Cyclohexene epoxidation with H2O2in the vapor and liquid phases over a vanadium-based metal-organic framework

Tae Ung Yoon; Sol Ahn; Ah Reum Kim; Justin M. Notestein; Omar K. Farha; Youn Sang Bae

doi:10.1039/d0cy00833h

Cyclohexene epoxidation with H₂O₂in the vapor and liquid phases over a vanadium-based metal-organic framework

Tae Ung Yoon, Sol Ahn, Ah Reum Kim, Justin M. Notestein, Omar K. Farha, Youn Sang Bae

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17 Scopus citations

Abstract

A metal-organic framework, MIL-47(V) containing coordinatively saturated V+IV sites linked together by terephthalic linkers, was prepared by a solvothermal method and evaluated as a catalyst in the epoxidation of cyclohexene. We have compared the catalytic activity in the condensed and gas phase oxidation of cyclohexene to discuss the effect of temperature and reaction phase in cyclohexene epoxidation over MIL-47(V). The catalysts were examined for the epoxidation of cyclohexene with H2O2 at 50, 65, 120, and 150 °C. We observed significant differences in product selectivity between liquid-phase and gas-phase operations and confirmed that the active sites are tightly incorporated into the MOF as node channels and thus resistant to leaching.

Original language	English (US)
Pages (from-to)	4580-4585
Number of pages	6
Journal	Catalysis Science and Technology
Volume	10
Issue number	14
DOIs	https://doi.org/10.1039/d0cy00833h
State	Published - Jul 21 2020

ASJC Scopus subject areas

Catalysis

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title = "Cyclohexene epoxidation with H2O2in the vapor and liquid phases over a vanadium-based metal-organic framework",

abstract = "A metal-organic framework, MIL-47(V) containing coordinatively saturated V+IV sites linked together by terephthalic linkers, was prepared by a solvothermal method and evaluated as a catalyst in the epoxidation of cyclohexene. We have compared the catalytic activity in the condensed and gas phase oxidation of cyclohexene to discuss the effect of temperature and reaction phase in cyclohexene epoxidation over MIL-47(V). The catalysts were examined for the epoxidation of cyclohexene with H2O2 at 50, 65, 120, and 150 °C. We observed significant differences in product selectivity between liquid-phase and gas-phase operations and confirmed that the active sites are tightly incorporated into the MOF as node channels and thus resistant to leaching.",

author = "Yoon, {Tae Ung} and Sol Ahn and Kim, {Ah Reum} and Notestein, {Justin M.} and Farha, {Omar K.} and Bae, {Youn Sang}",

note = "Funding Information: The authors gratefully acknowledge the financial support from the Inorganometallic Catalyst Design Center, an EFRC funded by the DOE, Office of Basic Energy Sciences (DESC0012702). This work was also supported by the National Research Foundation of Korea under Grant No. NRF-2019R1A2C2002313. Publisher Copyright: {\textcopyright} 2020 The Royal Society of Chemistry.",

year = "2020",

month = jul,

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doi = "10.1039/d0cy00833h",

language = "English (US)",

volume = "10",

pages = "4580--4585",

journal = "Catalysis Science and Technology",

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publisher = "Royal Society of Chemistry",

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TY - JOUR

T1 - Cyclohexene epoxidation with H2O2in the vapor and liquid phases over a vanadium-based metal-organic framework

AU - Yoon, Tae Ung

AU - Ahn, Sol

AU - Kim, Ah Reum

AU - Notestein, Justin M.

AU - Farha, Omar K.

AU - Bae, Youn Sang

N1 - Funding Information: The authors gratefully acknowledge the financial support from the Inorganometallic Catalyst Design Center, an EFRC funded by the DOE, Office of Basic Energy Sciences (DESC0012702). This work was also supported by the National Research Foundation of Korea under Grant No. NRF-2019R1A2C2002313. Publisher Copyright: © 2020 The Royal Society of Chemistry.

PY - 2020/7/21

Y1 - 2020/7/21

N2 - A metal-organic framework, MIL-47(V) containing coordinatively saturated V+IV sites linked together by terephthalic linkers, was prepared by a solvothermal method and evaluated as a catalyst in the epoxidation of cyclohexene. We have compared the catalytic activity in the condensed and gas phase oxidation of cyclohexene to discuss the effect of temperature and reaction phase in cyclohexene epoxidation over MIL-47(V). The catalysts were examined for the epoxidation of cyclohexene with H2O2 at 50, 65, 120, and 150 °C. We observed significant differences in product selectivity between liquid-phase and gas-phase operations and confirmed that the active sites are tightly incorporated into the MOF as node channels and thus resistant to leaching.

AB - A metal-organic framework, MIL-47(V) containing coordinatively saturated V+IV sites linked together by terephthalic linkers, was prepared by a solvothermal method and evaluated as a catalyst in the epoxidation of cyclohexene. We have compared the catalytic activity in the condensed and gas phase oxidation of cyclohexene to discuss the effect of temperature and reaction phase in cyclohexene epoxidation over MIL-47(V). The catalysts were examined for the epoxidation of cyclohexene with H2O2 at 50, 65, 120, and 150 °C. We observed significant differences in product selectivity between liquid-phase and gas-phase operations and confirmed that the active sites are tightly incorporated into the MOF as node channels and thus resistant to leaching.

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JO - Catalysis Science and Technology

JF - Catalysis Science and Technology

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Cyclohexene epoxidation with H₂O₂in the vapor and liquid phases over a vanadium-based metal-organic framework

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