基于triazine-Porphyrin的高性能光催化物的共有机框架
Xuxiao Liu1, Ruilian Qi2, Shumu Li3
1Department of Materials Science and Engineering, Beijing Jiaotong University, 100044 Beijing, China.
Journal of the American Chemical Society
|December 15, 2022
概括
研究人员开发了一种新的高合共有机框架 (COF),使用的是三胺-氨酸单元. 这种新型的多孔材料由于其有序的结构和高效的电荷分离,对有机反应具有很好的光催化活性.
科学领域:
- 材料科学
- 有机化学
- 纳米技术
背景情况:
- 共价有机框架 (COF) 是有序结构的多孔聚合物.
- 基于的COF通过希夫基反应等方法合成.
- 现有的方法在创建特定的COF架构方面存在局限性.
研究的目的:
- 开发一种新型的三素-氨酸高合COF (TA-Por-sp2-COF).
- 通过蓝色基团自我聚合来探索氨酸COF的新合成途径.
- 调查新COF结构的光催化性能.
主要方法:
- 合成TA-Por-sp2-COF使用基终结的氨酸前体.
- 在COF构造中使用蓝色组的自我聚合.
- 对二维拓结构和多孔性的描述.
主要成果:
- 成功构建了一个新的2D超合COF (TA-Por-sp2-COF).
- COF具有一个有序的结构,具有扩展的氨酸单元.
- 在有氧合和选择性氧化反应中表现出高光催化性能.
结论:
- 新型TA-Por-sp2-COF具有出色的光催化活性.
- 该材料的性能归因于其独特的结构,多孔性和电子性质.
- 这项工作提出了设计基于的先进COF的新策略.
更多相关视频
07:12Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
6.3K
08:42Microfluidic-based Synthesis of Covalent Organic Frameworks COFs: A Tool for Continuous Production of COF Fibers and Direct Printing on a Surface
Published on: July 10, 2017
13.5K
相关概念视频
Photochemical Electrocyclic Reactions: Stereochemistry
1.9K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Selection Rules: Photochemical Activation
1.9K
Cycloaddition Reactions: MO Requirements for Photochemical Activation
2.2K
Some cycloaddition reactions are activated by heat, while others are initiated by light. For example, a [2 + 2] cycloaddition between two ethylene molecules occurs only in the presence of light. It is photochemically allowed but thermally forbidden.
2.2K
Thermal and Photochemical Electrocyclic Reactions: Overview
2.4K
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
2.4K
