Crystallography Open Database

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7133138 CIFC62 H95 Cr Li N4 O5P -111.7699; 16.1506; 17.7227
97.669; 105.27; 108.783
2987.77D'Arpino, Alexander A; MacMillan, Samantha N.; Wolczanski, Peter T.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence via C-C bond formation amidst competing electrophilicity: [(cpta)CrMen]- (n = 0, 1) and [(pta)Cr]-
Chemical Communications, 2024
7133139 CIFC61 H90 Cr K N4 O8P -111.7863; 14.0237; 19.3145
85.096; 78.035; 75.843
3026.2D'Arpino, Alexander A; MacMillan, Samantha N.; Wolczanski, Peter T.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence via C-C bond formation amidst competing electrophilicity: [(cpta)CrMen]- (n = 0, 1) and [(pta)Cr]-
Chemical Communications, 2024
7133140 CIFC102 H140 Cr2 K2 N8 O5R -3 :H41.8744; 41.8744; 15.4776
90; 90; 120
23503.4D'Arpino, Alexander A; MacMillan, Samantha N.; Wolczanski, Peter T.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence via C-C bond formation amidst competing electrophilicity: [(cpta)CrMen]- (n = 0, 1) and [(pta)Cr]-
Chemical Communications, 2024
7133141 CIFC140 H202 Cr2 K2 N8 O17P -112.1161; 19.5547; 29.7051
82.767; 81.408; 78.704
6790.16D'Arpino, Alexander A; MacMillan, Samantha N.; Wolczanski, Peter T.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence via C-C bond formation amidst competing electrophilicity: [(cpta)CrMen]- (n = 0, 1) and [(pta)Cr]-
Chemical Communications, 2024
7133142 CIFC70 H63 B Cl3 F24 N2 O3 PP -112.6492; 13.6605; 21.8343
81.4; 78.136; 78.97
3600.1Karnbrock, Simon Bernhard Hugo; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: Stoichiometric C=O-bond cleavage in aldehydes and ketones
Chemical Communications, 2024
7133143 CIFC149 H136 B2 F48 N4 O6 P2P -113.6399; 16.8477; 19.2953
115.857; 102.316; 98.273
3754.1Karnbrock, Simon Bernhard Hugo; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: Stoichiometric C=O-bond cleavage in aldehydes and ketones
Chemical Communications, 2024
7133144 CIFC45 H60 Cl7 Ga2 N2 O3 PC 1 c 120.964; 12.2176; 20.1457
90; 93.743; 90
5148.9Karnbrock, Simon Bernhard Hugo; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: Stoichiometric C=O-bond cleavage in aldehydes and ketones
Chemical Communications, 2024
7133145 CIFC86 H85 B F24 N5 O3 PP -112.1449; 18.623; 20.405
70.624; 73.911; 75.97
4125.1Karnbrock, Simon Bernhard Hugo; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: Stoichiometric C=O-bond cleavage in aldehydes and ketones
Chemical Communications, 2024
7133146 CIFC91 H88 B F24 N2 O3 PP 1 21/n 113.9705; 31.6393; 19.2626
90; 93.898; 90
8494.7Karnbrock, Simon Bernhard Hugo; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: Stoichiometric C=O-bond cleavage in aldehydes and ketones
Chemical Communications, 2024
7133147 CIFC89.36 H97.27 B F24 N2 O3 P SiP -113.1456; 17.6698; 20.0734
95.272; 103.875; 91.26
4502.8Karnbrock, Simon Bernhard Hugo; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: Stoichiometric C=O-bond cleavage in aldehydes and ketones
Chemical Communications, 2024
