Search results for "etica"

showing 10 items of 14083 documents

Model building on the non-factorisable type IIA T6/(Z4×ΩR) orientifold

2016

We construct global semi-realistic supersymmetric models with intersecting D6-branes on the non-factorisable orientifold . The non-factorisable structure gives rise to differences compared to the factorisable case: additional conditions for the three-cycles to be Lagrangian and extra constraints on the wrapping numbers for building fractional cycles.

010308 nuclear & particles physicsStructure (category theory)General Physics and AstronomySupersymmetryConstruct (python library)Type (model theory)01 natural sciencessymbols.namesakeTheoretical physicsFactorizationOrientifoldMathematics::Category Theory0103 physical sciencessymbols010306 general physicsModel buildingLagrangianMathematicsFortschritte der Physik
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Measurement of the laser resonance ionization efficiency for lutetium

2019

Abstract The development of a highly efficient resonance ionization scheme for lutetium is presented. A laser ion source, based on the all-solid-state Titanium:sapphire laser system, was used at the 30 keV RISIKO off-line mass separator to characterize different possible optical excitation schemes in respect to their ionization efficiency. The developed laser resonance ionization scheme can be directly applied to the use at radioactive ion beam facilities, e. g. at the CERN-MEDICIS facility, for large-scale production of medical radioisotopes.

010308 nuclear & particles physicschemistry.chemical_elementMass spectrometry01 natural sciencesLutetiumIsotope separationlaw.inventionchemistrylawIonization0103 physical sciencesSapphireLaser resonancePhysics::Atomic PhysicsPhysical and Theoretical ChemistryAtomic physics010306 general physicsSpectroscopyRadiochimica Acta
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Effective characterization of the phase and intensity profiles of asymmetrically distorted light pulses in optical fiber systems

2009

International audience; We address the problem of characterization of light pulses that propagate in long-haul high-bit-rate optical communication systems under strongly perturbed conditions. We show that the conventional technique for characterization of the phase and intensity profile of such pulses becomes qualitatively inconsistent when the pulse's profile is asymmetrically distorted with respect to its center of mass. We resolve these inconsistencies by partially reformulating the conventional technique by means of appropriate pulse parameters, which we call upgraded parameters, that allow a fair characterization of the intensity and phase of all types of light pulses, including those …

010309 optics[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistry020210 optoelectronics & photonics0103 physical sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistry0202 electrical engineering electronic engineering information engineeringStatistical and Nonlinear Physics02 engineering and technology190.5530 060.5530 060.2330 060.2360 060.451001 natural sciencesAtomic and Molecular Physics and Optics
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Catalytic epoxidation using dioxidomolybdenum(VI) complexes with tridentate aminoalcohol phenol ligands

2019

Reaction of the tridentate aminoalcohol phenol ligands 2,4-di-tert-butyl-6-(((2 hydroxyethyl)(methyl)amino)methyl)phenol (H2L1) and 2,4-di-tert-butyl-6-(((1-hydroxybutan-2-yl)amino)methyl)phenol (H2L2) with [MoO2(acac)2] in methanol solutions resulted in the formation of [MoO2(L1)(MeOH)] (1) and [MoO2(L2)(MeOH)] (3), respectively. In contrast, the analogous reactions in acetonitrile afforded the dinuclear complexes [Mo2O2(μ-O)2(L1)2] (2) and [Mo2O2(μ-O)2(L2)2] (4). The corresponding reactions with the potentially tetradentate ligand 3-((3,5-di-tert-butyl-2-hydroxybenzyl)(methyl)amino)propane-1,2-diol (H3L3) led to the formation of the mononuclear complex [MoO2(L3)(MeOH)] (5) in methanol whi…

010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundkatalyytitepoxidationMaterials ChemistryPhenolMoietyPhysical and Theoretical ChemistryHydrogen peroxideAcetonitrileta116010405 organic chemistryLigandmolybdenum complexSubstrate (chemistry)kompleksiyhdisteettrinuclear structure0104 chemical scienceschemistrytridentate ligandMethanolmolybdeeniInorganica Chimica Acta
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The Taming of Redox‐Labile Phosphidotitanocene Cations

2019

International audience; Tame d0 phosphidotitanocene cations stabilized with a pendant tertiary phosphane arm are reported. These compounds were obtained by one-electron oxidation of d1 precursors with [Cp2Fe][BPh4]. The electronic structure of these compounds was studied experimentally (EPR, UV/Vis, and NMR spectroscopy, X-ray diffraction analysis) and through DFT calculations. The theoretical analysis of the bonding situation by using the electron localization function (ELF) shows the presence of π-interactions between the phosphido ligand and Ti in the d0 complexes, whereas dπ–pπ repulsion prevents such interactions in the d1 complexes. In addition, CH–π interactions were observed in seve…

010402 general chemistry01 natural sciencesRedoxTransition metal phosphidesCatalysisFrustrated Lewis pairlaw.inventionchemistry.chemical_compoundFrustrated Lewis Pair (FLP)[CHIM.ANAL]Chemical Sciences/Analytical chemistrylaw[CHIM.COOR]Chemical Sciences/Coordination chemistryPhosphorus LigandsElectron paramagnetic resonanceDiphenylacetyleneComputingMilieux_MISCELLANEOUSTitanium[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryLigandOrganic Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyElectron localization function0104 chemical sciencesHomolysis[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryDensity Functional Theory (DFT)Crystallographychemistry[CHIM.CHEM]Chemical Sciences/CheminformaticsChemistry – A European Journal
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Oxidovanadium(V) amine bisphenolates as epoxidation, sulfoxidation and catechol oxidation catalysts

2017

Air-stable oxidovanadium(V) complexes with tetradentate amine bisphenolate ligands were made by the reaction of VOSO4·xH2O and ligand precursors in MeOH solutions. Isolated compounds were studied as catechol oxidase models as well as catalysts for epoxidation and sulfoxidation reactions. All compounds can catalyse such oxidation reactions without notable structure-activity correlations. The 51V NMR studies indicate that the complexes turn to the number of different species during the catalytic experiments. peerReviewed

010402 general chemistry01 natural sciencesRedoxvanadiiniCatalysisInorganic ChemistryTurn (biochemistry)chemistry.chemical_compoundMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryCatechol oxidaseta216ta116Catecholbiologycatalysis010405 organic chemistryLigandoxo transferbiomimetic0104 chemical scienceschemistrykatalyysibiology.proteinvanadiumAmine gas treatingInorganic Chemistry Communications
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Gold/Isophorone Interaction Driven by Keto/Enol Tautomerization

2016

The binding behavior of isophorone (C9H14O) to Au adatoms and clusters deposited on MgO/Ag(001) thin films is investigated by scanning tunneling microscopy (STM) and density functional theory (DFT). The STM data reveal the formation of various metal/organic complexes, ranging from Au1/isophorone pairs to larger Au aggregates with molecules bound to their perimeter. DFT calculations find the energetically preferred keto-isophorone to be unreactive toward gold, while the enol-tautomer readily binds to Au monomers and clusters. The interaction is governed by electrostatic forces between the hydroxyl group of the enol and negative excess charges residing on the ad-gold. The activation barrier b…

010402 general chemistryPhotochemistry01 natural sciencesChemical reactionlaw.inventionchemistry.chemical_compoundlawketo-enol tautomerismgold compoundsMoleculePhysical and Theoretical Chemistryta116Isophoroneta114010405 organic chemistryKeto–enol tautomerismEnolTautomer0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsisophoroneGeneral EnergychemistryDensity functional theoryScanning tunneling microscopeJournal of Physical Chemistry C
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2,4,5-Triaryl imidazole probes for the selective chromo-fluorogenic detection of Cu(II). Prospective use of the Cu(II) complexes for the optical reco…

2019

The sensing behaviour toward metal cations and biothiols of two 2,4,5-triarylimidazole probes (3a and 3b) is tested in acetonitrile and in acetonitrile-water. In acetonitrile the two probes present charge-transfer absorption bands in the 320-350 nm interval. Among all cations tested only Cu(11) is able to induce bathochromic shifts of the absorption band in the two probes, which is reflected in marked colour changes. Colour modulations are ascribed to the formation of 1:1 Cu(II)-probe complexes in which the cation interacts with the imidazole acceptor heterocycle. Besides, the two probes present intense emission bands (at 404 and 437 nm for 3a and 3b respectively) in acetonitrile that are q…

010402 general chemistryPhotochemistryCu(II) detection01 natural sciencesCu(II) imagingInorganic ChemistryMetalchemistry.chemical_compoundBathochromic shiftMaterials ChemistryImidazolePhysical and Theoretical ChemistryAcetonitrileImidazole-based probesAqueous solutionScience & Technology010405 organic chemistryGSH imagingAcceptor0104 chemical sciences3. Good healthchemistryAbsorption bandvisual_artvisual_art.visual_art_mediumHypsochromic shiftBiothiols recognition
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9,10-Phenanthrenedione as Visible-Light Photoredox Catalyst: A Green Methodology for the Functionalization of 3,4-Dihydro-1,4-Benzoxazin-2- Ones thro…

2018

A visible-light photoredox functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones through a Friedel-Crafts reaction with indoles using an inexpensive organophotoredox catalyst is described. The reaction uses a dual catalytic system that is formed by a photocatalyst simple and cheap, 9,10-phenanthrenedione, and a Lewis acid, Zn(OTf)2. 5W white LEDs are used as visible-light source and oxygen from air as a terminal oxidant, obtaining the corresponding products with good yields. The reaction can be extended to other electron-rich arenes. Our methodology represents one of the most valuable and sustainable approach for the functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones, as compared to th…

010402 general chemistrylcsh:Chemical technology01 natural sciencesCatalysisCatalysislcsh:Chemistrychemistry.chemical_compoundCatàlisiTryptophollcsh:TP1-1185Lewis acids and basesorganic_chemistryPhysical and Theoretical ChemistryFriedel-Crafts reactionFriedel–Crafts reaction010405 organic chemistryindolesCombinatorial chemistry0104 chemical scienceschemistrylcsh:QD1-999visible-light photocatalysis14-benzoxazin-2-onesPhotocatalysisSurface modificationorganophotoredox catalysisQuímica orgànicaDerivative (chemistry)Visible spectrum
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Electrochemical Fluorocyclization of N-Allylcarboxamides to 2-Oxazolines by Hypervalent Iodine Mediator

2018

A resource saving protocol for the synthesis of 5-fluoromethyl-2-oxazolines by using electrochemistry has been realized. Thereby, a hypervalent iodine species I(III) is generated by anodic oxidation in the presence of Et3N·5HF and mediates the cyclization of N-allylcarboxamide to 5-fluoromethyl-2-oxazoline. This method allows application to various substrates furnishing the 2-oxazolines with yields up to 68%. The protocol is easy to conduct under constant current conditions offering a sustainable alternative over conventional reagent-based pathways.

010405 organic chemistryAnodic oxidationResource savingOrganic ChemistryHypervalent moleculechemistry.chemical_element010402 general chemistryIodineElectrochemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical scienceschemistryReagentPhysical and Theoretical ChemistryOrganic Letters
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