Non-aggregating phthalocyanines with bulky 2,4-di-tert-butylphenoxy-substituents

Agirtas M. S.

DYES AND PIGMENTS, vol.74, no.2, pp.490-493, 2007 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 74 Issue: 2
  • Publication Date: 2007
  • Doi Number: 10.1016/j.dyeing.2006.03.009
  • Journal Name: DYES AND PIGMENTS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.490-493
  • Keywords: phthalonitrile derivatives, phthalocyanine, nucleophilic displacement, metal complexes, aggregation, PORPHYRINS, COMPLEXES
  • Van Yüzüncü Yıl University Affiliated: No


In this paper, a bulky (2,4-di-tert-butylphenoxy)-substituted phthalonitrile was synthesized by nucleophilic displacement of nitro group in 4-nitro-phthalonitrile with 2,4-di-tert-butylphenol. Its cyclotetramerization in the presence of zinc(II), cobalt(II), nickel(II) or copper(II) ion with catalytic amount of DBU resulted in phthalocyanines being extensively soluble in number of organic solvents. Aggregation did not occur even in concentrations up to 1 x 10(-3) M. The new compounds were characterized by elemental analyses, UV-vis, IR and NMR spectra. (c) 2006 Elsevier Ltd. All rights reserved.