Search results for "ATAL"

showing 10 items of 10591 documents

Oxidative ortho-C-N Fusion of Aniline by OsO4. Isolation, Characterization of Oxo-Amido Osmium(VI) Complexes, and their Catalytic Activities for Oxid…

2008

In an unusual reaction of osmium(VIII) oxide with p-substituted aromatic amines (X-C6H4-NH2, where X = Me, H, Cl) in heptane afforded the brown osmium(VI)-oxo complexes [OsO(L)2] (1a-c, L = N-aryl-1,2-arylenediamide) in moderate yields. The ligand L is formed in situ via oxidative ortho-C-N fusion of arylamines. The reaction occurs in an inert atmosphere, and a part of Os(VIII) is used up for the oxidation of aromatic amine. Single crystal X-ray structure of a representative complex 1a is solved. The structural analysis has authenticated the ortho-C-N fusion of ArNH2 resulting in formation of the diamide ligand, L. The complex as a whole is penta-coordinated, and the coordination sphere has…

osmium(VI) kompleksitkatalyysiosmium(VI) complexes
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Ostaa vai tehdä itse -vertailut maatilataloudessa

2007

ostaminenvertailumaatilatalousulkoistaminentekeminenpäätöksenteko
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Organocatalisi: sviluppo di nuovi materiali supportati riciclabili ed ottimizzazione di reazioni in fase omogenea.

2011

ottimizzazione di reazioni in fase omogenea.organocatalisiSettore CHIM/06 - Chimica Organicaorganocatalisi; nuovi materiali supportati riciclabili; ottimizzazione di reazioni in fase omogenea.nuovi materiali supportati riciclabili
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Carbon Dioxide Activation and Reaction Induced by Electron Transfer at an Oxide-Metal Interface

2015

A model system has been created to shuttle electrons through a metal-insulator-metal (MIM) structure to induce the formation of a CO2 anion radical from adsorbed gas-phase carbon dioxide that subsequently reacts to form an oxalate species. The process is completely reversible, and thus allows the elementary steps involved to be studied at the atomic level. The oxalate species at the MIM interface have been identified locally by scanning tunneling microscopy, chemically by IR spectroscopy, and their formation verified by density functional calculations.

oxalateta114Inorganic chemistryOxidecarbon dioxideInfrared spectroscopychemistry.chemical_elementGeneral Chemistryelectron transferOxygenmetal-insulator-metal structureCatalysisOxalateIonlaw.inventionMetalElectron transferchemistry.chemical_compoundchemistrylawvisual_artvisual_art.visual_art_mediumScanning tunneling microscopeta116oxygenAngewandte Chemie International Edition
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An efficient method for selective oxidation of (oxime)Pt(II) to (oxime)Pt(IV) species using N,N-dichlorotosylamide

2016

The oxidation of (oxime)PtII species using the electrophilic chlorine-based oxidant N,N-dichlorotosylamide (4-CH3C6H4SO2NCl2) was studied. The reactions of trans-[PtCl2(oxime)2] (where oxime = acetoxime, cyclopentanone oxime, or acetaldoxime) with this oxidant led to trans-[PtCl4(oxime)2] products. The oxidation of trans-[Pt(o-OC6H4CH = NOH)2] at room temperature gave trans-[PtCl2(o-OC6H4CH = NOH)2], whereas the same reaction upon heating was accompanied by electrophilic substitution of the benzene rings. peerReviewed

oxidation010405 organic chemistryoxime ligandsMetals and Alloyschemistry.chemical_elementoxidative chlorination010402 general chemistryOxime01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisInorganic ChemistryElectrophilic substitutionchemistry.chemical_compoundchemistryElectrophileMaterials ChemistryChlorineOrganic chemistryAcetaldoximeBenzeneOrganometallic chemistryplatinum complexesTransition Metal Chemistry
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1,1prime-Binaphthyl-2-methylpyridinium-based peroxophosphotungstate salts: synthesis, characterization, and their use as oxidation catalysts

2009

A series of 1,1′-binaphthyl-2-methylammonium and pyridinium salts 6, 7, and 8 was synthesized through the coupling reaction of 2-(bromomethyl)-1,1′-binaphthalene (5) with the dendritic tetraallyl pyridinedicarbinol dendron 2 as well as triethylamine and 4-tert-butylpyridine. Tetraallyl pyridinedicarbinol dendron 2 was prepared by allylation of commercially available diethyl pyridine-3,5-dicarboxylate (1). The allylation of 2 with allyltrimethylsilane in the presence of boron trifluoride was unsuccessful, as tetraallyl pyridinedicarbinol trifluoroboron adduct 3 was obtained instead of expected hexaallylpyridine compound 4. The catalytic hydrogenation of allyl groups of the ammonium salt of 2…

oxidationCyclohexanolSalt (chemistry)010402 general chemistry01 natural sciencesCoupling reactionCatalysisdendrimersInorganic Chemistrychemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/Catalysis[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganic chemistrypolyoxometalatesTriethylamineBoron trifluorideComputingMilieux_MISCELLANEOUSchemistry.chemical_classification[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryThioanisole[CHIM.CATA]Chemical Sciences/Catalysishomogeneous catalysis0104 chemical scienceschemistryPyridinium
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Oxidation of aromatic alcohols in irradiated aqueous suspensions of commercial and home-prepared rutile TiO(2): a selectivity study.

