Search results for " organic"

showing 10 items of 5145 documents

DFT insights into the oxygen-assisted selective oxidation of benzyl alcohol on manganese dioxide catalysts

2020

Abstract The reactivity pattern of the MnO2 catalyst in the selective aerobic oxidation of benzyl alcohol is assessed by density functional theory (DFT) analysis of adsorption energies and activation barriers on a model Mn4O8 cluster. DFT calculations predict high reactivity of defective Mn(IV) sites ruling a surface redox mechanism, L-H type, involving gas-phase oxygen. Bare and promoted (i.e., CeOx and FeOx) MnOx materials with high surface exposure of Mn(IV) sites were synthesized to assess kinetic and mechanistic issues of the selective aerobic oxidation of benzyl alcohol on real catalysts (T, 333–363 K). According to DFT predictions, the experimental study shows: i) comparable activity…

inorganic chemicalsInorganic chemistrychemistry.chemical_elementAlcoholManganese010402 general chemistry01 natural sciencesRedoxCatalysisInorganic Chemistrychemistry.chemical_compoundAdsorptionBenzyl alcoholMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryReaction mechanismBenzoic acidDFT analysi010405 organic chemistryActive siteorganic chemicalsMnO2 catalyst0104 chemical scienceschemistrySettore CHIM/03 - Chimica Generale E InorganicaBenzyl alcoholActive sites; Benzyl alcohol; DFT analysis; MnO; 2; catalyst; Reaction mechanism; Selective oxidationSelective oxidation
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Design of PNIPAAM covalently grafted on halloysite nanotubes as a support for metal-based catalysts

2016

A thermo-responsive polymer such as poly(N-isopropylacrylamide) (PNIPAAM) was covalently grafted on the external surface of halloysite nanotubes (HNTs) by means of microwave irradiation. This nanomaterial was used as a support and stabilizer for palladium nanoparticles. The obtained HNT–PNIPAAM/PdNPs was characterized by means of TGA, SEM, EDS and TEM analyses. The palladium content of the catalyst was estimated to be 0.4 wt%. The stability of the catalytic material at different temperatures (below and above the PNIPAAM lower critical solution temperature) was tested in the Suzuki reaction under microwave irradiation. In addition, TEM analysis after five consecutive runs was performed. The …

inorganic chemicalsMaterials scienceGeneral Chemical Engineeringchemistry.chemical_element02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesHalloysiteLower critical solution temperatureNanomaterialsCatalysischemistry.chemical_compoundSuzuki reactionhalloysite PNIPAAM; microwave Suzuki reaction waterPolymer chemistryhalloysite PNIPAAMPhenylboronic acidSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationmicrowave Suzuki reaction waterSettore CHIM/06 - Chimica OrganicaGeneral ChemistryPolymer021001 nanoscience & nanotechnology0104 chemical scienceschemistryengineering0210 nano-technologyPalladiumNuclear chemistryRSC Advances
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Covalently modified nanoclays: synthesis, properties and applications

2020

Abstract Clay minerals are phyllosilicates of nanoscale dimensions. According to their ability to entrap and release organic moieties, they have found applications in several fields, such as drug carrier and delivery, support for catalyst, environmental remediation and filler for polymeric matrices. The possibility to modify, by covalent linkage, their surfaces gives the possibility to form new nanomaterials with improved properties respect to the pristine clay minerals. In this chapter, the modifications of the siloxane surfaces of the most representative clay minerals, namely montmorillonite, sepiolites, laponite and halloysite were reviewed and discussed.

inorganic chemicalsMaterials scienceSettore CHIM/06 - Chimica Organicaengineering.materialcomplex mixturesHalloysiteNanomaterialsCatalysismontmorillonite sepiolites laponite and halloysitechemistry.chemical_compoundMontmorilloniteChemical engineeringchemistryCovalent bondSiloxaneengineeringDrug carrierClay mineralsSettore CHIM/02 - Chimica Fisica
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Synergistic Anticancer Therapy by Ovalbumin Encapsulation-Enabled Tandem Reactive Oxygen Species Generation

