes with a new tetraaza m-xylyl-based macrocyclic ligand New J. Chem., 2015, 39, 2822 |
7054644 | CIF | C22 H40 Cl4 N4 O2 | P -1 | 7.9236; 10.168; 10.2931 62.925; 67.443; 69.428 | 665.97 | Khandar, Ali Akbar; Kirschbaum, Kristin; Abedi, Marjan; Mock, Kristi; Tracy, Greg; Spasojevic, Vojislav; Hosseini-Yazdi, Seyed Abolfazl Synthesis, characterization and crystal structures of mono and dinuclear macrocyclic cobalt(ii) complexes with a new tetraaza m-xylyl-based macrocyclic ligand New J. Chem., 2015, 39, 2822 |
7054645 | CIF | C22 H22 N6 O4 | P -1 | 4.8468; 9.2594; 12.245 69.536; 89.567; 85.993 | 513.51 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054646 | CIF | C24 H26 N6 O4 | P -1 | 5.5146; 6.81; 15.254 79.288; 85.259; 75.952 | 545.62 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054647 | CIF | C26 H30 N6 O4 | P -1 | 5.6196; 6.7825; 16.078 87.236; 82.669; 75.451 | 588.2 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054648 | CIF | C28 H34 N6 O4 | P -1 | 5.632; 6.845; 17.748 93.63; 98.988; 104.67 | 649.97 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054649 | CIF | C30 H38 N6 O4 | P -1 | 5.6047; 6.8589; 18.879 97.644; 91.164; 104.659 | 694.78 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054650 | CIF | C21 H20 N6 O4 | P 1 21/c 1 | 14.797; 4.5097; 29.886 90; 104.056; 90 | 1934.6 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054651 | CIF | C28 H32 N6 O8 | P -1 | 7.6142; 8.6608; 11.0348 102.357; 105.996; 93.866 | 677.09 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054652 | CIF | C24 H26 N6 O4 | P -1 | 5.0121; 7.8964; 15.1589 78.403; 88.333; 72.636 | 560.62 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054653 | CIF | C26 H30 N6 O4 | P -1 | 5.1024; 8.0128; 16.497 99.94; 93.967; 108.231 | 625.5 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054654 | CIF | C28 H34 N6 O4 | P -1 | 5.2731; 7.8464; 17.163 81.964; 88.938; 72.499 | 670.39 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054655 | CIF | C30 H38 N6 O4 | P -1 | 5.2955; 7.8185; 18.424 85.042; 83.543; 71.912 | 719.4 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054656 | CIF | C32 H40 N6 O8 | P -1 | 4.9161; 8.0077; 20.828 87.266; 88.665; 72.608 | 781.5 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
7054657 | CIF | C23 H22 N4 O4 | P 1 21/n 1 | 11.4449; 8.9002; 21.338 90; 94.855; 90 | 2165.7 | Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John Molecular electrostatic potential dependent selectivity of hydrogen bonding New J. Chem., 2015, 39, 822 |
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