Crystallography Open Database

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7117151 CIFC51 H50 N2 O2 S6C 1 2/c 137.215; 14.101; 9.619
90; 96.595; 90
5014.3Minh T. Nguyen; Bradley J. Holliday
Direct insights into metal-induced conductivity enhancement in conducting metallopolymers
Chem.Commun., 2015, 51, 8610
7117152 CIFC18.86 H19 Ag I0.14 N3.86P 1 21/n 19.6546; 10.6457; 17.115
90; 90.385; 90
1759.04Rachael Heath; Helge Muller-Bunz; Martin Albrecht
Silver(I) NHC mediated C-C bond activation of alkyl nitriles and catalytic efficiency in oxazoline synthesis
Chem.Commun., 2015, 51, 8699
7117153 CIFC19 H19 Ag N4P 1 21/n 19.59019; 10.57651; 17.1999
90; 90.1567; 90
1744.59Rachael Heath; Helge Muller-Bunz; Martin Albrecht
Silver(I) NHC mediated C-C bond activation of alkyl nitriles and catalytic efficiency in oxazoline synthesis
Chem.Commun., 2015, 51, 8699
7117154 CIFC20 H16 Cl F3 N2 O2P 1 21 110.4449; 7.9864; 11.2224
90; 93.069; 90
934.8Mingxia Ma; Yuanyuan Zhu; Quantao Sun; Xiaoyuan Li; Jinhuan Su; Long Zhao; Yanyan Zhao; Shuai Qiu; Wenjin Yan; Kairong Wang; Rui Wang
The asymmetric synthesis of CF3-containing spiro[pyrrolidin-3,2'-oxindole] through the organocatalytic 1,3-dipolar cycloaddition reaction
Chem.Commun., 2015, 51, 8789
7117155 CIFC11 H8 Br F3 N2 OP 1 21/n 16.8291; 12.139; 14.882
90; 101.467; 90
1209.1Mingxia Ma; Yuanyuan Zhu; Quantao Sun; Xiaoyuan Li; Jinhuan Su; Long Zhao; Yanyan Zhao; Shuai Qiu; Wenjin Yan; Kairong Wang; Rui Wang
The asymmetric synthesis of CF3-containing spiro[pyrrolidin-3,2'-oxindole] through the organocatalytic 1,3-dipolar cycloaddition reaction
Chem.Commun., 2015, 51, 8789
7117156 CIFC15 H11 N O SP 1 21/c 116.112; 7.8274; 9.593
90; 101.081; 90
1187.27Bhaskar Garg; Yong-Chien Ling
A highly selective phenothiazine-based fluorescence 'turn-on' indicator based on cyanide-promoted novel protection/deprotection mechanism
Chem.Commun., 2015, 51, 8809
7117157 CIFC29 H23 Br O2P -19.845; 10.37; 12.763
89.509; 70.585; 71.497
1158.5Ya-Jing Chen; Tian-Jiao Hu; Chen-Guo Feng; Guo-Qiang Lin
Synthesis of chiral cyclobutanes via rhodium/diene-catalyzed asymmetric 1,4-addition: a dramatic ligand effect on the diastereoselectivity
Chem.Commun., 2015, 51, 8773
7117158 CIFC15 H4 F4 I NP -17.4665; 9.3784; 10.5061
85.468; 75.25; 67.203
655.7Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117159 CIFC15 H8 I NF d d 218.421; 7.6185; 17.387
90; 90; 90
2440.1Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117160 CIFC15 H4 Br F4 NP 1 21/c 113.2997; 9.7019; 19.917
90; 102.415; 90
2509.8Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117161 CIFC15 H6 Br F2 NP -15.7972; 8.6736; 12.715
73.612; 85.418; 86.061
610.7Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117162 CIFC15 H8 Br NF d d 217.893; 7.5409; 17.168
90; 90; 90
2316.5Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117163 CIFC15 H9 NP -19.404; 9.48; 13.047
94.412; 102.356; 103.038
1097.3Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117164 CIFC16 H12 F2 N O4P 1 21/c 122.639; 5.0207; 11.438
90; 93.54; 90
1297.6Rui Guo; Haodong Yang; Pingping Tang
Silver-catalyzed Meerwein arylation: intermolecular and intramolecular fluoroarylation of styrenes
Chem.Commun., 2015, 51, 8829
7117166 CIFC10 H16 N4 O4 SC 1 2/c 19.642; 15.986; 9.334
90; 92.708; 90
1437Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117167 CIFC14 H14 N4 O4 SF d d 214.6766; 18.8388; 11.8862
90; 90; 90
3286.4Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117168 CIFC16 H18 N4 O4 SC 1 2/c 117.398; 7.4436; 14.051
90; 105.38; 90
1754.5Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117169 CIFC28 H28 N4 O5 SP b c n16.62; 8.218; 19.159
90; 90; 90
2616.8Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117170 CIFC28 H30 N4 O6 SP b c n16.933; 8.0337; 19.688
90; 90; 90
2678.3Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117171 CIFC14 H14 N4 O4 SeP 43 21 218.5107; 18.5107; 18.953
90; 90; 90
6494.2Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117172 CIFC17 H23 N4 O5.5 SeC 1 2/c 125.917; 8.7717; 17.5915
90; 100.377; 90
3933.8Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117173 CIFC26 H22 N4 O4 SeP -19.611; 10.852; 11.918
83.339; 72.175; 88.808
1175.2Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117174 CIFC28 H30 N4 O6 SeP b c n17.3442; 8.0712; 19.5768
90; 90; 90
2740.5Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117175 CIFC30 H24 O2C 1 2/c 131.067; 13.835; 15.67
90; 93.254; 90
6724Suman Kalyan Samanta; Eduard Preis; Christian W. Lehmann; Richard Goddard; Saientan Bag; Prabal K. Maiti; Gunther Brunklaus; Ullrich Scherf
One-step synthesis of a cyclic 2,17-dioxo[3,3](4,4') biphenylophane and first preparation of a microporous polymer network from a macrocyclic precursor by cyclotrimerization
Chem.Commun., 2015, 51, 9046
7117176 CIFC18 H11 F3 O SP 1 21 15.593; 8.107; 17.57
90; 95.029; 90
793.6Amparo Sanz-Marco; Gonzalo Blay; M. Carmen Munoz; Jose R. Pedro
Highly enantioselective copper(I)-catalyzed conjugate addition of 1,3-diynes to alpha,beta-unsaturated trifluoromethyl ketones
Chem.Commun., 2015, 51, 8958
7117177 CIFC29 H31 N3 O6P 1 21/c 119.2486; 10.9164; 12.4114
90; 93.117; 90
2604.09Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117178 CIFC116 H132 B4 F16 N12 O28 Pd2P -114.8562; 16.5839; 16.9982
117.401; 93.11; 114.691
3216.5Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117179 CIFC58 H62 Cl4 N6 O12 Pd2C 1 2/m 113.8958; 21.0537; 11.1192
90; 101.982; 90
3182.1Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117180 CIFC126 H150 N16 O38 Pd2 S4P 1 21/n 113.099; 17.179; 32.25
90; 91.566; 90
7254.4Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117181 CIFC24 H44 Cu7 I8 N8R -3 :H25.9051; 25.9051; 20.4603
90; 90; 120
11890.9Yao Kang; Wei-Hui Fang; Lei Zhang; Jian Zhang
A structure-directing method to prepare semiconductive zeolitic cluster-organic frameworks with Cu3I4 building units
Chem.Commun., 2015, 51, 8994
7117182 CIFC15 H29 Cu4 I4 N4I 4 2 218.5097; 18.5097; 36.1113
90; 90; 90
12372.1Yao Kang; Wei-Hui Fang; Lei Zhang; Jian Zhang
A structure-directing method to prepare semiconductive zeolitic cluster-organic frameworks with Cu3I4 building units
Chem.Commun., 2015, 51, 8994
7117183 CIFC26 H16 N2 O8 S UP 21 21 218.435; 12.595; 22.468
90; 90; 90
2387Shu-wen An; Lei Mei; Cong-zhi Wang; Chuan-qin Xia; Zhi-fang Chai; Wei-qun Shi
The first case of actinide triple helices: pH-dependent structural evolution and kinetically-controlled transformation of two supramolecular conformational isomers
Chem.Commun., 2015, 51, 8978
7117184 CIFC26 H18 N2 O9 S UP 1 21/c 114.395; 8.675; 20.368
90; 95.16; 90
2533.2Shu-wen An; Lei Mei; Cong-zhi Wang; Chuan-qin Xia; Zhi-fang Chai; Wei-qun Shi
The first case of actinide triple helices: pH-dependent structural evolution and kinetically-controlled transformation of two supramolecular conformational isomers
Chem.Commun., 2015, 51, 8978
7117185 CIFC11 H9 F3 N2 O3P -15.736; 7.686; 15.026
102.598; 92.769; 110.155
601.4Ai-Jie Cai; Yan Zheng; Jun-An Ma
Copper-triggered three-component reaction of CF3CHN2, nitriles, and aldehydes: highly diastereoselective synthesis of CF3-substituted oxazolines and vicinal amino alcohols
Chem.Commun., 2015, 51, 8946
7117186 CIFC11 H9 Cl F3 N O2P 1 21/c 17.764; 22.824; 7.398
90; 112.915; 90
1207.5Ai-Jie Cai; Yan Zheng; Jun-An Ma
Copper-triggered three-component reaction of CF3CHN2, nitriles, and aldehydes: highly diastereoselective synthesis of CF3-substituted oxazolines and vicinal amino alcohols
Chem.Commun., 2015, 51, 8946
7117188 CIFC46 H43 Cl3 S6P b c a9.4165; 19.7949; 45.588
90; 90; 90
8497.5Shu-Wei Chang; Masaki Horie
A donor-acceptor conjugated block copolymer of poly(arylenevinylene)s by ring-opening metathesis polymerization
Chem.Commun., 2015, 51, 9113
7117189 CIFC16 H17.13 Cu2 O19.5 S2P -17.6226; 8.0332; 19.2709
89.772; 88.902; 76.322
1146.36Xiao-Qin Wu; Jian-Gong Ma; Han Li; Di-Ming Chen; Wen Gu; Guang-Ming Yang; Peng Cheng
Metal-organic framework biosensor with high stability and selectivity in a bio-mimic environment
Chem.Commun., 2015, 51, 9161
7117190 CIFC17 H21 F4 N O4 SP 21 21 217.7459; 9.8069; 25.602
90; 90; 90
1944.8Chen Xie; Yanling Dai; Haibo Mei; Jianlin Han; Vadim A. Soloshonok; Yi Pan
Asymmetric synthesis of quaternary alpha-fluoro-beta-keto-amines via detrifluoroacetylative Mannich reactions
Chem.Commun., 2015, 51, 9149
7117191 CIFC22 H19 Br Cl3 N2 O4P 21 21 2110.2175; 12.1386; 19.641
90; 90; 90
2436Wu-Lin Yang; Yang-Zi Liu; Shuai Luo; Xingxin Yu; John S. Fossey; Wei-Ping Deng
The copper-catalyzed asymmetric construction of a dispiropyrrolidine skeleton via 1,3-dipolar cycloaddition of azomethine ylides to alpha-alkylidene succinimides
Chem.Commun., 2015, 51, 9212
7117192 CIFC24 H18 F6 O6P -18.917; 11.888; 12.165
62.137; 81.719; 78.834
1116.3Jingbo Wu; Scott T. Iacono; Gregory T. McCandless; Dennis W. Smith; Bruce M. Novak
