Crystallography Open Database

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7108141 CIFC27 H23 N O5P 1 21/c 17.0371; 18.781; 34.661
90; 90.2; 90
4580.9Yu-Ting Lee; Yeong-Jiunn Jang; Siang-en Syu; Shu-Chi Chou; Chia-Jui Lee; Wenwei Lin
Preparation of functional benzofurans and indoles via chemoselective intramolecular Wittig reactions
Chem.Commun., 2012, 48, 8135
7108142 CIFC36 H27 N O2P 1 21/n 110.6388; 17.7523; 14.6042
90; 103.685; 90
2679.89Yu-Ting Lee; Yeong-Jiunn Jang; Siang-en Syu; Shu-Chi Chou; Chia-Jui Lee; Wenwei Lin
Preparation of functional benzofurans and indoles via chemoselective intramolecular Wittig reactions
Chem.Commun., 2012, 48, 8135
7108143 CIFC37 H29 N O3P 1 21/c 114.8668; 11.2853; 18.3823
90; 109.591; 90
2905.58Yu-Ting Lee; Yeong-Jiunn Jang; Siang-en Syu; Shu-Chi Chou; Chia-Jui Lee; Wenwei Lin
Preparation of functional benzofurans and indoles via chemoselective intramolecular Wittig reactions
Chem.Commun., 2012, 48, 8135
7108144 CIFC36 H27 N O4 SP -19.443; 17.398; 19.97
66.139; 78.522; 76.82
2900Yu-Ting Lee; Yeong-Jiunn Jang; Siang-en Syu; Shu-Chi Chou; Chia-Jui Lee; Wenwei Lin
Preparation of functional benzofurans and indoles via chemoselective intramolecular Wittig reactions
Chem.Commun., 2012, 48, 8135
7108145 CIFC37 H26 Cl N O4P 1 21/n 114.182; 11.626; 17.884
90; 92.334; 90
2946Yu-Ting Lee; Yeong-Jiunn Jang; Siang-en Syu; Shu-Chi Chou; Chia-Jui Lee; Wenwei Lin
Preparation of functional benzofurans and indoles via chemoselective intramolecular Wittig reactions
Chem.Commun., 2012, 48, 8135
7108146 CIFC31 H31 N O4P -19.7424; 10.2579; 14.6034
109.778; 98.868; 98.878
1323.02Yu-Ting Lee; Yeong-Jiunn Jang; Siang-en Syu; Shu-Chi Chou; Chia-Jui Lee; Wenwei Lin
Preparation of functional benzofurans and indoles via chemoselective intramolecular Wittig reactions
Chem.Commun., 2012, 48, 8135
7108147 CIFC29 H18 Cl N O4 SP -18.1399; 12.4092; 12.5776
78.451; 87.408; 78.835
1221.15Yu-Ting Lee; Yeong-Jiunn Jang; Siang-en Syu; Shu-Chi Chou; Chia-Jui Lee; Wenwei Lin
Preparation of functional benzofurans and indoles via chemoselective intramolecular Wittig reactions
Chem.Commun., 2012, 48, 8135
7108150 CIFC34 H31 F8 I3 N2 O7P -19.3334; 11.853; 18.412
96.076; 96.664; 99.784
1977.2Javier Marti-Rujas; Luca Colombo; Jian Lu; Archan Dey; Giancarlo Terraneo; Pierangelo Metrangolo; Tullio Pilati; Giuseppe Resnati
Hydrogen and halogen bonding drive the orthogonal self-assembly of an organic framework possessing 2D channels
Chem.Commun., 2012, 48, 8207
7108151 CIFC36 H21 F8 I3 N4 O6P -19.004; 11.872; 19.283
94.51; 91.37; 107.65
1955.7Javier Marti-Rujas; Luca Colombo; Jian Lu; Archan Dey; Giancarlo Terraneo; Pierangelo Metrangolo; Tullio Pilati; Giuseppe Resnati
Hydrogen and halogen bonding drive the orthogonal self-assembly of an organic framework possessing 2D channels
Chem.Commun., 2012, 48, 8207
7108152 CIFC36 H19 Br4 F8 I3 N2 O2P -19.2497; 11.8502; 19.157
92.354; 94.75; 98.469
2066.76Javier Marti-Rujas; Luca Colombo; Jian Lu; Archan Dey; Giancarlo Terraneo; Pierangelo Metrangolo; Tullio Pilati; Giuseppe Resnati
Hydrogen and halogen bonding drive the orthogonal self-assembly of an organic framework possessing 2D channels
Chem.Commun., 2012, 48, 8207
7108153 CIFC24 H10 F8 I2 N2 O2P -19.3175; 10.3237; 13.5796
68.372; 74.546; 85.996
1169.78Javier Marti-Rujas; Luca Colombo; Jian Lu; Archan Dey; Giancarlo Terraneo; Pierangelo Metrangolo; Tullio Pilati; Giuseppe Resnati
Hydrogen and halogen bonding drive the orthogonal self-assembly of an organic framework possessing 2D channels
Chem.Commun., 2012, 48, 8207
7108154 CIFC36 H26 Cl2 Dy2 N6 O34 ZnC 1 2/c 117.3797; 16.6989; 21.4272
90; 107.578; 90
5928.3Peng-Fei Shi; Bin Zhao; Gang Xiong; Yin-Ling Hou; Peng Cheng
Fast capture and separation of, and luminescent probe for, pollutant chromate using a multi-functional cationic heterometal-organic framework
Chem.Commun., 2012, 48, 8231
7108155 CIFC70 H84 F12 N4 O20 P2P -111.139; 11.9736; 15.3398
110.014; 106.655; 94.675
1804.7Xuzhou Yan; Xiujuan Wu; Peifa Wei; Mingming Zhang; Feihe Huang
A chemical-responsive bis(m-phenylene)-32-crown-10/2,7-diazapyrenium salt [2]pseudorotaxane
Chem.Commun., 2012, 48, 8201
7108156 CIFC246 H388 K6 N12 Ni6 O18P 1 21/c 116.165; 21.255; 41.304
90; 95.56; 90
14125Bettina Horn; Christian Limberg; Christian Herwig; Michael Feist; Stefan Mebs
CO oxidation at nickel centres by N2O or O2 to yield a novel hexanuclear carbonate
Chem.Commun., 2012, 48, 8243
7108157 CIFC6 H14 Br Li N2 O4P 1 21/c 17.7723; 9.8812; 14.8483
90; 90.404; 90
1140.32Dario Braga; Fabrizia Grepioni; Lucia Maini; Davide Capucci; Saverio Nanna; Johan Wouters; Luc Aerts; Luc Quere
Combining piracetam and lithium salts: ionic co-crystals and co-drugs?
