Bowman-James Kristin
Department of Chemistry, University of Kansas, Lawrence, Kansas 66045, USA.
Acc Chem Res. 2005 Aug;38(8):671-8. doi: 10.1021/ar040071t.
A series of macrocyclic receptors were designed to probe the influence of four factors, hydrogen bonding, charge, dimensionality, and topology, on anion binding. Monocyclic and bicyclic polyammonium and polyamide receptors were synthesized from either 2,2'-diaminodiethylamine derivatives (dien) or 2,2',2''-aminoethylamine (tren) building blocks, plus aromatic or heterocyclic spacers. Supramolecular complexes of these hosts with three simple anion topologies were probed: spherical (halides), trigonal planar (nitrate), and tetrahedral (sulfate). Results indicate a number of corollaries with transition-metal coordination chemistry in terms of binding concepts such as the chelate effect and dual valencies, as well as geometries for anion complexes that are strikingly similar to those observed in transition-metal coordination chemistry.
设计了一系列大环受体,以探究氢键、电荷、维度和拓扑结构这四个因素对阴离子结合的影响。单环和双环多铵和聚酰胺受体由2,2'-二氨基二乙胺衍生物(二乙三胺)或2,2',2''-氨基乙胺(三亚乙基四胺)结构单元,加上芳族或杂环间隔基合成。研究了这些主体与三种简单阴离子拓扑结构形成的超分子配合物:球形(卤化物)、三角平面形(硝酸盐)和四面体(硫酸盐)。结果表明,在螯合效应和双价等结合概念方面,以及阴离子配合物的几何结构与过渡金属配位化学中观察到的结构惊人地相似,这与过渡金属配位化学有许多相似之处。