Crystallography Open Database

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7116816 CIFC20 H29 N O7P 1 21 114.4045; 6.2322; 23.4872
90; 103.762; 90		2048Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664
7116817 CIFC24 H31 N O7P 1 21 113.74; 6.188; 15.056
90; 113.998; 90		1169.5Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664
7116818 CIFC20 H29 N O7P 1 21 114.634; 6.2305; 11.855
90; 102.86; 90		1053.8Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664
7116819 CIFC32 H24 B2 N2P 1 21/n 19.938; 15.052; 16.599
90; 94.82; 90		2474.2Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116820 CIFC24 H18 B2 N2 SP -19.492; 10.356; 10.494
76.69; 80.05; 77.48		971.7Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116821 CIFC28 H25 B N2P n a 2111.268; 23.152; 8.5403
90; 90; 90		2228Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116822 CIFC20 H17 B N2P -110.344; 17.825; 18.052
94.99; 98.18; 90.06		3281.8Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116823 CIFC30 H38 N2 O5 S2P 1 21 113.0848; 13.5713; 16.2698
90; 94.205; 90		2881.38Yi Li; Marcel Hartmann; Constantin Gabriel Daniliuc; Armido Studer
Radical aminooxygenation of alkenes with N-fluoro-benzenesulfonimide (NFSI) and TEMPONa
Chem.Commun., 2015, 51, 5706
7116824 CIFC35 H47 I N2 ZnP n a m13.0009; 24.7338; 10.817
90; 90; 90		3478.33Matthew P. Blake; Nikolas Kaltsoyannis; Philip Mountford
Synthesis, molecular and electronic structure, and reactions of a Zn-Hg-Zn bonded complex
Chem.Commun., 2015, 51, 5743
7116825 CIFC36 H46 Fe N2 O2 ZnP b c a20.9493; 14.21072; 22.37442
90; 90; 90		6660.97Matthew P. Blake; Nikolas Kaltsoyannis; Philip Mountford
Synthesis, molecular and electronic structure, and reactions of a Zn-Hg-Zn bonded complex
Chem.Commun., 2015, 51, 5743
7116826 CIFC58 H82 Hg N4 Zn2P 1 21/n 112.784; 17.3101; 13.0055
90; 101.117; 90		2824.01Matthew P. Blake; Nikolas Kaltsoyannis; Philip Mountford
Synthesis, molecular and electronic structure, and reactions of a Zn-Hg-Zn bonded complex
Chem.Commun., 2015, 51, 5743
7116827 CIFC39 H45 Br6 N3 O3C 1 2/c 134.3269; 16.0953; 17.3532
90; 115.959; 90		8620.3Ryohei Yamakado; Shin-ichi Matsuoka; Masato Suzuki; Daisuke Takeuchi; Hyuma Masu; Isao Azumaya; Koji Takagi
Diastereoselective cyclization of an aminobenzoic acid derivative and chiroptical properties of triple-stranded helical bis(phenylethynyl)benzene
Chem.Commun., 2015, 51, 5710
7116830 CIFC18 H13 N3 OP 1 21/c 18.3217; 9.5453; 17.1799
90; 100.577; 90		1341.47Sreekumar Pankajakshan; Zhi Guang Chng; Rakesh Ganguly; Teck Peng Loh
Copper-catalyzed aerobic carboxygenation and N-arylation of [1,2,3]triazolo[1,5-a]pyridines towards pyridinium triazolinone ylides
Chem.Commun., 2015, 51, 5929
7116831 CIFC12 H9 N3 OC 1 2/c 111.477; 8.789; 19.955
90; 103.778; 90		1955Sreekumar Pankajakshan; Zhi Guang Chng; Rakesh Ganguly; Teck Peng Loh
Copper-catalyzed aerobic carboxygenation and N-arylation of [1,2,3]triazolo[1,5-a]pyridines towards pyridinium triazolinone ylides
Chem.Commun., 2015, 51, 5929
7116832 CIFC26 H23 NP 1 21/n 115.205; 7.3621; 18.007
90; 96.56; 90		2002.5Jia Zheng; Liangbin Huang; Zun Li; Wanqing Wu; Jianxiao Li; Huanfeng Jiang
Synthesis of 3-bromosubstituted pyrroles via palladium-catalyzed intermolecular oxidative cyclization of bromoalkynes with N-allylamines
Chem.Commun., 2015, 51, 5894
7116833 CIFC30 H22 O2P -111.7482; 13.7728; 15.9289
102.716; 104.883; 113.218		2134.1Shohei Eda; Fumiaki Eguchi; Hiroshi Haneda; Toshiyuki Hamura
A new synthetic route to substituted tetracenes and pentacenes via stereoselective [4+2] cycloadditions of 1,4-dihydro-1,4-epoxynaphthalene and isobenzofuran
Chem.Commun., 2015, 51, 5963
7116834 CIFC30 H22 O2P -110.448; 12.7886; 16.6149
84.832; 71.771; 84.18		2093.72Shohei Eda; Fumiaki Eguchi; Hiroshi Haneda; Toshiyuki Hamura
A new synthetic route to substituted tetracenes and pentacenes via stereoselective [4+2] cycloadditions of 1,4-dihydro-1,4-epoxynaphthalene and isobenzofuran
Chem.Commun., 2015, 51, 5963
7116835 CIFC42 H30 O2P 1 21/c 110.5584; 9.542; 29.2511
90; 91.525; 90		2945.95Shohei Eda; Fumiaki Eguchi; Hiroshi Haneda; Toshiyuki Hamura
A new synthetic route to substituted tetracenes and pentacenes via stereoselective [4+2] cycloadditions of 1,4-dihydro-1,4-epoxynaphthalene and isobenzofuran
Chem.Commun., 2015, 51, 5963
7116836 CIFC43 H38 Cl2 Li N8 O2 ScP -112.0145; 13.1895; 14.9239
64.581; 70.692; 88.526		1997Rachel H. Platel; Thiago Teixeira Tasso; Wen Zhou; Taniyuki Furuyama; Nagao Kobayashi; Daniel B. Leznoff
Metallophthalocyanin-ocenes: scandium phthalocyanines with an eta^5^-bound Cp ring
Chem.Commun., 2015, 51, 5986
7116837 CIFC37 H21 N8 ScP -18.976; 15.873; 19.618
83.59; 86.358; 83.85		2758Rachel H. Platel; Thiago Teixeira Tasso; Wen Zhou; Taniyuki Furuyama; Nagao Kobayashi; Daniel B. Leznoff
Metallophthalocyanin-ocenes: scandium phthalocyanines with an eta^5^-bound Cp ring
Chem.Commun., 2015, 51, 5986
7116838 CIFC45 H37 N8 O0.75 ScP b c m16.1402; 21.4116; 21.6902
90; 90; 90		7495.9Rachel H. Platel; Thiago Teixeira Tasso; Wen Zhou; Taniyuki Furuyama; Nagao Kobayashi; Daniel B. Leznoff
Metallophthalocyanin-ocenes: scandium phthalocyanines with an eta^5^-bound Cp ring
Chem.Commun., 2015, 51, 5986
7116839 CIFC32 H26 N4 Ni S2P b c a18.0049; 9.0457; 32.7494
90; 90; 90		5333.8Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116840 CIFC32 H26 N4 Ni S2P -19.7891; 11.7331; 12.5712
104.486; 99.689; 102.531		1326.3Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116841 CIFC32 H24 N4 Ni S2P -19.9075; 12.3331; 12.436
64.149; 69.893; 79.482		1283.19Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116842 CIFC33 H27 Cl3 N4 S2P -18.9232; 12.3869; 14.6782
75.749; 75.097; 86.521		1519.57Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116843 CIFC64 H48 N8 S4 Zn2P 1 21/n 115.1355; 14.9332; 24.9048
