Carbon dioxide reduction and carbon monoxide activation employing a reactive uranium(III) complex

被引:191
作者
Castro-Rodriguez, I [1 ]
Meyer, K [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
关键词
D O I
10.1021/ja053497r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The highly reactive, six-coordinate tris-aryloxide U(III) species, [((t-BuArO)3tacn)U] (1) reacts with CO2 in a 2e- reduction to produce CO and a dinuclear U(IV/IV) μ-oxygen bridged complex [{((t-BuArO)3tacn)U}2(μ-O)] (2). This reaction proceeds via a dinuclear CO2-bridged intermediate 3. Also, mononuclear 1 was treated with 1 atm of CO to yield dinuclear [{((t-BuArO)3tacn)U}2(μ-CO)] (4) with a CO ligand bridging two uranium ions in an unprecedented μ:η1,η1 fashion. The mixed-valent azido-bridged U(III/IV) complex 5 was synthesized from trivalent 1 and tetravalent [((t-BuArO)3tacn)U(N3)] and serves as an isostructural analogue of triatomic-bridged intermediate 3 as well as an electronic model for mixed-valent 4. Copyright © 2005 American Chemical Society.
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页码:11242 / 11243
页数:2
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