Issue 1, 2017

Functionalisation of ligands through click chemistry: long-lived NIR emission from organic Er(iii) complexes with a perfluorinated core and a hydrogen-containing shell

Abstract

Erbium complexes with a fluorinated organic core shell linked to a hydrogen-containing shell, have been synthesized using the click reaction between erbium(III) bis(perfluoro-4-azidophenyl)phosphinate and a series of alkynes. The erbium 1.5 μm emission lifetimes in the hydrogen-containing erbium complexes exceed 140 μs, the longest ever reported in hydrogenated organic erbium systems. The visible sensitisation for erbium emission indicates a successful strategy that broadens the usage of non-fluorinated chromophores in organic erbium systems and allows more choices for ligand functionalization with exceptional efficiency for erbium emission.

Graphical abstract: Functionalisation of ligands through click chemistry: long-lived NIR emission from organic Er(iii) complexes with a perfluorinated core and a hydrogen-containing shell

Supplementary files

Article information

Article type
Paper
Submitted
19 Oct 2016
Accepted
01 Dec 2016
First published
22 Dec 2016
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 128-131

Functionalisation of ligands through click chemistry: long-lived NIR emission from organic Er(III) complexes with a perfluorinated core and a hydrogen-containing shell

Y. Peng, J. X. Hu, H. Lu, R. M. Wilson, M. Motevalli, I. Hernández, W. P. Gillin, P. B. Wyatt and H. Q. Ye, RSC Adv., 2017, 7, 128 DOI: 10.1039/C6RA25494B

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