Search results for "Hammett equation"

showing 3 items of 3 documents

Organocatalysts Fold to Generate an Active Site Pocket for the Mannich Reaction

2017

Catalysts containing urea, thiourea and tertiary amine groups fold into a three-dimensional organized structure in solution both in the absence as well as in the presence of substrates or substrate analogues, as indicated by solution NMR and computational studies. These foldamer catalysts promote Mannich reactions with both aliphatic and aromatic imines and malonate esters. Hammett plot and secondary kinetic isotope effects provide evidence for the C-C bond forming event as the turnoverlimiting step of the Mannich reaction. Computational studies suggest two viable pathways for the C-C bond formation step, differing in the activation modes of the malonate and imine substrates. The results sh…

inorganic chemicalsorganocatalysis bifunctional cooperativity mechanism kinetics computationsTertiary aminecooperativityIminemechanism010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundHammett equationMannich reactionOrganic chemistryorganocatalysista116Mannich reactionbiology010405 organic chemistryChemistryFoldamerActive siteGeneral ChemistryCombinatorial chemistrycomputations0104 chemical sciencesbifunctionalMalonatekineticsOrganocatalysisbiology.protein
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Oxygenation of Alkane C−H Bonds with Methyl(trifluoromethyl)dioxirane:  Effect of the Substituents and the Solvent on the Reaction Rate

2005

[Chemical reaction: See text] The mechanism of the oxygenation of alkane C-H bonds with methyl(trifluoromethyl)dioxirane (1a) is studied through the effect of the substituent and solvent on the rate of oxygenation of 2-substituted adamantanes (2). The results suggest a remarkable electron deficiency at the reacting carbon atom in the transition state leading to the regular oxygenation products. The linearity of the Hammett plot reveals that the reaction mechanism does not change within a range of 0.15-0.67 units of sigma(I). A change in the solvent does not affect the distribution of the products, indicating a through-bond transmission of the substituent effect as the origin of the deactiva…

Reaction mechanismTrifluoromethylOrganic ChemistrySubstituentGeneral MedicineElectron deficiencyPhotochemistryMedicinal chemistryChemical reactionReaction ratechemistry.chemical_compoundHammett equationchemistryDioxiraneSolvent effectsThe Journal of Organic Chemistry
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Kinetik und Radikalausbeute beim Zerfall tertiärer Hyponitrite

1971

Der thermische Zerfall von Dicumylhyponitrit (1a) ist eine Reaktion erster Ordnung mit einer Aktivierungsenthalpie von 27.3 keal/Mol und einer Aktivierungsentropie von 8.5 cal/Mol·Grad in Isooctan. Die Radikalausbeute fur 1a betragt 84%, fur Di-tert.-butylhyponitrit 92%. Die Zerfallskonstanten substituierter Dicumylhyponitrite gehorchen bei Verwendung der σ+-Werte der Hammett-Beziehung mit σ=+ +0.34. Kinetic and Radical Efficiency for the Decomposition of Tertiary Hyponitrites The thermal decomposition of dicumylhyponitrite (1a) is a first order reaction with an activation enthalpy of 27.3 kcal/mole and an activation entropy of 8.5 e. u. in isooctane. The efficiency of radical formation is …

Inorganic ChemistryReaction rate constantHammett equationChemistryThermal decompositionFirst-order reactionEnthalpyPhysical chemistryActivation entropyKinetic energyDecompositionChemische Berichte
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