2022
DOI: 10.1039/d1nj05926b
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Ag supported on alumina for the epoxidation of 1-hexene with molecular oxygen: the effect of Ag+/Ag0

Abstract: Linear terminal olefins epoxidation is an important oxidation reaction that provides valuable chemical intermediates. Heterogeneous catalytic epoxidation with O2 is a “dream reaction” while it is still far away from...

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Cited by 6 publications
(3 citation statements)
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“…The epoxidation of long-chain linear α-olefins to produce industrially valuable epoxides plays a pivotal role in modern chemical industry, as it provides essential feedstock for the production of plasticizers, surfactants, and other fine chemicals [1][2][3][4]. Traditionally, this process relied on organic peracids as oxygen donors.…”
Section: Introductionmentioning
confidence: 99%
“…The epoxidation of long-chain linear α-olefins to produce industrially valuable epoxides plays a pivotal role in modern chemical industry, as it provides essential feedstock for the production of plasticizers, surfactants, and other fine chemicals [1][2][3][4]. Traditionally, this process relied on organic peracids as oxygen donors.…”
Section: Introductionmentioning
confidence: 99%
“…Epoxides are important raw materials in the chemical industry for the synthesis of glycols, epoxy resins, polyethers, etc. They are commonly synthesized through the oxidation of olefins by molecular oxygen or peroxides in the presence of metal catalysts. Epoxides can also be synthesized through the dehydrohalogenation of halohydrins through base-driven S N 2 substitution. However, due to the general consensus of pursuing a sustainable green process, new methods are continuously developed to replace the petrochemical-based routes. Glycerol, an oversupplied byproduct from biodiesel production, has therefore been considered as an alternative feedstock for the production of epoxides. The simplest route to achieve the set target would start with the halogenation of one of the hydroxyl groups to form chloro-propanediol under the presence of an organic acid catalyst such as acetic acid. Then, the base-driven S N 2 substitution can be applied to carry out the ring-closing epoxidation.…”
Section: Introductionmentioning
confidence: 99%
“…3,4 Although the epoxidation of ethylene and propylene with the oxidants of oxygen and hydrogen peroxide (H 2 O 2 ), respectively, has industrialized to date, the electron-deficient nature and steric hindrance retard the progress of long linear terminal olefin epoxidation. [5][6][7][8] Therefore, developing an environmentally friendly and easily available epoxidation process for long linear terminal olefins is desirable.…”
Section: Introductionmentioning
confidence: 99%