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Pentamethylcyclopentadienyl-dicarbollide derivatives of scandium

Journal Article · · Organometallics; (United States)
DOI:https://doi.org/10.1021/om00030a024· OSTI ID:6297763
; ;  [1]
  1. California Inst. of Technology, Pasadena (United States)

The reactions of [Cp*ScCl[sub 2]][sub x] (Cp* = ([eta][sup 5]-C[sub 5]Me[sub 5])) with Na[sub 2][C[sub 2]B[sub 9]H[sub 11]] or [Cp*ScMe[sub 2]][sub x] with C[sub 2]B[sub 9]H[sub 13], followed by treatment with THF yield Cp*(C[sub 2]B[sub 9]H[sub 11])Sc(THF)[sub 3]. Alkylation of Cp*(C[sub 2]B[sub 9]H[sub 11])Sc(THF)[sub 3] with LiCH(SiMe[sub 3])[sub 2] yields Cp*(C[sub 2]B[sub 9]H[sub 11])ScCH(SiMe[sub 3])[sub 2]Li(THF)[sub 3], and [C[Cp*(C[sub 2]B[sub 9]H[sub 11])ScCH(SiMe[sub 3])[sub 2]][sub 2]Li] - Li(THF)[sub 3], which is obtained by its recrystallization from pentane/toluene, has been characterized structurally. This alkyl derivative reacts slowly with H[sub 2] to yield [Cp*(C[sub 2]B[sub 9]H[sub 11])ScH][sub 2][Li(THF)[sub n]][sub 2], a surprisingly unreactive scandium hydride dimer. Once again, recrystallization from toluene affords a crystalline form with less coordinated THF, [Cp*(C[sub 2]B[sub 9]H[sub 11])ScH][sub 2]Li(THF)[sub 2][center dot] 3/2(C[sub 6]H[sub 5]CH[sub 3]), whose structure reveals that the two anionic [Cp*(C[sub 2]B[sub 9]H[sub 11])ScH][sup [minus]] fragments are held together by reciprocal B-H dative bonding from the dicarbollide ligand to the electron deficient scandium. The potential of pentamethylcyclopentadienyl-dicarbollide derivatives of scandium to serve as efficient [alpha] olefin polymerization catalysts is discussed. 16 refs., 2 fig., 2 tabs.

OSTI ID:
6297763
Journal Information:
Organometallics; (United States), Journal Name: Organometallics; (United States) Vol. 12:6; ISSN 0276-7333; ISSN ORGND7
Country of Publication:
United States
Language:
English