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

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

JOURNAL OF COORDINATION CHEMISTRY, cilt.38, sa.4, ss.287-293, 1996 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 38 Sayı: 4
  • Basım Tarihi: 1996
  • Doi Numarası: 10.1080/00958979608024523
  • Dergi Adı: JOURNAL OF COORDINATION CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.287-293
  • İstanbul Teknik Üniversitesi Adresli: Hayır

Özet

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.