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Original Articles

Synthesis and spectral properties of tetra- and octa-substituted lead phthalocyanines

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Pages 209-215 | Received 26 Sep 2005, Published online: 20 Feb 2007
 

Abstract

The novel four lead phthalocyanines were prepared from three different phthalonitrile derivatives, namely 3,4-dicyanophenylmalonate, 1-chloro-3,4-dicyano-6-(1,1-dicarbethoxy-methyl)benzene, 1-hexylthio-3,4-dicyano-6-(1,1-dicarbethoxy-methyl) benzene and metal salts (PbO or Pb(OAc)2·3H2O). Transesterification occurred when the reaction was carried out in hexanol in the presence of DBU. These new lead-phthalocyanines have been characterized by 1H NMR, FT-IR, UV-Vis and mass spectra. Two common points in these lead phthalocyanines are intense Q band absorptions in the near-IR region and relatively lower stability of the metal ion in the phthalocyanine cavity.

Acknowledgements

This work was supported by the Research Fund of the Technical University of Istanbul and State Planning Organization (DPT).

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