Utilization of a Meldrum's acid towards functionalized fluoropolymers possessing dual reactivity for thermal crosslinking and post-polymerization modification
Chem.Commun., 2015, 51, 9220
7117193 CIFC19 H14 B F2 N3 SP 1 21/c 113.4997; 13.9995; 10.1052
90; 111.458; 90
1777.4Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117194 CIFC23 H23 B F2 N3 SP 1 21/n 116.3271; 8.327; 16.9926
90; 109.759; 90
2174.2Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117195 CIFC20 H16 B F2 N3 O SP 1 21/c 110.5497; 19.995; 9.2865
90; 104.898; 90
1893.1Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117196 CIFC18 H11 B Cl F2 N3P 1 21/c 19.7361; 14.5464; 12.214
90; 111.146; 90
1613.33Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117197 CIFC90 H106 Cl4 N10 O92.75 V16P 1 21/a 121.2958; 21.33; 21.9581
90; 105.868; 90
9594.2Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117198 CIFC80 H80 Cl4 N4 O81.5 V16I 4/m m m14.9098; 14.9098; 38.069
90; 90; 90
8462.8Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117199 CIFC51.75 H64.75 Br4 Cl2 N7.25 O42.75 V8P -115.1975; 19.1532; 19.3115
103.817; 95.3294; 98.3478
5352.9Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117200 CIFC91 H119 Cl7 N9 O83.25 V16P -114.9214; 16.0334; 16.7794
79.476; 82.828; 81.284
3881.7Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117201 CIFC45 H109 Cr Mo6 N6 O29P -113.554; 13.7899; 21.0955
86.768; 88.944; 63.016
3508Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117202 CIFC62 H143 Br Cr Mo6 N5 O27P 1 21/c 124.0245; 13.9963; 26.7955
90; 94.54; 90
8981.8Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117203 CIFC69 H158 Br Cr Mo6 N8 O29P 113.2494; 14.7378; 14.8892
119.221; 103.752; 96.589
2371.5Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117204 CIFC46 H108 Cr Mo6 N5 O28P -113.6865; 13.7366; 21.5248
86.727; 83.692; 62.304
3561.4Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117205 CIFC67 H155 Br Mn Mo6 N9 O29P 113.2671; 14.756; 14.887
119.33; 103.729; 96.883
2370.4Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117206 CIFC8 H43 Cr Mo6 N2 O30P 1 21/n 115.0834; 11.5341; 23.0245
90; 98.122; 90
3965.47Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117207 CIFC62 H54 Cl6 P4 RuP -112.3129; 14.9215; 18.0053
67.588; 85.054; 78.028
2991.6Samantha G. Eaves; Sam J. Hart; Adrian C. Whitwood; Dmitry S. Yufit; Paul J. Low; Jason M. Lynam
Rapid Markovnikov addition of HCl to a pendant alkyne: evidence for a quinoidal cumulene
Chem.Commun., 2015, 51, 9362
7117208 CIFC63.5 H57 Cl5 P4 RuP -111.3506; 12.3819; 21.4222
80.7264; 74.684; 83.7147
2858.75Samantha G. Eaves; Sam J. Hart; Adrian C. Whitwood; Dmitry S. Yufit; Paul J. Low; Jason M. Lynam
Rapid Markovnikov addition of HCl to a pendant alkyne: evidence for a quinoidal cumulene
Chem.Commun., 2015, 51, 9362
7117210 CIFC67.99 H56.99 F11.99 N14 O P2 RuR -317.6408; 17.6408; 44.355
90; 90; 120
11953.9E. Rousset; D. Chartrand; I. Ciofini; V. Marvaud; G. S. Hanan
Red-light-driven photocatalytic hydrogen evolution using a ruthenium quaterpyridine complex
Chem.Commun., 2015, 51, 9261
7117211 CIFC60 H42 Cl2 N12 O5 RuP 41 3 221.1118; 21.1118; 21.1118
90; 90; 90
9409.7E. Rousset; D. Chartrand; I. Ciofini; V. Marvaud; G. S. Hanan
Red-light-driven photocatalytic hydrogen evolution using a ruthenium quaterpyridine complex
Chem.Commun., 2015, 51, 9261
7117212 CIFC17 H13 N3 OP 1 21/n 15.212; 17.471; 15.196
90; 92.267; 90
1382.6Liang Zhang; Mingzhu Zhao; Xiaoming Zhao
The synthesis of carbonyl 2-amino-pyrimidines via tandem regioselective heterocyclization of 1,3-diynes with guanidine and selective oxidation
Chem.Commun., 2015, 51, 9370
7117213 CIFAl4 H3 Na3 O19 P4P 1 21/m 17.537; 12.525; 9.7
90; 98.51; 90
905.6Yanjun Sun; Yan Yan; Yanyan Wang; Yi Li; Jiyang Li; Jihong Yu
High proton conduction in a new alkali metal-templated open-framework aluminophosphate
Chem.Commun., 2015, 51, 9317
7117214 CIFC96 H40 Cd5 O34R -3 c :H29.1653; 29.1653; 83.513
90; 90; 120
61520Hongming He; Yang Song; Chuanqi Zhang; Fuxing Sun; Rongrong Yuan; Zheng Bian; Lianxun Gao; Guangshan Zhu
A highly robust metal-organic framework based on an aromatic 12-carboxyl ligand with highly selective adsorption of CO2 over CH4
Chem.Commun., 2015, 51, 9463
7117215 CIFCl7 Cu10 O16 Pb2 Se4C 1 2/m 118.605; 6.204; 12.673
90; 109.869; 90
1376Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117216 CIFCl10 Cu12 O16 Pb2 Se4C 1 2/m 118.4956; 6.1454; 15.2985
90; 119.311; 90
1516.25Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117217 CIFCl11.6 Cu13.6 K1.6 O16 Pb0.4 Se4C 1 2/m 115.1158; 6.1853; 9.2672
90; 95.965; 90
861.75Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117218 CIFC15 H9 Ag Cl N9 O4I -4 3 d20.2313; 20.2313; 20.2313
90; 90; 90
8280.8Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117219 CIFC40 H27 Ag4 F12 N27 O12 S4P 1 21/n 110.6023; 18.0069; 33.316
90; 90.1374; 90
6360.5Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117220 CIFC24 H18 Ag2 F12 N18 P2P n m a10.6565; 16.8754; 19.1418
90; 90; 90
3442.3Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117221 CIFC30 H24 Cl2 N Ni O3 PP -110.2518; 11.9007; 13.0245
111.438; 97.586; 98.593
1432.11Wenfeng Lo; Chunhua Hu; Tyler Berenson; Nathaniel Tracer; Daniel Shlian; Michael Khaloo; Avraham Benhaim; Jianfeng Jiang
Oxidation of carbon monoxide in basic solution catalyzed by nickel cyano carbonyls under ambient conditions and the prototype of a CO-powered alkaline fuel cell
Chem.Commun., 2015, 51, 9432
7117222 CIFC20 H40 N4 Ni O2C 1 2/c 114.857; 10.303; 15.562
90; 99.009; 90
2352.7Wenfeng Lo; Chunhua Hu; Tyler Berenson; Nathaniel Tracer; Daniel Shlian; Michael Khaloo; Avraham Benhaim; Jianfeng Jiang
Oxidation of carbon monoxide in basic solution catalyzed by nickel cyano carbonyls under ambient conditions and the prototype of a CO-powered alkaline fuel cell
Chem.Commun., 2015, 51, 9432
7117223 CIFC62 H42 N6 Ni2 O18P 1 21/n 113.142; 12.337; 17.656
90; 108.519; 90
2714Jun Zhao; Yenan Wang; Wenwen Dong; Yapan Wu; Dongsheng Li; Bin Liu; Qichun Zhang
A new surfactant-introduction strategy for separating the pure single-phase of metal-organic frameworks
Chem.Commun., 2015, 51, 9479
7117224 CIFC36 H21 N4 Ni2 O8C m c a31.395; 13.702; 15.808
90; 90; 90
6800Jun Zhao; Yenan Wang; Wenwen Dong; Yapan Wu; Dongsheng Li; Bin Liu; Qichun Zhang
A new surfactant-introduction strategy for separating the pure single-phase of metal-organic frameworks
Chem.Commun., 2015, 51, 9479
7117225 CIFC18 H12 N2 O2P 1 21/n 17.72; 21.073; 8.161
90; 92.202; 90
1326.7David E. Stephens; Johant Lakey-Beitia; Gabriel Chavez; Carla Ilie; Hadi D. Arman; Oleg V. Larionov
Experimental and mechanistic analysis of the palladium-catalyzed oxidative C8-selective C-H homocoupling of quinoline N-oxides
Chem.Commun., 2015, 51, 9507
7117227 CIFC28 H31 N3C 1 2/c 131.282; 8.8017; 19.4725
90; 121.27; 90
4582.6Qian Gao; Peng Zhou; Feng Liu; Wen-Juan Hao; Changsheng Yao; Bo Jiang; Shu-Jiang Tu
Cobalt(II)/silver relay catalytic isocyanide insertion/cycloaddition cascades: a new access to pyrrolo[2,3-b]indoles
Chem.Commun., 2015, 51, 9519
7117228 CIFC23 H18 N2 O4P 1 21/c 110.8247; 12.1491; 14.009
90; 96.356; 90
1831Subrata Mukherjee; Santigopal Mondal; Atanu Patra; Rajesh G. Gonnade; Akkattu T. Biju
N-Heterocyclic carbene-catalyzed diastereoselective synthesis of beta-lactone-fused cyclopentanes using homoenolate annulation reaction
Chem.Commun., 2015, 51, 9559
7117229 CIFC24 H20 Cl3 N O3P 1 21/c 115.3285; 11.4221; 12.7961
90; 95.471; 90
2230.2Subrata Mukherjee; Santigopal Mondal; Atanu Patra; Rajesh G. Gonnade; Akkattu T. Biju
N-Heterocyclic carbene-catalyzed diastereoselective synthesis of beta-lactone-fused cyclopentanes using homoenolate annulation reaction
Chem.Commun., 2015, 51, 9559
7117230 CIFC50 H60 B F24 Na P6P 1 21/c 118.4514; 13.2631; 26.133
90; 90.826; 90
6394.7Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117231 CIFC62 H60 B F24 Na P6P -112.5084; 16.4798; 17.5637
79.047; 78.403; 81.625
3460.2Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117232 CIFC46 H48 Al F36 Li O4 P6P n a 2115.092; 27.737; 15.405
90; 90; 90
6448.6Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117233 CIFC48 H68 Cl Fe In N2 O4P 21 21 2110.3658; 18.6942; 23.794
90; 90; 90
4610.8Stephanie M. Quan; Paula L. Diaconescu
High activity of an indium alkoxide complex toward ring opening polymerization of cyclic esters
Chem.Commun., 2015, 51, 9643
7117234 CIFC27 H18 Br N3 OP 1 21 18.1413; 13.747; 10.606
90; 108.05; 90
1128.6Tianyou Qin; Lu Cheng; Sean Xiao-An Zhang; Weiwei Liao
Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction
Chem.Commun., 2015, 51, 9714
7117235 CIFC32 H24 N2 O SP -19.4724; 12.292; 12.563
104; 109.97; 102.72
1258.3Tianyou Qin; Lu Cheng; Sean Xiao-An Zhang; Weiwei Liao
Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction
Chem.Commun., 2015, 51, 9714
