Heterogeneously catalyzed phosphine-free heck cross-coupling reaction of aryl halides with reusable palladium(II) schiff base complex

The coupling between aryl halides with terminal alkenes (Heck reaction) has been investigated in the presence of a polystyrene-supported Schiff base palladium(II) catalyst. The present catalyst is air and moisture-stable and has significant catalytic activity in Heck cross-coupling reactions under operating conditions. Various aryl halides and terminal alkenes were coupled smoothly under air, to afford the corresponding cross-coupled products in excellent yields. Furthermore, the catalyst can be easily recovered quantitatively by simple filtration and reused up to seven cycles without losing its activity.

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Main Authors: Islam,Manirul, Mondal,Paramita, Tuhina,Kazi, Roy,Anupam S
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Química 2011
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000200018
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spelling oai:scielo:S0103-505320110002000182011-02-14Heterogeneously catalyzed phosphine-free heck cross-coupling reaction of aryl halides with reusable palladium(II) schiff base complexIslam,ManirulMondal,ParamitaTuhina,KaziRoy,Anupam S polystyrene schiff base palladium(II) complex heterogeneous catalysis Heck reaction The coupling between aryl halides with terminal alkenes (Heck reaction) has been investigated in the presence of a polystyrene-supported Schiff base palladium(II) catalyst. The present catalyst is air and moisture-stable and has significant catalytic activity in Heck cross-coupling reactions under operating conditions. Various aryl halides and terminal alkenes were coupled smoothly under air, to afford the corresponding cross-coupled products in excellent yields. Furthermore, the catalyst can be easily recovered quantitatively by simple filtration and reused up to seven cycles without losing its activity.info:eu-repo/semantics/openAccessSociedade Brasileira de QuímicaJournal of the Brazilian Chemical Society v.22 n.2 20112011-02-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000200018en10.1590/S0103-50532011000200018
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Islam,Manirul
Mondal,Paramita
Tuhina,Kazi
Roy,Anupam S
spellingShingle Islam,Manirul
Mondal,Paramita
Tuhina,Kazi
Roy,Anupam S
Heterogeneously catalyzed phosphine-free heck cross-coupling reaction of aryl halides with reusable palladium(II) schiff base complex
author_facet Islam,Manirul
Mondal,Paramita
Tuhina,Kazi
Roy,Anupam S
author_sort Islam,Manirul
title Heterogeneously catalyzed phosphine-free heck cross-coupling reaction of aryl halides with reusable palladium(II) schiff base complex
title_short Heterogeneously catalyzed phosphine-free heck cross-coupling reaction of aryl halides with reusable palladium(II) schiff base complex
title_full Heterogeneously catalyzed phosphine-free heck cross-coupling reaction of aryl halides with reusable palladium(II) schiff base complex
title_fullStr Heterogeneously catalyzed phosphine-free heck cross-coupling reaction of aryl halides with reusable palladium(II) schiff base complex
title_full_unstemmed Heterogeneously catalyzed phosphine-free heck cross-coupling reaction of aryl halides with reusable palladium(II) schiff base complex
title_sort heterogeneously catalyzed phosphine-free heck cross-coupling reaction of aryl halides with reusable palladium(ii) schiff base complex
description The coupling between aryl halides with terminal alkenes (Heck reaction) has been investigated in the presence of a polystyrene-supported Schiff base palladium(II) catalyst. The present catalyst is air and moisture-stable and has significant catalytic activity in Heck cross-coupling reactions under operating conditions. Various aryl halides and terminal alkenes were coupled smoothly under air, to afford the corresponding cross-coupled products in excellent yields. Furthermore, the catalyst can be easily recovered quantitatively by simple filtration and reused up to seven cycles without losing its activity.
publisher Sociedade Brasileira de Química
publishDate 2011
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000200018
work_keys_str_mv AT islammanirul heterogeneouslycatalyzedphosphinefreeheckcrosscouplingreactionofarylhalideswithreusablepalladiumiischiffbasecomplex
AT mondalparamita heterogeneouslycatalyzedphosphinefreeheckcrosscouplingreactionofarylhalideswithreusablepalladiumiischiffbasecomplex
AT tuhinakazi heterogeneouslycatalyzedphosphinefreeheckcrosscouplingreactionofarylhalideswithreusablepalladiumiischiffbasecomplex
AT royanupams heterogeneouslycatalyzedphosphinefreeheckcrosscouplingreactionofarylhalideswithreusablepalladiumiischiffbasecomplex
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