Crystallography Open Database

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Searching journal of publication like 'Chemical Communications' volume of publication is 48

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7107780 CIFC43 H58 B Br N2C 1 2/c 117.3321; 10.0841; 22.7728
90; 91.785; 90
3978.3Sarah Robinson; Jonathan McMaster; William Lewis; Alexander J. Blake; Stephen T. Liddle
Alkali-metal mediated reactivity of a diaminobromoborane: mono- and bis-borylation of naphthalene versus boryl lithium or hydroborane formation
Chem.Commun., 2012, 48, 5769
7107781 CIFC46 H57 B N2P 1 21/c 110.8044; 14.1728; 25.768
90; 98.594; 90
3901.51Sarah Robinson; Jonathan McMaster; William Lewis; Alexander J. Blake; Stephen T. Liddle
Alkali-metal mediated reactivity of a diaminobromoborane: mono- and bis-borylation of naphthalene versus boryl lithium or hydroborane formation
Chem.Commun., 2012, 48, 5769
7107782 CIFC82 H106 B2 N4P -18.9943; 15.0193; 15.0285
116.671; 90.773; 96.829
1796.17Sarah Robinson; Jonathan McMaster; William Lewis; Alexander J. Blake; Stephen T. Liddle
Alkali-metal mediated reactivity of a diaminobromoborane: mono- and bis-borylation of naphthalene versus boryl lithium or hydroborane formation
Chem.Commun., 2012, 48, 5769
7107783 CIFC44 H66 B Li N2 O2P 1 21/n 110.3828; 23.8027; 17.1319
90; 91.779; 90
4231.9Sarah Robinson; Jonathan McMaster; William Lewis; Alexander J. Blake; Stephen T. Liddle
Alkali-metal mediated reactivity of a diaminobromoborane: mono- and bis-borylation of naphthalene versus boryl lithium or hydroborane formation
Chem.Commun., 2012, 48, 5769
7107784 CIFC36 H51 B N2P n m a12.866; 14.546; 17.544
90; 90; 90
3283.3Sarah Robinson; Jonathan McMaster; William Lewis; Alexander J. Blake; Stephen T. Liddle
Alkali-metal mediated reactivity of a diaminobromoborane: mono- and bis-borylation of naphthalene versus boryl lithium or hydroborane formation
Chem.Commun., 2012, 48, 5769
7107785 CIFC10 H15 N SP -19.369; 10.7722; 11.8003
106.662; 102.457; 113.512
969.54Manohar Puppala; Annamalai Murali; Sundarababu Baskaran
Concise Synthesis of Bridged Azatricyclic Framework via Domino Semipinacol-Schmidt Reaction
Chem.Commun., 2012, 48, 5778-5780
7107786 CIFC18 H14 O4 P2P 1 21/n 112.0985; 7.6709; 18.3347
90; 100.317; 90
1674.07Amy J. Saunders; Ian R. Crossley; Martyn P. Coles; S. Mark Roe
Facile self-assembly of the first diphosphametacyclophane
Chem.Commun., 2012, 48, 5766
7107787 CIFC44 H44 Cl2 O10 P4 PtP -110.4564; 11.3437; 11.5627
87.512; 69.834; 64.064
1148.36Amy J. Saunders; Ian R. Crossley; Martyn P. Coles; S. Mark Roe
Facile self-assembly of the first diphosphametacyclophane
Chem.Commun., 2012, 48, 5766
7107788 CIFC80 H58 Br Fe N2 O4P 1 21 114.5514; 16.0909; 15.7159
90; 112.017; 90
3411.4Kenji Matsumoto; Hiromichi Egami; Takuya Oguma; Tsutomu Katsuki
What factors influence the catalytic activity of iron-salan complexes for aerobic oxidative coupling of 2-naphthols?
Chem.Commun., 2012, 48, 5823
7107789 CIFC136 H92 Fe2 N4 O5P 43 21 218.3252; 18.3252; 37.083
90; 90; 90
12453Kenji Matsumoto; Hiromichi Egami; Takuya Oguma; Tsutomu Katsuki
What factors influence the catalytic activity of iron-salan complexes for aerobic oxidative coupling of 2-naphthols?
Chem.Commun., 2012, 48, 5823
7107790 CIFC147 H234 Fe4 N8 O13P 21 21 2113.0266; 19.7736; 28.953
90; 90; 90
7457.8Kenji Matsumoto; Hiromichi Egami; Takuya Oguma; Tsutomu Katsuki
What factors influence the catalytic activity of iron-salan complexes for aerobic oxidative coupling of 2-naphthols?