7117236 CIFC33 H15 Cu6 N6 O19F m -3 m44.588; 44.588; 44.588
90; 90; 90
88645Wen-Yang Gao; Tony Pham; Katherine A. Forrest; Brian Space; Lukasz Wojtas; Yu-Sheng Chen; Shengqian Ma
The local electric field favours more than exposed nitrogen atoms on CO2 capture: a case study on the rht-type MOF platform
Chem.Commun., 2015, 51, 9636
7117237 CIFC69 H65 Au2 F6 N P SbP 1 21/c 116.83401; 18.4515; 19.639
90; 100.054; 90
6006.44Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117238 CIFC58.01 H55.02 Au2 F6 N P SbP b c n24.291; 17.933; 24.334
90; 90; 90
10600Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117239 CIFC66 H64 Au3 F6 N2 SbP 1 21/c 116.33309; 18.64797; 18.79354
90; 91.0581; 90
5723.14Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117240 CIFC32 H42 Cl3 N3 PdP 1 21/c 19.2943; 21.212; 18.121
90; 114.171; 90
3259.4Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117241 CIFC26 H30 Cl3 N3 PtP 21 21 235.0384; 9.1217; 16.6331
90; 90; 90
5316.1Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117242 CIFC32 H42 Cl3 N3 PtP 1 21/c 19.3227; 21.1418; 18.1068
90; 115.162; 90
3230.18Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117243 CIFC32 H41 Cl2 N3 PdP 1 21/c 19.7411; 22.3057; 14.8046
90; 98.163; 90
3184.2Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117244 CIFC33 H43 Cl4 N3 PdI 41/a :233.4882; 33.4882; 12.9635
90; 90; 90
14538Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117245 CIFC39 H49 Cl2 N3 PdP 1 21/c 114.8545; 17.1043; 14.8749
90; 102.243; 90
3693.4Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117246 CIFC22 H21 Cl2 N3 PdP 1 21/c 19.0414; 25.274; 10.5618
90; 120.856; 90
2071.9Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117247 CIFC44 H42 Br1.81 Cl2.18 N6 Pd2C 1 c 114.907; 15.9956; 18.4249
90; 99.438; 90
4333.9Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117248 CIFC26 H29 Cl2 N3 PdP 1 21/c 111.5869; 14.0962; 15.7142
90; 100.524; 90
2523.45Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117249 CIFC27 H31 Cl4 N3 PtP 1 21/c 116.5349; 11.8855; 14.5488
90; 91.162; 90
2858.62Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117250 CIFC22 H21 Cl2 N3 PtP 1 21/c 19.0255; 25.338; 10.5412
90; 120.716; 90
2072.5Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117251 CIFC79 H21 Cl2 NP 1 21/c 110.4764; 25.5317; 16.5265
90; 102.296; 90
4319.1Bolong Zhang; Jegadesan Subbiah; Yu-Ying Lai; Jonathan M. White; David J. Jones; Wallace W. H. Wong
One-pot selective synthesis of a fullerene bisadduct for organic solar cell applications
Chem.Commun., 2015, 51, 9837
7117252 CIFC21 H19 Cl N2 O3P 21 21 216.1999; 13.2765; 23.277
90; 90; 90
1916Santosh Agrawal; Nagaraju Molleti; Vinod K. Singh
Organocatalytic enantio- and diastereoselective synthesis of highly substituted ?-lactones via a Michael-cyclization cascade
Chem.Commun., 2015, 51, 9793
7117253 CIFC116 H150 Ag24 F12 N2 O16P 1 21/n 123.5527; 20.9694; 29.346
90; 95.231; 90
14433.2Kuan-Guan Liu; Su-Kun Chen; Yu-Mei Lin; Quan-Ming Wang
An organic anion template: a 24-nucleus silver cluster encapsulating a squarate dimer
Chem.Commun., 2015, 51, 9896
7117254 CIFC12 H18P -15.246; 6.1956; 7.9824
103.859; 98.602; 100.131
242.93Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117255 CIFC12 H18P -15.2512; 6.2279; 7.9892
103.846; 98.464; 99.919
245Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117256 CIFC12 H18P -15.2639; 6.2567; 8.0155
103.858; 98.504; 99.75
247.65Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117257 CIFC12 H18P -15.2748; 6.2602; 8.0316
103.949; 98.651; 99.531
248.77Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117258 CIFC12 H18P -15.2944; 6.2771; 8.0612
104.026; 98.839; 99.456
251.09Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117259 CIFC9 H9 Br3P -17.6628; 9.0535; 9.0675
119.828; 106.926; 95.17
500.73Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117260 CIFC9 H9 Br3P -17.6795; 9.0494; 9.0657
119.817; 106.887; 95.081
502.02Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117261 CIFC9 H9 Br3P -17.7114; 9.0669; 9.0829
119.802; 106.864; 95.034
506.39Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117262 CIFC9 H9 Br3P -17.7305; 9.0698; 9.0855
119.773; 106.867; 95.034
508.12Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117263 CIFC9 H9 Br3P -17.7631; 9.0805; 9.0999
119.76; 106.811; 95.019
512.06Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117264 CIFC9 H9 Cl3P -17.5031; 8.7681; 8.7862
119.731; 106.219; 95.51
462.5Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117265 CIFC9 H9 Cl3P -17.6629; 8.7822; 8.7994
119.644; 107.474; 96.23
466.72Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117266 CIFC9 H9 Cl3P -17.6799; 8.7893; 8.8083
119.651; 107.294; 96.335
469.01Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117267 CIFC9 H9 Cl3P -17.7076; 8.801; 8.8248
119.644; 107.231; 96.278
472.73Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117268 CIFC9 H9 Cl3P -17.7324; 8.8179; 8.8415
119.64; 107.114; 96.298
476.54Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117269 CIFC9 H9 I3P -17.9189; 9.5531; 9.5594
60.255; 66.67; 85.526
570.15Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117270 CIFC9 H9 I3P -17.9431; 9.5681; 9.5753
60.225; 66.662; 85.52
573.51Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117271 CIFC9 H9 I3P -17.97; 9.5781; 9.5874
60.223; 66.693; 85.452
577.07Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117272 CIFC9 H9 I3P -17.9901; 9.5851; 9.5953
60.221; 66.709; 85.445
579.51Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117273 CIFC9 H9 I3P -18.0247; 9.6025; 9.6148
60.183; 66.729; 85.377
584.24Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117274 CIFC35 H44 B2 N2 O2P 1 21/c 112.8272; 21.122; 14.0969
90; 93.392; 90
3812.7Marc-Andre Courtemanche; Alexander P. Pulis; Etienne Rochette; Marc-Andre Legare; Douglas W. Stephan; Frederic-Georges Fontaine
Intramolecular B/N frustrated Lewis pairs and the hydrogenation of carbon dioxide
Chem.Commun., 2015, 51, 9797
7117275 CIFC56 H78 B2 Cl4 F8 Ir2 N4C 1 2/c 119.338; 16.601; 18.949
90; 95.101; 90
6059.1Laura Rubio-Perez; Manuel Iglesias; Julen Munarriz; Victor Polo; Pablo J. Sanz Miguel; Jesus J. Perez-Torrente; Luis A. Oro
A bimetallic iridium(II) catalyst: [{Ir(IDipp)(H)}2][BF4]2 (IDipp = 1,3-bis(2,6-diisopropylphenylimidazol-2-ylidene))
Chem.Commun., 2015, 51, 9860
7117276 CIFC30 H34 N2 O2 SP 1 21/c 111.426; 16.485; 15.147
90; 100.185; 90
2808.1Stephanie Norsikian; Margaux Beretta; Alexandre Cannillo; Amelie Martin; Pascal Retailleau; Jean-Marie Beau
Synthesis of enantioenriched 1,2-trans-diamines using the borono-Mannich reaction with N-protected alpha-amino aldehydes
Chem.Commun., 2015, 51, 9991
7117277 CIFC38 H28 Co N4 O4P 1 21/n 19.3634; 21.379; 15.2
90; 101.912; 90
2977.2Sk Amanullah; Pradip Kumar Das; Subhra Samanta; Abhishek Dey
Tuning the thermodynamic onset potential of electrocatalytic O2 reduction reaction by synthetic iron-porphyrin complexes
Chem.Commun., 2015, 51, 10010
7117278 CIFC39 H42 Cl2 N O6 PP 1 21 19.921; 16.32; 11.549
90; 97.356; 90
1854.5Taichi Kano; Hiroki Maruyama; Ryu Sakamoto; Keiji Maruoka
Regioselectivity switch in chiral amine-catalysed asymmetric addition of aldehydes to reactive enals
Chem.Commun., 2015, 51, 10062
7117279 CIFC21 H19 N O4P 21 21 219.7332; 12.3327; 15.1571
90; 90; 90
1819.41Weiwei Luo; Jiannan Zhao; Jie Ji; Lili Lin; Xiaohua Liu; Hongjiang Mei; Xiaoming Feng
A catalytic asymmetric carbonyl-ene reaction of beta,gamma-unsaturated alpha-ketoesters with 5-methyleneoxazolines
Chem.Commun., 2015, 51, 10042
7117280 CIFC22 H19 N O4P 21 21 219.8442; 12.3537; 16.5313
90; 90; 90
2010.41Weiwei Luo; Jiannan Zhao; Jie Ji; Lili Lin; Xiaohua Liu; Hongjiang Mei; Xiaoming Feng
A catalytic asymmetric carbonyl-ene reaction of beta,gamma-unsaturated alpha-ketoesters with 5-methyleneoxazolines
Chem.Commun., 2015, 51, 10042
7117281 CIFC15 H21 N O3 SP 21 21 217.89498; 11.4535; 16.5401
90; 90; 90
1495.64Jin-Miao Tian; Yong-Hai Yuan; Yong-Qiang Tu; Fu-Min Zhang; Xiao-Bo Zhang; Shi-Heng Zhang; Shao-Hua Wang; Xiao-Ming Zhang
The design of a spiro-pyrrolidine organocatalyst and its application to catalytic asymmetric Michael addition for the construction of all-carbon quaternary centers
Chem.Commun., 2015, 51, 9979
7117283 CIFC48 H51 B F4 Ir N5P -110.3919; 13.6438; 15.4722
95.673; 95.753; 98.925
2141.59Mewis, Ryan E.; Fekete, Marianna; Green, Gary G. R.; Whitwood, Adrian C.; Duckett, Simon B.
Deactivation of signal amplification by reversible exchange catalysis, progress towards in vivo application.
Chemical communications (Cambridge, England), 2015, 51, 9857-9859
7117285 CIFC44 H34 Cl2 F9 N12 O10 S3 W2P 1 21/n 113.377; 15.6886; 25.1243
90; 102.402; 90
5149.7Brogden, David W.; Berry, John F.
Not all density functionals are created equal: the case of the missing electron in the oxidized [W-W[triple bond, length as m-dash]O](7+) core.
