Synthesis and properties of new phthalocyanines with tertiary or quaternarized aminoethylsulfanyl substituents


Dabak S., GUMUS G., Gul A. , BEKAROGLU O.

JOURNAL OF COORDINATION CHEMISTRY, vol.38, no.4, pp.287-293, 1996 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 38 Issue: 4
  • Publication Date: 1996
  • Doi Number: 10.1080/00958979608024523
  • Title of Journal : JOURNAL OF COORDINATION CHEMISTRY
  • Page Numbers: pp.287-293

Abstract

Metal-free- and metallo-phthalocyanines (M = Ni or Zn) carrying four dimethylaminoethylsulfanyl- or trimethylaminoethylsulfanyl- groups on peripheral positions have been synthesized from the corresponding phthalonitrile derivatives in the presence or the absence of the anhydrous metal salt [NiCl2 or Zn(CH3COO)(2)]. The new compounds have been characterized by elemental analyses, IR, NMR, and electronic spectroscopy and mass spectra. Phthalocyanines with quaternarized amino groups are soluble in aqueous solution over a wide pH range and these molecules are present as aggregated species in solution as confirmed by the blue shift of Q bands in their electronic spectra.