Chem.Commun., 2012, 48, 8219
7108158 CIFC6 H10 Cl Li N2 O2P 1 21/n 19.123; 12.1788; 8.1089
90; 101.855; 90
881.74Dario Braga; Fabrizia Grepioni; Lucia Maini; Davide Capucci; Saverio Nanna; Johan Wouters; Luc Aerts; Luc Quere
Combining piracetam and lithium salts: ionic co-crystals and co-drugs?
Chem.Commun., 2012, 48, 8219
7108159 CIFC6 H14 Cl Li N2 O4P 1 21/c 17.5347; 9.7992; 14.732
90; 91.596; 90
1087.3Dario Braga; Fabrizia Grepioni; Lucia Maini; Davide Capucci; Saverio Nanna; Johan Wouters; Luc Aerts; Luc Quere
Combining piracetam and lithium salts: ionic co-crystals and co-drugs?
Chem.Commun., 2012, 48, 8219
7108160 CIFC73 H80 F8 Si2P 19.5223; 10.2081; 18.3986
89.2381; 80.7371; 63.7452
1579.62Balaji Purushothaman; Sean R. Parkin; Mark J. Kendrick; Daniel David; Jeremy W. Ward; Liyang Yu; Natalie Stingelin; Oana D. Jurchescu; Oksana Ostroverkhova; John E. Anthony
Synthesis and charge transport studies of stable, soluble hexacenes
Chem.Commun., 2012, 48, 8261
7108161 CIFC18 H28 Mn2 N10 Nb O12P 21 21 210.4925; 11.4782; 12.3333
90; 90; 90
1485.36Dawid Pinkowicz; Michal Rams; Wojciech Nitek; Bernard Czarnecki; Barbara Sieklucka
Evidence for magnetic anisotropy of [Nb^IV^(CN)8]\4- in a pillared-layered Mn2Nb framework showing spin-flop transition
Chem.Commun., 2012, 48, 8323
7108162 CIFC18 H22 O8 Pd4C 1 2/c 130.142; 8.6063; 18.248
90; 90.703; 90
4733.4Kirill Monakhov; Christophe Gourlaouen; Pierre Braunstein
Stabilisation of a triply-bridging cyclopentadienyl ligand in a tetrapalladium cluster
Chem.Commun., 2012, 48, 8317
7108163 CIFC124 H134 Cu2 N4 O27 P4P -113.532; 15.708; 15.836
71.217; 70.92; 68.965
2888.2Jesus Ferrando-Soria; Maria Castellano; Rafael Ruiz-Garcia; Joan Cano; Miguel Julve; Francesc Lloret; Jorge Pasan; Catalina Ruiz-Perez; Laura Canadillas-Delgado; Yangling Li; Yves Journaux; Emilio Pardo
Redox switching of the antiferromagnetic coupling in permethylated dicopper(II) paracyclophanes
Chem.Commun., 2012, 48, 8401
7108164 CIFC56 H48 Ag6 F12 N16 O17 S4C 1 2/c 131.401; 10.116; 26.867
90; 119.53; 90
7426Cai-Yan Gao; Xin He; Liang Zhao; Mei-Xiang Wang
Dual templated synthesis of silver acetylide cluster-encapsulated supramolecular boxes
Chem.Commun., 2012, 48, 8368
7108165 CIFC59 H56 Ag5 B3 F12 N16 O2P -113.02; 15.085; 18.935
76.29; 84.39; 83.27
3578.7Cai-Yan Gao; Xin He; Liang Zhao; Mei-Xiang Wang
Dual templated synthesis of silver acetylide cluster-encapsulated supramolecular boxes
Chem.Commun., 2012, 48, 8368
7108166 CIFC102 Ge N9 O36 W10P b c a17.7471; 31.6276; 48.1971
90; 90; 90
27052.9Kosei Sugahara; Toshihiro Kimura; Keigo Kamata; Kazuya Yamaguchi; Noritaka Mizuno
A highly negatively charged Y-Keggin germanodecatungstate efficient for Knoevenagel condensation
Chem.Commun., 2012, 48, 8422-8424
7108167 CIFC16 Ge N4 O44 W10P 1 21/n 111.6252; 22.3313; 21.6699
90; 91.848; 90
5622.71Kosei Sugahara; Toshihiro Kimura; Keigo Kamata; Kazuya Yamaguchi; Noritaka Mizuno
A highly negatively charged Y-Keggin germanodecatungstate efficient for Knoevenagel condensation
Chem.Commun., 2012, 48, 8422-8424
7108168 CIFC29 H52 Cl6 P2 PtC 1 m 18.959; 17.604; 11.96
90; 110.056; 90
1771.9Emmanuel Nicolas; Xavier Le Goff; Stephane Bouchonnet; Nicolas Mezailles
Room Temperature Reversible CH Activation Mediated by a Pt(0) center, and Stoichiometric Biphenyl Formation via Solvent Activation
Chem.Commun., 2012, 48, 8350-8352
7108169 CIFC29 H54 Cl4 I2 P2 PtC 1 2/c 125.262; 9.278; 17.617
90; 117.018; 90
3678.5Emmanuel Nicolas; Xavier Le Goff; Stephane Bouchonnet; Nicolas Mezailles
