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.
Main Authors: | , , , |
---|---|
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 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
oai:scielo:S0103-50532011000200018 |
---|---|
record_format |
ojs |
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 |
_version_ |
1756403424280182784 |