Related Experiment Video
Updated: May 23, 2025

Isotopic Effect in Double Proton Transfer Process of Porphycene Investigated by Enhanced QM/MM Method
Published on: July 19, 2019
Concerted proton electron transfer or hydrogen atom transfer? an unequivocal strategy to discriminate these
Davide Zeppilli1, Laura Orian1,2
1Dipartimento di Scienze Chimiche, Università degli Studi di Padova, Via Marzolo 1, 35131 Padova, Italy. laura.orian@unipd.it.
Abstract:
Concerted proton electron transfer (CPET) and hydrogen atom transfer (HAT) are two important mechanisms in many fields of chemistry, which are characterized by the transfer of one proton and one electron. The distinction between these mechanisms may be challenging in several reactions; thus, different computational methods have been developed for this purpose. In this work, we present a computational strategy to distinguish the two mechanisms, rationalizing the factors controlling the reactivity in four different model reactions. Fist, the transition state SOMO (singly occupied molecular orbital) is visualized, presenting all the limits and ambiguities of this analysis. Then, the electron flow along the reaction path is evaluated through the intrinsic bond orbitals (IBOs); this analysis allows to describe correctly the mechanism of each reaction in agreement with previous studies. Furthermore, some structural modifications are applied to the transition state of each system and the energetic differences are rationalized in the framework of the activation strain analysis to understand the geometrical and electronic factors governing the reactivity and the selection of CPET or HAT mechanism. Lastly, the effect of the donor-acceptor distance is evaluated. It emerges that a combined computational analysis is crucial to understand not only the distinction between the two mechanisms, but also the molecular reasons why one mechanism is operative in a specific reaction.
More Related Videos
10:52Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics
Published on: April 12, 2019
10:03Proton Transfer and Protein Conformation Dynamics in Photosensitive Proteins by Time-resolved Step-scan Fourier-transform Infrared Spectroscopy
Published on: June 27, 2014
Related Concept Videos
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
Double Resonance Techniques: Overview
Spin decoupling is usually achieved by...
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Proton (¹H) NMR: Chemical Shift
Absorption signals of all the protium nuclei...
¹H NMR Chemical Shift Equivalence: Enantiotopic and Diastereotopic Protons
In chiral compounds such as 2-butanol, replacing the methylene hydrogens at C3 produces a pair of...