Search results for "Reactivity"

showing 10 items of 880 documents

A theoretical and experimental study of the formation mechanism of 4-X-chalcones by the Claisen–Schmidt reaction

2000

Abstract A theoretical and experimental study on the formation of 4-X-chalcones (X=H, Cl, F, OCH3, N(CH3)2) was carried out by the Claisen–Schmidt reaction. The influence of pH and temperature was analyzed. Under the adopted experimental conditions 4-X-chalcones were the only reaction products. In the theoretical study, the thermodynamic magnitudes and the reactivity indexes calculated with the AM1 method were used. The mechanism of Nayak and Rout was analyzed critically and a new mechanism was proposed, characterized by: (1) rapid nucleophilic attack of the catalyst (OH−) on the carbon atom of the methyl group of acetophenone; (2) attacks of the acetophenonate ion on the carbon atom of the…

ChemistryCondensed Matter PhysicsBiochemistryReaction rateElimination reactionchemistry.chemical_compoundReaction rate constantNucleophileComputational chemistrySchmidt reactionReactivity (chemistry)Physical and Theoretical ChemistryEquilibrium constantMethyl groupJournal of Molecular Structure: THEOCHEM
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Understanding the mechanism of the Povarov reaction. A DFT study

2014

The molecular mechanism of the Povarov reaction in acetonitrile has been studied at the MPWB1K/6-311G** level of theory. This reaction follows a domino process that comprises two sequential reactions: (i) a Lewis acid catalysed aza-Diels–Alder (A-DA) reaction between a N-aryl imine and a nucleophilic ethylene yielding a formal [4 + 2] cycloadduct; (ii) a stepwise 1,3-hydrogen shift at this intermediate affording the final tetrahydroquinoline. At this computational level, the Lewis acid catalysed A-DA reaction presents a two-step mechanism as a consequence of the large stabilisation of the corresponding zwitterionic intermediate. Our study allows establishing that the N-aryl substituent has …

ChemistryGeneral Chemical EngineeringImineGeneral ChemistryPhotochemistryReaction rateElimination reactionchemistry.chemical_compoundNucleophileComputational chemistryStepwise reactionReactivity (chemistry)Povarov reactionLewis acids and basesRSC Advances
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Electrochemical synthesis on boron-doped diamond

2012

Abstract Boron-doped diamond (BDD) is a novel and innovative electrode material. In protic media and particular aqueous electrolytes BDD exhibits a large over potential for the evolution of molecular hydrogen and oxygen. The large chemical window allows a variety of electrochemical conversions to be conducted. The anodic process treatment generates oxyl species directly which are known to be extremely reactive. Usually, the electrochemical mineralization of the organic components in the electrolyte occurs. However, with control of the reactivity of these intermediates the use in electroorganic synthesis can be realized. Until today mostly anodic conversions have been studied at BDD. Since h…

ChemistryGeneral Chemical EngineeringRadicalInorganic chemistrySupramolecular chemistrySubstrate (chemistry)DiamondElectrolyteengineering.materialElectrochemistryCombinatorial chemistrySolventElectrochemistryengineeringReactivity (chemistry)Electrochimica Acta
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A molecular electron density theory (MEDT) study of the role of halogens (X2= F2, Cl2, Br2and I2) on the aza-Michael-addition reactions

2020

Using the Molecular Electron Density Theory (MEDT), a set of uncatalyzed and X2 molecule-catalyzed (X2 = F2, Cl2, Br2, or I2) aza Michael addition reactions (aza-MARs) between pyrrolidine (PYR) and methyl acrylate (MA) have been studied in the gas phase and in dichloromethane (DCM) medium from the kinetics and molecular mechanism aspects. Analysis of the conceptual DFT reactivity indices indicates that the coordination of the X2 molecules to the oxygen of the MA's carbonyl group increases both the softness and the electrophilic character of MA, thus explaining the catalytic role of the X2 molecules. The nucleophilic attack of the nitrogen of PYR on the MA's β conjugated carbon is the rate-d…

ChemistryGeneral ChemistryTautomerMedicinal chemistryCatalysisCatalysischemistry.chemical_compoundReaction rate constantNucleophileMaterials ChemistryMichael reactionReactivity (chemistry)Lewis acids and basesMethyl acrylateNew Journal of Chemistry
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Oxidomolybdenum(IV), ‐(V), ‐(VI) Complexes with Relevance to Molybdenum Enzymes: Oxygen Atom Transfer, Redox Chemistry and EPR Spectroscopy

2010

The cis-dioxidomolybdenum(VI) complex Mo(NN′)2O2 (1) [(NN′) = N-(4-hydroxyphenyl)-2-pyrrolatocarbaldimine] transfers one oxygen atom to phosphanes PMenPh3–n (n = 0–3) to give quantitatively the respective phosphane oxides OPMenPh3–n (OAT, oxygen atom transfer). The kinetics of these OAT reactions has been investigated spectrophotometrically. When offering excess PMenPh3–n (n = 1–3), oxido(phoshane)molybdenum(IV) complexes Mo(NN′)2O(PMenPh3–n) 5a–5c are isolated and characterized by multinuclear NMR spectroscopy (1H, 13C, 31P, 15N), IR spectroscopy, UV/Vis spectroscopy and mass spectrometry. The redox chemistry of the molybdenum(IV) complexes 5a–5c and of molybdenum(VI) complex 1 has been pr…

ChemistryInorganic chemistryInfrared spectroscopychemistry.chemical_elementProtonationNuclear magnetic resonance spectroscopyRedoxlaw.inventionInorganic ChemistrylawMolybdenumPolymer chemistryReactivity (chemistry)Electron paramagnetic resonanceSpectroscopyEuropean Journal of Inorganic Chemistry
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Reactions of Carbonyl Compounds in Basic Solutions. Part 351: The Alkaline Hydrolysis and Reactivity – Structure – Spectra Correlations of (Z)-4-(Sub…

2002

The kinetics of the alkaline hydrolysis and the configuration, conformation and electronic structure were studied using IR, NMR spectroscopy, X-ray analysis and AM1 theoretical calculations for a series of (Z)-4-(substituted benzylidene)-2-phenyl-4H-oxazol-5-ones (1) and compared with analogous results reported for (E)-4-benzylidene-2-phenyl-4H-furan-5-ones (5) and related compounds.

