Search results for "Azo compound"

showing 10 items of 61 documents

A Molecular Electron Density Theory Study of the Reactivity of Azomethine Imine in [3+2] Cycloaddition Reactions

2017

The electronic structure and the participation of the simplest azomethine imine (AI) in [3+2] cycloaddition (32CA) reactions have been analysed within the Molecular Electron Density Theory (MEDT) using DFT calculations at the MPWB1K/6-311G(d) level. Electron localisation function (ELF) topological analysis reveals that AI has a pseudoradical structure, while the conceptual DFT reactivity indices characterise this TAC as a moderate electrophile and a good nucleophile. The non-polar 32CA reaction of AI with ethylene takes place through a one-step mechanism with low activation energy, 5.3 kcal/mol-1. A bonding evolution theory (BET) study indicates that this reaction takes place through a non-…

Models MolecularThiosemicarbazones[3+2] cycloaddition reactionsImineMolecular Conformationmolecular mechanismsazomethine iminePharmaceutical ScienceElectronsElectronic structureActivation energy010402 general chemistry01 natural sciencesArticlebonding evolution theoryAnalytical Chemistrychemistry.chemical_compoundNucleophileComputational chemistryDrug Discoveryconceptual density functional theoryMoleculeReactivity (chemistry)organic_chemistryelectron densityPhysical and Theoretical Chemistryazomethine imine; [3+2] cycloaddition reactions; molecular electron density theory; conceptual density functional theory; electron localisation function; bonding evolution theory; electron density; molecular mechanisms; chemical reactivityCycloaddition ReactionMolecular Structure010405 organic chemistrymolecular electron density theoryOrganic ChemistryCycloaddition0104 chemical scienceschemistryChemistry (miscellaneous)ElectrophileQuantum TheoryThermodynamicsMolecular MedicineDensity functional theoryImineselectron localisation functionAzo Compoundschemical reactivityMolecules; Volume 22; Issue 5; Pages: 750
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Azoxybenzene rearrangement catalyzed by solid acids

2008

Abstract For the first time, the potential of acidic cation-exchange resin (sulfonated polystyrene) to catalyze the Wallach rearrangement of azoxybenzene into 4-hydroxyazobenzene has been proved. This finding reveals an alternative reaction path possible in a heterogeneous process using solid acids and may help to clear some doubts concerning the rearrangement mechanism postulated so far. The resin-induced reaction was found to proceed exclusively in a non-polar medium. Reasonable yield was obtained particularly in isooctane due to favorable distribution of azoxybenzene throughout the resin's matrix. On the contrary, the HY type zeolite did not activate the rearrangement, most probably beca…

Steric effectsHeterogeneous catalysisZeoliteAzo compoundProcess Chemistry and TechnologyDFT calculationsWallach rearrangementHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundchemistryComputational chemistryYield (chemistry)Azoxybenzene rearrangementPolymer chemistryPolystyrenePhysical and Theoretical ChemistryZeoliteSulfonated polystyrene resinJournal of Molecular Catalysis A: Chemical
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New aspects in the histological examination of polyethylene wear particles in failed total joint replacements.

2002

The most important long-term complication in total joint replacements is aseptic osteolysis. Wear particles such as polyethylene (PE) debris are considered to be one of the causes that play a central role. Several studies indicated that PE can be visualised in paraffin-embedded tissue sections not only by polarised light, but also after oil red staining. To determine whether oil red staining enables sensitive detection of PE, we examined staining of mechanically-produced PE particles by oil red. Furthermore, we studied oil red staining of paraffin-embedded tissue specimens of patients with failed uncemented and cemented total knee and hip prostheses. We applied double labelling of sections …

MalePathologymedicine.medical_specialtyHistologyOsteolysisLightJoint ProsthesisTotal Joint ReplacementsAntigens Differentiation MyelomonocyticStainArthroplasty03 medical and health scienceschemistry.chemical_compound0302 clinical medicineAntigens CDMaterials TestingmedicineHumansColoring AgentsHistological examination030222 orthopedicsChemistryCell BiologyGeneral MedicineProstheses and ImplantsPolyethylenemedicine.diseaseImmunohistochemistry3. Good healthSurgeryStainingProsthesis FailureMicroscopy Electron030220 oncology & carcinogenesisImmunohistochemistryFemaleJointsAseptic processingPolyethylenesAzo CompoundsActa histochemica
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Kinetics of the lipoperoxyl radical-scavenging activity of indicaxanthin in solution and unilamellar liposomes

