堆积
超分子化学
配体(生物化学)
结晶学
氢键
分子间力
咪唑
晶体工程
金属有机骨架
晶体结构
化学
聚合物
金属
光致发光
固态
高分子化学
材料科学
立体化学
分子
有机化学
物理化学
生物化学
受体
光电子学
吸附
作者
Yu Zhang,Beibei Guo,Li Li,Shaofeng Liu,Gang Li
摘要
The newly designed organic ligand 2-(p-bromophenyl)-1H-imidazole-4,5-dicarboxylic acid (p-BrPhH3IDC) has been successfully prepared and its coordination features were explored. By the reactions of p-BrPhH3IDC with main group or transition metals, six metal–organic frameworks (MOFs), namely, [Ca(p-BrPhHIDC)(H2O)2]n (1), [Sr(p-BrPhHIDC)(H2O)]n (2), [Zn(p-BrPhHIDC)(H2O)]n (3), {[Co(p-BrPhH2IDC)2]·2H2O}n (4), [Cd1.5(p-BrPhHIDC)(p-BrPhH2IDC)(H2O)]n (5), and {[Cd2(p-BrPhHIDC)2(4,4′-bipy)]·4H2O}n (4,4′-bipy = 4,4′-bipyridine) (6) have been synthesized under hydro(solvo)thermal conditions. X-ray single-crystal analyses reveal that they have rich structural chemistry ranging from one-dimensional (1D) (3), two-dimensional (2D) (1, 2, 4, and 5) to three-dimensional (3D) polymers (6). Furthermore, the existence of intermolecular hydrogen bonds and/or π···π stacking interactions between the aromatic groups supplies the additional stabilization for the solid-state supramolecular structures of polymers 3, 4, and 5. The solid-state photoluminescence properties of the polymers 1–6 have been investigated as well.
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