Synthesis and characterization of new polymeric phthalocyanines substituted with pyridine through methyleneoxy bridges by microwave irradiation

Kantekin H., BIYIKHOGLU Z.

DYES AND PIGMENTS, vol.77, no.2, pp.432-436, 2008 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 77 Issue: 2
  • Publication Date: 2008
  • Doi Number: 10.1016/j.dyepig.2007.07.004
  • Journal Name: DYES AND PIGMENTS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.432-436
  • Karadeniz Technical University Affiliated: Yes


A tetranitrile monomer was synthesized by nucleophilic aromatic substitution of pyridine-2,6-diyldimethanol onto 4-nitrophthalonitrile. A metal-free phthalocyanine polymer was prepared by the reaction of a tetranitrile monomer with 4,4'-[pyridine-2,6-diylbis(methyleneoxy)]diphthalonitrile in DMAE. Ni(II), Co(II), Cu(I)-phthalocyanine polymers were prepared by reaction of the tetranitrile compound with the chlorides of Ni(II), Co(II) and Cu(I) in DMAE. The Zn(II)-phthalocyanine polymer was prepared by reaction of the tetranitrile compound with the acetates of Zn(II) in DMAE. The new compounds were characterized by a combination of IR, H-1 NMR, C-13 NMR, UV-vis, elemental analysis and MS spectral data. @ 2007 Elsevier Ltd. All rights reserved.