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相关概念视频

Photochemical Electrocyclic Reactions: Stereochemistry01:26

Photochemical Electrocyclic Reactions: Stereochemistry

1.8K
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
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Cycloaddition Reactions: MO Requirements for Photochemical Activation01:12

Cycloaddition Reactions: MO Requirements for Photochemical Activation

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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.
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Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

2.3K
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.
2.3K
The Photochemical Reaction Center01:29

The Photochemical Reaction Center

4.1K
Reaction centers are pigment-protein complexes that initiate energy conversion from photons to chemical entities. Therefore, photochemical reaction center is a more appropriate term that describes these complexes. The Nobel laureates Robert Emerson and William Arnold provided the first experimental evidence of photochemical reaction centers by demonstrating the participation of nearly 2,500 chlorophyll molecules for the release of just one molecule of oxygen. Despite thousands of photosynthetic...
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相关实验视频

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Microfluidic-based Synthesis of Covalent Organic Frameworks COFs: A Tool for Continuous Production of COF Fibers and Direct Printing on a Surface
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一个可逆光色共价有机框架.

Xue-Tian Li1, Meng-Jing Li1, Yuan-Liang Tian1

  • 1College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Shandong Normal University, Jinan, 250014, P. R. China.

Nature communications
|October 1, 2024
PubMed
概括

一个新的共价有机框架 (COF) 呈现可逆光色,随着光和空气暴露而改变颜色. 这种稳定,与水结合的材料显示出防伪和光学切换应用的潜力.

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High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal
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科学领域:

  • 材料科学 材料科学 材料科学
  • 有机化学 有机化学
  • 纳米技术 纳米技术

背景情况:

  • 聚合有机框架 (COF) 是具有多种应用的晶体多孔材料.
  • 在COF中,光色是未被充分探索的领域,具有显著的潜力.

研究的目的:

  • 合成一种具有光色特性的新型酸结合COF.
  • 调查观察到的光色变异的稳定性和机制.
  • 探索光色COF的潜在应用.

主要方法:

  • 在超声波辅助下合成DBTB-DETH-COF.
  • 在光和空气下对光色表现的描述.
  • 长时间和多个周期的稳定性测试.
  • 谱学和电化学分析 (EPR,XPS,电化学,短暂吸收) 来阐明光色机制.

主要成果:

  • 通过超声波快速合成与水相关的DBTB-DETH-COF.
  • 由光和空气触发的可逆光色 (黄色到橄) 已被证明,具有超过50个周期.
  • 在暴露于光线15天后,COF具有出色的结构稳定性.
  • 通过先进的表征技术提供了对光色过程的详细机械洞察.

结论:

  • 合成的DBTB-DETH-COF表现出稳定和可逆的光色.
  • 该材料在防伪油墨和光学开关等应用中表现有前途.
  • 这项工作扩大了稳定的有机光色材料的范围,并扩大了COF的应用.