Bondy Chantelle R, Gale Philip A, Loeb Stephen J
Department of Chemistry and Biochemistry, University of Windsor, Ontario, Canada.
J Am Chem Soc. 2004 Apr 28;126(16):5030-1. doi: 10.1021/ja039712q.
A new class of synthetic receptors for anions can be prepared by arranging urea hydrogen-bond donor groups on a simple metal-organic scaffold. The complex cation [PtL4]2+ (L = 8-(n-butylurea)iso-quinoline) can adopt four conformations reminiscent of calix[4]arene-based receptors; "cone", "partial cone", "1,2-alternate", or "1,3-alternate". 1H NMR solution data and solid-state X-ray structures show that a "1,2-alternate" conformation is used to bind spherical halide ions while a "cone" conformation is involved in strong binding with the tetrahedral oxy-anions such as the sulfate ion; even in a strongly competitive solvent such as DMSO.
通过在简单的金属有机骨架上排列尿素氢键供体基团,可以制备出一类新型的阴离子合成受体。配合物阳离子[PtL4]2+(L = 8-(正丁基脲)异喹啉)可以呈现出四种构象,让人联想到基于杯[4]芳烃的受体;“锥式”、“部分锥式”、“1,2-交替式”或“1,3-交替式”。1H NMR溶液数据和固态X射线结构表明,“1,2-交替式”构象用于结合球形卤离子,而“锥式”构象则参与与四面体氧阴离子(如硫酸根离子)的强结合;即使在二甲基亚砜等强竞争性溶剂中也是如此。