Search results for "Quadricyclane"

showing 2 items of 2 documents

On the role of interfacial hydrogen bonds in "on-water" catalysis.

2014

Numerous experiments have demonstrated that many classes of organic reactions exhibit increased reaction rates when performed in heterogeneous water emulsions. Despite enormous practical importance of the observed "on-water" catalytic effect and several mechanistic studies, its microscopic origins remains unclear. In this work, the second generation Car-Parrinello molecular dynamics method is extended to self-consistent charge density-functional based tight-binding in order to study "on-water" catalysis of the Diels-Alder reaction between dimethyl azodicarboxylate and quadricyclane. We find that the stabilization of the transition state by dangling hydrogen bonds exposed at the aqueous inte…

Chemical Physics (physics.chem-ph)Aqueous solutionHydrogen bondGeneral Physics and AstronomyFOS: Physical sciencesCondensed Matter - Soft Condensed MatterPhotochemistryCatalysisReaction rateMolecular dynamicschemistry.chemical_compoundchemistryOrganic reactionBiological Physics (physics.bio-ph)Physics - Chemical PhysicsSoft Condensed Matter (cond-mat.soft)Density functional theoryPhysics - Biological PhysicsPhysical and Theoretical ChemistryQuadricyclaneThe Journal of chemical physics
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Understanding the Participation of Quadricyclane as Nucleophile in Polar [2σ + 2σ + 2π] Cycloadditions toward Electrophilic π Molecules

2008

The formal [2sigma + 2sigma + 2pi] cycloaddition of quadricyclane, 1, with dimethyl azodicarboxylate, 2, in water has been studied using DFT methods at the B3LYP/6-31G** and MPWB1K/6-31G** levels. In the gas phase, the reaction of 1 with 2 has a two-stage mechanism with a large polar character and an activation barrier of 23.2 kcal/mol. Inclusion of water through a combined discrete-continuum model changes the mechanism to a two-step model where the first nucleophilic attack of 1 to 2 is the rate-limiting step with an activation barrier of 14.7 kcal/mol. Analysis of the electronic structure of the transition state structures points out the large zwitterionic character of these species. A DF…

Reaction ratechemistry.chemical_compoundReaction mechanismchemistryNucleophileComputational chemistryStereochemistryZwitterionOrganic ChemistryElectrophileQuadricyclaneSolvent effectsCycloadditionThe Journal of Organic Chemistry
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