skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Synthesis of hydride and alkyl compounds containing the Cp*Os([eta][sup 3]-allyl) fragment. Crystal structures of Cp*Os([eta][sup 3]-C[sub 8]H[sub 13])Br[sub 2] and [Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])Me(H[sub 2]O)][BF[sub 4]]

Journal Article · · Organometallics
DOI:https://doi.org/10.1021/om990150m· OSTI ID:5937175
; ; ;  [1]
  1. Univ. of Illinois, Urbana, IL (United States). School of Chemical Sciences

Treatment of Cp*[sub 2]Os[sub 2]Br[sub 4] with 3-bromo-2-methylpropene or 1,3-cyclooctadiene affords the 2-methylpropenyl and cyclooctenyl products Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])Br[sub 2] and Cp*Os([eta][sup 3]-C[sub 8]H[sub 13])Br[sub 2], respectively. The monoalkyl complexes Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])MeBr and Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])(CH[sub 2]SiMe[sub 3])-Br can be generated by treating Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])Br[sub 2] with MgMe[sub 2] or LiCH[sub 2]SiMe[sub 3]. The dimethyl complex Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])Me[sub 2] can be synthesized from Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])Br[sub 2] by addition of methyllithium. In contrast, addition of ethyllithium to Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])Br[sub 2] yields the ethylene complex Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])([eta][sup 2]-C[sub 2]H[sub 4]) and a small amount of Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])H[sub 2]. The latter dihydride can be synthesized in better yield by treating Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])Br[sub 2] with LiAlH[sub 4]. When the dimethyl complex Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])Me[sub 2] is protonated with HBF[sub 4] in the presence of H[sub 2]O the aqua complex [Cp*Os([eta][sup 3]-C[sub 4]H[sub 7])Me(H[sub 2]O)][BF[sub 4]] is formed.

Sponsoring Organization:
USDOE; USDOE, Washington, DC (United States)
OSTI ID:
5937175
Journal Information:
Organometallics, Vol. 18:17; ISSN 0276-7333
Country of Publication:
United States
Language:
English