Search results for "Redox"

showing 10 items of 619 documents

Relationship between Electron Affinity and Half-Wave Reduction Potential: A Theoretical Study on Cyclic Electron-Acceptor Compounds.

2016

A high-level ab initio protocol to compute accurate electron affinities and half-wave reduction potentials is presented and applied for a series of electron-acceptor compounds with potential interest in organic electronics and redox flow batteries. The comprehensive comparison between the theoretical and experimental electron affinities not only proves the reliability of the theoretical G3(MP2) approach employed but also calls into question certain experimental measurements, which need to be revised. By using the thermodynamic cycle for the one-electron attachment reaction A+e- →A- , theoretical estimates for the first half-wave reduction potential have been computed along the series of ele…

chemistry.chemical_classification010304 chemical physicsChemistryAb initioSolvationElectronElectron acceptor010402 general chemistry01 natural sciencesRedoxAtomic and Molecular Physics and Optics0104 chemical sciencesReduction (complexity)Ab initio quantum chemistry methodsComputational chemistryChemical physicsElectron affinity0103 physical sciencesPhysical and Theoretical ChemistryChemphyschem : a European journal of chemical physics and physical chemistry
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Visible Light-Induced Sulfonylation/Arylation of Styrenes in a Double Radical Three-Component Photoredox Reaction

2019

Simultaneous sulfonylation/arylation of styrene derivatives is achieved in a photoredox-catalyzed three-component reaction using visible light. A broad variety of difunctionalized products is accessible in mostly excellent yields and high diastereoselectivity. The developed reaction is scalable and suitable for the modification of styrene-functionalized biomolecules. Mechanistic investigations suggest the transformation to be operating through a designed sequence of radical formation and radical combination.

chemistry.chemical_classification010405 organic chemistryChemistryBiomoleculeOrganic ChemistryPhotoredox catalysisGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical sciencesStyrenechemistry.chemical_compoundRadical formationVisible spectrum
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Electrocarboxylation of Benzyl Halides through Redox Catalysis on the Preparative Scale

2006

The electrocarboxylation of benzyl halides to the corresponding carboxylic acids through homogeneous charge-transfer catalysis was investigated both theoretically and experimentally to determine the influence of the operative parameters on the yield of the process and on the catalyst consumption. Theoretical considerations, based on fast kinetics of redox catalysis, were confirmed by the electrocarboxylation of 1-phenyl-1-chloroethane catalyzed by 1,3-benzenedicarboxylic acid di methyl ester performed at a carbon cathode under different operative conditions. We obtained high yields of the target carboxylic acid and experienced a low catalyst consumption by operating with optimized [RX]bulk/…

chemistry.chemical_classification010405 organic chemistryChemistryCarboxylic acidOrganic ChemistryInorganic chemistryHalideHomogeneous catalysisGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryElectrochemistry01 natural sciencesRedoxCatalysis0104 chemical sciencesCatalysisCarboxylationYield (chemistry)benzyl halides • carbon dioxide • carboxylation • electrochemistry • homogeneous catalysisComputingMilieux_MISCELLANEOUS
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Comparative studies of oxidation processes on Group 10 Metals Dithiolene Derivatives in the formation of coordination polymers

2018

This document is the Accepted Manuscript Version of a Published Work that appeared in final form in "Crystal Growth and Design", copyright © 2018 American Chemical Society after peer review and techical editing by publisher. To access the final and published work see "Comparative Studies of Oxidation Processes on Group 10 Metals Dithiolene Derivatives in the Formation of Coordination Polymers Oscar Castillo, Esther Delgado, Carlos J. Gómez-García, Diego Hernández, Elisa Hernández, Pilar Herrasti, Avelino Martín, and Félix Zamora Crystal Growth & Design 2018 18 (4), 2486-2494

chemistry.chemical_classification010405 organic chemistryDianionic tetranickel dithiolene clusterFísicaGeneral ChemistryPolymerQuímica010402 general chemistryCondensed Matter Physics01 natural sciencesMedicinal chemistryRedoxGroup 10 metal dithiolene Ion-Pairs0104 chemical sciencesCoordination polymerschemistryGroup (periodic table)General Materials ScienceGroup 10 metal dithiolene compounds
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Introduction: Protein Oligomerization and the Formation of Macromolecular Assemblies

2019

The ability of biomolecules to link together to form higher order assemblies underlies much of cellular structure and function. Here we emphasise protein oligomerisation and discuss some of the principles of molecular interaction, from early considerations through to the present day. A few protein examples are presented, selected from our research interests, to highlight assembly features, ranging from the hemoglobins, the hemocyanins to the peroxiredoxins, collagen, the encapsulins and ferritins.

chemistry.chemical_classification0303 health sciencesBiomoleculemedicine.medical_treatmentHemocyanin02 engineering and technology021001 nanoscience & nanotechnologyStructure and function03 medical and health scienceschemistrymedicineBiophysicsProtein oligomerization0210 nano-technologyPeroxiredoxin030304 developmental biologyMacromolecule
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Redox Biochemistry of the Genetic Code.

