Crystallography Open Database

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7054425 CIFC30 H38 N3 Ni S8C 1 2 116.624; 7.8685; 28.101
90; 102.325; 90		3591.1Le 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 CIFC17 H17 N3 S4P 21 21 218.5565; 11.6085; 37.5518
90; 90; 90		3729.95Le 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 CIFC30 H33 N3P 1 21/c 113.508; 24.193; 7.507
90; 94.864; 90		2444Vishnoi, 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 CIFC48 H42 N12 O21P -110.766; 13.96; 17.294
102.357; 98.189; 100.935		2447Vishnoi, 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 CIFC16 H19 Fe N3 O3P 1 21/n 19.8538; 12.9015; 12.7365
90; 97.033; 90		1606.99Liu, 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 CIFC17 H21 Fe N3 O3P 1 21/c 112.5421; 14.1112; 9.8489
90; 92.506; 90		1741.43Liu, 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 CIFC17 H23 Fe N3 O4P -17.6098; 9.9244; 12.4142
94.402; 97.669; 107.436		879.69Liu, 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 CIFC14 H17 Fe N4 O3.5P -16.06; 12.5298; 20.6252
80.833; 87.615; 87.665		1543.82Liu, 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 CIFC21 H19 Fe N5 O7P n a 2143.0383; 5.8461; 8.4347
90; 90; 90		2122.22Liu, 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 CIFC22 H21 Fe N5 O7P -19.4141; 11.4937; 11.5265
109.571; 96.214; 105.601		1104.49Liu, 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 CIFC23 H23 Fe N5 O7P -17.4108; 13.2305; 13.7738
63.098; 74.466; 78.581		1155.71Liu, 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 CIFC23 H23 Fe N5 O7P -111.0568; 11.2915; 11.3242
77.032; 73.612; 62.236		1192.99Liu, 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 CIFC24 H25 Fe N5 O7P n a 2122.3748; 5.7925; 19.342
90; 90; 90		2506.8Liu, 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 CIFC20 H18 Fe N6 O7P -18.4026; 10.9599; 12.3548
107.976; 102.058; 92.43		1051.35Liu, 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 CIFC22 H27 Co N2 O9P 1 21/c 115.959; 11.194; 13.281
90; 100.678; 90		2331.5Mitra, Merry; Raghavaiah, Pallepogu; Ghosh, Rajarshi
A mononuclear cobalt(iii) complex and its catecholase activity
New J. Chem., 2015, 39, 200
7054460 CIFC6 H26 As2 N9 Na9 Ni3 O73 W18P 63/m13.9035; 13.9035; 33.499
90; 90; 120		5608Liu, 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 CIFC6 H37 As2 Mn3 N9 Na9 O78.5 W18P 63/m13.9494; 13.9494; 33.76
90; 90; 120		5689.1Liu, 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 CIFC6 H34 As2 Co3 N9 Na9 O77 W18P 63/m13.9307; 13.9307; 33.554
90; 90; 120		5639.2Liu, 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 CIFC4 H6 N6 O4P 1 21/n 16.9708; 14.408; 7.8104
90; 105.99; 90		754.1Fischer, 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 CIFC4 H8 N12 O4P 1 21/n 17.5509; 7.844; 18.562
90; 94.987; 90		1095.3Fischer, 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 CIFC4 H10 N12 O7P 1 21 18.0286; 8.0668; 9.6666
90; 90.004; 90		626.06Fischer, 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 CIFC4 H2 Cl2 N4 O4P 21 21 216.985; 8.4845; 13.8574
90; 90; 90		821.25Fischer, 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 CIFC4 H2 Cl2 N4 O3P 1 21/n 18.2678; 11.2186; 8.5693
90; 99.912; 90		782.97Fischer, 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 CIFC4 H6 N6 O3C 1 2/c 112.844; 8.919; 6.988
90; 112.147; 90		741.5Fischer, 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 CIFC4 K2 N10 O4P -17.1412; 7.2056; 11.498
89.658; 73.514; 64.814		508.88Fischer, 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 CIFC6 H12 N16 O4C 1 2/c 114.7455; 11.7557; 10.6941
90; 129.904; 90		1422.05Fischer, 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 CIFC6 H14 N18 O4P 1 21/n 17.0135; 31.347; 7.9795
90; 115.793; 90		1579.5Fischer, 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 CIFC4 H4 K2 N10 O5P 1 21/c 17.4337; 21.6146; 7.5901
90; 97.741; 90		1208.44Fischer, 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 CIFC4 H10 N14 O3P -13.7659; 11.0046; 14.3912
97.056; 95.04; 98.978		581.14Fischer, 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 CIFC4 H8 N12 O3P b c a14.5573; 7.5523; 19.5093
90; 90; 90		2144.9Fischer, 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 CIFC19 H11 F4 N O2P 1 21/n 18.3016; 12.104; 16.4292
90; 98.436; 90		1632.99Huo, 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 CIFC9 H16 N2 O3P -16.9516; 8.1294; 9.6234
74.586; 80.157; 83.657		515.35Maton, 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 CIFC8 H15 Cl N2P 1 21/c 16.77997; 14.4971; 9.8785
90; 100.572; 90		954.47Maton, 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 CIFC9 H17 Cl N2R -319.8873; 19.8873; 14.4048
90; 90; 120		4933.9Maton, 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 CIFC32 H22 N2 OP 1 21/c 112.3316; 21.3475; 8.8212
90; 92.34; 90		2320.2Jayabharathi, Jayaraman; Ramanathan, Periyasamy; Thanikachalam, Venugopal
Synthesis and optical properties of phenanthromidazole derivatives for organic electroluminescent devices
New J. Chem., 2015, 39, 142
7054491 CIFC30 H47 F N4 OP 1 21/c 19.575; 20.505; 15.88
90; 105.413; 90		3006Ghosh, 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 CIFC12 H14 O5 PbI b a 216.2354; 19.1181; 8.2268
90; 90; 90		2553.5Bo, 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 CIFC24 H24 O9 Pb3P 1 21/c 118.7933; 17.7755; 8.2471
90; 99.723; 90		2715.45Bo, 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 CIFC36 H36 O13 Pb4P n a 2118.4043; 30.9956; 6.9963
90; 90; 90		3991.1Bo, 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 CIFC40 H44 Fe N8 O2 Se2P -110.594; 14.2967; 14.5177
84.866; 68.83; 77.339		2000.46Nguyen, 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 CIFC38 H36 Fe N8 O3 Se2P 1 21/c 112.203; 19.513; 15.887
90; 90.858; 90		3782.5Nguyen, 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 CIFC27 H41 Au N P S2P b c a12.3157; 19.6569; 22.945
90; 90; 90		5554.7Altaf, 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 CIFC29.33 H26 N3 O6.17R -328.3533; 28.3533; 15.9781
90; 90; 120		11124.1Haddad, 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 CIFC17 H19 F I3 N3 O3P -18.1001; 9.6437; 13.9228
87.481; 77.694; 77.279		1036.5Zou, 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 CIFC24 H29 Fe N4 O4 SP 1 21/c 119.0809; 11.3904; 23.6108
90; 107.42; 90		4896.2Masárová, 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 CIFC24 H29 Fe N4 O4 SP 1 21/c 119.165; 11.6749; 22.449
90; 107.772; 90		4783.2Masárová, 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 CIFC24 H29 Fe N4 O4 SP 1 21/c 119.334; 11.456; 23.831
90; 107.131; 90		5044.2Masárová, 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 CIFC28 H25 Fe N4 O2 SP 21 21 217.5011; 13.0676; 24.704
90; 90; 90		2421.5Masárová, 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 CIFC28 H25 Fe N4 O2 SP 21 21 217.5422; 13.5725; 24.6626
90; 90; 90		2524.62Masárová, 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 CIFC20 H19 Fe N6 O6 SP b c n15.903; 14.218; 19.6342
90; 90; 90		4439.5Masárová, 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 CIFC23 H29 Fe N6 O4P 1 21/n 111.0321; 11.3322; 18.9441
90; 96.974; 90		2350.8Masárová, 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 CIFC36 H53 Fe N4 O2 SP 1 21/c 118.2879; 11.8974; 17.3763
90; 96.903; 90		3753.3Masárová, 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 CIFC23 H27 Fe N4 O4 SP 1 21/n 111.5785; 11.6541; 18.2132
90; 106.508; 90		2356.33Masárová, 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 CIFC18 H21 Cl2 N5 ZnP -17.927; 10.615; 12.92
78.84; 74.08; 70.62		979.9Štefane, 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 CIFC28 H26 Cl2 N6 ZnP 1 21/c 18.8955; 14.5691; 21.5718
90; 91.451; 90		2794.8Štefane, 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 CIFC24 H29 Cl2 N5 Ni O2P -16.4217; 11.6331; 34.4621
89.715; 85.211; 82.58		2543.95Štefane, 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 CIFC27 H23 Cu N3 O4 SC 1 2/c 126.919; 8.723; 22.424
90; 107.99; 90		5008.1Li, 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 CIFC29 H33 N3 Ni O7 SP 1 21/n 114.759; 13.805; 14.772
90; 96.14; 90		2992.5Li, 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 CIFC11 H10 N2 O2P 1 21/c 115.6778; 3.9598; 17.4076
90; 108.928; 90		1022.24Song, 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 CIFC11 H10 N2 O2I 1 2/a 113.7381; 8.877; 17.564
90; 103.368; 90		2083.9Song, 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 CIFC11 H10 N2 O2P 1 21/c 13.92; 10.792; 23.124
90; 93.463; 90		976.5Song, 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 CIFC32 H28 N6 O Ti2P 1 21/c 113.8001; 14.107; 14.966
90; 93.4; 90		2908.4Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan
Titanocene(iii) pseudohalides: an ESR and structural study
New J. Chem., 2015, 39, 576
7054518 CIFC30 H36 N2 O3 S2 Ti2P 1 21/c 19.842; 19.9841; 15.283
90; 99.947; 90		2960.7Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan
Titanocene(iii) pseudohalides: an ESR and structural study
New J. Chem., 2015, 39, 576
7054519 CIFC51 H78 N3 Si6 Ti3P -114.5932; 14.925; 15.54
74.368; 83.551; 61.471		2863.2Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan
Titanocene(iii) pseudohalides: an ESR and structural study
New J. Chem., 2015, 39, 576
7054520 CIFC36 H52 N6 Si4 Ti2P -17.598; 11.523; 25.0561
77.795; 89.851; 84.089		2132.3Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan
Titanocene(iii) pseudohalides: an ESR and structural study
New J. Chem., 2015, 39, 576
7054521 CIFC47 H60 N6 Si4 Ti2P -111.475; 11.6289; 18.8461
92.434; 99.597; 96.7		2457.8Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan
Titanocene(iii) pseudohalides: an ESR and structural study
New J. Chem., 2015, 39, 576
7054522 CIFC32 H52 Cl2 Si4 Ti2P -18.828; 9.427; 12.2471
71.689; 78.624; 89.462		947.09Křižan, Martin; Honzíček, Jan; Vinklárek, Jaromír; Růžičková, Zdeňka; Erben, Milan
Titanocene(iii) pseudohalides: an ESR and structural study