Chem.Commun., 2012, 48, 5823
7107791 CIFC113 H92 Cl2 Fe2 N4 O8P 1 21 112.5225; 25.289; 15.7743
90; 95.27; 90
4974.3Kenji Matsumoto; Hiromichi Egami; Takuya Oguma; Tsutomu Katsuki
What factors influence the catalytic activity of iron-salan complexes for aerobic oxidative coupling of 2-naphthols?
Chem.Commun., 2012, 48, 5823
7107792 CIFC102 H92 Fe2 N4 O9C 1 2 126.435; 12.5897; 18.562
90; 125.357; 90
5038.2Kenji Matsumoto; Hiromichi Egami; Takuya Oguma; Tsutomu Katsuki
What factors influence the catalytic activity of iron-salan complexes for aerobic oxidative coupling of 2-naphthols?
Chem.Commun., 2012, 48, 5823
7107793 CIFC79 H62 Br Cl2 Fe N2 O5P 21 21 2114.237; 19.981; 22.218
90; 90; 90
6320.3Kenji Matsumoto; Hiromichi Egami; Takuya Oguma; Tsutomu Katsuki
What factors influence the catalytic activity of iron-salan complexes for aerobic oxidative coupling of 2-naphthols?
Chem.Commun., 2012, 48, 5823
7107794 CIFC111 H86.5 Br1.5 Fe2 N4 O6.5P 21 21 2113.6693; 25.349; 27.02
90; 90; 90
9362.5Kenji Matsumoto; Hiromichi Egami; Takuya Oguma; Tsutomu Katsuki
What factors influence the catalytic activity of iron-salan complexes for aerobic oxidative coupling of 2-naphthols?
Chem.Commun., 2012, 48, 5823
7107795 CIFC13 H13 Br N2 O5P 1 21 15.413; 17.675; 7.539
90; 96.083; 90
717.2Gaosheng; Yang; Yang Gaosheng; Chongrong Luo; Xiaolong Mu; Tingting Wang; Xin-Yuan Liu
Highly efficient enantioselective three-component synthesis of 2-amino-4H-chromenes catalysed by chiral tertiary amine-thioureas
Chem.Commun., 2012, 48, 5880
7107796 CIFC11 H8 Br N3 O3P 1 21 19.397; 5.142; 12.852
90; 109.634; 90
584.9Gaosheng; Yang; Yang Gaosheng; Chongrong Luo; Xiaolong Mu; Tingting Wang; Xin-Yuan Liu
Highly efficient enantioselective three-component synthesis of 2-amino-4H-chromenes catalysed by chiral tertiary amine-thioureas
Chem.Commun., 2012, 48, 5880
7107797 CIFC10 H6 N2 OP 1 21/c 111.833; 9.268; 7.28
90; 95.842; 90
794.2Gaosheng; Yang; Yang Gaosheng; Chongrong Luo; Xiaolong Mu; Tingting Wang; Xin-Yuan Liu
Highly efficient enantioselective three-component synthesis of 2-amino-4H-chromenes catalysed by chiral tertiary amine-thioureas
Chem.Commun., 2012, 48, 5880
7107798 CIFC54 H48 N2 O14 Zn2I 41/a :225.502; 25.502; 49.611
90; 90; 90
32265Lei Chen; Ke Tan; Ya-Qian Lan; Shun-Li Li; Kui-Zhan Shao; Zhong-Min Su
Unusual microporous polycatenane-like metal-organic frameworks for the luminescent sensing of Ln3+ cations and rapid adsorption of iodine
Chem.Commun., 2012, 48, 5919
7107799 CIFC39.63 H36.38 N1.19 O13.19 Zn2I 41/a :224.337; 24.337; 39.257
90; 90; 90
23252Lei Chen; Ke Tan; Ya-Qian Lan; Shun-Li Li; Kui-Zhan Shao; Zhong-Min Su
Unusual microporous polycatenane-like metal-organic frameworks for the luminescent sensing of Ln3+ cations and rapid adsorption of iodine
Chem.Commun., 2012, 48, 5919
7107800 CIFC42 H56 N12 O2P -110.711; 11.5603; 18.6159
76.538; 90.023; 62.401
1970.9Domasevitch, Konstantin V.; Solntsev, Pavlo V.; Krautscheid, Harald; Zhylenko, Iryna S.; Rusanov, Eduard B.; Chernega, Alexander N.
Facile access to a series of large polycondensed pyridazines and their utility for the supramolecular synthesis of coordination polymers
Chem.Commun., 2012, 48, 5847
7107801 CIFC30 H38 N6 OP 1 21/c 117.8207; 6.1397; 24.7531
90; 100.451; 90
2663.4Domasevitch, Konstantin V.; Solntsev, Pavlo V.; Krautscheid, Harald; Zhylenko, Iryna S.; Rusanov, Eduard B.; Chernega, Alexander N.
