Organometallic coordination networks based on π-bonded transition metal quinonoid complexes

被引:0
|
作者
Reingold, Jeffrey A.
Son, Seung Uk
Carpenter, Gene B.
Sweigart, Dwight A. [1 ]
机构
[1] Brown Univ, Dept Chem, Providence, RI 02912 USA
[2] Sungkyunkwan Univ, Dept Chem, Suwon 440746, South Korea
基金
美国国家科学基金会;
关键词
coordination networks; hydrogen-bonding; quinone complexes; organometalloligand; polymers; self-assembly;
D O I
10.1007/s10904-006-9024-0
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Hydroquinones pi-bonded to the transition metal fragments Mn(CO)(3)(+), Rh(COD)(+), and Rh [P(OPh)(3)](2)(+) are readily deprotonated to afford anionic eta(4)-quinone complexes that function as organometalloligands by binding to metal ions through the quinone oxygen atoms. The resulting supramolecular assemblies display a variety of interesting and potentially useful network topologies.
引用
收藏
页码:1 / 13
页数:13
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