Toggle Main Menu Toggle Search

Open Access padlockePrints

The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Circularly Polarized Luminescence from Helically Chiral N,N,O,O-Boron Chelated Dipyrromethenes

Lookup NU author(s): Rua Alnoman, Dr Sandra Rihn, Fiona Black, Dr Paul Waddell, Professor William Clegg, Dr Julian Knight, Dr Michael HallORCiD

Downloads


Licence

This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

Helically chiral N,N,O,O-boron chelated dipyrromethenes show solution-phase circularly polarized luminescence (CPL) in the red region of the visible spectrum (λem(max) from 621 to 663 nm). The parent dipyrromethene is desymmetrised through O-chelation of boron by the 3,5-ortho-phenolic substituents, inducing a helical chirality in the fluorophore. The combination of high luminescence dissymmetry factors (|glum| up to 4.7 x10-3) and fluorescence quantum yields (ΦF up to 0.73) results in exceptionally efficient circularly polarized red emission from these simple small organic fluorophores, enabling future application in CPL-based bioimaging.


Publication metadata

Author(s): Alnoman RB, Rihn S, OConnor DC, Black FA, Costello B, Waddell PG, Clegg W, Peacock RD, Herrebout W, Knight JG, Hall MJ

Publication type: Article

Publication status: Published

Journal: Chemistry - A European Journal

Year: 2016

Volume: 22

Issue: 1

Pages: 93-96

Print publication date: 04/01/2016

Online publication date: 11/11/2015

Acceptance date: 09/11/2015

Date deposited: 01/12/2015

ISSN (print): 0947-6539

ISSN (electronic): 1521-3765

Publisher: Wiley

URL: http://dx.doi.org/10.1002/chem.201504484

DOI: 10.1002/chem.201504484


Altmetrics

Altmetrics provided by Altmetric


Funding

Funder referenceFunder name
Newcastle University (NCL)
Department of Chemistry, Faculty of Science, Taibah University, Saudi Arabia
BB/K013971/1BBSRC
BB/K013971/1Biotechnology and Biological Sciences Research Council (BBSRC)

Share