Abstract
Reaction of the crystallographically characterised [Y(C5Me5)(OC6H3Bu(t)2)2] 2 with LiCH(SiMe3)2 affords the mixed alkyl-alkoxide species [Y(C5Me5){CH(SiMe3)2}(OC6H3Bu(t)2)] 3 which, on subsequent hydrogenation, gives the hydride bridged dimer [{Y(C5Me5)(OC6H3Bu(t)2)(mu-H)}2] 4; Y-89 NMR spectra of these, and related complexes, allows C5Me5, OC6H3Bu(t)2 and CH(SiMe3)2 group contributions to be determined.
Original language | English |
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Pages (from-to) | 642-644 |
Number of pages | 3 |
Journal | Journal of the Chemical Society-Chemical Communications |
Issue number | 9 |
Publication status | Published - 1-May-1991 |
Keywords
- RAY CRYSTAL-STRUCTURE
- HIGHLY REACTIVE ORGANOLANTHANIDES
- ORGANOYTTRIUM HYDRIDE CHEMISTRY
- PERMETHYLYTTROCENE DERIVATIVES
- COMPLEXES
- BIS(PENTAMETHYLCYCLOPENTADIENYL)
- METAL
- HYDROCARBYLS
- ARYLOXIDES
- BONDS