2007

Abstract The reaction of the phytochemical indicaxanthin with lipoperoxyl radicals generated in methyl linoleate methanol solution by 2,20-azobis(2,4-dimethylvaleronitrile), and in aqueous soybean phosphatidylcholine unilamellar liposomes by 2,20-azobis(2- amidinopropane)hydrochloride, was studied. The molecule acts as a chain-terminating lipoperoxyl radical scavenger in solution, with a calculated inhibition constant of 3.63 £ 105M21 s21, and a stoichiometric factor approaching 2. Indicaxanthin incorporated in liposomes prevented lipid oxidation, inducing clear-cut lag periods and decrease of the propagation rate. Both effects were concentration-dependent, but not linearly related to the p…

Indicaxanthin membranes radical scavenger liposomesLipid PeroxidesAntioxidant12-DipalmitoylphosphatidylcholinePyridinesmedicine.medical_treatmentRadicalLipid Bilayersalpha-TocopherolAmidinesContext (language use)In Vitro TechniquesBiochemistryAntioxidantsLipid peroxidationchemistry.chemical_compoundLipid oxidationSuspensionsPhosphatidylcholineNitrilesmedicineOrganic chemistryLiposomeDose-Response Relationship DrugMolecular StructureMethanolDrug SynergismGeneral MedicineFree Radical ScavengersBetaxanthinsSolutionsKineticschemistryLinoleic AcidsLiposomesPhosphatidylcholinesSolventsLipid PeroxidationIndicaxanthinAzo CompoundsOxidation-ReductionNuclear chemistry
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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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A study on the adsorption voltammetry of titanium with various heterocyclic azo-compounds

1994

The voltammetric behaviour of various heterocyclic azo-compounds and their Ti-complexes was investigated at a stationary Hg electrode. In moderately acidic solutions Ti(IV) reacts with pyridylazo-compounds (PAR, 5-Br-PADAP, PAN), thiazolylazo-compounds (TAR, 5-Me-TAR, TAN, 4-Me-TAP) and pyrazolylazo-compounds (MDR, ERB) to form Ti-complexes, which are strongly adsorbed onto the Hg-electrode. These complexes are reduced at potentials more negative than those corresponding to the reduction of their respective ligands. The conditions for determining titanium by adsorption voltammetry using TAR and MDR as complexing agents were investigated in detail, as was the influence of foreign ions on the…

Detection limitMERCUREAzo compoundTrace AmountsChemistryInorganic chemistrychemistry.chemical_elementBiochemistryAnalytical Chemistrychemistry.chemical_compoundAdsorptionElectrodeVoltammetryTitaniumFresenius' Journal of Analytical Chemistry
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Azo-Dyes Photocatalytic Degradation in Aqueous Suspension of TiO2 Under Solar Irradiation

2002

Abstract The photodegradation of two common and very stable azo-dyes, i.e. methyl-orange (C14H14N3SO3Na) and orange II (C16H11N2SO4Na), is reported. The photocatalytic oxidation was carried out in aqueous suspensions of polycrystalline TiO2 irradiated by sunlight. Compound parabolic collectors, installed at the “Plataforma Solar de Almeria” (PSA, Spain) were used as the photoreactors and two identical reacting systems allowed to perform photoreactivity runs for the two dyes at the same time and under the same irradiation conditions. The disappearance of colour and substrates together with the abatement of total organic carbon content was monitored. The main sulfonate-containing intermediate…

Environmental EngineeringPhotochemistryHealth Toxicology and MutagenesisPhotochemistryHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundMethyl orangeEnvironmental ChemistryIrradiationColoring AgentsPhotodegradationTitaniumAqueous solutionBenzenesulfonatesPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryPollutionchemistryTitanium dioxideSunlightPhotocatalysisIndicators and ReagentsAzo CompoundsOxidation-ReductionWater Pollutants Chemical
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Demonstration of dihydro-orotate dehydrogenase inNeurospora crassa hyphae with a cytochemical procedure

1971

Dihydro-orotate dehydrogenase activity was demonstrated in the hyphae of the fungusNeurospora crassa by a cytochemical technique. The activity was slightly stronger in the hyphal tips thus demonstrating the more intense metabolic activity in these parts of the mycelium. Several control reactions showed that the staining reaction was specific.

