Coordination chemistry in the solid state

被引:28
作者
Bruce, PG
机构
[1] School of Chemistry, University of St Andrews, St Andrews
来源
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 1996年 / 354卷 / 1706期
关键词
D O I
10.1098/rsta.1996.0015
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Salts, e.g. LiPF6, may be dissolved in solid polymers, e.g. (CH2-CH2-O)(n). Dissolution is driven by the complexation of the cations by the donor groups on the polymer chains. The resulting solids are coordination compounds with infinite ligands. They form a vital bridge between coordination chemistry in solution and more classical solid-state chemistry. The solid coordination compounds are often referred to as polymer electrolytes. In this paper I present a view of the coordination chemistry of these fascinating compounds which yield elegant structures as well as forming the basis of high technology devices for the 21st century. Topics covered include: the forces driving complexation; the major ligands and complexes; the structures of several model systems; and the physical properties and applications of the materials.
引用
收藏
页码:415 / 436
页数:22
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