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Journal ArticleDOI

Photoisomerization in different classes of azobenzene

TLDR
This critical review details the studies completed to date on the 3 main classes of azobenzene derivatives and explains the mechanism behind the isomerization mechanism.
Abstract
Azobenzene undergoes trans → cisisomerization when irradiated with light tuned to an appropriate wavelength. The reverse cis →transisomerization can be driven by light or occurs thermally in the dark. Azobenzene's photochromatic properties make it an ideal component of numerous molecular devices and functional materials. Despite the abundance of application-driven research, azobenzene photochemistry and the isomerization mechanism remain topics of investigation. Additional substituents on the azobenzene ring system change the spectroscopic properties and isomerization mechanism. This critical review details the studies completed to date on the 3 main classes of azobenzene derivatives. Understanding the differences in photochemistry, which originate from substitution, is imperative in exploiting azobenzene in the desired applications.

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Citations
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Journal ArticleDOI

Reversibly tuning hydrogel stiffness through photocontrolled dynamic covalent crosslinks

TL;DR: By controlling the stability of dynamic covalent crosslinks with adjacent photoswitches, the stiffness of an adaptable hydrogel is tuned reversibly.
Journal ArticleDOI

Determining the Photoisomerization Quantum Yield of Photoswitchable Molecules in Solution and in the Solid State.

TL;DR: This work shows how to determine the photoisomerization quantum yield in the solid state and in solution when taking thermal processes into account and allows for rapid and accurate determination of the isomerization process for this important class of molecules.
Journal ArticleDOI

Switching the Proton Conduction in Nanoporous, Crystalline Materials by Light.

TL;DR: It is foreseen that photoswitchable proton-conducting materials may find its application in advanced, remote-controllable chemical sensors, and a variety of devices based on the conductivity of protons or other charged molecules, which can be interfaced with biological systems.
Journal ArticleDOI

Aktivierung molekularer Schalter mit sichtbarem Licht

TL;DR: Grundlegende Eigenschaften molekularer systeme durch Bestrahlung mit Licht zu beeinflussen, verspricht vielfaltige Moglichkeiten im Bereich der Material-and Biowissenschften.
Journal ArticleDOI

Light-enhanced liquid-phase exfoliation and current photoswitching in graphene–azobenzene composites

TL;DR: It is shown that the large conformational change associated with the trans–cis photochemical isomerization of alkyl-substituted azobenzenes can be used to improve the efficiency of liquid-phase exfoliation of graphite, with the photochromic molecules acting as dispersion-stabilizing agents.
References
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Journal ArticleDOI

Photomechanics: directed bending of a polymer film by light.

TL;DR: It is shown that a single film of a liquid-crystal network containing an azobenzene chromophore can be repeatedly and precisely bent along any chosen direction by using linearly polarized light.
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A Reëxamination of the Hammett Equation.

H. H. Jaffé
- 01 Oct 1953 - 
Journal ArticleDOI

Light-driven motion of liquids on a photoresponsive surface

TL;DR: The light-driven motion of a fluid substance in a surface-modified glass tube suggests potential applicability to microscale chemical process systems.
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Design and synthesis of chromophores and polymers for electro-optic and photorefractive applications

TL;DR: The ability of nonlinear optical materials to transmit, process and store information forms the basis of emerging optoelectronic and photonic technologies as discussed by the authors, where organic chromophore-containing polymers, in which the refractive index can be controlled by light or an electric field, are expected to play an important role.
Journal ArticleDOI

Ultrafast Dynamics of Photochromic Systems.

TL;DR: Reaction dynamics of the photochromic systems such as spiropyran, flugide and diarylethene derivatives in femto- to nano-second time region was reviewed and mechanisms of rapid reaction channels in various phases were discussed.
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