Search results for "PHOTOISOMERIZATION"

showing 10 items of 73 documents

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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ChemInform Abstract: Modified Photobehavior of Carboxylic Acid Derivatives Induced by Protonation.

1987

Abstract A series of carboxylic acid derivatives 1–6 containing a second interacting function have been converted into the corresponding O -protonated species or acylium ions upon treatment with 96% sulfuric acid or oleum, respectively, at room temperature. The resulting stable cations have been spectroscopically characterized and submitted to irradiation. Cis-trans photoisomerization was observed in the ionic speciesderived from trans -crotonic, fumaric and maleic acids, and maleic anhydride. By contrast protonated crotonolactone 5a+ was found to be photostable. Finally, protonated α-bromobutyrolactone 6a+ was clean and efficiently dehydrohalogenated to 5a+ upon irradiation. Since the norm…

chemistry.chemical_classificationchemistry.chemical_compoundchemistryPhotoisomerizationCarboxylic acidIonic bondingMaleic anhydrideSulfuric acidProtonationGeneral MedicineMedicinal chemistryOleumIonChemInform
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Photochemical behavior in azobenzene having acidic groups. Preparation of magnetic photoresponsive gels

2011

[EN] The photochemistry of three azobenzenes representing contrasting photochemical behaviors is described in the present work. Thus, Methyl Orange (MO, 4-[[(4-dimethylamino)phenyl]-azo]benzenesulfonic acid sodium salt, hereinafter (1) and 4-hydroxyazobenzene-4'-sulfonic acid (2) undergo in water fast photochemical proton shift, with decays in the microsecond timescale. In contrast to the previous cases, azobenzene-4,4'-dicarboxylic acid (3) undergoes photoisomerization in water. This photochemical behavior allows the preparation of aqueous gels with Aerosil as gelating agent (5% weight) exhibiting high cyclability and photoreversible isomerization of the trans to cis (300 nm irradiation) a…

PhotoisomerizationMagnetismGeneral Chemical EngineeringGeneral Physics and Astronomy02 engineering and technology010402 general chemistryPhotochemistry01 natural scienceschemistry.chemical_compoundQUIMICA ORGANICABenzenesulfonic acidPhotoisomerizationMethyl orangeMagnetite nanoparticlesAqueous solutionAzobenzeneMultifunctional materialsLaser flash photolysisGeneral Chemistry021001 nanoscience & nanotechnologyPhotoresponsive gel0104 chemical sciencesAzobenzenechemistry0210 nano-technologyIsomerizationIron oxide nanoparticlesJournal of Photochemistry and Photobiology A: Chemistry
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Femtosecond structural dynamics drives the trans/cis isomerization in photoactive yellow protein

2016

Many biological processes depend on detecting and responding to light. The response is often mediated by a structural change in a protein that begins when absorption of a photon causes isomerization of a chromophore bound to the protein. Pande et al. used x-ray pulses emitted by a free electron laser source to conduct time-resolved serial femtosecond crystallography in the time range of 100 fs to 3 ms. This allowed for the real-time tracking of the trans-cis isomerization of the chromophore in photoactive yellow protein and the associated structural changes in the protein.Science, this issue p. 725A variety of organisms have evolved mechanisms to detect and respond to light, in which the re…

0301 basic medicinePhotoreceptorsTime FactorsPhotoisomerizationLightProtein ConformationPhotochemistryPhotoreceptors MicrobialMYOGLOBINProtein structureMicrobialX-RAY-DIFFRACTIONPHOTOISOMERIZATIONMOTIONSchromophoresta116MultidisciplinarySPECTROSCOPYCrystallographyChemistryPhotochemical ProcessesTime resolved crystallographyTIMEMultidisciplinary SciencesPicosecondFemtosecondphotoactive proteinsScience & Technology - Other Topicsddc:500IsomerizationStereochemistryGeneral Science & TechnologyConjugated systemArticle03 medical and health sciencesBacterial ProteinsIsomerismEXCITATIONx-ray crystallographyPhotonsScience & TechnologyPHOTOCYCLEta114CHROMOPHOREta1182PATHWAYSChromophore030104 developmental biologyfree-electron laserssense organstrans-cis isomerization
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A theoretical study of the lowest electronic states of azobenzene: the role of torsion coordinate in the cis-trans photoisomerization

2003

In the present paper we report the results of a multiconigurational computational study on potential- energy curves of azobenzene along the NN twisting to clarify the role of this coordinate in the decay of the S2(pp*) and S1(np*) states. We have found that there is a singlet state, S3 at the trans geometry, on the basis of the doubly excited coniguration n 2 p* 2 , that has a deep minimum at about 90 of twisting, where it is the lowest excited singlet state. The existence of this state provides an explanation for the short lifetime of S2(pp*) and for the wavelength-dependence of azobenzene photochem- istry. We have characterized the S1(np*) state by calcu- lating its vibrational frequencie…

