Photoisomerization of Azobenzene

trans-Azobenzene → cis-Azobenzene

概要

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.

日常の例

Azobenzene-based molecular motors can move objects millions of times their own mass when triggered by light.

産業上の重要性

アゾベンゼン光スイッチは分子マシン、ドラッグデリバリーシステム、液晶ディスプレイ、データ記憶の研究に使用される。

特性

タイプ
Photochemical
可逆的
はい
エネルギー
吸熱性
ΔH
50.0 kJ/mol

関連する反応

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.