New J. Chem., 2015, 39, 576
7054523 CIFC21 H30 N8 O11 V2P -19.616; 12.119; 12.594
90.497; 98.27; 113.05		1333Ma, 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 CIFC23 H32 N8 O12 S VP -19.9813; 12.3482; 13.298
103.22; 93.546; 100.63		1558.9Ma, 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 CIFC22 H18 N3 O5.5 VR -3 :H21.563; 21.563; 24.14
90; 90; 120		9720Ma, 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 CIFC42 H33 F10 O3 P3 Pt S2P -111.1223; 13.6579; 16.7386
67.229; 81.64; 71.075		2217.22Cervantes, Ruy; Tiburcio, Jorge; Torrens, Hugo
cis and trans influences on [Pt(SRF)(triphos)]+complexes (SRF= polyfluorobenzothiolate)
New J. Chem., 2015, 39, 631
7054527 CIFC41 H38 F3 O3 P3 Pt S2P 1 21/n 110.2751; 19.9018; 19.3686
90; 93.744; 90		3952.3Cervantes, Ruy; Tiburcio, Jorge; Torrens, Hugo
cis and trans influences on [Pt(SRF)(triphos)]+complexes (SRF= polyfluorobenzothiolate)
New J. Chem., 2015, 39, 631
7054528 CIFC41 H34 F7 O3 P3 Pt S2P 1 21/n 110.188; 19.711; 21.039
90; 96.02; 90		4201.7Cervantes, Ruy; Tiburcio, Jorge; Torrens, Hugo
cis and trans influences on [Pt(SRF)(triphos)]+complexes (SRF= polyfluorobenzothiolate)
New J. Chem., 2015, 39, 631
7054529 CIFC9 H8 N12 O8P -18.0665; 8.3119; 13.9189
90.693; 104.018; 118.084		790.11Wu, 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 CIFC8 H8 N8 O9P 1 21/c 117.582; 10.4936; 15.8405
90; 111.304; 90		2722.8Wu, 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 CIFC16 H28 N2 O SP 1 21/c 120.6963; 4.89894; 16.9658
90; 97.371; 90		1705.95Yadav, 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 CIFC17 H30 N2 O SP 1 21/c 123.237; 4.9497; 15.6429
90; 90.966; 90		1798.9Yadav, 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 CIFC18 H32 N2 O SP 1 21/c 122.1166; 19.4545; 9.42062
90; 101.186; 90		3976.38Yadav, 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 CIFC17 H30 N2 O SP -14.9139; 8.2041; 23.1603
84.043; 87.033; 78.743		910.3Yadav, 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 CIFC15 H26 N2 O5P 110.036; 11.838; 15.884
79.36; 78.98; 74.71		1768.7Shi, 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 CIFC20 H24 N2 O6C 1 2/c 129.7753; 4.8973; 13.9889
90; 103.74; 90		1981.47Parveen, 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 CIFC23 H8 Br N O9 Ru3P -110.13; 10.886; 11.806
95.962; 105.519; 93.803		1241.6Ma, 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 CIFC32 H17 Br N2 O4 Ru2C 1 2/c 124.724; 10.628; 23.593
90; 115.263; 90		5607Ma, 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 CIFC28 H16 Br2 N2C 1 2/c 123.277; 6.251; 14.611
90; 92.423; 90		2124Ma, 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 CIFC21 H8 Br N O7 Ru3P -17.181; 9.6498; 16.7441
95.889; 98.26; 104.031		1102.52Ma, 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 CIFC22 H14 O4 Ru2P 1 21/c 19.241; 13.168; 8.138
90; 112.245; 90		916.6Ma, 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 CIFC27 H16 Br N O5 Ru2P 1 21/c 113.5255; 12.8602; 15.6149
90; 114.691; 90		2467.7Ma, 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 CIFC69 H59.33 Eu2 N12 O11.67C 1 2/c 146.333; 17.299; 32.343
90; 123.542; 90		21607Das, 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 CIFC80 H104 Li N8 Nd O3P -112.6452; 15.0817; 20.7038
101.662; 97.13; 106.03		3648Yakovenko, 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 CIFC46 H68 N5 Nd O Si2P 1 21/c 123.9499; 19.4258; 21.8709
90; 116.878; 90		9076.1Yakovenko, 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 CIFC26 H28 Br2 F8 N4C 1 2 113.0391; 6.8246; 15.9891
90; 92.828; 90		1421.08Yi, 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 CIFC18 H18 Br F7 N2 OP b c a13.647; 12.4533; 22.0643
90; 90; 90		3749.83Yi, 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 CIFC18 H33 B10 N5 O5P 21 21 217.32285; 13.0124; 26.9145
90; 90; 90		2564.62Matuszewski, 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 CIFC4 H16.86 Fe2 N12 O8.43 S5P b c a12.6104; 10.35013; 37.1231
90; 90; 90		4845.28Sanina, 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 CIFC4 H16 Fe4 N16 O14 S8P -16.2712; 10.4132; 12.1912
86.462; 88.363; 87.613		793.65Sanina, 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 CIFC13.4 H24.5 Cl0 Cu N1.5 O5.92 Y0.5P -19.4934; 13.2045; 14.699
76.486; 85.811; 83.394		1777.66Ahmed, 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 CIFC12 H12 Cu4 N10P 1 21/c 115.368; 8.37; 13.71
90; 101.697; 90		1727Xu, 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 CIFC6 H8 Cu N4F d d 215.836; 24.736; 7.948
90; 90; 90		3113.4Xu, 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 CIFC12 H18 Cl O4 PC 1 2/c 133.1; 11.236; 8.061
90; 97.58; 90		2971.8Dar, 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 CIFC12 H18 Br O4 PC 1 2/c 133.434; 11.241; 7.946
90; 97.374; 90		2962Dar, 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 CIFC12 H18 I O4 PC 1 2/c 134.091; 11.245; 8.001
90; 97.511; 90		3041Dar, 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 CIFC20 H27 O4 PC 1 2/c 133.71; 6.824; 17.253
90; 90.834; 90		3968Dar, 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 CIFC39 H48 N O4 PP 1 21/c 113.664; 10.956; 23.642
90; 98.563; 90		3500Dar, 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 CIFC21 H27 O5 PP -16.69; 9.064; 17.502
79.175; 89.61; 82.167		1032.5Dar, 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 CIFC19 H23 O5 PC 1 2/c 141.181; 11.01; 8.186
90; 92.162; 90		3709Dar, 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 CIFC8 H6.5 N5 O1.75C 1 2/c 126.008; 6.836; 22.709
90; 123.384; 90		3371.3Chen, 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 CIFC16 H16 Mn N10 O6C 1 2/c 119.315; 8.088; 11.97
90; 94.203; 90		1864.9Chen, 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 CIFC16 H16 N10 O6 ZnC 1 2/c 119.02; 8.0801; 11.953
90; 94.235; 90		1832Chen, 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 CIFC16 H16 Cd N10 O6C 1 2/c 119.4542; 8.1626; 12.0696
90; 94.203; 90		1911.46Chen, 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 CIFC9 H8 N5 O1.5P 1 21/n 16.8792; 20.841; 13.359
90; 103.471; 90		1862.6Chen, 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 CIFC30 H32 Br Cl2 Cu N6P 1 21/c 113.3142; 15.6092; 14.3394
90; 98.779; 90		2945.16Chou, 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 CIFC30 H32 Cl4 Cu2 N6P 1 21/c 125.9994; 15.1102; 17.1561
90; 107.436; 90		6430.2Chou, 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 CIFC29 H30 Ag Cl N6 O4P -110.2448; 12.581; 13.3336
71.022; 86.393; 66.479		1485.7Chou, 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 CIFC43 H53 B Co F4 N6 O6 P2 S2P 1 21/c 113.3203; 25.2381; 15.0807
90; 109.346; 90		4783.5Jing, 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 CIFC42 H47 B F4 N6 Ni O5 P2 S2P -19.43; 12.8553; 21.7668
93.409; 91.482; 111.218		2452.3Jing, 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 CIFC24 H34 O4 S4P -14.919; 7.285; 18.574
84.19; 86.42; 84.08		657.7Turbiez, 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 CIFC19 H27 F N2 O4P 4310.1585; 10.1585; 19.0174
90; 90; 90		1962.5Hassoun, 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 CIFC32 H40 F4 N4 O7P 21 21 215.35; 20.2; 29.927
90; 90; 90		3234.2Hassoun, 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 CIFC17 H15 Cu N7 O8P 1 21/n 112.4021; 12.3286; 13.1324
90; 105.544; 90		1934.5Ma, 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 CIFC42 H34 Cu2 N14 O18P -110.272; 15.184; 16.2
100.009; 99.61; 108.045		2299.2Ma, 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 CIFC36 H36 N4 O12 S4P 1 21/c 113.0584; 17.2823; 17.4795
90; 94.228; 90		3934.02Mačková, 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 CIFC44 H52 N4 O12 S4P -111.0672; 12.3077; 18.3099
101.125; 95.076; 102.421		2367.8Mačková, 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 CIFC48 H58 N6 O12 S4P 42/n :213.2452; 13.2452; 14.9787
90; 90; 90		2627.79Mačková, 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 CIFC52 H36 N4 O12 S4P 41 21 212.73537; 12.73537; 28.8831
90; 90; 90		4684.54Mačková, 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 CIFC48 H60 N4 O12 S4P 1 21/c 127.261; 16.3468; 17.9466
90; 139.366; 90		5208.2Mačková, 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 CIFC36 H20 N4 O12 S4C 1 2/c 111.2845; 18.1827; 18.8706
90; 105.953; 90		3722.8Mačková, 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 CIFC44 H52 N4 O12 S4P 1 21 112.64786; 14.04823; 13.3958
90; 101.233; 90		2334.57Mačková, 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 CIFC48 H56 N8 O12 S4C 1 2/m 128.7209; 19.3593; 13.9154
90; 136.11; 90		5364Mačková, 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 CIFC150.6 H206.4 N8 O14.6P -115.65; 17.82; 26.44
70.56; 86.08; 87.57		6936Gattuso, 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 CIFC26 H25 N3 O2 SP 1 21/c 115.6352; 16.2677; 8.8947
90; 103.891; 90		2196.2Sharma, Shilpa; Pradeep, Chullikkattill. P.; Dhir, Abhimanew
Dansyl-carbazole AIEE material for selective recognition of thiourea derivatives
New J. Chem., 2015, 39, 1822
7054587 CIFC55 H41 Er N2 O6P 1 21/c 114.9946; 17.0429; 22.7907
90; 128.291; 90		4571.3Martín-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 CIFC55 H41 Er N2 O6P -115.2886; 17.7424; 20.7735
73.91; 70.046; 68.647		4857.3Martín-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 CIFC50 H44 B Cu N7 S2P 1 21/c 113.9619; 25.3276; 12.567
90; 104.037; 90		4311.3Harding, 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 CIFC60 H48 B Cu N7 S2P 1 21/c 117.804; 18.099; 17.81
90; 119.686; 90		4986Harding, 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 CIFC50 H42 B Cu N7 S2P 1 21/c 113.9204; 25.042; 12.6285
90; 102.523; 90		4297.5Harding, 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 CIFC16 H17 N O4 SP 1 21/c 115.7805; 5.0908; 21.06
90; 110.851; 90		1581.06Ragab, Sherif Shaban; Swaminathan, Subramani; Garcia-Amorós, Jaume; Captain, Burjor; Raymo, Françisco M.
