Issue 39, 2009
From the journal:

Chemical Communications

Meso-alkylidenyl-thia(p-benzi)porphyrins and their unusual protonation selectivity†

Seung-Doo Jeong,a   Kee Jong Park,a   Hyun-Jin Kima  and  Chang-Hee Lee*a  

* Corresponding authors

a Department of Chemistry Kangwon National University, Chun-Chon 200-701, Korea
E-mail: chhlee@kangwon.ac.kr
Fax: +82-33-250-7582
Tel: +82-33-250-8490

Abstract

Meso-alkylidenyl-thia(p-benzi)porphyrin and its ring expanded analog containing exocyclic C–C double bonds at meso-positions, undergo initial protonation at the exocyclic alkylidene α-carbon.

Graphical abstract: Meso-alkylidenyl-thia(p-benzi)porphyrins and their unusual protonation selectivity

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Article information

DOI
https://doi.org/10.1039/B911695H
Article type
Communication
Submitted
16 Jun 2009
Accepted
22 Jul 2009
First published
13 Aug 2009

Chem. Commun., 2009, 5877-5879

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Meso-alkylidenyl-thia(p-benzi)porphyrins and their unusual protonation selectivity

S. Jeong, K. J. Park, H. Kim and C. Lee, Chem. Commun., 2009, 5877 DOI: 10.1039/B911695H

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