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

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

Turkish Journal of Chemistry, vol.45, no.1, pp.17-25, 2021 (SCI-Expanded) identifier identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 45 Issue: 1
  • Publication Date: 2021
  • Doi Number: 10.3906/kim-2007-47
  • Journal Name: Turkish Journal of Chemistry
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Chemical Abstracts Core, TR DİZİN (ULAKBİM)
  • Page Numbers: pp.17-25
  • Keywords: Synthesis, diethylamino, phthalocyanine, electrochemistry, ELECTROPOLYMERIZABLE METAL-FREE, DNA PHOTOCLEAVAGE, DNA/BSA BINDING, PHTHALOCYANINES, BEARING, BIOSENSOR, ZINC(II)
  • Recep Tayyip Erdoğan University Affiliated: Yes

Abstract

© 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.