Bimolecular photoactivation of NBD fluorescence
New J. Chem., 2015, 39, 1570
7054593 CIFC26 H25 Cl2 N5 Ni O9P 1 21/c 115.5059; 11.4074; 16.1421
90; 100.036; 90		2811.56Song, 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 CIFC26 H25 Cl2 Co N5 O9P 1 21/c 115.5452; 11.45475; 16.1105
90; 99.8494; 90		2826.46Song, 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 CIFC39 H55 Cl6 N5 O8P -111.307; 13.8002; 17.341
70.683; 73.734; 71.237		2371.71Pike, 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 CIFC54 H82 Cl4 P2 RuP 1 21/c 119.2677; 14.6496; 22.219
90; 122.706; 90		5277.3Yu, 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 CIFC51 H76 Cl2 P2 RuR -346.1591; 46.1591; 13.9447
90; 90; 120		25730.9Yu, 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 CIFC28 H45 Cl2 O P RuP 1 21/c 111.4775; 19.2194; 25.7969
90; 96.478; 90		5654.2Yu, 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 CIFC53 H44 Cl2 P2 RuP -110.2241; 12.7121; 20.0557
72.94; 76.718; 81.407		2415.8Yu, 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 CIFC17 H16 OP 1 21/c 16.6764; 16.5673; 11.6107
90; 92.308; 90		1283.22Yu, 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 CIFC53 H80 Cl2 P2 RuR -347.1514; 47.1514; 13.6692
90; 90; 120		26318.6Yu, 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 CIFC55 H78 Cl2 P2 RuR -346.042; 46.042; 14.0313
90; 90; 120		25759.5Yu, 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 CIFC51 H75 Cl2 F P2 RuR -345.479; 45.479; 14.179
90; 90; 120		25398Yu, 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 CIFC26 H25 N3 O4P -110.1589; 11.3338; 11.6688
68.322; 67.396; 82.841		1152.4Yan, 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 CIFC25 H24 N4 O3P -17.3752; 10.9275; 14.5614
101.707; 92.769; 98.544		1132.64Yan, 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 CIFC24 H21 N3 O2P -17.7356; 10.8256; 13.5508
112.683; 90.907; 107.741		985.67Yan, 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 CIFC32 H34 N4 O3P -19.5274; 10.4205; 14.7518
77.254; 82.096; 84.377		1411.4Yan, 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 CIFC24 H21 N3 O2P -17.2287; 11.0934; 14.0509
107.981; 99.534; 105.146		996.58Yan, 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 CIFC27 H25 N3 O6P -18.4482; 10.4238; 13.9303
86.458; 77.239; 86.317		1192.54Yan, 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 CIFC34 H36 Al2 N2 O4P 1 21/c 111.552; 12.366; 22.149
90; 97.83; 90		3134.53Forder, 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 CIFC102 H95 Al4 Cl8 N4 O8P b n 2112.0601; 22.5938; 35.5013
90; 90; 90		9673.5Forder, 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 CIFC69 H100 Al2 N2 O4P 1 21/n 113.632; 19.128; 25.491
90; 99.037; 90		6564.3Forder, 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 CIFC14 H13 N O2C 1 2/c 122.383; 5.781; 17.844
90; 99.915; 90		2274.5Forder, 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 CIFC16 H17 N O2P 1 21/a 19.505; 11.258; 13.533
90; 109.058; 90		1368.76Forder, 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 CIFC14 H11 Cl2 N O2P 1 21/n 18.041; 8.647; 18.742
90; 95.121; 90		1297.94Forder, 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 CIFC30 H45 N O2P 1 21/c 19.96; 24.276; 12.226
90; 104.981; 90		2855.64Forder, 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 CIFC48 H42 Eu2 I6 N2 O16P 1 21/c 18.3983; 25.31; 14.1228
90; 105.357; 90		2894.8Monteiro, 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 CIFC25 H26 Mo N4 O7 SP -18.782; 11.521; 14.083
106.769; 98.537; 91.636		1345.3Maurya, 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 CIFC24 H26 Mo N6 O7 SP -17.3114; 13.174; 13.6623
98.512; 91.457; 90.513		1300.9Maurya, 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 CIFC10 H13 N4 O3 ZnP 4/n c c :213.4761; 13.4761; 27.254
90; 90; 90		4949.5Zhu, 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 CIFC19 H33 N3 O7P 1 21 19.4237; 11.6936; 9.8675
90; 95.103; 90		1083.06Kwon, 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 CIFC29 H47 N5 O9P 1 21 19.4408; 11.5247; 15.054
90; 91.567; 90		1637.3Kwon, 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 CIFC39 H59 N7 O10C 1 2 131.232; 8.842; 18.831
90; 95.848; 90		5173Kwon, 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 CIFC29 H45 N5 O8P 21 21 219.2829; 17.955; 23.143
90; 90; 90		3857.3Kwon, 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 CIFC2 H8 O8 ZnP 31 2 17.42; 7.42; 12.11
90; 90; 120		577.41Mei, 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 CIFC2 H8 O8 ZnP 32 2 17.42; 7.42; 12.11
90; 90; 120		577.41Mei, 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 CIFC15 H18 Cl2 N4 O2 PdP -19.8262; 9.8965; 9.9887
104.009; 99.865; 110.767		845.09Kumar, 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 CIFC15 H20 N4 O2 PdP 1 21/c 19.606; 15.616; 10.6058
90; 104.624; 90		1539.4Kumar, 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 CIFC17 H24 N4 O4 PdP 1 21/n 110.4774; 10.9664; 16.1533
90; 99.73; 90		1829.31Kumar, 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 CIFC17 H24 N4 O2 PdP 1 21/c 19.864; 10.537; 17.033
90; 106.046; 90		1701.4Kumar, 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 CIFC41 H66 N2 O4 TiC 1 2/c 116.43; 26.165; 21.2458
90; 105.579; 90		8797.8Gao, 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 CIFC80 H92 Eu3 N11 O38P 1 21/n 115.4724; 14.1459; 24.04
90; 90.188; 90		5261.6Li, 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 CIFDy0.5 Mn O3 Yb0.5P n m a5.8352; 7.3473; 5.2561
90; 90; 90		225.34Zhang, 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 CIFC28 H25 F6 N5 O2 SP 1 21/c 18.2512; 30.1101; 11.634
90; 102.212; 90		2825Guo, 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 CIFC23 H23 Cl N2 O2P -19.2721; 10.3272; 10.7817
81.614; 81.335; 89.456		1009.62Sutariya, 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 CIFC23 H23 Cl N2 O2P 1 21/n 113.9521; 6.6102; 21.977
90; 106.352; 90		1944.9Sutariya, 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 CIFC14 H34 Co N4 O18 S2P -16.7203; 8.2504; 12.3358
84.469; 79.593; 85.31		668.13Kammoun, 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 CIFC14 H34 Cu N4 O18 S2P -16.8292; 8.1314; 12.3445
85.429; 81.437; 85.436		674.11Kammoun, 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 CIFC14 H32 Fe N4 O17 S2P 1 21/n 16.6706; 26.5804; 15.2009
90; 92.254; 90		2693.14Kammoun, 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 CIFC14 H34 N4 Ni O18 S2P -16.6415; 8.2264; 12.2601
84.337; 79.491; 85.886		654.4Kammoun, 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 CIFC22 H33 Co2 I3 N4 OP 1 21/n 111.6864; 17.6541; 14.7499
90; 113.152; 90		2798.02Khandar, 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 CIFC22 H34 Cl4 Co N4P 21 21 218.8736; 13.6929; 21.0647
90; 90; 90		2559.47Khandar, 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 CIFC22 H40 Cl4 N4 O2P -17.9236; 10.168; 10.2931
62.925; 67.443; 69.428		665.97Khandar, 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 CIFC22 H22 N6 O4P -14.8468; 9.2594; 12.245
69.536; 89.567; 85.993		513.51Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054646 CIFC24 H26 N6 O4P -15.5146; 6.81; 15.254
79.288; 85.259; 75.952		545.62Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054647 CIFC26 H30 N6 O4P -15.6196; 6.7825; 16.078
87.236; 82.669; 75.451		588.2Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054648 CIFC28 H34 N6 O4P -15.632; 6.845; 17.748