Room Temperature Reversible CH Activation Mediated by a Pt(0) center, and Stoichiometric Biphenyl Formation via Solvent Activation
Chem.Commun., 2012, 48, 8350-8352
7108170 CIFC41 H66 P2 PtP 1 21/c 111.772; 13.486; 25.007
90; 104.899; 90
3836.6Emmanuel Nicolas; Xavier Le Goff; Stephane Bouchonnet; Nicolas Mezailles
Room Temperature Reversible CH Activation Mediated by a Pt(0) center, and Stoichiometric Biphenyl Formation via Solvent Activation
Chem.Commun., 2012, 48, 8350-8352
7108171 CIFC61 H110 P4 Pt2P -111.408; 17.246; 18.454
78.329; 72.921; 85.186
3397.7Emmanuel Nicolas; Xavier Le Goff; Stephane Bouchonnet; Nicolas Mezailles
Room Temperature Reversible CH Activation Mediated by a Pt(0) center, and Stoichiometric Biphenyl Formation via Solvent Activation
Chem.Commun., 2012, 48, 8350-8352
7108172 CIFC106 H124 Cl2 Li14 O4 S8 Si4P -113.929; 16.604; 24.31
98.031; 94.466; 96.054
5511.6Stefan Spirk; Ferdinand Belaj; Natascha Hurkes; Rudolf Pietschnig
A 32 vertex polyhedron via supramolecular assembly of silanedithiolate silanolate units
Chem.Commun., 2012, 48, 8398
7108173 CIFC116 H148 Cl2 Li14 O4 S8 Si4I -415.287; 15.287; 25.661
90; 90; 90
5997Stefan Spirk; Ferdinand Belaj; Natascha Hurkes; Rudolf Pietschnig
A 32 vertex polyhedron via supramolecular assembly of silanedithiolate silanolate units
Chem.Commun., 2012, 48, 8398
7108174 CIFC126 H130 Cl2 Li14 O4 S8 Si4P -114.445; 16.804; 27.691
102.661; 90.088; 110.203
6132.7Stefan Spirk; Ferdinand Belaj; Natascha Hurkes; Rudolf Pietschnig
A 32 vertex polyhedron via supramolecular assembly of silanedithiolate silanolate units
Chem.Commun., 2012, 48, 8398
7108175 CIFC108 H184 N18 O65 S12 Zr6F m -3 m49.964; 49.964; 49.964
90; 90; 90
124730Volodymyr Bon; Volodymyr Senkovskyy; Irena Senkovska; Stefan Kaskel
Zr(IV) and Hf(IV) Metal-Organic Frameworks with reo-topology
Chem.Commun., 2012, 48, 8407
7108176 CIFC108 H148 Hf6 N18 O47 S12F m -3 m49.84; 49.84; 49.84
90; 90; 90
123804Volodymyr Bon; Volodymyr Senkovskyy; Irena Senkovska; Stefan Kaskel
Zr(IV) and Hf(IV) Metal-Organic Frameworks with reo-topology
Chem.Commun., 2012, 48, 8407
7108177 CIFC129 H207 Gd5 N12 O34P 1 21/n 121.8094; 29.6604; 23.9915
90; 114.834; 90
14084.4Robyn Fairbairn; Ross McLellan; Ruaraidh McIntosh; Stephanie Taylor; Euan Brechin; Scott Dalgarno
Calixarene-supported rare-earth clusters: heteroatom bridge influences cluster composition
Chem.Commun., 2012, 48, 8493
7108178 CIFC53.5 H53.5 Fe2 P2P -114.0951; 17.492; 19.8743
107.86; 90.2326; 103.78
4513.86Takahiro Sasamori; Michiyasu Sakagami; Masatoshi Niwa; Heisuke Sakai; Yukio Furukawa; Norihiro Tokitoh
Synthesis of a stable 1,2-bis(ferrocenyl)diphosphene
Chem.Commun., 2012, 48, 8562
7108179 CIFC33 H39 N6 O3I b a 217.778; 26.576; 12.4884
90; 90; 90
5900.4Vladimir B. Arion; Anatolie Dobrov; Simone Goeschl; Michael A. Jakupec; Bernhard K. Keppler; Peter Rapta
Ruthenium(II)- and osmium(II)-arene-based paullones bearing a TEMPO free-radical unit as potential anticancer drugs
Chem.Commun., 2012, 48, 8559
7108181 CIFC44 H44 Cl2 O4P 18.4671; 8.9149; 13.1177
91.426; 100.286; 102.834
947.8L.R.Nassimbeni; Hong Su; Tanith-Lee Curtin
Enhanced enantioselectivity of 3-methylcyclohexanone by mixed diol host compounds
Chem.Commun., 2012, 48, 8526
7108182 CIFC44 H44 Cl2 O4P 18.5231; 8.7974; 13.1011
91.629; 99.871; 102.048
944.37L.R.Nassimbeni; Hong Su; Tanith-Lee Curtin
Enhanced enantioselectivity of 3-methylcyclohexanone by mixed diol host compounds
Chem.Commun., 2012, 48, 8526
7108183 CIFC44 H46 O4P 1 21/n 16.2924; 17.7601; 16.1586
90; 94.047; 90
1801.28L.R.Nassimbeni; Hong Su; Tanith-Lee Curtin
