Issue 20, 2010

Rational design of visible and NIR distyryl-BODIPYdyes from a novel fluorinated platform

Abstract

A new series of distyryl-BODIPY has been rationally designed and synthesised from a novel fluorinated platform, 8-pentafluorophenylBODIPY, which has enhanced reactivity in the presence of both electron rich, and for the first time, electron deficient aldehydes. The pentafluorobenzene leads to larger red shifts of absorption and emission compared to previously reported analogues. The reactivity and spectroscopic results have been rationalised with quantum mechanics calculation. The fluorescence sensitivity of one derivative to acidity is also presented.

Graphical abstract: Rational design of visible and NIR distyryl-BODIPY dyes from a novel fluorinated platform

Supplementary files

Article information

Article type
Paper
Submitted
31 Mar 2010
Accepted
30 Jun 2010
First published
17 Aug 2010

Org. Biomol. Chem., 2010,8, 4546-4553

Rational design of visible and NIR distyryl-BODIPY dyes from a novel fluorinated platform

O. Galangau, C. Dumas-Verdes, R. Méallet-Renault and G. Clavier, Org. Biomol. Chem., 2010, 8, 4546 DOI: 10.1039/C004812G

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