Results 21 to 30 of about 23,102 (300)

Reprocessable Photodeformable Azobenzene Polymers [PDF]

open access: yesMolecules, 2021
Photodeformable azobenzene (azo) polymers are a class of smart polymers that can efficiently convert light energy into mechanical power, holding great promise in various photoactuating applications. They are typically of crosslinked polymer networks with highly oriented azo mesogens embedded inside. Upon exposure to the light of appropriate wavelength,
openaire   +3 more sources

Azobenzene as Antimicrobial Molecules

open access: yesMolecules, 2022
Azo molecules, characterized by the presence of a -N=N- double bond, are widely used in various fields due to their sensitivity to external stimuli, ch as light. The emergence of bacterial resistance has pushed research towards designing new antimicrobial molecules that are more efficient than those currently in use.
Di Martino, Miriam   +5 more
openaire   +4 more sources

Fluorescent Azobenzene-Containing Compounds: From Structure to Mechanism

open access: yesCrystals, 2021
The reversible photoisomerization of azobenzenes has been extensively studied to construct systems with optical responsiveness; however, this process limits the luminescence of these compounds.
Lulu Xue   +9 more
doaj   +1 more source

Columnar Aggregates of Azobenzene Stars: Exploring Intermolecular Interactions, Structure, and Stability in Atomistic Simulations

open access: yesMolecules, 2021
We present a simulation study of supramolecular aggregates formed by three-arm azobenzene (Azo) stars with a benzene-1,3,5-tricarboxamide (BTA) core in water.
Markus Koch   +2 more
doaj   +1 more source

Molecular Factors Controlling the Isomerization of Azobenzenes in the Cavity of a Flexible Coordination Cage

open access: yesJournal of the American Chemical Society, 2020
Photoswitchable molecules are employed for many applications, from the development of active materials to the design of stimuli-responsive molecular systems and light-powered molecular machines.
L. Pesce   +4 more
semanticscholar   +1 more source

Continuous flow synthesis of azobenzenes via Baeyer–Mills reaction

open access: yesBeilstein Journal of Organic Chemistry, 2022
Azobenzene, as one of the most prominent molecular switches, is featured in many applications ranging from photopharmacology to information or energy storage.
Jan H. Griwatz   +2 more
doaj   +1 more source

Light-Activating PROTACs in Cancer: Chemical Design, Challenges, and Applications

open access: yesApplied Sciences, 2022
Nonselective cell damage remains a significant limitation of radiation therapies in cancer. Decades of successful integration of radiation therapies with other medicinal chemistry strategies significantly improved therapeutic benefits in cancer ...
Arvind Negi   +2 more
doaj   +1 more source

Halogen bonding stabilizes a cis-azobenzene derivative in the solid state: A crystallographic study [PDF]

open access: yes, 2017
Crystals of trans- and cis-isomers of a fluorinated azobenzene derivative have been prepared and characterized by single-crystal X-ray diffraction. The presence of F atoms on the aromatic core of the azobenzene increases the lifetime of the metastable ...
Fernandez-Palacio F.   +6 more
core   +1 more source

Electrochemical Site-Selective Alkylation of Azobenzenes with (Thio)Xanthenes

open access: yesMolecules, 2022
Herein, we first report an electrochemical methodology for the site-selective alkylation of azobenzenes with (thio)xanthenes in the absence of any transition metal catalyst or external oxidant. A variety of groups are compatible with this electrochemical
Qiang Zhong   +5 more
doaj   +1 more source

Photo-responsive graphene and carbon nanotubes to control and tackle biological systems [PDF]

open access: yes, 2018
Photo-responsive multifunctional nanomaterials are receiving considerable attention for biological applications because of their unique properties. The functionalization of the surface of carbon nanotubes (CNTs) and graphene, among other carbon based ...
Cardano, Francesca   +2 more
core   +1 more source

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