Search results for "Photoswitch"

showing 10 items of 13 documents

N,N′-Disubstituted Indigos as Readily Available Red-Light Photoswitches with Tunable Thermal Half-Lives

2017

Some rare indigo derivatives have been known for a long time to be photochromic upon irradiation with red light, which should be advantageous for many applications. However, the absence of strategies to tune their thermal half-lives by modular molecular design as well as the lack of proper synthetic methods to prepare a variety of such molecules from the parent indigo dye have so far precluded their use. In this work, several synthetic protocols for N-functionalization have been developed, and a variety of N-alkyl and N-aryl indigo derivatives have been prepared. By installation of electron-withdrawing substituents on the N-aryl moieties, the thermal stability of the Z-isomers could be enha…

010405 organic chemistryChemistryIndigos photoswitchesIndigo dyeGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisIndigo0104 chemical sciencesPhotochromismchemistry.chemical_compoundColloid and Surface ChemistryThermal[CHIM]Chemical SciencesMoleculeOrganic chemistryThermal stabilityIrradiationAbsorption (electromagnetic radiation)Journal of the American Chemical Society
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A photoswitchable helical peptide with light-controllable interface/transmembrane topology in lipidic membranes

2021

Summary The spontaneous insertion of helical transmembrane (TM) polypeptides into lipid bilayers is driven by three sequential equilibria: solution-to-membrane interface (MI) partition, unstructured-to-helical folding, and MI-to-TM helix insertion. A bottleneck for understanding these three steps is the lack of experimental approaches to perturb membrane-bound hydrophobic polypeptides out of equilibrium rapidly and reversibly. Here, we report on a 24-residues-long hydrophobic α-helical polypeptide, covalently coupled to an azobenzene photoswitch (KCALP-azo), which displays a light-controllable TM/MI equilibrium in hydrated lipid bilayers. FTIR spectroscopy reveals that trans KCALP-azo folds…

BiomoleculesMembranesMultidisciplinaryPhotoisomerizationPhotoswitchPhotoabsorptionScienceQArticleFolding (chemistry)chemistry.chemical_compoundCrystallographyMembraneAzobenzenechemistryMembrane topologyHelixLipid bilayer
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Tuning Azoheteroarene Photoswitch Performance through Heteroaryl Design

2017

International audience; Photoswitchable compounds, which can be reversibly switched between two isomers by light, continue to attract significant attention for a wide array of applications. Azoheteroarenes represent a relatively new but understudied type of photoswitch, where one of the aryl rings from the conventional azobenzene class has been replaced with a five-membered heteroaromatic ring. Initial studies have suggested the azoheteroarenes – the arylazopyrazoles in particular – to have excellent photoswitching properties (quantitative switching and long Z isomer half-life). Here we present a systematic computational and experimental study to elucidate the origin of the long thermal hal…

CHEMICAL-REACTIONSMOLECULAR SWITCHESFUNCTIONAL RESPONSE THEORYChemistry Multidisciplinary010402 general chemistryRing (chemistry)Photochemistry01 natural sciencesBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryAZO-COMPOUNDSPHOTOISOMERIZATION[CHIM]Chemical SciencesTO-TRANS ISOMERIZATIONAZOBENZENEScience & TechnologyPhotoswitch010405 organic chemistryArylSOLAR THERMAL STORAGEGeneral ChemistryCombinatorial chemistry0104 chemical sciencesChemistrychemistryAzobenzenePhysical SciencesEXCITATION-ENERGIESVISIBLE-LIGHT03 Chemical Sciences
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A photoswitchable helical peptide with light-controllable interface / transmembrane topology in lipidic membranes

2021

AbstractAccording to the three-step model, the spontaneous insertion and folding of helical transmembrane (TM) polypeptides into lipid bilayers is driven by three sequential equilibria: solution-to-membrane interface (MI) partition, unstructured-to-helical folding, and MI-to-TM helix insertion. However, understanding these three steps with molecular detail has been challenged by the lack of suitable experimental approaches to rapidly and reversibly perturb membrane-bound hydrophobic polypeptides out of equilibrium. Here, we report on a 24-residues-long hydrophobic α-helical polypeptide, covalently coupled to an azobenzene photoswitch (KCALP-azo), which displays a light-controllable TM/MI eq…

Folding (chemistry)chemistry.chemical_compoundCrystallographyMembraneAzobenzenechemistryPhotoswitchPhotoisomerizationMembrane topologyHelixLipid bilayer
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Photo-switching and -cyclisation of hydrogen bonded liquid crystals based on resveratrol

2020

A series of hydrogen-bonded liquid crystals based on resveratrol and resveratrone is reported and investigated with respect to their photo-switchability (at 405 nm) and photo-cyclisation (at 300 nm).

Materials scienceHydrogenMetals and AlloysChemiechemistry.chemical_elementGeneral ChemistryResveratrolPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryLiquid crystalMaterials ChemistryCeramics and CompositesSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhotoswitching Liquid Crystals Hydrogen Bonding Packing Analysis
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Light-responsive hybrid material based on luminescent core-shell quantum dots and steroidal organogel

2016

We report the synthesis of a smart novel hybrid with reversible photoswitchable luminescence properties modulated by light. The combination of a low molecular weight organogelator (LMOG) and CdSe/ZnS core-shell semiconductor nanoparticles capped with trioctylphosphine oxide ligands produces a luminescent, stable and transparent material. Modulation of the luminescence properties was successfully achieved using a diarylethene photochromic compound, with good resistance to fatigue ca. 22 cycles. Interestingly, the morphology of the organogel fibers was preserved in the hybrid, while a partial luminescence quenching of the nanoparticle was observed. This material could have implication for on-…

Materials scienceOrganogelNanoparticleNanotechnology02 engineering and technology010402 general chemistry01 natural sciences//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundPhotochromismPhotoswitchableDiaryletheneQuantum DotsMaterials Chemistry//purl.org/becyt/ford/1.4 [https]Quenching (fluorescence)Otras Ciencias QuímicasCiencias QuímicasGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryChemical engineeringQuantum dot0210 nano-technologyHybrid materialLuminescenceTrioctylphosphine oxideCIENCIAS NATURALES Y EXACTAS
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Wavelength-Gated Adaptation of Hydrogel Properties via Photo-Dynamic Multivalency in Associative Star Polymers.