90; 106.399; 90		5400Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116844 CIFC205 H172 N24 O4 S12 Zn6P -113.3649; 18.2896; 18.8109
96.448; 99.538; 94.693		4482.1Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116845 CIFC34 H26 N4 Ni O4P -19.2124; 11.1476; 14.7168
86.166; 76.5; 70.682		1386.77Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116846 CIFC34 H24 N4 Ni O4C 1 2/c 134.4732; 9.868; 7.9143
90; 100.724; 90		2645.28Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116847 CIFC34 H26 N4 O4P 1 2/c 120.8248; 7.2192; 19.4469
90; 105.825; 90		2812.81Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116848 CIFC68 H48 N8 O8 Zn2C 1 2/c 123.8065; 16.6644; 42.744
90; 100.563; 90		16670.1Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116849 CIFC105 H75 Cl9 N12 O12 Zn3C 1 2/c 118.1355; 21.5289; 25.5659
90; 100.008; 90		9830Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116850 CIFC136 H96 N16 O16 Zn4I 2 2 215.3648; 19.7305; 23.6393
90; 90; 90		7166.4Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116851 CIFC136 H96 N16 O16 Zn4I 2 2 215.337; 19.7279; 23.6518
90; 90; 90		7156.2Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116852 CIFC36 H15 As B F15 OP 1 21/n 113.134; 16.309; 14.601
90; 96.167; 90		3109.5Ralf Kather; Tomas Svoboda; Maren Wehrhahn; Elena Rychagova; Enno Lork; Libor Dostal; Sergey Ketkov; Jens Beckmann
Lewis-acid induced disaggregation of dimeric arylantimony oxides
Chem.Commun., 2015, 51, 5932
7116853 CIFC36 H15 B F15 O SbP 1 21/n 112.248; 17.312; 15.058
90; 95.34; 90		3179Ralf Kather; Tomas Svoboda; Maren Wehrhahn; Elena Rychagova; Enno Lork; Libor Dostal; Sergey Ketkov; Jens Beckmann
Lewis-acid induced disaggregation of dimeric arylantimony oxides
Chem.Commun., 2015, 51, 5932
7116854 CIFC30 H19 B F15 N2 O SbP -19.814; 10.784; 16.68
84.08; 87.26; 77.49		1713.6Ralf Kather; Tomas Svoboda; Maren Wehrhahn; Elena Rychagova; Enno Lork; Libor Dostal; Sergey Ketkov; Jens Beckmann
Lewis-acid induced disaggregation of dimeric arylantimony oxides
Chem.Commun., 2015, 51, 5932
7116855 CIFC25 H24 N2 O2 S3P 1 21/n 111.461; 12.938; 15.619
90; 93.48; 90		2311.8Chuan Liu; Qin Yin; Li-Xin Dai; Shu-Li You
Synthesis of pyrroloindolines and furoindolines via cascade dearomatization of indole derivatives with carbenium ion
Chem.Commun., 2015, 51, 5971
7116856 CIFC93 H97 Al N10 O2 UP 1 21/c 121.6483; 15.4318; 24.4807
90; 98.594; 90		8086.5Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116857 CIFC74 H88 Al N9 O3 UP 1 21/n 112.5004; 40.0423; 14.2199
90; 105.173; 90		6869.57Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116858 CIFC124 H124 Li2 N18 O4 U2P -111.963; 14.243; 17.926
99.705; 90.311; 114.231		2736Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116859 CIFC84.47 H84.47 Li0.87 N16.49 O2 UC 1 c 114.2782; 24.4176; 22.8717
90; 90.634; 90		7973.5Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116860 CIFC62 H62 B0 N12 Na O2 UC 1 c 114.427; 24.602; 23.182
90; 90.881; 90		8227Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116861 CIFC77 H76 K N15 O2 UP 21 21 2113.693; 21.7419; 24.2382
90; 90; 90		7216Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116862 CIFC18 H11.33 Co O6.67P -3 1 c16.789; 16.789; 15.144
90; 90; 120		3696.8Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116863 CIFC18 H11.33 Co O6.67R -3 c :H17.431; 17.431; 48.043
90; 90; 120		12641.7Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116864 CIFC18 H11.33 Co O6.67P -3 1 c16.7639; 16.7639; 14.9592
90; 90; 120		3640.7Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116865 CIFC18 H11.33 Co O6.67P -3 1 c16.7335; 16.7335; 14.9637
90; 90; 120		3628.6Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116866 CIFC18 H11.33 Co O6.67R -3 c :H17.2813; 17.2813; 47.354
90; 90; 120		12247.3Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116867 CIFC18 H11.33 Co O6.67R -3 c :H17.3321; 17.3321; 47.616
90; 90; 120		12387.6Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116870 CIFC54 H52P 21 21 2113.2582; 14.2403; 42.561
90; 90; 90		8035.5K. W. J. Heard; J. J. Morrison; L. Weston; C. H. Lo; L. Pirvu; J. Raftery; M. S. Little; J. J. W. McDouall; S. G. Yeates; P. Quayle
An orthogonal C-H borylation - cross-coupling strategy for the preparation of tetrasubstituted 'A2B2'-chrysene derivatives with tuneable photophysical properties
Chem.Commun., 2015, 51, 6115
7116871 CIFC42 H42 Cl2P 1 21/c 115.5669; 11.5716; 18.0171
90; 96.615; 90		3223.9K. W. J. Heard; J. J. Morrison; L. Weston; C. H. Lo; L. Pirvu; J. Raftery; M. S. Little; J. J. W. McDouall; S. G. Yeates; P. Quayle
An orthogonal C-H borylation - cross-coupling strategy for the preparation of tetrasubstituted 'A2B2'-chrysene derivatives with tuneable photophysical properties
Chem.Commun., 2015, 51, 6115
7116872 CIFC20 H8 Cl2 F6P -18.5128; 11.4844; 13.1495
97.59; 96.803; 103.045		1226.68K. W. J. Heard; J. J. Morrison; L. Weston; C. H. Lo; L. Pirvu; J. Raftery; M. S. Little; J. J. W. McDouall; S. G. Yeates; P. Quayle
An orthogonal C-H borylation - cross-coupling strategy for the preparation of tetrasubstituted 'A2B2'-chrysene derivatives with tuneable photophysical properties
Chem.Commun., 2015, 51, 6115
7116873 CIFC34 H45 Fe N2P -110.1306; 11.1529; 13.6025
93.475; 92.686; 101.503		1500.52Shenglai Yao; Tibor Szilvasi; Nils Lindenmaier; Yun Xiong; Shigeyoshi Inoue; Mario Adelhardt; Jorg Sutter; Karsten Meyer; Matthias Driess
Reductive cleavage of P4 by iron(I) centres: synthesis and structural characterisation of Fe2(P2)2 complexes with two bridging P22- ligands
Chem.Commun., 2015, 51, 6153
7116874 CIFC54 H74 Fe2 N4 P4P 1 21/n 114.4521; 12.9461; 14.8567
