Direct synthesis of cyclic carbonates from olefins and CO2 catalyzed by a MoO2(acac)2-quaternary ammonium salt system

Fawang Chen; Tao Dong; Tiegang Xu; Xiaofang Li; Changwen Hu

doi:10.1039/c1gc15549k

Direct synthesis of cyclic carbonates from olefins and CO₂ catalyzed by a MoO₂(acac)₂-quaternary ammonium salt system

Fawang Chen
, Tao Dong
, Tiegang Xu
, Xiaofang Li^*
, Changwen Hu

^*Corresponding author for this work

School of Chemistry and Chemical Engineering

Beijing Institute of Technology

Research output: Contribution to journal › Article › peer-review

89 Citations (Scopus)

Abstract

A highly efficient synthesis of cyclic carbonates from olefins and CO₂ has been achieved by the use of a molybdenyl acetylacetonate (MoO₂(acac)₂)–quaternary ammonium salt catalytic system with tert-butyl hydroperoxide as an oxidant through a one-pot multistep process. This simple and cheap method can be applied to various olefins, such as 1-octene, 1-hexene, allyl chloride, cyclohexene and styrene, affording the highest yields in comparison with the data reported previously except for styrene. A plausible mechanism is proposed based on the results.

Original language	English
Pages (from-to)	2518-2524
Number of pages	7
Journal	Green Chemistry
Volume	13
Issue number	9
DOIs	https://doi.org/10.1039/c1gc15549k
Publication status	Published - 30 Aug 2011

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abstract = "A highly efficient synthesis of cyclic carbonates from olefins and CO2 has been achieved by the use of a molybdenyl acetylacetonate (MoO2(acac)2){\textendash}quaternary ammonium salt catalytic system with tert-butyl hydroperoxide as an oxidant through a one-pot multistep process. This simple and cheap method can be applied to various olefins, such as 1-octene, 1-hexene, allyl chloride, cyclohexene and styrene, affording the highest yields in comparison with the data reported previously except for styrene. A plausible mechanism is proposed based on the results.",

author = "Fawang Chen and Tao Dong and Tiegang Xu and Xiaofang Li and Changwen Hu",

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AU - Chen, Fawang

AU - Dong, Tao

AU - Xu, Tiegang

AU - Li, Xiaofang

AU - Hu, Changwen

PY - 2011/8/30

Y1 - 2011/8/30

N2 - A highly efficient synthesis of cyclic carbonates from olefins and CO2 has been achieved by the use of a molybdenyl acetylacetonate (MoO2(acac)2)–quaternary ammonium salt catalytic system with tert-butyl hydroperoxide as an oxidant through a one-pot multistep process. This simple and cheap method can be applied to various olefins, such as 1-octene, 1-hexene, allyl chloride, cyclohexene and styrene, affording the highest yields in comparison with the data reported previously except for styrene. A plausible mechanism is proposed based on the results.

AB - A highly efficient synthesis of cyclic carbonates from olefins and CO2 has been achieved by the use of a molybdenyl acetylacetonate (MoO2(acac)2)–quaternary ammonium salt catalytic system with tert-butyl hydroperoxide as an oxidant through a one-pot multistep process. This simple and cheap method can be applied to various olefins, such as 1-octene, 1-hexene, allyl chloride, cyclohexene and styrene, affording the highest yields in comparison with the data reported previously except for styrene. A plausible mechanism is proposed based on the results.

UR - https://www.scopus.com/pages/publications/80052330257

U2 - 10.1039/c1gc15549k

DO - 10.1039/c1gc15549k

M3 - Article

AN - SCOPUS:80052330257

SN - 1463-9262

VL - 13

SP - 2518

EP - 2524

JO - Green Chemistry

JF - Green Chemistry

IS - 9

ER -

Direct synthesis of cyclic carbonates from olefins and CO₂ catalyzed by a MoO₂(acac)₂-quaternary ammonium salt system

Abstract

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