Crystallography Open Database

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Searching journal of publication like 'Chem.Commun.' volume of publication is 51

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7116708 CIFC23 H40 Cl Ir N2P 1 21/n 111.8497; 12.2144; 16.718
90; 91.591; 90
2418.8Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116709 CIFC15 H28 Cl Cu N2P 1 21/c 16.043; 18.944; 15.635
90; 100.45; 90
1760.2Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116710 CIFC30.5 H57 Cl5 N4 Pd2P -18.6743; 15.139; 15.947
86.794; 85.946; 80.765
2059.7Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116711 CIFC15 H28 Au Cl N2P 1 21/n 111.3202; 12.8913; 12.5373
90; 90.2151; 90
1829.6Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116712 CIFC31 H56 Au F3 N4 O3 SP 1 21/c 113.2941; 9.5096; 14.5324
90; 93.61; 90
1833.56Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116713 CIFC6 H6 Fe Na3 O17C 1 2/c 117.4212; 12.5545; 14.9217
90; 101.047; 90
3203.1Qingchun Ge; Tai-Shung Chung
Oxalic acid complexes: promising draw solutes for forward osmosis (FO) in protein enrichment
Chem.Commun., 2015, 51, 4854
7116714 CIFC6 H10 Cr Na3 O17C 1 2/c 117.2551; 12.4639; 15.1228
90; 100.454; 90
3198.4Qingchun Ge; Tai-Shung Chung
Oxalic acid complexes: promising draw solutes for forward osmosis (FO) in protein enrichment
Chem.Commun., 2015, 51, 4854
7116715 CIFC24 H18P n a 217.4869; 19.718; 11.2222
90; 90; 90
1656.7Lingzhi Li; Ming Chen; Haoke Zhang; Han Nie; Jing Zhi Sun; Anjun Qin; Ben Zhong Tang
Influence of the number and substitution position of phenyl groups on the aggregation-enhanced emission of benzene-cored luminogens
Chem.Commun., 2015, 51, 4830
7116716 CIFC20 H25 NP 21 21 2110.529; 11.655; 12.596
90; 90; 90
1545.7Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116717 CIFC26 H29 N SP 1 21/c 17.535; 14.973; 18.844
90; 95.77; 90
2115.2Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116718 CIFC20 H25 N SP 1 21/n 18.104; 8.358; 24.688
90; 96.2; 90
1662.4Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116719 CIFC20 H25 N SP 1 21/n 17.812; 11.736; 18.668
90; 96.49; 90
1700.5Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116720 CIFC32 H28 O4P 1 21/n 110.2761; 15.204; 15.2549
90; 96.857; 90
2366.34Murat Cakici; Zhi-Gang Gu; Martin Nieger; Jochen Burck; Lars Heinke; Stefan Brase
Planar-chiral building blocks for metal-organic frameworks
Chem.Commun., 2015, 51, 4796
7116729 CIFC48.93 H35.72 Cu2 N2 O8.93P -110.7482; 12.23; 16.366
95.11; 96.968; 102.936
2066.2Yuichi Takasaki; Satoshi Takamizawa
Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption
Chem.Commun., 2015, 51, 5024
7116730 CIFC48 H32 Cu2 N2 O8P -110.4745; 11.6064; 17.037
97.583; 104.918; 90.081
1982.5Yuichi Takasaki; Satoshi Takamizawa
Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption
Chem.Commun., 2015, 51, 5024
7116731 CIFC48 H32 Cu2 N2 O8P -110.6065; 11.6485; 17.4513
80.612; 75.215; 89.821
2055.1Yuichi Takasaki; Satoshi Takamizawa
Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption
Chem.Commun., 2015, 51, 5024
7116732 CIFC36 H24 Co3 N13 Na O15.25P 6313.1191; 13.1191; 16.014
90; 90; 120
2386.92Ru-Xin Yao; Xin Cui; Jun Wang; Xian-Ming Zhang
A homochiral magnet based on D3 symmetric [(NaO3)Co3] clusters: from spontaneous resolution to absolute chiral induction
Chem.Commun., 2015, 51, 5108
7116733 CIFC36 H27 Co3 N13 Na O15P 6313.1177; 13.1177; 16.005
90; 90; 120
2385.07Ru-Xin Yao; Xin Cui; Jun Wang; Xian-Ming Zhang
A homochiral magnet based on D3 symmetric [(NaO3)Co3] clusters: from spontaneous resolution to absolute chiral induction
Chem.Commun., 2015, 51, 5108
7116734 CIFC6 H5 B K N3P -19.5267; 9.9704; 10.1727
81.041; 68.165; 83.636
884.51Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989
7116735 CIFC28 H36 B4 K4 N12 O2P 1 21/c 17.5693; 25.062; 22.116
90; 94.3; 90
4183.6Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989

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