Chemical communications (Cambridge, England), 2015, 51, 9153-9156
7117286 CIFC90 H189 N30 Na5 O162 S10 U20 V20P c c n32.023; 27.232; 28.774
90; 90; 90
25092G. A. Senchyk; E. M. Wylie; S. Prizio; J. E. S. Szymanowski; G. E. Sigmon; P. C. Burns
Hybrid uranyl-vanadium nano-wheels
Chem.Commun., 2015, 51, 10134
7117287 CIFC48 H90 N16 O51 U2 V16C 1 2/c 123.656; 14.981; 27.97
90; 112.886; 90
9132G. A. Senchyk; E. M. Wylie; S. Prizio; J. E. S. Szymanowski; G. E. Sigmon; P. C. Burns
Hybrid uranyl-vanadium nano-wheels
Chem.Commun., 2015, 51, 10134
7117288 CIFC28 H24 O2P 1 21 19.6751; 10.2214; 10.6522
90; 96.993; 90
1045.6Meng Zhang; Xianpeng Yin; Tian Tian; Yun Liang; Weina Li; Yue Lan; Jian Li; Meimei Zhou; Yong Ju; Guangtao Li
AIE-induced fluorescent vesicles containing amphiphilic binding pockets and the FRET triggered by host-guest chemistry
Chem.Commun., 2015, 51, 10210
7117289 CIFC60 H51 P10P -110.102; 13.842; 19.518
90.19; 93.99; 93.2
2718.3Heidi Schneider; David Schmidt; Udo Radius
The reductive P-P coupling of primary and secondary phosphines mediated by N-heterocyclic carbenes
Chem.Commun., 2015, 51, 10138
7117290 CIFC42 H42 P6R -3 :H13.896; 13.896; 20.034
90; 90; 120
3350.3Heidi Schneider; David Schmidt; Udo Radius
The reductive P-P coupling of primary and secondary phosphines mediated by N-heterocyclic carbenes
Chem.Commun., 2015, 51, 10138
7117291 CIFC90 H111 B Cl F15 Ge P4 Pt2P -113.4568; 18.179; 18.421
92.687; 105.972; 96.846
4286.5Norio Nakata; Noriko Sekizawa; Akihiko Ishii
Cationic dinuclear platinum and palladium complexes with bridging hydrogermylene and hydrido ligands
Chem.Commun., 2015, 51, 10111
7117292 CIFC90 H112 B F15 Ge P4 Pt2P -113.4434; 18.197; 18.3865
92.576; 106.152; 97.311
4269.9Norio Nakata; Noriko Sekizawa; Akihiko Ishii
Cationic dinuclear platinum and palladium complexes with bridging hydrogermylene and hydrido ligands
Chem.Commun., 2015, 51, 10111
7117293 CIFC96 H116 B Cl F16 Ge P4 Pd2P n a 2124.942; 32.139; 11.1842
90; 90; 90
8965Norio Nakata; Noriko Sekizawa; Akihiko Ishii
Cationic dinuclear platinum and palladium complexes with bridging hydrogermylene and hydrido ligands
Chem.Commun., 2015, 51, 10111
7117294 CIFC33 H48 B F4 P2 RhP 1 21 110.6347; 29.6678; 10.7567
90; 105.968; 90
3262.88E. Louise Hazeland; Andy M. Chapman; Paul G. Pringle; Hazel A. Sparkes
A one-step, modular route to optically-active diphos ligands
Chem.Commun., 2015, 51, 10206
7117295 CIFC30 H34 Cl4 O2 P2 PtP 21 21 219.8749; 10.7553; 29.0217
90; 90; 90
3082.3E. Louise Hazeland; Andy M. Chapman; Paul G. Pringle; Hazel A. Sparkes
A one-step, modular route to optically-active diphos ligands
Chem.Commun., 2015, 51, 10206
7117296 CIFC6 H7 Cu2 N9 O2.5C 1 2/c 124.258; 9.4877; 16.473
90; 118.79; 90
3322.7Chao Huang; Jie Wu; Chuanjun Song; Ran Ding; Yan Qiao; Hongwei Hou; Junbiao Chang; Yaoting Fan
Reversible conversion of valence-tautomeric copper metal-organic frameworks dependent single-crystal-to-single-crystal oxidation/reduction: a redox-switchable catalyst for C-H bonds activation reaction
Chem.Commun., 2015, 51, 10353
7117297 CIFC6 H8 Cu2 N9 O3C 1 2/c 124.321; 9.4098; 16.628
90; 119.24; 90
3320.5Chao Huang; Jie Wu; Chuanjun Song; Ran Ding; Yan Qiao; Hongwei Hou; Junbiao Chang; Yaoting Fan
Reversible conversion of valence-tautomeric copper metal-organic frameworks dependent single-crystal-to-single-crystal oxidation/reduction: a redox-switchable catalyst for C-H bonds activation reaction
Chem.Commun., 2015, 51, 10353
7117298 CIFC6 H4 Cu2 N9 O1.5C 1 2/c 124.338; 9.4877; 16.502
90; 119.89; 90
3303.6Chao Huang; Jie Wu; Chuanjun Song; Ran Ding; Yan Qiao; Hongwei Hou; Junbiao Chang; Yaoting Fan
Reversible conversion of valence-tautomeric copper metal-organic frameworks dependent single-crystal-to-single-crystal oxidation/reduction: a redox-switchable catalyst for C-H bonds activation reaction
Chem.Commun., 2015, 51, 10353
7117299 CIFC12 H19 Cu2 N10 OC 1 2/c 124.225; 9.6254; 16.37
90; 118.54; 90
3353.2Chao Huang; Jie Wu; Chuanjun Song; Ran Ding; Yan Qiao; Hongwei Hou; Junbiao Chang; Yaoting Fan
Reversible conversion of valence-tautomeric copper metal-organic frameworks dependent single-crystal-to-single-crystal oxidation/reduction: a redox-switchable catalyst for C-H bonds activation reaction
Chem.Commun., 2015, 51, 10353
7117300 CIFC12 H18 Cu2 N10 O0.5C 1 c 124.349; 9.2334; 16.959
90; 119.41; 90
3321.4Chao Huang; Jie Wu; Chuanjun Song; Ran Ding; Yan Qiao; Hongwei Hou; Junbiao Chang; Yaoting Fan
Reversible conversion of valence-tautomeric copper metal-organic frameworks dependent single-crystal-to-single-crystal oxidation/reduction: a redox-switchable catalyst for C-H bonds activation reaction
Chem.Commun., 2015, 51, 10353
7117301 CIFC81 H49 O20 Tb3P 1 2/c 110.8511; 28.8803; 19.155
90; 123.902; 90
4982.3Hang Xu; Chun-Shuai Cao; Bin Zhao
A water-stable lanthanide-organic framework as a recyclable luminescent probe for detecting pollutant phosphorus anions
Chem.Commun., 2015, 51, 10280
7117302 CIFC20 H18 O2P b c a15.2594; 10.4298; 19.4355
90; 90; 90
3093.2Kegong Ji; Xiang Liu; Bowen Du; Fang Yang; Jinming Gao
Gold-catalyzed selective oxidation of 4-oxahepta-1,6-diynes to 2H-pyran-3(6H)-ones and chromen-3(4H)-ones via beta-gold vinyl cation intermediates
Chem.Commun., 2015, 51, 10318
7117303 CIFC164 H261 Cu31 N64 O35 PP -120.4153; 22.91; 25.8662
103.685; 94.975; 110.593
10809.7Gellert Mezei
Incarceration of one or two phosphate or arsenate species within nanojars, capped nanojars and nanohelicages: helical chirality from two closely-spaced, head-to-head PO4^3-^ or AsO4^3-^ ions
Chem.Commun., 2015, 51, 10341
7117304 CIFC145 H227 As Cu31 N64 O35P -120.4878; 22.9195; 25.7171
103.64; 95.22; 110.663
10777.1Gellert Mezei
Incarceration of one or two phosphate or arsenate species within nanojars, capped nanojars and nanohelicages: helical chirality from two closely-spaced, head-to-head PO4^3-^ or AsO4^3-^ ions
Chem.Commun., 2015, 51, 10341
7117305 CIFC117 H196 Cu30 N61 O42 PP 1 21/c 119.9142; 28.2823; 33.9811
90; 106.132; 90
18385.2Gellert Mezei
Incarceration of one or two phosphate or arsenate species within nanojars, capped nanojars and nanohelicages: helical chirality from two closely-spaced, head-to-head PO4^3-^ or AsO4^3-^ ions
Chem.Commun., 2015, 51, 10341
7117306 CIFC104 H149 Br1.5 Cu15 N39.5 O19 P2P 1 21/c 117.1774; 24.4; 33.549
90; 103.254; 90
13686.8Gellert Mezei
Incarceration of one or two phosphate or arsenate species within nanojars, capped nanojars and nanohelicages: helical chirality from two closely-spaced, head-to-head PO4^3-^ or AsO4^3-^ ions
Chem.Commun., 2015, 51, 10341
7117307 CIFC110 H154 As2 Br2 Cu15 N40 O20C 1 2/c 117.3262; 25.319; 31.9199
90; 102.256; 90
13683.6Gellert Mezei
Incarceration of one or two phosphate or arsenate species within nanojars, capped nanojars and nanohelicages: helical chirality from two closely-spaced, head-to-head PO4^3-^ or AsO4^3-^ ions
Chem.Commun., 2015, 51, 10341
7117308 CIFC16 H13 Cl Fe SP -15.7825; 8.6085; 14.043
99.114; 99.532; 94.734
676.43Zongjun Qiao; Nanyang Ge; Xuefeng Jiang
CO2-promoted oxidative cross-coupling reaction for C-S bond formation via masked strategy in an odourless way
Chem.Commun., 2015, 51, 10295
7117309 CIFC22 H40 Cu F2 N4 O8 S4P -17.5312; 8.2038; 13.344
92.852; 93.152; 107.116
784.9Zongjun Qiao; Nanyang Ge; Xuefeng Jiang
CO2-promoted oxidative cross-coupling reaction for C-S bond formation via masked strategy in an odourless way
Chem.Commun., 2015, 51, 10295
7117310 CIFC17.75 H24 N2 O3.5 PtC 1 2/c 133.626; 12.052; 24.064
90; 134.007; 90
7014Mohamed E. Moustafa; Paul D. Boyle; Richard J. Puddephatt
A biomimetic phenol substituent effect on the reaction of a dimethylplatinum(II) complex with oxygen: proton coupled electron transfer and multiple proton relay
Chem.Commun., 2015, 51, 10334
7117311 CIFC75 H72 F9 N16 O21 S3 Yb Zn4P 4/n c c23.3111; 23.3111; 19.866
90; 90; 90
10795.3Quan-Wen Li; Jun-Liang Liu; Jian-Hua Jia; Yan-Cong Chen; Jiang Liu; Long-Fei Wang; Ming-Liang Tong
'Half-sandwich' Yb^III^ single-ion magnets with metallacrowns
Chem.Commun., 2015, 51, 10291
7117312 CIFC100 H100 F9 N19 O24 S3 Yb Zn4P 1 21/c 116.1341; 42.5371; 18.4653
90; 93.131; 90
12653.8Quan-Wen Li; Jun-Liang Liu; Jian-Hua Jia; Yan-Cong Chen; Jiang Liu; Long-Fei Wang; Ming-Liang Tong
'Half-sandwich' Yb^III^ single-ion magnets with metallacrowns
Chem.Commun., 2015, 51, 10291
7117313 CIFC23 H16 N2 O3C 1 2/c 126.382; 8.7432; 15.937
90; 97.035; 90
3648.4Ahmed Kamal; Chada Narsimha Reddy; Malasala Satyaveni; D. Chandrasekhar; Jagadeesh Babu Nanubolu; Kiran Kumar Singarapud; Ram Awatar Maurya
Cu(OAc)2-Et3N mediated oxidative coupling of alpha-azido ketones with pyridinium ylides: utilizing in situ generated imines for regioselective synthesis of imidazo[1,2-a]pyridines
Chem.Commun., 2015, 51, 10475
7117314 CIFC45 H36 O4C 1 2/c 120.81; 13.789; 12.317
90; 90.752; 90
3534Zhaozhong Yi; Hitoshi Okuda; Yasuhito Koyama; Ryota Seto; Satoshi Uchida; Hiromitsu Sogawa; Shigeki Kuwata; Toshikazu Takata
