Reductive Reactivity of the Tetravalent Uranium Complex [(η5-C5Me5)(η8-C8H8)U]2(μ-η3:η3-C8H8)
- 20 November 2008
- journal article
- research article
- Published by American Chemical Society (ACS) in Organometallics
- Vol. 28 (1), 236-243
- https://doi.org/10.1021/om800747s
Abstract
No abstract availableKeywords
This publication has 64 references indexed in Scilit:
- Two-electron reductive reactivity of trivalent uranium tetraphenylborate complexes of (C5Me5)1− and (C5Me4H)1−Journal of Organometallic Chemistry, 2007
- Actinide Hydride Complexes as Multielectron Reductants: Analogous Reduction Chemistry from [(C5Me5)2UH]2, [(C5Me5)2UH2]2, and [(C5Me5)2ThH2]2Organometallics, 2007
- Methyl Displacements from Cyclopentadienyl Ring Planes in Sterically Crowded (C5Me5)3M ComplexesInorganic Chemistry, 2005
- [(C5Me5)2U][(µ-Ph)2BPh2] as a four electron reductantChemical Communications, 2005
- Structure, Reactivity, and Density Functional Theory Analysis of the Six-Electron Reductant, [(C5Me5)2U]2(μ-η6:η6-C6H6), Synthesized via a New Mode of (C5Me5)3M ReactivityJournal of the American Chemical Society, 2004
- Chemistry of Tris(pentamethylcyclopentadienyl) f-Element Complexes, (C5Me5)3MChemical Reviews, 2002
- Multiple Syntheses of (C5Me5)3UOrganometallics, 2002
- How Much Steric Crowding Is Possible in Tris(η5-pentamethylcyclopentadienyl) Complexes? Synthesis and Structure of (C5Me5)3UCl and (C5Me5)3UF1Journal of the American Chemical Society, 2000
- Arene-Bridged Diuranium Complexes: Inverted Sandwiches Supported by δ BackbondingJournal of the American Chemical Society, 2000
- Formal Three-Electron Reduction by an f-Element Complex: Formation of [{(C5Me5)(C8H8)U}2(C8H8)] from Cyclooctatetraene and [(C5Me5)3U]Angewandte Chemie, 2000