Synthesis of phthalocyanines crosswise-substituted with two alkylsulfanyl and two amino groups


Dabak S., Bekaroglu O.

NEW JOURNAL OF CHEMISTRY, vol.21, no.2, pp.267-271, 1997 (Journal Indexed in SCI) identifier

  • Publication Type: Article / Article
  • Volume: 21 Issue: 2
  • Publication Date: 1997
  • Title of Journal : NEW JOURNAL OF CHEMISTRY
  • Page Numbers: pp.267-271

Abstract

Crosswise-substituted phthalocyanines (4, 4a-c) with two nitro and two dodecylsulfanyl groups are synthesized by a 2:2 condensation of 1,3-dihydro-1,3-diimino-6-(n-dodecylsulfanyl)isoiminoindolenine (2) with 6-nitro-1,3,3-trichloroisoindolenine (3) in the presence of sodium methoxide, hydroquinone and triethylamine. Nitro substituents are reduced to amines by sodium sulfide and condensation of the amine groups with ferrocenylaldehyde results in a new pc with two ferrocenylimino substituents, The novel compounds are characterized by UV/vis, mass and H-1-NMR spectroscopy.