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Novel Schiff base cobalt(ii) phthalocyanine with appliance of MWCNTs on GCE: enhanced electrocatalytic activity behaviour of α-amino acids

A novel tetra-4-{(E)-[(8-aminonaphthalen-1-yl)imino]methyl}-2-methoxyphenol Co(ii) phthalocyanine (CoTANImMMPPc) was synthesized using a precursor protocol and characterized via electroanalytical and spectroscopic techniques. The FT-IR spectra of the synthesized compounds showed significant peaks co...

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Autores principales: Mounesh, Sharan Kumar, T. M., Praveen Kumar, N. Y., Reddy, K. R. Venugopala, Chandrakala, K. B., Arunkumar, L., Vidyasagar, C. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9032359/
https://www.ncbi.nlm.nih.gov/pubmed/35479120
http://dx.doi.org/10.1039/d1ra01815a
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author Mounesh,
Sharan Kumar, T. M.
Praveen Kumar, N. Y.
Reddy, K. R. Venugopala
Chandrakala, K. B.
Arunkumar, L.
Vidyasagar, C. C.
author_facet Mounesh,
Sharan Kumar, T. M.
Praveen Kumar, N. Y.
Reddy, K. R. Venugopala
Chandrakala, K. B.
Arunkumar, L.
Vidyasagar, C. C.
author_sort Mounesh,
collection PubMed
description A novel tetra-4-{(E)-[(8-aminonaphthalen-1-yl)imino]methyl}-2-methoxyphenol Co(ii) phthalocyanine (CoTANImMMPPc) was synthesized using a precursor protocol and characterized via electroanalytical and spectroscopic techniques. The FT-IR spectra of the synthesized compounds showed significant peaks corresponding to the functional groups of the precursors and phthalocyanine (Pc) compound. The mass and NMR spectra confirmed the formation of the target precursor compounds. A film of CoTANImMMPPc was deposited on the surface of an electrode and applied for the detection and monitoring of l-alanine and l-arginine. The cyclic voltammetric studies of l-alanine and l-arginine using the (CoTANImMMPPc/MWCNTs/GC) electrode showed a linear response in the range of 50–500 nM and the limit of detection was found to be 1.5 and 1.2 nM, respectively. Differential pulse voltammetry and chronoamperometry showed that the catalytic response for l-alanine and l-arginine is in the range of 50–500 nM with an LoD of 1.8 and 2.3 nM, respectively. The oxidation-active CoTANImMMPPc film significantly enhanced the current response in the chronoamperometric method and displayed a selective and sensitive response towards l-alanine and l-arginine in the presence of various other bio-molecules. The developed electrode showed good working stability and was applied for the analysis of real samples, which yielded satisfactory results. Therefore, CoTANImMMPPc-MWCNTs/GCE shows good analytical performance, is economical and produced via a simple synthetic method and can be applied as a sensor for the detection of l-alanine and l-arginine.
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spelling pubmed-90323592022-04-26 Novel Schiff base cobalt(ii) phthalocyanine with appliance of MWCNTs on GCE: enhanced electrocatalytic activity behaviour of α-amino acids Mounesh, Sharan Kumar, T. M. Praveen Kumar, N. Y. Reddy, K. R. Venugopala Chandrakala, K. B. Arunkumar, L. Vidyasagar, C. C. RSC Adv Chemistry A novel tetra-4-{(E)-[(8-aminonaphthalen-1-yl)imino]methyl}-2-methoxyphenol Co(ii) phthalocyanine (CoTANImMMPPc) was synthesized using a precursor protocol and characterized via electroanalytical and spectroscopic techniques. The FT-IR spectra of the synthesized compounds showed significant peaks corresponding to the functional groups of the precursors and phthalocyanine (Pc) compound. The mass and NMR spectra confirmed the formation of the target precursor compounds. A film of CoTANImMMPPc was deposited on the surface of an electrode and applied for the detection and monitoring of l-alanine and l-arginine. The cyclic voltammetric studies of l-alanine and l-arginine using the (CoTANImMMPPc/MWCNTs/GC) electrode showed a linear response in the range of 50–500 nM and the limit of detection was found to be 1.5 and 1.2 nM, respectively. Differential pulse voltammetry and chronoamperometry showed that the catalytic response for l-alanine and l-arginine is in the range of 50–500 nM with an LoD of 1.8 and 2.3 nM, respectively. The oxidation-active CoTANImMMPPc film significantly enhanced the current response in the chronoamperometric method and displayed a selective and sensitive response towards l-alanine and l-arginine in the presence of various other bio-molecules. The developed electrode showed good working stability and was applied for the analysis of real samples, which yielded satisfactory results. Therefore, CoTANImMMPPc-MWCNTs/GCE shows good analytical performance, is economical and produced via a simple synthetic method and can be applied as a sensor for the detection of l-alanine and l-arginine. The Royal Society of Chemistry 2021-05-06 /pmc/articles/PMC9032359/ /pubmed/35479120 http://dx.doi.org/10.1039/d1ra01815a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Mounesh,
Sharan Kumar, T. M.
Praveen Kumar, N. Y.
Reddy, K. R. Venugopala
Chandrakala, K. B.
Arunkumar, L.
Vidyasagar, C. C.
Novel Schiff base cobalt(ii) phthalocyanine with appliance of MWCNTs on GCE: enhanced electrocatalytic activity behaviour of α-amino acids
title Novel Schiff base cobalt(ii) phthalocyanine with appliance of MWCNTs on GCE: enhanced electrocatalytic activity behaviour of α-amino acids
title_full Novel Schiff base cobalt(ii) phthalocyanine with appliance of MWCNTs on GCE: enhanced electrocatalytic activity behaviour of α-amino acids
title_fullStr Novel Schiff base cobalt(ii) phthalocyanine with appliance of MWCNTs on GCE: enhanced electrocatalytic activity behaviour of α-amino acids
title_full_unstemmed Novel Schiff base cobalt(ii) phthalocyanine with appliance of MWCNTs on GCE: enhanced electrocatalytic activity behaviour of α-amino acids
title_short Novel Schiff base cobalt(ii) phthalocyanine with appliance of MWCNTs on GCE: enhanced electrocatalytic activity behaviour of α-amino acids
title_sort novel schiff base cobalt(ii) phthalocyanine with appliance of mwcnts on gce: enhanced electrocatalytic activity behaviour of α-amino acids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9032359/
https://www.ncbi.nlm.nih.gov/pubmed/35479120
http://dx.doi.org/10.1039/d1ra01815a
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