Exact helical polymer synthesis by a two-point-covalent-linking protocol between C2-chiral spirobifluorene and C2- or Cs-symmetric anthraquinone monomers
Chem.Commun., 2015, 51, 10423
7117315 CIFC46 H56 Cu2 N22 O10 Tb2P 19.6495; 11.9679; 12.5126
78.879; 85.44; 79.309
1391.83Xing-Cai Huang; Veacheslav Vieru; Liviu F. Chibotaru; Wolfgang Wernsdorfer; Shang-Da Jiang; Xin-Yi Wang
Determination of magnetic anisotropy in a multinuclear Tb^III^-based single-molecule magnet
Chem.Commun., 2015, 51, 10373
7117316 CIFC46 H56 Cu2 N22 O10 Tb2P 19.6455; 11.9723; 12.5139
78.864; 85.397; 79.256
1391.56Xing-Cai Huang; Veacheslav Vieru; Liviu F. Chibotaru; Wolfgang Wernsdorfer; Shang-Da Jiang; Xin-Yi Wang
Determination of magnetic anisotropy in a multinuclear Tb^III^-based single-molecule magnet
Chem.Commun., 2015, 51, 10373
7117317 CIFC30 H30 N2 O4I 4117.4485; 17.4485; 16.711
90; 90; 90
5087.67Jianlin Zhang; Yulong Zhang; Lili Lin; Qian Yao; Xiaohua Liu; Xiaoming Feng
Catalytic asymmetric desymmetrization of N-arylmaleimides: efficient construction of both atom chirality and axial chirality
Chem.Commun., 2015, 51, 10554
7117318 CIFC65 H115 N2 O6 P5 Re6 S2 Se8P 1 21 112.8853; 12.9302; 25.069
90; 92.4338; 90
4173Jessica L. Durham; Wade B. Wilson; Daniel N. Huh; Robert McDonald; Lisa F. Szczepura
Organometallic rhenium(III) chalcogenide clusters: coordination of N-heterocyclic carbenes
Chem.Commun., 2015, 51, 10536
7117319 CIFC55 H80 Cl4 N4 P2 Re6 S8P 1 21/c 116.6282; 16.7446; 25.1262
90; 92.1776; 90
6990.9Jessica L. Durham; Wade B. Wilson; Daniel N. Huh; Robert McDonald; Lisa F. Szczepura
Organometallic rhenium(III) chalcogenide clusters: coordination of N-heterocyclic carbenes
Chem.Commun., 2015, 51, 10536
7117320 CIFC19 H13 N OP 1 21/c 18.3956; 21.0394; 8.2906
90; 105.859; 90
1408.7Pengchong Xue; Jiabao Sun; Peng Chen; Panpan Wang; Boqi Yao; Peng Gong; Zhenqi Zhang; Ran Lu
Luminescence switching of a persistent room-temperature phosphorescent pure organic molecule in response to external stimuli
Chem.Commun., 2015, 51, 10381
7117321 CIFC14 H17 N3 O3P -19.212; 12.624; 12.927
94.78; 109.99; 105.42
1336.5Lingliang Long; Yanjun Wu; Lin Wang; Aihua Gong; Feilong Hu; Chi Zhang
A fluorescent probe for hypochlorite based on the modulation of the unique rotation of the N-N single bond in acetohydrazide
Chem.Commun., 2015, 51, 10435
7117322 CIFC20 H21 N3 O3P 1 21/c 113.1553; 6.9401; 21.0792
90; 109.629; 90
1812.67Lingliang Long; Yanjun Wu; Lin Wang; Aihua Gong; Feilong Hu; Chi Zhang
A fluorescent probe for hypochlorite based on the modulation of the unique rotation of the N-N single bond in acetohydrazide
Chem.Commun., 2015, 51, 10435
7117327 CIFC24 H23 N O4P -19.9379; 10.0008; 10.8276
96.918; 104.753; 99.92
1009.72Min Tang; Dong Xing; Haoxi Huang; Wenhao Hu
Divergent synthesis of chiral heterocycles via sequencing of enantioselective three-component reactions and one-pot subsequent cyclization reactions
Chem.Commun., 2015, 51, 10612
7117328 CIFC25 H22 Br N O5P -19.6542; 10.7705; 12.1323
87.694; 71.902; 69.127
1116.89Min Tang; Dong Xing; Haoxi Huang; Wenhao Hu
Divergent synthesis of chiral heterocycles via sequencing of enantioselective three-component reactions and one-pot subsequent cyclization reactions
Chem.Commun., 2015, 51, 10612
7117329 CIFC28 H25 N O7P -19.1316; 11.5658; 12.884
87.471; 84.937; 78.96
1329.8Min Tang; Dong Xing; Haoxi Huang; Wenhao Hu
Divergent synthesis of chiral heterocycles via sequencing of enantioselective three-component reactions and one-pot subsequent cyclization reactions
Chem.Commun., 2015, 51, 10612
7117333 CIFC24 H256 Cl14 Gd24 O217 Zn4F m -3 m37.4763; 37.4763; 37.4763
90; 90; 90
52634.5Xiu-Ying Zheng; Shi-Qiang Wang; Wen Tang; Gui-Lin Zhuang; Xiang-Jian Kong; Yan-Ping Ren; La-Sheng Long; Lan-Sun Zheng
Two nanosized 3d-4f clusters featuring four Ln6 octahedra encapsulating a Zn4 tetrahedron
Chem.Commun., 2015, 51, 10687
7117334 CIFC24 H216 Cl14 O197 Sm24 Zn4F m -3 m37.8651; 37.8651; 37.8651
90; 90; 90
54289.7Xiu-Ying Zheng; Shi-Qiang Wang; Wen Tang; Gui-Lin Zhuang; Xiang-Jian Kong; Yan-Ping Ren; La-Sheng Long; Lan-Sun Zheng
Two nanosized 3d-4f clusters featuring four Ln6 octahedra encapsulating a Zn4 tetrahedron
Chem.Commun., 2015, 51, 10687
7117337 CIFC12 H9 N3 O2 SP 1 21/n 18.412; 15.9905; 8.469
90; 91.55; 90
1138.8Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117338 CIFC12 H9 N3 O2 SP 1 21/n 18.337; 15.8027; 8.4626
90; 91.44; 90
1114.6Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117339 CIFC12 H9 N3 O2 SP 1 21/n 18.2031; 15.4235; 8.4569
90; 90.851; 90
1069.9Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117340 CIFC12 H9 N3 O2 SP 1 21/n 18.116; 15.121; 8.4699
90; 90.38; 90
1039.4Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117341 CIFC12 H9 N3 O2 SP 1 21/n 18.0755; 14.874; 8.4734
90; 89.76; 90
1017.8Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117342 CIFC12 H9 N3 O2 SP 1 21/n 18.0025; 14.448; 8.4923
90; 89.15; 90
981.8Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117343 CIFC12 H9 N3 O2 SP 1 21/n 18.45062; 15.9403; 8.46555
90; 91.0663; 90
1140.16Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117344 CIFC12 H9 N3 O2 SP 1 21/n 17.9246; 14.028; 8.4897
90; 88.75; 90
943.5Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117345 CIFC12 H9 N3 O2 SP 1 21/n 17.8626; 13.721; 8.4707
90; 88.55; 90
913.5Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117346 CIFC12 H9 N3 O2 SP 1 21/n 18.5322; 16.412; 8.4958
90; 91.78; 90
1189.1Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117347 CIFC12 H9 N3 O2 SP 1 21/n 18.546; 16.42; 8.5053
90; 91.78; 90
1192.9Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117348 CIFC34 H50 Br2 Cl2 N3 PP 1 21/c 112.1055; 25.0614; 14.662
90; 123.958; 90
3689.5Thomas Simler; Andreas A. Danopoulos; Pierre Braunstein
N-Heterocyclic carbene-phosphino-picolines as precursors of anionic 'pincer' ligands with dearomatised pyridine backbones; transmetallation from potassium to chromium
Chem.Commun., 2015, 51, 10699
7117349 CIFC148 H220 K4 N12 O4 P4P -112.9906; 14.5542; 21.8297
72.803; 78.663; 70.389
3692.3Thomas Simler; Andreas A. Danopoulos; Pierre Braunstein
N-Heterocyclic carbene-phosphino-picolines as precursors of anionic 'pincer' ligands with dearomatised pyridine backbones; transmetallation from potassium to chromium
Chem.Commun., 2015, 51, 10699
7117350 CIFC29 H41 Cl Cr N3 PP 1 21/c 18.37; 23.052; 17.18
90; 116.249; 90
2973Thomas Simler; Andreas A. Danopoulos; Pierre Braunstein
N-Heterocyclic carbene-phosphino-picolines as precursors of anionic 'pincer' ligands with dearomatised pyridine backbones; transmetallation from potassium to chromium
Chem.Commun., 2015, 51, 10699
7117354 CIFC44 H50 N4 S Si2P -17.6707; 15.0819; 18.167
105.557; 94.548; 95.487
2003.3A. Belen Marco; Diego Cortizo-Lacalle; Cristian Gozalvez; Mikel Olano; Ainhoa Atxabal; Xiangnan Sun; Manuel Melle-Franco; Luis E. Hueso; Aurelio Mateo-Alonso
An electron-conducting pyrene-fused phenazinothiadiazole
Chem.Commun., 2015, 51, 10754
7117355 CIFC37 H30 Al Cl6 P3P -110.7482; 11.7146; 16.2326
108.178; 100.829; 99.8863
1848.28Chitra Gurnani; Nemanja Dordevic; Senthilkumar Muthaiah; Dusan Dimic; Rakesh Ganguly; Milena Petkovic; Dragoslav Vidovic
Extending the chemistry of carbones: P-N bond cleavage via an SN2'-like mechanism
Chem.Commun., 2015, 51, 10762
7117356 CIFC19 H20 Cl2 F6 N4 P SbP b c a11.63; 19.1931; 21.194
90; 90; 90
4730.8Chitra Gurnani; Nemanja Dordevic; Senthilkumar Muthaiah; Dusan Dimic; Rakesh Ganguly; Milena Petkovic; Dragoslav Vidovic
Extending the chemistry of carbones: P-N bond cleavage via an SN2'-like mechanism
Chem.Commun., 2015, 51, 10762
7117357 CIFC24 H26 Br N O4P 1 21 110.7238; 7.4576; 13.759
90; 93.502; 90
1098.3Shutao Sun; Ying Mao; Hongxiang Lou; Lei Liu
Copper(II)/amine synergistically catalyzed enantioselective alkylation of cyclic N-acyl hemiaminals with aldehydes
Chem.Commun., 2015, 51, 10691
7117358 CIFC23 H24 Br N O4P 21 21 215.1792; 11.1118; 36.24
90; 90; 90
2085.6Shutao Sun; Ying Mao; Hongxiang Lou; Lei Liu
Copper(II)/amine synergistically catalyzed enantioselective alkylation of cyclic N-acyl hemiaminals with aldehydes
Chem.Commun., 2015, 51, 10691
7117359 CIFC19 H22 Cl NP n a 217.4474; 16.4971; 12.9089
90; 90; 90
1585.99YoungKu Kang; Matthew T. Richers; Conrad H. Sawicki; Daniel Seidel
C-H functionalization of cyclic amines: redox-annulations with alpha,beta-unsaturated carbonyl compounds
Chem.Commun., 2015, 51, 10648
7117360 CIFC20 H23 Br NP 1 21/c 113.9903; 6.5457; 19.158
90; 103.355; 90
1706.97YoungKu Kang; Matthew T. Richers; Conrad H. Sawicki; Daniel Seidel
C-H functionalization of cyclic amines: redox-annulations with alpha,beta-unsaturated carbonyl compounds
Chem.Commun., 2015, 51, 10648
7117361 CIFC444 H1061 Cl9 In84 Mn23 N148 O7 Se150R -3 c :H34.7264; 34.7264; 155.851
90; 90; 120
162765Yu-Hong Wang; Jing Wu; Xiao-Wei Zhao; Li-Wen Qian; Qin-Yu Zhu; Jie Dai
A nano-scale triangular ring cluster of indium-selenide: the structure and templating effect
Chem.Commun., 2015, 51, 10668
7117362 CIFC46 H98 O Si10P -19.4329; 11.2567; 29.197
85.049; 83.862; 67.021
