Search results for "azobenzene"

showing 10 items of 84 documents

1D coordination polymer based on copper(II)-containing tetrameric 1,2,3-triazole ligand from click chemistry: Magnetic and catalytic properties

2019

Abstract A novel tetrameric tetra[O-((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)]-pentaerythritol (TBTP) has been synthesized using click chemistry strategy. TBTP was characterized and used as ligand to form new Cu(II) complexes, forming 1-D coordination polymers. Two square planar complexes were characterized by single-crystal X-ray diffraction, presenting formula [Cu(TBTP)][Cu(NO3)4] (1) and [Cu(TBTP)](NO3)2 (2). In both structures, a cationic 1-D coordination polymer (CP) has been formed. The CP contain a 1:1 Cu(II)/TBTP ratio with four neutral triazole groups coordinating the Cu(II) center, forming a Cu N bonds ranging 1.988(2)–2.001(2) A. The study of the magnetic properties of compounds 1…

123-Triazole010405 organic chemistryCoordination polymerLigandCationic polymerizationTriazole010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographyAnilineAzobenzenechemistryMaterials ChemistryClick chemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
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Influence of End Groups on the Stimulus-Responsive Behavior of Poly[oligo(ethylene glycol) methacrylate] in Water

2010

The influence of the chemical structure of both end groups onto the lower critical solution temperature (LCST) of poly[oligo(ethylene glycol) monomethyl ether methacrylate] (POEGMA) in water was systematically investigated. POEGMA of Mn = 3550 g/mol and Mw/Mn = 1.14 prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization was equipped with two different functional end groups in a one-step postpolymerization reaction combining activated esters, functional amines, and functional methane thiosulfonates. As end groups, n-propyl, n-hexadecyl, di(n-octadecyl), poly(ethylene glycol)-550 (PEG), 1H,1H-perfluorononyl, azobenzene, and trimethylethylammonium groups were system…

Polymers and PlasticsChemistryOrganic ChemistryChain transferLower critical solution temperatureMicelleInorganic ChemistryHydrophobic effectEnd-groupchemistry.chemical_compoundPolymerizationAzobenzenePolymer chemistryMaterials ChemistryEthylene glycolMacromolecules
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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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Efficient light-induced phase transitions in halogen-bonded liquid crystals

2016

Here, we present a new family of light-responsive, fluorinated supramolecular liquid crystals (LCs) showing efficient and reversible light-induced LC-to-isotropic phase transitions. Our materials design is based on fluorinated azobenzenes, where the fluorination serves to strengthen the noncovalent interaction with bond-accepting stilbazole molecules, and increase the lifetime of the cis-form of the azobenzene units. The halogen-bonded LCs were characterized by means of X-ray diffraction, hot-stage polarized optical microscopy, and differential scanning calorimetry. Simultaneous analysis of light-induced changes in birefringence, absorption, and optical scattering allowed us to estimate tha…

Phase transitionMaterials scienceGeneral Chemical Engineering116 Chemical sciencesSupramolecular chemistry02 engineering and technology010402 general chemistry01 natural sciencesArticlechemistry.chemical_compoundDifferential scanning calorimetryLiquid crystalMaterials ChemistryMoleculeHalogen Bonding Liquid Crystals Photoresponsive Supramolecular Chemistryta216ta116ta215Birefringenceta114General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographyAzobenzenechemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologieAbsorption (chemistry)0210 nano-technology
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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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Impact of the molecular structure of an indandione fragment containing azobenzene derivatives on the morphology and electrical properties of thin fil…

2016

Abstract The solution casting method is low-cost processing method. Moreover, it is possible to prepare amorphous thin films by using this method, and thus, both optical quality and electrical properties could be improved in compare to polycrystalline films made by thermal evaporation in vacuum. Therefore, low-molecular-weight compounds that form amorphous structure from solution could be promising in organic electronics. In this work film morphology, molecule energy levels, and charge carrier mobility in thin films of indandione fragment containing azobenzene derivatives were studied. Deep charge carrier trapping states that drastically influenced charge carrier mobility were observed for …

010302 applied physicsOrganic electronicsMaterials science02 engineering and technology021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesAmorphous solidchemistry.chemical_compoundAzobenzenechemistryElectron affinity0103 physical sciencesOrganic chemistryPhysical chemistryGeneral Materials ScienceCharge carrierCrystalliteThin filmIonization energy0210 nano-technologyMaterials Chemistry and Physics
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<title>Optically induced switching of dicyclohexylamino substituted azobenzene derivatives in thin ordered films</title>

2005

During the last years, there has been an increasing interest in the photoinduced switching effects. Among the objects of concern azobenzene derivatives, isomerizing under UV and visible light, occupy a prominent position. To understand the photoresponse of these materials in the condensed phase, their spectroscopic and electrical properties are studied. It is shown that the photoresponse depends on the orientation of the molecules and their packing. A number of novel azobenzene derivatives containing a N,N-dicyclohexyl sulfonamide moiety is synthesized. The derivatives differ in the length of alkyl chains between the azobenzene moiety and SH or COOH groups. The morphology and the photoinduc…

chemistry.chemical_classificationchemistry.chemical_compoundchemistryAzobenzenePhase (matter)MonolayerMoleculeMoietySelf-assembled monolayerPhotochemistryAlkylVisible spectrumSPIE Proceedings
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Photocontrolled On-Surface Pseudorotaxane Formation with Well-Ordered Macrocycle Multilayers.

