Search results for "EMT"

showing 10 items of 413 documents

Time resolved CARS measurements of I2 in solid Kr

2006

Dephasing is a central concept in condensed phase spectroscopy. It determines how long a system will maintain its coherence. The dephasing time of a system is determined by dynamic intermolecular interactions, and therefore measurements of dephasing time can provide information on interactions and couplings between a molecule and its environment. This chapter illustrates the application of the femtosecond coherent anti-Stokes Raman scattering (CARS) method to investigate the vibrational dephasing of I 2 in solid krypton. Dephasing of vibrational states between v = 2 and v = 16 is studied in the temperature range T = 2.6–32 K. The low vibrational states show dephasing times on the order of a…

Condensed matter physicsPhononDephasingKryptonIntermolecular forcechemistry.chemical_elementsymbols.namesakechemistryPicosecondFemtosecondsymbolsAtomic physicsSpectroscopyRaman scattering
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Tracking the time-evolution of the electron distribution function in Copper by femtosecond broadband optical spectroscopy

2019

Multitemperature models are nowadays often used to quantify the ultrafast electron-phonon (boson) relaxations and coupling strengths in advanced quantum solids. To test their applicability and limitations, we perform systematic studies of carrier relaxation dynamics in copper, a prototype system for which the two-temperature model (TTM) was initially considered. Using broadband time-resolved optical spectroscopy, we study the time evolution of the electron distribution function, $f(E)$, over a large range of excitation densities. Following intraband optical excitation, $f(E)$ is found to be athermal over several 100 fs, with a substantial part of the absorbed energy already being transferre…

Coupling constantCondensed Matter - Materials ScienceMaterials scienceTime evolutionGeneral Physics and AstronomyMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesElectron01 natural sciences0103 physical sciencesFemtosecondAtomic physics010306 general physicsSpectroscopyUltrashort pulseExcitationBoson
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Exciton Interactions and Femtosecond Relaxation in Chlorophyll a−Water and Chlorophyll a−Dioxane Aggregates

1998

Chlorophyll a (Chl a) in hydrocarbon solution with a small amount of dioxane or water shows red-shifted absorption bands at 686 nm and at 700 nm (dioxane) and at 745 nm (water), indicative of self-organized aggregate structures in solution. To study the relationship between the structure and spectral properties of the aggregates, several one-dimensional model structures of Chl a−dioxane and Chl a−water aggregates were computed by the molecular mechanics method. Three overall structures ranging from stick to a ring shape were energetically favored for the dioxane system. All these structures contain structural heterogeneity that consists of repeating dimers that further form tetramer substru…

CrystallographyChlorophyll achemistry.chemical_compoundTetramerChemical physicsChemistryExcitonFemtosecondRelaxation (NMR)Physical and Theoretical ChemistryAbsorption (chemistry)FluorescenceExcitationThe Journal of Physical Chemistry A
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Duration of first-line antiretroviral therapy with tenofovir and emtricitabine combined with atazanavir/ritonavir, efavirenz or lopinavir/ritonavir i…

2013

Objectives: To explore the durability of three first-line tenofovir/emtricitabine-based regimens in combination with atazanavir/ritonavir, efavirenz or lopinavir/ritonavir in HIV-1-infected patients. Patients and methods: A retrospective, longitudinal, multicentre analysis of adult patients enrolled in the Antiretroviral Resistance Cohort Analysis (ARCA), a national prospective observational cohort of HIV-1-infected patients followed up at more than 100 clinical and laboratory units in Italy. Patients eligible were those starting first-line antiretroviral therapy between 1 June 2004 and 15 April 2011 and who were followed up for at least 6 months. The primary endpoint was durability, define…

