Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5567
Title: Phthalocyanine pendented polyaniline via amide linkage for an electrochemical sensing of H2O2
Authors: Sudhakara, Sarvajith Malali
DEVENDRACHARI, MRUTHYUNJAYACHARI CHATTANAHALLI
Kotresh, Harish Makri Nimbegondi
Khan, Fasiulla
Dept. of Chemistry
Keywords: Phthalocyanine
Polyaniline
Non-enzymatic sensor
Hydrogen peroxide
Electrocatalyst
Electrochemical sensor
2021-JAN-WEEK3
TOC-JAN-2021
2021
Issue Date: Feb-2021
Publisher: Elsevier B.V.
Citation: Microchemical Journal, 161, 105781.
Abstract: Cobalt phthalocyanines are known to be the better electrocatalyst for a wide range of organic, inorganic, and biomolecular analytes. The synthesis of electrocatalysts through phthalocyanine (Pc) functionalization involves a single-step reaction to a multi-step reaction. The functionalization of Pc catalyst with the conducting polymer involves either simple electronic interactions or direct covalent bonding. Here we are reporting covalently connected tetra carboxy cobalt phthalocyanine (TCCoPc) pendent via amide linking to the conducting polyaniline (PANI) backbone. The synthesized electrocatalyst is extensively utilized for the sensing of biologically active H2O2 on the surface of the catalyst modified glassy carbon electrode (GCE). The synthesized molecule was characterized by various spectroscopic techniques and the detailed electrochemical activity of the synthesized molecule for the sensing of H2O2 was investigated using linear sweep voltammetry and chronoamperometry techniques, by fabricating on the GCE. The superlative catalytic activity of the synthesized molecule is might be due to the synergetic effect of pendanted macrocyclic Pc molecule with the redox-active demeanor of central cobalt metal atom and anchoring of the metal-centered Pc through amide linking with the conducting PANI.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5567
https://doi.org/10.1016/j.microc.2020.105781
ISSN: 0026-265X
1095-9149
Appears in Collections:JOURNAL ARTICLES

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