2834.5Tomoyuki Kosai; Shintaro Ishida; Takeaki Iwamoto
Transformation of azulenes to bicyclic [4]dendralene and heptafulvene derivatives via photochemical cycloaddition of dialkylsilylene
Chem.Commun., 2015, 51, 10707
7117363 CIFC31 H58 Si5P -19.5864; 10.9534; 18.638
105.877; 92.815; 110.499
1740.2Tomoyuki Kosai; Shintaro Ishida; Takeaki Iwamoto
Transformation of azulenes to bicyclic [4]dendralene and heptafulvene derivatives via photochemical cycloaddition of dialkylsilylene
Chem.Commun., 2015, 51, 10707
7117364 CIFC66 H43 N5P -19.45; 16.69; 19.57
82.49; 88.39; 74.9
2954.4Chenglong Li; Shipan Wang; Weiping Chen; Jinbei Wei; Guochun Yang; Kaiqi Ye; Yu Liu; Yue Wang
High performance full color OLEDs based on a class of molecules with dual carrier transport channels and small singlet-triplet splitting
Chem.Commun., 2015, 51, 10632
7117365 CIFC40 H41 N3 O12P 1 21/c 110.8958; 17.3981; 19.868
90; 91.143; 90
3765.6Qi-Lin Wang; Tian Cai; Jing Zhou; Fang Tian; Xiao-Ying Xu; Li-Xin Wang
An unprecedented base-promoted domino reaction of methyleneindolinones and N-tosyloxycarbamates for the construction of bispirooxindoles and spiroaziridine oxindoles
Chem.Commun., 2015, 51, 10726
7117366 CIFC24 H24 N2 O7P -16.647; 12.469; 14.173
87.147; 79.429; 89.31
1153Qi-Lin Wang; Tian Cai; Jing Zhou; Fang Tian; Xiao-Ying Xu; Li-Xin Wang
An unprecedented base-promoted domino reaction of methyleneindolinones and N-tosyloxycarbamates for the construction of bispirooxindoles and spiroaziridine oxindoles
Chem.Commun., 2015, 51, 10726
7117367 CIFC25 H30 B F4 Fe N3P -18.5466; 9.9789; 14.7438
104.047; 91.109; 101.147
1193.92Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117368 CIFC24 H27 Fe N3F d d 221.0171; 49.949; 7.7045
90; 90; 90
8088.1Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117369 CIFC21 H21 Fe N3P 1 21/n 17.2798; 16.749; 14.796
90; 103.923; 90
1751.1Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117370 CIFC22 H24 B F4 Fe N3P b c a9.213; 9.618; 47.215
90; 90; 90
4184Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117371 CIFC25 H29 Au Cl Fe N3C 1 2/c 129.3929; 9.2832; 17.3954
90; 90.428; 90
4746.4Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117372 CIFC22 H23 Au Cl Fe N3P 1 21/c 124.435; 7.515; 11.492
90; 93.546; 90
2106.2Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117373 CIFC12 H78 La4 N4 O53 P12P 1 21/c 114.274; 18.624; 12.53
90; 115.14; 90
3015.4Ricardo F. Mendes; Patricia Silva; Margarida M. Antunes; Anabela A. Valente; Filipe A. Almeida Paz
Sustainable synthesis of a catalytic active one-dimensional lanthanide-organic coordination polymer
Chem.Commun., 2015, 51, 10807
7117374 CIFC30 H22 F18 N2 O10 TbP 1 21/c 111.7995; 15.2788; 24.2492
90; 116.868; 90
3899.77Leilei Li; Shuang Liu; Han Li; Wei Shi; Peng Cheng
Influence of external magnetic field and magnetic-site dilution on the magnetic dynamics of a one-dimensional Tb(III)-radical complex
Chem.Commun., 2015, 51, 10933
7117375 CIFC21 H44 O2 P2 PdP c a 2115.9351; 14.7211; 21.273
90; 90; 90
4990.3S. Chantal E. Stieber; Nuria Huguet; Takeharu Kageyama; Ivana Jevtovikj; Piyal Ariyananda; Alvaro Gordillo; Stephan A. Schunk; Frank Rominger; Peter Hofmann; Michael Limbach
Acrylate formation from CO2 and ethylene: catalysis with palladium and mechanistic insight
Chem.Commun., 2015, 51, 10907
7117376 CIFC30 H58 P2 PdC 1 c 111.1923; 16.4379; 16.7601
90; 101.082; 90
3026S. Chantal E. Stieber; Nuria Huguet; Takeharu Kageyama; Ivana Jevtovikj; Piyal Ariyananda; Alvaro Gordillo; Stephan A. Schunk; Frank Rominger; Peter Hofmann; Michael Limbach
Acrylate formation from CO2 and ethylene: catalysis with palladium and mechanistic insight
Chem.Commun., 2015, 51, 10907
7117377 CIFC31.5 H56 O2 P2 PdC 1 2/c 128.266; 13.8216; 18.2436
90; 118.016; 90
6292.2S. Chantal E. Stieber; Nuria Huguet; Takeharu Kageyama; Ivana Jevtovikj; Piyal Ariyananda; Alvaro Gordillo; Stephan A. Schunk; Frank Rominger; Peter Hofmann; Michael Limbach
Acrylate formation from CO2 and ethylene: catalysis with palladium and mechanistic insight
Chem.Commun., 2015, 51, 10907
7117378 CIFC39 H56 F2 O4 P2 PdP 1 21/n 117.3557; 17.2752; 27.49
90; 106.717; 90
7893.8S. Chantal E. Stieber; Nuria Huguet; Takeharu Kageyama; Ivana Jevtovikj; Piyal Ariyananda; Alvaro Gordillo; Stephan A. Schunk; Frank Rominger; Peter Hofmann; Michael Limbach
Acrylate formation from CO2 and ethylene: catalysis with palladium and mechanistic insight
Chem.Commun., 2015, 51, 10907
7117379 CIFC19 H18 O2P 1 21 19.8399; 7.9143; 10.7479
90; 112.006; 90
776.02Naoya Kanbayashi; Kazuki Hosoda; Masanori Kato; Koichiro Takii; Taka-aki Okamura; Kiyotaka Onitsuka
Enantio- and diastereoselective asymmetric allylic alkylation catalyzed by a planar-chiral cyclopentadienyl ruthenium complex
Chem.Commun., 2015, 51, 10895
7117380 CIFC18 H12 Br Cl O3C 1 2/c 113.884; 10.515; 22.936
90; 96.166; 90
3329.1Dattatraya H. Dethe; Ganesh M. Murhade
FeCl3 mediated synthesis of substituted indenones by a formal [2+2] cycloaddition/ring opening cascade of o-keto-cinnamates
Chem.Commun., 2015, 51, 10891
7117381 CIFC37 H35 B3 F20 N2 OP 1 21/c 115.3212; 15.0201; 17.8636
90; 98.982; 90
4060.5Liam D. Curless; Ewan R. Clark; Jessica Cid; Alessandro Del Grosso; Michael J. Ingleson
Complete reductive cleavage of CO facilitated by highly electrophilic borocations
Chem.Commun., 2015, 51, 10903
7117382 CIFC36 H32 B2 F20 N2P -18.7661; 13.7257; 15.8543
82.373; 83.288; 81.661
1861.44Liam D. Curless; Ewan R. Clark; Jessica Cid; Alessandro Del Grosso; Michael J. Ingleson
Complete reductive cleavage of CO facilitated by highly electrophilic borocations
Chem.Commun., 2015, 51, 10903
7117383 CIFC16 H24 Gd3 Mn2 N48 O16P n -3 n17.1065; 17.1065; 17.1065
90; 90; 90
5005.9Huan-Cheng Hu; Xiao-Min Kang; Chun-Shuai Cao; Peng Cheng; Bin Zhao
First tetrazole-bridged d-f heterometallic MOFs with a large magnetic entropy change
Chem.Commun., 2015, 51, 10850
7117384 CIFC27 H21 Cl2 I N P2 PdP 1 21 19.2622; 18.511; 9.5911
90; 112.413; 90
1520.2Chen Tan; Peng Wang; Huan Liu; Xiao-Li Zhao; Yong Lu; Ye Liu
Bifunctional ligands in combination with phosphines and Lewis acidic phospheniums for the carbonylative Sonogashira reaction
Chem.Commun., 2015, 51, 10871
7117385 CIFC34 H32 Au Cl F3 N O3 P2 SP b c a17.0157; 15.2244; 27.1217
90; 90; 90
7026Chen Tan; Peng Wang; Huan Liu; Xiao-Li Zhao; Yong Lu; Ye Liu
Bifunctional ligands in combination with phosphines and Lewis acidic phospheniums for the carbonylative Sonogashira reaction
Chem.Commun., 2015, 51, 10871
7117386 CIFC29 H30 Au Cl F3 N O4 P2 SP 1 21/c 118.0468; 13.1909; 14.8731
90; 112.083; 90
3280.86Chen Tan; Peng Wang; Huan Liu; Xiao-Li Zhao; Yong Lu; Ye Liu
Bifunctional ligands in combination with phosphines and Lewis acidic phospheniums for the carbonylative Sonogashira reaction
Chem.Commun., 2015, 51, 10871
7117387 CIFC134.75 H221 N32 O23.75P 1 21 116.51; 27.312; 17.957
90; 96.33; 90
8048E. Prigorchenko; M. Oeren; S. Kaabel; M. Fomitsenko; I. Reile; I. Jarving; T. Tamm; F. Topic; K. Rissanen; R. Aav
Template-controlled synthesis of chiral cyclohexylhemicucurbit[8]uril
Chem.Commun., 2015, 51, 10921
7117388 CIFC95 H156 Cr6 F8 N2 O30 Zn2P 1 21/c 123.6326; 22.5386; 37.8111
90; 126.954; 90
16094.2Antonio Fernandez; Eufemio Moreno Pineda; Jesus Ferrando-Soria; Eric J. L. McInnes; Grigore A. Timco; Richard E. P. Winpenny
A hybrid organic-inorganic molecular daisy chain
Chem.Commun., 2015, 51, 11126
7117389 CIFC21 H25 Cl Cu N5 SP 1 21/n 111.2265; 14.264; 12.7921
90; 97.221; 90
2032.2B. N. Sanchez-Eguia; M. Flores-Alamo; M. Orio; I. Castillo
Side-on cupric-superoxo triplet complexes as competent agents for H-abstraction relevant to the active site of PHM
Chem.Commun., 2015, 51, 11134
7117390 CIFC52 H66 Cu2 F6 N10 O8 S4C 1 2/c 147.532; 11.8821; 29.711
90; 135.477; 90
11766B. N. Sanchez-Eguia; M. Flores-Alamo; M. Orio; I. Castillo
Side-on cupric-superoxo triplet complexes as competent agents for H-abstraction relevant to the active site of PHM
Chem.Commun., 2015, 51, 11134
7117391 CIFC42 H50 Br Cl3 Cu2 N10 O8 S2P 1 21/c 18.1746; 23.0559; 13.4166
90; 103.092; 90
2462.94B. N. Sanchez-Eguia; M. Flores-Alamo; M. Orio; I. Castillo
Side-on cupric-superoxo triplet complexes as competent agents for H-abstraction relevant to the active site of PHM
Chem.Commun., 2015, 51, 11134
7117392 CIFC58 H64 Cu2 F6 N10 O8 S4P 1 21/n 111.6838; 26.1913; 15.5908
90; 111.737; 90
4431.8B. N. Sanchez-Eguia; M. Flores-Alamo; M. Orio; I. Castillo
Side-on cupric-superoxo triplet complexes as competent agents for H-abstraction relevant to the active site of PHM
Chem.Commun., 2015, 51, 11134
7117393 CIFC27 H27 N3 O2 SP 1 21/c 19.0312; 13.3378; 19.5264
90; 99.689; 90
2318.53Guorong Sheng; Kai Huang; Shicong Ma; Jing Qian; Ping Lu; Yanguang Wang
Preparation of 3-aryl-2-aminoindoles, 3-allyl-3-amino-2-iminoindolines, and tetrahydro-[1,4]diazepino[2,3-b]indoles from 3-diazoindolin-2-imines
Chem.Commun., 2015, 51, 11056
7117394 CIFC22 H40 Cu2 F6 N6 O9 S2P 21 21 2112.6647; 15.6022; 17.2534
90; 90; 90
3409.2Mohammad S. Askari; MaylisOriob; Xavier Ottenwaelder
