PolyU Institutional Repository >
Applied Biology and Chemical Technology >
ABCT Theses >
Please use this identifier to cite or link to this item:
|Title: ||Green approaches to catalytic epoxidation of olefins|
|Authors: ||Tong, Kit-ho|
|Subjects: ||Hong Kong Polytechnic University -- Dissertations|
Alkenes -- Oxidation.
|Issue Date: ||2004 |
|Publisher: ||The Hong Kong Polytechnic University|
|Abstract: ||Epoxides are useful intermediates for the synthesis of a range of chemicals with a variety of commercial applications. Epoxidation of olefins is an important reaction in organic chemistry. Many studies have shown that high yield and selectivity of epoxide can be obtained efficiently by different catalyzed reaction systems. Nevertheless, most of the reported studies needed to use organic solvents and/or toxic catalyst. The work presented in this thesis aims to develop some simple, inexpensive, environmentally friendly and scalable methods for olefin epoxidation Chapter 2 shows a chemoenzymatic approach for the in situ generation of hydrogen peroxide in the epoxidation of olefins. In this system, hydrogen peroxide can be simply produced by enzymatic oxidation of glucose in aqueous medium. Water-soluble olefins were oxidized with oxygen/glucose/glucose oxidase and Mnᶦ ᶦ/HCO₃⁻ to afford excellent yields of epoxides. By using sodium dodecylsulfate (SDS), lipophilic olefins could be effectively epoxidized with similar conditions without the need for an organic co-solvent. The use of immobilized GOx was explored and it was found that chemically immobilized GOx on silica gel was stable and could be reused up to ten cycles. Ionic liquids are considered as "green" or "clean" solvents as they are non-volatile and potentially easily recycled. In Chapter 3, a simple catalytic system, manganese sulfate/bicarbonate, was developed to epoxidize olefins with hydrogen peroxide in the room temperature ionic liquid, 1-butyl-3-methylimidazolium. The ionic liquid itself can be easily recovered and re-used. Epoxidation of terminal olefins remains a challenging task in organic chemistry. In Chapter 4, a useful method for the epoxidation of unactivated olefins using a modified bis-phenanthroline iron dimer as catalyst in ionic liquids as the reaction medium was developed. By using this catalytic system, a wide range of terminal olefins could be simply oxidized to epoxides by peracetic acid in minutes. The ionic liquid could be easily recycled and re-used. The mechanism of the reaction was discussed.|
|Degree: ||Ph.D., Dept. of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, 2004.|
|Description: ||x, 133 leaves : ill. ; 30 cm.|
PolyU Library Call No.: [THS] LG51 .H577P ABCT 2004 Tong
|Rights: ||All rights reserved.|
|Appears in Collections:||ABCT Theses|
PolyU Electronic Theses
All items in the PolyU Institutional Repository are protected by copyright, with all rights reserved, unless otherwise indicated.
No item in the PolyU IR may be reproduced for commercial or resale purposes.