Issue 16, 1998

Transition metal imide/organic imine metathesis reactions: unexpected observations

Abstract

Mixtures of [Ti(NBut)Cl2(py)3] 1 and PhC(NAr)H (Ar = C6H3Me2-2,6 or C6H4Me-4) gave quantitative conversion to [Ti(NAr)Cl2(py)3] and PhC(NBut)H, the products of Ti[double bond, length half m-dash]NBut/C[double bond, length half m-dash]NAr transition metal imide/organic imine meta-thesis; examination of the kinetics for Ar = C6H4Me-4 showed that the rate limiting step for this process is zero order in [1], demonstrating that these reactions do not involve metal imide particiption in the rate limiting step.

Article information

Article type
Paper

Chem. Commun., 1998, 1669-1670

Transition metal imide/organic imine metathesis reactions: unexpected observations

J. M. McInnes, Chem. Commun., 1998, 1669 DOI: 10.1039/A803719A

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