Allylic C–H acetoxylation of terminal alkenes over TiO2 supported palladium nanoparticles using molecular oxygen as the oxidant

Zhenzhong Zhang, Qixun Wu, Taishin Hashiguchi, Tamao Ishida, Haruno Murayama, Makoto Tokunaga

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

A method for synthesizing linear allylic acetates from terminal alkenes over TiO2 supported Pd nanoparticles (NPs) has been developed, in which O2 serves as the sole oxidant. Good catalytic activity was performed when using allylbenzene as a substrate and the catalyst can be reused at least five times without activity losing. The catalytic system has a broad substrate scope including transformation of 1,3-butadiene into 1,4-diacetoxy-2-butene, which is an important industrial intermediate for production of 1,4-butanediol. In contrast to previous reports that the Pd-catalyzed allylic acetoxylation is generally promoted by PdII species, the XAFS measurements suggest that this reaction is catalyzed over Pd0 NPs. Additionally, XPS analysis of the catalyst confirms the interaction between Pd and TiO2, which probably promote the initial catalytic procedure.

Original languageEnglish
Pages (from-to)18-22
Number of pages5
JournalCatalysis Communications
Volume87
DOIs
Publication statusPublished - Dec 5 2016

Fingerprint

Molecular oxygen
Palladium
Alkenes
Oxidants
Olefins
Nanoparticles
Catalysts
Substrates
Butadiene
Butenes
Catalyst activity
Acetates
X ray photoelectron spectroscopy
allylbenzene
1,3-butadiene
2-butene
1,4-butanediol

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)
  • Process Chemistry and Technology

Cite this

Allylic C–H acetoxylation of terminal alkenes over TiO2 supported palladium nanoparticles using molecular oxygen as the oxidant. / Zhang, Zhenzhong; Wu, Qixun; Hashiguchi, Taishin; Ishida, Tamao; Murayama, Haruno; Tokunaga, Makoto.

In: Catalysis Communications, Vol. 87, 05.12.2016, p. 18-22.

Research output: Contribution to journalArticle

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