Synthesis, DFT Calculations, Photophysical, Photochemical Properties of Peripherally Metallophthalocyanines Bearing (2-(Benzo[d] [1,3] Dioxol-5-Ylmethoxy) Phenoxy) Substituents

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Solğun D., Yıldıko Ü., Ağırtaş M. S.

Polycyclic Aromatic Compounds, cilt.42, sa.9, ss.6444-6462, 2022 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 42 Sayı: 9
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1080/10406638.2021.1983618
  • Dergi Adı: Polycyclic Aromatic Compounds
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aerospace Database, Applied Science & Technology Source, CAB Abstracts, Chemical Abstracts Core, Communication Abstracts, Food Science & Technology Abstracts, Metadex, Pollution Abstracts, Veterinary Science Database, Civil Engineering Abstracts
  • Sayfa Sayıları: ss.6444-6462
  • Anahtar Kelimeler: Phthalocyanines, fluorescence, DFT, aggregation, the docking study, HOMO-LUMO, MOLECULAR-STRUCTURE, FT-IR, ZINC(II) PHTHALOCYANINE, COPPER-PHTHALOCYANINE, VIBRATIONAL-SPECTRA, MULLIKEN ANALYSIS, NBO, NLO, MEP
  • Van Yüzüncü Yıl Üniversitesi Adresli: Evet

Özet

© 2021 Taylor & Francis Group, LLC.4-(2-(benzo[d] [1,3] dioxol-5-ylmethoxy) phenoxy) phthalonitrile was first prepared as a starting material. Then, this new phthalonitrile derivative was reacted with Zn and Co salts to obtain new phthalocyanine complexes. Phthalocyanine complexes were evaluated by fluorescence emission, extinction, and absorption measurements. Aggregation studies show compliance with the lambert-beer law in the concentration range studied for peripheral phthalocyanine compounds. The density functional theory calculations of the metallophthalocyanines compounds were performed using the B3LYP method- LanL2DZ basis set to derive structural optimization, HOMO-LUMO energy parameters, and nonlinear Optical properties. The calculated values of metallophthalocyanines with different center atoms were obtained close to each other. Molecular electronic surface maps of the studied compounds are mapped and discussed. The HOMO-LUMO energy gaps of our compounds studied are around 2.1 eV. The docking studies were performed with the phthalonitrile.