CyclopropanesTime FactorsPyridinesPyridineDrug ResistanceLopinavir/ritonavirLongitudinal StudieHIV InfectionsPharmacologyAntiviral therapyDeoxycytidineLopinavirCohort Studieschemistry.chemical_compoundimmune system diseasesRetrospective StudieOrganophosphonateMedicineEmtricitabineHIV InfectionPharmacology (medical)ViralLongitudinal StudiesProspective StudiesProspective cohort studyvirus diseasesLopinavirInfectious DiseasesAnti-Retroviral AgentsItalyAlkynesCombinationOligopeptideHIV/AIDSDrug Therapy CombinationOligopeptidesmedicine.drugHumanMicrobiology (medical)Benzoxazinemedicine.medical_specialtyEfavirenzTime Factorantiretroviral therapyAtazanavir SulfateOrganophosphonatesfirst-line therapy tenofovir emtricitabine atazanavir/ritonavirSettore MED/17 - MALATTIE INFETTIVEEmtricitabineDurabilityDrug TherapyInternal medicineDrug Resistance ViralDrug utilizationHumansAntiviral therapy; Drug utilization; Durability; HIV/AIDS; Tenofovir/emtricitabine; Adenine; Anti-Retroviral Agents; Benzoxazines; Cohort Studies; Deoxycytidine; Drug Resistance Viral; Drug Therapy Combination; HIV Infections; HIV-1; Humans; Italy; Longitudinal Studies; Lopinavir; Oligopeptides; Organophosphonates; Prospective Studies; Pyridines; Retrospective Studies; Ritonavir; Time Factors; Pharmacology; Pharmacology (medical); Infectious DiseasesTenofovirRetrospective StudiesAntiviral therapy; Drug utilization; Durability; HIV/AIDS; Tenofovir/emtricitabine; Adenine; Anti-Retroviral Agents; Atazanavir Sulfate; Benzoxazines; Cohort Studies; Deoxycytidine; Drug Resistance Viral; Drug Therapy Combination; Emtricitabine; HIV Infections; HIV-1; Humans; Italy; Longitudinal Studies; Lopinavir; Oligopeptides; Organophosphonates; Prospective Studies; Pyridines; Retrospective Studies; Ritonavir; Tenofovir; Time FactorsPharmacologyRitonavirbusiness.industryAdenineAtazanavirBenzoxazinesRegimenProspective StudiechemistryHIV-1RitonavirAnti-Retroviral AgentCohort StudieTenofovir/emtricitabinebusiness
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Rotational Raman spectroscopy of ethylene using a femtosecond time-resolved pump-probe technique.

2005

154309; Femtosecond Raman-induced polarization spectroscopy (RIPS) was conducted at low pressure (250 mb at 295 K and 400 mb at 373 K) in ethylene. The temporal signal, resulting from the beating between pure rotational coherences, was measured with a heterodyne detection. The temporal traces were converted to the frequency domain using a Fourier transformation and then analyzed thanks to the D2hTDS software (http://www.u-bourgogne.fr/LPUB/shTDS.html) dedicated to X2Y4 molecules with D2h symmetry. The effective Hamiltonian was expanded up to order 2, allowing the determination of five parameters with an rms of 0.017 cm(-1). Special care was taken in the precise modeling of intensities, taki…

DYNAMICSLIQUID WATERTENSORIAL FORMALISMGeneral Physics and Astronomy02 engineering and technology01 natural sciencessymbols.namesakeMOLECULESOpticsINDUCED POLARIZATION SPECTROSCOPYPolarizability0103 physical sciencesCOHERENCEHeterodyne detectionPhysical and Theoretical ChemistrySpectroscopySPECTRUM010304 chemical physicsChemistrybusiness.industry021001 nanoscience & nanotechnologyPolarization (waves)Fourier transformFrequency domainFemtosecondsymbolsZEOLITEMODESCO2Atomic physics0210 nano-technologyRaman spectroscopybusinessThe Journal of chemical physics
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Ultrafast Optical Demagnetization manipulates Nanoscale Spin Structure in Domain Walls

2012

During ultrafast demagnetization of a magnetically ordered solid, angular momentum has to be transferred between the spins, electrons, and phonons in the system on femto- and picosecond timescales. Although the intrinsic spin-transfer mechanisms are intensely debated, additional extrinsic mechanisms arising due to nanoscale heterogeneity have only recently entered the discussion. Here we use femtosecond X-ray pulses from a free-electron laser to study thin film samples with magnetic domain patterns. We observe an infrared-pump-induced change of the spin structure within the domain walls on the sub-picosecond timescale. This domain-topography-dependent contribution connects the intrinsic dem…

DYNAMICSMagnetic domainGeneral Physics and AstronomyMAGNETIZATION REVERSALPhysics::OpticsLarge scale facilities for research with photons neutrons and ionsNanotechnology02 engineering and technologyElectronFILMS01 natural sciencesArticleGeneral Biochemistry Genetics and Molecular BiologyOptical pumping0103 physical sciencesddc:530010306 general physicsPhysics[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]MultidisciplinaryCondensed matter physicsSpins[PHYS.PHYS]Physics [physics]/Physics [physics]Demagnetizing fieldALLOYGeneral Chemistry021001 nanoscience & nanotechnologyPicosecondFemtosecondX-RAYLASER0210 nano-technologyUltrashort pulse
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The primary structural photoresponse of phytochrome proteins captured by a femtosecond X-ray laser

