Search results for "Calculation"

showing 10 items of 594 documents

Unexpected Reaction of the Unsaturated Cluster Host and Catalyst [Pd3(3-CO)(dppm)3]2+ with the Hydroxide Ion: Spectroscopic and Kinetic Evidence of a…

2006

The title cluster, [Pd(3)(mu(3)-CO)(dppm)(3)](2+) (dppm=bis(diphenylphosphino)methane), reacts with one equivalent of hydroxide anions (OH(-)), from tetrabutylammonium hydroxide (Bu(4)NOH), to give the paramagnetic [Pd(3)(mu(3)-CO)(dppm)(3)](+) species. Reaction with another equivalent of OH(-) leads to the zero-valent compound [Pd(3)(mu(3)-CO)(dppm)(3)](0). From electron paramagnetic resonance analysis of the reaction medium using the spin-trap agent 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), the 2-tetrahydrofuryl or methyl radicals, deriving from the tetrahydrofuran (THF) or dimethyl sulfoxide (DMSO) solvent, respectively, were detected. For both [Pd(3)(mu(3)-CO)(dppm)(3)](2+) and [Pd(3)(mu…

RadicalInner sphere electron transfersolvent effects[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistryCatalysislaw.inventionAdductchemistry.chemical_compoundlawElectron paramagnetic resonancehydroxide anionsTetrahydrofuranComputingMilieux_MISCELLANEOUS010405 organic chemistryTetrabutylammonium hydroxideOrganic Chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryGeneral Chemistrypalladium0104 chemical scienceschemistrydensity functional calculationsHydroxidecluster compoundsSolvent effects
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Propan-2-ol dehydration on H-ZSM-5 and H-Y zeolite: a DFT study

2012

The catalytic dehydration of propan-2-ol over H-Y and H-ZMS-5 aluminated zeolite models, mimicking both internal cavities and external surfaces, was studied by DFT calculations to investigate the reaction mechanism. After the adsorption of propan-2-ol on the zeolite, the dehydration mechanism starts with alcohol protonation, occurring by one acidic –OH group of the zeolite fragment, followed by a concerted β-elimination to give propene. The catalytic activity is affected by the size of the zeolite cavity, which is larger in the H-Y than in the H-ZMS-5 zeolite. The adsorption energy of the reagent, as an example, decreases in the order: H-Y cavity ≃ H-ZMS-5 surface > H-ZMS-5 cavity, pointing…

Reaction mechanismChemistryDFT and MP2 calculationsPhotochemistryCatalysisReaction modelingCatalysisGibbs free energyPropenePropan-2-ol dehydrationsymbols.namesakechemistry.chemical_compoundAdsorptionSettore CHIM/03 - Chimica Generale E InorganicaReagentsymbolsPhysical and Theoretical ChemistryZSM-5ZeoliteConfinement effect
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Oxygen-assisted hydroxymatairesinol dehydrogenation: a selective secondary-alcohol oxidation over a gold catalyst.

2013

Selective dehydrogenation of the biomass-derived lignan hydroxymatairesinol (HMR) to oxomatairesinol (oxoMAT) was studied over an Au/Al(2)O(3) catalyst. The reaction was carried out in a semi-batch glass reactor at 343 K under two different gas atmospheres, namely produced through synthetic air or nitrogen. The studied reaction is, in fact, an example of secondary-alcohol oxidation over an Au catalyst. Thus, the investigated reaction mechanism of HMR oxidative dehydrogenation is useful for the fundamental understanding of other secondary-alcohol dehydrogenation over Au surfaces. To investigate the elementary catalytic steps ruling both oxygen-free- and oxygen-assisted dehydrogenation of HMR…

Reaction mechanismMolecular Structure010405 organic chemistryChemistryOrganic ChemistryDiastereomerGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysisLignans0104 chemical sciencesCatalysisOxygenAdsorptionHydroxymatairesinolAlcohol oxidationAlcoholsdehydrogenation density functional calculations gold catalysisReactivity (chemistry)DehydrogenationAdsorptionGoldOxidation-ReductionChemistry (Weinheim an der Bergstrasse, Germany)
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DFT and experimental studies on structure and spectroscopic parameters of 3,6-diiodo-9-ethyl-9H-carbazole

2015

The first report on crystal and molecular structure of 3,6-diiodo-9-ethyl-9H-carbazole is presented. Experimental room-temperature X-ray and 13C chemical shift studies were supported by advanced theoretical calculations using density functional theory (DFT). The 13C nuclear magnetic shieldings were predicted at the non-relativistic and relativistic level of theory using the zeroth-order regular approximation (ZORA). Theoretical relativistic calculations of chemical shifts of carbons C3 and C6, directly bonded to iodine atoms, produced a reasonable agreement with experiment (initial deviation from experiment of 44.3 dropped to 4.25 ppm). The changes in ring aromatic character via simple harm…

Relativistic Effects3Simple harmonic motionDFT calculations010402 general chemistryRing (chemistry)13C NMR spectra01 natural sciencesMolecular physicsChemical shift indexCrystalZORA6-diiodo-9-ethyl-9H-carbazoleComputational chemistrycarbazoleFaculty of ScienceMolecule/dk/atira/pure/core/keywords/TheFacultyOfSciencePhysical and Theoretical Chemistry010405 organic chemistryChemistryChemical shiftAromaticityQuantum ChemistryCondensed Matter Physicscomputational chemistry0104 chemical sciencesZORA GIAO NMR calculationsNMR spectrocopyDensity functional theoryX-ray structureNMR; chemical shiftStructural Chemistry
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Molecular modeling and experimental studies on structure and NMR parameters of 9-benzyl-3,6-diiodo-9H-carbazole

