Issue 24, 1984

Lithium η3-aza-allyl) type complexes derived from the metallation of 2-(Me3Si)3 –nCHnC5H4N; influence of solvent and degree of substitution, n= 1 or 2, on the nature of the product

Abstract

Metallation of 2-Me3Si)2CHC5N ([double bond, length half m-dash]RH) with LiBun in hexane yields RLi·RH, (1), whreas RH with LiBun and tmeda (tetramethylethylenediamine; 1 equiv.) in hexane affords Rli(tmeda), (2); the related 2-(Me3Si)CH2C5H4N ([double bond, length half m-dash]R′H) with LiBun in a hexane–diethyl ether mixture gives [{LiR′(OEt2)}2], (3): compounds (1)–(3), shown by X-ray crystallography to have novel η3-aza-allyl ligand geometries, are regarded as models for the bonding in the products of metallation of systems CH3-C(R″)[double bond, length half m-dash]NR‴.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1708-1710

Lithium η3-aza-allyl) type complexes derived from the metallation of 2-(Me3Si)3 –nCHnC5H4N; influence of solvent and degree of substitution, n= 1 or 2, on the nature of the product

D. Colgan, R. I. Papasergio, C. L. Raston and A. H. White, J. Chem. Soc., Chem. Commun., 1984, 1708 DOI: 10.1039/C39840001708

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