Controlled nitrene transfer from a tyrosinase-like arylnitroso-copper complex
Chem.Commun., 2015, 51, 11206
7117395 CIFC29 H44 Cl2 Cu F3 N4 O6 SP b c n34.9331; 10.1199; 20.5135
90; 90; 90
7251.9Mohammad S. Askari; MaylisOriob; Xavier Ottenwaelder
Controlled nitrene transfer from a tyrosinase-like arylnitroso-copper complex
Chem.Commun., 2015, 51, 11206
7117396 CIFC39 H41 Mn N8 O7 UI 1 2/a 125.9044; 13.2058; 23.7598
90; 99.772; 90
8010Lucile Chatelain; Floriana Tuna; Jacques Pecaut; Marinella Mazzanti
A zig-zag uranyl(V)-Mn(II) single chain magnet with a high relaxation barrier
Chem.Commun., 2015, 51, 11309
7117397 CIFC44 H56 Co N4 O4 UP 4215.8348; 15.8348; 16.3777
90; 90; 90
4106.56Lucile Chatelain; Floriana Tuna; Jacques Pecaut; Marinella Mazzanti
A zig-zag uranyl(V)-Mn(II) single chain magnet with a high relaxation barrier
Chem.Commun., 2015, 51, 11309
7117398 CIFC13 H12 N3 O2.5P b c n23.2307; 11.1515; 9.2568
90; 90; 90
2398.04Hai Qian; Ivan Aprahamian
An emissive and pH switchable hydrazone-based hydrogel
Chem.Commun., 2015, 51, 11158
7117399 CIFC14 H12 N2 O2P -15.032; 9.7091; 12.6168
89.6; 89.102; 79.669
606.34Hai Qian; Ivan Aprahamian
An emissive and pH switchable hydrazone-based hydrogel
Chem.Commun., 2015, 51, 11158
7117400 CIFC18 H76 Cu9 N36 O88 P2 W18P 63/m20.64; 20.64; 14.742
90; 90; 120
5439Yan-Qing Jiao; Hong-Ying Zang; Xin-Long Wang; En-Long Zhou; Bai-Qiao Song; Chun-Gang Wang; Kui-Zhan Shao; Zhong-Min Su
Self-assembled arrays of polyoxometalate-based metal-organic nanotubes for proton conduction and magnetism
Chem.Commun., 2015, 51, 11313
7117401 CIFC18 H23 N O7 SP 1 21 19.5125; 13.887; 14.68
90; 90.249; 90
1939.2Shizhou Liu; Mengchao Tong; Yang Yu; Hexin Xie; Hao Li; Wei Wang
Construction of an all-carbon quaternary stereocenter by organocatalytic enantioselective alpha-functionalization of alpha-substituted beta-ketocarbonyls with electron deficient vinylarenes
Chem.Commun., 2015, 51, 11221
7117403 CIFC23 H31 NP -19.3731; 9.7689; 11.5285
85.605; 74.318; 69.692
952.97Yuya Suzuki; Masato Kageyama; Ryuichi Morisawa; Yasuo Dobashi; Hiroshi Hasegawa; Satoshi Yokojima; Osamu Kitagawa
The synthesis of optically active N-C axially chiral tetrahydroquinoline and its response to an acid-accelerated molecular rotor
Chem.Commun., 2015, 51, 11229
7117404 CIFC29 H24 Cl N O5P 21 21 216.6033; 13.917; 27.99
90; 90; 90
2572.2Guofeng Li; Wangsheng Sun; Jingyi Li; Fengjing Jia; Liang Hong; Rui Wang
Organocatalytic enantioselective formal arylation of azlactones using quinones as the aromatic partner
Chem.Commun., 2015, 51, 11280
7117405 CIFC H8 I3 N O PbP 1 21/m 110.469; 4.6557; 11.214
90; 101.251; 90
536.07Gregory H. Imler; Xia Li; Bolei Xu; Graham E. Dobereiner; Hai-Lung Dai; Yi Rao; Bradford B. Wayland
Solid state transformation of the crystalline monohydrate (CH3NH3)PbI3(H2O) to the (CH3NH3)PbI3 perovskite
Chem.Commun., 2015, 51, 11290
7117406 CIFC93.14 H86.24 Br11.98 Cl1.87 N24 O3.42 Zn5.99C 1 2 133.964; 14.5897; 33.787
90; 104.936; 90
16177Timothy R. Ramadhar; Shao-Liang Zheng; Yu-Sheng Chen; Jon Clardy
The crystalline sponge method: MOF terminal ligand effects
Chem.Commun., 2015, 51, 11252
7117407 CIFC95.1 H90 Cl13.31 N24 O3.78 Zn6C 1 2 133.391; 14.3975; 33.897
90; 105.272; 90
15720.4Timothy R. Ramadhar; Shao-Liang Zheng; Yu-Sheng Chen; Jon Clardy
The crystalline sponge method: MOF terminal ligand effects
Chem.Commun., 2015, 51, 11252
7117408 CIFC26 H41 N2 O5 P Si3 WP n a 2120.7398; 9.2018; 17.6394
90; 90; 90
3366.36Nora C. Breit; Tibor Szilvasi; Shigeyoshi Inoue
Facile rotation around a silicon-phosphorus double bond enabled through coordination to tungsten
Chem.Commun., 2015, 51, 11272
7117409 CIFC52 H82 N4 O10 P2 Si6 W2I 1 2/a 118.8405; 10.1491; 34.9207
90; 92.318; 90
6671.87Nora C. Breit; Tibor Szilvasi; Shigeyoshi Inoue
Facile rotation around a silicon-phosphorus double bond enabled through coordination to tungsten
Chem.Commun., 2015, 51, 11272
7117410 CIFC12 H13 N O2P 1 21/c 19.1916; 12.6389; 9.1878
90; 100.21; 90
1050.5Yanxin Yang; Maotong Xu; Datong Song
Organocatalysts with carbon-centered activity for CO2 reduction with boranes
Chem.Commun., 2015, 51, 11293
7117411 CIFC52 H45 N5 O3 ZnC 1 2/c 124.4775; 12.968; 26.5412
90; 94.383; 90
8400.2MiLosz Pawlicki; Karolina Hurej; Katarzyna Kwiecinska; Ludmila Szterenberg; Lechoslaw Latos-Grazynski
A fused meso-aminoporphyrin: a switchable near-IR chromophore
Chem.Commun., 2015, 51, 11362
7117412 CIFC26 H22 N3 O4P 21 21 216.9776; 12.8353; 25.7684
90; 90; 90
2307.81Tianyu Huang; Lili Lin; Xiaolei Hu; Jianfeng Zheng; Xiaohua Liu; Xiaoming Feng
Kinetic resolution of 2,3-epoxy 3-aryl ketones via catalytic asymmetric ring-opening with pyrazole derivatives
Chem.Commun., 2015, 51, 11374
7117414 CIFC16 H37 Fe N10 Ni O6C 1 2/m 113.863; 12.502; 10.093
90; 133.02; 90
1278.92Beata Nowicka; Mateusz Reczynski; Michal Rams; Wojciech Nitek; Jan Zukrowski; Czeslaw Kapusta; Barbara Sieklucka
Hydration-switchable charge transfer in the first bimetallic assembly based on the [Ni(cyclam)]^3+^ - magnetic CN-bridged chain {(H3O)[Ni^III^(cyclam)][Fe^II^(CN)6]^.^5H2O}n
Chem.Commun., 2015, 51, 11485
7117415 CIFC91 H136 N4 Pt2 Sn2P 1 21/c 115.6296; 19.9002; 30.4007
90; 100.5; 90
9297.3Christian P. Sindlinger; Lars Wesemann
Dimeric platinum-stannylene complexes by twofold ligand transfer from an NHC adduct to an organotin(II) hydride
Chem.Commun., 2015, 51, 11421
7117416 CIFC18 H22 F6 N3 P PtP 1 21/c 110.9042; 12.0936; 15.9712
90; 93.73; 90
2101.68Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117417 CIFC19 H22 F6 N3 O P PtP -19.141; 9.5731; 13.2139
108.296; 97.486; 95.712
1076.33Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117418 CIFC21 H26 F6 N3 O2 P PtP 1 21/n 110.94969; 14.36; 15.746
90; 96.7748; 90
2458.57Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117419 CIFC15 H21 I N2 O2 PtP 1 21/n 111.1595; 11.6084; 13.5382
90; 103.102; 90
1708.1Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117420 CIFC21 H24 N2 O2 Pt SP 1 21/c 114.3479; 9.0481; 16.1964
90; 109.574; 90
1981.12Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117421 CIFC25 H27 N2 O6 Pt SP -17.2201; 13.2276; 14.0336
70.675; 80.551; 84.13
1245.94Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117422 CIFC118 H143 Mg3 N12P 63/m15.9267; 15.9267; 24.086
90; 90; 120
5291.1Jani O. Moilanen; Benjamin M. Day; Thomas Pugh; Richard A. Layfield
Open-shell doublet character in a hexaazatrinaphthylene trianion complex
Chem.Commun., 2015, 51, 11478
7117423 CIFC22 H19 Cl2 F6 N O3 S2 SbP -19.106; 10.58; 15.856
102.819; 97.906; 112.771
1330.3S. Menichetti; S. Cecchi; P. Procacci; M. Innocenti; L. Becucci; L. Franco; C. Viglianisi
Thia-bridged triarylamine heterohelicene radical cations as redox-driven molecular switches
Chem.Commun., 2015, 51, 11452
7117424 CIFC21 H17 N O3 S2P b c a10.641; 14.807; 23.076
90; 90; 90
3635.9S. Menichetti; S. Cecchi; P. Procacci; M. Innocenti; L. Becucci; L. Franco; C. Viglianisi
Thia-bridged triarylamine heterohelicene radical cations as redox-driven molecular switches
Chem.Commun., 2015, 51, 11452
7117425 CIFC21 H17 F6 N S2 SbP 1 21/n 18.543; 15.622; 16.383
90; 94.989; 90
2178.2S. Menichetti; S. Cecchi; P. Procacci; M. Innocenti; L. Becucci; L. Franco; C. Viglianisi
Thia-bridged triarylamine heterohelicene radical cations as redox-driven molecular switches
Chem.Commun., 2015, 51, 11452
7117426 CIFC24 H22 O SiP 1 c 18.624; 15.417; 7.309
90; 104.681; 90
940.1Ryo Shintani; Hiroki Kurata; Kyoko Nozaki
Rhodium-catalyzed intramolecular alkynylsilylation of alkynes
Chem.Commun., 2015, 51, 11378
7117427 CIFC58 H64 Cl Mg N2 O SbP 1 21/n 113.7235; 16.6434; 23.277
90; 106.733; 90
5091.5Alexander Hinz; Axel Schulz; Alexander Villinger
Accessing heavy allyl-analogous [(TerN)2E]- (E = Sb, Bi) ions and their reactivity towards ECl3
Chem.Commun., 2015, 51, 11437
7117428 CIFC58 H64 Bi Cl Mg N2 OP 1 21/n 113.7359; 16.6363; 23.257
90; 106.645; 90
5091.9Alexander Hinz; Axel Schulz; Alexander Villinger
Accessing heavy allyl-analogous [(TerN)2E]- (E = Sb, Bi) ions and their reactivity towards ECl3
Chem.Commun., 2015, 51, 11437
7117429 CIFC48 H50 Bi Cl2 N2 SbP b c a14.6206; 15.5222; 18.7038
90; 90; 90
4244.7Alexander Hinz; Axel Schulz; Alexander Villinger
Accessing heavy allyl-analogous [(TerN)2E]- (E = Sb, Bi) ions and their reactivity towards ECl3
Chem.Commun., 2015, 51, 11437
7117435 CIFC13 H10 N2 OC 1 2/c 117.9438; 6.3301; 19.758
90; 113.492; 90
2058.2Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit
KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones.
Chemical communications (Cambridge, England), 2015, 51, 11658-11661
7117436 CIFC13 H12 N2 OC 1 2/c 118.9282; 6.0959; 20.6755
90; 116.768; 90
2130Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit
KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones.
Chemical communications (Cambridge, England), 2015, 51, 11658-11661
7117437 CIFC13 H11 Cl N2 OP 1 21 113.4732; 9.5123; 19.795
90; 109.801; 90
2386.95Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit
KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones.