Enhanced enantioselectivity of 3-methylcyclohexanone by mixed diol host compounds
Chem.Commun., 2012, 48, 8526
7108184 CIFC58 H80 Cl N9 O9P -19.3945; 17.0675; 18.9451
109.827; 96.627; 93.298
2823.3and; Nicholas G. White; Paul D. Beer
A catenane host system containing integrated triazole C-H hydrogen bond donors for anion recognition
Chem.Commun., 2012, 48, 8499
7108185 CIFC72 H90 Cl N9 O16.5P -111.4693; 16.2473; 20.3444
97.255; 105.022; 99.338
3556.2and; Nicholas G. White; Paul D. Beer
A catenane host system containing integrated triazole C-H hydrogen bond donors for anion recognition
Chem.Commun., 2012, 48, 8499
7108186 CIFC19 H22 O4P -17.3712; 8.0916; 13.8262
94.596; 98.403; 90.318
813.06Xue-Song Xu; Zhen-Wu Li; Yi-Jun Zhang; Xiao-Shui Peng; Henry N. C. Wong
Total synthesis of (+/-)-pallambins C and D
Chem.Commun., 2012, 48, 8517
7108187 CIFC14 H24 O4P 3214.4194; 14.4194; 6.0541
90; 90; 120
1090.1Xue-Song Xu; Zhen-Wu Li; Yi-Jun Zhang; Xiao-Shui Peng; Henry N. C. Wong
Total synthesis of (+/-)-pallambins C and D
Chem.Commun., 2012, 48, 8517
7108188 CIFC18 H30 O5P -18.331; 8.783; 13.724
93.33; 106.838; 101.942
932.8Xue-Song Xu; Zhen-Wu Li; Yi-Jun Zhang; Xiao-Shui Peng; Henry N. C. Wong
Total synthesis of (+/-)-pallambins C and D
Chem.Commun., 2012, 48, 8517
7108189 CIFC18 H30 O8 SP 1 21/n 114.724; 6.79; 22.394
90; 108.516; 90
2123Xue-Song Xu; Zhen-Wu Li; Yi-Jun Zhang; Xiao-Shui Peng; Henry N. C. Wong
Total synthesis of (+/-)-pallambins C and D
Chem.Commun., 2012, 48, 8517
7108190 CIFC20 H36 O3 SiP 1 21 111.6292; 7.7435; 12.2967
90; 90.516; 90
1107.3Xue-Song Xu; Zhen-Wu Li; Yi-Jun Zhang; Xiao-Shui Peng; Henry N. C. Wong
Total synthesis of (+/-)-pallambins C and D
Chem.Commun., 2012, 48, 8517
7108191 CIFC16 H17 N SiP 1 21/m 19.2798; 6.9773; 10.569
90; 94.586; 90
682.13Yuichiro Tokoro; Hyeonuk Yeo; Kazuo Tanaka; Yoshiki Chujo
Synthesis of benzo[h]quinoline-based neutral pentacoordinate organosilicon complexes
Chem.Commun., 2012, 48, 8541
7108192 CIFC18 H13 N SiP -112.5359; 14.647; 16.586
90.159; 109.894; 98.672
2826.1Yuichiro Tokoro; Hyeonuk Yeo; Kazuo Tanaka; Yoshiki Chujo
Synthesis of benzo[h]quinoline-based neutral pentacoordinate organosilicon complexes
Chem.Commun., 2012, 48, 8541
7108193 CIFC13 H8 F3 N SiP 1 21/n 18.112; 14.615; 9.2149
90; 97.739; 90
1082.5Yuichiro Tokoro; Hyeonuk Yeo; Kazuo Tanaka; Yoshiki Chujo
Synthesis of benzo[h]quinoline-based neutral pentacoordinate organosilicon complexes
Chem.Commun., 2012, 48, 8541
7108194 CIFC30 H21 N SiP 1 21/n 113.1959; 19.4826; 35.67
90; 92.882; 90
9158.8Yuichiro Tokoro; Hyeonuk Yeo; Kazuo Tanaka; Yoshiki Chujo
Synthesis of benzo[h]quinoline-based neutral pentacoordinate organosilicon complexes
Chem.Commun., 2012, 48, 8541
7108195 CIFC34 H17 F12 N SiP n a 217.3912; 19.057; 21.384
90; 90; 90
3012Yuichiro Tokoro; Hyeonuk Yeo; Kazuo Tanaka; Yoshiki Chujo
Synthesis of benzo[h]quinoline-based neutral pentacoordinate organosilicon complexes
Chem.Commun., 2012, 48, 8541
7108196 CIFC30 H24 Cl3 N O3P -111.125; 11.134; 11.495
91.983; 103.98; 93.387
1377.5Danqing Zheng; Shaoyu Li; Jie Wu
Generation of 3-(1H-pyrrol-3-yl)-1H-inden-1-ones via a tandem reaction of 1-(2-alkynylphenyl)-2-enone, 2-isocyanoacetate, and water
Chem.Commun., 2012, 48, 8568
7108197 CIFC30 H78 Br6 N8 O12 S3P 21 317.789; 17.789; 17.789
90; 90; 90
5629.3Musabbir A. Saeed; Avijit Pramanik; Bryan M. Wong; Syed Ataul Haque; Douglas R. Powell; Dillip Kumar Chand; Md. Alamgir Hossain
Self-assembly of ordered water tetramers in an encapsulated [Br(H2O)12]^-^ complex
Chem.Commun., 2012, 48, 8631
