1980Journal of the Chemical Society Chemical CommunicationsRequires access

The mechanism of the secondary alkylation of dinitrogen and the relationship between structure and reactivity in the alkylation of co-ordinated dinitrogen

J. Chatt, Wasif Hussain, G. Jeffery Leigh, Heinrich Neukomm, Christopher J. Pickett, Douglas A. Rankin

Open publisher page 26 citations

Abstract

Dinitrogen loss from a range of bis(N2)-complexes of Mo and W is the common rate-determining step in the primary alkylation of the remaining co-ordinated N2, whereas the second alkylation of co-ordinated N2 is a typical SN2 reaction; the rates of these reactions are sensitive to both the metal and the coligands, and those factors which encourage the first alkylation are those which inhibit the second.

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What this paper is about

Dinitrogen loss from a range of bis(N2)-complexes of Mo and W is the common rate-determining step in the primary alkylation of the remaining co-ordinated N2, whereas the second alkylation of co-ordinated N2 is a typical SN2 reaction; the rates of these reactions are sensitive to both the metal and the coligands, and those factors which encourage the first alkylation are those which inhibit the second.

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Available abstract

Dinitrogen loss from a range of bis(N2)-complexes of Mo and W is the common rate-determining step in the primary alkylation of the remaining co-ordinated N2, whereas the second alkylation of co-ordinated N2 is a typical SN2 reaction; the rates of these reactions are sensitive to both the metal and the coligands, and those factors which encourage the first alkylation are those which inhibit the second.

Key concepts: Alkylation, SN2 reaction, Chemistry, Reactivity (psychology), Metal, Primary (astronomy), Stereochemistry, Medicinal chemistry

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