Chemical communications (Cambridge, England), 2015, 51, 11658-11661
7117438 CIFC14 H14 N2 O SC 1 2/c 120.924; 5.7267; 23.879
90; 112.393; 90
2645.5Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit
KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones.
Chemical communications (Cambridge, England), 2015, 51, 11658-11661
7117439 CIFC17 H15 Fe N3C 1 2/c 135.793; 5.7087; 13.346
90; 99.709; 90
2687.9Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit
KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones.
Chemical communications (Cambridge, England), 2015, 51, 11658-11661
7117440 CIFC22 H17 N O4P -17.3977; 11.6656; 20.3981
76.247; 83.564; 88.301
1699.07Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K.
A supramolecular approach for designing emissive solid-state carbazole arrays.
Chemical communications (Cambridge, England), 2015, 51, 11603-11606
7117441 CIFC46.67 H42 Co2 N3.34 O12P 1 21/n 110.148; 14.9006; 28.1544
90; 92.505; 90
4253.2Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K.
A supramolecular approach for designing emissive solid-state carbazole arrays.
Chemical communications (Cambridge, England), 2015, 51, 11603-11606
7117442 CIFC25 H20 Cu N2 O5C 1 2/c 127.7412; 11.114; 15.0069
90; 102.921; 90
4509.7Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K.
A supramolecular approach for designing emissive solid-state carbazole arrays.
Chemical communications (Cambridge, England), 2015, 51, 11603-11606
7117443 CIFC50 H47 N5 O12 Zn2P 21 21 2110.2867; 17.0328; 26.8808
90; 90; 90
4709.8Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K.
A supramolecular approach for designing emissive solid-state carbazole arrays.
Chemical communications (Cambridge, England), 2015, 51, 11603-11606
7117444 CIFC39 H37 Cl N2 O5 SiP -19.8459; 10.5371; 19.8151
94.748; 98.528; 110.714
1881.2Kim, Sooyeon; Fujitsuka, Mamoru; Tohnai, Norimitsu; Tachikawa, Takashi; Hisaki, Ichiro; Miyata, Mikiji; Majima, Tetsuro
The unprecedented J-aggregate formation of rhodamine moieties induced by 9-phenylanthracenyl substitution.
Chemical communications (Cambridge, England), 2015, 51, 11580-11583
7117445 CIFC30 H34 N6 O8P -19.0281; 11.3963; 16.9166
109.458; 90.63; 102.206
1597.7Li, Yi-Jin; Li, Xue; Zhang, Shao-Xiao; Zhao, Yu-Long; Liu, Qun
Copper(ii)-catalyzed oxidative [3+2] cycloaddition reactions of secondary amines with α-diazo compounds: a facile and efficient synthesis of 1,2,3-triazoles.
Chemical communications (Cambridge, England), 2015, 51, 11564-11567
7117446 CIFC22 H18 O3P 1 21/c 18.6642; 20.3575; 10.1977
90; 115.123; 90
1628.53Khoobi, Mehdi; Molaverdi, Fatemeh; Jafarpour, Farnaz; Abbasnia, Masoumeh; Kubicki, Maciej; Shafiee, Abbas
A one-pot domino C-H, C-C activation in coumarins: a fast track to 2,3-diaryl benzo[b]furans.
Chemical communications (Cambridge, England), 2015, 51, 11713-11716
7117447 CIFC22 H29 N O6P 21 21 218.4147; 11.96874; 21.5473
90; 90; 90
2170.1Zhou, Yuhang; Lin, Lili; Yin, Chengkai; Wang, Zhengmeng; Liu, Xiaohua; Feng, Xiaoming
The N,N'-dioxide/Ni(ii)-catalyzed asymmetric inverse-electron-demand hetero-Diels-Alder reaction of methyleneindolinones with hetero-substituted alkenes.
Chemical communications (Cambridge, England), 2015, 51, 11689-11692
7117448 CIFC30 H49 N O Si2P -112.502; 15.8137; 17.4136
74.497; 75.487; 76.75
3162.7Liu, Yan-Hua; Liu, Yue-Jin; Yan, Sheng-Yi; Shi, Bing-Feng
Ni(ii)-catalyzed dehydrative alkynylation of unactivated (hetero)aryl C-H bonds using oxygen: a user-friendly approach.
Chemical communications (Cambridge, England), 2015, 51, 11650-11653
7117449 CIFC54 H50 Cl0 Cu2 F0 N6 P2C 1 2/c 126.589; 17.564; 29.171
90; 106.352; 90
13072.1Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117450 CIFC144 H124 B4 Cl0 Cu4 F16 N12 O0 P4P -115.189; 15.957; 23.446
107.923; 101.304; 104.447
5001.1Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117451 CIFC172 H140 B0 Cl0 Cu4 F0 N12 P4P -115.705; 17.816; 21.535
107.871; 104.457; 97.386
5413.8Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117452 CIFC176 H148 B4 Cl0 Cu4 F16 N12 P4P -115.582; 17.047; 22.619
102.262; 104.435; 102.171
5460.5Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117453 CIFC146 H128 B4 Cl12 Cu4 F16 N12 P4P -113.887; 15.375; 18.799
101.562; 105.589; 101.967
3639.7Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117454 CIFC108 H102 B0 Cl0 Cu4 F0 N12 P4C 1 2/c 125.7551; 20.5086; 24.6987
90; 95.409; 90
12987.8Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117455 CIFC17 H20 N2 O2P -19.074; 9.586; 10.271
105.491; 97.554; 108.975
790.5García-González, Ma Carmen; Hernández-Vázquez, Eduardo; Gordillo-Cruz, Raúl E; Miranda, Luis D.
Ugi-derived dehydroalanines as a pivotal template in the diversity oriented synthesis of aza-polyheterocycles.
Chemical communications (Cambridge, England), 2015, 51, 11669-11672
7117456 CIFC18 H22 N2 O2P 1 21/c 19.1496; 9.3085; 19.945
90; 95.325; 90
1691.4García-González, Ma Carmen; Hernández-Vázquez, Eduardo; Gordillo-Cruz, Raúl E; Miranda, Luis D.
Ugi-derived dehydroalanines as a pivotal template in the diversity oriented synthesis of aza-polyheterocycles.
Chemical communications (Cambridge, England), 2015, 51, 11669-11672
7117457 CIFC21 H22 N2 O2P -19.2332; 10.3088; 10.7141
105.017; 100.269; 102.043
933.7García-González, Ma Carmen; Hernández-Vázquez, Eduardo; Gordillo-Cruz, Raúl E; Miranda, Luis D.
Ugi-derived dehydroalanines as a pivotal template in the diversity oriented synthesis of aza-polyheterocycles.
Chemical communications (Cambridge, England), 2015, 51, 11669-11672
7117458 CIFC27 H18 O6P 131.1904; 31.2132; 51.976
72.71; 77.555; 60.912
42068Zentner, Cassandra A.; Lai, Holden W. H.; Greenfield, Joshua T.; Wiscons, Ren A.; Zeller, Matthias; Campana, Charles F.; Talu, Orhan; FitzGerald, Stephen A.; Rowsell, Jesse L. C.
High surface area and Z' in a thermally stable 8-fold polycatenated hydrogen-bonded framework.
Chemical communications (Cambridge, England), 2015, 51, 11642-11645
7117459 CIFC27 H18 O6I 1 2 131.419; 30.116; 45.32
90; 90.412; 90
42881Zentner, Cassandra A.; Lai, Holden W. H.; Greenfield, Joshua T.; Wiscons, Ren A.; Zeller, Matthias; Campana, Charles F.; Talu, Orhan; FitzGerald, Stephen A.; Rowsell, Jesse L. C.
High surface area and Z' in a thermally stable 8-fold polycatenated hydrogen-bonded framework.
Chemical communications (Cambridge, England), 2015, 51, 11642-11645
7117460 CIFC21 H26 O3P 21 21 215.7682; 7.7444; 39.9505
90; 90; 90
1784.64Akira Matsumoto; Keisuke Asano; Seijiro Matsubara
A chiral phosphoric acid catalyst for asymmetric construction of 1,3-dioxanes
Chem.Commun., 2015, 51, 11693
7117465 CIFC48 H88 N12 O12P 21 21 219.4643; 19.6586; 31.9809
90; 90; 90
5950.2Julien Maury; Bryden A. F. Le Bailly; James Raftery; Jonathan Clayden
Conformational cooperativity between helical domains of differing geometry in oligoamide-oligourea foldamer chimeras
Chem.Commun., 2015, 51, 11802
7117466 CIFC27 H27 N3 O9 SP -18.3006; 9.3862; 17.717
86.352; 87.532; 77.772
1345.68Cong-Shuai Wang; Ren-Yi Zhu; Yu-Chen Zhang; Feng Shi
Catalytic chemoselective [3+3] cycloadditions of azomethine ylides with quinone monoimides leading to the construction of a dihydrobenzoxazine scaffold
Chem.Commun., 2015, 51, 11798
7117467 CIFC28 H21 Cl2 N3 O7 SP -18.4575; 12.5061; 13.4396
80.3987; 85.8752; 78.3825
1371.8Cong-Shuai Wang; Ren-Yi Zhu; Yu-Chen Zhang; Feng Shi
Catalytic chemoselective [3+3] cycloadditions of azomethine ylides with quinone monoimides leading to the construction of a dihydrobenzoxazine scaffold
Chem.Commun., 2015, 51, 11798
7117468 CIFC35 H36 Br N3 O3 SP 1 21 19.4805; 15.3417; 11.8162
90; 111.93; 90
1594.3Chao-You Liu; Fu-She Han
Organocatalytic asymmetric reaction of indol-2-yl carbinols with enamides: synthesis of chiral 2-indole-substituted 1,1-diarylalkanes
Chem.Commun., 2015, 51, 11844
7117469 CIFC31 H10 Al F36 N O4 SP 1 21/c 114.2945; 19.666; 19.9786
90; 134.333; 90
4017.3Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang
Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures
Chem.Commun., 2015, 51, 11822
7117470 CIFC69.8 H27.6 Al2 Cl3.61 F72 N2 O8 S2P 1 21/n 113.604; 20.135; 16.634
90; 93.113; 90
4549.6Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang
Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures
Chem.Commun., 2015, 51, 11822
7117471 CIFC71.56 H27.11 Al2 Cl3.11 F72 N2 O8 S2P 1 21/c 110.415; 15.3696; 28.611
90; 93.362; 90
4572Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang
Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures
Chem.Commun., 2015, 51, 11822
7117472 CIFC62 H24 Al2 F72 N2 O8P 1 21/c 127.656; 11.298; 25.57
90; 94.846; 90
7961Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang
Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures
Chem.Commun., 2015, 51, 11822
7117473 CIFC96 H109 Cl Li N4 O6 P4 Pd YP -113.4049; 15.2317; 22.79
99.348; 98.546; 99.455
4455Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117474 CIFC96 H109 Cl Li Lu N4 O6 P4 PdP 1 21/n 113.559; 28.87; 22.627
90; 90.84; 90
8856Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117475 CIFC96 H109 Cl Li Lu N4 O6 P4 PdP -113.332; 15.349; 21.771
88.53; 80.9; 83.96
4374.4Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117476 CIFC94.4 H105.8 Cl Li Lu N4 O5.6 P4 PdP -113.414; 15.386; 22.048
88.38; 80.4; 84.17
4463.2Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117477 CIFC124 H124 Li N6 O4 P6 Pd2 YP 1 21/c 128.427; 14.576; 29.04
90; 106.14; 90
11559Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117478 CIFC124 H124 Li Lu N6 O4 P6 Pd2P 1 21/c 128.3174; 14.561; 29.0288
90; 105.984; 90
11506.7Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117479 CIFC100 H116 Li N4 O7 P4 YP 1 21/c 114.911; 24.635; 26.155
90; 104.1; 90
9318Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761

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