Crystallography Open Database

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7119895 CIFC14 H22 N2 O6 ZnP 21 21 216.166; 15.763; 17.831
90; 90; 90		1733.1Karak, Suvendu; Kumar, Sushil; Bera, Saibal; Díaz, David Díaz; Banerjee, Subhrashis; Vanka, Kumar; Banerjee, Rahul
Interplaying anions in a supramolecular metallohydrogel to form metal organic frameworks.
Chemical communications (Cambridge, England), 2017, 53, 3705-3708
7119896 CIFC12 H17 N5 O2 ZnP 6117.764; 17.764; 10.4098
90; 90; 120		2844.8Karak, Suvendu; Kumar, Sushil; Bera, Saibal; Díaz, David Díaz; Banerjee, Subhrashis; Vanka, Kumar; Banerjee, Rahul
Interplaying anions in a supramolecular metallohydrogel to form metal organic frameworks.
Chemical communications (Cambridge, England), 2017, 53, 3705-3708
7119897 CIFC12 H19 Br N2 O3 ZnP 21 21 216.2078; 14.2553; 17.0701
90; 90; 90		1510.6Karak, Suvendu; Kumar, Sushil; Bera, Saibal; Díaz, David Díaz; Banerjee, Subhrashis; Vanka, Kumar; Banerjee, Rahul
Interplaying anions in a supramolecular metallohydrogel to form metal organic frameworks.
Chemical communications (Cambridge, England), 2017, 53, 3705-3708
7119898 CIFC12 H18 N2 O2P 1 21 17.7667; 5.8151; 13.6758
90; 102.312; 90		603.45Karak, Suvendu; Kumar, Sushil; Bera, Saibal; Díaz, David Díaz; Banerjee, Subhrashis; Vanka, Kumar; Banerjee, Rahul
Interplaying anions in a supramolecular metallohydrogel to form metal organic frameworks.
Chemical communications (Cambridge, England), 2017, 53, 3705-3708
7119899 CIFC12 H19 N3 O6 ZnP 1 21 16.1863; 16.8458; 15.5108
90; 96.948; 90		1604.56Karak, Suvendu; Kumar, Sushil; Bera, Saibal; Díaz, David Díaz; Banerjee, Subhrashis; Vanka, Kumar; Banerjee, Rahul
Interplaying anions in a supramolecular metallohydrogel to form metal organic frameworks.
Chemical communications (Cambridge, England), 2017, 53, 3705-3708
7119900 CIFC68.5 H112.5 Dy Li N4 O6P 1 21/c 117.9746; 15.7488; 26.9666
90; 107.71; 90		7271.9Long, Jérôme; Shestakov, Boris G.; Liu, Dan; Chibotaru, Liviu F.; Guari, Yannick; Cherkasov, Anton V.; Fukin, Georgy K.; Trifonov, Alexander A.; Larionova, Joulia
An organolanthanide(iii) single-molecule magnet with an axial crystal-field: influence of the Raman process over the slow relaxation.
Chemical communications (Cambridge, England), 2017, 53, 4706-4709
7119901 CIFC67 H109 Er Li N4 O6P 1 21/c 116.8819; 15.9384; 27.699
90; 103.719; 90		7240.4Long, Jérôme; Shestakov, Boris G.; Liu, Dan; Chibotaru, Liviu F.; Guari, Yannick; Cherkasov, Anton V.; Fukin, Georgy K.; Trifonov, Alexander A.; Larionova, Joulia
An organolanthanide(iii) single-molecule magnet with an axial crystal-field: influence of the Raman process over the slow relaxation.
Chemical communications (Cambridge, England), 2017, 53, 4706-4709
7119902 CIFC69 H114 Li N4 O7 TbP 1 21/c 118.126; 15.536; 26.498
90; 107.529; 90		7115Long, Jérôme; Shestakov, Boris G.; Liu, Dan; Chibotaru, Liviu F.; Guari, Yannick; Cherkasov, Anton V.; Fukin, Georgy K.; Trifonov, Alexander A.; Larionova, Joulia
An organolanthanide(iii) single-molecule magnet with an axial crystal-field: influence of the Raman process over the slow relaxation.
Chemical communications (Cambridge, England), 2017, 53, 4706-4709
7119903 CIFC65.89 H106.71 Dy Li N4 O6.94P 21 21 2116.1232; 17.3948; 24.3737
90; 90; 90		6835.84Long, Jérôme; Shestakov, Boris G.; Liu, Dan; Chibotaru, Liviu F.; Guari, Yannick; Cherkasov, Anton V.; Fukin, Georgy K.; Trifonov, Alexander A.; Larionova, Joulia
An organolanthanide(iii) single-molecule magnet with an axial crystal-field: influence of the Raman process over the slow relaxation.