Facile access to a series of large polycondensed pyridazines and their utility for the supramolecular synthesis of coordination polymers
Chem.Commun., 2012, 48, 5847
7107802 CIFC20 H22 N4 O2P 1 21/c 15.0227; 13.5312; 12.4146
90; 94.498; 90
841.14Domasevitch, Konstantin V.; Solntsev, Pavlo V.; Krautscheid, Harald; Zhylenko, Iryna S.; Rusanov, Eduard B.; Chernega, Alexander N.
Facile access to a series of large polycondensed pyridazines and their utility for the supramolecular synthesis of coordination polymers
Chem.Commun., 2012, 48, 5847
7107803 CIFC23 H22 Cl3 Cu2 I2 N5I 41/a m d :222.3792; 22.3792; 13.1261
90; 90; 90
6573.93Domasevitch, Konstantin V.; Solntsev, Pavlo V.; Krautscheid, Harald; Zhylenko, Iryna S.; Rusanov, Eduard B.; Chernega, Alexander N.
Facile access to a series of large polycondensed pyridazines and their utility for the supramolecular synthesis of coordination polymers
Chem.Commun., 2012, 48, 5847
7107804 CIFC28 H30 Cl2 Cu2 N8P 43 21 215.9327; 15.9327; 12.4522
90; 90; 90
3161Domasevitch, Konstantin V.; Solntsev, Pavlo V.; Krautscheid, Harald; Zhylenko, Iryna S.; Rusanov, Eduard B.; Chernega, Alexander N.
Facile access to a series of large polycondensed pyridazines and their utility for the supramolecular synthesis of coordination polymers
Chem.Commun., 2012, 48, 5847
7107805 CIFC24 H14 O2P -15.986; 7.803; 17.433
85.512; 82.285; 85.93
802.9Kazuki Niimi; Hiroki Mori; Eigo Miyazaki; Itaru Osaka; Hayato Kakizoe; Kazuo Takimiya; Chihaya Adachi
[2,2']Bi[naphtho[2,3-b]furanyl]: a versatile organic semiconductor with a furan-furan junction
Chem.Commun., 2012, 48, 5892
7107806 CIFC23 H32 O3P 21 21 2111.061; 11.333; 16.323
90; 90; 90
2046.2Daniel Morton; Allison R. Dick; Debashis Ghosh; Huw M. L. Davies
Convenient method for the functionalization of the 4- and 6-positions of the androgen skeleton
Chem.Commun., 2012, 48, 5838
7107813 CIFC134 H329 Ag34 F6 N O45 S26 W6P -4 21 c37.905; 37.905; 35.309
90; 90; 90
50732Kun Zhou; Chao Qin; Hai-Bin Li; Li-Kai Yan; Xin-Long Wang; Guo-Gang Shan; Zhong-Min Su; Chuang Xu; Xiu-Li Wang
Assembly of a luminescent core-shell nanocluster featuring a Ag34S26 shell and a W6O21^6-^ polyoxoanion core
Chem.Commun., 2012, 48, 5844
7107814 CIFC93 H113 N7 O12P 1 21/c 128.663; 11.665; 28.056
90; 115.997; 90
8431David A. Leigh; Paul J. Lusby; Alexandra M. Z. Slawin; D. Barney Walker
Half-rotation in a kinetically locked [2]catenane induced by transition metal ion substitution
Chem.Commun., 2012, 48, 5826
7107815 CIFC97 H117 N9 O12 PdP -113.579; 17.669; 19.456
77.683; 74.61; 81.063
4372.8David A. Leigh; Paul J. Lusby; Alexandra M. Z. Slawin; D. Barney Walker
Half-rotation in a kinetically locked [2]catenane induced by transition metal ion substitution
Chem.Commun., 2012, 48, 5826
7107816 CIFC237 H246 Ce4 N44 O60F d d d :218.303; 46.917; 91.25
90; 90; 90
78358Yang Jiao; Jing Zhang; Lejie Zhang; Zhihua Lin; Cheng He; Chun-ying Duan
Metal-organic polyhedra containing 36 and 24 folds of amide groups for selective luminescent recognition of natural disaccharides
Chem.Commun., 2012, 48, 6022
7107817 CIFC377 H416 Ce8 N82 O111P -127.2839; 42.094; 46.93
67.993; 80.406; 89.908
49163Yang Jiao; Jing Zhang; Lejie Zhang; Zhihua Lin; Cheng He; Chun-ying Duan