7108198 CIFC120 H118 Ag2 Au6 B4 F16 N10 O P6 S2C 1 2/c 133.623; 17.0023; 23.3618
90; 105.93; 90
12842.3Li-Qin Mo; Jian-Hua Jia; Li-jia Sun; Quan-Ming Wang
Solvent-induced intercluster rearrangements and the reversible luminescence responses in sulfide bridged gold(I)-silver(I) clusters
Chem.Commun., 2012, 48, 8691
7108199 CIFC103 H85.5 Ag2 Au6 B4 F16 N6.5 P6 S2F d d 247.6833; 72.663; 13.6472
90; 90; 90
47285Li-Qin Mo; Jian-Hua Jia; Li-jia Sun; Quan-Ming Wang
Solvent-induced intercluster rearrangements and the reversible luminescence responses in sulfide bridged gold(I)-silver(I) clusters
Chem.Commun., 2012, 48, 8691
7108200 CIFC99 H86 Ag2 Au6 B4 F16 N12 O2 P6 S2P -114.5234; 14.6396; 28.6409
75.378; 89.089; 67.769
5432.7Li-Qin Mo; Jian-Hua Jia; Li-jia Sun; Quan-Ming Wang
Solvent-induced intercluster rearrangements and the reversible luminescence responses in sulfide bridged gold(I)-silver(I) clusters
Chem.Commun., 2012, 48, 8691
7108201 CIFC97 H88 Ag2 Au6 B4 F16 N12 O4 P6 S2P 1 2/c 113.4471; 22.4381; 18.2824
90; 104.442; 90
5342Li-Qin Mo; Jian-Hua Jia; Li-jia Sun; Quan-Ming Wang
Solvent-induced intercluster rearrangements and the reversible luminescence responses in sulfide bridged gold(I)-silver(I) clusters
Chem.Commun., 2012, 48, 8691
7108202 CIFC0 H33 Ge3.3 K6 N11 O0 Si4.7 ZnP -19.0694; 11.4274; 15.8894
77.468; 81.547; 87.07
1589.76Markus Waibel; Thomas Henneberger; Thomas F. Faessler
[(eta^2^-(Si/Ge)4)Zn(eta^2^-(Si/Ge)4)]^6-^ ‒ novel Zintl clusters with mixed Si/Ge tetrahedra bridged by a Zn atom
Chem.Commun., 2012, 48, 8676
7108203 CIFGe3.86 H33 K6 N11 Si4.14 ZnP 1 21 19.543; 12.2351; 13.8927
90; 103.145; 90
1579.6Markus Waibel; Thomas Henneberger; Thomas F. Faessler
[(eta^2^-(Si/Ge)4)Zn(eta^2^-(Si/Ge)4)]^6–^ ‒ novel Zintl clusters with mixed Si/Ge tetrahedra bridged by a Zn atom
Chem.Commun., 2012, 48, 8676
7108204 CIFC37 H30 F6 N P SP -19.6816; 17.8079; 20.1801
73.46; 76.508; 84.393
3241.4Na Zhao; Zhiyong Yang; Jacky W. Y. Lam; Herman H. Y. Sung; Ni Xie; Sijie Chen; Huimin Su; Meng Gao; Ian D. Williams; Kam Sing Wong; Ben Zhong Tang
Benzothiazolium-functionalized tetraphenylethene: an AIE luminogen with tunable solid-state emission
Chem.Commun., 2012, 48, 8637
7108205 CIFC43 H42 F6 N O1.5 P SP -19.7467; 17.3887; 23.849
72.962; 85.952; 83.053
3833.6Na Zhao; Zhiyong Yang; Jacky W. Y. Lam; Herman H. Y. Sung; Ni Xie; Sijie Chen; Huimin Su; Meng Gao; Ian D. Williams; Kam Sing Wong; Ben Zhong Tang
Benzothiazolium-functionalized tetraphenylethene: an AIE luminogen with tunable solid-state emission
Chem.Commun., 2012, 48, 8637
7108206 CIFC41 H38 F6 N O2 P SP -19.6552; 17.4019; 23.8103
72.469; 84.653; 82.064
3772.6Na Zhao; Zhiyong Yang; Jacky W. Y. Lam; Herman H. Y. Sung; Ni Xie; Sijie Chen; Huimin Su; Meng Gao; Ian D. Williams; Kam Sing Wong; Ben Zhong Tang
Benzothiazolium-functionalized tetraphenylethene: an AIE luminogen with tunable solid-state emission
Chem.Commun., 2012, 48, 8637
7108207 CIFC44 H41 Fe N2 P3P 1 21/n 114.8559; 14.3443; 18.85
90; 109.03; 90
3797.4Tufan K. Mukhopadhyay; Russell K. Feller; Francisca N. Rein; Neil J. Henson; Nathan C. Smythe; Ryan J. Trovitch; John C. Gordon
Investigation of formally zerovalent Triphos iron complexes
Chem.Commun., 2012, 48, 8670
7108208 CIFC75 H74 Cl2 Fe P6P -110.3077; 10.9001; 15.4955
71.483; 84.083; 77.596
1611.2Tufan K. Mukhopadhyay; Russell K. Feller; Francisca N. Rein; Neil J. Henson; Nathan C. Smythe; Ryan J. Trovitch; John C. Gordon
Investigation of formally zerovalent Triphos iron complexes
Chem.Commun., 2012, 48, 8670
7108209 CIFC102 H160 N6 O7 U2C 1 2/c 123.955; 20.947; 23.302
