Coordination and Redox Isomerization in the Reduction of a Uranium(III) Monoarene Complex1. (30th May 2014)

• Record Type: Journal Article
• Authors: La Pierre, Henry S.; Kameo, Hajime; Halter, Dominik P.; Heinemann, Frank W.; Meyer, Karsten
• Is Part Of: Angewandte Chemie. Volume 126:Number 28(2014)
• Page Start: 7282
• Page End: 7285
• Publication Date: 2014-05-30
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201402048
• Languages: English
• ISSNs: 0044-8249

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Synthetic studies on the redox chemistry of trivalent uranium monoarene complexes were undertaken with a complex derived from the chelating tris(aryloxide)arene ligand (^{Ad, Me}ArO)₃mes³⁻. Cyclic voltammetry of [{(^{Ad, Me}ArO)₃mes}U^III] (<bold>1</bold>) revealed a nearly reversible and chemically accessible reduction at −2.495 V vs. Fc/Fc⁺—the first electrochemical evidence for a formally divalent uranium complex. Chemical reduction of <bold>1</bold> indicates that reduction induces coordination and redox isomerization to form a uranium(IV) hydride, and addition of a crown ether results in hydride insertion into the coordinated arene to afford uranium(IV) complexes. This stoichiometric reaction sequence provides structural insight into the mechanism of arene functionalization at diuranium inverted sandwich complexes.</p> </abstract>