Metal-organic polyhedra containing 36 and 24 folds of amide groups for selective luminescent recognition of natural disaccharides
Chem.Commun., 2012, 48, 6022
7107818 CIFAl H63 K14 Nb18 O85P 21 21 2118.582; 18.646; 24.646
90; 90; 90
8539Yu Hou; Todd Alam; Mark A. Rodriguez; May Nyman
Aqueous compatibility of group IIIA monomers and Nb-polyoxoanions
Chem.Commun., 2012, 48, 6004
7107819 CIFGa H62 K14 Na Nb18 O85P 21 21 2118.6023; 18.6225; 24.567
90; 90; 90
8510.5Yu Hou; Todd Alam; Mark A. Rodriguez; May Nyman
Aqueous compatibility of group IIIA monomers and Nb-polyoxoanions
Chem.Commun., 2012, 48, 6004
7107820 CIFGa H70 Nb18 O89 Rb15P -115.0863; 17.94; 19.1713
63.539; 82.135; 79.927
4563.3Yu Hou; Todd Alam; Mark A. Rodriguez; May Nyman
Aqueous compatibility of group IIIA monomers and Nb-polyoxoanions
Chem.Commun., 2012, 48, 6004
7107821 CIFCs13 Ga H24 Na2 Nb18 O66P 42/n c m :216.8515; 16.8515; 28.919
90; 90; 90
8212.2Yu Hou; Todd Alam; Mark A. Rodriguez; May Nyman
Aqueous compatibility of group IIIA monomers and Nb-polyoxoanions
Chem.Commun., 2012, 48, 6004
7107822 CIFC84.5 H136 B2 Cl6 O28 P2P 21 21 2116.0969; 22.4367; 27.7516
90; 90; 90
10022.8Matthieu Jouffroy; Rafael Gramage-Doria; Dominique Armspach; Dominique Matt; Loic Toupet
Regioselective opening of proximally sulfato-capped cyclodextrins
Chem.Commun., 2012, 48, 6028
7107823 CIFC68 H116 Cl N O32P 1 21 115.297; 15.7262; 16.671
90; 90.778; 90
4010.1Matthieu Jouffroy; Rafael Gramage-Doria; Dominique Armspach; Dominique Matt; Loic Toupet
Regioselective opening of proximally sulfato-capped cyclodextrins
Chem.Commun., 2012, 48, 6028
7107824 CIFC18 H26 N O5 P S Si2 WP -19.2854; 9.7913; 15.3748
72.585; 74.551; 77.633
1271.74Rainer Streubel; Jose Manuel Villalba Franco; Gregor Schnakenburg; Arturo Espinosa Ferao
The difference between the reactivity of a terminal phosphinidene and a Li/Cl phosphiniodenoid complex in cycloaddition chemistry ‒ in the importance of template-induced selectivity
Chem.Commun., 2012, 48, 5986
7107825 CIFC18 H26 N O5 P S Si2 WP -18.7938; 10.6257; 14.0699
107.332; 94.398; 96.224
1239.35Rainer Streubel; Jose Manuel Villalba Franco; Gregor Schnakenburg; Arturo Espinosa Ferao
The difference between the reactivity of a terminal phosphinidene and a Li/Cl phosphiniodenoid complex in cycloaddition chemistry ‒ in the importance of template-induced selectivity
Chem.Commun., 2012, 48, 5986
7107826 CIFC55 H37 Cl3 N2 O2P -110.887; 11.448; 17.595
102.152; 96.56; 104.691
2040.9Gang Li; Hieu M. Duong; Zhonghan Zhang; Jinchong Xiao; Lei Liu; Yanli Zhao; Hua Zhang; Fengwei Huo; Shuzhou Li; Jan Ma; Fred Wudl; Qichun Zhang
Approaching a stable, green twisted heteroacene through 'clean reaction' strategy
Chem.Commun., 2012, 48, 5974
7107827 CIFC32 H22 N4 O6 ZnP 64 2 216.5528; 16.5528; 25.5559
90; 90; 120
6064.1Feng Luo; Ming-Sheng Wang; Pei-Xin Li; Guo-Cong Guo; Ming-Biao Luo; Gong-Ming Sun; Yu-Mei Song
Functionalizing the pore wall of chiral porous metal-organic frameworks by distinct -H, -OH, -NH2, -NO2, -COOH shutters showing selective adsorption of CO2, tunable photoluminescence, and direct white-light emission
Chem.Commun., 2012, 48, 5989
7107828 CIFC32 H22 N4 O6 ZnP 62 2 216.5276; 16.5276; 25.3959
90; 90; 120
6007.8Feng Luo; Ming-Sheng Wang; Pei-Xin Li; Guo-Cong Guo; Ming-Biao Luo; Gong-Ming Sun; Yu-Mei Song
