Crystallography Open Database

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7133028 CIFC43 H59 B Ge N4P -19.5039; 14.0108; 16.3294
90.542; 90.684; 106.025
2089.55Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, Structural and Reactivity Studies of Boryl-Ethynyl Silylene
Chemical Communications, 2024
7133029 CIFC86 H118 B2 N8 O2 Si2P 1 21/n 113.5861; 20.8352; 14.9701
90; 100.035; 90
4172.7Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, Structural and Reactivity Studies of Boryl-Ethynyl Silylene
Chemical Communications, 2024
7133030 CIFC48 H59 B F5 N5 SiP 1 21/c 119.2831; 10.4515; 24.172
90; 103.424; 90
4738.5Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, Structural and Reactivity Studies of Boryl-Ethynyl Silylene
Chemical Communications, 2024
7133031 CIFCs6 Na3 Nd O54 W10P -111.3552; 15.4905; 16.9027
101.371; 104.424; 91.701
2813.17Colliard, Ian; Deblonde, Gauthier J.-P.
Characterization of the first Peacock-Weakley polyoxometalate containing a transplutonium element: curium bis-pentatungstate [Cm(W5O18)2]9-
Chemical Communications, 2024
7133032 CIFCm Cs8 Na O50 W10P -111.46121; 14.46007; 17.5536
101.11; 99.4298; 103.293
2711.36Colliard, Ian; Deblonde, Gauthier J.-P.
Characterization of the first Peacock-Weakley polyoxometalate containing a transplutonium element: curium bis-pentatungstate [Cm(W5O18)2]9-
Chemical Communications, 2024
7133033 CIFC33 H26 N4 O6P 1 21/c 112.5972; 10.0613; 21.8687
90; 90.553; 90
2771.6Zhu, Shugao; Huang, Wenliang; Liu, Shihan; Yu, Rongjing; Ma, Yufeng; Wang, Hong; Zhang, Rui; Liu, Bin; Lan, Yu; Shen, Ruwei
Synthesis of Benzooxepane-Fused Cyclobutene Derivatives via Pd-Catalyzed Cascade Reactions of Haloarenes and Diynylic Ethers
Chemical Communications, 2024
7133034 CIFC42 H68 O8P 1 21 16.1621; 11.6465; 13.7206
90; 102.517; 90
961.28Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step Synthesis of (−)-Larikaempferic Acid Methyl Ester Enabled by Skeletal Rearrangement
Chemical Communications, 2024
7133035 CIFC21 H34 O4P 21 21 216.9015; 11.1195; 24.8315
90; 90; 90
1905.6Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step Synthesis of (−)-Larikaempferic Acid Methyl Ester Enabled by Skeletal Rearrangement
Chemical Communications, 2024
7133036 CIFC21 H34 O4I 1 2 120.0209; 6.9482; 29.3036
90; 107.026; 90
3897.74Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step Synthesis of (−)-Larikaempferic Acid Methyl Ester Enabled by Skeletal Rearrangement
Chemical Communications, 2024
7133037 CIFC23 H28 F3 N O8 SP 1 21 112.4612; 10.5196; 20.4828
90; 107.749; 90
2557.22Moore, Jonathan Christopher; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective de novo synthesis of 14-hydroxy-6-oxomorphinans
Chemical Communications, 2024
7133038 CIFC23 H28 F3 N O8 SP 1 21 111.0308; 11.6724; 11.0847
90; 116.773; 90
1274.22Moore, Jonathan Christopher; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective de novo synthesis of 14-hydroxy-6-oxomorphinans
Chemical Communications, 2024
7133039 CIFC19 H23 N O3P 1 21 110.163; 13.6943; 11.4184
90; 92.889; 90
1587.14Moore, Jonathan Christopher; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective de novo synthesis of 14-hydroxy-6-oxomorphinans
Chemical Communications, 2024
7133040 CIFC19 H24 O2 SP 1 21/n 111.562; 5.6279; 26.4527
90; 92.458; 90
1719.7Suryawanshi, Sharad Madhukar; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and β-dicarbonyls
Chemical Communications, 2024
7133041 CIFC16 H24 O2P c a 2110.399; 13.561; 9.888
90; 90; 90
1394.4Suryawanshi, Sharad Madhukar; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and β-dicarbonyls
Chemical Communications, 2024
7133042 CIFC17 H18 O2P 1 21/c 111.0571; 10.1834; 11.8525
90; 102.1; 90
1304.93Suryawanshi, Sharad Madhukar; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and β-dicarbonyls
Chemical Communications, 2024
7133043 CIFC12 H14 O4P 1 21/n 15.8827; 24.9167; 8.1339
90; 110.149; 90