93.63; 98.988; 104.67		649.97Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054649 CIFC30 H38 N6 O4P -15.6047; 6.8589; 18.879
97.644; 91.164; 104.659		694.78Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054650 CIFC21 H20 N6 O4P 1 21/c 114.797; 4.5097; 29.886
90; 104.056; 90		1934.6Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054651 CIFC28 H32 N6 O8P -17.6142; 8.6608; 11.0348
102.357; 105.996; 93.866		677.09Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054652 CIFC24 H26 N6 O4P -15.0121; 7.8964; 15.1589
78.403; 88.333; 72.636		560.62Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054653 CIFC26 H30 N6 O4P -15.1024; 8.0128; 16.497
99.94; 93.967; 108.231		625.5Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054654 CIFC28 H34 N6 O4P -15.2731; 7.8464; 17.163
81.964; 88.938; 72.499		670.39Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054655 CIFC30 H38 N6 O4P -15.2955; 7.8185; 18.424
85.042; 83.543; 71.912		719.4Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054656 CIFC32 H40 N6 O8P -14.9161; 8.0077; 20.828
87.266; 88.665; 72.608		781.5Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054657 CIFC23 H22 N4 O4P 1 21/n 111.4449; 8.9002; 21.338
90; 94.855; 90		2165.7Aakeröy, Christer B.; Wijethunga, Tharanga K.; Desper, John
Molecular electrostatic potential dependent selectivity of hydrogen bonding
New J. Chem., 2015, 39, 822
7054658 CIFC26 H20 Cl F N4 O2P b c a7.8846; 27.1172; 20.7714
90; 90; 90		4441.1Turkoglu, Gulsen; Berber, Halil; Kani, Ibrahim
Synthesis, crystal structure, optical and electrochemical properties of novel diphenylether-based formazan derivatives
New J. Chem., 2015, 39, 2728
7054659 CIFC15 H19 N O3P 1 21 19.7435; 6.5523; 11.959
90; 105.802; 90		734.64Rodríguez, Isabel; Calaza, M. Isabel; Jiménez, Ana I.; Cativiela, Carlos
Synthesis of enantiomerically pure δ-benzylproline derivatives
New J. Chem., 2015, 39, 3310
7054660 CIFC11 H17 N O9 ZnP b c a12.3453; 12.0038; 20.971
90; 90; 90		3107.7Karmakar, Anirban; Guedes da Silva, M. Fátima C.; Hazra, Susanta; Pombeiro, Armando J. L.
Zinc amidoisophthalate complexes and their catalytic application in the diastereoselective Henry reaction
New J. Chem., 2015, 39, 3004
7054661 CIFC11 H21 N O11 ZnP -17.0755; 11.1714; 12.1991
73.152; 82.48; 72.042		877Karmakar, Anirban; Guedes da Silva, M. Fátima C.; Hazra, Susanta; Pombeiro, Armando J. L.
Zinc amidoisophthalate complexes and their catalytic application in the diastereoselective Henry reaction
New J. Chem., 2015, 39, 3004
7054662 CIFC15 H13 N O7 ZnP 21 21 215.2989; 15.3102; 19.3432
90; 90; 90		1569.3Karmakar, Anirban; Guedes da Silva, M. Fátima C.; Hazra, Susanta; Pombeiro, Armando J. L.
Zinc amidoisophthalate complexes and their catalytic application in the diastereoselective Henry reaction
New J. Chem., 2015, 39, 3004
7054663 CIFC15 H17 N O9 ZnP -18.9796; 10.1531; 10.6054
89.721; 77.398; 71.835		894.5Karmakar, Anirban; Guedes da Silva, M. Fátima C.; Hazra, Susanta; Pombeiro, Armando J. L.
Zinc amidoisophthalate complexes and their catalytic application in the diastereoselective Henry reaction
New J. Chem., 2015, 39, 3004
7054664 CIFC11 H10 Br N3 OP 1 21/n 113.5334; 12.3004; 28.098
90; 102.177; 90		4572.1Bustos, Carlos; Molins, Elies; Cárcamo, Juan-Guillermo; Aguilar, Marcelo N.; Sánchez, Christian; Moreno-Villoslada, Ignacio; Nishide, Hiroyuki; Mesías-Salazar, Angela; Zarate, Ximena; Schott, Eduardo
New 3,4,5-trisubstituted isoxazole derivatives with potential biological properties
New J. Chem., 2015, 39, 4295
7054665 CIFC11 H10 N4 O3C 1 2/c 111.765; 11.314; 17.774
90; 95.75; 90		2354Bustos, Carlos; Molins, Elies; Cárcamo, Juan-Guillermo; Aguilar, Marcelo N.; Sánchez, Christian; Moreno-Villoslada, Ignacio; Nishide, Hiroyuki; Mesías-Salazar, Angela; Zarate, Ximena; Schott, Eduardo
New 3,4,5-trisubstituted isoxazole derivatives with potential biological properties
New J. Chem., 2015, 39, 4295
7054666 CIFC16 H16 N2 O S2P 1 21/n 15.0508; 33.692; 8.9618
90; 100.081; 90		1501.5Biswal, Debanjana; Pramanik, Nikhil Ranjan; Chakrabarti, Syamal; Chakraborty, Nirmalya; Acharya, Krishnendu; Mandal, Sudhanshu Sekhar; Ghosh, Saktiprosad; Drew, Michael G. B.; Mondal, Tapan Kumar; Biswas, Sujan
Lewis base controlled supramolecular architectures via non-covalent interactions of dioxomolybdenum(vi) complexes with an ONS donor ligand: DFT calculations and biological study
New J. Chem., 2015, 39, 2778
7054667 CIFC20 H22 Mo N2 O4 S2P 1 21/n 114.489; 7.1442; 21.09
90; 91.518; 90		2182.3Biswal, Debanjana; Pramanik, Nikhil Ranjan; Chakrabarti, Syamal; Chakraborty, Nirmalya; Acharya, Krishnendu; Mandal, Sudhanshu Sekhar; Ghosh, Saktiprosad; Drew, Michael G. B.; Mondal, Tapan Kumar; Biswas, Sujan
Lewis base controlled supramolecular architectures via non-covalent interactions of dioxomolybdenum(vi) complexes with an ONS donor ligand: DFT calculations and biological study
New J. Chem., 2015, 39, 2778
7054668 CIFC21 H21 Cl3 Mo N4 O3 S2P -19.7755; 10.9369; 12.4981
99.619; 96.272; 90.833		1308.81Biswal, Debanjana; Pramanik, Nikhil Ranjan; Chakrabarti, Syamal; Chakraborty, Nirmalya; Acharya, Krishnendu; Mandal, Sudhanshu Sekhar; Ghosh, Saktiprosad; Drew, Michael G. B.; Mondal, Tapan Kumar; Biswas, Sujan
Lewis base controlled supramolecular architectures via non-covalent interactions of dioxomolybdenum(vi) complexes with an ONS donor ligand: DFT calculations and biological study
New J. Chem., 2015, 39, 2778
7054669 CIFC22 H22 Mo N4 O3 S2P 1 21/n 114.272; 11.291; 14.874
90; 102.868; 90		2336.7Biswal, Debanjana; Pramanik, Nikhil Ranjan; Chakrabarti, Syamal; Chakraborty, Nirmalya; Acharya, Krishnendu; Mandal, Sudhanshu Sekhar; Ghosh, Saktiprosad; Drew, Michael G. B.; Mondal, Tapan Kumar; Biswas, Sujan
Lewis base controlled supramolecular architectures via non-covalent interactions of dioxomolybdenum(vi) complexes with an ONS donor ligand: DFT calculations and biological study
New J. Chem., 2015, 39, 2778
7054670 CIFC23.33 H24.96 Mo N3 O4 S2P -17.505; 13.022; 14.463
106.162; 101.97; 105.956		1242.1Biswal, Debanjana; Pramanik, Nikhil Ranjan; Chakrabarti, Syamal; Chakraborty, Nirmalya; Acharya, Krishnendu; Mandal, Sudhanshu Sekhar; Ghosh, Saktiprosad; Drew, Michael G. B.; Mondal, Tapan Kumar; Biswas, Sujan
Lewis base controlled supramolecular architectures via non-covalent interactions of dioxomolybdenum(vi) complexes with an ONS donor ligand: DFT calculations and biological study
New J. Chem., 2015, 39, 2778
7054671 CIFC21 H19 Mo N3 O3 S2P -111.2231; 14.2627; 14.4636
103.729; 97.022; 106.223		2114.93Biswal, Debanjana; Pramanik, Nikhil Ranjan; Chakrabarti, Syamal; Chakraborty, Nirmalya; Acharya, Krishnendu; Mandal, Sudhanshu Sekhar; Ghosh, Saktiprosad; Drew, Michael G. B.; Mondal, Tapan Kumar; Biswas, Sujan
Lewis base controlled supramolecular architectures via non-covalent interactions of dioxomolybdenum(vi) complexes with an ONS donor ligand: DFT calculations and biological study
New J. Chem., 2015, 39, 2778
7054672 CIFC42 H80 N24 O28C 1 2/m 114.8304; 19.0315; 12.5878
90; 94.618; 90		3541.3Zhao, Wenxuan; Wang, Chuanzeng; Zhang, Yunqian; Xue, Saifeng; Zhu, Qianjiang; Tao, Zhu
Supramolecular assembly of a methyl-substituted cucurbit[6]uril and its potential applications in selective sorption
New J. Chem., 2015, 39, 2433
7054673 CIFC24 H18 Cu2 N10 O6 S2P b c a13.3215; 12.3215; 16.7717
90; 90; 90		2752.9Hazra, Susanta; Karmakar, Anirban; Guedes da Silva, Maria de Fátima C.; Dlháň, L'ubor; Boča, Roman; Pombeiro, Armando J. L.
