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HERO ID
6922697
Reference Type
Journal Article
Title
Lewis Acid Ionic Liquid Immobilized on Chitosan for Synthesis of Dichlorophenylphosphine
Author(s)
Qiu, X; Xie, Yu; Wang, XY; Cao, QY; Tang, X; Hu, J; Hong, X; Yan, SiF; ,
Year
2013
Is Peer Reviewed?
Yes
Journal
Asian Journal of Chemistry
ISSN:
0970-7077
EISSN:
0975-427X
Publisher
ASIAN JOURNAL OF CHEMISTRY
Location
SAHIBABAD
Volume
25
Issue
3
Page Numbers
1673-1678
Language
English
Web of Science Id
WOS:000312621400109
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84875144901&partnerID=40&md5=5ad282ae7e0ff64bc425e0e136764206
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Abstract
Lewis acid ionic liquid immobilized on chitosan as a new catalyst was prepared via the synthesis of 1-triniethoxy-silylpropy1-3-methylindazolium-chloride-AlCl3, 1-trimethoxy-silylpropyl-3-methylindazolium-chloride-InCl3 and 1-trimethoxy-silylpropyl-3-methylindazolium-chloride-FeCl3 and then grafting them to chitosan respectively. Their catalytic activities were investigated in the synthesis of dichlorophenylphosphine. The results showed when the three catalysts' amounts were 0.0225, 0.0195 and 0.015 g respectively, the substrate of benzene could be completely transformed into dichlorophenylphosphine on the conditions of the phosphorus trichloride 0.22 g, the molar ratio of phosphorus trichloride to benzene 1.8:1, the reaction temperature 75 degrees C and the reaction time 120 min. Moreover, the molar ratios of ionic liquid moiety to benzene were merely 0.285, 0.187 and 0.172% respectively, which were much lower than that of the corresponding pure ionic liquids to benzene. The catalyst can be reused for many times with fine catalytic efficiency. In addition, the new catalyst using chitosan with the higher deacetylation degree as carrier could improve catalytic activity and reusability.
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