Issue 22, 1983

Isomerization and dealkylation reactions of nickel(II) complexes of macrocyclic tertiary amine ligands: X-ray crystal structures of {Ni[1,4,8,11-tetra(2-cyanoethyl)-1,4,8,11-tetra-azacyclotetradecane](NCMe)2}(ClO4)2·H2O and {Ni[1,8-di (2-carbamoylethyl)-4-(2-cyanoethyl)-1,4,8,11-tetra-azacyclotetradecane]}(ClO4)2

Abstract

Nitrogen inversion reactions have been observed in nickel(II) complexes of macrocyclic tertiary tetra-amine ligands in which the nitrogen substituents are either 2-cyanoethyl or 2-carbamoylethyl; under certain conditions dealkylative loss of the cyanoethyl substituent occurs but loss of a carbamoyl substituent has not been observed for nickel(II) although it has for copper(II).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 1358-1360

Isomerization and dealkylation reactions of nickel(II) complexes of macrocyclic tertiary amine ligands: X-ray crystal structures of {Ni[1,4,8,11-tetra(2-cyanoethyl)-1,4,8,11-tetra-azacyclotetradecane](NCMe)2}(ClO4)2·H2O and {Ni[1,8-di (2-carbamoylethyl)-4-(2-cyanoethyl)-1,4,8,11-tetra-azacyclotetradecane]}(ClO4)2

E. K. Barefield, G. M. Freeman and D. G. V. Derveer, J. Chem. Soc., Chem. Commun., 1983, 1358 DOI: 10.1039/C39830001358

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements