Search results for "TRANSITION"

showing 10 items of 3988 documents

Ring splitting of azetidin-2-ones via radical anions

2012

The radical anions of azetidin-2-ones, generated by UV-irradiation in the presence of triethylamine, undergo ring-splitting via N-C4 or C3-C4 bond breaking, leading to open-chain amides. This reactivity diverges from that found for the neutral excited states, which is characterised by alpha-cleavage. The preference for beta-cleavage is supported by DFT theoretical calculations on the energy barriers associated with the involved transition states. Thus, injection of one electron into the azetidin-2-one moiety constitutes a complementary activation strategy which may be exploited to produce new chemistry.

AnionsAZETIDINESFree RadicalsUltraviolet RaysElectronVINYL ETHERSRing (chemistry)PhotochemistryBiochemistryPolarizable continuum modelchemistry.chemical_compoundN-(ARYLIDENE(OR ALKYLIDENE)AMINO)-2-AZETIDINONESQUIMICA ORGANICAMoietyReactivity (chemistry)BETA-LACTAM RINGPhysical and Theoretical ChemistryTriethylamineDNA PHOTOLYASEMolecular StructureSTEREOCONTROLLED SYNTHESISOrganic ChemistryTransition stateSTEREOSELECTIVE-SYNTHESISchemistryPOLARIZABLE CONTINUUM MODELExcited stateQuantum TheoryPHOTOCHEMICAL-REACTIONSBUILDING-BLOCKS
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Computed positron lifetimes in vacancies and vacancy-iron clusters in gold

1983

Abstract Annihilation characteristics are calculated for positrons trapped in clean and impurity decorated vacancy clusters in Au. The positron lifetime depends strongly on the structure of the clusters. In a strongly relaxed vacancy cluster, the lifetime can become smaller than the lifetime in a single vacancy. The substitution of some neighbour atoms of a vacancy cluster by Fe atoms has only a minor effect on the positron lifetimes.

AnnihilationCondensed Matter::OtherChemistryGeneral EngineeringMetalCondensed Matter::Materials SciencePositronTransition metalImpurityvisual_artVacancy defectPhysics::Atomic and Molecular Clustersvisual_art.visual_art_mediumCluster (physics)Physics::Accelerator PhysicsAtomic physicsPositron annihilationRadiation Effects
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Intramolecular electronic excitation energy transfer in donor∕acceptor dyads studied by time and frequency resolved single molecule spectroscopy

2008

Electronic excitation energy transfer has been studied by single molecule spectroscopy in donor/acceptor dyads composed of a perylenediimide donor and a terrylenediimide acceptor linked by oligo(phenylene) bridges of two different lengths. For the shorter bridge (three phenylene units) energy is transferred almost quantitatively from the donor to the acceptor, while for the longer bridge (seven phenylene units) energy transfer is less efficient as indicated by the occurrence of donor and acceptor emission. To determine energy transfer rates and efficiencies at the single molecule level, several methods have been employed. These comprise time-correlated single photon counting techniques at r…

AnthracenesTime FactorsLightMolecular StructurePhotochemistryChemistryTemperatureGeneral Physics and AstronomyElectronsP680ElectronImidesAcceptorMolecular electronic transitionSpectrometry FluorescenceEnergy TransferPhenyleneIntramolecular forceExcited statePolycyclic Aromatic HydrocarbonsPhysical and Theoretical ChemistryAtomic physicsPeryleneExcitationThe Journal of Chemical Physics
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Multi-disciplinary, Inter-disciplinary, Anti-disciplinary. Transition Knowledges in Design Education

2023

The environmental issues are recently proving to be the center and the connecting element of all the states of crisis, only apparently diversified (energy, political, migration); after the lucid forward-looking analysis of Maldonado in the 70s, the vision proposed in 2019 by the exhibition Broken Nature opens new spaces to the “design hope” activated by design, emphasizing the broad responsibility that the designer must take on contemporary challenges. The complex scenarios of the “transition” (environmental, cultural, productive) are also based on the ability of disciplinary encroachment and on the most radical forms of “anti-disciplinary” innovation, which in some cases opens to design fo…

Anti-disciplinary · Design Education · Design Culture · Complexity · TransitionSettore ICAR/13 - Disegno Industriale
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The cryogenic anticoincidence detector for ATHENA-XMS: preliminary results from the new prototype

2012

ATHENA has been the re-scoped IXO mission, and one of the foreseen focal plane instrument was the X-ray Microcalorimeter Spectrometer (XMS) working in the energy range 0.3-10 keV, which was a kilo-pixel array based on TES (Transition Edge Sensor) detectors. The need of an anticoincidence (AC) detector is legitimated by the results performed with GEANT4 simulations about the impact of the non x-ray background onto XMS at L2 orbit (REQ. < 0.02 cts/cm2/s/keV). Our consortium has both developed and tested several samples, with increasing area, in order to match the large area of the XMS (64 mm2). Here we show the preliminary results from the last prototype. The results achieved in this work off…

Anticoincidence detectorLow temperature DetectorAnticoincidence detectorsAstrophysicsOrbital mechanicslaw.inventionOpticslawElectronicOptical and Magnetic MaterialsElectrical and Electronic EngineeringAnticoincidence detectors; High Energy Astrophysics; Low temperature Detectors; TES; Electronic Optical and Magnetic Materials; Condensed Matter Physics; Computer Science Applications1707 Computer Vision and Pattern Recognition; Applied Mathematics; Electrical and Electronic EngineeringPhysicsLow temperature DetectorsSpectrometerbusiness.industryApplied MathematicsElectronic Optical and Magnetic MaterialBolometerDetectorComputer Science Applications1707 Computer Vision and Pattern RecognitionCondensed Matter PhysicsApplied MathematicCardinal pointMillimeterSatelliteTransition edge sensorHigh Energy AstrophysicbusinessTESHigh Energy AstrophysicsSPIE Proceedings
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Structure and Phase Transitions in Ethylenediammonium Dichloride and its Salts with Antimony Trichloride

2000

During the mixing of ethylenediammonium dichloride and antimony trichloride except of reported earlier [NH3(CH2)2NH3]5(Sb2Cl11)2 · 4 H2O a new salt [NH3(CH2)2NH3](SbCl4)2 was obtained. The crystals are monoclinic at 295 K, space group C2/m, a = 13.829(3), b = 7.408(1), c = 7.588(2) A; β = 103.18(3)°; V = 756.9(3) A3; Z = 2; dc = 2.585, dm = 2.56(2) g · cm–3. The structure consists of anionic sublattice built of Sb2Cl82– units composed of two SbCl52– square pyramids connected by edge. The ethylenediammonium cations are located in anionic cavities. The cations are disordered. Each methylene carbon atom is split between two positions. The X-ray diffraction, DSC, TGA and dilatometric methods we…

Antimony trichloridePhase transitionCarbon atomChemistrychemistry.chemical_elementCrystal structureFirst orderInorganic Chemistrychemistry.chemical_compoundCrystallographyAntimonyPolymer chemistryMethyleneMonoclinic crystal systemZeitschrift für anorganische und allgemeine Chemie
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Selective oxidation of propane over alkali-doped Mo-V-Sb-O catalysts

2009

[EN] Alkali metal-doped MoVSbO catalysts have been prepared by impregnation of a MoVSbO-mixed oxide (prepared previously by a hydrothermal synthesis) and finally activated at 500 or 600 degrees C in N-2. The catalysts have been characterized and tested for the selective oxidation of propane and propylene. Alkali-doped catalysts improved in general the catalytic performance of MoVSbO, resulting more selective to acrylic acid and less selective to acetic acid than the corresponding alkali-free MoVSbO catalysts. However, the specific behaviour strongly depends on both the alkali metal added and/or the final activation temperature. At isoconversion conditions, catalysts activated at 600 degrees…

AntimonyCarboxylic acidIndustrial catalystsInorganic chemistryLithiumHeterogeneous catalysisAcetic acidCatalysisCatalysisPropeneAcrylic acidchemistry.chemical_compoundAcetic acidTransition metalAcrylic acidchemistry.chemical_classificationMolybdenumSodiumVanadiumGeneral ChemistryCaesiumchemistryPotassiumMetal oxidesPropane oxidation
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Sb-implanted ZnO ultra-thin films

2017

Mild heating of the Zn(C5F6HO2)(2)center dot 2H(2)O center dot CH3(OCH2CH2)(2)OCH3 precursor allowed MOCVD deposition of ZnO films, in a low-pressure horizontal hot-wall reactor, on ITO substrates. The ZnO films were subsequently implanted with Sb ions. XRD measurements provided evidence that they consist of hexagonal, (002) and (101) oriented, crystals. UV-vis spectra showed that the transmittance of these films in the visible region is about 90%. The Sb implanted ZnO film showed a current-voltage characteristic that resembles that of a rectifying diode. This study represents the first example of Sb-implantation in ZnO films obtained by MOCVD.

AntimonyMaterials scienceCondensed Matter Physic02 engineering and technology010402 general chemistrySettore ING-INF/01 - Elettronica01 natural sciencesSettore FIS/03 - Fisica Della MateriaSpectral lineIonTransmittanceZnO filmDeposition (phase transition)Mechanics of MaterialGeneral Materials ScienceMetalorganic vapour phase epitaxyThin filmFilmDiodeDiodeHexagonal crystal systembusiness.industryMechanical Engineering021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesMechanics of MaterialsMOCVDZnOZnO film; antimony; diodeOptoelectronicsMaterials Science (all)0210 nano-technologybusinessMaterials Science in Semiconductor Processing
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Calculation of the surface concentration of Zn(I) from the anodic voltammetric peak of zinc combined with the QCM results

2004

Deconvolution of voltammograms of anodic dissolution of zinc has proved to be possible through the electrochemical quartz crystal microbalance data and the F(dm/dQ) function. This deconvolution allows to calculate the surface concentration of Zn(I) and to obtain an estimation for the kinetic constant of the second single-electron transfer. Keywords: Zinc anodic dissolution, EQCM, Surface concentration, Deconvolution and kinetic constant

Aqueous solutionChemistryAnalytical chemistrychemistry.chemical_elementQuartz crystal microbalanceZincElectrochemistryAnodelcsh:Chemistrylcsh:Industrial electrochemistrylcsh:QD1-999Transition metalElectrochemistryDeconvolutionCyclic voltammetrylcsh:TP250-261Electrochemistry Communications
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Analysis of an impedance function of zinc anodic dissolution

2004

Zinc anodic dissolution has been studied by means of electrochemical impedance spectroscopy (EIS). The kinetic study of the oxidation mechanism has allowed us to propose a theoretical impedance function for this system in deaerated sulphate medium. Relevant information on the faradaic process is provided by analysis of the theoretical impedance function. Kinetic parameters of this system can be calculated from the fitting of experimental data to the faradaic impedance function deduced theoretically. The physical measurements of this function are analysed by means of the dependence of simulated EIS spectra on kinetic parameters.

Aqueous solutionChemistryGeneral Chemical EngineeringFaradaic impedanceAnalytical chemistrychemistry.chemical_elementZincKinetic energyAnalytical ChemistryDielectric spectroscopyReaction rate constantTransition metalElectrochemistryElectrical impedanceJournal of Electroanalytical Chemistry
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