Search results for "IAT"

showing 10 items of 33873 documents

Origin of Enzymatic Kinetic Isotope Effects in Human Purine Nucleoside Phosphorylase

2017

Here we report a study of the effect of heavy isotope labeling on the reaction catalyzed by human purine nucleoside phosphorylase (hPNP) to elucidate the origin of its catalytic effect and of the enzymatic kinetic isotope effect (EKIE). Using quantum mechanical and molecular mechanical (QM/MM) molecular dynamics (MD) simulations, we study the mechanism of the hPNP enzyme and the dynamic effects by means of the calculation of the recrossing transmission coefficient. A free energy surface (FES), as a function of both a chemical and an environmental coordinate, is obtained to show the role of the environment on the chemical reaction. Analysis of reactive and nonreactive trajectories allows us …

010304 chemical physicsChemistryPurine nucleoside phosphorylasevariational transition state theoryGeneral Chemistry010402 general chemistryenzyme catalysis01 natural sciencesChemical reactionCatalysis0104 chemical sciencesEnzyme catalysisCatalysisSolventMolecular dynamicsComputational chemistryenzymatic kinetic isotope effect0103 physical sciencesKinetic isotope effectMoleculeQM/MM methodsprotein motionsACS Catalysis
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Hexacarbonyls of Mo, W, and Sg: Metal–CO Bonding Revisited

2017

Calculations of the first bond dissociation energies (FBDEs) and other molecular properties of M(CO)6, where M = Mo, W, and Sg, have been performed using a variety of nonrelativistic and relativistic methods, such as ZORA-DFT, X2c+AMFI-CCSD(T), and Dirac–Coulomb density functional theory. The aim of the study is to assist experiments on the measurements of the FBDE of Sg(CO)6. We have found that, different from the results published earlier, the metal–CO bond in Sg(CO)6 should be weaker than that in W(CO)6. A comparison of the relativistic and nonrelativistic FBDE values, as well as molecular orbital and vibrational frequency analyses within both the nonrelativistic and relativistic approac…

010304 chemical physicsChemistryScalar (mathematics)010402 general chemistry01 natural sciencesBond-dissociation energy0104 chemical sciencesInorganic ChemistryMetalMolecular vibrationvisual_art0103 physical sciencesvisual_art.visual_art_mediumPhysical chemistryMolecular orbitalDensity functional theoryPhysical and Theoretical ChemistryAtomic physicsInorganic Chemistry
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Bond Dissociation Energies for Diatomic Molecules Containing 3d Transition Metals: Benchmark Scalar-Relativistic Coupled-Cluster Calculations for 20 …

2017

Benchmark scalar-relativistic coupled-cluster calculations for dissociation energies of the 20 diatomic molecules containing 3d transition metals in the 3dMLBE20 database ( J. Chem. Theory Comput. 2015 , 11 , 2036 ) are reported. Electron correlation and basis set effects are systematically studied. The agreement between theory and experiment is in general satisfactory. For a subset of 16 molecules, the standard deviation between computational and experimental values is 9 kJ/mol with the maximum deviation being 15 kJ/mol. The discrepancies between theory and experiment remain substantial (more than 20 kJ/mol) for VH, CrH, CoH, and FeH. To explore the source of the latter discrepancies, the …

010304 chemical physicsElectronic correlationChemistryThermodynamics010402 general chemistry01 natural sciencesDiatomic moleculeHeterolysisBond-dissociation energyDissociation (chemistry)0104 chemical sciencesComputer Science ApplicationsCoupled cluster0103 physical sciencesMoleculePhysical and Theoretical ChemistryAtomic physicsBasis setJournal of Chemical Theory and Computation
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Carbonyl compounds of Tc, Re, and Bh: Electronic structure, bonding, and volatility.

2018

Calculations of molecular properties of M(CO)5 and MH(CO)5, where M = Tc, Re, and Bh, and of the products of their decomposition, M(CO)4 and MH(CO)4, were performed using density functional theory and coupled-cluster methods implemented in the relativistic program suits such as ADF, DIRAC, and ReSpect. The calculated first M—CO bond dissociation energies (FBDEs) of Bh(CO)5 and BhH(CO)5 turned out to be significantly weaker than those of the corresponding Re homologs. The reason for that is the relativistic destabilization and expansion of the 6d AOs, responsible for weaker σ-forth and π-back donations in the Bh compounds. The relativistic FBDEs of M(CO)5 have, therefore, a Λ-shape behavior …

010304 chemical physicsGeneral Physics and Astronomychemistry.chemical_elementBohriumInteraction modelElectronic structure010403 inorganic & nuclear chemistry01 natural sciencesBond-dissociation energy0104 chemical sciencesAdsorptionchemistry0103 physical sciencesMoleculePhysical chemistryDensity functional theoryPhysical and Theoretical ChemistryVolatility (chemistry)The Journal of chemical physics
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Matrix isolation and quantum chemical studies on the H2O2–SO2complex

2004

Complexation and photochemical reactions of hydrogen peroxide and sulfur dioxide have been studied in solid Ar, Kr and Xe. Complexes between H2O2 and SO2 are characterized using Fourier transform infrared spectroscopy and ab initio calculations. In solid Ar, the H2O2–SO2 complex absorptions are found at wavenumbers of 3572.8, 3518.7, 3511.2, 3504.3, 1340.3, 1280.2 and 1149.9 cm−1. In Kr and Xe matrices, the bonded OH stretching frequencies deviate from the values in Ar, and we propose that the matrix surrounding influences the structure of the H2O2–SO2 complex. UV photolysis of the H2O2–SO2 was also studied in solid Ar, Kr and Xe. This photolysis produces mainly a complex between sulfur tri…

