Search results for "Redox"

showing 10 items of 619 documents

Topological effects of a rigid chiral spacer on the electronic interactions in donor-acceptor ensembles

2005

Two triads (donor-spacer-acceptor), etTTF-BN-C 6 0 (6) and ZnP-BN-C 6 0 (7), in which electron donors (i.e., exTTF or ZnP) are covalently linked to C 6 0 through a chiral binaphthyl bridge (BN), have been prepared in a multistep synthetic procedure starting from a highly soluble enantiomerically pure binaphthyl building block (1). Unlike other oligomeric bridges, with hinaphthyl bridges, the conjugation between the donor and the acceptor units is broken and geometric conformational changes are facilitated. Consequently, distances and electronic interactions between the donor and C 6 0 are drastically changed. Both donor-spacer-acceptor (D-s-A) systems (i.e., 6 and 7) exhibit redox processes…

FullereneStereochemistryOrganic ChemistryTriad (anatomy)Donor-Acceptor EnsemblesGeneral ChemistrySettore CHIM/06 - Chimica OrganicaFluorescenceAcceptorRedoxCatalysischemistry.chemical_compoundmedicine.anatomical_structurePhotophysicschemistryFullereneCovalent bondUltrafast laser spectroscopymedicineTetrathiafulvalene
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Synthesis of Silver Gallium Selenide (AgGaSe2) Nanotubes and Nanowires by Template-Based Electrodeposition

2020

In this work, a systematic investigation of the different parameters that control the electrodeposition processes was carried out at the aim to synthetizing AgGaSe₂ nanostructures. We found that pH is a key parameter to control both the morphology and composition of the nanostructures. Low pH favours mainly the formation of Ag2Se nanotubes with a scarce mechanical stability, while multi-phase nanowires well anchored to the substrate were obtained at higher pH. We also found that it was necessary to increase dramatically the concentration of the gallium precursor into the deposition bath in order to obtain AgGaSe₂ owing to lower redox potential of the Ga3+/Ga couple than Ag2+/Ag and Se4+/Se.…

Ga ElectrodepositionMorphology (linguistics)NanostructureMaterials scienceBiomedical EngineeringNanowirechemistry.chemical_elementBioengineeringGeneral ChemistrySubstrate (electronics)Condensed Matter PhysicsRedoxTemplate ElectrosynthesiAmorphous solidNanowireNanotubeSettore ING-IND/23 - Chimica Fisica ApplicataChemical engineeringchemistryAgGaSe2General Materials ScienceGalliumDeposition (law)Journal of Nanoscience and Nanotechnology
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Insights into the anion effect on the self assembly of perylene bisimide diimidazolium salts

2017

Abstract We studied how changing the anion affects the self-assembly of three diimidazolium salts bearing a perylene bisimide spacer. In particular we used [BF 4 − ] and [NTf 2 − ] based salts together with a mixed salt bearing both [I − ] and [BF 4 − ] anions. Thermal as well as concentration and temperature dependent spectroscopic investigations revealed that changing the anion impacts on solid state and solution aggregation, leading to articulate thermotropic behaviors and contrasting solvent effects, respectively. We also studied the electrochemical behavior of the salts to verify if changing the anion alters the redox properties of the salts. Finally, different anions also lead to very…

General Chemical EngineeringDiimidazolium saltSalt (chemistry)010402 general chemistryPhotochemistryElectrochemistry01 natural sciencesThermotropic crystalRedoxIonchemistry.chemical_compoundAnion effectPolymer chemistryChemical Engineering (all)chemistry.chemical_classification010405 organic chemistryProcess Chemistry and TechnologyDiimidazolium saltsAnion effect; Diimidazolium salts; Perylene bisimide; Self assembly; Chemical Engineering (all); Process Chemistry and TechnologySettore CHIM/06 - Chimica OrganicaSelf assembly0104 chemical scienceschemistryPerylene bisimideSelf-assemblySolvent effectsPeryleneDyes and Pigments
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Electro- and magneto-electrochemistry of zeolite Y- and MCM-41-associated bipyrylium ion

2005

Abstract The electrochemical response of bipyrylium bication [1,4-bis(3,5-diphenyl-4-pyrylium)phenylene] associated with Y and MCM-41 aluminosilicates (BTP@Y and BTP@MCM, respectively) is described using polymer-film electrodes immersed into Et 4 N +  + MeCN and Bu 4 N +  + MeCN electrolytes. BTP@MCM provides a solution-like response in all electrolytes consisting in two successive strongly comproportionation mediated one-electron reduction processes near to +0.05 and −0.12 V vs. Ag|AgCl. The response of BTP@Y in Bu 4 N +  + MeCN is restricted to a unique reduction process near to −0.40 V, while in Et 4 N +  + MeCN, it differs significantly: here, two reduction processes at −0.22 and −0.36 …