Orotic AcidMicroscopyFormatesStaining and LabelingbiologyHyphaHistocytochemistryChemistryfungiCrassaDehydrogenaseCell BiologyDihydro-orotate dehydrogenasebiology.organism_classificationStainingNeurosporaBiochemistryAnatomyOxidoreductasesMetabolic activityAzo CompoundsDevelopmental biologyMyceliumThe Histochemical Journal
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Surface-relief gratings in halogen-bonded polymer-azobenzene complexes A concentration-dependence study

2017

In recent years, supramolecular complexes comprising a poly(4-vinylpyridine) backbone and azobenzene-based halogen bond donors have emerged as a promising class of materials for the inscription of light-induced surface-relief gratings (SRGs). The studies up to date have focused on building supramolecular hierarchies, i.e., optimizing the polymer–azobenzene noncovalent interaction for efficient surface patterning. They have been conducted using systems with relatively low azobenzene content, and little is known about the concentration dependence of SRG formation in halogen-bonded polymer–azobenzene complexes. Herein, we bridge this gap, and study the concentration dependence of SRG formation…

Polymers116 Chemical sciencesPharmaceutical Science02 engineering and technologyPhotoresponsiveMicroscopy Atomic Force01 natural sciencesAnalytical Chemistrylaw.inventionchemistry.chemical_compoundHalogenslawDrug DiscoverySupramolecularPolymerchemistry.chemical_classificationHalogen bondMolecular StructureAzobenzenePolymer021001 nanoscience & nanotechnologyAzobenzeneChemistry (miscellaneous)HalogenHalogenMolecular MedicineHalogen bonding0210 nano-technologyMaterials scienceSurface PropertiesChemieSupramolecular chemistry010402 general chemistrySurface-relief gratingArticleAzo Compoundlcsh:QD241-441lcsh:Organic chemistryOptical microscopeMoleculePhysical and Theoretical ChemistryThin filmta114Organic Chemistry0104 chemical sciencesCrystallographychemistrysurface-relief grating; azobenzene; halogen bonding; supramolecular; photoresponsiveSettore CHIM/07 - Fondamenti Chimici Delle TecnologieAzo CompoundsMOLECULES
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Azobenzene Polyesters Used as Gate-Like Scaffolds in Nanoscopic Hybrid Systems

2012

The synthesis and characterisation of new capped silica mesoporous nanoparticles for on-command delivery applications is reported. Functional capped hybrid systems consist of MCM-41 nanoparticles functionalised on the external surface with polyesters bearing azobenzene derivatives and rhodamine¿B inside the mesopores. Two solid materials, Rh-PAzo8-S and Rh-PAzo6-S, containing two closely related polymers, PAzo8 and PAzo6, in the pore outlets have been prepared. Materials Rh-PAzo8-S and Rh-PAzo6-S showed an almost zero release in water due to steric hindrance imposed by the presence of anchored bulky polyesters, whereas a large delivery of the cargo was observed in the presence of an esteras…

TECNOLOGIA DE ALIMENTOSazo compoundsPolyestersenzymesNanoparticlemesoporous materialspolyestersCatalysischemistry.chemical_compoundDrug Delivery SystemsQUIMICA ORGANICAPolymer chemistryHumanschemistry.chemical_classificationOrganic ChemistryQUIMICA INORGANICAGeneral ChemistryPolymerMesoporous silicaHydrogen-Ion ConcentrationSilicon DioxideControlled releaseMesoporous materialsEnzymesPolyesterAzobenzenechemistryChemical engineeringDrug deliveryDrug deliverydrug deliveryNanoparticlesCamptothecinMesoporous materialAzo CompoundsPorosityHeLa Cells
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