Issue 11, 2018

Self-assembly of singlet-emitting double-helical silver dimers: the curious coordination chemistry and fluorescence of bisquinolylpyridone

Abstract

2,6-Bis(2-quinolyl)-4(1H)-pyridone 1, a novel quinoline analogue of the well-known ligand 2-terpyridone, shows unusual fluorescence with a large Stokes shift and low energy emission. Pyridine-pyridone tautomerism is investigated by NMR and theoretical methods and indicates that the low energy emission is from the pyridine form. 1 reacts with Ag(I) salts to give a double helical Ag2N6 core showing a BLUE shift in fluorescence with respect to the free ligand, which has been characterised experimentally and theoretically as involving an unusual mixed MLCT/ILCT excited state and emission from a singlet state.

Graphical abstract: Self-assembly of singlet-emitting double-helical silver dimers: the curious coordination chemistry and fluorescence of bisquinolylpyridone

Supplementary files

Article information

Article type
Paper
Submitted
15 Dec 2017
Accepted
06 Feb 2018
First published
09 Feb 2018
This article is Open Access
Creative Commons BY license

Dalton Trans., 2018,47, 3906-3912

Self-assembly of singlet-emitting double-helical silver dimers: the curious coordination chemistry and fluorescence of bisquinolylpyridone

C. M. A. Farrow, G. R. Akien, N. R. Halcovitch, J. A. Platts and M. P. Coogan, Dalton Trans., 2018, 47, 3906 DOI: 10.1039/C7DT04744D

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements