氧化物被固定在离子液体修饰的二氧化上,作为与过氧化的异质环氧化催化剂
Kazuya Yamaguchi1, Chie Yoshida, Sayaka Uchida
1Department of Applied Chemistry, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan.
Journal of the American Chemical Society
|January 13, 2005
概括
在改性上固定过氧化物使得olefins的高效异质环氧化成为可能. 催化剂可重复使用,并防止金属漏,证实了真正的异质催化剂.
科学领域:
- 不同质的催化剂.
- 绿色化学是一种绿色化学.
背景情况:
- 均质环氧化催化剂经常遭受浸出和分离困难.
- 开发强大的异质催化剂对于可持续的化学合成至关重要.
研究的目的:
- 开发一种可回收的异质催化剂,用于olefin环氧化.
- 为了证明固定过氧状态催化剂的稳定性和可重复使用性.
主要方法:
- 过氧化物被固定在离子液改性SiO2.2上.
- 测试催化剂在氧化各种olefins中的性能.
- 分析反应过物以检测的泄.
主要成果:
- 固定过氧化状态催化剂有效地环氧化了广泛的烯酸.
- 在催化剂去除后反应的完全停止证实了异质性质.
- 没有观察到可检测的溶解到反应溶液中.
- 催化剂在经过多次重复使用周期后保持了性能.
结论:
- 在离子液改性SiO2上固定化的氧化物是一种高效和可重复使用的异质环氧化催化剂.
- 催化剂的设计可以防止金属漏,确保真正的异质催化,并简化产品的净化.
相关概念视频
Catalysis
The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Diols are compounds with two hydroxyl groups. In addition to syn dihydroxylation, diols can also be synthesized through the process of anti dihydroxylation. The process involves treating an alkene with a peroxycarboxylic acid to form an epoxide. Epoxides are highly strained three-membered rings with oxygen and two carbons occupying the corners of an equilateral triangle. This step is followed by ring-opening of the epoxide in the presence of an aqueous acid to give a trans diol.
Preparation of Epoxides
Overview
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Sharpless Epoxidation
The conversion of allylic alcohols into epoxides using the chiral catalyst was discovered by K. Barry Sharpless and is known as Sharpless epoxidation. The use of a chiral catalyst enables the formation of one enantiomer of the product in excess. This chiral catalyst is mainly a chiral complex of titanium tetraisopropoxide and tartrate ester (specific stereoisomer). The stereoisomer used in the chiral catalyst dictates the formation of the enantiomer of the product. In other words, the use of...
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Heterogeneous catalysis involves a catalyst in a different phase from the reactants. It is a process where the catalyst and the reactants are in distinct phases, typically solid and gas or liquid.Most heterogeneous catalysts are metals, metal oxides, or acids. The list includes transition metals like iron (Fe), cobalt (Co), nickel (Ni), palladium (Pd), platinum (Pt), chromium (Cr), manganese (Mn), tungsten (W), silver (Ag), and copper (Cu). These metals possess partially vacant d orbitals that...


