Highly Active Thiol-functionalized SBA-15 Supported Palladium catalyst for Sonogashira and Suzuki-Miyaura Cross-coupling Reactions

Highly ordered mesoporous silica SBA-15 with pendent 3-mercaptopropyl groups has been prepared by condensation of surface silanols and (3-mercaptopropyl)trimethoxysilane. Treatment of the mercaptopropylated SBA-15 with (CH3CN)2PdCl2 gave a heterogeneous Pd-catalyst. The immobilized Pd-catalyst se...

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Main Authors: Sarkar, Shaheen M., Lutfor, M. R., M. M., Yusoff
Format: Article
Published: Royal Society of Chemistry 2015
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Online Access:http://umpir.ump.edu.my/id/eprint/8101/
http://dx.doi.org/10.1039/C4RA13322F
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spelling my.ump.umpir.81012018-02-14T04:01:50Z http://umpir.ump.edu.my/id/eprint/8101/ Highly Active Thiol-functionalized SBA-15 Supported Palladium catalyst for Sonogashira and Suzuki-Miyaura Cross-coupling Reactions Sarkar, Shaheen M. Lutfor, M. R. M. M., Yusoff Q Science (General) Highly ordered mesoporous silica SBA-15 with pendent 3-mercaptopropyl groups has been prepared by condensation of surface silanols and (3-mercaptopropyl)trimethoxysilane. Treatment of the mercaptopropylated SBA-15 with (CH3CN)2PdCl2 gave a heterogeneous Pd-catalyst. The immobilized Pd-catalyst served as an efficient heterogeneous catalyst for Sonogashira and Suzuki–Miyaura cross coupling reactions of aryl halides. Furthermore, the SBA-15 supported Pd-catalyst was recovered by a simple filtration from the reaction mixture and reused five times without significant loss of its catalytic activity. Royal Society of Chemistry 2015 Article PeerReviewed Sarkar, Shaheen M. and Lutfor, M. R. and M. M., Yusoff (2015) Highly Active Thiol-functionalized SBA-15 Supported Palladium catalyst for Sonogashira and Suzuki-Miyaura Cross-coupling Reactions. RSC Advances, 5. pp. 1295-1300. ISSN 2046-2069 http://dx.doi.org/10.1039/C4RA13322F DOI: 10.1039/C4RA13322F
institution Universiti Malaysia Pahang
building UMP Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Pahang
content_source UMP Institutional Repository
url_provider http://umpir.ump.edu.my/
topic Q Science (General)
spellingShingle Q Science (General)
Sarkar, Shaheen M.
Lutfor, M. R.
M. M., Yusoff
Highly Active Thiol-functionalized SBA-15 Supported Palladium catalyst for Sonogashira and Suzuki-Miyaura Cross-coupling Reactions
description Highly ordered mesoporous silica SBA-15 with pendent 3-mercaptopropyl groups has been prepared by condensation of surface silanols and (3-mercaptopropyl)trimethoxysilane. Treatment of the mercaptopropylated SBA-15 with (CH3CN)2PdCl2 gave a heterogeneous Pd-catalyst. The immobilized Pd-catalyst served as an efficient heterogeneous catalyst for Sonogashira and Suzuki–Miyaura cross coupling reactions of aryl halides. Furthermore, the SBA-15 supported Pd-catalyst was recovered by a simple filtration from the reaction mixture and reused five times without significant loss of its catalytic activity.
format Article
author Sarkar, Shaheen M.
Lutfor, M. R.
M. M., Yusoff
author_facet Sarkar, Shaheen M.
Lutfor, M. R.
M. M., Yusoff
author_sort Sarkar, Shaheen M.
title Highly Active Thiol-functionalized SBA-15 Supported Palladium catalyst for Sonogashira and Suzuki-Miyaura Cross-coupling Reactions
title_short Highly Active Thiol-functionalized SBA-15 Supported Palladium catalyst for Sonogashira and Suzuki-Miyaura Cross-coupling Reactions
title_full Highly Active Thiol-functionalized SBA-15 Supported Palladium catalyst for Sonogashira and Suzuki-Miyaura Cross-coupling Reactions
title_fullStr Highly Active Thiol-functionalized SBA-15 Supported Palladium catalyst for Sonogashira and Suzuki-Miyaura Cross-coupling Reactions
title_full_unstemmed Highly Active Thiol-functionalized SBA-15 Supported Palladium catalyst for Sonogashira and Suzuki-Miyaura Cross-coupling Reactions
title_sort highly active thiol-functionalized sba-15 supported palladium catalyst for sonogashira and suzuki-miyaura cross-coupling reactions
publisher Royal Society of Chemistry
publishDate 2015
url http://umpir.ump.edu.my/id/eprint/8101/
http://dx.doi.org/10.1039/C4RA13322F
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score 13.211869