Search results for "Methyl vinyl ketone"

showing 5 items of 5 documents

Methyl vinyl ketone+OH and methacrolein+OH oxidation reactions: a master equation analysis of the pressure- and temperature-dependent rate constants.

2006

High-level electronic structure calculations and master equation analyses were carried out to obtain the pressure- and temperature-dependent rate constants of the methyl vinyl ketone+OH and methacrolein+OH reactions. The balance between the OH addition reactions at the high-pressure limit, the OH addition reactions in the fall-off region, and the pressure-independent hydrogen abstractions involved in these multiwell and multichannel systems, has been shown to be crucial to understand the pressure and temperature dependence of each global reaction. In particular, the fall-off region of the OH addition reactions contributes to the inverse temperature dependence of the rate constants in the Ar…

Arrhenius equationAddition reactionHydrogenChemistryOrganic Chemistrychemistry.chemical_elementMethacroleinGeneral ChemistryPhotochemistryHydrogen atom abstractionRedoxCatalysischemistry.chemical_compoundsymbols.namesakeReaction rate constantMethyl vinyl ketonesymbolsChemistry (Weinheim an der Bergstrasse, Germany)
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Enthalpies of formation of isoprene’s major oxidation byproducts

2005

Abstract The theoretical enthalpies of formation ( Δ f H 298 . 15 ∘ ) of methyl vinyl ketone (MVK, CH 2 CHC(O)CH 3 ), methacrolein (MACR, CH 2 C(CH 3 )CHO), and the radical products formed in their corresponding OH radical oxidations have been calculated with DFT (MPW1K/6-31+G(d,p)) and multilevel (MCCM-UT-CCSD(T)//MPW1K/6-31+G(d,p)) methods. The bond dissociation energies ( BDE , DH 298 . 15 0 ) of the H-atoms that can be abstracted from the MVK and MACR molecules, and the C–O forming bonds of the OH addition products are also calculated. The regioselectivity of the global reaction is discussed in terms of bond strength.

Bond strengthGeneral Physics and AstronomyRegioselectivityMethacroleinPhotochemistryBond-dissociation energyMedicinal chemistryStandard enthalpy of formationchemistry.chemical_compoundchemistryMethyl vinyl ketoneMoleculePhysical and Theoretical ChemistryIsopreneChemical Physics Letters
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Theoretical study of the formation reaction of the methyl vinyl ketone: A conformational approach

2005

The formation reaction of both isomers of the methyl vinyl ketone (MVK) from the corresponding alkoxy radicals was investigated by means of theoretical methods based on quantum chemistry. Perturbative unrestricted Moller–Plesset (UMP2) and density functional methods B3LYP and BH and HLYP were used to obtain the stationary points on the potential energy surface. In addition to this, the interconversion reaction between both isomers of the MVK was studied, characterizing the corresponding transition state. A conformational study was done, and the energy and geometry of the stationary points located were analyzed by means of ab initio calculations. © 2005 Wiley Periodicals, Inc. Int J Quantum …

RadicalCondensed Matter PhysicsQuantum chemistryAtomic and Molecular Physics and Opticschemistry.chemical_compoundchemistryComputational chemistryAb initio quantum chemistry methodsMethyl vinyl ketonePotential energy surfaceAlkoxy groupPhysical and Theoretical ChemistryQuantumIsopreneInternational Journal of Quantum Chemistry
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Pressure dependence in the methyl vinyl ketone + OH and methacrolein + OH oxidation reactions: an electronic structure study.

2005

High-level electronic structure calculations were carried out for the study of the reaction pathways in the OH-initiated oxidations of methyl vinyl ketone (MVK) and methacrolein (MACR). For the two conformers of MVK (called synperiplanar and antiperiplanar), the addition channels of OH to the terminal and central carbon atom of the double bond dominate the overall rate constant, whereas the abstraction of the methyl hydrogen atoms has no significant kinetic role. In the case of MACR, only the antiperiplanar conformer is important in its reactivity. In addition, the lower Gibbs free energy barrier for MACR corresponds to the aldehydic hydrogen abstraction reaction, which will be somewhat mor…

chemistry.chemical_classificationDouble bondChemistryHydroxyl RadicalMethacroleinElectronsHydrogen atom abstractionPhotochemistryAtomic and Molecular Physics and OpticsButanonesGibbs free energysymbols.namesakechemistry.chemical_compoundReaction rate constantModels ChemicalAlkane stereochemistryMethyl vinyl ketonesymbolsPressureOrganic chemistryThermodynamicsReactivity (chemistry)Physical and Theoretical ChemistryAcroleinOxidation-ReductionChemphyschem : a European journal of chemical physics and physical chemistry
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ChemInform Abstract: A New Tandem Cross Metathesis-Intramolecular Aza-Michael Reaction for the Synthesis of α,α-Difluorinated Lactams.

2012

Difluorinated amides are treated with methyl vinyl ketone or analogous esters to produce the desired γ- and δ-lactam units including optically active versions.

chemistry.chemical_compoundTandemChemistryIntramolecular forceMethyl vinyl ketoneMichael reactionSalt metathesis reactionOrganic chemistryGeneral MedicineOptically activeMetathesisPyrrole derivativesChemInform
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