Search results for "Redox"

showing 10 items of 619 documents

Effects of anions size on the redox behavior of poly(o-toluidine) in acid solutions. An in situ vis-NIR cyclic spectroelectrogravimetry study

2014

International audience; The combination of different in situ techniques allows a more complete analysis combining several physical and chemical processes of polymer-modified electrodes to be obtained. The hybrid technique -cyclic electrogravimetry coupled with visible-near infrared spectroscopy- was used to study in depth the electrochemistry of poly(o-toluidine) (POT) thin films. In this work, a POT modified electrode was polarized between the pernigraniline and leucoemeraldine forms in 0.5 M HNO3 and 0.5 M HClO4 solutions. The electrochromic properties of View the MathML sourcePOT-CIO4− and View the MathML sourcePOT-NO3− were localized in the experimental potential range associated to the…

chemistry.chemical_classificationMaterials scienceGeneral Chemical EngineeringInorganic chemistryInfrared spectroscopy02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesRedox6. Clean water0104 chemical scienceschemistryElectrochromismElectrogravimetryElectrodeElectrochemistry[CHIM]Chemical SciencesThin film0210 nano-technology[CHIM.OTHE]Chemical Sciences/Other
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Redox active polymers with phenothiazine moieties for nanoscale patterning via conductive scanning force microscopy

2011

Redox active polymers with phenothiazine moieties have been synthesized by Atomic Transfer Radical Polymerization (ATRP). These novel polymers reveal bistable behaviour upon application of a bias potential above the oxidation threshold value. Using conductive Scanning Force Microscopy, two distinguishable conductivity levels were induced on a nanoscale level. These levels were related to a high conducting “On” and a low conducting “Off” state. The “On” state is generated by the oxidation of the phenothiazine side chains to form stable phenothiazine radical cations. The formation and stability of the radical sites was examined by cyclic voltammetry, electron spin resonance and optical spectr…

chemistry.chemical_classificationMaterials scienceRadical polymerizationAnalytical chemistryChemiePolymerPhotochemistryRedoxlaw.inventionchemistry.chemical_compoundchemistrylawPhenothiazineSide chainGeneral Materials ScienceCyclic voltammetryThin filmElectron paramagnetic resonance
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Chiroptical inversion of a planar chiral redox-switchable rotaxane.

2019

Reversible redox-switching of a planar chiral [2]rotaxane with a tetrathiafulvalene-bearing crown ether macrocycle generates a complete sign reversal of the main band in the ECD spectrum, as shown by experiment and rationalised by DFT calculations.

chemistry.chemical_classificationMaterials scienceRotaxane010405 organic chemistryGeneral Chemistry547Planar chirality010402 general chemistryElectrochemistry01 natural sciences0104 chemical sciencesChiral column chromatographyCrystallographychemistry.chemical_compoundChemistry500 Naturwissenschaften und Mathematik::540 Chemie::547 Organische Chemieredox-switchablechemistryElectronic effectrotaxanechiroptical inversionEnantiomermakromolekyylitTetrathiafulvaleneCrown etherChemical science
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Tuneable Transient Thermogels Mediated by a pH- and Redox-Regulated Supramolecular Polymerization.

2017

A multistimuli-responsive transient supramolecular polymerization of β-sheet-encoded dendritic peptide monomers in water is presented. The amphiphiles, which contain glutamic acid and methionine, undergo a glucose oxidase catalyzed, glucose-fueled transient hydrogelation in response to an interplay of pH and oxidation stimuli, promoted by the production of reactive oxygen species (ROS). Adjusting the enzyme and glucose concentration allows tuning of the assembly and the disassembly rates of the supramolecular polymers, which dictate the stiffness and transient stability of the hydrogels. The incorporation of triethylene glycol chains introduces thermoresponsive properties to the materials. …

chemistry.chemical_classificationMethioninebiologyStereochemistrytechnology industry and agricultureSupramolecular chemistrymacromolecular substances02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesRedoxCatalysis0104 chemical sciencesSupramolecular polymerschemistry.chemical_compoundMonomerPolymerizationchemistrySelf-healing hydrogelsbiology.proteinBiophysicsGlucose oxidase0210 nano-technologyAngewandte Chemie (International ed. in English)
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The Quest for Mononuclear Gold(II) and Its Potential Role in Photocatalysis and Drug Action.

2017

The chemistry of gold strongly focuses on the ubiquitous oxidation states +I and +III. The intermediate oxidation state +II is generally avoided in mononuclear gold species. In recent years, gold(II) has been increasingly suggested as a key intermediate in artificial photosynthesis systems, with gold(III) moieties acting as electron acceptors, as well as in gold-catalyzed photoredox catalysis and radical chemistry. This Minireview provides a concise summary of confirmed and characterized mononuclear open-shell gold(II) complexes. Recent findings on structural motifs and reactivity patterns will be discussed. Exciting developments in the fields of photosynthesis, photocatalysis, and potentia…

chemistry.chemical_classificationMolecular Structure010405 organic chemistryChemistryRadicalChemistry PharmaceuticalPhotoredox catalysisElectronsGeneral ChemistryElectron acceptor010402 general chemistryPhotochemical Processes01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesArtificial photosynthesisElectron transferOxidation statePhotocatalysisOrganic chemistryReactivity (chemistry)Organogold CompoundsAngewandte Chemie (International ed. in English)
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Chemistry and reactivity of mononuclear manganese oxamate complexes: Oxidative carbon-carbon bond cleavage of vic-diols by dioxygen and aldehydes cat…

