Infrared Spectroscopy of Extreme Coordination: The Carbonyls of U+ and UO2+

被引:64
|
作者
Ricks, Allen M. [1 ]
Gagliardi, Laura [2 ,3 ]
Duncan, Michael A. [1 ]
机构
[1] Univ Georgia, Dept Chem, Athens, GA 30602 USA
[2] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Inst Supercomp, Minneapolis, MN 55455 USA
关键词
IR PHOTODISSOCIATION SPECTROSCOPY; 32-ELECTRON PRINCIPLE; METAL-CARBONYLS; COMPLEXES; URANIUM; URANYL; MOLECULES; SPECTRA; CATIONS; ATOMS;
D O I
10.1021/ja1077365
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Uranium and uranium dioxide carbonyl cations produced by laser vaporization are studied with mass-selected ion infrared spectroscopy in the C-O stretching region. Dissociation patterns, spectra, and quantum chemical calculations establish that the fully coordinated ions are U(CO)(8)(+) and UO2(CO)(5)(+), with D-4d square antiprism and D-5h, pentagonal bipyramid structures. Back-bonding in U(CO)(8)(+) causes a red-shifted CO stretch, but back-donation is inefficient for UO2(CO)(5)(+), producing a blue-shifted CO stretch characteristic of nonclassical carbonyls.
引用
收藏
页码:15905 / 15907
页数:3
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