2021

New findings on the chemistry of the amino acids, their role in protein folding, and their sequential primordial introduction have uncovered concealed causalities in genetic code evolution. The genetically encoded amino acids successively provided (i) membrane anchors, (ii) halophilic protein folds, (iii) mesophilic protein folds, (iv) metal ligation, and (v) antioxidation.

chemistry.chemical_classification0303 health sciencesModels GeneticChemistryProteinsGenetic codeBiochemistryRedoxHalophileEnzyme catalysisAmino acidEvolution Molecular03 medical and health sciences0302 clinical medicineBiochemistryAbiogenesisGenetic CodeProtein foldingAmino AcidsMolecular BiologyOxidation-Reduction030217 neurology & neurosurgery030304 developmental biologyTrends in biochemical sciences
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Contribution of exofacial thiol groups in the reducing activity of Lactococcus lactis

2010

Lactococcus lactis can decrease the redox potential at pH 7 (E(h7)) from 200 to -200 mV in oxygen free Man-Rogosa-Sharpe media. Neither the consumption of oxidizing compounds or the release of reducing compounds during lactic acid fermentation were involved in the decrease in E(h7) by the bacteria. Thiol groups located on the bacterial cell surface appear to be the main components that are able to establish a greater exchange current between the Pt electrode and the bacteria. After the final E(h7) (-200 mV) was reached, only thiol-reactive reagents could restore the initial E(h7) value. Inhibition of the proton motive force showed no effect on maintaining the final E(h7) value. These result…

chemistry.chemical_classification0303 health sciencesbiology030306 microbiologyChemistryChemiosmosisLactococcus lactisCell Biologybiology.organism_classificationBiochemistryRedoxBacterial cell structureLactic acid03 medical and health scienceschemistry.chemical_compoundBiochemistryThiolFermentationMolecular BiologyBacteria030304 developmental biologyFEBS Journal
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Nickel‐Mediated Photoreductive Cross Coupling of Carboxylic Acid Derivatives for Ketone Synthesis**

2021

A simple photochemical, nickel-catalyzed synthesis of ketones starting from carboxylic acids is presented. Hantzsch-ester (HE) functions as a cheap, green and strong photoreductant upon visible-light excitation to facilitate radical generation and also engages in the Ni-catalytic cycle to restore the reactive species. With this dual role, HE allows for the coupling of a large variety of radicals (1°,2°, benzylic, α-oxy & α-amino) with aroyl and alkanoyl moieties, a new feature in the synthesis of ketones through dual nickel photoredox catalysis. With both precursors deriving from abundant carboxylic acids, this protocol is a welcome addition to the organic chemistry toolbox. The reactio…

chemistry.chemical_classification540 Chemistry and allied sciencesRadicalCarboxylic acidOrganic ChemistryKetone synthesisCarboxylic AcidsPhotoredox catalysischemistry.chemical_elementGeneral ChemistryKetonesCombinatorial chemistryCatalysisMetalCoupling (electronics)NickelchemistryNickel540 ChemieReagentvisual_artvisual_art.visual_art_mediumPhotocatalysisOxidation-ReductionChemistry – A European Journal
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Kinetic and Mechanistic Aspects of a Poly(o-toluidine)-Modified Gold Electrode. 1. Simultaneous Cyclic Spectroelectrochemistry and Electrogravimetry …

2012

International audience; Electrodeposited poly(o-toluidine) (POT) on gold electrodes was investigated in a 0.5 M H2SO4 aqueous solution using cyclic electrogravimetry with in situ vis-NIR spectroscopy. This coupling of different techniques allows the electrical, color, and mass changes during the electrochemical reactions of these polymers to be correlated. Therefore, this is a powerful tool to obtain valuable information on the physical models of polymer films and their electrochemical properties. The accurate analysis of the results from these techniques showed the contribution of three different redox transitions (leucoemeraldine-polaron transition, polaron-bipolaron transition, and bipol…

chemistry.chemical_classificationAqueous solutionInorganic chemistry02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesRedox0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAbsorbancechemistry.chemical_compoundGeneral EnergychemistryElectrogravimetryElectrode[CHIM]Chemical SciencesPhysical and Theoretical Chemistry0210 nano-technology[CHIM.OTHE]Chemical Sciences/OtherDerivative (chemistry)
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Speciation of the oxidation states of plutonium in aqueous solutions by UV/Vis spectroscopy, CE-ICP-MS and CE-RIMS

2007

For the speciation of the plutonium oxidation states in aqueous solutions, the online coupling of capillary electrophoresis (CE) with inductively coupled plasma mass spectrometry (ICP-MS) has been developed. Depending on the radius/electrical charge ratio, the oxidation states III, IV, V, and VI of plutonium are separated by CE, based on the different migration times through the capillary and are detected by ICP-MS. The detection limit is 20 ppb,i.e.109–1010atoms (10-12–10-13g) for one oxidation state with an uncertainty of the reproducibility of the migration times of ≤1% and ≤5% for the peak area. The redox kinetics of the different plutonium oxidation states in the presence of humic subs…

chemistry.chemical_classificationAqueous solutionInorganic chemistryAnalytical chemistrychemistry.chemical_elementMass spectrometryRedoxPlutoniumCapillary electrophoresischemistryOxidation stateHumic acidPhysical and Theoretical ChemistryInductively coupled plasma mass spectrometryRadiochimica Acta
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