Issue 16, 2005
From the journal:

Chemical Communications

Straightforward synthesis of sulfur bridged oligopyrrolic macrocycles

David Sanchez-Garcia,a   Thomas Köhler,a   Daniel Seidel,a   Vincent Lyncha  and  Jonathan L. Sessler*a  

* Corresponding authors

a Department of Chemistry and Biochemistry and Institute for Cellular and Molecular Biology, 1 University Station-A5300, The University of Texas, Austin, Texas, USA
E-mail: sessler@mail.utexas.edu
Fax: +1 512 471 7550
Tel: +1 512 471 5009

Abstract

Di- and trisulfide linked oligopyrrolic macrocycles are obtained when appropriate α,α′-free pyrrolic precursors are reacted with sulfur dichloride; these systems represent the first examples of what might be a general new class of porphyrin analogues.

Graphical abstract: Straightforward synthesis of sulfur bridged oligopyrrolic macrocycles

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Article information

DOI
https://doi.org/10.1039/B500735F
Article type
Communication
Submitted
18 Jan 2005
Accepted
17 Feb 2005
First published
01 Mar 2005

Chem. Commun., 2005, 2122-2124

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Straightforward synthesis of sulfur bridged oligopyrrolic macrocycles

D. Sanchez-Garcia, T. Köhler, D. Seidel, V. Lynch and J. L. Sessler, Chem. Commun., 2005, 2122 DOI: 10.1039/B500735F

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