摘要
Two crystalline metal-organic frameworks, [Cd2(o-BTC)(H2O)2]n (1) and [Pb2(o-BTC)]n (2) (o-BTC = benzene-1,2,3,4-tetracarboxylic), were synthesized under hydrothermal conditions and characterized by analytical, spectroscopic and single crystal X-ray diffraction studies, which reveal three-dimensional reticular structures via M2+ and carboxylate ligands. All carboxyl groups of o-BTC are deprotonated, in agreement with the IR data. The Cd2+ centers of 1 have one coordination environment, while Pb2+ centers of 2 have two coordination environments. Both 1 and 2 form 3D interpenetrated grid structures along the b and c axes, respectively.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 1437-1442 |
| 页数 | 6 |
| 期刊 | Journal of Coordination Chemistry |
| 卷 | 61 |
| 期 | 9 |
| DOI | |
| 出版状态 | 已出版 - 2008 |
指纹
探究 'Structurally different cadmium(II) and lead(II) supramolecular polymers with the same benzene-1,2,3,4-tetracarboxylate dianion as bridging ligands from hydrothermal reactions' 的科研主题。它们共同构成独一无二的指纹。引用此
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