Issue 35, 2006
From the journal:

Chemical Communications

Synthesis of functionalized thia analogues of phlorins and covalently linked phlorin–porphyrin dyads†

Iti Gupta,a   Roland Fröhlichb  and  M. Ravikanth*a  

* Corresponding authors

a Department of Chemistry, Indian Institute of Technology, Mumbai, India
E-mail: ravikanth@chem.iitb.ac.in
Fax: +91-22-25767152
Tel: +91-22-25767176

b Organisch-Chemisches Institut, Universität Münster, Corrensstraße 40, D-48149 Münster, Germany

Abstract

The 21,23-dithia and 21-thia analogues of phlorins and mono-functionalized thiaphlorins were synthesized using easily available precursors and the mono-functionalized thiaphlorins were used further to synthesize the first examples of three covalently linked thiaphlorin–porphyrin dyads.

Graphical abstract: Synthesis of functionalized thia analogues of phlorins and covalently linked phlorin–porphyrin dyads

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B607013B
Article type
Communication
Submitted
17 May 2006
Accepted
03 Jul 2006
First published
01 Aug 2006

Chem. Commun., 2006, 3726-3728

Permissions

Request permissions

Synthesis of functionalized thia analogues of phlorins and covalently linked phlorin–porphyrin dyads

I. Gupta, R. Fröhlich and M. Ravikanth, Chem. Commun., 2006, 3726 DOI: 10.1039/B607013B

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