2006

[EN] Two new mononuclear octahedral manganese(III) complexes with the tetradentate equatorial ligand o-phenylenebis(oxamate) (opba) and two aquo (1a) or two pyridine (1b) axial ligands have been synthesized and characterized structurally, magnetically, and electrochemically. The cyclovoltammogram of 1a in acetonitrile (25 degrees C, 0.1 M Bu4NPF6) shows an irreversible one-electron oxidation peak at a high anodic potential (E-ap = 1.03 V versus SCE), while that of 1b shows two well-separated one-electron oxidation peaks at moderate to high anodic potentials (E-ap = 0.92 and 1.27 V versus SCE), the first redox-wave being quasireversible in nature. The access to formally high-valent Mn-IV and…

chemistry.chemical_classificationO-O bond activationManganesePivalic acidLigandStereochemistryProcess Chemistry and Technologychemistry.chemical_elementManganeseC-C bond activationMedicinal chemistryAldehydeRedoxCatalysischemistry.chemical_compoundchemistryCarbon–carbon bondOxidationsFISICA APLICADAPyridinePhysical and Theoretical ChemistryBond cleavageRedox properties
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Facile access to foldable redox-active flavin-peptide conjugates

2021

A convenient approach for the synthesis of foldable redox-active flavin peptide conjugates was established. A model β-hairpin oligopeptide motif was utilized to demonstrate that azidolysine side-chains are readily functionalised with an alkyne-bearing flavine derivative. The folding equilibrium of the peptide backbone as well as the redox behaviour of the flavin moieties remains intact after the conjugation.

chemistry.chemical_classificationOligopeptideChemistryOrganic ChemistryPeptideFlavin groupBiochemistryRedoxCombinatorial chemistryFolding (chemistry)chemistry.chemical_compoundRedox activeheterocyclic compoundsPhysical and Theoretical ChemistryPeptidesDerivative (chemistry)Conjugate
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Multiplicity of Reaction Pathways in the Processes of Oxygen Transfer to Secondary Amines by Mo(VI) and W(VI) Peroxo Complexes.

1996

Oxidation of N,N-benzylmethylamine, N,N-benzylisopropylamine, and N,N-benzyl-tert-butylamine by both anionic and neutral Mo(VI) and W(VI) oxodiperoxo complexes yields the corresponding nitrones quantitatively. The oxidation reactions employing anionic oxidants were performed in CHCl(3) and follow second-order kinetics, first order with respect to the amine and to the oxidant. The data were rationalized on the basis of a rate-determining nucleophilic attack of the amine onto the peroxide oxygen of the oxidant, with a transition state in which N-O bond formation and O-O bond cleavage occur in a concerted way (electrophilic oxygen transfer mechanism). This attack yields the corresponding hydro…

chemistry.chemical_classificationOrganic ChemistryPhotochemistryRedoxPeroxideNitronechemistry.chemical_compoundNucleophilechemistryIntramolecular forcePolymer chemistryElectrophileAmine gas treatingBond cleavageThe Journal of organic chemistry
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The synergy between the CsPbBr3 nanoparticle surface and the organic ligand becomes manifest in a demanding carbon–carbon coupling reaction

2020

We demonstrate here the suitability of CsPbBr3nanoparticles as photosensitizers for a demanding photoredox catalytic homo- and cross-coupling of alkyl bromides at room temperature by merely using visible light and an electron donor, thanks to the cooperative action between the nanoparticle surface and organic capping. Fil: Rosa-Pardo, Ignacio. Instituto de Ciencia Molecular; España. Universidad de Valencia; España Fil: Casadevall, Carla. Barcelona Institute Of Science And Technology. Institut Català D'investigació Química.; España Fil: Schmidt, Luciana Carina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigac…

chemistry.chemical_classificationPEROVSKITE CsPbBr3LigandChemistryMetals and AlloysReinforced carbon–carbonNanoparticleElectron donorGeneral ChemistryPhotochemistryCatalysisCoupling reactionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysis//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundCARBON-CARBON COUPLING//purl.org/becyt/ford/1.4 [https]Materials ChemistryCeramics and CompositesPHOTOREDOXAlkylVisible spectrumChemical Communications
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2021

Ruthenium(II) polypyridine complexes are among the most popular sensitizers in photocatalysis, but they face some severe limitations concerning accessible excited-state energies and photostability that could hamper future applications. In this study, the borylation of heteroleptic ruthenium(II) cyanide complexes with alpha-diimine ancillary ligands is identified as a useful concept to elevate the energies of photoactive metal-to-ligand charge-transfer (MLCT) states and to obtain unusually photorobust compounds suitable for thermodynamically challenging energy transfer catalysis as well as oxidative and reductive photoredox catalysis. B(C6F5)(3) groups attached to the CN- ligands stabilize t…

chemistry.chemical_classificationPhotoisomerization010405 organic chemistryChemistryPinacolPhotoredox catalysischemistry.chemical_elementContext (language use)010402 general chemistryPhotochemistry01 natural sciencesBorylation0104 chemical sciencesCoordination complexRutheniumCatalysischemistry.chemical_compoundJACS Au
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