Search results for "Associative substitution"

showing 4 items of 4 documents

Hydrolysis of Phosphotriesters: A Theoretical Analysis of the Enzymatic and Solution Mechanisms

2012

A theoretical study on the alkaline hydrolysis of paraoxon, one of the most popular organophosphorus pesticides, in aqueous solution and in the active site of Pseudomonas diminuta phosphotriesterase (PTE) is presented. Simulations by means of hybrid quantum mechanics/molecular mechanics (QM/MM) potentials show that the hydrolysis of paraoxon takes place through an A(N)D(N) or associative mechanism both in solution and in the active site of PTE. The results correctly reproduce the magnitude of the activation free energies and can be used to rationalize the observed kinetic isotope effects (KIEs) for the hydrolysis of paraoxon in both media. Enzymatic hydrolysis of O,O-diethyl p-chlorophenyl …

StereochemistryReaction mechanismsMolecular dynamicsParaoxonCatalysisEnzyme catalysisHydrolysisComputational chemistryCatalytic DomainPseudomonasEnzymatic hydrolysismedicinebiologyParaoxonLigandChemistryHydrolysisOrganic ChemistryLeaving groupActive siteEnzyme catalysisGeneral ChemistryAssociative substitutionModels TheoreticalSolutionsZincPhosphoric Triester Hydrolasesbiology.proteinQuantum chemistrymedicine.drugChemistry - A European Journal
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Der austausch des cyclopentadienylliganden im methylcyclopentadienylmangan(I)tricarbonyl. Untersuchungen zur konkurrierenden komplexbildung mit methy…

1981

Abstract Exchange of the cyclopentadienyl ligand in methylcyclopentadienylmanganese(I) tricarbonyl with methyl-substituted benzenes is catalysed by AlCl 3 + HCl and leads to the cations [arene-Mn(CO) 3 ] + . The methylbenzenes isomerize and disproportionate during the reaction. The distribution of the arenes between the solution and the complex ions has been determined. The different complexing abilities of the arenes lead to the proposal of an associative mechanism for the ligand exchange.

Inorganic ChemistryCyclopentadienyl complexChemistryStereochemistryLigandOrganic ChemistryMaterials ChemistryAssociative substitutionPhysical and Theoretical ChemistryBiochemistryMedicinal chemistryComplex ionsJournal of Organometallic Chemistry
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Structural and Theoretical Basis for Ligand Exchange on Thiolate Monolayer Protected Gold Nanoclusters

2012

Ligand exchange reactions are widely used for imparting new functionality on or integrating nanoparticles into devices. Thiolate-for-thiolate ligand exchange in monolayer protected gold nanoclusters has been used for over a decade; however, a firm structural basis of this reaction has been lacking. Herein, we present the first single-crystal X-ray structure of a partially exchanged Au(102)(p-MBA)(40)(p-BBT)(4) (p-MBA = para-mercaptobenzoic acid, p-BBT = para-bromobenzene thiol) with p-BBT as the incoming ligand. The crystal structure shows that 2 of the 22 symmetry-unique p-MBA ligand sites are partially exchanged to p-BBT under the initial fast kinetics in a 5 min timescale exchange reacti…

Models Molecularchemistry.chemical_classificationta114LigandMetal NanoparticlesBridging ligandGeneral ChemistryAssociative substitutionCrystal structureCrystallography X-RayLigandsBiochemistryArticleCatalysisNanoclustersCrystallographyColloid and Surface ChemistrychemistryMonolayerSolventsThiolThermodynamicsDensity functional theoryGoldJournal of the American Chemical Society
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Electrochemical and DFT studies of the oxidative decomposition of the trihydride complexes Cp*M(dppe)H3 (M = Mo, W) in acetonitrile

2006

International audience; A detailed electrochemical study of the oxidative decomposition of the trihydride complexes Cp*M(dppe)H3 (M = Mo, W) in acetonitrile is presented. For the Mo complex, the decomposition occurs by four different pathways involving classical and non-classical tautomers, whereas only the classical form is accessible for the W derivative. Each of the decomposition pathways has been quantitatively assessed by analyses of the linear sweep voltammograms. In addition to the previously established (B. Pleune, D. Morales, R. Meunier-Prest, P. Richard, E. Collange, J. C. Fettinger and R. Poli, J. Am. Chem. Soc., 1999, 121, 2209–2225) deprotonation, disproportionation, and H2 red…

StereochemistryDisproportionation010402 general chemistryElectrochemistry01 natural sciencesMedicinal chemistryDFTCatalysisReductive eliminationTungstenchemistry.chemical_compoundDeprotonationComplexMaterials Chemistrypentamethylcyclopentadienyl[CHIM.COOR]Chemical Sciences/Coordination chemistryAcetonitrileComputingMilieux_MISCELLANEOUSMolybdenumPhenylphosphinoethane010405 organic chemistryChemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryGeneral ChemistryAssociative substitutionRate-determining stepTautomer0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryTrihydridoPentamethylcyclopentadienyl ligand
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