2016

The photoinduced pseudorotaxane formation between a photoresponsive axle and a tetralactam macrocycle was investigated in solution and on glass surfaces with immobilized multilayers of macrocycles. In the course of this reaction, a novel photoswitchable binding station with azobenzene as the photoswitchable unit and diketopiperazine as the binding station was synthesized and studied by NMR and UV/Vis spectroscopy. Glass surfaces have been functionalized with pyridine-terminated SAMs and subsequently with multilayers of macrocycles through layer-by-layer self assembly. A preferred orientation of the macrocycles could be confirmed by NEXAFS spectroscopy. The photocontrolled deposition of the …

Supramolecular chemistryTetralactam macrocyclesurface chemistry02 engineering and technology010402 general chemistryLinear dichroismPhotochemistry01 natural sciencessupramolecular chemistryCatalysischemistry.chemical_compoundSpectroscopyta116pseudorotaxanesphotochemistryOrganic ChemistryGeneral Chemistry021001 nanoscience & nanotechnologyXANES0104 chemical sciencesazobenzeneAzobenzenechemistryNexafs spectroscopySelf-assembly0210 nano-technologyChemistry (Weinheim an der Bergstrasse, Germany)
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The spectrum of allergic (cross-)sensitivity in clinical patch testing with 'para amino' compounds

2002

Background: Allergic contact sensitization to ‘para amino’ compounds is frequent and the spectrum of cross-reactivity between members of this chemical group is variable. Methods: A retrospective analysis of clinical patch test data obtained with a special test series in the centres of the Information Network of Departments of Dermatology (IVDK) between 1995 and 1999. Results: In the 638 patients tested with the above test panel positive reactions were observed most often to p-aminoazobenzene (16.2%), p-phenylenediamine (14.1%), p-toluylenediamine (10.0%), followed by 4,4′-diaminodiphenylmethane (8.5%), Disperse Orange 3 (8.4%) and p-aminophenol (3.1%). Among the 544 patients tested with p-p…

medicine.medical_specialtyAllergyConcordanceCross sensitivityStatistics as TopicImmunologyCross ReactionsPhenylenediaminesAminophenolsmedicine.disease_causeCross-reactivity030207 dermatology & venereal diseases03 medical and health scienceschemistry.chemical_compoundSulfanilamide0302 clinical medicineGermanySulfanilamidesmedicineHumansImmunology and AllergyAminesRetrospective Studiesbusiness.industryPatch testp-PhenylenediamineAllergensPatch Testsmedicine.diseaseDermatology3. Good healthchemistryP-Aminoazobenzenep-Aminoazobenzene030220 oncology & carcinogenesisDermatitis Allergic ContactImmunologybusiness4-Aminobenzoic AcidContact dermatitisAllergy
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Halogen bonding stabilizes a cis-azobenzene derivative in the solid state : A crystallographic study

2017

Crystals oftrans- andcis-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 metastablecis-isomer, allowing single crystals of thecis-azobenzene to be grown. Structural analysis on thecis-azobenzene, complemented with density functional theory calculations, highlights the active role of the halogen-bond contact (N...I synthon) in promoting the stabilization of thecis-isomer. The presence of a long aliphatic chain on the azobenzene unit induces a phase segregation that stabilizes the molecular arrangement for both thetrans- andcis-i…

Materials Chemistry2506 Metals and Alloys116 Chemical sciencesCrystal structure010402 general chemistryPhotochemistry01 natural sciencesazobenzene; halogen bonding; isomerization; Electronic Optical and Magnetic Materials; Atomic and Molecular Physics and Optics; 2506; Materials Chemistry2506 Metals and Alloysisomerizationchemistry.chemical_compoundPhase (matter)Atomic and Molecular PhysicsMaterials ChemistryElectronicOptical and Magnetic MaterialsHalogen bondta114010405 organic chemistryChemistrySynthonMetals and AlloysAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallographyazobenzeneAzobenzenehalogen bondingDensity functional theorySettore CHIM/07 - Fondamenti Chimici Delle Tecnologieand Optics2506IsomerizationDerivative (chemistry)
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