Photoisomerization of Azobenzene
trans-Azobenzene → cis-Azobenzene
概述
UV light (340 nm) converts the thermodynamically stable trans isomer of azobenzene to the cis form through rotation around the N=N bond. Visible light (450 nm) or thermal relaxation converts it back. The large geometric change (9 Å to 5.5 Å end-to-end distance) makes azobenzene a versatile molecular switch.
日常示例
Azobenzene-based molecular motors can move objects millions of times their own mass when triggered by light.
工业重要性
偶氮苯光异构化用于光控药物释放、液晶光开关和光驱动分子马达等智能材料和纳米机器领域。
属性
- 可逆
- 是
- 能量
- 吸热
- ΔH
- 50.0 kJ/mol
相关反应
Cis-Trans Isomerization of Retinal
Silver Chloride Photodecomposition
Luminol Chemiluminescence
Firefly Bioluminescence (Luciferin Oxidation)
Photolysis of Water (Vacuum UV)
Photochemical Smog Formation (NO₂ Photolysis)
Photodegradation of Methylene Blue by TiO₂
Photodissociation of Chlorine Gas
Silver Bromide Photodecomposition
Chlorophyll Fluorescence
Frequently Asked Questions
What is the equation for Photoisomerization of Azobenzene?
The balanced equation is: trans-Azobenzene → cis-Azobenzene.
What type of reaction is Photoisomerization of Azobenzene?
Photoisomerization of Azobenzene is a photochemical reaction. It is reversible under certain conditions.
Is Photoisomerization of Azobenzene exothermic or endothermic?
Photoisomerization of Azobenzene is endothermic (absorbs energy). The enthalpy change (ΔH) is 50.0 kJ/mol.