Functionalizing the pore wall of chiral porous metal-organic frameworks by distinct -H, -OH, -NH2, -NO2, -COOH shutters showing selective adsorption of CO2, tunable photoluminescence, and direct white-light emission
Chem.Commun., 2012, 48, 5989
7107829 CIFC32 H21 N4 O8 ZnP 64 2 216.5764; 16.5764; 25.3058
90; 90; 120
6021.87Feng Luo; Ming-Sheng Wang; Pei-Xin Li; Guo-Cong Guo; Ming-Biao Luo; Gong-Ming Sun; Yu-Mei Song
Functionalizing the pore wall of chiral porous metal-organic frameworks by distinct -H, -OH, -NH2, -NO2, -COOH shutters showing selective adsorption of CO2, tunable photoluminescence, and direct white-light emission
Chem.Commun., 2012, 48, 5989
7107830 CIFC32 H21 N4 O7 ZnP 62 2 216.5744; 16.5744; 25.2582
90; 90; 120
6009.1Feng Luo; Ming-Sheng Wang; Pei-Xin Li; Guo-Cong Guo; Ming-Biao Luo; Gong-Ming Sun; Yu-Mei Song
Functionalizing the pore wall of chiral porous metal-organic frameworks by distinct -H, -OH, -NH2, -NO2, -COOH shutters showing selective adsorption of CO2, tunable photoluminescence, and direct white-light emission
Chem.Commun., 2012, 48, 5989
7107831 CIFC32 H23 N5 O6 ZnP 64 2 216.5764; 16.5764; 25.2504
90; 90; 120
6008.7Feng Luo; Ming-Sheng Wang; Pei-Xin Li; Guo-Cong Guo; Ming-Biao Luo; Gong-Ming Sun; Yu-Mei Song
Functionalizing the pore wall of chiral porous metal-organic frameworks by distinct -H, -OH, -NH2, -NO2, -COOH shutters showing selective adsorption of CO2, tunable photoluminescence, and direct white-light emission
Chem.Commun., 2012, 48, 5989
7107832 CIFC32 H23 N5 O6 ZnP 62 2 216.5755; 16.5755; 25.117
90; 90; 120
5976.3Feng Luo; Ming-Sheng Wang; Pei-Xin Li; Guo-Cong Guo; Ming-Biao Luo; Gong-Ming Sun; Yu-Mei Song
Functionalizing the pore wall of chiral porous metal-organic frameworks by distinct -H, -OH, -NH2, -NO2, -COOH shutters showing selective adsorption of CO2, tunable photoluminescence, and direct white-light emission
Chem.Commun., 2012, 48, 5989
7107833 CIFC32 H21 N5 O8 ZnP 64 2 216.5597; 16.5597; 25.787
90; 90; 120
6124Feng Luo; Ming-Sheng Wang; Pei-Xin Li; Guo-Cong Guo; Ming-Biao Luo; Gong-Ming Sun; Yu-Mei Song
Functionalizing the pore wall of chiral porous metal-organic frameworks by distinct -H, -OH, -NH2, -NO2, -COOH shutters showing selective adsorption of CO2, tunable photoluminescence, and direct white-light emission
Chem.Commun., 2012, 48, 5989
7107834 CIFC32 H21 N5 O8 ZnP 62 2 216.5094; 16.5094; 25.701
90; 90; 120
6066.6Feng Luo; Ming-Sheng Wang; Pei-Xin Li; Guo-Cong Guo; Ming-Biao Luo; Gong-Ming Sun; Yu-Mei Song
Functionalizing the pore wall of chiral porous metal-organic frameworks by distinct -H, -OH, -NH2, -NO2, -COOH shutters showing selective adsorption of CO2, tunable photoluminescence, and direct white-light emission
Chem.Commun., 2012, 48, 5989
7107835 CIFC33 H21 N4 O8 ZnP 64 2 216.5097; 16.5097; 25.4661
90; 90; 120
6011.34Feng Luo; Ming-Sheng Wang; Pei-Xin Li; Guo-Cong Guo; Ming-Biao Luo; Gong-Ming Sun; Yu-Mei Song
Functionalizing the pore wall of chiral porous metal-organic frameworks by distinct -H, -OH, -NH2, -NO2, -COOH shutters showing selective adsorption of CO2, tunable photoluminescence, and direct white-light emission
Chem.Commun., 2012, 48, 5989

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