Positional isomeric and N-donor auxiliary chelating ligand effect on engineering crystalline architectures of four lead(II) complexes with diverse fluorescent properties
作者:Wei Liang、Zhaoyin Zhong、Zi-Cai Pan、Qing-Hua Meng、Ye Deng、Kou-Lin Zhang
DOI:10.1080/00958972.2013.815747
日期:2013.8.1
chelating ligand (bipy/phen) effect on engineering of crystalline architectures of four Pb(II) complexes with a pair of methyl-substituted 3-sulfobenzoic isomers: [Pb(4-msba)(phen)(H2O)] (1), [Pb(4-msba)(bipy)(H2O)]·H2O (2), [Pb(5-msba)(phen)2]·9H2O (3), and [Pb2(5-msba)2(bipy)2(H2O)2] (4) (4/5-msba = 4/5-methyl-3-sulfobenzoate, phen = 1,10-phenanthroline and bipy = 2,2′-bipyridine). The lead(II) ions exhibit
这项工作研究了取代基的位置和 N 供体辅助螯合配体(bipy/phen)对具有一对甲基取代的 3-磺基苯甲酸异构体的四种 Pb(II) 配合物的晶体结构工程的影响:[Pb (4-msba)(phen)(H2O)] (1), [Pb(4-msba)(bipy)(H2O)]·H2O (2), [Pb(5-msba)(phen)2]·9H2O (3) 和 [Pb2(5-msba)2(bipy)2(H2O)2] (4) (4/5-msba = 4/5-methyl-3-sulfobenzoate, phen = 1,10-菲咯啉和bipy = 2,2'-联吡啶)。铅 (II) 离子在 1-4 中表现出半定向几何形状。甲基的位置以及辅助螯合配体影响磺酸盐的配位模式,从而决定结构。随着甲基在芳环中的位置从 4 变为 5,结构从 1 和 2 的二维片状化合物变为 3 和 4 的 0-D 二聚体。水簇(H