90; 117.653; 90
10357Anna-Corina Schmidt; Alexey V. Nizovtsev; Andreas Scheurer; Frank W. Heinemann; Karsten Meyer
Uranium-Mediated Reductive Conversion of CO2 to CO and Carbonate in a Single-Vessel, Closed Synthetic Cycle
Chem.Commun., 2012, 48, 8634
7108210 CIFC96 H138 N6 O7 U2P n n a16.3; 21.497; 25.42
90; 90; 90
8907Anna-Corina Schmidt; Alexey V. Nizovtsev; Andreas Scheurer; Frank W. Heinemann; Karsten Meyer
Uranium-Mediated Reductive Conversion of CO2 to CO and Carbonate in a Single-Vessel, Closed Synthetic Cycle
Chem.Commun., 2012, 48, 8634
7108211 CIFC106 H147 N6 O9 U2P 1 21/n 117.0385; 23.9304; 24.1626
90; 95.986; 90
9798.3Anna-Corina Schmidt; Alexey V. Nizovtsev; Andreas Scheurer; Frank W. Heinemann; Karsten Meyer
Uranium-Mediated Reductive Conversion of CO2 to CO and Carbonate in a Single-Vessel, Closed Synthetic Cycle
Chem.Commun., 2012, 48, 8634
7108212 CIFC292 H372 K4 N12 O24 U4P -118.9925; 20.0409; 21.895
71.285; 65.118; 63.811
6690Anna-Corina Schmidt; Alexey V. Nizovtsev; Andreas Scheurer; Frank W. Heinemann; Karsten Meyer
Uranium-Mediated Reductive Conversion of CO2 to CO and Carbonate in a Single-Vessel, Closed Synthetic Cycle
Chem.Commun., 2012, 48, 8634
7108213 CIFC48 H18 F8 N11 S8P 1 21/n 122.0041; 7.0211; 31.0684
90; 95.8755; 90
4774.6Sang Chul Lee; Akira Ueda; Hiromichi Kamo; Kazuyuki Takahashi; Mikio Uruichi; Kaoru Yamamoto; Kyuya Yakushi; Akiko Nakao; Reiji Kumai; Kensuke Kobayashi; Hironori Nakao; Youichi Murakami; Hatsumi Mori
Charge-order driven proton arrangement in a hydrogen-bonded charge-transfer complex based on a pyridyl-substituted TTF derivative
Chem.Commun., 2012, 48, 8673
7108214 CIFC11 H7 N S4P 21 21 213.971; 11.487; 25.411
90; 90; 90
1159.1Sang Chul Lee; Akira Ueda; Hiromichi Kamo; Kazuyuki Takahashi; Mikio Uruichi; Kaoru Yamamoto; Kyuya Yakushi; Akiko Nakao; Reiji Kumai; Kensuke Kobayashi; Hironori Nakao; Youichi Murakami; Hatsumi Mori
Charge-order driven proton arrangement in a hydrogen-bonded charge-transfer complex based on a pyridyl-substituted TTF derivative
Chem.Commun., 2012, 48, 8673
7108215 CIFC11 H8 B F4 N O S4P -16.801; 7.939; 14.424
90.83; 96.2; 92.08
773.6Sang Chul Lee; Akira Ueda; Hiromichi Kamo; Kazuyuki Takahashi; Mikio Uruichi; Kaoru Yamamoto; Kyuya Yakushi; Akiko Nakao; Reiji Kumai; Kensuke Kobayashi; Hironori Nakao; Youichi Murakami; Hatsumi Mori
Charge-order driven proton arrangement in a hydrogen-bonded charge-transfer complex based on a pyridyl-substituted TTF derivative
Chem.Commun., 2012, 48, 8673
7108216 CIFC27 H23 N3 O6P 21 21 2110.2839; 15.4819; 15.8271
90; 90; 90
2519.9Xiao-nan Zhang; Hong-Ping Deng; Long Huang; Yin Wei; Min Shi
Phosphine-catalyzed asymmetric [4+1] annulation of Morita-Baylis-Hillman carbonates with dicyano-2-methylenebut-3-enoates
Chem.Commun., 2012, 48, 8664
7108217 CIFC14 H10 Au2 F12 N2C 1 2/c 115.891; 10.75; 12.404
90; 106.369; 90
2033.1David Zopes; Corinna Hegemann; Wieland Tyrra; Sanjay Mathur
[(CF3)4Au2(C5H5N)2] ‒ a new alkyl gold(II) derivative with a very short Au-Au bond
Chem.Commun., 2012, 48, 8805
7108218 CIFC26 H28 Ca3 N2 O16C 1 2/c 116.552; 10.961; 18.691
90; 111.514; 90
3155Arijit Mallick; Tanay Kundu; Rahul Banerjee
Correlation between coordinated water content and proton conductivity in Ca-BTC-based metal-organic frameworks
Chem.Commun., 2012, 48, 8829
7108219 CIFC29 H9 Ca3 N3 O14.98C 1 2 116.2817; 13.5141; 15.7591
90; 93.254; 90
3461.92Arijit Mallick; Tanay Kundu; Rahul Banerjee
Correlation between coordinated water content and proton conductivity in Ca-BTC-based metal-organic frameworks