ChemistryKineticsOrganic chemistryReactivity (chemistry)General ChemistryElectronic structureNuclear magnetic resonance spectroscopyAlkaline hydrolysis (body disposal)Medicinal chemistrySpectral lineJournal of Chemical Research
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Synthesis, reactivity and structures of ruthenium carbonyl clusters with telluride and hydride ligands

2002

The reaction of [Cp* 2 Nb(Te 2 H)] ( 1 ) (Cp*=C 5 Me 5 ) with [Ru 3 (CO) 12 ] in boiling toluene gave [Ru 3 (μ 2 -H) 2 (CO) 9 (μ 3 -Te)] ( 2 ), [Ru 6 (μ 3 -H)(CO) 15 (μ 3 -Te) 3 ][Cp* 2 Nb(CO) 2 ] ( 3 ) and [Ru 5 (μ 2 -H)(CO) 14 (μ 4 -Te)][Cp* 2 Nb(CO) 2 ] ( 4 ) along with already known [Ru 4 (CO) 11 (μ 4 -Te) 2 ] ( 5 ). Complexes 2 – 4 were analytically and spectroscopically characterized and X-ray diffraction analyses of 3 and 4 were carried out. The anion of 3 is built up of a triangular hexametallic core of C 3 v symmetry, in which the central Ru 3 triangle, being bridged by a μ 3 -H ligand, is composed of three corner-linked Ru 3 Te tetrahedra. The main structural feature of the anion …

ChemistryLigandOrganic ChemistryCluster chemistrychemistry.chemical_elementCrystal structureBiochemistrySquare pyramidal molecular geometryRutheniumInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronTellurideMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryJournal of Organometallic Chemistry
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Synthesis, Molecular Structure, and Reactivity of Rhodium(I) Complexes with Diazoalkanes and Related Substrates as Ligands

2003

A series of (diazoalkane)rhodium(I) compounds of the general composition trans-[RhCl(N2CRR‘)(PiPr3)2] with R = R‘ = Ph, p-C6H4Me, p-C6H4Cl and R = Ph, R‘ = p-C6H4Me, o-C6H4Me, CH3, CH2Ph, CF3 has been prepared from the dimer [RhCl(PiPr3)2]2 (1) and the diazoalkane. This preparative route has also been extended to complexes in which the N2C unit(s) of 1,4-C6H4{C(Ph)N2}2, 9-diazofluorene, 9,10-anthraquinone-9-diazide, and 3-methyl-1,4-naphthoquinone-1-diazide is (are) linked to a 14-electron [RhCl(PiPr3)2] fragment. While C(CO2Et)2N2 behaves as expected and affords upon treatment with 1 the complex trans-[RhCl{N2C(CO2Et)2}(PiPr3)2), CH(CO2Et)N2 reacts with the same starting material to give t…

ChemistryLigandStereochemistryDimerOrganic Chemistrychemistry.chemical_elementMedicinal chemistryRhodiumInorganic Chemistrychemistry.chemical_compoundMoleculeReactivity (chemistry)Physical and Theoretical ChemistryDerivative (chemistry)Organometallics
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Structurally simple complexes of CO2

2015

The ability to bind CO2 through the formation of low-energy, easily-broken, bonds could prove invaluable in a variety of chemical contexts. For example, weak bonds to CO2 would greatly decrease the cost of the energy-intensive sorbent-regeneration step common to most carbon capture technologies. Furthermore, exploration of this field could lead to the discovery of novel CO2 chemistry. Reduction of complexed carbon dioxide might generate chemical feedstocks for the preparation of value-added products, particularly transportation fuels or fuel precursors. Implementation on a large scale could help to drastically reduce CO2 concentrations in the atmosphere. However, literature examples of weak…

ChemistryMetals and AlloysGeneral ChemistryCombinatorial chemistryCatalysisFrustrated Lewis pairSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAdductMetalchemistry.chemical_compoundvisual_artMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumOrganic chemistryReactivity (chemistry)Amine gas treatingCarbeneChemical Communications
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N-benzoylindole-2,3-quinodimethane: Diels-Alder reactivity and synthetic applications for [b]annellated indoles

1991

Abstract The Diels-Alder reactivity of in situ generated N -benzoylindole-2,3-quinodimethane has been expanded considerably to include reactions with carbon- and hetero-dienophiles which furnish a variety of [ b ]annellated indoles as well as functionalized and annellated carbazoles. The frontier molecular orbital theory was found to be a useful model for the prediction of the experimental results under consideration of reactivity aspects.

ChemistryOrganic ChemistryDrug DiscoveryDiels alderOrganic chemistryFrontier molecular orbital theoryReactivity (chemistry)BiochemistryCycloadditionQuinoneTetrahedron
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