化学
单斜晶系
结晶学
氢键
螯合作用
晶体结构
发光
菲咯啉
金属
立体化学
无机化学
分子
有机化学
材料科学
光电子学
作者
Changkun Xia,Yuanyuan Min,Wen Sun,Kai Yang,Yunlong Wu
标识
DOI:10.1080/00958972.2018.1428312
摘要
Two dinuclear Fe(III) metal–organic complexes with tetracarboxylate and chelating N-donor ligands, [Fe(Hbtec)(phen)(H2O)]2·2H2O (1) and [Fe(Hbtec)(bpy)(H2O)]2·2H2O (2) (H4btec = 1,2,3,5-benzenetetracarboxylic acid, phen = 1,10-phenanthroline, bpy = 2,2′-bipyridine) have been prepared and characterized by elemental analysis, IR spectroscopic, and X-ray diffraction methods. Both complexes crystallize in the monoclinic space group P21/c with two Fe(III) ions bridged by two Hbtec3− ligands into a dinuclear unit. Hydrogen bonding connects the dinuclear units into a 3-D framework. The dinuclear units are 10-connected nodes that produce a 3-D framework with topology Schläfli symbol as (312·428·55). Thermal stabilities and luminescent properties of the two complexes have also been investigated.
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