2015

A combined experimental and theoretical study has been performed on 9-benzyl-3,6-diiodo-9H-carbazole. Experimental X-ray (100.0 K) and room-temperature 13C NMR studies were supported by advanced density functional theory (DFT) calculations. The non relativistic structure optimization was performed and the 13C nuclear magnetic shieldings were predicted at the relativistic level of theory using the Zeroth Order Regular Approximation (ZORA). The changes in the benzene and pyrrole rings compared to the unsubstituted carbazole or the parent molecules were discussed in terms of aromaticity changes using the harmonic oscillator model of aromaticity (HOMA) and the nucleus independent chemical shift…

Relativistic EffectsNICSMolecular modelGIAO NMR CalculationsDFT calculationsZORAchemistry.chemical_compoundComputational chemistrycarbazoleFaculty of ScienceHOMAMolecule13 C NMR spectra/dk/atira/pure/core/keywords/TheFacultyOfSciencePhysical and Theoretical ChemistryBenzeneHarmonic oscillator9-Benzyl-3CarbazoleChemical shiftAromaticityQuantum Chemistry6-diiodo-9H-carbazoleCondensed Matter Physicscomputational chemistryNMR spectrocopychemistryPhysical chemistryDensity functional theoryX-ray structureNMR; chemical shiftStructural Chemistry
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The hyperfine structure in the rotational spectra of D2(17)O and HD(17)O: Confirmation of the absolute nuclear magnetic shielding scale for oxygen

2015

Guided by theoretical predictions, the hyperfine structures of the rotational spectra of mono- and bideuterated-water containing (17)O have been experimentally investigated. To reach sub-Doppler resolution, required to resolve the hyperfine structure due to deuterium quadrupole coupling as well as to spin-rotation (SR) and dipolar spin-spin couplings, the Lamb-dip technique has been employed. The experimental investigation and in particular, the spectral analysis have been supported by high-level quantum-chemical computations employing coupled-cluster techniques and, for the first time, a complete experimental determination of the hyperfine parameters involved was possible. The experimental…

RotationGeneral Physics and AstronomyOxygen Isotopesquantum-chemical calculationParamagnetismrotational spectroscopyPhysics::Atomic PhysicsDeuterium OxidePhysical and Theoretical ChemistryHyperfine structureOxygen-17ChemistrySpectrum AnalysisWaterDeuterium17O NMR shieldinghyperfine parameterModels ChemicalDeuteriumElectromagnetic shieldingQuadrupoleQuantum TheoryDiamagnetismRotational spectroscopyAtomic physicsElectromagnetic PhenomenaLamb-dip technique
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Water Splitting on Multifaceted SrTiO3 Nanocrystals: Calculations of Raman Vibrational Spectrum

2022

The financial support of M-ERA.net SunToChem project is greatly acknowledged by L.L.R. and Y.A.M. This paper is partly based upon COST (European Cooperation in Science and Technology) Action 18234 Short Term Scientific Mission. The support is greatly acknowledged by E.K. and V.K. The Institute of Solid State Physics, University of Latvia (Latvia) as the Centre of Excellence has received funding from the European Union’s Horizon 2020 Frame-work Programme H2020-WIDESPREAD-01-2016-2017-Teaming Phase2 under grant agreement No. 739508, project CAMART2. The computer resources were provided by the Stuttgart Supercomputing Center (HLRS project DEFTD 12939) and Latvian Super Cluster (LASC).

STOCondensed Matter::Materials ScienceRaman calculation:NATURAL SCIENCES [Research Subject Categories]General Materials Sciencestepped surfacePhysics::Chemical PhysicsSTO; Raman calculation; DFT; stepped surfaceDFTMaterials
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The influence of substitution in the quinoxaline nucleus on 1,3-dipolar cycloaddition reactions

2013

The reaction mechanism of 1,3-dipolar cycloadditions of both symmetric and unsymmetric benzo-condensed diazines with a nitrilimine dipole, to give two different mono- and bis-cycloadducts, in tetrahydrofuran (THF) solution, was studied by DFT calculatio ns. The results obtained show that each 1,3-dipolar cycloaddition reaction always proceeds by a two steps mechanism, in which the first intermediate shows only one covalent bond between the beta carbon of the nitrilimine and the aromatic nitrogen of the diazine molecule. The structure and energy content of the two transition states of the two cycloaddition steps, in the case of the unsymmetric benzo-condensed diazine, nicely explains why the…

Settore CHIM/03 - Chimica Generale E InorganicaSettore CHIM/08 - Chimica FarmaceuticaDFT calculations 13-Dipolar cycloaddition reactions Quinoxalines Reaction mechanism
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The molecular structure of N-hydroxyurea

1996

Ab initio calculations were performed on the tautomers and conformers of N-hydroxyurea using a 6-31G** basis set. The minimum-energy structures have been found and the importance of the intramolecular hydrogen bond as the stabilizing factor was pointed out. © 1996 John Wiley & Sons, Inc.

Settore CHIM/03 - Chimica Generale E Inorganicaab initio calculationsmolecular structureN-hydroxyurea
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Prediction of driving performance of a hybrid vehicle with CVT transmission

2009

The purpose of this work is the description of the phenomenology of driving behaviour of a production car characterized by a hybrid powertrain and a continuously variable transmission (CVT), along with a theoretical study of consumption that provides results in agreement with the experimental ones obtained and reported by the Car Maker.

Settore ING-IND/14 - Progettazione Meccanica E Costruzione Di MacchineHybrid VehicleConsumption calculationCVT
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