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Physico-analytical studies on some heterocyclic azo dyes and their metal complexes with some transition metals

In this investigation, the azo dyes; 2-(3′-phenyl-5′-pyrazolyl azo) schaffer acid (la) and 2-(3′-phenyl-5′-pyrazolyl azo) resorcinol (Ib); were prepared through diazotizing 3-phenyl-5-aminopyrazole (PAP) and coupling the resulting diazonium salt with Schäffer acid and resorcinol respectively. The pr...

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Autores principales: El-Seify, Fathy A., Azab, Hassan A., Degedy, Fikrea S., Abdel-Mageed, Khalid A., El-Dossoki, Farid I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9153159/
https://www.ncbi.nlm.nih.gov/pubmed/35637518
http://dx.doi.org/10.1186/s13065-022-00833-x
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author El-Seify, Fathy A.
Azab, Hassan A.
Degedy, Fikrea S.
Abdel-Mageed, Khalid A.
El-Dossoki, Farid I.
author_facet El-Seify, Fathy A.
Azab, Hassan A.
Degedy, Fikrea S.
Abdel-Mageed, Khalid A.
El-Dossoki, Farid I.
author_sort El-Seify, Fathy A.
collection PubMed
description In this investigation, the azo dyes; 2-(3′-phenyl-5′-pyrazolyl azo) schaffer acid (la) and 2-(3′-phenyl-5′-pyrazolyl azo) resorcinol (Ib); were prepared through diazotizing 3-phenyl-5-aminopyrazole (PAP) and coupling the resulting diazonium salt with Schäffer acid and resorcinol respectively. The prepared azo dyes are characterized using both IR spectra and the elemental analysis (C, H, N and S). The prepared azo dyes are used as chromogenic reagents for the spectrophotometric determination of copper (II), nickel (II), cobalt (II) and zinc (II) ions. The conditional acid dissociation constants of these azo dyes (la and Ib) and the stability constants of its metal ion complexes have been determined by spectro-analytical methods. The effect of pH, time, organic solvent and the foreign ions on the spectrophotometric determination of these ions and their complexes with the azo dyes under study were studied. The stoichiometric ratio (M:L) of the formed complexes was also determined. The molar absorptivity, the Sandell's sensitivity values, the obeyance of Beers law and the stability constants of the formed complexes have been also determined and discussed.
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spelling pubmed-91531592022-06-01 Physico-analytical studies on some heterocyclic azo dyes and their metal complexes with some transition metals El-Seify, Fathy A. Azab, Hassan A. Degedy, Fikrea S. Abdel-Mageed, Khalid A. El-Dossoki, Farid I. BMC Chem Research In this investigation, the azo dyes; 2-(3′-phenyl-5′-pyrazolyl azo) schaffer acid (la) and 2-(3′-phenyl-5′-pyrazolyl azo) resorcinol (Ib); were prepared through diazotizing 3-phenyl-5-aminopyrazole (PAP) and coupling the resulting diazonium salt with Schäffer acid and resorcinol respectively. The prepared azo dyes are characterized using both IR spectra and the elemental analysis (C, H, N and S). The prepared azo dyes are used as chromogenic reagents for the spectrophotometric determination of copper (II), nickel (II), cobalt (II) and zinc (II) ions. The conditional acid dissociation constants of these azo dyes (la and Ib) and the stability constants of its metal ion complexes have been determined by spectro-analytical methods. The effect of pH, time, organic solvent and the foreign ions on the spectrophotometric determination of these ions and their complexes with the azo dyes under study were studied. The stoichiometric ratio (M:L) of the formed complexes was also determined. The molar absorptivity, the Sandell's sensitivity values, the obeyance of Beers law and the stability constants of the formed complexes have been also determined and discussed. Springer International Publishing 2022-05-30 /pmc/articles/PMC9153159/ /pubmed/35637518 http://dx.doi.org/10.1186/s13065-022-00833-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
El-Seify, Fathy A.
Azab, Hassan A.
Degedy, Fikrea S.
Abdel-Mageed, Khalid A.
El-Dossoki, Farid I.
Physico-analytical studies on some heterocyclic azo dyes and their metal complexes with some transition metals
title Physico-analytical studies on some heterocyclic azo dyes and their metal complexes with some transition metals
title_full Physico-analytical studies on some heterocyclic azo dyes and their metal complexes with some transition metals
title_fullStr Physico-analytical studies on some heterocyclic azo dyes and their metal complexes with some transition metals
title_full_unstemmed Physico-analytical studies on some heterocyclic azo dyes and their metal complexes with some transition metals
title_short Physico-analytical studies on some heterocyclic azo dyes and their metal complexes with some transition metals
title_sort physico-analytical studies on some heterocyclic azo dyes and their metal complexes with some transition metals
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9153159/
https://www.ncbi.nlm.nih.gov/pubmed/35637518
http://dx.doi.org/10.1186/s13065-022-00833-x
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