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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

Stimuli-Responsive Materials for Tissue Engineering and Drug Delivery.

TL;DR: Smart materials as controlled drug release vehicles for tissue engineering are described, highlighting their potential for the delivery of precise quantities of drugs at specific locations and times promoting the controlled repair or remodeling of tissues.
Journal ArticleDOI

Efficient cycling utilization of solar-thermal energy for thermochromic displays with controllable heat output

TL;DR: In this paper, the closed-cycle utilization of photo-thermal energy for thermochromic displays by optimizing the solid-state high-rate heat output of solar thermal storage (STS) films was investigated.
Journal ArticleDOI

NIR-triggered drug release from switchable rotaxane-functionalized silica-covered Au nanorods.

TL;DR: An NIR-triggered drug delivery system was developed by capping photo-switchable azobenzene-based rotaxane onto Au nanorod-mesoporous silica core-shell hybrids, showing significant drug spreading to the adjacent tissues.
Journal ArticleDOI

A Highly Efficient Near-Infrared-Emissive Copolymer With a N=N Double-Bond π-Conjugated System Based on a Fused Azobenzene-Boron Complex

TL;DR: It is proposed that N=N double bonds should be attractive and functional building blocks for designing π-conjugated materials.
Journal ArticleDOI

Palladium-Catalyzed Direct Ortho-Nitration of Azoarenes Using NO2 as Nitro Source

TL;DR: A palladium-catalyzed direct ortho-nitration reaction of azoarenes was developed in which NO2 was used as both nitro source and oxidant for the first time.
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.
Journal ArticleDOI

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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