Accessing the Free Energy Profile of a Ring Closure in a Proline-Catalyzed Reaction Using a Reactive Force Field

Pierre Hubin, Denis Jacquemin, Laurence Leherte, Daniel P. Vercauteren

Résultats de recherche: Contribution à un journal/une revueArticle

Résumé

The free energy profile of a ring closure involving a carboxylate and an iminium functional group in a proline-derived compound is determined by applying the adaptive biasing force scheme along molecular dynamics simulations. As the reaction considered implies the formation of a covalent bond, the system is modeled with a reactive force field (FF), namely ReaxFF. The impact of the surrounding water molecules on the reaction mechanism is investigated in detail using three FF models for the water molecules. In particular, a hybrid reactive/non-reactive FF is used to assess explicit solvent effects while avoiding solute–solvent reactions. Combined with existing experimental observations, our results provide an explanation for the role of water molecules in the proline-catalyzed aldol reaction, which is one of the hallmark reactions in organocatalysis.

langue originaleAnglais
Numéro d'article16
Pages (de - à)1-10
Nombre de pages10
journalTheoretical Chemistry Accounts
Volume135
Numéro de publication1
Les DOIs
Etat de la publicationPublié - 1 janv. 2016

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    Investigation of proline-catalyzed aldol reactions using a reactive force field

    HUBIN, P., Vercauteren, D. & Jacquemin, D.

    1/10/121/10/16

    Projet: Projet de thèse

    PAI n°P7/05 - FS2: Systèmes supramoléculaires fonctionnels (PAI P7/05)

    CHAMPAGNE, B., De Vos, D., Van der Auweraer, M., Jérôme, C., Lazzaroni, R., Marin, G., Jonas, A., Du Prez, F., Vanderzande, D., Van Tendeloo, G., Van Speybroeck, V., NENON, S. & STAELENS, N.

    1/04/1230/09/17

    Projet: Recherche

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  • Thèses de l'étudiant

    Investigation of proline-catalyzed aldol reactions using a reactive force field

    Author: Hubin, P., 26 oct. 2016

    Superviseur: Vercauteren, D. (Promoteur), Jacquemin, D. (Personne externe) (Copromoteur), Champagne, B. (Président), Harvey, J. (Personne externe) (Jury), Lanners, S. (Jury) & Hénin, J. (Personne externe) (Jury)

    Thèse de l'étudiant: Doc typesDocteur en Sciences

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