General Chemical EngineeringInorganic chemistryComproportionationElectrolyteElectrochemistryRedoxAnalytical Chemistrychemistry.chemical_compoundCrystallographyElectron transferchemistryPhenyleneElectrochemistryMagnetoelectrochemistryAcetonitrileJournal of Electroanalytical Chemistry
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Electrochemical treatment of aqueous solutions containing one or many organic pollutants at boron doped diamond anodes. Theoretical modeling and expe…

2012

The electrochemical oxidation of organics in water at boron doped diamonds (BDD) was experimentally investigated with the aim to discuss the correlations among the conversion of the pollutants and the instantaneous current efficiency ICE with the operative conditions. A simple theoretical model previously developed for the oxidation of oxalic acid accounting for the cases of mass transfer control, oxidation reaction control and mixed kinetic regimes was adopted and extended to challenge its predictive capability in the case of organics of different nature and in systems with more pollutants. A quite good agreement, between theoretical predictions and experimental data pertaining to the elec…

General Chemical EngineeringRadicalChlorine compoundOxalic acidInorganic chemistryPollution Anodic oxidationElectrochemistryCarboxylic acidRedoxIndustrial and Manufacturing Engineeringchemistry.chemical_compoundElectron transferAOPs; BDD; Diamond anode; Oxygen evolution; Theoretical models Boron; Carboxylic acids; Chlorine compounds; Diamonds; Electrochemical oxidation; Electron transitions; Free radical reactions; Pollution Anodic oxidationMass transferDiamond anodeEnvironmental ChemistryAOPElectron transitionAqueous solutionOxygen evolutionGeneral ChemistrySettore ING-IND/27 - Chimica Industriale E TecnologicaFree radical reactionTheoretical models BoronElectrochemical oxidationchemistryDiamondBDDOxygen evolutionChemical Engineering Journal
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Size-activity relationship of iridium particles supported on silica for the total oxidation of volatile organic compounds (VOCs)

2019

12 Figures, 2 Tables.-- Datos suplementarios disponibles en línea en la página web del editor.-- © 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/

General Chemical EngineeringTotal oxidationInorganic chemistryShort chain alkaneschemistry.chemical_element02 engineering and technologyIridium010402 general chemistry01 natural sciencesRedoxIndustrial and Manufacturing Engineeringlaw.inventionCatalysisMetalSize-activity relationshiplawEnvironmental ChemistryCalcinationIridiumVOCSilicaGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryvisual_artvisual_art.visual_art_mediumParticle size0210 nano-technologyPlatinumPalladiumChemical Engineering Journal
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Determination of the depth profile distribution of guest species in microporous materials using the voltammetry of immobilized particles methodology:…

2014

A model for determining the in-depth profile distribution of electroactive species hosted in inorganic microporous matrixes using the voltammetry of immobilized particles methodology is described. The method, based on the analysis of cyclic voltammetric data at different potential scan rates, allows us to determine the in-depth profile variation of the concentration of electroactive guest species as well as the evaluation of the (oxidized form)/(reduced form) concentration ratio in cases where two oxidation states of the electroactive species coexist. The application to Maya blue-type materials prepared from lapachol, a naphtoquinonic dye, and palygorskite and kaolinite clays is reported. T…

General Physics and AstronomyPalygorskiteMicroporous materialElectrochemistryRedoxchemistry.chemical_compoundAdsorptionchemistryChemical engineeringmedicineOrganic chemistryKaolinitePhysical and Theoretical ChemistryVoltammetrymedicine.drugLapacholPhysical chemistry chemical physics : PCCP
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Redox regulation of genome stability by effects on gene expression, epigenetic pathways and DNA damage/repair

2015

Reactive oxygen and nitrogen species (e.g. H2O2, nitric oxide) confer redox regulation of essential cellular signaling pathways such as cell differentiation, proliferation, migration and apoptosis. In addition, classical regulation of gene expression or activity, including gene transcription to RNA followed by translation to the protein level, by transcription factors (e.g. NF-κB, HIF-1α) and mRNA binding proteins (e.g. GAPDH, HuR) is subject to redox regulation. This review will give an update of recent discoveries in this field, and specifically highlight the impact of reactive oxygen and nitrogen species on DNA repair systems that contribute to genomic stability. Emphasis will be placed …

