Issue 14, 2013

Synthesis of unsymmetrical carboxyphthalocyanines by palladium-catalyzed hydroxycarbonylation of iodo-substituted precursors

Abstract

Phthalocyanines (Pcs) containing a carboxylic acid functionality directly bound to the macrocycle have been synthesized, in one step and in good yields, from iodo-substituted Pc precursors. This methodology represents a convenient alternative to the commonly used method based on two consecutive oxidations of hydroxymethyl Pcs.

Graphical abstract: Synthesis of unsymmetrical carboxyphthalocyanines by palladium-catalyzed hydroxycarbonylation of iodo-substituted precursors

Supplementary files

Article information

Article type
Communication
Submitted
20 Dec 2012
Accepted
07 Feb 2013
First published
26 Feb 2013

Org. Biomol. Chem., 2013,11, 2237-2240

Synthesis of unsymmetrical carboxyphthalocyanines by palladium-catalyzed hydroxycarbonylation of iodo-substituted precursors

Í. Aguirre de Carcer García, A. M. Sevim, A. de la Escosura and T. Torres, Org. Biomol. Chem., 2013, 11, 2237 DOI: 10.1039/C3OB27468C

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