90; 105.421; 90		2679.6Shenglai Yao; Tibor Szilvasi; Nils Lindenmaier; Yun Xiong; Shigeyoshi Inoue; Mario Adelhardt; Jorg Sutter; Karsten Meyer; Matthias Driess
Reductive cleavage of P4 by iron(I) centres: synthesis and structural characterisation of Fe2(P2)2 complexes with two bridging P22- ligands
Chem.Commun., 2015, 51, 6153
7116875 CIFC43 H69 Fe K0.5 N2 O4 P2P 1 21/c 113.2205; 18.4486; 18.4434
90; 90.303; 90		4498.28Shenglai Yao; Tibor Szilvasi; Nils Lindenmaier; Yun Xiong; Shigeyoshi Inoue; Mario Adelhardt; Jorg Sutter; Karsten Meyer; Matthias Driess
Reductive cleavage of P4 by iron(I) centres: synthesis and structural characterisation of Fe2(P2)2 complexes with two bridging P22- ligands
Chem.Commun., 2015, 51, 6153
7116876 CIFC19 H18 Cl O2P 43 21 211.6351; 11.6351; 48.952
90; 90; 90		6626.9Yang Yang; Jinpeng Li; Biao Du; Changchun Yuan; Bo Liu; Song Qin
An entry to vinylcyclopropane through palladium-catalyzed intramolecular cyclopropanation of alkenes with unstabilized allylic tosylhydrazones
Chem.Commun., 2015, 51, 6179
7116877 CIFC19 H17 Br N2 O3P 21 21 215.613; 16.048; 18.9931
90; 90; 90		1710.8Srimanta Manna; Rishikesh Narayan; Christopher Golz; Carsten Strohmann; Andrey P. Antonchick
Regioselective annulation of nitrosopyridine with alkynes: straightforward synthesis of N-oxide-imidazopyridines
Chem.Commun., 2015, 51, 6119
7116878 CIFC56 H72 S8 Si4C 1 2/c 143.196; 6.377; 24.5113
90; 115.408; 90		6099Kengo Asai; Aiko Fukazawa; Shigehiro Yamaguchi
A cyclic octithiophene containing beta,beta'-linkages
Chem.Commun., 2015, 51, 6096
7116879 CIFC46 H45 B F15 P3 PdP 1 21/n 19.7351; 29.7778; 16.3484
90; 104.943; 90		4579Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116880 CIFC33 H53 Cl P2 PdP 1 21/c 112.3466; 11.6819; 23.5089
90; 91.4208; 90		3389.7Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116881 CIFC36 H61 P3 PdC 1 2/c 128.976; 14.6255; 31.853
90; 106.946; 90		12913Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116882 CIFC54 H61 B F15 P3 PdP 1 21/c 114.7706; 13.9199; 28.5994
90; 93.208; 90		5871Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116883 CIFC60 H58 B F24 P3 PdP 1 21/n 113.1862; 12.7167; 37.1231
90; 94.967; 90		6201.6Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116884 CIFC68 H74 B F24 P3 PdP -113.7002; 17.7228; 18.52
65.531; 74.7; 88.259		3931.8Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116885 CIFC29 H46 O5 SiP -110.3975; 11.144; 13.6268
113.777; 91.585; 102.55		1398.6Hideki Abe; Yuri Horii; Megumi Hagiwara; Toyoharu Kobayashi; Hisanaka Ito
Stereoselective synthesis of a highly oxygenated decahydrocyclopenta[g]chromene derivative: the common tricyclic framework of leucosceptrine and leucosesterterpenone
Chem.Commun., 2015, 51, 6108
7116886 CIFC74 H127 Cl3 Mg3 O11P -114.3956; 15.2219; 18.5435
88.65; 74.452; 85.197		3900.96Baofei Pan; Junjie Zhang; Jinhua Huang; John T. Vaughey; Lu Zhang; Sang-Don Han; Anthony K. Burrell; Zhengcheng Zhang; Chen Liao
A Lewis acid-free and phenolate-based magnesium electrolyte for rechargeable magnesium batteries
Chem.Commun., 2015, 51, 6214
7116887 CIFC16 H12 Cl N O3P -110.3981; 10.4368; 15.4169
78.123; 81.589; 61.978		1442.9Wen-Zhen Zhang; Tian Xia; Xu-Tong Yang; Xiao-Bing Lu
Synthesis of oxazolidine-2,4-diones by a tandem phosphorus-mediated carboxylative condensation-cyclization reaction using atmospheric carbon dioxide
Chem.Commun., 2015, 51, 6175
7116888 CIFC28 H20 O2P -110.5146; 11.1198; 18.1537
73.905; 80.721; 89.893		2010.6Jing Wang; Dekun Qin; Jingbo Lan; Yangyang Cheng; Shuai Zhang; Qiang Guo; Jie Wu; Di Wu; Jingsong You
Rh-catalysed direct cyclisation of 1,4-naphthoquinone and 9,10-phenanthraquinone with alkyne: facile access to 1,8-dioxapyrenes and 1,12-dioxaperylenes as orange and red-emitting luminophores
Chem.Commun., 2015, 51, 6337
7116889 CIFC29 H31 N O3P 1 21/c 113.186; 14.909; 12.985
90; 110.29; 90		2394.3Kai Zhang; Hang Wang; Jingfeng Zheng; Lei Yu; Hanfeng Ding
Hypervalent iodine mediated alkene difunctionalization of vinylphenols: diastereoselective synthesis of substituted indoles and indolizines
Chem.Commun., 2015, 51, 6399
7116890 CIFC29 H23 Br N2 SP -19.2263; 11.3952; 12.1843
99.988; 101.997; 95.944		1221.01Ying Zhang; Jun-Hao Wang; Ji Zheng; Dan Li
A Br-substituted phenanthroimidazole derivative with aggregation induced emission from intermolecular halogen-hydrogen interactions
Chem.Commun., 2015, 51, 6350
7116891 CIFC29 H24 N2 SP 1 21/n 18.6586; 22.4244; 12.0588
90; 100.455; 90		2302.51Ying Zhang; Jun-Hao Wang; Ji Zheng; Dan Li
A Br-substituted phenanthroimidazole derivative with aggregation induced emission from intermolecular halogen-hydrogen interactions
Chem.Commun., 2015, 51, 6350
7116892 CIFC28 H28 Cl N O9P -111.5552; 11.6532; 11.9655
77.69; 68.849; 63.172		1338.48Marie Cordier; Aurelie Dos Santos; Laurent El Kaim; Noisette Narboni
Passerini/Tsuji-Trost strategies towards achieving lactams and cyclopentane derivatives
Chem.Commun., 2015, 51, 6411
7116893 CIFC19 H20 I N OP 1 21/c 110.6819; 9.4115; 17.492
90; 92.723; 90		1756.5Renhong Sun; Jun Liu; Shuang Yang; Ming Chen; Ning Sun; Haoyi Chen; Xin Xie; Xu You; Shi Li; Yuanhong Liu
Cp2TiCl2-catalyzed cis-hydroalumination of propargylic amines with Red-Al: stereoselective synthesis of Z-configured allylic amines
Chem.Commun., 2015, 51, 6426
7116894 CIFC16 H26 Al O4 TiP -19.6563; 9.8287; 10.6494
64.408; 74.407; 73.803		862.5Renhong Sun; Jun Liu; Shuang Yang; Ming Chen; Ning Sun; Haoyi Chen; Xin Xie; Xu You; Shi Li; Yuanhong Liu
Cp2TiCl2-catalyzed cis-hydroalumination of propargylic amines with Red-Al: stereoselective synthesis of Z-configured allylic amines
Chem.Commun., 2015, 51, 6426
7116895 CIFC18 H16 O3 S3P -14.5264; 13.238; 14.614
85.804; 82.143; 84.097		861.3Hai-Bin Yang; Yu-Chao Yuan; Yin Wei; Min Shi