Genome instabilityRedox signalingRNA UntranslatedEpigenetic regulation of neurogenesisDNA RepairHuR mRNA-binding protein in the 3′-untranslated regionClinical BiochemistryHDAC histone deacetylaseReview ArticleAP-1 activator protein 1BiochemistryApe-1 apurinic/apyrimidinic endonuclease 1GPx-1 glutathione peroxidase-1Epigenesis GeneticHistonesTrx thioredoxinPHD prolylhydroxylaseBER base excision repairlcsh:QH301-705.5HO-1 heme oxygenase-1EpigenomicsGeneticsRegulation of gene expressionNox member of the NADPH oxidase familylcsh:R5-920JmjC Jumonji C domain-containing histone demethylasesHIF-1α hypoxia inducible factor-1α5-hmC 5-hydroxymethylcytosineddc:Cell biologyMMP matrix metalloproteinaseGrx glutaredoxinGAPDH glyceraldehyde-3-phosphate dehydrogenaseNrf2 nuclear factor erythroid related factor 2DNA methylationEpigeneticslcsh:Medicine (General)Oxidation-ReductionSignal Transduction5-mC 5-methylcytosineDNA repairDNA damageNF-κB nuclear factor-κBBiologyGenomic InstabilityRNS reactive nitrogen speciesROS reactive oxygen speciesNER nucleotide excision repairSOD superoxide dismutaseOxyR transcription factor (hydrogen peroxide-inducible genes activator)HumansEpigeneticsOrganic ChemistryPETN pentaerithrityl tetranitrateGene regulationOxidative StressDNMT DNA methyltransferaseGene Expression Regulationlcsh:Biology (General)AREs AU-rich elementsHAT histone acetyltransferaseKeap1 kelch-like ECH-associated protein 1BiomarkersCOPD chronic obstructive pulmonary disorderDNA DamageRedox Biology
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IMPROVEMENT IN REDOX HOMEOSTASIS AFTER CYTOREDUCTIVE SURGERY IN COLORECTAL ADENOCARCINOMA

2021

Colorectal cancer (CRC) as one the most common cancer type is associated with oxidative stress. Surgery is the only curative modality for early-stage CRC. The aim of this study was to evaluate the oxidative damage biomarkers as well as enzymatic and nonenzymatic antioxidants in patients with CRC before and after tumor resection and in healthy controls. 60 patients with stage I/II colorectal adenocarcinoma and 43 healthy controls were recruited in this study. We measured plasma levels of oxidative damage biomarkers, including advanced oxidation protein products (AOPP), advanced glycation end products (AGEs), malondialdehyde (MDA), and oxidized low-density lipoprotein (ox-LDL) at baseline and…

Glycation End Products AdvancedMale0301 basic medicineAgingAntioxidantColorectal cancermedicine.medical_treatmentmedicine.disease_causeBiochemistryGastroenterologychemistry.chemical_compoundPostoperative Complications0302 clinical medicineMalondialdehydeHomeostasischemistry.chemical_classificationbiologyGlutathione peroxidaseCytoreduction Surgical ProceduresGeneral MedicineMiddle AgedCatalaseMalondialdehydecolorectal cancer colorectal surgery cytoreductive surgery redox homeostasisLipoproteins LDLCatalase030220 oncology & carcinogenesisFemaleColorectal NeoplasmsResearch ArticleAdultmedicine.medical_specialtyArticle SubjectAdenocarcinomaSuperoxide dismutase03 medical and health sciencesInternal medicinemedicineHumansAgedGlutathione PeroxidaseQH573-671business.industryCell Biologymedicine.diseaseOxidative Stress030104 developmental biologychemistrybiology.proteinCytologybusinessOxidative stressLipoprotein
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On the Mechanistic Origins of the pH-Dependency in Au-Catalyzed Glycerol Electro-Oxidation: Insight from First Principles Calculations

2021

Electrocatalytic oxidation of glycerol (EOG) is an attractive approach to convert surplus glycerol to value-added products. Experiments have shown that EOG activity and selectivity depend on the electrocatalyst, but also on the electrode potential, the pH, and the electrolyte. For broadly employed gold (Au) electrocatalysts, experiments have demonstrated high EOG activity under alkaline conditions with glyceric acid as a primary product, whereas under acidic and neutral conditions Au is rather inactive producing only small amounts of dihydroxyacetone. In the present computational work, we have performed an extensive mechanistic study to understand the pH- and potential-dependency of Au-cata…

Glyceric acidchemistry.chemical_compoundReaction mechanismchemistryInorganic chemistryHydroxideDihydroxyacetoneSelectivityElectrocatalystRedoxElectrode potential
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