Chemical communications (Cambridge, England), 2017, 53, 4706-4709
7119904 CIFC37 H27 Br N2 O2P 1 21 117.9007; 13.4705; 18.9244
90; 98.1603; 90		4517.1Zhu, Guodong; Wu, Shiqi; Bao, Xiaoze; Cui, Longchen; Zhang, Yanpeng; Qu, Jingping; Chen, Hongbo; Wang, Baomin
Asymmetric [3+2] cycloaddition of 3-amino oxindole-based azomethine ylides with α,β-ynones: a straightforward approach to spirooxindoles incorporating 2,5-dihydropyrroles and pyrroles.
Chemical communications (Cambridge, England), 2017, 53, 4714-4717
7119905 CIFC24 H18 Cl N O2 SP -19.5389; 10.7066; 11.237
66.541; 73.749; 85.725		1009.82Mao, Xi; Tong, Tao; Fan, Senbao; Fang, Liting; Wu, Jingyi; Wang, Xiaoxia; Kang, Honglan; Lv, Xin
One-pot synthesis of thiazino[2,3,4-hi]indole derivatives through a tandem oxidative coupling/heteroannulation process.
Chemical communications (Cambridge, England), 2017, 53, 4718-4721
7119906 CIFC26 H30 N2 O3 SP -18.774; 10.058; 14.512
96.541; 105.912; 108.607		1138.4Wani, Imtiyaz Ahmad; Sayyad, Masthanvali; Ghorai, Manas K.
Domino ring-opening cyclization (DROC) of activated aziridines and epoxides with nitrones via dual-catalysis "on water".
Chemical communications (Cambridge, England), 2017, 53, 4386-4389
7119907 CIFC16 H17 N O2P 1 21 15.4942; 18.284; 6.781
90; 103.824; 90		661.5Wani, Imtiyaz Ahmad; Sayyad, Masthanvali; Ghorai, Manas K.
Domino ring-opening cyclization (DROC) of activated aziridines and epoxides with nitrones via dual-catalysis "on water".
Chemical communications (Cambridge, England), 2017, 53, 4386-4389
7119908 CIFC23 H24 N2 O3 SP 1 21/n 19.9562; 12.5624; 16.3026
90; 92.165; 90		2037.6Wani, Imtiyaz Ahmad; Sayyad, Masthanvali; Ghorai, Manas K.
Domino ring-opening cyclization (DROC) of activated aziridines and epoxides with nitrones via dual-catalysis "on water".
Chemical communications (Cambridge, England), 2017, 53, 4386-4389
7119909 CIFC108.75 H87.75 Ag7 B7 F28 N38.25 O2.25P -325.3416; 25.3416; 16.5233
90; 90; 120		9189.6Li, Cheng-Peng; Zhou, Hang; Wang, Si; Yuan, Hong-Han; Zhang, Su-Zhen; Du, Miao
A nanoporous Ag(i) coordination polymer for selective adsorption of carcinogenic dye Acid Red 26.
Chemical communications (Cambridge, England), 2017, 53, 4767-4770
7119910 CIFC102 H72 Ag7 Cl7 N36 O28P -325.4554; 25.4554; 16.5591
90; 90; 120		9292.39Li, Cheng-Peng; Zhou, Hang; Wang, Si; Yuan, Hong-Han; Zhang, Su-Zhen; Du, Miao
A nanoporous Ag(i) coordination polymer for selective adsorption of carcinogenic dye Acid Red 26.
Chemical communications (Cambridge, England), 2017, 53, 4767-4770
7119911 CIFC27 H40 I N2 O3 PP 1 21/c 124.2819; 9.3561; 25.4208
90; 90.908; 90		5774.5Li, Shiwu; Gao, Meng; Wang, Shuxia; Hu, Rongrong; Zhao, Zujin; Qin, Anjun; Tang, Ben Zhong
Light up detection of heparin based on aggregation-induced emission and synergistic counter ion displacement.
Chemical communications (Cambridge, England), 2017, 53, 4795-4798
7119912 CIFC42 H36 I19 K5 N6 O16 Pb6 Zn2P -112.038; 12.491; 16.889
93.07; 103.47; 90.98		2465Liu, Jian-Jun; Guan, Ying-Fang; Li, Ling; Chen, Yong; Dai, Wen-Xin; Huang, Chang-Cang; Lin, Mei-Jin
Construction of a bicontinuous donor-acceptor hybrid material at the molecular level by inserting inorganic nanowires into porous MOFs.
Chemical communications (Cambridge, England), 2017, 53, 4481-4484
7119913 CIFC14 H12 I N2 O4 Zn0.5P 1 2/n 118.7223; 5.7758; 20.8283
90; 91.165; 90		2251.8Liu, Jian-Jun; Guan, Ying-Fang; Li, Ling; Chen, Yong; Dai, Wen-Xin; Huang, Chang-Cang; Lin, Mei-Jin
Construction of a bicontinuous donor-acceptor hybrid material at the molecular level by inserting inorganic nanowires into porous MOFs.
