Synthesis of peripheral and non-peripheral substituted metallophthalocyanines containing (E)-3-(5-bromo-2-hydroxphenyl)-1-o-tolyprop-2-en-1-one: Investigation of the photophysical and photochemical properties

KANTEKİN H., Sarkı G., Ömeroğlu İ., Yalazan H., KAHRİMAN N., Durmuş M.

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, vol.252, 2021 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 252
  • Publication Date: 2021
  • Doi Number: 10.1016/j.saa.2021.119474
  • Journal Name: Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, CAB Abstracts, Chemical Abstracts Core, Chimica, Compendex, EMBASE, INSPEC, MEDLINE, Veterinary Science Database
  • Keywords: Phthalocyanine, Chalcone, Photodynamic therapy, Fluorescence, Singlet oxygen, Photodegradation, METAL-FREE, PHTHALOCYANINES SYNTHESIS, CHALCONE DERIVATIVES, FLAVONOIDS, ZINC(II)
  • Karadeniz Technical University Affiliated: Yes


© 2021 Elsevier B.V.In this study, the novel peripherally (5–7) and non-peripherally (9–11) metallo (zinc, magnesium and lead) phthalocyanine derivatives were synthesized from their (E)-4-(4-bromo-2-(3-oxo-3-o-tolyprop-1-enyl)phenoxy) substituted phthalonitrile precursors (4 and 8). These novel phthalocyanine derivatives including chalcone groups were characterized by spectroscopic techniques such as FT-IR, UV–vis, 1H NMR, 13C NMR and MALDI-TOF mass spectra. In the next stage, the photophysical and photochemical properties of synthesized compounds were searched in DMSO which is not cause toxic effects at a certain concentration in biological applications. As a result of investigations, it was determined that phthalocyanine complexes did not demonstrate aggregation in DMSO solutions.