Amine-catalyzed tunable reactions of allenoates with dithioesters: formal [4+2] and [2+2] cycloadditions for the synthesis of 2,3-dihydro-1,4-oxathiines and enantioenriched thietanes
Chem.Commun., 2015, 51, 6430
7116896 CIFC22 H27 N O4 SC 1 2/c 131.687; 6.2286; 23.0782
90; 106.427; 90		4368.9Hai-Bin Yang; Yu-Chao Yuan; Yin Wei; Min Shi
Amine-catalyzed tunable reactions of allenoates with dithioesters: formal [4+2] and [2+2] cycloadditions for the synthesis of 2,3-dihydro-1,4-oxathiines and enantioenriched thietanes
Chem.Commun., 2015, 51, 6430
7116897 CIFC212.07 H84 Cl4 O66.07 Ru11.36P -116.3234; 16.3914; 18.3063
64.293; 83.74; 83.301		4373.8Chia-Hsiang Chen; Amineh Aghabali; Catalina Suarez; Marilyn M. Olmstead; Alan L. Balch; Luis Echegoyen
Synthesis and characterization of bis-triruthenium cluster derivatives of an all equatorial [60]fullerene tetramalonate
Chem.Commun., 2015, 51, 6489
7116898 CIFC97 H40 O25 Ru3P 1 21/c 122.538; 34.0435; 18.4298
90; 92.787; 90		14124Chia-Hsiang Chen; Amineh Aghabali; Catalina Suarez; Marilyn M. Olmstead; Alan L. Balch; Luis Echegoyen
Synthesis and characterization of bis-triruthenium cluster derivatives of an all equatorial [60]fullerene tetramalonate
Chem.Commun., 2015, 51, 6489
7116899 CIFC37 H25 N2 O4 ZnP -19.8824; 11.548; 15.648
89.784; 76.441; 75.603		1678.7Suresh Sanda; Srinivasulu Parshamoni; Soumava Biswas; Sanjit Konar
Highly selective detection of palladium and picric acid by a luminescent MOF: a dual functional fluorescent sensor
Chem.Commun., 2015, 51, 6576
7116900 CIFC31 H39 Cl2 N3 NiP 21 21 2113.6222; 14.2676; 15.7854
90; 90; 90		3068Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116901 CIFC32 H39 Br2 Cl2 N3 NiP 1 21/n 19.787; 26.3927; 13.7739
90; 108.906; 90		3365.9Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116902 CIFC39 H47 Cl N3 Ni O2P -19.7349; 12.3308; 15.6197
87.49; 75.776; 85.562		1811.45Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116903 CIFC39 H47 Br N3 Ni O2P -19.8908; 12.3807; 15.5767
86.987; 75.727; 85.167		1841Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116904 CIFC37 H49 Br N3 Ni O1.5P -19.7274; 14.232; 14.9719
111.974; 99.695; 101.376		1816.3Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116905 CIFC44 H44 Cu5 N6 O14P 1 21/n 16.2137; 16.2226; 22.6452
90; 91.2531; 90		2282.1Christian Plenk; Jasmin Krause; Martin Beck; Eva Rentschler
Rational linkage of magnetic molecules using click chemistry
Chem.Commun., 2015, 51, 6524
7116906 CIFC23 H17 F3 O SP -19.4049; 10.3048; 10.563
79.807; 74.337; 82.314		966.1Dao-Qian Chen; Pin Gao; Ping-Xin Zhou; Xian-Rong Song; Yi-Feng Qiu; Xue-Yuan Liu; Yong-Min Liang
Regioselective access to CF3S-substituted dihydrofurans from homopropargylic alcohols with trifluoromethanesulfenamide
Chem.Commun., 2015, 51, 6637
7116907 CIFC64 H82 N8 S8P -4 3 n22.6217; 22.6217; 22.6217
90; 90; 90		11576.5Yunus Zorlu; Ufuk Kumru; Umit Isci; Burcin Divrik; Erwann Jeanneau; Florian Albrieux; Yavuz Dede; Vefa Ahsen; Fabienne Dumoulin
1,4,8,11,15,18,22,25-Alkylsulfanyl phthalocyanines: effect of macrocycle distortion on spectroscopic and packing properties
Chem.Commun., 2015, 51, 6580
7116908 CIFC80 H114 N8 S8P -112.7956; 17.1258; 18.8008
112.281; 91.994; 94.129		3793.8Yunus Zorlu; Ufuk Kumru; Umit Isci; Burcin Divrik; Erwann Jeanneau; Florian Albrieux; Yavuz Dede; Vefa Ahsen; Fabienne Dumoulin
1,4,8,11,15,18,22,25-Alkylsulfanyl phthalocyanines: effect of macrocycle distortion on spectroscopic and packing properties
Chem.Commun., 2015, 51, 6580
7116909 CIFC12 H9 N3 O2P b c a11.5359; 15.7377; 23.975
90; 90; 90		4352.6Cheng Xu; Feng-Cheng Jia; Qun Cai; Deng-Kui Li; Zhi-Wen Zhou; An-Xin Wu
Intramolecular decarboxylative coupling as the key step in copper-catalyzed domino reaction: facile access to 2-(1,3,4-oxadiazol-2-yl)aniline derivatives
Chem.Commun., 2015, 51, 6629
7116910 CIFC25 H19 N OP c a 2113.273; 18.584; 7.3811
90; 90; 90		1820.7Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116911 CIFC24 H32 Cl NP 21 21 217.0083; 8.9587; 32.914
90; 90; 90		2066.5Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116912 CIFC20 H20 F3 N OP -110.018; 10.446; 35.11
83.334; 86.119; 76.252		3542Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116913 CIFC21 H31 Cl N O2P -17.085; 12.661; 12.767
94.479; 93.887; 100.786		1117.6Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116914 CIFC22 H19 N2P 1 21/n 19.7108; 11.3687; 14.8851
90; 97.059; 90		1630.85Likui Xiang; Yanning Niu; Xiaobo Pang; Xiaodong Yang; Rulong Yan
I2-catalyzed synthesis of substituted imidazoles from vinyl azides and benzylamines
Chem.Commun., 2015, 51, 6598
7116915 CIFC12 H14 Br N OP b c a8.8904; 13.0832; 19.2524
90; 90; 90		2239.3Rahul Kisan Kawade; Deepak B. Huple; Rong-Jing Lin; Rai-Shung Liu
Cu-catalyzed oxidative Povarov reactions between N-alkyl N-methylanilines and saturated oxa- and thiacycles
Chem.Commun., 2015, 51, 6625
7116916 CIFC16 H14 Co2 O7P -18.893; 16.495; 19.797
101.28; 102.13; 103.697		2664.8Pierangelo Gobbo; Tommaso Romagnoli; Stephanie M. Barbon; Jacquelyn T. Price; Jennifer Keir; Joe B. Gilroy; Mark S. Workentin
Expanding the scope of strained-alkyne chemistry: a protection-deprotection strategy via the formation of a dicobalt-hexacarbonyl complex
Chem.Commun., 2015, 51, 6647
7116917 CIFC16 H14 Co2 O7P -19.074; 12.983; 16.699
110.879; 96.205; 98.023		1793.4Pierangelo Gobbo; Tommaso Romagnoli; Stephanie M. Barbon; Jacquelyn T. Price; Jennifer Keir; Joe B. Gilroy; Mark S. Workentin
Expanding the scope of strained-alkyne chemistry: a protection-deprotection strategy via the formation of a dicobalt-hexacarbonyl complex
Chem.Commun., 2015, 51, 6647
7116918 CIFC23 H17 Co2 N O11C 1 2/c 139.343; 8.101; 16.72
90; 110.966; 90		4976Pierangelo Gobbo; Tommaso Romagnoli; Stephanie M. Barbon; Jacquelyn T. Price; Jennifer Keir; Joe B. Gilroy; Mark S. Workentin