2020

Abstract The anticancer efficacy of photodynamic therapy (PDT) is limited due to the hypoxic features of solid tumors. We report synergistic PDT/chemotherapy with integrated tandem Fenton reactions mediated by ovalbumin encapsulation for improved in vivo anticancer therapy via an enhanced reactive oxygen species (ROS) generation mechanism. O2 .− produced by the PDT is converted to H2O2 by superoxide dismutase, followed by the transformation of H2O2 to the highly toxic .OH via Fenton reactions by Fe2+ originating from the dissolution of co‐loaded Fe3O4 nanoparticles. The PDT process further facilitates the endosomal/lysosomal escape of the active agents and enhances their intracellular deliv…

inorganic chemicalsNanomedicines | Hot PaperOvalbuminmedicine.medical_treatmentRadicalsynergisticcisplatinPhotodynamic therapyAntineoplastic Agents010402 general chemistry01 natural sciencesCatalysisSuperoxide dismutasechemistry.chemical_compoundMicemedicineAnimalsHumansResearch Articleschemistry.chemical_classificationCisplatinReactive oxygen speciesOxidase testPhotosensitizing Agentsbiology010405 organic chemistryFenton reactionsDrug SynergismGeneral MedicineGeneral ChemistryhypoxicEndocytosis0104 chemical sciencesOvalbuminchemistryphotodynamic therapybiology.proteinBiophysicsMCF-7 CellsReactive Oxygen SpeciesNicotinamide adenine dinucleotide phosphatemedicine.drugResearch Article
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Acetylcholine-responsive cargo release using acetylcholinesterase-capped nanomaterials

2019

[EN] Mesoporous silica nanoparticles capped with acetylcholinesterase, through boronic ester linkages, selectively release an entrapped cargo in the presence of acetylcholine.

inorganic chemicalsNanoparticlemacromolecular substances010402 general chemistry01 natural sciencesCatalysisNanomaterialschemistry.chemical_compoundQUIMICA ORGANICAQUIMICA ANALITICAMaterials ChemistrymedicineBIOQUIMICA Y BIOLOGIA MOLECULAR010405 organic chemistryQUIMICA INORGANICAtechnology industry and agricultureMetals and AlloysGeneral ChemistryMesoporous silicaCombinatorial chemistryAcetylcholinesterase0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsstomatognathic diseaseschemistryCeramics and CompositesAcetylcholinemedicine.drug
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From Mono- to Poly-Substituted Frameworks: A Way of Tuning the Acidic Character of C-c-H in o-Carborane Derivatives

2009

[EN] The incorporation of iodine atoms onto the boron vertices of the o-carborane framework causes, according to spectroscopic data, a uniform increase in the acidic character of the C-c-H (C-c= cluster carbon) vertices, whereas the incorporation of methyl groups onto the boron vertices of the o-carborane framework reduces their acidity. Methyl groups when attached to boron are electron-withdrawing in boron clusters, whereas iodine atoms bonded to boron act as electron donors. This has been proven on B-methyl and B-iodinated o-carboranes with NMR spectroscopy measurements and DFT calculations of natural bond orbital (NBO) charges. which show a Cumulative buildup of positive cluster only tot…

inorganic chemicalsNatural bond orbital chargesInorganic chemistrychemistry.chemical_elementElectron010402 general chemistryIodine01 natural sciencesCatalysisQUIMICA ANALITICACluster (physics)BoronCarboranesBoron010405 organic chemistryOrganic ChemistryGeneral ChemistryNuclear magnetic resonance spectroscopy3. Good health0104 chemical sciencesCrystallographyDensity functional calculationschemistryCarboraneCarbonNatural bond orbitalIodine
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Identifying Iron-Bearing Nanoparticle Precursor for Thermal Transformation into the Highly Active Hematite Photo-Fenton Catalyst

2020

Funding: This reseach was funded by the European Regional Development Fund within the Activity 1.1.1.2 “Post-doctoral Research Aid” of the Specific Aid Objective 1.1.1 “To increase the research and innovative capacity of scientific institutions of Latvia and the ability to attract external financing, investing in human resources and infrastructure” of the Operational Programme “Growth and Employment” (No. 1.1.1.2/VIAA/1/16/157).

