Related Experiment Video
Updated: Aug 7, 2026

Reductive Electropolymerization of a Vinyl-containing Poly-pyridyl Complex on Glassy Carbon and Fluorine-doped Tin Oxide Electrodes
Published on: January 30, 2015
Products and reaction sequences in tetrahydrofuran exposed to low-energy electrons
Claudia Jäggle1, Petra Swiderek, Simon-Philippe Breton
1Universität Bremen, Fachbereich 2 (Chemie/Biologie), Leobener Strasse/NW 2, Postfach 330440, 28334 Bremen, Germany.
Abstract:
Electron-stimulated reactions in solid films of tetrahydrofuran (THF), condensed on Kr spacers deposited on a Pt substrate, or directly onto the substrate, were induced and monitored simultaneously with use of high-resolution electron-energy-loss spectroscopy in the ranges of vibrational and electronic excitations. The spectra of the molecular films obtained after a certain time of exposure to electrons at incident energies of 14 and 15.5 eV were analyzed and different products were identified. Besides an aldehyde, which is the main product, olefins, conjugated olefins, as well as CO were identified. Closer investigation of the reactions of propionaldehyde, as a model aldehyde, demonstrates that CO appears in THF as a secondary product (i.e., from the intermediate aldehyde). On the basis of the cross sections for the formation of an aldehyde from THF, of CO from propionaldehyde, and for the loss of propionaldehyde under electron impact, the reaction sequences were evaluated with the help of a kinetic model. This analysis suggests that some CO could also be formed directly from THF (i.e., without involvement of an intermediate aldehyde).
Related Concept Videos
Thermal and Photochemical Electrocyclic Reactions: Overview
Energy Diagrams, Transition States, and Intermediates
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
Deactivation Processes: Jablonski Diagram
Radical Reactivity: Overview
Fast Reactions

