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Activation of carbon dioxide by new mixed sandwich uranium(iii) complexes incorporating cyclooctatetraenyl and pyrrolide, phospholide, or arsolide ligands†
Rachel J. Kahan,F. Geoffrey N. Cloke,S. Mark Roe,François Nief
New Journal of Chemistry Pub Date : 04/22/2015 00:00:00 , DOI:10.1039/C5NJ00590F
Abstract

A series of uranium(III) mixed-sandwich complexes of the type [U(COTTIPS2)(CpEMe4)] (CpEMe4 = EC4Me4, E is N, P or As, and COTTIPS2 = C8H6{1,4-SiiPr3}), featuring a heterocyclic five membered ring, have been synthesised and their X-ray crystal structures determined. The redox properties of these complexes have been assessed using cyclic voltammetry and the results compared to the purely carbocyclic mixed-sandwich analogues. The reactions of [U(COTTIPS2)(CpNMe4)] and [U(COTTIPS2)(CpPMe4)] with CO2 afford the structurally characterised carbamate and phosphacarbonate complexes [U(COTTIPS2)]2(μ-O)(μ-η11-O2CEC4Me4)2 (E = N and P respectively), arising from CO2 reduction and insertion.

Graphical abstract: Activation of carbon dioxide by new mixed sandwich uranium(iii) complexes incorporating cyclooctatetraenyl and pyrrolide, phospholide, or arsolide ligands
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