PhotoisomerizationAzobenzeneMulticonfigurational wave function methodschemistry.chemical_compoundsymbols.namesakeAzobenzenechemistryExcited statePhotoisomerizationddc:540symbolsDensity functional theoryExcited electronic statesSinglet statePhysical and Theoretical ChemistryAtomic physicsRaman spectroscopyIsomerizationCis–trans isomerism
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Photoswitchable Smectic Liquid-Crystalline Elastomers

2005

We succeeded in the synthesis of azo side chain containing polysioxanes with broad smectic C* and A phases. In these polymers the phase transition temperatures can be shifted reversibly by up to 17°C by irradiation with UV (cis) or VIS (trans) light. Thin films of these polymers in the smectie phase (both on substrates and as free-standing films) orient perfectly in a homeotropic manner. As a consequence, the aze chromophores do no longer absorb during a perpendicular illumination with light (dichroism). It is thus possible to crosslink these films photochemically to prepare photoswitchable smectic LC elastomers.

chemistry.chemical_classificationMaterials scienceAzo compoundPolymers and PlasticsPhotoisomerizationOrganic ChemistryHomeotropic alignmentPolymerDichroismPhotochemistryCis trans isomerizationchemistry.chemical_compoundchemistryPhase (matter)Polymer chemistryMaterials ChemistrySide chainMacromolecular Rapid Communications
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Competing Ring-Photoisomerization Pathways in the 1,2,4-Oxadiazole Series. An Unprecedented Ring-Degenerate Photoisomerization

2002

The irradiation of some 5-alkyl-3-amino-1,2,4-oxadiazoles at lambda = 254 nm in methanol in the presence of triethylamine (TEA) gave ring-photoisomerization both into 2-alkyl-5-amino-1,3,4-oxadiazoles and, unprecedently, into the ring-degenerate 3-alkyl-5-amino-1,2,4-oxadiazoles. The competing ring contraction-ring expansion route and the internal cyclization-isomerization mechanism explain the results.

chemistry.chemical_compoundReaction mechanismchemistryPhotoisomerizationOrganic ChemistryOxadiazoleMethanolRing (chemistry)PhotochemistryTriethylamineIsomerizationChemical synthesisThe Journal of Organic Chemistry
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Some photochemical transformations of polymers

1969

Abstract Several light-induced reactions of polymers are described. The light-sensitive groups are part of the macromolecules. Photoisomerization of polyvinylbutyral produces a polymer with vinylbutyrate-groups. At exposure to light, furan and benzofuran are added to the carbonyl-groups of polyvinylbenzophenone. Polymers with azido-groups are prepared, which eliminate nitrogen at irradiation. Light-sensitive films can be cast from polymers with o-quinonediazide-groups.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsPhotoisomerizationOrganic ChemistryGeneral Physics and Astronomychemistry.chemical_elementPolymerPhotochemistryNitrogenchemistry.chemical_compoundchemistryFuranPolymer chemistryMaterials ChemistryIrradiationBenzofuranMacromoleculeEuropean Polymer Journal
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Conformational preferences and synthesis of isomers Z and E of oxazole-dehydrophenylalanine

2016

Dehydrophenylalanine, ΔPhe, is the most commonly studied α,β-dehydroamino acid. In nature, further modifications of the α,β-dehydroamino acids were found, for example, replacement of the C-terminal amide group by oxazole ring. The conformational properties of oxazole-dehydrophenylalanine residue (ΔPhe-Ozl), both isomers Z and E, were investigated. To determine all possible conformations, theoretical calculations were performed using Ac-(Z/E)-ΔPhe-Ozl(4-Me) model compounds at M06-2X/6-31++G(d,p) level of theory. Ac-(Z/E)-ΔPhe-Ozl-4-COOEt compounds were synthesized and the conformational preferences of each isomer, Z and E, were investigated using FTIR and NMR-NOE in solutions of increasing p…

Ramachandran diagramHantzsch reactioncis–trans isomerizationdehydroamino acidsphotoisomerizationBiopolymers
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Theoretical Study of the Electronic Spectrum of trans-Stilbene

1997

The electronic spectrum of trans-stilbene in the energy range up to 6 eV has been studied using multiconfigurational second-order perturbation theory (CASPT2). The study includes a geometry determination of the ground state. In all, 12 singlet and one triplet excited states were studied. The calculated spectrum makes it possible to assign the valence excited singlet states corresponding to the three bands observed in the low-energy region of the one-photon absorption spectrum. The most intense feature of the calculated spectrum corresponds to the 11Ag → 21Bu transition at 4.07 eV. The weakly allowed 11Bu state was found 0.3 eV below 21Bu. Transition to the 31Ag state, computed at 4.95 eV, i…

symbols.namesakeValence (chemistry)PhotoisomerizationAbsorption spectroscopyChemistryExcited stateRydberg formulasymbolsTrans stilbeneSinglet statePhysical and Theoretical ChemistryAtomic physicsGround stateThe Journal of Physical Chemistry A
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