2020

Abstract Responsive materials, such as switchable hydrogels, have been largely engineered for maximum changes between two states. In contrast, adaptive systems target distinct functional plateaus between these maxima. Here, we demonstrate how the photostationary state (PSS) of an E/Z‐arylazopyrazole photoswitch can be tuned by the incident wavelength across a wide color spectrum, and how this behavior can be exploited to engineer the photo‐dynamic mechanical properties of hydrogels based on multivalent photoswitchable interactions. We show that these hydrogels adapt to the wavelength‐dependent PSS and the number of arylazopyrazole units by programmable relationships. Hence, our material des…

Materials sciencePhotoswitch010405 organic chemistryArylazopyrazoleSoft roboticsNanotechnologyHydrogelsGeneral ChemistryMaterial Design010402 general chemistry01 natural sciencesWavelength-Gated EngineeringCatalysis0104 chemical sciencesWavelengthPhotostationary stateAdaptive systemSelf-healing hydrogelsPhotoswitchAdaptation (computer science)Photoresponsive SystemsAdaptive MaterialsResearch ArticlesResearch ArticleAngewandte Chemie (International ed. in English)
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Trans-to-cis photoisomerization of cyclocurcumin in different environments rationalized by computational photochemistry

2020

International audience; Cyclocurcumin is a turmeric component that attracted much less attention compared to the well known curcumin. In spite of the less deep charcaterization of its properties, cyclocurcumin has shown promising anticancer effects when used in combination with curcumin. Especially, due to its peculiar molecular structure, cyclocurcumin can be regarded as an almost ideal photoswitch, whose capabilities can also be exploited for relevant biological applications. Here, by means of state-of-the-art computational methods for electronic excited-state calculations (TD-DFT, MS-CASPT2, XMS-CASPT2) we analyze in detail the absorption and photoisomerization pathways leading from the …

PhotoswitchPhotoisomerizationChemistryGeneral Physics and Astronomy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesFluorescence0104 chemical sciencesExcited state[CHIM]Chemical SciencesMoleculePhysical and Theoretical ChemistrySolvent effects0210 nano-technologyGround stateCis–trans isomerismPhysical Chemistry Chemical Physics
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A NOT gate in a cis-trans photoisomerization model

2007

We numerically study the implementation of a NOT gate by laser pulses in a model molecular system presenting two electronic surfaces coupled by non adiabatic interactions. The two states of the bit are the fundamental states of the cis-trans isomers of the molecule. The gate is classical in the sense that it involves a one-qubit flip so that the encoding of the outputs is based on population analysis which does not take the phases into account. This gate can also be viewed as a double photo-switch process with the property that the same electric field controls the two isomerizations. As an example, we consider one-dimensional cuts in a model of the retinal in rhodopsin already proposed in t…

PhysicsQuantum Physicseducation.field_of_study010304 chemical physicsPhotoisomerizationPhotoswitchPopulationFOS: Physical sciencesSpectral densityPulse durationLaser01 natural sciencesAtomic and Molecular Physics and Opticslaw.inventionlawElectric fieldQubit0103 physical sciences[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Atomic physicsQuantum Physics (quant-ph)010306 general physicseducation
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Supramolecular hierarchy among halogen and hydrogen bond donors in light-induced surface patterning

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. Herein, we unambiguously show that one of these characteristic features, namely high directionality, renders halogen bonding the interaction of choice when developing azobenzene-containing supramolecular polymers for light-induced surface patterning. The study is conducted by using an extensive library of azobenzene molecules that differ only in terms of the bond-donor unit. We introduce a new tetrafluorophenol-containing azobenzene photoswitch capable of forming strong hydrogen bonds, and show that an io…

RELIEF GRATINGSDENSITY-FUNCTIONAL THEORY CALCULATIONSMaterials sciencePHOTOINDUCED BIREFRINGENCE116 Chemical sciencesta221Supramolecular chemistryPhotochemistrysupramolecular chemistryDENSITY-FUNCTIONAL THEORYchemistry.chemical_compoundMaterials ChemistryMoleculeTHERMAL-ISOMERIZATIONPOLARIZATION DEPENDENCECO-CRYSTALSLIQUID-CRYSTAL ORDERta218chemistry.chemical_classificationta214Halogen bondta114PhotoswitchHydrogen bondPolymers Halogen Bonding Supramolecular Chemistry Photoresponsive AzobenzeneGeneral Chemistryhydrogen bondingPOLYMER-AZOBENZENE COMPLEXESSupramolecular polymersSOLID-STATEchemistryAzobenzeneHALOGEN BONDINGHalogenlight-induced surface patterningSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePHOTONIC APPLICATIONSPOLYMER-AZOBENZENE COMPLEXES; DENSITY-FUNCTIONAL THEORY; LIQUID-CRYSTAL ORDER; RELIEF GRATINGS; SOLID-STATE; PHOTOINDUCED BIREFRINGENCE; POLARIZATION DEPENDENCE; THERMAL-ISOMERIZATION; PHOTONIC APPLICATIONS; CO-CRYSTALSJournal of Materials Chemistry C
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