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Oxidation and reduction data of four subphthalocyanines with axially coordinated ferrocenylcarboxylic acids

Redox data obtained from cyclic voltammetry experiments of the Fe(II/III) and ring-based oxidation and reductions of subphthalocyanines containing a ferrocenylcarboxylic acid as axial ligand, is presented in this data in brief article. The Fe(II/III) oxidation of ferrocenylsubphthalocyanines which c...

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Autores principales: Swarts, Pieter J., Conradie, Jeanet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7298653/
https://www.ncbi.nlm.nih.gov/pubmed/32566713
http://dx.doi.org/10.1016/j.dib.2020.105816
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author Swarts, Pieter J.
Conradie, Jeanet
author_facet Swarts, Pieter J.
Conradie, Jeanet
author_sort Swarts, Pieter J.
collection PubMed
description Redox data obtained from cyclic voltammetry experiments of the Fe(II/III) and ring-based oxidation and reductions of subphthalocyanines containing a ferrocenylcarboxylic acid as axial ligand, is presented in this data in brief article. The Fe(II/III) oxidation of ferrocenylsubphthalocyanines which containing the electron-withdrawing fluorine atoms at the peripheral and non-peripheral positions, are ca. 0.100 V more positive than Fe(II/III) oxidation of ferrocenylsubphthalocyanines containing hydrogens at the peripheral and non-peripheral positions. For more insight into the reported data, see the related research article “Redox and photophysical properties of four subphthalocyanines containing ferrocenylcarboxylic acid as axial ligands” [1].
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spelling pubmed-72986532020-06-19 Oxidation and reduction data of four subphthalocyanines with axially coordinated ferrocenylcarboxylic acids Swarts, Pieter J. Conradie, Jeanet Data Brief Chemistry Redox data obtained from cyclic voltammetry experiments of the Fe(II/III) and ring-based oxidation and reductions of subphthalocyanines containing a ferrocenylcarboxylic acid as axial ligand, is presented in this data in brief article. The Fe(II/III) oxidation of ferrocenylsubphthalocyanines which containing the electron-withdrawing fluorine atoms at the peripheral and non-peripheral positions, are ca. 0.100 V more positive than Fe(II/III) oxidation of ferrocenylsubphthalocyanines containing hydrogens at the peripheral and non-peripheral positions. For more insight into the reported data, see the related research article “Redox and photophysical properties of four subphthalocyanines containing ferrocenylcarboxylic acid as axial ligands” [1]. Elsevier 2020-06-03 /pmc/articles/PMC7298653/ /pubmed/32566713 http://dx.doi.org/10.1016/j.dib.2020.105816 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Chemistry
Swarts, Pieter J.
Conradie, Jeanet
Oxidation and reduction data of four subphthalocyanines with axially coordinated ferrocenylcarboxylic acids
title Oxidation and reduction data of four subphthalocyanines with axially coordinated ferrocenylcarboxylic acids
title_full Oxidation and reduction data of four subphthalocyanines with axially coordinated ferrocenylcarboxylic acids
title_fullStr Oxidation and reduction data of four subphthalocyanines with axially coordinated ferrocenylcarboxylic acids
title_full_unstemmed Oxidation and reduction data of four subphthalocyanines with axially coordinated ferrocenylcarboxylic acids
title_short Oxidation and reduction data of four subphthalocyanines with axially coordinated ferrocenylcarboxylic acids
title_sort oxidation and reduction data of four subphthalocyanines with axially coordinated ferrocenylcarboxylic acids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7298653/
https://www.ncbi.nlm.nih.gov/pubmed/32566713
http://dx.doi.org/10.1016/j.dib.2020.105816
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