Expanding the scope of strained-alkyne chemistry: a protection-deprotection strategy via the formation of a dicobalt-hexacarbonyl complex
Chem.Commun., 2015, 51, 6647
7116919 CIFC28 H17 OP b c n11.6165; 12.7592; 12.4644
90; 90; 90		1847.44Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116920 CIFC58.5 H37.5 Cl7.5 O2P -111.5782; 14.3354; 16.4867
96.3005; 101.787; 113.704		2395.88Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116921 CIFC52 H41 OP 1 21/n 110.6594; 21.7535; 16.0991
90; 100.123; 90		3674.93Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116922 CIFC57 H46 Cl15 OP 1 21/c 113.966; 19.591; 21.6636
90; 109.308; 90		5593.9Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116923 CIFC21 H22 N2 O4 SP 1 21/c 113.153; 17.8912; 9.1269
90; 109.86; 90		2020Xin-Hua Hao; Pin Gao; Xian-Rong Song; Yi-Feng Qiu; Dong-Po Jin; Xue-Yuan Liu; Yong-Min Liang
Metal-free nitro-carbocyclization of 1,6-enynes with tBuONO and TEMPO
Chem.Commun., 2015, 51, 6839
7116924 CIFC45 H40 Ag0 Cl7 F0 N5 O11 P0 Sb U Zn0P -110.3488; 15.1997; 16.7191
89.696; 77.054; 84.978		2552.93Christina M. Davis; Kei Ohkubo; I-Ting Ho; Zhan Zhang; Masatoshi Ishida; Yuanyuan Fang; Vincent M. Lynch; Karl M. Kadish; Jonathan L. Sessler; Shunichi Fukuzumi
Near-infrared-induced electron transfer of an uranyl macrocyclic complex without energy transfer to dioxygen
Chem.Commun., 2015, 51, 6757
7116925 CIFC32 H31 B Fe N7 SP 1 21/n 19.3767; 16.0545; 19.6816
90; 96.784; 90		2942.1M. Sallmann; B. Braun; C. Limberg
Dioxygenation of cysteamine to hypotaurine at a tris(pyrazolyl)borate iron(II) unit - cysteamine dioxygenase mimicking?
Chem.Commun., 2015, 51, 6785
7116926 CIFC36 H52 Eu2 N8 O22P -113.2205; 13.9973; 14.9
99.68; 91.009; 117.103		2405.6Yin-Ling Hou; Hang Xu; Rui-Rui Cheng; Bin Zhao
Controlled lanthanide-organic framework nanospheres as reversible and sensitive luminescent sensors for practical applications
Chem.Commun., 2015, 51, 6769
7116927 CIFC33 H47 N7 O22 Tb2P -113.009; 13.7701; 15.0439
99.513; 90.402; 116.522		2368.1Yin-Ling Hou; Hang Xu; Rui-Rui Cheng; Bin Zhao
Controlled lanthanide-organic framework nanospheres as reversible and sensitive luminescent sensors for practical applications
Chem.Commun., 2015, 51, 6769
7116928 CIFC19 H19 F3 N2P b c a10.9173; 8.53033; 34.7268
90; 90; 90		3234.04Kazuki Isa; Maki Minakawa; Motoi Kawatsura
Palladium-catalyzed amination of 2,3,3-trifluoroallyl esters: synthesis of trifluoromethylenamines via an intramolecular fluorine shift and CF3 group construction
Chem.Commun., 2015, 51, 6761
7116929 CIFC55 H77 Ge N O4 SiP -111.9476; 13.7236; 16.2518
81.454; 83.839; 80.731		2591.21Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116930 CIFC50 H66 Ge N O3 SiP -110.074; 14.516; 18.777
109.23; 96.79; 97.99		2527.7Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116931 CIFC45 H55 Ge N O3 SiP 1 21/n 110.7047; 21.7462; 17.079
90; 92.615; 90		3971.6Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116932 CIFC45 H55 N O3 SiP 1 21/n 112.369; 21.768; 14.724
90; 96.32; 90		3940.3Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116933 CIFC53 H70 Li N O5 SiP 1 21/c 111.531; 24.287; 17.056
90; 98.37; 90		4725.7Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116934 CIFC32 H26 N2 O2P 1 21/c 118.889; 7.1199; 18.6541
90; 104.646; 90		2427.2Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116935 CIFC42 H30 N2P -111.0719; 11.9763; 12.7664
95.06; 92.632; 117.362		1490.4Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116936 CIFC30.3 H25.6 Cl0.6 N4 O2 RhP -19.6401; 11.069; 12.562
82.69; 77.98; 83.72		1295.6Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116937 CIFC30 H21 Cl N2P -18.8053; 11.2771; 12.0975
67.401; 89.113; 83.151		1100.51Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116938 CIFC32 H26 N2 OP 1 21/c 19.9489; 17.1959; 14.4905
90; 109.121; 90		2342.3Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116939 CIFC72 H60 Ag O4 P4 ReR 3 :H14.2192; 14.2192; 51.1145
90; 90; 120		8950F. Deiser; F. Kraus; H. Schmidbaur
Bis(triphenylphosphine)silver(I) perrhenate, a cyclic dimer
Chem.Commun., 2015, 51, 6746
7116940 CIFC72 H60 Ag2 O8 P4 Re2P -112.1764; 12.4966; 13.2647
89.938; 62.745; 68.528		1635.6F. Deiser; F. Kraus; H. Schmidbaur
Bis(triphenylphosphine)silver(I) perrhenate, a cyclic dimer
Chem.Commun., 2015, 51, 6746
7116941 CIFC28.84 H42.57 N O6 S SiP 1 21/c 115.627; 13.4083; 15.769
90; 110.208; 90		3100.7Urszula K. Klimczak; Bartosz K. Zambron
Effective 1,5-stereocontrol in Pd(0)/InI promoted reactions of chiral N-Ts-4-vinylazetidin-2-ones with aldehydes. An efficient entry into nonracemic semi-protected (3Z)-2,6-anti-enediols
Chem.Commun., 2015, 51, 6796
7116942 CIFC22 H12 K N9 O1.94P 42/n :220.9259; 20.9259; 9.6322
90; 90; 90		4217.9Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116943 CIFC22 K N9 O2P 1 2/a 120.904; 15.931; 9.711
90; 104.65; 90		3129Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116944 CIFC22 K N9 O6P 1 2/a 120.656; 15.978; 16.801
90; 100.68; 90		5449Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116945 CIFC22 K N9 O8.5P 1 2/n 124.131; 19.458; 16.672
90; 122.52; 90		6601Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116946 CIFC10 H9 N OP b c a15.005; 12.061; 18.219
90; 90; 90		3297.2Yanli Xu; Weigao Hu; Xiaodong Tang; Jinwu Zhao; Wanqing Wu; Huanfeng Jiang
Palladium-catalyzed Csp2-H carbonylation of aromatic oximes: selective access to benzo[d][1,2]oxazin-1-ones and 3-methyleneisoindolin-1-ones
Chem.Commun., 2015, 51, 6843
7116947 CIFC10 H18 B16 Cu O5P m -3 n28.973; 28.973; 28.973
90; 90; 90		24321Clingerman, Daniel J.; Morris, William; Mondloch, Joseph E.; Kennedy, Robert D.; Sarjeant, Amy A.; Stern, Charlotte; Hupp, Joseph T.; Farha, Omar K.; Mirkin, Chad A.
