Related Experiment Video
Updated: Sep 23, 2025

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
Published on: July 27, 2022
Electron paramagnetic resonance spectroscopic studies of the electron transfer reaction of Hantzsch ester and a
K Sebők-Nagy1, D Rózsár2, L G Puskás2
1Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences Temesvári Krt. 62 H-6726 Szeged Hungary pali.tibor@brc.mta.hu.
Abstract:
The oxidation of Hantzsch ester by a pyrylium cation takes place via electron-proton-electron transfer. The reaction was investigated with EPR spectroscopy using TEMPO and DMPO for inhibition and spin trapping, respectively, of the radicals appearing during the reaction. The present in-depth EPR study of the radical reactions of a NADH analogue indicate a complex electron transfer mechanism in the title reaction.
More Related Videos
Related Concept Videos
Acid Halides to Esters: Alcoholysis
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals
Thermal and Photochemical Electrocyclic Reactions: Overview
π Electron Effects on Chemical Shift: Overview

