Issue 12, 2016

Dual nucleophilic substitution at a W(ii) η2-coordinated diiodo acetylene leading to an amidinium carbyne complex

Abstract

The synthesis and reactivity of a W(II) C2I2 complex towards various nucleophiles are described. Soft, aprotic nucleophiles like 4-dimethylaminopyridine (DMAP) lead to substitution of one CO at tungsten, whereas reaction with an excess of benzylamine results in a dual nucleophilic substitution at the alkyne moiety involving the rearrangement to a novel cationic amidinium carbyne complex.

Graphical abstract: Dual nucleophilic substitution at a W(ii) η2-coordinated diiodo acetylene leading to an amidinium carbyne complex

Supplementary files

Article information

Article type
Communication
Submitted
18 Dec 2015
Accepted
30 Dec 2015
First published
04 Jan 2016

Chem. Commun., 2016,52, 2616-2619

Dual nucleophilic substitution at a W(II) η2-coordinated diiodo acetylene leading to an amidinium carbyne complex

K. Helmdach, J. Rüger, A. Villinger and W. W. Seidel, Chem. Commun., 2016, 52, 2616 DOI: 10.1039/C5CC10397E

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