Efficient Epoxidation of Olefins with
99% Selectivity and Use of Hydrogen Peroxide
Keigo Kamata,1
Koji Yonehara,2
Yasutaka Sumida,2
Kazuya Yamaguchi,1
Shiro Hikichi,1
Noritaka Mizuno1*
Epoxides are an important class of industrial chemicals that
have been used as chemical intermediates. Catalytic epoxidation
of olefins affords an interesting production technology. We
found a widely usable green route to the production of epoxides:
A silicotungstate compound, [

-SiW
10O
34(H
2O)
2]
4, is synthesized
by protonation of a divacant, lacunary, Keggin-type polyoxometalate
of [

-SiW
10O
36]
8 and exhibits high catalytic performance
for the epoxidation of various olefins, including propylene,
with a hydrogen peroxide (H
2O
2) oxidant at 305 kelvin. The effectiveness
of this catalyst is evidenced by

99% selectivity to epoxide,

99% efficiency of H
2O
2 utilization, high stereospecificity,
and easy recovery of the catalyst from the homogeneous reaction
mixture.
1 Department of Applied Chemistry, School of Engineering, University of Tokyo, 7-3-1 Hongo, Bunkyoku, Tokyo 113-8656, Japan.
2 Strategic Technology Research, Nippon Shokubai, 5-8 Nishi Otabi-cho, Suita, Osaka 564-8512, Japan.
* To whom correspondence should be addressed. E-mail: tmizuno{at}mail.ecc.u-tokyo.ac.jp