Sulfonated Schiff base dinuclear and polymeric copper(ii) complexes: crystal structures, magnetic properties and catalytic application in Henry reaction
New J. Chem., 2015, 39, 3424
7054674 CIFC26 H18 Cu2 N6 O6 S4P -17.2488; 8.5638; 13.1244
83.205; 89.661; 70.551		762.35Hazra, Susanta; Karmakar, Anirban; Guedes da Silva, Maria de Fátima C.; Dlháň, L'ubor; Boča, Roman; Pombeiro, Armando J. L.
Sulfonated Schiff base dinuclear and polymeric copper(ii) complexes: crystal structures, magnetic properties and catalytic application in Henry reaction
New J. Chem., 2015, 39, 3424
7054675 CIFC14 H11 Cu N5 O4 SP 1 21/c 18.5179; 15.1779; 12.2602
90; 92.219; 90		1583.86Hazra, Susanta; Karmakar, Anirban; Guedes da Silva, Maria de Fátima C.; Dlháň, L'ubor; Boča, Roman; Pombeiro, Armando J. L.
Sulfonated Schiff base dinuclear and polymeric copper(ii) complexes: crystal structures, magnetic properties and catalytic application in Henry reaction
New J. Chem., 2015, 39, 3424
7054676 CIFC29 H28 Dy F12 N5 Ni O11P 1 21/c 117.8522; 10.6611; 19.9365
90; 106.854; 90		3631.4Lu, Xing-Yun; Liu, Yu-Qing; Deng, Xiao-Wei; Zhu, Zhao-Xia; Yao, Min-Xia; Jing, Su
Synthesis, structures and magnetism of heterodinuclear Ni‒Ln complexes: field-induced single-molecule magnet behavior in the dysprosium analogue
New J. Chem., 2015, 39, 3467
7054677 CIFC29 H28 F12 Gd N5 Ni O11P 1 21/c 118.351; 10.8682; 19.911
90; 106.184; 90		3813.7Lu, Xing-Yun; Liu, Yu-Qing; Deng, Xiao-Wei; Zhu, Zhao-Xia; Yao, Min-Xia; Jing, Su
Synthesis, structures and magnetism of heterodinuclear Ni‒Ln complexes: field-induced single-molecule magnet behavior in the dysprosium analogue
New J. Chem., 2015, 39, 3467
7054678 CIFC29 H28 F12 N5 Ni O11 TbP 1 21/c 117.8821; 10.8892; 20.0534
90; 106.038; 90		3752.9Lu, Xing-Yun; Liu, Yu-Qing; Deng, Xiao-Wei; Zhu, Zhao-Xia; Yao, Min-Xia; Jing, Su
Synthesis, structures and magnetism of heterodinuclear Ni‒Ln complexes: field-induced single-molecule magnet behavior in the dysprosium analogue
New J. Chem., 2015, 39, 3467
7054679 CIFC61 H49 F9 N9 O8 Yb ZnC 1 2/c 123.852; 13.2551; 41.053
90; 104.55; 90		12563Yu, Chao; Zhang, Zhao; Liu, Lin; Li, Hongyan; He, Yani; Lü, Xingqiang; Wong, Wai-Kwok; Jones, Richard A.
PMMA-supported hybrid materials doped with highly near-infrared (NIR) luminescent complexes [Zn(L1)(Py)Ln(L2)3] (Ln = Nd, Yb or Er)
New J. Chem., 2015, 39, 3698
7054680 CIFC17 H27 I N2 PtP 1 21/c 112.0156; 12.0304; 13.4566
90; 102.37; 90		1900Ghosh, Biswa Nath; Lentz, Dieter; Schlecht, Sabine
Substituent effects in solution speciation of the mononuclear and dinuclear trimethylplatinum(iv) iodide complexes of pyridines
New J. Chem., 2015, 39, 3536
7054681 CIFC15 H23 I N2 PtP 1 21/n 111.1252; 12.8648; 12.2536
90; 98.742; 90		1733.4Ghosh, Biswa Nath; Lentz, Dieter; Schlecht, Sabine
Substituent effects in solution speciation of the mononuclear and dinuclear trimethylplatinum(iv) iodide complexes of pyridines
New J. Chem., 2015, 39, 3536
7054682 CIFC15 H17 I N4 PtP -19.7124; 10.2867; 10.3892
70.911; 66.286; 73.069		882.64Ghosh, Biswa Nath; Lentz, Dieter; Schlecht, Sabine
Substituent effects in solution speciation of the mononuclear and dinuclear trimethylplatinum(iv) iodide complexes of pyridines
New J. Chem., 2015, 39, 3536
7054683 CIFC18 H26 I2 N4 Pt2P 1 21/n 18.88211; 12.088; 22.6364
90; 99.0938; 90		2399.85Ghosh, Biswa Nath; Lentz, Dieter; Schlecht, Sabine
Substituent effects in solution speciation of the mononuclear and dinuclear trimethylplatinum(iv) iodide complexes of pyridines
New J. Chem., 2015, 39, 3536
7054684 CIFC18 H26 I2 N4 Pt2P 1 21/c 18.0595; 11.2505; 13.6434
90; 106.09; 90		1188.63Ghosh, Biswa Nath; Lentz, Dieter; Schlecht, Sabine
Substituent effects in solution speciation of the mononuclear and dinuclear trimethylplatinum(iv) iodide complexes of pyridines
New J. Chem., 2015, 39, 3536
7054685 CIFC18 H32 I2 N2 O2 Pt2P 1 21/n 110.407; 11.7649; 20.7823
90; 98.377; 90		2517.4Ghosh, Biswa Nath; Lentz, Dieter; Schlecht, Sabine
Substituent effects in solution speciation of the mononuclear and dinuclear trimethylplatinum(iv) iodide complexes of pyridines
New J. Chem., 2015, 39, 3536
7054686 CIFC20 H36 I2 N2 Pt2P n a m10.7003; 12.7871; 18.4091
90; 90; 90		2518.8Ghosh, Biswa Nath; Lentz, Dieter; Schlecht, Sabine
Substituent effects in solution speciation of the mononuclear and dinuclear trimethylplatinum(iv) iodide complexes of pyridines
New J. Chem., 2015, 39, 3536
7054687 CIFC28 H52 N4 O7P 18.999; 14.013; 14.873
66.19; 75.21; 73.6		1624.6M. B. Reddy, Madhusudana; Basuroy, K.; Chandrappa, S.; Dinesh, B.; Vasantha, B.; A. Venkatesha, Manjunath; Balaram, P.
Structural characterization of folded and extended conformations in peptides containing γ amino acids with proteinogenic side chains: crystal structures of γn, (αγ)nand γγδγ sequences
New J. Chem., 2015, 39, 3319
7054688 CIFC34 H64 N4 O9P 1 21 110.6075; 10.735; 19.1418
90; 105.348; 90		2101.97M. B. Reddy, Madhusudana; Basuroy, K.; Chandrappa, S.; Dinesh, B.; Vasantha, B.; A. Venkatesha, Manjunath; Balaram, P.
Structural characterization of folded and extended conformations in peptides containing γ amino acids with proteinogenic side chains: crystal structures of γn, (αγ)nand γγδγ sequences
New J. Chem., 2015, 39, 3319
7054689 CIFC49 H88 N8 O12P 1 21 19.5742; 10.8563; 28.0245
90; 93.811; 90		2906.44M. B. Reddy, Madhusudana; Basuroy, K.; Chandrappa, S.; Dinesh, B.; Vasantha, B.; A. Venkatesha, Manjunath; Balaram, P.
Structural characterization of folded and extended conformations in peptides containing γ amino acids with proteinogenic side chains: crystal structures of γn, (αγ)nand γγδγ sequences
New J. Chem., 2015, 39, 3319
7054690 CIFC39 H74 N4 O7P 15.0768; 8.924; 25.12
98.67; 94.399; 99.374		1104M. B. Reddy, Madhusudana; Basuroy, K.; Chandrappa, S.; Dinesh, B.; Vasantha, B.; A. Venkatesha, Manjunath; Balaram, P.
Structural characterization of folded and extended conformations in peptides containing γ amino acids with proteinogenic side chains: crystal structures of γn, (αγ)nand γγδγ sequences
New J. Chem., 2015, 39, 3319
7054691 CIFC27 H52 N4 O5P 1 21 15.0056; 15.829; 20.317
90; 93.452; 90		1606.9M. B. Reddy, Madhusudana; Basuroy, K.; Chandrappa, S.; Dinesh, B.; Vasantha, B.; A. Venkatesha, Manjunath; Balaram, P.
