0000000000646187

AUTHOR

Zafar Ahmed

0000-0002-4737-6238

showing 2 related works from this author

ortho -Fluorination of azophenols increases the mesophase stability of photoresponsive hydrogen-bonded liquid crystals

2018

Photoresponsive liquid crystals (LCs) whose alignment can be controlled with UV-Visible light are appealing for a range of photonic applications. From the perspective of exploring the interplay between the light response and the self-assembly of the molecular components, supramolecular liquid crystals are of particular interest. They allow elaborating the structure-property relationships that govern the optical performance of LC materials by subtle variation of the chemical structures of the building blocks. Herein we present a supramolecular system comprising azophenols and stilbazoles as hydrogen-bond donors and acceptors, respectively, and show that ortho-fluorination of the azophenol dr…

Solid-state chemistryMaterials scienceHydrogen116 Chemical sciencesChemieSupramolecular chemistrychemistry.chemical_element02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesLiquid crystalMaterials ChemistryThermal stabilityLight responsebusiness.industryFluorine Liquid Crystals Supramolecular Chemistry Hydrogen bonding PhotoresponsiveMesophaseGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhotonics0210 nano-technologybusinessJournal of Materials Chemistry C
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Towards low-energy-light-driven bistable photoswitches : ortho-fluoroaminoazobenzenes

2021

AbstractThermally stable photoswitches that are driven with low-energy light are rare, yet crucial for extending the applicability of photoresponsive molecules and materials towards, e.g., living systems. Combined ortho-fluorination and -amination couples high visible light absorptivity of o-aminoazobenzenes with the extraordinary bistability of o-fluoroazobenzenes. Herein, we report a library of easily accessible o-aminofluoroazobenzenes and establish structure–property relationships regarding spectral qualities, visible light isomerization efficiency and thermal stability of the cis-isomer with respect to the degree of o-substitution and choice of amino substituent. We rationalize the exp…

aromaattiset yhdisteetMaterials sciencephotochemistryBistabilityLightbusiness.industry010405 organic chemistry116 Chemical sciences010402 general chemistry01 natural sciencesfluori0104 chemical sciencesLow energyIsomerismLight drivenOptoelectronicsvalokemiaPhysical and Theoretical Chemistrybusiness
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