Polyaniline-supported palladium(ii)-schiff base complex as efficient catalyst for mizoroki-heck cross-coupling reaction

Mizoroki-Heck cross-coupling reaction of 4-bromoacetophenone with methyl acrylate were investigated as a model system of heterogeneous reaction in order to evaluate the performance of polyaniline supported N,N’-bis(3,5-di-tert-butylsalicylidene)propane-1,3-diaminepalladium(II) complex as catalyst. T...

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Main Authors: Che Soh, Siti Kamilah, Shamsuddin, Mustaffa
Format: Article
Language:English
Published: Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia (UTM) 2012
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Online Access:http://eprints.utm.my/id/eprint/29093/1/MustaffaShamsuddin2012_Polyaniline-SupportedPalladium%28II%29-SchiffBaseComplexasEfficientCatalystforMizoroki-HeckCross-CouplingReaction.pdf
http://eprints.utm.my/id/eprint/29093/
http://mjfas.ibnusina.utm.my/index.php/jfs/article/viewFile/283/213
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spelling my.utm.290932013-03-13T03:45:59Z http://eprints.utm.my/id/eprint/29093/ Polyaniline-supported palladium(ii)-schiff base complex as efficient catalyst for mizoroki-heck cross-coupling reaction Che Soh, Siti Kamilah Shamsuddin, Mustaffa QD Chemistry Mizoroki-Heck cross-coupling reaction of 4-bromoacetophenone with methyl acrylate were investigated as a model system of heterogeneous reaction in order to evaluate the performance of polyaniline supported N,N’-bis(3,5-di-tert-butylsalicylidene)propane-1,3-diaminepalladium(II) complex as catalyst. The reactions were carried out in both N,N-dimethylacetamide (DMAc) and water-DMAc mixed solvent. The performances of the catalyst in both media are comparable, giving more than 90 % conversion after 24 hours of reaction with 100 % selectivity and high isolated product yields of cinnamic esters were obtained. The used of mixed solvent gave more advantages such as less organic solvent was required and an enhanced recyclability in which the supported catalyst could be reusable at least four times without noticeable decrease in the product conversion. The properties of the catalyst was characterized by various techniques such as FTIR spectroscopy, TG-DTA, AAS, BET surface area, XRD and FESEM. Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia (UTM) 2012 Article PeerReviewed application/pdf en http://eprints.utm.my/id/eprint/29093/1/MustaffaShamsuddin2012_Polyaniline-SupportedPalladium%28II%29-SchiffBaseComplexasEfficientCatalystforMizoroki-HeckCross-CouplingReaction.pdf Che Soh, Siti Kamilah and Shamsuddin, Mustaffa (2012) Polyaniline-supported palladium(ii)-schiff base complex as efficient catalyst for mizoroki-heck cross-coupling reaction. Malaysian Journal of Fundamental and Applied Sciences, 8 (2). pp. 94-100. ISSN 1823-626X http://mjfas.ibnusina.utm.my/index.php/jfs/article/viewFile/283/213
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
language English
topic QD Chemistry
spellingShingle QD Chemistry
Che Soh, Siti Kamilah
Shamsuddin, Mustaffa
Polyaniline-supported palladium(ii)-schiff base complex as efficient catalyst for mizoroki-heck cross-coupling reaction
description Mizoroki-Heck cross-coupling reaction of 4-bromoacetophenone with methyl acrylate were investigated as a model system of heterogeneous reaction in order to evaluate the performance of polyaniline supported N,N’-bis(3,5-di-tert-butylsalicylidene)propane-1,3-diaminepalladium(II) complex as catalyst. The reactions were carried out in both N,N-dimethylacetamide (DMAc) and water-DMAc mixed solvent. The performances of the catalyst in both media are comparable, giving more than 90 % conversion after 24 hours of reaction with 100 % selectivity and high isolated product yields of cinnamic esters were obtained. The used of mixed solvent gave more advantages such as less organic solvent was required and an enhanced recyclability in which the supported catalyst could be reusable at least four times without noticeable decrease in the product conversion. The properties of the catalyst was characterized by various techniques such as FTIR spectroscopy, TG-DTA, AAS, BET surface area, XRD and FESEM.
format Article
author Che Soh, Siti Kamilah
Shamsuddin, Mustaffa
author_facet Che Soh, Siti Kamilah
Shamsuddin, Mustaffa
author_sort Che Soh, Siti Kamilah
title Polyaniline-supported palladium(ii)-schiff base complex as efficient catalyst for mizoroki-heck cross-coupling reaction
title_short Polyaniline-supported palladium(ii)-schiff base complex as efficient catalyst for mizoroki-heck cross-coupling reaction
title_full Polyaniline-supported palladium(ii)-schiff base complex as efficient catalyst for mizoroki-heck cross-coupling reaction
title_fullStr Polyaniline-supported palladium(ii)-schiff base complex as efficient catalyst for mizoroki-heck cross-coupling reaction
title_full_unstemmed Polyaniline-supported palladium(ii)-schiff base complex as efficient catalyst for mizoroki-heck cross-coupling reaction
title_sort polyaniline-supported palladium(ii)-schiff base complex as efficient catalyst for mizoroki-heck cross-coupling reaction
publisher Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia (UTM)
publishDate 2012
url http://eprints.utm.my/id/eprint/29093/1/MustaffaShamsuddin2012_Polyaniline-SupportedPalladium%28II%29-SchiffBaseComplexasEfficientCatalystforMizoroki-HeckCross-CouplingReaction.pdf
http://eprints.utm.my/id/eprint/29093/
http://mjfas.ibnusina.utm.my/index.php/jfs/article/viewFile/283/213
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score 13.209306