Structural characterization of folded and extended conformations in peptides containing γ amino acids with proteinogenic side chains: crystal structures of γn, (αγ)nand γγδγ sequences
New J. Chem., 2015, 39, 3319
7054692 CIFC20 H38 N2 O5P 1 21 15.1643; 30.0027; 7.5724
90; 94.261; 90		1170.05M. B. Reddy, Madhusudana; Basuroy, K.; Chandrappa, S.; Dinesh, B.; Vasantha, B.; A. Venkatesha, Manjunath; Balaram, P.
Structural characterization of folded and extended conformations in peptides containing γ amino acids with proteinogenic side chains: crystal structures of γn, (αγ)nand γγδγ sequences
New J. Chem., 2015, 39, 3319
7054693 CIFC34 H64 N4 O7P 1 21 15.1182; 50.153; 7.4046
90; 97.675; 90		1883.68M. B. Reddy, Madhusudana; Basuroy, K.; Chandrappa, S.; Dinesh, B.; Vasantha, B.; A. Venkatesha, Manjunath; Balaram, P.
Structural characterization of folded and extended conformations in peptides containing γ amino acids with proteinogenic side chains: crystal structures of γn, (αγ)nand γγδγ sequences
New J. Chem., 2015, 39, 3319
7054694 CIFC20 H38 N2 O5C 1 2 128.9383; 5.1419; 18.4128
90; 120.323; 90		2364.96M. B. Reddy, Madhusudana; Basuroy, K.; Chandrappa, S.; Dinesh, B.; Vasantha, B.; A. Venkatesha, Manjunath; Balaram, P.
Structural characterization of folded and extended conformations in peptides containing γ amino acids with proteinogenic side chains: crystal structures of γn, (αγ)nand γγδγ sequences
New J. Chem., 2015, 39, 3319
7054695 CIFC33 H63 N5 O8P 19.901; 10.527; 10.553
100.403; 106.665; 93.047		1029.9M. B. Reddy, Madhusudana; Basuroy, K.; Chandrappa, S.; Dinesh, B.; Vasantha, B.; A. Venkatesha, Manjunath; Balaram, P.
Structural characterization of folded and extended conformations in peptides containing γ amino acids with proteinogenic side chains: crystal structures of γn, (αγ)nand γγδγ sequences
New J. Chem., 2015, 39, 3319
7054696 CIFC16 H32 Cd N8 O4 PdC 1 2/c 118.57; 10.3191; 17.2851
90; 133.39; 90		2407Şenocak, Ayşegül; Karadağ, Ahmet; Soylu, Mustafa Serkan; Andaç, Ömer
Two novel cyanido-bridged polymeric complexes with suspension bridge type connections and a series of related complex salts: crystallographic and thermal characterizations
New J. Chem., 2015, 39, 3675
7054697 CIFC10 H16 N6 Ni O2 ZnP b c n11.463; 8.9492; 14.7436
90; 90; 90		1512.5Şenocak, Ayşegül; Karadağ, Ahmet; Soylu, Mustafa Serkan; Andaç, Ömer
Two novel cyanido-bridged polymeric complexes with suspension bridge type connections and a series of related complex salts: crystallographic and thermal characterizations
New J. Chem., 2015, 39, 3675
7054698 CIFC10 H16 Cd N6 Ni O2C 1 2/c 110.8081; 10.4606; 14.2364
90; 107.209; 90		1537.5Şenocak, Ayşegül; Karadağ, Ahmet; Soylu, Mustafa Serkan; Andaç, Ömer
Two novel cyanido-bridged polymeric complexes with suspension bridge type connections and a series of related complex salts: crystallographic and thermal characterizations
New J. Chem., 2015, 39, 3675
7054699 CIFC16 H36 Cd N8 Ni O6P 21 21 219.6656; 14.9615; 17.9211
90; 90; 90		2591.6Şenocak, Ayşegül; Karadağ, Ahmet; Soylu, Mustafa Serkan; Andaç, Ömer
Two novel cyanido-bridged polymeric complexes with suspension bridge type connections and a series of related complex salts: crystallographic and thermal characterizations
New J. Chem., 2015, 39, 3675
7054700 CIFC32 H32 Be2 N4 O6P -18.5367; 8.8067; 10.1596
106.505; 92.538; 97.889		722.6Reglinski, John; Kennedy, Alan R.; Steel, Graham
Tetradentate Schiff base beryllium complexes
New J. Chem., 2015, 39, 2437
7054701 CIFC18 H18 Be N2 O2C 1 c 17.6771; 17.9229; 11.3182
90; 98.385; 90		1540.7Reglinski, John; Kennedy, Alan R.; Steel, Graham
Tetradentate Schiff base beryllium complexes
New J. Chem., 2015, 39, 2437
7054702 CIFC18 H16 N2 O2 SP b n a7.4296; 19.375; 22.676
90; 90; 90		3264.2Salahifar, Eslam; Nematollahi, Davood
Electrochemical generation of a Michael acceptor: a green method for the synthesis of 4-amino-3-(phenylsulfonyl)diphenylamine derivatives
New J. Chem., 2015, 39, 3852
7054703 CIFC19 H21 N3 OP 1 21/n 110.1735; 14.3043; 11.2897
90; 96.376; 90		1632.8Singh, Nongthombam Geetmani; Nagarajaprakash, Rammamorthy; Rani, Jims World Star; Kathing, Chingrishon; Nongrum, Ridaphun; Nongkhlaw, Rishanlang
Nickel nanoparticles assisted regioselective synthesis of pyrazoloquinolinone and triazoloquinazolinone derivatives
New J. Chem., 2015, 39, 3908
7054704 CIFC17 H17 Cl N4 OP -16.0023; 12.317; 12.46
67.981; 77.245; 80.977		830.1Singh, Nongthombam Geetmani; Nagarajaprakash, Rammamorthy; Rani, Jims World Star; Kathing, Chingrishon; Nongrum, Ridaphun; Nongkhlaw, Rishanlang
Nickel nanoparticles assisted regioselective synthesis of pyrazoloquinolinone and triazoloquinazolinone derivatives
New J. Chem., 2015, 39, 3908
7054707 CIFC102 H90 N16 O19 Pb2 TbP 1 21/n 112.3263; 20.7018; 18.2517
90; 91.642; 90		4655.49Pan, Mei; Yan, Cheng; Chen, Ling; Zhang, Lu-Yin; Yin, Shao-Yun; Zhu, Yi-Xuan; Wu, Kai; Hou, Ya-Jun; Su, Cheng-Yong
Photoluminescence and white-light emission in two series of heteronuclear Pb(ii)‒Ln(iii) complexes
New J. Chem., 2015, 39, 3770
7054708 CIFC102 H90 Eu N16 O19 Pb2P 1 21/n 112.31597; 20.8623; 18.2267
90; 91.689; 90		4681.12Pan, Mei; Yan, Cheng; Chen, Ling; Zhang, Lu-Yin; Yin, Shao-Yun; Zhu, Yi-Xuan; Wu, Kai; Hou, Ya-Jun; Su, Cheng-Yong
Photoluminescence and white-light emission in two series of heteronuclear Pb(ii)‒Ln(iii) complexes
New J. Chem., 2015, 39, 3770
7054709 CIFC108 H100 N20 O28 Pb Tb2P -111.7061; 13.0527; 17.955
87.73; 88.01; 89.886		2739.65Pan, Mei; Yan, Cheng; Chen, Ling; Zhang, Lu-Yin; Yin, Shao-Yun; Zhu, Yi-Xuan; Wu, Kai; Hou, Ya-Jun; Su, Cheng-Yong
Photoluminescence and white-light emission in two series of heteronuclear Pb(ii)‒Ln(iii) complexes
New J. Chem., 2015, 39, 3770
7054710 CIFC36 H42 Cl2 N8 O10 Ru SP -111.0785; 11.9068; 16.6733
76.422; 75.205; 79.014		2047Bhat, Satish S.; Revankar, Vidyanand K.; Khan, Ayesha; Butcher, Raymond J.; Thatipamula, Krishnachary
Supramolecular architecture and photophysical and biological properties of ruthenium(ii) polypyridyl complexes
New J. Chem., 2015, 39, 3646
7054711 CIFC18 H17 Cu Mo4 N6 O14P 1 21/c 110.6473; 19.752; 13.407
90; 113.396; 90		2587.7Li, Shaobin; Zhang, Li; Ma, Huiyuan; Pang, Haijun; Zhao, Chunyan
Tuning the topology structures of polymolybdate-based hybrids from interpenetrated framework to interdigitated architecture via changing polymolybdate clusters
New J. Chem., 2015, 39, 3528
7054712 CIFC36 H40 Cu Mo12 N12 O44 PP -111.158; 12.946; 13.292
97.478; 112.381; 104.018		1668.8Li, Shaobin; Zhang, Li; Ma, Huiyuan; Pang, Haijun; Zhao, Chunyan
Tuning the topology structures of polymolybdate-based hybrids from interpenetrated framework to interdigitated architecture via changing polymolybdate clusters
New J. Chem., 2015, 39, 3528
7054713 CIFC48 H44 Cu4 Mo12 N16 O42 SiP -110.9784; 14.048; 14.5469
110.234; 107.408; 102.658		1873.7Li, Shaobin; Zhang, Li; Ma, Huiyuan; Pang, Haijun; Zhao, Chunyan
Tuning the topology structures of polymolybdate-based hybrids from interpenetrated framework to interdigitated architecture via changing polymolybdate clusters
New J. Chem., 2015, 39, 3528
7054714 CIFC4 H4 O2P -15.0156; 6.9262; 7.0836
112.956; 97.227; 107.388		207.85Saraswatula, Viswanadha G.; Bhattacharya, Suman; Saha, Binoy K.
Can the thermal expansion be controlled by varying the hydrogen bond dimensionality in polymorphs?
New J. Chem., 2015, 39, 3345
7054715 CIFC4 H4 O2P -15.0359; 6.9758; 7.1152
112.963; 97.033; 107.706		210.8Saraswatula, Viswanadha G.; Bhattacharya, Suman; Saha, Binoy K.
Can the thermal expansion be controlled by varying the hydrogen bond dimensionality in polymorphs?