Stabilization of a highly porous metal-organic framework utilizing a carborane-based linker.
Chemical communications (Cambridge, England), 2015, 51, 6521-6523
7116948 CIFC12 H30 B24P 1 21/c 111.9932; 19.6594; 12.4615
90; 118.684; 90		2577.6Clingerman, Daniel J.; Morris, William; Mondloch, Joseph E.; Kennedy, Robert D.; Sarjeant, Amy A.; Stern, Charlotte; Hupp, Joseph T.; Farha, Omar K.; Mirkin, Chad A.
Stabilization of a highly porous metal-organic framework utilizing a carborane-based linker.
Chemical communications (Cambridge, England), 2015, 51, 6521-6523
7116949 CIFC75 H63 Mn3 N12 O12P -112.281; 12.919; 30.425
94.65; 93.93; 92.4		4794.5Bloch, Witold M.; Burgun, Alexandre; Doonan, Christian J.; Sumby, Christopher J.
Probing post-synthetic metallation in metal-organic frameworks: insights from X-ray crystallography.
Chemical communications (Cambridge, England), 2015, 51, 5486-5489
7116950 CIFC77 H69 Cl5.25 Mn5.5 N13 O16.5P 1 21/m 112.338; 33.33; 25.857
90; 97.45; 90		10543Bloch, Witold M.; Burgun, Alexandre; Doonan, Christian J.; Sumby, Christopher J.
Probing post-synthetic metallation in metal-organic frameworks: insights from X-ray crystallography.
Chemical communications (Cambridge, England), 2015, 51, 5486-5489
7116951 CIFC37.5 H33 Cl Mn2 N6 O7.5P 1 21/m 112.355; 33.452; 12.952
90; 97.63; 90		5306Bloch, Witold M.; Burgun, Alexandre; Doonan, Christian J.; Sumby, Christopher J.
Probing post-synthetic metallation in metal-organic frameworks: insights from X-ray crystallography.
Chemical communications (Cambridge, England), 2015, 51, 5486-5489
7116952 CIFC21 H22 N4 O4P 21 21 215.9906; 15.7335; 21.9353
90; 90; 90		2067.5Bag, Subhendu Sekhar; Jana, Subhashis; Yashmeen, Afsana; De, Suranjan
Triazolo-β-aza-ε-amino acid and its aromatic analogue as novel scaffolds for β-turn peptidomimetics.
Chemical communications (Cambridge, England), 2015, 51, 5242-5245
7116961 CIFC42 H46 N4 O13 S3P 21 21 218.6884; 19.6749; 25.149
90; 90; 90		4299.1Zhiyuan Hu; Rory L. Arrowsmith; James A. Tyson; Vincenzo Mirabello; Haobo Ge; Ian M. Eggleston; Stanley W. Botchway; G. Dan Pantos; Sofia I. Pascu
A fluorescent Arg-Gly-Asp (RGD) peptide-naphthalenediimide (NDI) conjugate for imaging integrin alpha-v-beta3in vitro
Chem.Commun., 2015, 51, 6901
7116963 CIFC120 H76 O36 S12 Zr6F m -3 m32.7165; 32.7165; 32.7165
90; 90; 90		35018.7Bo Gui; Ka-Kit Yee; Yan-Lung Wong; Shek-Man Yiu; Matthias Zeller; Cheng Wang; Zhengta Xu
Tackling poison and leach: catalysis by dangling thiol-palladium functions within a porous metal-organic solid
Chem.Commun., 2015, 51, 6917
7116964 CIFC72 H80 Cl2 N4 Ni2P 1 21/n 116.1963; 12.2535; 16.3252
90; 94.689; 90		3229.1Wei Gao; Lan Xin; Zhiqiang Hao; Guodong Li; Ji-Hu Su; Lijing Zhou; Ying Mu
The ligand redox behavior and role in 1,2-bis[(2,6-diisopropylphenyl)imino]-acenaphthene nickel-TMA(MAO) systems for ethylene polymerization
Chem.Commun., 2015, 51, 7004
7116965 CIFC64.5 H63 Cl N2 Ni PP -111.2339; 13.5323; 19.012
72.179; 88.564; 84.99		2741Wei Gao; Lan Xin; Zhiqiang Hao; Guodong Li; Ji-Hu Su; Lijing Zhou; Ying Mu
The ligand redox behavior and role in 1,2-bis[(2,6-diisopropylphenyl)imino]-acenaphthene nickel-TMA(MAO) systems for ethylene polymerization
Chem.Commun., 2015, 51, 7004
7116966 CIFC38 H46 Al Br2 N2 NiP b c n13.7598; 18.9444; 14.2281
90; 90; 90		3708.9Wei Gao; Lan Xin; Zhiqiang Hao; Guodong Li; Ji-Hu Su; Lijing Zhou; Ying Mu
The ligand redox behavior and role in 1,2-bis[(2,6-diisopropylphenyl)imino]-acenaphthene nickel-TMA(MAO) systems for ethylene polymerization
Chem.Commun., 2015, 51, 7004
7116967 CIFC18 H10 O2P 21 21 215.2561; 9.121; 24.027
90; 90; 90		1151.9Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116968 CIFC54 H32P 1 21/c 19.2045; 16.8399; 22.397
90; 90.064; 90		3471.6Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116969 CIFC78 H81.4P -17.6054; 18.7609; 21.2252
72.252; 84.027; 87.9		2868.66Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116970 CIFC66.15 H56.83 Cl0.45P 1 21/c 19.3755; 26.1158; 20.0039
90; 101.625; 90		4797.5Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116971 CIFC62 H36P -110.1459; 14.0677; 15.4819
66.782; 77.518; 85.704		1982.63Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116972 CIFC68 H54 Cl4C 1 2/c 147.051; 9.3095; 27.9099
90; 125.063; 90		10006.5Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116973 CIFC44 H56 O6 S2P -19.2441; 9.4374; 11.5116
81.533; 81.481; 87.419		982.09Michal Hucko; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak
2,14-Dithiacalix[4]arene and its homooxa analogues: synthesis and dynamic NMR study of conformational behaviour
Chem.Commun., 2015, 51, 7051
7116974 CIFC43 H54 O5 S2P 1 21/a 113.3707; 18.8446; 16.9728
90; 107.545; 90		4077.62Michal Hucko; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak
2,14-Dithiacalix[4]arene and its homooxa analogues: synthesis and dynamic NMR study of conformational behaviour
Chem.Commun., 2015, 51, 7051
7116975 CIFC32 H30 N OI 41/a :227.745; 27.745; 6.4943
90; 90; 90		4999Subham Bhattacharjee; Santanu Bhattacharya
Role of synergistic pi-pi stacking and X-H^...^Cl (X = C, N, O) H-bonding interactions in gelation and gel phase crystallization
Chem.Commun., 2015, 51, 7019
7116976 CIFC30 H40 Cl2.08 N2 O3P -19.7572; 11.9316; 13.8051
89.961; 102.504; 110.06		1469.11Subham Bhattacharjee; Santanu Bhattacharya
