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Title: Tris(Cyclopentadienyl)Uranium-t-Butyl: Synthesis, reactions, and mechanisms

Thesis/Dissertation ·
DOI:https://doi.org/10.2172/10159968· OSTI ID:10159968
 [1]
  1. Univ. of California, Berkeley, CA (United States)

Compounds (RC5H4)3U(t-Bu) were prepared for R = H, Me, Et. Their decomposition products in aromatic solvents are consistent with a radical decomposition pathway induced by solvent-assisted U-C bond homolysis. NMR was used to study the reactions of (RC5H4)3UCl with t-BuLi (R = t-Bu, Me3Si). Reactions of (MeC5H4)3U(t-Bu) with Lewis bases and fluorocarbons were studied. Analogous reaction chemistry between (RC5H4)3ThX systems and t-BuLi was also studied, and reactivity differences between U and Th are discussed. Synthesis of sterically crowded (RC5H4)4U compounds is next considered. Reaction of the trivalent (RC5H4)3U with (RC5H4)2Hg results in formation of (RC5H4)4U. Steric congestion, cyclopentadienyl ligand exchange, and electron transfer are discussed. (DLC)

Research Organization:
Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC03-76SF00098
OSTI ID:
10159968
Report Number(s):
LBL-34031; ON: DE93015036
Resource Relation:
Other Information: TH: Thesis (Ph.D.); PBD: Apr 1993
Country of Publication:
United States
Language:
English