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Lee, Jae Sung
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Oxidative coupling of methyl benzoate with palladium/heteropolyacid catalysts

Alternative Title
Oxidative coupling of methyl benzoate with palladium/heteropolyacid catalysts
Author(s)
Lee, Si HoonLee, Kyung HeeLee, Jae SungJung, Jae DoShim, Jong Sub
Issued Date
1997-01
DOI
10.1016/S1381-1169(96)00160-4
URI
https://scholarworks.unist.ac.kr/handle/201301/12597
Fulltext
http://www.sciencedirect.com/science/article/pii/S1381116996001604
Citation
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, v.115, no.2, pp.241 - 246
Abstract
The oxidative coupling of methyl benzoate in the presence of a catalyst system comprising of Pd(OAc)(2) and a vanadium-containing heteropolyacid produced 2,2'-biphenic acid dimethyl ester with a high selectivity. The mode of coordination of methyl benzoate to palladium and the non-coordinating nature of the heteropolyacid appeared to be responsible for the unusual selectivity. Addition of Hg(OAc)(2) or triphenyl phosphine increased greatly the conversion of methyl benzoate without impairing the selectivity to the 2,2'-isomer. The catalyst deactivated with reaction time, mainly due to water produced from the reaction
Publisher
ELSEVIER SCIENCE BV
ISSN
1381-1169

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