Issue 38, 2021

Steric effects on acetate-assisted cyclometallation of meta-substituted N-phenyl and N-benzyl imidazolium salts at [MCl2Cp*]2 (M = Ir, Rh)

Abstract

meta-Substituted N-phenyl,N′-methyl and N-benzyl,N′-methyl imidazolium salts undergo acetate-assisted cyclometallation to provide mixtures of ortho and para substituted cyclometallated complexes. The effect of the substituents on the isomer ratios is discussed; steric effects are more important in the 6-membered rings derived from the N-benzyl imidazolium salts than 5-membered rings from the N-phenyl salts. Comparisons are made to steric effects with some other common directing groups.

Graphical abstract: Steric effects on acetate-assisted cyclometallation of meta-substituted N-phenyl and N-benzyl imidazolium salts at [MCl2Cp*]2 (M = Ir, Rh)

Supplementary files

Article information

Article type
Paper
Submitted
11 Aug 2021
Accepted
31 Aug 2021
First published
31 Aug 2021
This article is Open Access
Creative Commons BY license

Dalton Trans., 2021,50, 13505-13515

Steric effects on acetate-assisted cyclometallation of meta-substituted N-phenyl and N-benzyl imidazolium salts at [MCl2Cp*]2 (M = Ir, Rh)

D. L. Davies, K. Singh and N. Tamosiunaite, Dalton Trans., 2021, 50, 13505 DOI: 10.1039/D1DT02677A

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