OCTAKIS(ALKYLTHIO)-SUBSTITUTED PHTHALOCYANINES AND THEIR INTERACTIONS WITH SILVER(I) AND PALLADIUM(II) IONS

GUREK A., BEKAROGLU O.

JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, no.9, pp.1419-1423, 1994 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: Issue: 9
  • Publication Date: 1994
  • Doi Number: 10.1039/dt9940001419
  • Journal Name: JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aquatic Science & Fisheries Abstracts (ASFA), Chimica, Communication Abstracts, Compendex, EMBASE, MEDLINE
  • Page Numbers: pp.1419-1423
  • Istanbul Technical University Affiliated: No

Abstract

Metal-free phthalocyanines and metal phthalocyaninates (M = Ni, Cu, Co or Zn) carrying eight alkylthio-groups on peripheral positions have been synthesised from 4,5-bis(alkylthio)phthalonitrile and 1,8-diazabicyclo[5.4.0]undec-7-ene (dbu) or the corresponding anhydrous metal salt [NiCl2, CuCl, CoCl2 or Zn(O2CMe)2]. The resulting compounds reacted with silver(I) or palladium(II) salts to form complexes with a phthalocyanine:metal ratio of 1:4. Spectrophotochemical investigation of these reactions revealed that complexation with Ag(I) results in aggregation, while the addition of Pd(II) destroys the aggregation and yields a new Q band at 720 nm.