New J. Chem., 2015, 39, 3345
7054716 CIFC4 H4 O2P -15.058; 7.0169; 7.1325
112.92; 96.962; 108.002		213.14Saraswatula, Viswanadha G.; Bhattacharya, Suman; Saha, Binoy K.
Can the thermal expansion be controlled by varying the hydrogen bond dimensionality in polymorphs?
New J. Chem., 2015, 39, 3345
7054717 CIFC4 H4 O2P -15.0673; 7.0638; 7.163
113.064; 96.689; 108.347		215.3Saraswatula, Viswanadha G.; Bhattacharya, Suman; Saha, Binoy K.
Can the thermal expansion be controlled by varying the hydrogen bond dimensionality in polymorphs?
New J. Chem., 2015, 39, 3345
7054718 CIFC4 H4 O2P 1 21 13.9158; 7.1104; 7.871
90; 100.59; 90		215.42Saraswatula, Viswanadha G.; Bhattacharya, Suman; Saha, Binoy K.
Can the thermal expansion be controlled by varying the hydrogen bond dimensionality in polymorphs?
New J. Chem., 2015, 39, 3345
7054719 CIFC4 H4 O2P 1 21 13.8248; 7.0987; 7.7801
90; 101.058; 90		207.32Saraswatula, Viswanadha G.; Bhattacharya, Suman; Saha, Binoy K.
Can the thermal expansion be controlled by varying the hydrogen bond dimensionality in polymorphs?
New J. Chem., 2015, 39, 3345
7054720 CIFC4 H4 O2P 1 21 13.8518; 7.0956; 7.7924
90; 100.862; 90		209.16Saraswatula, Viswanadha G.; Bhattacharya, Suman; Saha, Binoy K.
Can the thermal expansion be controlled by varying the hydrogen bond dimensionality in polymorphs?
New J. Chem., 2015, 39, 3345
7054721 CIFC4 H4 O2P 1 21 13.8856; 7.1138; 7.8353
90; 100.93; 90		212.65Saraswatula, Viswanadha G.; Bhattacharya, Suman; Saha, Binoy K.
Can the thermal expansion be controlled by varying the hydrogen bond dimensionality in polymorphs?
New J. Chem., 2015, 39, 3345
7054722 CIFC4 H4 O2P 1 21 13.8912; 7.1141; 7.8453
90; 100.8; 90		213.33Saraswatula, Viswanadha G.; Bhattacharya, Suman; Saha, Binoy K.
Can the thermal expansion be controlled by varying the hydrogen bond dimensionality in polymorphs?
New J. Chem., 2015, 39, 3345
7054723 CIFC4 H4 O2P 1 21 13.9127; 7.1074; 7.8489
90; 100.422; 90		214.67Saraswatula, Viswanadha G.; Bhattacharya, Suman; Saha, Binoy K.
Can the thermal expansion be controlled by varying the hydrogen bond dimensionality in polymorphs?
New J. Chem., 2015, 39, 3345
7054724 CIFC4 H4 O2P 1 21 13.9417; 7.1096; 7.878
90; 100.25; 90		217.25Saraswatula, Viswanadha G.; Bhattacharya, Suman; Saha, Binoy K.
Can the thermal expansion be controlled by varying the hydrogen bond dimensionality in polymorphs?
New J. Chem., 2015, 39, 3345
7054725 CIFC20 H28 N2 O S2P -18.9476; 10.2758; 12.1482
98.043; 95.114; 110.648		1023.3Tarakci, Deniz Kutlu; Berber, Savaş; Zorlu, Yunus; Atilla, Devrim; Ahsen, Vefa; Dumoulin, Fabienne
The synthesis of an octasubstituted monohydroxylated phthalocyanine designed to investigate the effect of the presence of active moieties
New J. Chem., 2015, 39, 3929
7054726 CIFC10 H15 N4 O6 PP b c a8.8012; 13.0262; 25.0491
90; 90; 90		2871.8Gholivand, Khodayar; Molaei, Foroogh
Synthesis and structural study of some new phosphorus(v) hydrazide compounds: spectroscopic evidence and a theoretical approach
New J. Chem., 2015, 39, 3747
7054727 CIFC14 H15 N2 O5 PP -15.757; 8.9928; 14.7059
78.99; 86.504; 87.806		745.67Gholivand, Khodayar; Molaei, Foroogh
Synthesis and structural study of some new phosphorus(v) hydrazide compounds: spectroscopic evidence and a theoretical approach
New J. Chem., 2015, 39, 3747
7054728 CIFC10 H15 N4 O5 PP 1 21/c 112.2908; 7.0588; 17.6586
90; 109.425; 90		1444.82Gholivand, Khodayar; Molaei, Foroogh
Synthesis and structural study of some new phosphorus(v) hydrazide compounds: spectroscopic evidence and a theoretical approach
New J. Chem., 2015, 39, 3747
7054731 CIFC18 H31 Cl Ni O3 P2P -112.2454; 14.3018; 14.9082
71.876; 69.05; 71.933		2258.4García-Eleno, Marco A.; Padilla-Mata, Esteban; Estudiante-Negrete, Fabiola; Pichal-Cerda, Francisco; Hernández-Ortega, Simón; Toscano, Rubén A.; Morales-Morales, David
Single step, high yield synthesis of para-hydroxy functionalized POCOP ligands and their Ni(ii) pincer derivatives
New J. Chem., 2015, 39, 3361
7054732 CIFC22.5 H40 Cl2 Ni O3 P2P 1 21/n 110.159; 20.23; 13.9587
90; 102.917; 90		2796.2García-Eleno, Marco A.; Padilla-Mata, Esteban; Estudiante-Negrete, Fabiola; Pichal-Cerda, Francisco; Hernández-Ortega, Simón; Toscano, Rubén A.; Morales-Morales, David
Single step, high yield synthesis of para-hydroxy functionalized POCOP ligands and their Ni(ii) pincer derivatives
New J. Chem., 2015, 39, 3361
7054733 CIFC30 H23 Cl Ni O3 P2P 1 21/c 115.125; 10.058; 17.403
90; 90.493; 90		2647.4García-Eleno, Marco A.; Padilla-Mata, Esteban; Estudiante-Negrete, Fabiola; Pichal-Cerda, Francisco; Hernández-Ortega, Simón; Toscano, Rubén A.; Morales-Morales, David
Single step, high yield synthesis of para-hydroxy functionalized POCOP ligands and their Ni(ii) pincer derivatives
New J. Chem., 2015, 39, 3361
7054734 CIFC29 H43 Cl Ni O4 P2P 1 21/c 18.0299; 27.236; 15.128
90; 101.306; 90		3244.3García-Eleno, Marco A.; Padilla-Mata, Esteban; Estudiante-Negrete, Fabiola; Pichal-Cerda, Francisco; Hernández-Ortega, Simón; Toscano, Rubén A.; Morales-Morales, David
Single step, high yield synthesis of para-hydroxy functionalized POCOP ligands and their Ni(ii) pincer derivatives
New J. Chem., 2015, 39, 3361
7054735 CIFC18 H31 Cl Ni O3 P2P -112.2454; 14.3018; 14.9082
71.876; 69.05; 71.933		2258.4Koleša-Dobravc, Tanja; Meden, Anton; Perdih, Franc
Influence of noncovalent interactions on the structures of metal‒organic hybrids based on a [VO2(2,6-pydc)]−tecton with cations of imidazole, pyridine and its derivatives
New J. Chem., 2015, 39, 4265
7054736 CIFC22.5 H40 Cl2 Ni O3 P2P 1 21/n 110.159; 20.23; 13.9587
90; 102.917; 90		2796.2Koleša-Dobravc, Tanja; Meden, Anton; Perdih, Franc
Influence of noncovalent interactions on the structures of metal‒organic hybrids based on a [VO2(2,6-pydc)]−tecton with cations of imidazole, pyridine and its derivatives
New J. Chem., 2015, 39, 4265
7054737 CIFC30 H23 Cl Ni O3 P2P 1 21/c 115.125; 10.058; 17.403
90; 90.493; 90		2647.4Koleša-Dobravc, Tanja; Meden, Anton; Perdih, Franc
Influence of noncovalent interactions on the structures of metal‒organic hybrids based on a [VO2(2,6-pydc)]−tecton with cations of imidazole, pyridine and its derivatives
New J. Chem., 2015, 39, 4265
7054738 CIFC29 H43 Cl Ni O4 P2P 1 21/c 18.0299; 27.236; 15.128
90; 101.306; 90		3244.3Koleša-Dobravc, Tanja; Meden, Anton; Perdih, Franc
Influence of noncovalent interactions on the structures of metal‒organic hybrids based on a [VO2(2,6-pydc)]−tecton with cations of imidazole, pyridine and its derivatives
New J. Chem., 2015, 39, 4265
7054739 CIFC12 H13 N2 O8 VP -16.7436; 8.14; 13.7971
103.904; 97.539; 95.474		722.45Koleša-Dobravc, Tanja; Meden, Anton; Perdih, Franc
Influence of noncovalent interactions on the structures of metal‒organic hybrids based on a [VO2(2,6-pydc)]−tecton with cations of imidazole, pyridine and its derivatives
New J. Chem., 2015, 39, 4265
7054740 CIFC12 H9 N2 O6 VP -17.9144; 12.5749; 13.4045
88.379; 89.985; 74.931		1287.63Koleša-Dobravc, Tanja; Meden, Anton; Perdih, Franc
Influence of noncovalent interactions on the structures of metal‒organic hybrids based on a [VO2(2,6-pydc)]−tecton with cations of imidazole, pyridine and its derivatives
New J. Chem., 2015, 39, 4265
7054741 CIFC12 H11 N2 O8 VP 1 21/m 17.8481; 6.421; 13.8887
90; 95.055; 90		697.17Koleša-Dobravc, Tanja; Meden, Anton; Perdih, Franc
