一个多孔的安德森型聚氧甲基金属有机框架作为一个多功能平台,用于选择性氧化合氨基
Hong-Ru Tan1, Xiang Zhou2, Hanqi You1
1State Key Laboratory for Modification of Chemical Fibers and Polymer Materials & College of Chemistry and Chemical Engineering, Donghua University, Shanghai 201620, P. R. China. syzhao8@dhu.edu.cn.
Dalton transactions (Cambridge, England : 2003)
|November 7, 2023
概括
本研究介绍了POMOF-1,一种新的多孔金属有机框架,用于高效的异质催化. POMOF-1通过氧化合增强了含N的化合物合成,显示出更好的产量和可回收性.
科学领域:
- 材料科学 材料科学 材料科学
- 催化剂是一种催化剂.
- 超分子化学 超分子化学
背景情况:
- 带有多孔框架的异质催化剂通过协同效应和受限的微环境提供了增强的性能.
- 在金属有机框架 (MOF) 中集成的多氧金属 (POM) 是设计先进催化材料的有希望的策略.
研究的目的:
- 设计和合成一种基于多氧金属酸盐的多孔金属有机框架 (POMOF-1),用于多功能催化.
- 通过选择性氧化合反应,研究POMOF-1在通过选择性氧化合反应合成含N化合物的催化性能.
主要方法:
- 使用安德森型[CrMo6O18(PET) 2]构建块和Y3+和L链接器合成POMOF-1.
- 使用POMOF-1作为异质催化剂,使用H2O2作为氧化合反应的氧化剂.
- 研究了N-形成,与酒精的氧化交叉合,以及氧化同型合反应.
主要成果:
- POMOF-1有效地催化了氨基的转化为胺,伊胺和亚,产量和选择性很高.
- 在N-成型中达到高达95%的产量,与同质催化剂相比,产量增加了四倍.
- 在5个循环中,POMOF-1表现出强度和可回收性,触媒活性和结构完整性损失最小.
结论:
- POMOF-1的合理设计创造了一个用于增强异质催化剂的多功能平台.
- 在POMOF-1内部的协同效应和限制效应显著提高了催化活性和选择性.
- 将催化活性POM与多孔MOF相结合是开发强大,可回收和高效的催化剂的可行策略.
相关概念视频
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
10.3K
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.
10.3K
Oxidation and Reduction of Organic Molecules
6.7K
Energy production within a cell involves many coordinated chemical pathways. Most of these pathways are combinations of oxidation and reduction reactions, which occur at the same time. An oxidation reaction strips an electron from an atom in a compound, and the addition of this electron to another compound is a reduction reaction. Because oxidation and reduction usually occur together, these pairs of reactions are called redox reactions.
The removal of an electron from a molecule, results in a...
The removal of an electron from a molecule, results in a...
6.7K
Properties of Organometallic Compounds
1.0K
Organometallic compounds are compounds that contain a carbon–metal bond. Carbon belongs to an organyl group like alkyl, aryl, allyl, or benzyl groups. The metal can be from Group I or Group II of the periodic table, a transition metal, or a semimetal.
1.0K
Preparation of Amines: Reduction of Oximes and Nitro Compounds
3.7K
Oximes can be reduced to primary amines using catalytic hydrogenation, hydride reduction, or sodium metal reduction. The reduction of aliphatic and aromatic nitro compounds to primary amines takes place by either catalytic hydrogenation or by using active metals like Fe, Zn, and Sn in the presence of an acid.
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
3.7K
Radical Oxidation of Allylic and Benzylic Alcohols
2.0K
Activated manganese(IV) oxide can selectively oxidize allylic and benzylic alcohols via a radical intermediate mechanism. Primary allylic alcohols are oxidized to aldehydes, while secondary allylic alcohols yield ketones. The redox reaction of potassium permanganate with an Mn(II) salt such as manganese sulfate (under either alkaline or acidic conditions), followed by thorough drying, yields the oxidizing agent: activated MnO2. While MnO2 is insoluble in the solvents used for the reaction, the...
2.0K
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate
11.7K
Alkenes can be dihydroxylated using potassium permanganate. The method encompasses the reaction of an alkene with a cold, dilute solution of potassium permanganate under basic conditions to form a cis-diol along with a brown precipitate of manganese dioxide.
11.7K