1119.28Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiaobing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide
Chemical Communications, 2024
7133044 CIFC18 H18 O4P 1 21/n 15.845; 17.181; 7.9441
90; 107.273; 90
761.8Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiaobing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide
Chemical Communications, 2024
7133045 CIFC15 H16 O4P 1 21/c 110.828; 7.9485; 15.2171
90; 95.439; 90
1303.8Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiaobing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide
Chemical Communications, 2024
7133046 CIFC17 H18 O5P -15.8137; 8.5017; 16.6639
99.886; 92.872; 108.302
765.58Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiaobing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide
Chemical Communications, 2024
7133047 CIFC35 H15 B F15 N OP 1 21/n 110.78652; 21.7974; 17.9089
90; 105.265; 90
4062.15Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable N-borylenamines
Chemical Communications, 2024
7133048 CIFC29 H8 B F15 N2I 1 2/a 113.6313; 19.4305; 24.194
90; 99.003; 90
6329.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable N-borylenamines
Chemical Communications, 2024
7133049 CIFC35 H12 B F15 N4 O2P 1 21/c 112.0468; 16.3233; 15.715
90; 95.2169; 90
3077.45Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable N-borylenamines
Chemical Communications, 2024
7133050 CIFC30 H11 B Cl3 F15 N2C 1 2/c 134.981; 9.9268; 19.229
90; 109.205; 90
6305.7Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable N-borylenamines
Chemical Communications, 2024
7133051 CIFC27 H7 B F15 NP -111.505; 12.536; 17.074
77.759; 87.576; 77.117
2345.9Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable N-borylenamines
Chemical Communications, 2024
7133052 CIFC33 H11 B F15 NP -19.3635; 12.334; 13.652
108.894; 103.287; 96.811
1419.5Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable N-borylenamines
Chemical Communications, 2024
7133053 CIFC33 H11 B F15 NP -110.152; 10.204; 14.905
100.952; 99.276; 103.819
1437.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable N-borylenamines
Chemical Communications, 2024
7133054 CIFC38 H21 B F15 N3P 1 21/c 112.1553; 18.4902; 15.9842
90; 111.521; 90
3342.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable N-borylenamines
Chemical Communications, 2024
7133055 CIFC58.06 H70.12 Cl4.12 F4 I2 N6 O9 SeI 1 2/a 121.6338; 28.0204; 21.9354
90; 98.596; 90
13147.6Liu, Chuan-Zhi; Zhang, Chi; Li, Zhongyi; Chen, Jiale; Wang, Tonglu; Zhang, Xiang-Kung; Yan, Meng; Zhai, Bin
Multiple Non-covalent Interactions Directed Supramolecular Double Helices: The Orthogonality of Hydrogen, Halogen and Chalcogen Bonding
Chemical Communications, 2024
7133056 CIFC32 H34 F3 I N4 O5 SeP -19.5768; 10.0412; 18.3416
96.6; 101.321; 98.752
1690.13Liu, Chuan-Zhi; Zhang, Chi; Li, Zhongyi; Chen, Jiale; Wang, Tonglu; Zhang, Xiang-Kung; Yan, Meng; Zhai, Bin
Multiple Non-covalent Interactions Directed Supramolecular Double Helices: The Orthogonality of Hydrogen, Halogen and Chalcogen Bonding
Chemical Communications, 2024
7133057 CIFC56 H46 Cd2 N6 O10P 21 21 219.6443; 17.67; 36.653
90; 90; 90
6246.2Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical Chiral MOFs with the Induced Chirality of AIE Ligands Exhibiting the Non-reciprocal CPL
Chemical Communications, 2024
7133058 CIFC55 H42 Cd2 N6 O10P 21 21 219.6554; 17.7129; 36.6589
90; 90; 90
6269.6Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical Chiral MOFs with the Induced Chirality of AIE Ligands Exhibiting the Non-reciprocal CPL
Chemical Communications, 2024
7133059 CIFC45 H39 N4 O13 Zn4P 21 21 2113.6565; 29.6834; 14.1762
90; 90; 90
5746.6Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical Chiral MOFs with the Induced Chirality of AIE Ligands Exhibiting the Non-reciprocal CPL
Chemical Communications, 2024
7133060 CIFC45 H34 N4 O13 Zn4P 21 21 2113.6827; 14.1989; 29.77
90; 90; 90
