Results 71 to 80 of about 7,520 (264)

Thermally Bistable Stiff Stilbene Photoswitches and Polymer Applications

open access: yesThe Chemical Record, EarlyView.
Thermally stable photoswitches offer new opportunities for controlling polymer structures and functions under nonequilibrium conditions. This Personal Account highlights stiff stilbene (SS) and sterically hindered stiff stilbene (HSS) photoswitches, which combine large structural changes with exceptional thermal bistability.
Keiichi Imato
wiley   +1 more source

Fluorescence switching of photochromic diarylethenes [PDF]

open access: yesOptical Materials, 2003
Fluorescence switching performance of photochromic diarylethenes has been studied. A bisbenzothienylethene having m-terphenyl substituents underwent reversible photochromic reactions in the amorphous solid state and exhibited fluorescence intensity change and shift of the emission band with the photochromic reaction.
Tsuyoshi Kawai   +3 more
openaire   +1 more source

Photo-induced and thermal reactions in thin films of an azobenzene derivative on Bi(111) [PDF]

open access: yes, 2014
Azobenzene is a prototypical molecular switch which can be interconverted with UV and visible light between a trans and a cis isomer in solution. While the ability to control their conformation with light is lost for many molecular photoswitches in the ...
Bronner, Christopher, Tegeder, Petra
core   +1 more source

Light‐Programmable Interfaces: From Molecular Photoswitching to Adaptive Membrane Separations

open access: yesAdvanced Materials Interfaces, Volume 13, Issue 10, 19 May 2026.
This review advances an interface‐centered framework for light‐responsive membranes, linking molecular photoswitches (azobenzene (AZO), spiropyran (SP), diarylethene (DAE), donor–acceptor Stenhouse adducts (DASA), photoacid) to integration strategies in polymeric, porous, self‐assembled, and mixed‐matrix systems.
Liangliang Zhang   +6 more
wiley   +1 more source

Improving the Fatigue Resistance of Diarylethene Switches

open access: yesJournal of the American Chemical Society, 2015
When applying photochromic switches as functional units in light-responsive materials or devices, an often disregarded yet crucial property is their resistance to fatigue during photoisomerization. In the large family of diarylethene photoswitches, formation of an annulated isomer as a byproduct of the photochromic reaction turns out to prevent the ...
Martin Herder   +5 more
openaire   +3 more sources

Photochemical investigation of a photochromic diarylethene compound that can be used as a wide range actinometer [PDF]

open access: yes, 2010
The photochromic diarylethene derivative 1,2-bis(5-(4-ethynylphenyl)-2-methylthiophen-3-yl)perfluorocyclopentene (1) was submitted to photochemical, thermal stability and fatigue resistance studies in acetonitrile, also to evaluate its possible ...
Ballardini, Roberto   +5 more
core  

Discrimination between FRET and non-FRET quenching in a photochromic CdSe quantum dot/dithienylethene dye system [PDF]

open access: yes, 2014
A photochromic Förster resonance energy transfer (FRET) system was employed to disentangle the fluorescence quenching mechanisms in quantum dot/photochromic dye hybrids.
Dworak, Lars   +4 more
core   +1 more source

Phototunable Polarization Volume Gratings Driven by Chiral Hydrazone Switches

open access: yesAdvanced Optical Materials, Volume 14, Issue 19, 22 May 2026.
Chiral hydrazone photoswitches incorporated into polarization volume gratings enable light‐driven, reversible modulation of optical properties. UV and blue light irradiation reversibly alter the hydrazone isomer ratio, leading to tunable diffraction efficiency and spectral response across the visible spectrum.
Artem Boichuk   +4 more
wiley   +1 more source

Click chemistry towards thermally reversible photochromic 4,5-bisthiazolyl-1,2,3-triazoles

open access: yesBeilstein Journal of Organic Chemistry, 2019
Three new diarylethenes were synthesized from 1,2-bis(5-methyl-2-(4-substituted-phenyl)thiazol-4-yl)ethyne and benzyl azide through Ru(I)-catalyzed Huisgen cyclization reactions.
Chenxia Zhang   +4 more
doaj   +1 more source

Carbon Dot Self‐Assembly: Bottom‐Up Fabrication, Morphological Evolution, Luminescence Regulation, and Advanced Applications

open access: yesAggregate, Volume 7, Issue 5, May 2026.
The self‐assembly of carbon dots, which enables precise control over their macroscopic architectures and collective properties, profoundly enhances their functionality. This review systematically summarizes the field through four key aspects—morphology control, luminescence modulation, assembly mechanisms, and advanced applications—and thereby offers a
Kai Chen   +5 more
wiley   +1 more source

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