通过原子层沉积修饰的金属有机框架的选
Ryan A Hackler, Riddhish Pandharkar1, Magali S Ferrandon
1Department of Chemistry, Chemical Theory Center, and Supercomputing Institute, University of Minnesota-Twin Cities, 207 Pleasant Street SE, Minneapolis, Minnesota 55455, United States.
Journal of the American Chemical Society
|November 17, 2020
概括
这项研究使用了高通量选,以找到最好的金属氧化物聚合物用于转化. 在NU-1000 MOF中和的组合显示出高活性和对所需产品的选择性.
科学领域:
- 材料科学
- 催化剂
- 纳米技术
背景情况:
- 金属有机框架 (MOF) 为催化提供可调节的多孔结构.
- 原子层沉积 (ALD) 允许精确地将金属集群纳入MOF.
- 转化对于生产有价值的化学品至关重要.
研究的目的:
- 选各种金属氧化物集群进行催化异构和化.
- 确定选择性propyne转换的最佳单金属和双金属集群.
- 调查集群组成对反应选择性和稳定性的作用.
主要方法:
- 通过ALD将各种金属氧化物集群 (≥8个原子) 纳入NU-1000 MOF.
- 对合成的MOF催化剂进行高通量选.
- 催化活性分析以异构化为烯和化为烯.
主要成果:
- 铜 (Cu) 和 (Co) 集群在化中最活跃.
- - (Co-Zn) 双金属集群,以及 (Zn) 和 (Cd) 单金属集群,在异构化到中最活跃.
- 与单个金属相比,NU-1000中的Co-Zn集群减少了过度化到和焦化.
结论:
- 高通量选对于发现小分子转换的最佳金属集群是有效的.
- 在MOF中,特定的金属组合 (例如Co-Zn) 可以提高催化过程中的选择性和稳定性.
- 了解金属特异性机制是设计高效的异构和化催化剂的关键.
相关概念视频
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
3.7K
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
3.7K
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
8.6K
Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
8.6K
Reduction of Alkenes: Catalytic Hydrogenation
13.5K
Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
13.5K
Preparation of Alkynes: Dehydrohalogenation
17.3K
Introduction
Alkynes can be prepared by dehydrohalogenation of vicinal or geminal dihalides in the presence of a strong base like sodium amide in liquid ammonia. The reaction proceeds with the loss of two equivalents of hydrogen halide (HX) via two successive E2 elimination reactions.
Alkynes can be prepared by dehydrohalogenation of vicinal or geminal dihalides in the presence of a strong base like sodium amide in liquid ammonia. The reaction proceeds with the loss of two equivalents of hydrogen halide (HX) via two successive E2 elimination reactions.
17.3K
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
19.9K
Introduction
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
19.9K
Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration
9.9K
Introduction
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.
9.9K