Chem.Commun., 2012, 48, 8829
7108220 CIFC24 H28 Ca3 O18 S4C 1 2/c 115.547; 13.6128; 18.981
90; 101.88; 90
3931.1Arijit Mallick; Tanay Kundu; Rahul Banerjee
Correlation between coordinated water content and proton conductivity in Ca-BTC-based metal-organic frameworks
Chem.Commun., 2012, 48, 8829
7108221 CIFC9 H6 Ca O7P -16.8656; 9.1287; 9.9209
101.341; 99.683; 111.95
545.11Arijit Mallick; Tanay Kundu; Rahul Banerjee
Correlation between coordinated water content and proton conductivity in Ca-BTC-based metal-organic frameworks
Chem.Commun., 2012, 48, 8829
7108222 CIFC18 H6 Ca3 O12R -3 :H8.9636; 8.9636; 19.2832
90; 90; 120
1341.76Arijit Mallick; Tanay Kundu; Rahul Banerjee
Correlation between coordinated water content and proton conductivity in Ca-BTC-based metal-organic frameworks
Chem.Commun., 2012, 48, 8829
7108223 CIFC180 Co6 N12 O44 Zn8F 4 3 241.5687; 41.5687; 41.5687
90; 90; 90
71828.9Teng Zhang; Feijie Song; Wenbin Lin
Blocking bimolecular activation pathways leads to different regioselectivity in metal-organic framework catalysis
Chem.Commun., 2012, 48, 8766
7108224 CIFC150 Co5 N10 O41 Zn4I 2 2 217.9269; 19.2699; 50.45
90; 90; 90
17427.9Teng Zhang; Feijie Song; Wenbin Lin
Blocking bimolecular activation pathways leads to different regioselectivity in metal-organic framework catalysis
Chem.Commun., 2012, 48, 8766
7108225 CIFC37.5 H44 Cl N5 O S SiP c c n30.13; 13.543; 19.002
90; 90; 90
7754Ting Wang; Qing-Jie Zhao; Hong-Gang Hu; Shi-Chong Yu; Xiang Liu; Li Liu; Qiu-Ye Wu
Spirolactonized Si-rhodamine: a novel NIR fluorophore utilized as a platform to construct Si-rhodamine-based probes
Chem.Commun., 2012, 48, 8781
7108226 CIFC54.5 H33 Cl N2P 21 21 2112.456; 16.127; 20.503
90; 90; 90
4119Remi Chauvin; Arnaud Rives; Iaroslav Baglai; Volodymyr Malytskyi; Valerie Maraval; Nathalie Saffon; Zoia Voitenko
Highly pi electron-rich macro-aromatics: bis(p-aminophenyl)-carbo-benzenes and their DBA acyclic references
Chem.Commun., 2012, 48, 8763
7108227 CIFC56 H64 N2 Si2P -17.4967; 7.7637; 21.2257
97.551; 93.735; 96.544
1212.66Remi Chauvin; Arnaud Rives; Iaroslav Baglai; Volodymyr Malytskyi; Valerie Maraval; Nathalie Saffon; Zoia Voitenko
Highly pi electron-rich macro-aromatics: bis(p-aminophenyl)-carbo-benzenes and their DBA acyclic references
Chem.Commun., 2012, 48, 8763
7108228 CIFC60 H72 N2 Si2P -19.2348; 9.3293; 15.6051
104.252; 91.728; 95.653
1294.7Remi Chauvin; Arnaud Rives; Iaroslav Baglai; Volodymyr Malytskyi; Valerie Maraval; Nathalie Saffon; Zoia Voitenko
Highly pi electron-rich macro-aromatics: bis(p-aminophenyl)-carbo-benzenes and their DBA acyclic references
Chem.Commun., 2012, 48, 8763
7108229 CIFC67 H75 I N6 S6R -3 c :H17.8042; 17.8042; 47.6257
90; 90; 120
13074.3Yih-Chern Horng; Pin-Shen Huang; Chang-Chih Hsieh; Chih-Hong Kuo; Ting-Shen Kuo
Selective encapsulation of volatile and reactive methyl iodide
Chem.Commun., 2012, 48, 8844
7108230 CIFC34 H41 Cl2 N3P -111.274; 11.548; 11.946
95.33; 93.62; 99.07
1524.4Yih-Chern Horng; Pin-Shen Huang; Chang-Chih Hsieh; Chih-Hong Kuo; Ting-Shen Kuo
Selective encapsulation of volatile and reactive methyl iodide
Chem.Commun., 2012, 48, 8844
7108231 CIFC36 H42 F9 N3 O9 S3P 1 21/m 19.8069; 20.416; 10.8597
90; 100.45; 90
2138.2Yih-Chern Horng; Pin-Shen Huang; Chang-Chih Hsieh; Chih-Hong Kuo; Ting-Shen Kuo
Selective encapsulation of volatile and reactive methyl iodide
Chem.Commun., 2012, 48, 8844
7108232 CIFC36 H48 I3 N3P -110.014; 10.358; 18.774
86.51; 88.14; 81.26
1921Yih-Chern Horng; Pin-Shen Huang; Chang-Chih Hsieh; Chih-Hong Kuo; Ting-Shen Kuo
