Jump to main content
Jump to site search

Issue 14, 2013
Previous Article Next Article

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

Author affiliations

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

Back to tab navigation

Supplementary files

Publication details

The article was received on 20 Dec 2012, accepted on 07 Feb 2013 and first published on 26 Feb 2013


Article type: Communication
DOI: 10.1039/C3OB27468C
Org. Biomol. Chem., 2013,11, 2237-2240

  •   Request permissions

    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

Search articles by author

Spotlight

Advertisements