Role of synergistic pi-pi stacking and X-H^...^Cl (X = C, N, O) H-bonding interactions in gelation and gel phase crystallization
Chem.Commun., 2015, 51, 7019
7116977 CIFC17 H16 N2 O3 SC 1 2/c 126.8782; 8.2244; 19.4674
90; 132.644; 90		3165.5Jisu Jeong; Donggun Lee; Sukbok Chang
Copper-catalyzed oxygen atom transfer of N-oxides leading to a facile deoxygenation procedure applicable to both heterocyclic and amine N-oxides
Chem.Commun., 2015, 51, 7035
7116978 CIFC18 H14 F3 N3 O3P 1 21/n 111.296; 13.615; 11.516
90; 105.89; 90		1703Devalina Ray; T. Manikandan; Arup Roy; Krishna N. Tripathi; Ravi P. Singh
Ligand-promoted intramolecular dehydrogenative cross-coupling using a Cu catalyst: direct access to polycyclic heteroarenes
Chem.Commun., 2015, 51, 7065
7116981 CIFC39 H29 N O3 P2P 21 21 2111.279; 16.1962; 17.5843
90; 90; 90		3212.2G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116982 CIFC39 H29 N O4 P2P 21 21 2111.281; 16.1001; 17.7437
90; 90; 90		3222.7G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116983 CIFC40 H31 N O4 P2P 21 21 2111.1755; 15.95; 18.117
90; 90; 90		3229.3G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116984 CIFC40 H30 Cl N O4 P2P -19.9475; 13.0705; 14.9853
106.24; 94.143; 110.585		1719.37G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116985 CIFC42 H32 Br Cl6 N O4 P2P -111.5145; 13.3968; 14.6374
86.833; 75.632; 87.59		2183G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116986 CIFC39 H33 N O4 P2P 21 21 2111.335; 17.7472; 16.1457
90; 90; 90		3247.9G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116987 CIFC39 H33 N O4 P2P 21 21 2111.3101; 17.7378; 16.0426
90; 90; 90		3218.4G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116988 CIFC39 H33 Cl N O4 P2P -19.7782; 12.6735; 15.218
72.422; 88.076; 69.077		1673.42G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116989 CIFC39 H33 N O4 P2P 21 21 2111.326; 15.94; 17.593
90; 90; 90		3176.2G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116990 CIFC28 H19 N3P 1 21/c 115.3114; 12.9392; 10.8302
90; 102.639; 90		2093.7Lijun Shi; Xiang Zhong; Houde She; Ziqiang Lei; Fuwei Li
Manganese catalyzed C-H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity
Chem.Commun., 2015, 51, 7136
7116991 CIFC17 H10 Mn N3 O4P 1 21/c 111.7689; 10.7605; 13.511
90; 107.25; 90		1634.1Lijun Shi; Xiang Zhong; Houde She; Ziqiang Lei; Fuwei Li
Manganese catalyzed C-H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity
Chem.Commun., 2015, 51, 7136
7116992 CIFC12 H22 B10P 21 21 219.009; 12.9189; 14.1739
90; 90; 90		1649.65Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116993 CIFC13 H24 B10 O2P 1 21/c 17.3151; 13.218; 19.6674
90; 93.078; 90		1898.92Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116994 CIFC12 H22 B10 OC 1 2/c 124.2272; 13.0711; 23.5734
90; 108.334; 90		7086.2Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116995 CIFC10 H20 B10P b c a24.322; 8.2628; 15.382
90; 90; 90		3091.3Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116996 CIFC13 H24 B10 O2P 1 21/n 17.0474; 19.9445; 13.4339
90; 94.295; 90		1882.92Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116997 CIFC70 H66 Cl4 N6 O4P -110.963; 10.985; 15.643
94.45; 104.45; 119.51		1542Chenhao Zhang; Ke Shi; Kang Cai; Jiajun Xie; Ting Lei; Qifan Yan; Jie-Yu Wang; Jian Pei; Dahui Zhao
Cyano- and chloro-substituted coronene diimides as solution-processable electron-transporting semiconductors
Chem.Commun., 2015, 51, 7144
7116998 CIFC36 H36 As Cl2 N SiP -18.8947; 12.7255; 15.2825
78.686; 73.993; 70.48		1556.81Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7116999 CIFC38 H40 Br2 N Sb SiP -110.1762; 11.2391; 15.5145
95.865; 95.903; 100.813		1720.21Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117000 CIFC44 H52 Br2 N Sb SiP 1 21/c 110.104; 17.041; 23.615
90; 101.92; 90		3978.4Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117001 CIFC38 H40 Bi Br2 N SiP -110.1646; 11.259; 15.5011
95.931; 96.15; 100.498		1720.51Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117002 CIFC44 H52 Bi Br2 N SiP 1 21/c 110.13; 17.182; 23.696
90; 102.26; 90		4030.3Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117003 CIFC51 H42 Bi Br2 N SiP -110.3779; 12.172; 18.3157
82.925; 88.322; 66.682		2108Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117004 CIFC82 H90 B Bi2 N3 SiP -113.6508; 14.2481; 20.2258
97.059; 95.917; 112.943		3545.8Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117005 CIFC63.5 H73.5 As B N3 SiP -112.3574; 12.667; 19.7946
99.963; 104.228; 100.574		2874Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117006 CIFC65.25 H80 As B N3 SiP -112.4034; 13.37; 20.102
77.434; 77.587; 65.731		2936.5Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117007 CIFC98 H128 N2 Sb2 Si2P -112.6918; 13.6933; 14.0983
72.74; 77.066; 67.955		2151.2Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117008 CIFC52 H72 B2 Bi2 N4P -110.501; 12.7973; 21.8679
88.502; 76.645; 67.584		2636.9Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117018 CIFC27 H36 Br2 F6 In N2 SbP -19.5651; 10.502; 18.1036
94.315; 95.583; 115.957		1613.18Bastien Michelet; Jean-Remy Colard-Itte; Guillaume Thiery; Regis Guillot; Christophe Bour; Vincent Gandon
Dibromoindium(III) cations as a pi-Lewis acid: characterization of [IPr^.^InBr2][SbF6] and its catalytic activity towards alkynes and alkenes
Chem.Commun., 2015, 51, 7401
7117019 CIFC36 H24 Co3 Mn3 N17 Na O19R -317.343; 17.343; 31.6652