7133148 CIFC79 H74 B F24 N2 O3 PP -113.9743; 16.814; 19.335
115.292; 106.112; 94.371
3845.7Karnbrock, Simon Bernhard Hugo; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: Stoichiometric C=O-bond cleavage in aldehydes and ketones
Chemical Communications, 2024
7133149 CIFC79 H64 B F24 N2 O3 PP 1 21/c 112.366; 20.9073; 29.743
90; 97.228; 90
7628.6Karnbrock, Simon Bernhard Hugo; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: Stoichiometric C=O-bond cleavage in aldehydes and ketones
Chemical Communications, 2024
7133150 CIFC28 H30 N2 O4C 1 c 114.4111; 20.2712; 10.3678
90; 129.444; 90
2338.94Sakai, Dan; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Stereoselective synthesis of 6/7/6-fused heterocycles with multiple stereocenters via internal redox reaction/inverse electron-demand hetero-Diels–Alder reaction sequence
Chemical Communications, 2024
7133151 CIFC29 H32 Cl2 N2 O4P -19.9028; 11.7064; 11.8877
89.667; 74.086; 77.512
1291.8Sakai, Dan; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Stereoselective synthesis of 6/7/6-fused heterocycles with multiple stereocenters via internal redox reaction/inverse electron-demand hetero-Diels–Alder reaction sequence
Chemical Communications, 2024
7133152 CIFC31 H46 F N S Si2P 1 21 18.1462; 13.1951; 15.8775
90; 96.946; 90
1694.15Zhou, Pengfei; Liang, Xinyao; Xu, Zekun; Chen, Honggu; Wei, Zongwu; Liang, Taoyuan; Jiang, Jun; Zhang, Zhuan
Regiodivergent C–H Alkynylation of 2-Arylthiazoles Switched by RuII and PdII Catalysis
Chemical Communications, 2024
7133153 CIFC22 H29 N O S SiP -18.798; 12.4654; 21.0908
104.49; 90.974; 91.921
2237.4Zhou, Pengfei; Liang, Xinyao; Xu, Zekun; Chen, Honggu; Wei, Zongwu; Liang, Taoyuan; Jiang, Jun; Zhang, Zhuan
Regiodivergent C–H Alkynylation of 2-Arylthiazoles Switched by RuII and PdII Catalysis
Chemical Communications, 2024
7133154 CIFC38 H39 N O8P 21 21 217.7775; 19.6476; 22.0751
90; 90; 90
3373.28Sun, Chunzhao; Inokuma, Tsubasa; Tsuji, Daisuke; Yamaoka, Yousuke; Akagi, Reiko; Yamada, Ken-ichi
Total Synthesis of 1,4a-di-epi-ent-Pancratistatin, Exemplifying a Stereodivergent Approach to Pancratistatin Isomers
Chemical Communications, 2024
7133155 CIFC51 H39 Cl2 N O13P 1 21 110.8258; 13.1828; 15.3126
90; 79.363; 90
2147.78Sun, Chunzhao; Inokuma, Tsubasa; Tsuji, Daisuke; Yamaoka, Yousuke; Akagi, Reiko; Yamada, Ken-ichi
Total Synthesis of 1,4a-di-epi-ent-Pancratistatin, Exemplifying a Stereodivergent Approach to Pancratistatin Isomers
Chemical Communications, 2024
7133156 CIFC6 H22 Br5 In N2 O2P n m a20.264; 7.9353; 11.0226
90; 90; 90
1772.4Biswas, Shuva; Mandal, Arnab; Swain, Diptikanta; Biswas, Kanishka
Synthesis and Soft Crystal Structure-Induced Broad Emission in (NH3C6H12NH3)InBr5·2H2O
Chemical Communications, 2024
7133157 CIFC6 H22 Br5 In N2 O2P 1 21/n 17.8333; 20.223; 10.9317
90; 91.232; 90
1731.3Biswas, Shuva; Mandal, Arnab; Swain, Diptikanta; Biswas, Kanishka
Synthesis and Soft Crystal Structure-Induced Broad Emission in (NH3C6H12NH3)InBr5·2H2O
Chemical Communications, 2024

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