Issue 27, 2019

Luminescent iridium(iii) complexes of N-heterocyclic carbene ligands prepared using the ‘click reaction’

Abstract

A series of imidazolium salt, N-heterocyclic carbene (NHC) ligand precursors, combined with 1,2,3-triazoles were synthesized using the Cu(I) catalyzed azide–alkyne cycloaddition ‘click reaction’. These pro-ligands were prepared from imidazolium molecules that were functionalized with either a terminal alkyne or azide group. Methylation of the triazole unit with methyl iodide produced a series of imidazolium/triazolium NHC pro-ligands. From these pro-ligands a family of luminescent Ir(III) complexes of the general form [Ir(ppy)2(C^N)]+ or [Ir(ppy)2(C^C)]+ (where ppy is 2-phenylpyridine and C^N represents a bidentate imidazolylidene/triazole ligand and C^C represents a bidentate imidazolylidene/triazolylidene ligand) were prepared. The electrochemical, photophysical and electrochemiluminescence properties of the complexes have been evaluated and a preliminary study of two of these compounds as luminescent probes for cell imaging studies was conducted in A549 human lung adenocarcinoma basal epithelial cells. Co-localisation studies with the commercial dye MitoTracker CMXRos were consistent with mitochondrial uptake for these compounds.

Graphical abstract: Luminescent iridium(iii) complexes of N-heterocyclic carbene ligands prepared using the ‘click reaction’

Supplementary files

Article information

Article type
Paper
Submitted
30 Mar 2019
Accepted
24 May 2019
First published
30 May 2019

Dalton Trans., 2019,48, 9998-10010

Luminescent iridium(III) complexes of N-heterocyclic carbene ligands prepared using the ‘click reaction’

R. E. Karmis, S. Carrara, A. A. Baxter, C. F. Hogan, M. D. Hulett and P. J. Barnard, Dalton Trans., 2019, 48, 9998 DOI: 10.1039/C9DT01362H

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.

Social activity

Spotlight

Advertisements