Synthesis of nonperipherally tetra-[5-(diethylamino)-2-formylphenoxy] substituted metallophthalocyanines and their electrochemistry

Creative Commons License

KELEŞ T., Ünlüer D., BIYIKLIOĞLU Z., ÜNVER Y.

Turkish Journal of Chemistry, cilt.45, sa.1, ss.17-25, 2021 (SCI-Expanded) identifier identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 45 Sayı: 1
  • Basım Tarihi: 2021
  • Doi Numarası: 10.3906/kim-2007-47
  • Dergi Adı: Turkish Journal of Chemistry
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Chemical Abstracts Core, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.17-25
  • Anahtar Kelimeler: Synthesis, diethylamino, phthalocyanine, electrochemistry, ELECTROPOLYMERIZABLE METAL-FREE, DNA PHOTOCLEAVAGE, DNA/BSA BINDING, PHTHALOCYANINES, BEARING, BIOSENSOR, ZINC(II)
  • Recep Tayyip Erdoğan Üniversitesi Adresli: Evet

Özet

© This work is licensed under a Creative Commons Attribution 4.0 International License.3-[5-(diethylamino)-2-formylphenoxy]phthalonitrile (n-TY-CN), metallophthalocyanines n-TY-Co, n-TY-Cu, and n-TY-Mn bearing [5-(diethylamino)-2-formylphenoxy] groups at nonperipheral positions were prepared for the first time. These compounds were characterized with IR, NMR (only for n-TY-CN), mass and UV-vis (except n-TY-CN) spectroscopy. Voltammetric characterizations of n-TY-Co, n-TY-Cu, and n-TY-Mn revealed that while n-TY-Co, n-TY-Cu, and n-TY-Mn showed characteristic Pc ring and/or metal-based reduction reaction, n-TY-Co, n-TY-Cu, and n-TY-Mn were coated on the working electrode during the oxidation processes owing to the cationic electropolymerizations of the [5-(diethylamino)-2-formylphenoxy] substituents.