2019

Phytochrome proteins control the growth, reproduction, and photosynthesis of plants, fungi, and bacteria. Light is detected by a bilin cofactor, but it remains elusive how this leads to activation of the protein through structural changes. We present serial femtosecond X-ray crystallographic data of the chromophore-binding domains of a bacterial phytochrome at delay times of 1 ps and 10 ps after photoexcitation. The data reveal a twist of the D-ring, which leads to partial detachment of the chromophore from the protein. Unexpectedly, the conserved so-called pyrrole water is photodissociated from the chromophore, concomitant with movement of the A-ring and a key signaling aspartate. The chan…

DYNAMICSQH301-705.5ScienceEXCITED-STATEDIFFRACTION010402 general chemistryPhotosynthesisphytochromes01 natural sciencesCofactor03 medical and health scienceschemistry.chemical_compoundDeinococcus radioduransPROTON-TRANSFERREVEALSSFXCRYSTAL-STRUCTUREBiology (General)Bilin030304 developmental biologyISOMERIZATION0303 health sciencesbiologyPhytochromeD-RINGChemistryCRYSTALLOGRAPHYinitial photoresponsQRChromophore0104 chemical sciencesPhotoexcitationFemtosecondbiology.proteinBiophysics1182 Biochemistry cell and molecular biologyMedicine3111 BiomedicinevalokemiaproteiinitSignal transductionröntgenkristallografia
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Application of time-resolved spectroscopy to concentration measurements in gas mixtures

2001

1296-2147; Concentration measurements using femtosecond Raman Induced Polarization Spectroscopy (RIPS) are performed in binary gas mixtures CO2-N2 and CO2-N2O at room temperature. The principle of these measurements is based on the nonlinear rotational time response of each molecular component of the mixture, The general form of this molecular response is a series of periodic transients with a period related to the rotational constant Be The relative strength of the individual responses allows an accurate determination of the concentration. Two techniques are presented using either two pulses (one pump and one probe) or three pulses (two pumps and one probe). (C) 2001 Academie des sciences/…

DYNAMICSmolecular concentrationMaterials scienceAnalytical chemistryGeneral Physics and Astronomy01 natural sciencesInduced polarizationsymbols.namesakeINDUCED POLARIZATION SPECTROSCOPYfemtosecond laser0103 physical sciencesMOLECULE010306 general physicsSpectroscopyPOPULATIONINTERFERENCE010304 chemical physicsTriatomic moleculeFEMTOSECONDDiatomic moleculeINVERSE RAMAN-SPECTROSCOPYROTATIONAL COHERENCEFemtosecondsymbolsCO2Rotational spectroscopyTime-resolved spectroscopyRaman spectroscopystimulated Raman effect
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Femtosecond laser induced breakdown spectroscopy of air–methane mixtures

2013

Abstract Femtosecond laser pulses are used in order to induce dielectric breakdown in gaseous mixtures, namely in some reactive air–methane mixtures. The light emitted from the laser induced plasma was analyzed while the main emission features are identified and assigned. From the analysis of the emission spectra, a linear relationship was found to hold between the intensity of some spectral features and methane content. Finally, the use of femtosecond laser induced breakdown as a tool for the in situ determination of the composition of gaseous mixtures (e.g., equivalence ratio) is also discussed.

Dielectric strengthChemistryAnalytical chemistryPhysics::OpticsGeneral Physics and AstronomyPlasmaLaserMethanelaw.inventionchemistry.chemical_compoundlawFemtosecondLaser-induced breakdown spectroscopyEmission spectrumPhysical and Theoretical ChemistryIntensity (heat transfer)Chemical Physics Letters
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Diffractive optics for spectral tuning of second harmonic and supercontinuum generated in nonlinear crystals

2011

It is shown that diffractive lenses can tune the spectrum of femtosecond pulses after nonlinear optical processes. We focus on spectra of second-order pulses generated in birefringent crystals and supercontinuum in sapphire crystals. The tunability is achieved by changing the relative distance between the nonlinear crystal and the diffractive lens.

DiffractionBirefringenceMaterials sciencebusiness.industryPhysics::OpticsNonlinear opticsSecond-harmonic generationSupercontinuumOpticsCondensed Matter::SuperconductivityFemtosecondSapphireOptoelectronicsStimulated emissionbusiness2011 10th Euro-American Workshop on Information Optics
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