Selective encapsulation of volatile and reactive methyl iodide
Chem.Commun., 2012, 48, 8844
7108233 CIFC17 H24 N2 O5 SP 43 21 29.2214; 9.2214; 46.482
90; 90; 90
3952.6Gowri Priya; Amol Kotmale; Rupesh Gawade; Deepti Mishra; Sourav Pal; Vedavati Puranik; Pattuparambil Rajamohanan; Gangadhar J.Sanjayan
Helical folding in heterogeneous foldamers without inter-residual backbone hydrogen-bonding
Chem.Commun., 2012, 48, 8922
7108234 CIFC15 H20 N2 O5 SP 21 21 217.894; 10.947; 19.78
90; 90; 90
1709.3Gowri Priya; Amol Kotmale; Rupesh Gawade; Deepti Mishra; Sourav Pal; Vedavati Puranik; Pattuparambil Rajamohanan; Gangadhar J.Sanjayan
Helical folding in heterogeneous foldamers without inter-residual backbone hydrogen-bonding
Chem.Commun., 2012, 48, 8922
7108235 CIFC27 H34 N4 O7 S2P 21 21 2111.077; 16.02; 17.325
90; 90; 90
3074.4Gowri Priya; Amol Kotmale; Rupesh Gawade; Deepti Mishra; Sourav Pal; Vedavati Puranik; Pattuparambil Rajamohanan; Gangadhar J.Sanjayan
Helical folding in heterogeneous foldamers without inter-residual backbone hydrogen-bonding
Chem.Commun., 2012, 48, 8922
7108236 CIFC26 H32 N4 O6 S2P 1 21 17.3385; 38.88; 9.7776
90; 94.613; 90
2780.7Gowri Priya; Amol Kotmale; Rupesh Gawade; Deepti Mishra; Sourav Pal; Vedavati Puranik; Pattuparambil Rajamohanan; Gangadhar J.Sanjayan
Helical folding in heterogeneous foldamers without inter-residual backbone hydrogen-bonding
Chem.Commun., 2012, 48, 8922
7108237 CIFC29 H39 N5 O5 S2P 21 21 219.3121; 17.991; 18.154
90; 90; 90
3041.4Gowri Priya; Amol Kotmale; Rupesh Gawade; Deepti Mishra; Sourav Pal; Vedavati Puranik; Pattuparambil Rajamohanan; Gangadhar J.Sanjayan
Helical folding in heterogeneous foldamers without inter-residual backbone hydrogen-bonding
Chem.Commun., 2012, 48, 8922
7108238 CIFC12 H11 Br O3P 1 21/c 113.2003; 11.6716; 7.281
90; 91.843; 90
1121.19Hikaru Yanai; Takeo Taguchi
Organic acid induced olefination reaction of lactones
Chem.Commun., 2012, 48, 8967
7108239 CIFC18 H22 O3 SiP 1 21/c 119.733; 12.199; 7.4044
90; 100.236; 90
1754Hikaru Yanai; Takeo Taguchi
Organic acid induced olefination reaction of lactones
Chem.Commun., 2012, 48, 8967
7108240 CIFC13 H19 N O4P 21 21 217.7341; 8.49; 20.9282
90; 90; 90
1374.2Wanfang Li; Weizheng Fan; Xin Ma; Xiaoming Tao; Xiaoming Li; Xiaomin Xie; Zhaoguo Zhang
Ru-catalyzed hydrogenation of 3,5-diketo amides: simultaneous control of chemo- and enantioselectivity
Chemical Communications, 2012, 48, 8976
7108241 CIFC21 H29 B F2 N2 O SP -18.8415; 11.6778; 11.996
104.113; 110.686; 103.033
1055.38Min Zhang; Yangchun Wu; Shengzhou Zhang; Hongnian Zhu; Qiong Wu; Lijuan Jiao; Erhong Hao
A nitroolefin functionalized BODIPY chemodosimeter for biothiols driven by an unexpected conjugated addition mechanism
Chem.Commun., 2012, 48, 8925
7108242 CIFC32 H19 N3 SP -16.8928; 9.1948; 20.413
96.347; 95.242; 100.897
1254.24Antoine Leliege; Charles-Henri Le Regent; Magali Allain; Philippe Blanchard; Jean Roncali
Structural modulation of internal charge transfer in small molecular donors for organic solar cells
Chem.Commun., 2012, 48, 8907-8909
7108243 CIFC80 H51.38 O15.19 P5P 1 21/n 120.628; 16.0821; 35.467
90; 93.754; 90
11740.6Anastasiya A. Yurkova; Ekaterina A. Khakina; Sergey I. Troyanov; Alexander Chernyak; Lyubov Shmygleva; Alexander S. Peregudov; Vyacheslav M. Martynenko; Yury A. Dobrovolskiy; Pavel A. Troshin
Arbuzov chemistry with chlorofullerene C60Cl6: a powerful method for selective synthesis of highly functionalized [60]fullerene derivatives
Chem.Commun., 2012, 48, 8916

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