Chemical communications (Cambridge, England), 2017, 53, 4481-4484
7119927 CIFC32 H31 F3 N2 O2P 1 21 18.7183; 18.007; 9.5051
90; 106.811; 90		1428.4Tinsley, Ian C.; Spaniol, Jacqueline M.; Wheeler, Kraig A.
Mapping the structural boundaries of quasiracemate fractional crystallization using 2-substituted diarylamides.
Chemical communications (Cambridge, England), 2017, 53, 4601-4604
7119928 CIFC30 H28 Br N3 O4P 1 21 18.2953; 9.5761; 17.2423
90; 101.342; 90		1342.92Tinsley, Ian C.; Spaniol, Jacqueline M.; Wheeler, Kraig A.
Mapping the structural boundaries of quasiracemate fractional crystallization using 2-substituted diarylamides.
Chemical communications (Cambridge, England), 2017, 53, 4601-4604
7119929 CIFC16 H17 N O2P 21 21 215.8757; 14.464; 15.887
90; 90; 90		1350.2Tinsley, Ian C.; Spaniol, Jacqueline M.; Wheeler, Kraig A.
Mapping the structural boundaries of quasiracemate fractional crystallization using 2-substituted diarylamides.
Chemical communications (Cambridge, England), 2017, 53, 4601-4604
7119930 CIFC31 H28 F3 I N2 O2P 21 21 219.4943; 16.1705; 18.3454
90; 90; 90		2816.52Tinsley, Ian C.; Spaniol, Jacqueline M.; Wheeler, Kraig A.
Mapping the structural boundaries of quasiracemate fractional crystallization using 2-substituted diarylamides.
Chemical communications (Cambridge, England), 2017, 53, 4601-4604
7119931 CIFC30 H29 F N2 O2P 15.354; 8.3824; 13.8585
96.477; 93.829; 105.841		591.42Tinsley, Ian C.; Spaniol, Jacqueline M.; Wheeler, Kraig A.
Mapping the structural boundaries of quasiracemate fractional crystallization using 2-substituted diarylamides.
Chemical communications (Cambridge, England), 2017, 53, 4601-4604
7119932 CIFC31 H28 F3 N3 O4P 1 21 18.3035; 9.6853; 17.333
90; 101.057; 90		1368.1Tinsley, Ian C.; Spaniol, Jacqueline M.; Wheeler, Kraig A.
Mapping the structural boundaries of quasiracemate fractional crystallization using 2-substituted diarylamides.
Chemical communications (Cambridge, England), 2017, 53, 4601-4604
7119933 CIFC42 H40 Eu F6 N16 O12 S2P -111.2812; 14.038; 18.1066
89.495; 82.741; 73.516		2726.47Edwards, Alyn C.; Mocilac, Pavle; Geist, Andreas; Harwood, Laurence M.; Sharrad, Clint A.; Burton, Neil A.; Whitehead, Roger C.; Denecke, Melissa A.
Hydrophilic 2,9-bis-triazolyl-1,10-phenanthroline ligands enable selective Am(iii) separation: a step further towards sustainable nuclear energy.
Chemical communications (Cambridge, England), 2017, 53, 5001-5004
7119934 CIFC46 H62 O6 S2P 1 21/c 114.9364; 7.6637; 18.4671
90; 97.593; 90		2095.36Khambhati, D. P.; Sachinthani, K. A. N.; Rheingold, A. L.; Nelson, T. L.
Regioselective copper-catalyzed direct arylation of benzodithiophene-S,S-tetraoxide.
Chemical communications (Cambridge, England), 2017, 53, 5107-5109
7119938 CIFC29 H34 F2 N6 O6P 21 21 215.1466; 22.4076; 25.6853
90; 90; 90		2962.1Mamone, M.; Gonçalves, R S B; Blanchard, F.; Bernadat, G.; Ongeri, S.; Milcent, T.; Crousse, B.
N-Difluoromethyl-triazole as a constrained scaffold in peptidomimetics.
Chemical communications (Cambridge, England), 2017, 53, 5024-5027
7119939 CIFC56 H46 F10 N6 O2 UP b c n14.8944; 9.8978; 32.5727
90; 90; 90		4801.9Brewster, James T.; He, Qing; Anguera, Gonzalo; Moore, Matthew D.; Ke, Xian-Sheng; Lynch, Vincent M.; Sessler, Jonathan L.
Synthesis and characterization of a dipyriamethyrin-uranyl complex.