5783.7Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical Chiral MOFs with the Induced Chirality of AIE Ligands Exhibiting the Non-reciprocal CPL
Chemical Communications, 2024
7133061 CIFC4 H6 Na O14 Re U2C 1 2/m 115.2417; 8.1267; 15.0583
90; 113.798; 90
1706.6Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024
7133062 CIFC8 H12 Na2 O30 Tc2 U4C 1 2/m 115.2356; 8.1216; 15.0053
90; 114.061; 90
1695.39Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024
7133063 CIFC4 H18 O32 Re2 U5P -17.7354; 8.4717; 12.782
94.029; 99.086; 109.92
770.66Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024
7133064 CIFC4 H6 O32 Tc2 U5P -17.7451; 8.4501; 12.7565
93.982; 99.211; 109.708
768.96Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024
7133065 CIFC8 H20 O25.75 Tc U4P b c n14.371; 13.8231; 14.8033
90; 90; 90
2940.7Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024
7133066 CIFC13 H8 Br N SP 1 21/c 111.7154; 14.3463; 7.0036
90; 102.82; 90
1147.77Maeda, Bumpei; Akiyoshi, Ryohei; Tanaka, Daisuke; Sato, Kohei; Murakami, Kei
Synthesis of N-β-brominated alkenyl isothiocyanates via dehydrogenation of alkyl isothiocyanates
Chemical Communications, 2024
7133067 CIFC15 H10 Br N SP b c a7.4897; 18.6819; 19.2474
90; 90; 90
2693.13Maeda, Bumpei; Akiyoshi, Ryohei; Tanaka, Daisuke; Sato, Kohei; Murakami, Kei
Synthesis of N-β-brominated alkenyl isothiocyanates via dehydrogenation of alkyl isothiocyanates
Chemical Communications, 2024
7133068 CIFC36 H44 N4 O13 S3P 1 21 117.0638; 4.9924; 23.7104
90; 101.092; 90
1982.14Zhao, Chenyang; Li, Zujian; Ji, Lukang; Wang, Han-Xiao; Ouyang, Guanghui; Liu, Minghua
Aggregate-state-dependent photochromism and circularly polarized luminescence of a chiral biquinoline amphiphile
Chemical Communications, 2024
7133069 CIFC26 H32 Br2.31 I1.69 N6 O2 ZnP -18.6011; 12.1473; 17.1881
71.236; 80.474; 79.466
1660.7Rit, Arnab; Manna, Subarna; Sahoo, Sangita
Synthesis of Quinazolinone Scaffolds via Zinc(II) Stabilized Amidyl Radical Promoted Deaminative Approach
Chemical Communications, 2024
7133070 CIFC107 H97 Cl3 O4P -110.8817; 15.6992; 25.2074
92.731; 92.591; 108.886
4061.44Hirano, Junichiro; Miyoshi, Sayaka; Yashima, Eiji; Ikai, Tomoyuki; Shinokubo, Hiroshi; Fukui, Norihito
Synthesis of sterically congested double helicene by alkyne cycloisomerization
Chemical Communications, 2024
7133071 CIFC11 H17 N O S2P 1 21/c 115.8974; 7.835; 9.4791
90; 100.682; 90
1160.2Cheng, Yuhe; Hyodo, Tadashi; Yamaguchi, Kentaro; Ohwada, Tomohiko; Otani, Yuko
Complete Amide Cis-Trans Switching Synchronized with Disulfide Bond Formation and Cleavage in a Proline-Mimicking System
Chemical Communications, 2024
7133072 CIFC19 H20 N2 O4P -18.1324; 11.0134; 20.24
77.534; 79.396; 80.934
1726.67Greaney, Michael; Liu, Zi
Aminoarylation of Alkynes using Diarylanilines
Chemical Communications, 2024
7133073 CIFC15 H11 N SP -19.2993; 9.8997; 13.2708
82.308; 83.479; 77.987
1179.57George III, Gary C.; Kruse, Samantha; Forbes, Tori; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide
Chemical Communications, 2024
7133074 CIFC15 H11 N SP -19.2758; 9.9051; 13.2567
82.254; 83.462; 77.957
1175.69George III, Gary C.; Kruse, Samantha; Forbes, Tori; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide
Chemical Communications, 2024
7133075 CIFC15 H11 N SP -19.2177; 9.9216; 13.2043
82.062; 83.369; 77.928
1164.89George III, Gary C.; Kruse, Samantha; Forbes, Tori; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide
Chemical Communications, 2024
7133076 CIFC15 H11 N SP -19.1868; 9.9277; 13.1688
81.952; 83.305; 77.93
1158.19George III, Gary C.; Kruse, Samantha; Forbes, Tori; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide
Chemical Communications, 2024
7133077 CIFC15 H11 N SP -19.2356; 9.9171; 13.2232
82.118; 83.407; 77.923
1168.48George III, Gary C.; Kruse, Samantha; Forbes, Tori; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide
Chemical Communications, 2024

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