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HERO ID
4321580
Reference Type
Journal Article
Title
beta-Diketimine appended periodic mesoporous organosilica as a scaffold for immobilization of palladium acetate: An efficient green catalyst for Wacker type reaction
Author(s)
Borah, P; Zhao, Y
Year
2014
Is Peer Reviewed?
Yes
Journal
Journal of Catalysis
ISSN:
0021-9517
EISSN:
1090-2694
Volume
318
Page Numbers
43-52
Language
English
DOI
10.1016/j.jcat.2014.07.019
Web of Science Id
WOS:000343360800005
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84906100031&doi=10.1016%2fj.jcat.2014.07.019&partnerID=40&md5=8855b962f06226ebf0c4e2e317036823
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Abstract
A series of β-diketimine appended periodic mesoporous organosilicas (PMOs) were prepared and characterized. These PMOs were found to be an excellent scaffold for the immobilization of palladium acetate [Pd(OAc)2] through the complexation between Pd(OAc)2 and iminic nitrogen atoms of β-diketiminate, leading to the formation of efficient heterogeneous catalysts (Pd/PMOs) for the oxidation of styrene. Catalytic evaluations show that, in liquid phase using H2O2 as oxidant, Pd/PMOs could promote styrene to undergo Wacker type reaction with a high selectivity of up to 100% toward the formation of acetophenone, a useful chemical with high demand in the global market. The novel solid catalyst offers a good catalytic recyclability with consistently high catalytic activity. In addition, it was experimentally demonstrated that H2O2 plays an important role to prevent unwanted catalyst deactivation. Thus, the current work presents a convenient approach for the direct production of acetophenone from styrene. © 2014 Elsevier Inc. All rights reserved.
Keywords
beta-Diketimine; Heterogeneous catalysis; Palladium acetate; Periodic mesoporous silica; Wacker reaction
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