2008

WOS: 000256241700021

oxidationPhotochemistryUltraviolet RaysAlcoholAnisolesAldehydeAlcohols Oxidation Photocatalysis Rutile SelectivityCatalysisCatalysisalcoholschemistry.chemical_compoundX-Ray DiffractionOrganic chemistryReactivity (chemistry)chemistry.chemical_classificationTitaniumSettore ING-IND/24 - Principi Di Ingegneria ChimicaAqueous solutionalcohols;oxidation;photocatalysis;rutile;selectivityMolecular StructureOrganic ChemistryselectivityWaterGeneral ChemistrychemistryBenzyl alcoholPhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelectivityrutilephotocatalysisOxidation-ReductionBenzyl AlcoholChemistry (Weinheim an der Bergstrasse, Germany)
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DFT Prediction of Enhanced Reducibility of Monoclinic Zirconia upon Rhodium Deposition.

2018

Oxides are an important class of materials and are widely used, for example, as supports in heterogeneous catalysis. In a number of industrial catalytic processes, oxide supports actively participate in chemical transformations by releasing lattice oxygen anions. While this is intuitively understood for reducible oxides, the reducibility of irreducible oxides may be modified via nanoengineering or upon inclusion of foreign species. Our calculations predict that the ability of irreducible monoclinic zirconia to release oxygen improves substantially upon deposition of rhodium. Through a comprehensive screening of Rh/ZrO2 with different size of the rhodium species, we find that a Rh adatom and…

oxidation-reduction reactionMaterials scienceOxidechemistry.chemical_element02 engineering and technologyNanoengineering010402 general chemistryHeterogeneous catalysis01 natural sciencesOxygencatalystsRhodiumCatalysischemistry.chemical_compoundkatalyytitnanorakenteetnanostructuresCubic zirconiahapetus-pelkistysreaktioPhysical and Theoretical Chemistryta116ta114tiheysfunktionaaliteoriazirkoniumoksidi021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral Energychemistry13. Climate actionoksiditoxideszirconium dioxidePhysical chemistry0210 nano-technologyMonoclinic crystal systemThe journal of physical chemistry. C, Nanomaterials and interfaces
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Controlling Oxidative Addition and Reductive Elimination at Tin(I) via Hemi-Lability.

2021

We report on the synthesis of a distannyne supported by a pincer ligand bearing pendant amine donors that is capable of reversibly activating E–H bonds at one or both of the tin centres through dissociation of the hemi-labile N–Sn donor/acceptor interactions. This chemistry can be exploited to sequentially (and reversibly) assemble mixed-valence chains of tin atoms of the type ArSn{Sn(Ar)H} n SnAr ( n = 1, 2). The experimentally observed (decreasing) propensity towards chain growth with increasing chain length can be rationalized both thermodynamically and kinetically by the electron-withdrawing properties of the –Sn(Ar)H– backbone units generated via oxidative addition. peerReviewed

oxidative additionchemistry.chemical_element010402 general chemistry01 natural sciencesCatalysisDissociation (chemistry)Reductive eliminationreversibilityNucleophilic aromatic substitutiontinPolymer chemistryPincer ligandkemiallinen synteesiChemistry010405 organic chemistryreductive eliminationliganditkompleksiyhdisteetGeneral ChemistryGeneral MedicineAcceptorOxidative addition3. Good health0104 chemical scienceshemi-labile ligandorgaaniset tinayhdisteettinaAmine gas treatingTinAngewandte Chemie (International ed. in English)
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Oxidative Stress and Antioxidant Levels in Patients with Anorexia Nervosa after Oral Re-alimentation: A Systematic Review and Exploratory Meta-analys…

2015

Oxidative stress markers seem to be higher in patients with anorexia nervosa (AN) than healthy controls, but the potentially beneficial effects of weight gain is not known. We calculated random effects standardised mean differences (SMDs) as effect size measures of oxidative stress marker changes after re-alimentation reported in two or more studies, summarising others descriptively. Seven longitudinal studies (n = 104) were included. After a median follow-up period of 8 weeks, AN patients significantly increased their body mass index (15.1 ± 2.1 to 17.1 ± 2.2, p < 0.0001). This weight gain was followed by a significant increase in serum levels of the antioxidant albumin (studies = 6, SM…

oxidative streantioxidantSuperoxide DismutaseMedicine (all)weight gainCatalaseAntioxidantsanorexia nervosaOxidative StressClinical PsychologyPsychiatry and Mental HealthAlbuminsApolipoprotein B-100albumin; anorexia nervosa; antioxidant; ApoB; oxidative stress; refeeding; weight gain; Albumins; Anorexia Nervosa; Antioxidants; Apolipoprotein B-100; Biomarkers; Catalase; Humans; Longitudinal Studies; Superoxide Dismutase; Weight Gain; Oxidative Stress; Clinical Psychology; Psychiatry and Mental Health; Medicine (all)HumansLongitudinal StudiesApoBApoB; albumin; anorexia nervosa; antioxidant; oxidative stress; refeeding; weight gainBiomarkersalbuminrefeeding
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