inorganic chemicalsPhoto-FentonGoethiteMaterials scienceHematiteNanoparticlelcsh:Chemical technology010402 general chemistry01 natural sciences7. Clean energyCatalysishematiteCatalysislcsh:Chemistryphoto-Fenton:NATURAL SCIENCES:Physics [Research Subject Categories]Goethitegoethitelcsh:TP1-1185Reactivity (chemistry)Physical and Theoretical ChemistryAqueous solutionWater purification010405 organic chemistryHematite0104 chemical sciencesAmorphous solidlcsh:QD1-999Chemical engineering13. Climate actionvisual_artvisual_art.visual_art_mediumwater purificationVisible spectrumCatalysts
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Tailoring polymers through interplay of ligands within precatalysts: 8-(Nitro/benzhydryl-arylimino)-7,7-dimethyl-5,6-dihydroquinolylnickel halides in…

2017

A series of 8-(nitro/benzhydryl-substituted arylimino)-7,7-dimethyl-5,6-dihydroquinolines and the corresponding nickel halide complexes were synthesized and characterized. Molecular structures of representative nickel complexes were determined by single crystal X-ray diffraction, showing the dinuclear dimers with distorted square-pyramidal geometry around the nickel center. The binding energies determined by X-ray photoelectron spectroscopy (XPS) indicate the effective coordination between the sp2-nitrogen and nickel atoms as well as the influence of both the halogen ligands and the substituents within dihydroquinolines on the strength of the NiN bond. Ethylene polymerization with the nicke…

inorganic chemicalsPolymers and PlasticsMethylaluminoxaneSubstituentHalidechemistry.chemical_element010402 general chemistry01 natural sciencesvinylene groupnickelchemistry.chemical_compoundBromideVinylene groupPolymer chemistryMaterials ChemistryOrganic chemistrynitro substituent010405 organic chemistryChemistryLigandOrganic Chemistryhomogeneous catalysis0104 chemical sciencesNickelPolymerizationpolymerization
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Oxidative Dehydrogenation of Ethanol on Gold : Combination of Kinetic Experiments and Computation Approach to Unravel the Reaction Mechanism

2021

Abstract Selective alcohol dehydrogenation on heterogeneous catalysts is a key industrial reaction for production of aldehydes, ketones, and carboxylic compounds. Design of catalysts with improved activity and selectivity requires understanding of the reaction mechanism and kinetics. Herein, experiments, density functional theory (DFT) and kinetic modelling were combined to elucidate the mechanism and kinetics of ethanol oxidative dehydrogenation to acetaldehyde on gold catalysts. Catalytic experiments clearly emphasized the role of oxygen in this reaction. Ethanol conversion was rather independent on the gold cluster size. Formation of minor products, acetic acid and ethyl acetate was stru…

inorganic chemicalsReaction mechanismetanoliethanol oxidationEthyl acetatemechanismAlcohol010402 general chemistryHydrogen atom abstractionreaktiomekanismit01 natural sciences7. Clean energyDFTCatalysiskultaCatalysischemistry.chemical_compoundAcetic acidComputational chemistryDehydrogenationPhysical and Theoretical Chemistryasetaldehydikemialliset reaktiot010405 organic chemistryAcetaldehydegold0104 chemical scienceschemistrykineticskatalyysi
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Heterogeneous borrowing hydrogen reactions with Pd/C and ZnO: Diol scope

2017

Abstract A borrowing hydrogen reaction with different diols was employed for the preparation of complex beta- gamma- or epsilon-amino alcohols from p-toluidine and tetrahydroquinoline with the aim of better understanding the applicability of the Pd/C ZnO heterogeneous catalyst.

inorganic chemicalsScope (project management)010405 organic chemistryChemistryorganic chemicalsOrganic ChemistryDiolBorrowing hydrogen010402 general chemistryHeterogeneous catalysis01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundDrug DiscoveryOrganic chemistryheterocyclic compoundsBeta (finance)Tetrahedron Letters
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