90; 90; 120		8248.2Jiang Liu; Mei Qu; Rodolphe Clerac; Xian Ming Zhang
A two-dimensional honeycomb coordination network based on fused triacontanuclear heterometallic {Co12Mn18} wheels
Chem.Commun., 2015, 51, 7356
7117020 CIFGd2 H8 O7C m c m16.583; 12.975; 7.3106
90; 90; 90		1573Yan Yang; Qian-Chong Zhang; Yin-Yin Pan; La-Sheng Long; Lan-Sun Zheng
Magnetocaloric effect and thermal conductivity of Gd(OH)3 and Gd2O(OH)4(H2O)2
Chem.Commun., 2015, 51, 7317
7117021 CIFGd H3 O3P 63/m6.2993; 6.2993; 3.6057
90; 90; 120		123.91Yan Yang; Qian-Chong Zhang; Yin-Yin Pan; La-Sheng Long; Lan-Sun Zheng
Magnetocaloric effect and thermal conductivity of Gd(OH)3 and Gd2O(OH)4(H2O)2
Chem.Commun., 2015, 51, 7317
7117022 CIFC8 H10 N14 O4P -15.4207; 6.797; 10.53
82.822; 77.868; 71.33		358.65Jiaheng Zhang; Damon A. Parrish; Jean'ne M. Shreeve
Curious cases of 3,6-dinitropyrazolo[4,3-c]pyrazole-based energetic cocrystals with high nitrogen content: an alternative to salt formation
Chem.Commun., 2015, 51, 7337
7117023 CIFC8 H10 N14 O4P 1 21/c 16.2903; 7.2315; 15.5555
90; 92.037; 90		707.15Jiaheng Zhang; Damon A. Parrish; Jean'ne M. Shreeve
Curious cases of 3,6-dinitropyrazolo[4,3-c]pyrazole-based energetic cocrystals with high nitrogen content: an alternative to salt formation
Chem.Commun., 2015, 51, 7337
7117024 CIFC54 H40 Cd Cl2 N12 O10P 43 21 215.8664; 15.8664; 21.7986
90; 90; 90		5487.6Fan Yang; Qi-Kui Liu; Dan Wu; An-Yan Li; Yu-Bin Dong
p-Benzoquinone adsorption-separation, sensing and its photoinduced transformation within a robust Cd(II)-MOF in a SC-SC fashion
Chem.Commun., 2015, 51, 7443
7117025 CIFC56 H46 Cd Cl2 N12 O11P 43 21 215.8983; 15.8983; 21.6675
90; 90; 90		5476.59Fan Yang; Qi-Kui Liu; Dan Wu; An-Yan Li; Yu-Bin Dong
p-Benzoquinone adsorption-separation, sensing and its photoinduced transformation within a robust Cd(II)-MOF in a SC-SC fashion
Chem.Commun., 2015, 51, 7443
7117026 CIFC54 H41.2 Cd Cl2 N12 O10P 41 21 215.90821; 15.90821; 21.6184
90; 90; 90		5470.99Fan Yang; Qi-Kui Liu; Dan Wu; An-Yan Li; Yu-Bin Dong
p-Benzoquinone adsorption-separation, sensing and its photoinduced transformation within a robust Cd(II)-MOF in a SC-SC fashion
Chem.Commun., 2015, 51, 7443
7117027 CIFC24 H20 N9 P SnP -110.756; 11.0605; 12.354
91.668; 108.414; 116.545		1222.1Benjamin Peerless; Theo Keane; Anthony J. H. M. Meijer; Peter Portius
Homoleptic low-valent polyazides of group 14 elements
Chem.Commun., 2015, 51, 7435
7117028 CIFC24 H20 Ge N9 PP -17.7712; 11.4711; 14.2003
93.278; 99.357; 100.865		1221.59Benjamin Peerless; Theo Keane; Anthony J. H. M. Meijer; Peter Portius
Homoleptic low-valent polyazides of group 14 elements
Chem.Commun., 2015, 51, 7435
7117029 CIFC16 H17 O3 PP 1 21 15.826; 17.749; 14.404
90; 93.154; 90		1487.2Junli Hou; Yang Chen; Dongmei Ma; Burghard Cordes; Jingyun Wang; Xin Wang; Fritz E. Kuhn; Hao Guo; Mingdong Zhou
Methyltrioxorhenium-catalyzed highly selective dihydroxylation of 1,2-allenylic diphenyl phosphine oxides
Chem.Commun., 2015, 51, 7439
7117030 CIFC16 H17 O3 PP 1 21 15.8589; 17.826; 14.463
90; 93.258; 90		1508.1Junli Hou; Yang Chen; Dongmei Ma; Burghard Cordes; Jingyun Wang; Xin Wang; Fritz E. Kuhn; Hao Guo; Mingdong Zhou
Methyltrioxorhenium-catalyzed highly selective dihydroxylation of 1,2-allenylic diphenyl phosphine oxides
Chem.Commun., 2015, 51, 7439
7117031 CIFC27 H19 B F2 N2 SP -110.1096; 12.4472; 18.3814
95.587; 95.919; 96.9		2269.9Xiaoqing Wang; Qingsong Liu; Hui Yan; Zhipeng Liu; Mingguang Yao; Qingfu Zhang; Shuwen Gong; Weijiang He
Piezochromic luminescence behaviors of two new benzothiazole-enamido boron difluoride complexes: intra- and inter-molecular effects induced by hydrostatic compression
Chem.Commun., 2015, 51, 7497
7117032 CIFC66 H66 B2 F4 N8 O S2C 1 2 129.997; 8.4716; 12.7084
90; 112.788; 90		2977.4Xiaoqing Wang; Qingsong Liu; Hui Yan; Zhipeng Liu; Mingguang Yao; Qingfu Zhang; Shuwen Gong; Weijiang He
Piezochromic luminescence behaviors of two new benzothiazole-enamido boron difluoride complexes: intra- and inter-molecular effects induced by hydrostatic compression
Chem.Commun., 2015, 51, 7497
7117033 CIFC9.66667 H13 Br N4.33333 PP -110.1735; 12.6747; 16.2901
83.778; 72.596; 73.177		1918.05Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117034 CIFC21 H20 Br N4 PP 1 21/c 112.2417; 4.8288; 33.91
90; 98.281; 90		1983.6Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117035 CIFC10 H12 F3 N4 O3 P SP -18.2477; 8.4833; 10.7821
97.866; 104.396; 93.252		720.59Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117036 CIFC49 H48 B N4 O PP -111.0003; 13.6439; 14.0585
77.876; 79.118; 87.493		2025.82Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117037 CIFC46 H42 B Cl2 N4 PP -111.012; 13.4813; 13.8114
78.513; 77.138; 87.889		1958.84Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117038 CIFC20 H24 Au Cl F6 N8 O6 P2 S2C 1 2/c 120.7657; 14.6302; 13.2427
90; 123.628; 90		3349.9Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117039 CIFC88 H0.5 Cl12 Co14 N48 O4P -117.9278; 18.574; 28.0345
74.801; 87.6211; 61.281		7861.1Fu-Ping Huang; Peng-Fei Yao; Hai-Ye Li; Qing Yu; He-Dong Bian; Hong Liang
An intuitional hierarchical assembly of cluster-organic frameworks with a thickness of 1.97 nm from a discrete Co14 cluster
Chem.Commun., 2015, 51, 7598

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All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.