Preparation, characterization, electrochemistry and in situ spectroelectrochemistry of novel alpha-tetra[7-oxo-3-(2-chloro-4-fluorophenyl)coumarin]-substituted metal-free, cobalt and zinc phthalocyanines

Alemdar A., ÖZKAYA A. R., Bulut M.

SYNTHETIC METALS, cilt.160, ss.1556-1565, 2010 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 160
  • Basım Tarihi: 2010
  • Doi Numarası: 10.1016/j.synthmet.2010.05.025
  • Dergi Adı: SYNTHETIC METALS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1556-1565
  • Anahtar Kelimeler: Phthalocyanines, Coumarin, alpha-Substitution, Spectroelectrochemistry, ELECTROCATALYTIC PROPERTIES, WATER, REDUCTION, AGGREGATION, DERIVATIVES, ASSIGNMENT, COMPLEXES, ALUMINUM, SOLVENT, SERIES
  • Marmara Üniversitesi Adresli: Evet

Özet

In this study, a novel ligand, 7-(2,3-dicyanophenoxy)-3-(2-chloro-4-fluorophenyl)coumarin was synthesized by the reaction of 3-(2-chloro-4-fluorophenyI)-7-hydroxycoumarin with 1,2-dicyano-3-nitrobenzen in dry DMF as the solvent in the presence of K(2)CO(3) as the base. The preparation of the corresponding phthalocyanines H(2)Pc, CoPc and ZnPc, substituted with 7-oxo-3-(2-chloro-4-fluorophenyl)coumarin functional groups at a positions of the Pc ring, was achieved by the cyclotetramerization of the coumarin ligand without any metal salts or with the relevant metal(11) acetates in 2-N,N-dimethylaminoethanol. The structures of the compounds were confirmed by elemental analysis, UV-vis, IR, MALDI-TOF mass and 1H NMR spectra. In addition, aggregation and redox properties of the novel phthalocyanines with four halogenated coumarinoxy substituents at a positions of the phthalocyanine ring were compared with those of previously reported corresponding ones with beta-substitution, by UV-vis spectroscopy, in situ spectroelectrochemistry and voltammetry. Remarkable differences in these properties between alpha- and beta-substituted compounds were detected, and discussed in detail. (C) 2010 Elsevier B.V. All rights reserved.