010304 chemical physicsPhotodissociationMatrix isolationGeneral Physics and Astronomy010402 general chemistry7. Clean energy01 natural sciences0104 chemical scienceschemistry.chemical_compoundMatrix (mathematics)chemistryComputational chemistryAb initio quantum chemistry methods0103 physical sciencesSulfur trioxidePhysical chemistryPhysical and Theoretical ChemistryFourier transform infrared spectroscopyHydrogen peroxideSulfur dioxidePhys. Chem. Chem. Phys.
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Effect of molecular Stokes shift on polariton dynamics

2021

When the enhanced electromagnetic field of a confined light mode interacts with photoactive molecules, the system can be driven into the regime of strong coupling, where new hybrid light-matter states, polaritons, are formed. Polaritons, manifested by the Rabi split in the dispersion, have shown potential for controlling the chemistry of the coupled molecules. Here, we show by angle-resolved steady-state experiments accompanied by multi-scale molecular dynamics simulations that the molecular Stokes shift plays a significant role in the relaxation of polaritons formed by organic molecules embedded in a polymer matrix within metallic Fabry-Pérot cavities. Our results suggest that in the case …

010304 chemical physicsScatteringRelaxation (NMR)Physics::OpticsGeneral Physics and Astronomy010402 general chemistry7. Clean energy01 natural sciencesMolecular physics0104 chemical sciencessymbols.namesakeMolecular dynamicsMolecular vibrationStokes shift0103 physical sciencesPolaritonsymbolsRadiative transferPhysical and Theoretical ChemistryExcitationThe Journal of Chemical Physics
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Exotic SiO(2)H(2) Isomers: Theory and Experiment Working in Harmony.

2016

Replacing carbon with silicon can result in dramatic and unanticipated changes in isomeric stability, as the well-studied CO2H2 and the essentially unknown SiO2H2 systems illustrate. Guided by coupled-cluster calculations, three SiO2H2 isomers have been detected and spectroscopically characterized in a molecular beam discharge source using rotational spectroscopy. The cis,trans conformer of dihydroxysilylene HOSiOH, the ground-state isomer, and the high-energy, metastable dioxasilirane c-H2SiO2 are abundantly produced in a dilute SiH4/O2 electrical discharge, enabling precise structural determinations of both by a combination of isotopic measurements and calculated vibrational corrections. …

010304 chemical physicsSiliconChemistrychemistry.chemical_element010402 general chemistry01 natural sciencesDissociation (chemistry)0104 chemical sciencesComputational chemistryMetastability0103 physical sciencesRotational spectrumPhysical chemistryGeneral Materials ScienceElectric dischargeRotational spectroscopyPhysical and Theoretical ChemistryMolecular beamConformational isomerismThe journal of physical chemistry letters
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Neutron imaging and tomography: Applications in food science

2018

International audience; Neutron imaging and tomography allow observing the structure of large objects (from few to hundred centimeters) at a resolution around 100 μm. This non-destructive method is based on the detection of the transmission of a neutron beam through an object in 2D (imaging) or 3D after rotating the sample (tomography). The components of the object attenuate the neutron beam differently, depending on their composition, and produce accurate pictures of objects which give information about their structure. Neutron imaging has been used for quality control purposes in industries (aircraft, motor engineering...), but also find application from materials sciences (fuel cells, li…

010308 nuclear & particles physicsNeutron imagingPhysicsQC1-99902 engineering and technologyNeutron radiation021001 nanoscience & nanotechnologyObject (computer science)01 natural sciencesSample (graphics)0103 physical sciencesFuel cellsTomographyFood science0210 nano-technology[SDV.AEN]Life Sciences [q-bio]/Food and NutritionEPJ Web of Conferences
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High Gradient Performance of an S-Band Backward Traveling Wave Accelerating Structure for Medical Hadron Therapy Accelerators

2018

The high-gradient performance of an accelerating structure prototype for a medical proton linac is presented. The structure was designed and built using technology developed by the CLIC collaboration and the target application is the TULIP (Turning Linac for Proton therapy) proposal developed by the TERA foundation. The special feature of this design is to produce gradient of more than 50 MV /m in low-β accelerating structures (v/c=0.38). The structure was tested in an S-band test stand at CERN. During the tests, the structure reached over above 60 MV/m at 1.2 μs pulse length and breakdown rate of about 5x10⁻⁶ bpp. The results presented include ultimate performance, long term behaviour and …

010308 nuclear & particles physicsU01 Medical Applications[PHYS.PHYS.PHYS-ACC-PH]Physics [physics]/Physics [physics]/Accelerator Physics [physics.acc-ph]08 Applications of Accelerators Tech Transfer and Industrial RelationscavityAccelerators and Storage Rings01 natural sciencesAccelerator Physicsradiation0103 physical scienceslinac010306 general physicsaccelerating-gradientproton
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A Study of Milk Particles Size Variation with pH Change using Dynamic Light Scattering

2019

A very simple experimental setup for a Dynamic Light Scattering measurement was used to measure the average size of the milk proteins in aqueous suspensions at 20 °C. The PH of the suspensions was adjusted using Calcium lactate, in its most common form of pentahydrate C6H10CaO6•5H2O. The mean size variation of the suspended particles in time has been monitored and reveals a fast increase over a time interval of less than ten of seconds.

010309 opticsMaterials scienceVariation (linguistics)Dynamic light scatteringlcsh:TA1-2040Chemical physics0103 physical sciences02 engineering and technologylcsh:Engineering (General). Civil engineering (General)021001 nanoscience & nanotechnology0210 nano-technology01 natural sciencesMATEC Web of Conferences
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