Chemical communications (Cambridge, England), 2017, 53, 4981-4984
7119940 CIFC58 H52 Cl4 F10 N6P -18.5433; 18.7105; 19.0289
68.396; 82.032; 77.23		2752.6Brewster, James T.; He, Qing; Anguera, Gonzalo; Moore, Matthew D.; Ke, Xian-Sheng; Lynch, Vincent M.; Sessler, Jonathan L.
Synthesis and characterization of a dipyriamethyrin-uranyl complex.
Chemical communications (Cambridge, England), 2017, 53, 4981-4984
7119945 CIFC44 H32 Br2 N2 O4 S2P -18.5964; 9.7097; 11.6415
94.704; 111.769; 91.394		897.79Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119946 CIFC44 H32 Br2 N2 O4 S2P -18.6797; 9.6861; 11.3175
93.296; 109.136; 92.301		895.67Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119947 CIFC44 H32 Br2 N2 O4 S2P -18.5964; 9.7099; 11.6456
94.705; 111.845; 91.391		897.64Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119948 CIFC44 H32 Br2 N2 O4 S2P -18.5989; 9.7109; 11.6303
94.667; 111.698; 91.429		897.77Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119949 CIFC44 H32 Br2 N2 O4 S2P -18.616; 9.6963; 11.5069
94.172; 110.426; 91.735		896.9Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119950 CIFC44 H32 Br2 N2 O4 S2P -111.5732; 12.7765; 13.1918
97.696; 108.46; 99.643		1787.27Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119951 CIFC44 H32 Br2 N2 O4 S2P -18.6501; 9.691; 11.4533
93.968; 109.971; 91.879		898.58Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119952 CIFC30 H23 Br N2 O4 S2P 1 21/n 19.6864; 8.4793; 31.9276
90; 96.433; 90		2605.8Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119953 CIFC44 H32 Br2 N2 O4 S2P -18.5906; 9.7077; 11.6448
94.709; 111.858; 91.399		896.67Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119954 CIFC44 H32 Br2 N2 O4 S2P -18.5997; 9.7097; 11.6134
94.602; 111.523; 91.472		897.61Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119955 CIFC44 H32 Br2 N2 O4 S2P -18.6159; 9.7052; 11.5522
94.355; 110.91; 91.578		898.21Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119956 CIFC44 H32 Br2 N2 O4 S2P -18.612; 9.7121; 11.5828
94.47; 111.179; 91.55		899.02Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119957 CIFC44 H32 Br2 N2 O4 S2P -18.5966; 9.7095; 11.6614
94.75; 111.998; 91.366		897.81Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119958 CIFC44 H32 Br2 N2 O4 S2P -111.5487; 12.7694; 13.171
97.689; 108.313; 99.485		1782.67Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119959 CIFC44 H32 Br2 N2 O4 S2P -18.5953; 9.7096; 11.6335
94.661; 111.729; 91.425		897.34Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119960 CIFC44 H32 Br2 N2 O4 S2P -18.5791; 9.7036; 11.6537
94.725; 111.977; 91.443		894.95Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119961 CIFC44 H32 Br2 N2 O4 S2P -18.595; 9.707; 11.6561
94.748; 111.956; 91.375		897.27Khorasani, S.; Fernandes, M. A.
A synthetic co-crystal prepared by cooperative single-crystal-to-single-crystal solid-state Diels-Alder reaction.
Chemical communications (Cambridge, England), 2017, 53, 4969-4972
7119962 CIFC21 H17 Br N2 O4P 1 21 112.61; 5.974; 12.888
90; 106.487; 90		931Rout, Subhrajit; Das, Arko; Singh, Vinod K.
An asymmetric vinylogous Mukaiyama-Michael reaction of α,β-unsaturated 2-acyl imidazoles catalyzed by chiral Sc(iii)- or Er(iii)-pybox complexes.
Chemical communications (Cambridge, England), 2017, 53, 5143-5146
7119963 CIFC16 H16 N2 O3 SP 21 21 217.683; 10.196; 19.34
90; 90; 90		1515Rout, Subhrajit; Das, Arko; Singh, Vinod K.
An asymmetric vinylogous Mukaiyama-Michael reaction of α,β-unsaturated 2-acyl imidazoles catalyzed by chiral Sc(iii)- or Er(iii)-pybox complexes.
Chemical communications (Cambridge, England), 2017, 53, 5143-5146
7119964 CIFC18 H17 Cl N2 O3P 21 21 2110.8555; 12.1442; 12.5528
90; 90; 90		1654.85Rout, Subhrajit; Das, Arko; Singh, Vinod K.
An asymmetric vinylogous Mukaiyama-Michael reaction of α,β-unsaturated 2-acyl imidazoles catalyzed by chiral Sc(iii)- or Er(iii)-pybox complexes.
Chemical communications (Cambridge, England), 2017, 53, 5143-5146

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