Influence of noncovalent interactions on the structures of metal‒organic hybrids based on a [VO2(2,6-pydc)]−tecton with cations of imidazole, pyridine and its derivatives
New J. Chem., 2015, 39, 4265
7054742 CIFC12 H12 N3 O7 VP 1 21/m 18.1855; 6.5443; 13.8669
90; 97.755; 90		736.03Koleša-Dobravc, Tanja; Meden, Anton; Perdih, Franc
Influence of noncovalent interactions on the structures of metal‒organic hybrids based on a [VO2(2,6-pydc)]−tecton with cations of imidazole, pyridine and its derivatives
New J. Chem., 2015, 39, 4265
7054743 CIFC12 H10 N3 O6 VP 1 21/c 114.4966; 7.3713; 14.6252
90; 118.696; 90		1370.88Koleša-Dobravc, Tanja; Meden, Anton; Perdih, Franc
Influence of noncovalent interactions on the structures of metal‒organic hybrids based on a [VO2(2,6-pydc)]−tecton with cations of imidazole, pyridine and its derivatives
New J. Chem., 2015, 39, 4265
7054744 CIFC14 H16 N3 O7 VP b c m8.1715; 29.4539; 6.6398
90; 90; 90		1598.08Koleša-Dobravc, Tanja; Meden, Anton; Perdih, Franc
Influence of noncovalent interactions on the structures of metal‒organic hybrids based on a [VO2(2,6-pydc)]−tecton with cations of imidazole, pyridine and its derivatives
New J. Chem., 2015, 39, 4265
7054745 CIFC10 H8 N3 O6 VC 1 2 19.3492; 12.426; 6.436
90; 129.421; 90		577.59Koleša-Dobravc, Tanja; Meden, Anton; Perdih, Franc
Influence of noncovalent interactions on the structures of metal‒organic hybrids based on a [VO2(2,6-pydc)]−tecton with cations of imidazole, pyridine and its derivatives
New J. Chem., 2015, 39, 4265
7054747 CIFC17 H21 B N2 O2P 1 21/c 113.3088; 6.012; 19.833
90; 108.647; 90		1503.59Adamczyk-Woźniak, Agnieszka; Czerwińska, Karolina; Madura, Izabela D.; Matuszewska, Alicja; Sporzyński, Andrzej; Żubrowska-Zembrzuska, Anna
Piperazine derivatives of boronic acids ‒ potential bifunctional biologically active compounds
New J. Chem., 2015, 39, 4308
7054748 CIFC18 H23 B N2 O3I 1 2/a 112.1978; 19.2053; 15.5424
90; 96; 90		3621.05Adamczyk-Woźniak, Agnieszka; Czerwińska, Karolina; Madura, Izabela D.; Matuszewska, Alicja; Sporzyński, Andrzej; Żubrowska-Zembrzuska, Anna
Piperazine derivatives of boronic acids ‒ potential bifunctional biologically active compounds
New J. Chem., 2015, 39, 4308
7054749 CIFC17 H19 B Cl2 N2 O2P -17.9155; 10.313; 11.8333
88.456; 72.897; 69.37		860.88Adamczyk-Woźniak, Agnieszka; Czerwińska, Karolina; Madura, Izabela D.; Matuszewska, Alicja; Sporzyński, Andrzej; Żubrowska-Zembrzuska, Anna
Piperazine derivatives of boronic acids ‒ potential bifunctional biologically active compounds
New J. Chem., 2015, 39, 4308
7054750 CIFC17 H20 B N3 O4P 1 21/n 110.32568; 9.10656; 18.03844
90; 90.7068; 90		1696.05Adamczyk-Woźniak, Agnieszka; Czerwińska, Karolina; Madura, Izabela D.; Matuszewska, Alicja; Sporzyński, Andrzej; Żubrowska-Zembrzuska, Anna
Piperazine derivatives of boronic acids ‒ potential bifunctional biologically active compounds
New J. Chem., 2015, 39, 4308
7054751 CIFC12 H21 B N2 O3P n a 2112.87751; 10.18562; 10.36536
90; 90; 90		1359.58Adamczyk-Woźniak, Agnieszka; Czerwińska, Karolina; Madura, Izabela D.; Matuszewska, Alicja; Sporzyński, Andrzej; Żubrowska-Zembrzuska, Anna
Piperazine derivatives of boronic acids ‒ potential bifunctional biologically active compounds
New J. Chem., 2015, 39, 4308
7054752 CIFC27 H33 B N2 O3P 1 21/c 124.60371; 11.76829; 17.52165
90; 93.8287; 90		5061.96Adamczyk-Woźniak, Agnieszka; Czerwińska, Karolina; Madura, Izabela D.; Matuszewska, Alicja; Sporzyński, Andrzej; Żubrowska-Zembrzuska, Anna
Piperazine derivatives of boronic acids ‒ potential bifunctional biologically active compounds
New J. Chem., 2015, 39, 4308
7054753 CIFCs6 O16 P4 Y2P 1 21 110.1897; 10.3703; 10.5504
90; 107.526; 90		1063.11Wang, Ying; Lian, Zhipeng; Su, Xin; Yang, Zhihua; Pan, Shilie; Yan, Qingfeng; Zhang, Fangfang
Cs6RE2(PO4)4(RE = Y and Gd): two new members of the alkali rare-earth double phosphates
New J. Chem., 2015, 39, 4328
7054754 CIFCs6 Gd2 O16 P4P 1 21 110.2819; 10.4257; 10.5785
90; 107.649; 90		1080.6Wang, Ying; Lian, Zhipeng; Su, Xin; Yang, Zhihua; Pan, Shilie; Yan, Qingfeng; Zhang, Fangfang
Cs6RE2(PO4)4(RE = Y and Gd): two new members of the alkali rare-earth double phosphates
New J. Chem., 2015, 39, 4328
7054755 CIFC16 H14 N2 O10 Zn2P 1 21/n 19.0342; 8.2698; 11.623
90; 100.9; 90		852.7Wang, Fengqin; Dong, Caifu; Wang, Chengmiao; Yu, Zongchao; Guo, Shukun; Wang, Zechuan; Zhao, Yongnan; Li, Guodong
Fluorescence detection of aromatic amines and photocatalytic degradation of rhodamine B under UV light irradiation by luminescent metal‒organic frameworks
New J. Chem., 2015, 39, 4437
7054756 CIFC8 H11 Cd N O7P -17.7683; 8.6089; 8.6695
84.04; 76.23; 66.04		514.6Wang, Fengqin; Dong, Caifu; Wang, Chengmiao; Yu, Zongchao; Guo, Shukun; Wang, Zechuan; Zhao, Yongnan; Li, Guodong
Fluorescence detection of aromatic amines and photocatalytic degradation of rhodamine B under UV light irradiation by luminescent metal‒organic frameworks
New J. Chem., 2015, 39, 4437
7054757 CIFC11 H5 Cl4 N3 O2P 1 21/n 17.4698; 9.5364; 18.73
90; 90.05; 90		1334.2Poorfreidoni, Alireza; Ranjbar-Karimi, Reza; Kia, Reza
Regiochemistry of nucleophilic substitution of pentachloropyridine with N and O bidentate nucleophiles
New J. Chem., 2015, 39, 4398
7054758 CIFC18 H30 B2 F8 Fe N6 S6C 1 2/c 122.662; 11.13; 18.004
90; 134.54; 90		3236.7Pilia, Luca; Espa, Davide; Concas, Giorgio; Congiu, Francesco; Marchiò, Luciano; Laura Mercuri, M.; Serpe, Angela; Deplano, Paola
Tuning the oxidation state and magnetic and coordination behaviour of iron and cobalt complexes by O/S variation in mono-thio and dithio-oxamide chelating ligands
New J. Chem., 2015, 39, 4716
7054759 CIFC12 H20 B Cl2 F4 Fe N4 O2 S2P 1 21/c 19.978; 12.495; 17.672
90; 97.174; 90		2186Pilia, Luca; Espa, Davide; Concas, Giorgio; Congiu, Francesco; Marchiò, Luciano; Laura Mercuri, M.; Serpe, Angela; Deplano, Paola
Tuning the oxidation state and magnetic and coordination behaviour of iron and cobalt complexes by O/S variation in mono-thio and dithio-oxamide chelating ligands
New J. Chem., 2015, 39, 4716
7054760 CIFC34 H30 Fe N6 O P S5C 1 c 19.59; 31.06; 12.91
90; 97.82; 90		3810Pilia, Luca; Espa, Davide; Concas, Giorgio; Congiu, Francesco; Marchiò, Luciano; Laura Mercuri, M.; Serpe, Angela; Deplano, Paola
Tuning the oxidation state and magnetic and coordination behaviour of iron and cobalt complexes by O/S variation in mono-thio and dithio-oxamide chelating ligands
New J. Chem., 2015, 39, 4716
7054761 CIFC18 H30 Fe I5.6 N6 S6P -18.487; 13.97; 16.988
73.85; 77.69; 76.69		1858.6Pilia, Luca; Espa, Davide; Concas, Giorgio; Congiu, Francesco; Marchiò, Luciano; Laura Mercuri, M.; Serpe, Angela; Deplano, Paola
Tuning the oxidation state and magnetic and coordination behaviour of iron and cobalt complexes by O/S variation in mono-thio and dithio-oxamide chelating ligands
New J. Chem., 2015, 39, 4716
7054762 CIFC36 H60 Co2 I14 N12 S12C 1 2/c 114.543; 42.417; 14.52
90; 115.476; 90		8086Pilia, Luca; Espa, Davide; Concas, Giorgio; Congiu, Francesco; Marchiò, Luciano; Laura Mercuri, M.; Serpe, Angela; Deplano, Paola
Tuning the oxidation state and magnetic and coordination behaviour of iron and cobalt complexes by O/S variation in mono-thio and dithio-oxamide chelating ligands
New J. Chem., 2015, 39, 4716

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