Issue 8, 2010
From the journal:

New Journal of Chemistry

Dithienophosphole-capped π-conjugated oligomers†‡§

Stefan Durben,a   Thomas Lindera  and  Thomas Baumgartner*a  

* Corresponding authors

a Department of Chemistry, University of Calgary, 2500 University Dr. NW, Calgary AB, Canada
E-mail: thomas.baumgartner@ucalgary.ca
Fax: +1 403-289-9488

Abstract

The synthesis of a 2-monobrominated dithieno[3,2-b:2′,3′-d]phosphole has opened the access to a series of highly luminescent π-conjugated oligomers that link two dithienophosphole units via a variety of aromatic spacers. The nature of the linking mode was found to have a significant impact on the photophysical properties of the system as a whole, either considerably improving the molar absorptivity of the new extended chromophores, or providing luminescent materials with red-shifted emission features and substantial photoluminescence quantum yields.

Graphical abstract: Dithienophosphole-capped π-conjugated oligomers

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C0NJ00026D
Article type
Paper
Submitted
15 Jan 2010
Accepted
02 Mar 2010
First published
31 Mar 2010

New J. Chem., 2010,34, 1585-1592

Permissions

Request permissions

Dithienophosphole-capped π-conjugated oligomers

S. Durben, T. Linder and T. Baumgartner, New J. Chem., 2010, 34, 1585 DOI: 10.1039/C0NJ00026D

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