Results 11 to 20 of about 30,490 (251)

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.
Miriam Di Martino   +5 more
doaj   +4 more sources

Photomechanical Azobenzene Crystals [PDF]

open access: yesCrystals, 2019
Photomechanically responsive materials are promising candidates for future smart actuator applications. The photo-responsive behaviors originate from the photoisomerization of photochromic molecules.
Takuya Taniguchi   +2 more
doaj   +2 more sources

Dihydroazulene‐Azobenzene‐Dihydroazulene Triad Photoswitches [PDF]

open access: yesChemistry – A European Journal, 2021
AbstractPhotoswitch triads comprising two dihydroazulene (DHA) units in conjugation with a central trans‐azobenzene (AZB) unit were prepared in stepwise protocols starting from meta‐ and para‐disubstituted azobenzenes. The para‐connected triad had significantly altered optical properties and lacked the photoactivity of the separate photochromes.
Alvis Mengots   +9 more
openaire   +6 more sources

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

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

Supramolecular hierarchy among halogen and hydrogen bond donors in light-induced surface patterning [PDF]

open access: yes, 2015
Halogen bonding, a noncovalent interaction possessing several unique features compared to the more familiar hydrogen bonding, is emerging as a powerful tool in functional materials design.
Barrett C. J.   +10 more
core   +1 more source

Surface-Relief Gratings in Halogen-Bonded Polymer–Azobenzene Complexes: A Concentration-Dependence Study

open access: yesMolecules, 2017
In recent years, supramolecular complexes comprising a poly(4-vinylpyridine) backbone and azobenzene-based halogen bond donors have emerged as a promising class of materials for the inscription of light-induced surface-relief gratings (SRGs). The studies
Jelle E. Stumpel   +6 more
doaj   +1 more source

Building Triazolated Macrocycles from Bis-Propargylated Calix[4]arenes and Bis-Azidomethylated Azobenzene or Stilbene

open access: yesMolbank, 2023
Copper(I)-catalyzed azide-alkyne cycloaddition was employed to construct biscalixarene assemblies from the calix[4]arene dipropargyl ethers and 4,4′-bis-azidomethylated azobenzene or stilbene.
Ivan Lentin   +6 more
doaj   +1 more source

Coordination networks incorporating halogen-bond donor sites and azobenzene groups [PDF]

open access: yes, 2016
Two Zn coordination networks, [Zn(1)(Py)2]2(2-propanol)n (3) and [Zn(1)2(Bipy)2](DMF)2n (4), incorporating halogen-bond (XB) donor sites and azobenzene groups have been synthesized and fully characterized.
Fernandez-Palacio F.   +6 more
core   +1 more source

Thermal stability improvement of azobenzene for the integration of photochemical and solar thermochemical energy conversion

open access: yesCase Studies in Thermal Engineering, 2023
Azobenzene is a typical photoisomerization material that is widely used in photochemical energy conversion. However, it's generally operated below 200 °C to avoid thermal decomposition.
Shaopeng Guo   +3 more
doaj   +1 more source

Home - About - Disclaimer - Privacy