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Antimicrobial and Dyeing Properties of Reactive Dyes with Thiazolidinon-4-one Nucleus

Four imines, the condensation products of 2,4-dioxo-4-phenylbutanal with four primary amines, were condensed with mercapto acetic acid to obtain thiazolidinon-4-ones which on subsequent condensation with vanillin and isatin separately yielded eight thiazolidin-4-one derivatives. The chemical structu...

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Detalles Bibliográficos
Autores principales: Ayalew, Hailemichael, Reda, Gebremedihin, Gashaw, Tsegaye, Babu, Neelaiah, Upadhyay, Raj Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041016/
https://www.ncbi.nlm.nih.gov/pubmed/24955258
http://dx.doi.org/10.1155/2014/894250
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author Ayalew, Hailemichael
Reda, Gebremedihin
Gashaw, Tsegaye
Babu, Neelaiah
Upadhyay, Raj Kumar
author_facet Ayalew, Hailemichael
Reda, Gebremedihin
Gashaw, Tsegaye
Babu, Neelaiah
Upadhyay, Raj Kumar
author_sort Ayalew, Hailemichael
collection PubMed
description Four imines, the condensation products of 2,4-dioxo-4-phenylbutanal with four primary amines, were condensed with mercapto acetic acid to obtain thiazolidinon-4-ones which on subsequent condensation with vanillin and isatin separately yielded eight thiazolidin-4-one derivatives. The chemical structures of the synthesized compounds were elucidated by elemental analysis, molecular weight determination, IR and (1)H and (13)C NMR spectral measurements. Antibacterial and antifungal properties were studied in vitro against two bacteria and two fungi. The dyeing potential of synthesized reactive dyes was investigated with regard to silk, wool, cotton, and polyester fabrics under hot and cold dyeing conditions.
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spelling pubmed-40410162014-06-22 Antimicrobial and Dyeing Properties of Reactive Dyes with Thiazolidinon-4-one Nucleus Ayalew, Hailemichael Reda, Gebremedihin Gashaw, Tsegaye Babu, Neelaiah Upadhyay, Raj Kumar ISRN Org Chem Research Article Four imines, the condensation products of 2,4-dioxo-4-phenylbutanal with four primary amines, were condensed with mercapto acetic acid to obtain thiazolidinon-4-ones which on subsequent condensation with vanillin and isatin separately yielded eight thiazolidin-4-one derivatives. The chemical structures of the synthesized compounds were elucidated by elemental analysis, molecular weight determination, IR and (1)H and (13)C NMR spectral measurements. Antibacterial and antifungal properties were studied in vitro against two bacteria and two fungi. The dyeing potential of synthesized reactive dyes was investigated with regard to silk, wool, cotton, and polyester fabrics under hot and cold dyeing conditions. Hindawi Publishing Corporation 2014-03-04 /pmc/articles/PMC4041016/ /pubmed/24955258 http://dx.doi.org/10.1155/2014/894250 Text en Copyright © 2014 Hailemichael Ayalew et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ayalew, Hailemichael
Reda, Gebremedihin
Gashaw, Tsegaye
Babu, Neelaiah
Upadhyay, Raj Kumar
Antimicrobial and Dyeing Properties of Reactive Dyes with Thiazolidinon-4-one Nucleus
title Antimicrobial and Dyeing Properties of Reactive Dyes with Thiazolidinon-4-one Nucleus
title_full Antimicrobial and Dyeing Properties of Reactive Dyes with Thiazolidinon-4-one Nucleus
title_fullStr Antimicrobial and Dyeing Properties of Reactive Dyes with Thiazolidinon-4-one Nucleus
title_full_unstemmed Antimicrobial and Dyeing Properties of Reactive Dyes with Thiazolidinon-4-one Nucleus
title_short Antimicrobial and Dyeing Properties of Reactive Dyes with Thiazolidinon-4-one Nucleus
title_sort antimicrobial and dyeing properties of reactive dyes with thiazolidinon-4-one nucleus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041016/
https://www.ncbi.nlm.nih.gov/pubmed/24955258
http://dx.doi.org/10.1155/2014/894250
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