Issue 18, 1989

Lipophilic lithium alkoxides or dialkylboroxides; X-ray structures of [Li(µ-OR′)]2 and Li(OBR2)(tmeda), [tmeda =(Me2NCH2)2, R = CH(SiMe3)2, R′= CBut3 or BR2]

Abstract

Treatment of But3COH or BR2OH [R = CH(SiMe3)2] with LiBun yields the colourless crystalline [Li(µ-OR′)]2, [R′= CBut3(1) or BR2(2)]; the dialkylboroxide (2) reacts with tmeda [tmeda =(Me2NCH2)2], MeCOCI, or [Ti(η-C5H5)2Cl2] to yield Li(OBR2)(tmeda)(3), BR2OH, or [Ti(η-C5H5)2(Cl)(OBR2)], respectively; X-ray data on complexes (1)–(3) are compared with those for related LiO compounds, the two-co-ordinate lithium environment in (1) and (2), and the exceedingly short Li–O [1.677(5)Å] and O–B [1.308(8)Å] distances in (3) being noteworthy.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1312-1314

Lipophilic lithium alkoxides or dialkylboroxides; X-ray structures of [Li(µ-OR′)]2 and Li(OBR2)(tmeda), [tmeda =(Me2NCH2)2, R = CH(SiMe3)2, R′= CBut3 or BR2]

G. Beck, P. B. Hitchcock, M. F. Lappert and I. A. MacKinnon, J. Chem. Soc., Chem. Commun., 1989, 1312 DOI: 10.1039/C39890001312

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