Issue 16, 2012

Strong π-delocalization and substitution effect on electronic properties of dithienylpyrrole-containing bipyridineligands and corresponding ruthenium complexes

Abstract

The first dithienylpyrrole (DTP)-based bipyridine ligands has been prepared and coordinated with ruthenium to give the corresponding homoleptic complexes. Bipyridine was bound at pyrrole (DTP1) or thiophene (DTP2) ring. A strong bathochromic effect was obtained by switching from pyrrole to thiophene for ligands and complexes. Interestingly the DTP2 series offered a wide absorption window from UV to visible domain with an almost constant absorbance. These effects are due to a larger extent of delocalization as supported by DFT calculations and photophysical measurements.

Graphical abstract: Strong π-delocalization and substitution effect on electronic properties of dithienylpyrrole-containing bipyridine ligands and corresponding ruthenium complexes

Supplementary files

Article information

Article type
Paper
Submitted
07 Dec 2011
Accepted
24 Jan 2012
First published
06 Mar 2012

Dalton Trans., 2012,41, 4833-4844

Strong π-delocalization and substitution effect on electronic properties of dithienylpyrrole-containing bipyridine ligands and corresponding ruthenium complexes

S. Noureen, S. Caramori, A. Monari, X. Assfeld, R. Argazzi, C. A. Bignozzi, M. Beley and P. C. Gros, Dalton Trans., 2012, 41, 4833 DOI: 10.1039/C2DT12367C

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