6533b851fe1ef96bd12a8f47
RESEARCH PRODUCT
On the role of interfacial hydrogen bonds in "on-water" catalysis.
Thomas D. KühneThomas D. KühneKristof KarhanRustam Z. Khaliullinsubject
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 ChemistryQuadricyclanedescription
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 interfaces plays a significantly smaller role in "on-water" catalysis than has been suggested previously.
year | journal | country | edition | language |
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2014-01-01 | The Journal of chemical physics |