Search results for "PHOTOISOMERIZATION"

showing 10 items of 73 documents

TiO2-induced photoisomerization of caffeic acid

2014

Settore CHIM/07 - Fondamenti Chimici Delle TecnologiePhotoisomerization Caffeic acid Titanium dioxide
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A theoretical study of the electronic spectrum of cis-stilbene

1999

Abstract The valence and Rydberg electronic excited singlet states of cis -stilbene have been studied using multiconfigurational second-order perturbation theory (CASPT2). The study includes a geometry determination of the ground state. The geometry of the lowest 1 B state has also been optimized, leading to a structure where the two benzyl groups are nearly perpendicular. The calculated vertical spectrum is in agreement with the occurrence of three main bands in the observed one-photon absorption spectrum. Below the relatively intense transition to the 2 1 B (HOMO→LUMO) state at 4.61 eV, two weak transitions have been computed at 4.11–4.45 eV, which correspond to transitions to the 1 1 B a…

Valence (chemistry)Absorption spectroscopyPhotoisomerizationChemistryAtomic and Molecular Physics and OpticsAnalytical Chemistrysymbols.namesakeExcited stateSinglet fissionRydberg formulasymbolsSinglet stateAtomic physicsGround stateInstrumentationSpectroscopySpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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Temperature and light sensitive copolymers containing azobenzene moieties prepared via a polymer analogous reaction

2009

Abstract Four different series of polyacrylamides containing different amounts of azobenzene moieties have been synthesized via a polymer analogous reaction of poly(pentafluorophenylacrylate) (PPFPA). All copolymers were designed to exhibit a lower critical solution temperature (LCST) in aqueous solution, which was dependent on (i) the amount of incorporated chromophoric azobenzene groups and (ii) the isomerization state of the respective azobenzene group. Higher LCST values were measured for UV-irradiated solutions of the copolymers in comparison to the non-irradiated copolymer solutions. A maximum difference in the LCST of up to 7 °C was found for the copolymer poly(N,N-dimethylacrylamide…

chemistry.chemical_classificationAzo compoundPolymers and PlasticsPhotoisomerizationOrganic ChemistryPolymerLower critical solution temperatureCis trans isomerizationchemistry.chemical_compoundchemistryAzobenzenePolymer chemistryMaterials ChemistryCopolymerIsomerizationPolymer
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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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One is Enough: Influencing Polymer Properties with a Single Chromophoric Unit

2011

1) Institute for Technical and Macromolecular Chemistry, University of Hamburg, Bundesstrasse 45, D-­‐20146 Hamburg, Germany 2) WCU program of C2E2, School of Chemical and Biological, Engineering, College of Engineering, Seoul National University, Seoul, Korea Designing a polymer usually involves the incorporation of multiple functional units into a polymer chain, which mutually determine the polymer properties. By combining various functional units, a myriad of polymer properties can be fine-­‐ tuned. Classical polymer chemistry teaches us that a single functional group -­‐-­‐ in particular the end-­‐group of a polymer chain -­‐-­‐ does not contribute to the polymer properties, as is indee…

chemistry.chemical_classificationMaterials sciencePhotoisomerizationPolymer scienceResearch areasGeneral ChemistryPolymerChromophorePhotochemistryCatalysischemistry.chemical_compoundAzobenzenechemistryChain (algebraic topology)Functional groupMoleculeAngewandte Chemie International Edition
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Direct Surface Relief Formation in Polymer Films

2013

Due to active development of nanoelectronics, the studies of methods of nanorelief surface formation in different materials, in particular polymers are very important. Organic polymer films in consequence of their dielectric and optical properties have been used as basis of these devices. In this paper, the possibility of UV optical record and electron beam lithography in different type of polymeric films was studied. Mechanisms of molecular structure changes: photoisomerization, destruction, cross-linking and oxidation have been discussed. The results of UV illumination of polyurethanes, polyacrylates, and some block-copolymers were described. The element analysis of polybutadiene block co…

chemistry.chemical_classificationMaterials sciencePhotoisomerizationbusiness.industryMechanical EngineeringPolymerDielectricPolybutadieneOpticschemistryNanoelectronicsMechanics of MaterialsCopolymerOptoelectronicsMoleculeGeneral Materials SciencebusinessElectron-beam lithographyKey Engineering Materials
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UV optical record and electron beam lithography in polymer films

2012

Possibility of UV optical record and electron beam lithography in different type of organic polymer films was studied. Mechanisms of molecular structure changes: photoisomerization, destruction, cross-linking and oxidation have been discussed. The results of UV illumination of polyurethanes, polyacrilates, and some block-copolymers are described. The element analysis of polyisoprene block copolymer was performed before and after UV illumination, and the changes in transmission spectra of the polymer film were measured. The resolution of electron beam lithography on polymer films was studied. In the polyisoprene block copolymer film the oxidation polymerization was ascertain at UV-illuminati…

chemistry.chemical_classificationMaterials sciencePhotoisomerizationbusiness.industryResolution (electron density)PolymerOpticsPolymerizationchemistryCopolymerOptoelectronicsMoleculeX-ray lithographybusinessElectron-beam lithographyIOP Conference Series: Materials Science and Engineering
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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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Heterocyclic rearrangements in constrained media. A zeolite-directed photorearrangement of 1,2,4-oxadiazoles

2005

[reaction: see text] The first intrazeolite-photoinduced rearrangement of a five-membered heterocycle is reported. A completely different behavior compared to solution irradiations has been observed. The zeolite's role in directing the photoreaction of 3-phenyl-1,2,4-oxadiazoles toward the formation of the corresponding 1,3,4-oxadiazoles in a ring contraction-ringexpansion route is discussed.

chemistry.chemical_classificationModels MolecularOxadiazolesRING-PHOTOISOMERIZATIONMolecular StructurePHOTOCHEMICAL BEHAVIORChemistryPhotochemistryUltraviolet RaysOrganic ChemistryPATHWAYSSettore CHIM/06 - Chimica OrganicaRing (chemistry)PhotochemistryHeterocyclic compoundCyclizationZeolitesZeolite
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Living Light-Induced Crystallization-Driven Self-Assembly for Rapid Preparation of Semiconducting Nanofibers.

2018

Well-defined nanostructures composed of conjugated polymers have attracted significant attention due to their intriguing electronic and optical properties. However, precise control of the size and uniformity of these semiconducting nanostructures is still rare and challenging, despite recent advances in strategies to obtain self-assembled nanostructures with narrow dispersions. Herein, we demonstrate the preparation of fluorescent conjugated block copolymers by one-shot polymerization and rapid formation of nanofibers in a few minutes via light-induced crystallization-driven self-assembly, driven by facile cis-to- trans photoisomerization of its poly( p-phenylenevinylene) blocks. Furthermor…

chemistry.chemical_classificationNanostructurePhotoisomerizationNanotechnology02 engineering and technologyGeneral ChemistryPolymerConjugated system010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCatalysis0104 chemical sciencesColloid and Surface ChemistryPolymerizationchemistryNanofiberCopolymerSelf-assembly0210 nano-technologyJournal of the American Chemical Society
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