Ohi Hiromi, Tachi Yoshimitsu, Itoh Shinobu
Department of Chemistry, Graduate School of Science, Osaka City University, 3-3-138 Sugimoto, Sumiyoshi-ku, Osaka 558-8585, Japan.
Inorg Chem. 2004 Jul 26;43(15):4561-3. doi: 10.1021/ic049468j.
By By combining a tripodal tripyridine ligand containing a 1,3,5-triethylbenzene spacer (L) with several divalent transition-metal chlorides, we have selectively prepared a capsule-type supramolecular complex, [PdII3(L)2Cl6] x 2H2O, and one-dimensional (1D) coordination polymer complexes, ([CuII(L)Cl2] x C2H5OH)n, ([CoII3(L)2Cl6] x 2CH2Cl2)n, and ([ZnII3(L)2Cl6] x 2H2O)n, with a zigzag polymer chain, a linear polymer chain, and a ladder polymer chain structure, respectively. All the structures were established in detail by single-crystal X-ray diffraction analysis, and the factors inducing the structural differences among the complexes are discussed by taking account of the differences in coordination geometry (square planar vs tetrahedral) as well as metal-ligand binding strength in the complexes.
通过将含有1,3,5 - 三乙苯间隔基的三脚架型三联吡啶配体(L)与几种二价过渡金属氯化物相结合,我们选择性地制备了一种胶囊型超分子配合物[PdII3(L)2Cl6]·2H2O以及一维(1D)配位聚合物配合物([CuII(L)Cl2]·C2H5OH)n、([CoII3(L)2Cl6]·2CH2Cl2)n和([ZnII3(L)2Cl6]·2H2O)n,它们分别具有之字形聚合物链、线性聚合物链和梯形聚合物链结构。所有结构均通过单晶X射线衍射分析详细确定,并通过考虑配合物中配位几何结构(平面正方形与四面体)的差异以及金属 - 配体结合强度的差异来讨论导致配合物结构差异的因素。