Related Experiment Video
Updated: Jul 14, 2026

Hyperpolarized Xenon for NMR and MRI Applications
Published on: September 6, 2012
Energetics and volume changes in electron attachment to pyrazine in supercritical xenon
Richard A Holroyd1, Jack M Preses, Masaru Nishikawa
1Chemistry Department, Brookhaven National Laboratory, Upton, New York 11973, USA.
Abstract:
The attachment of electrons to pyrazine occurs reversibly over a wide range of pressures at and above room temperature in supercritical xenon. The rate constant for attachment increases with pressure at low pressures, passes through a maximum, and levels off at values of 1-3x10(12) m(-1) s(-1) at high pressure. The activation volumes for attachment (DeltaVa*) are quite small but show maxima near the compressibility maxima. In contrast, DeltaVa* is always negative for this reaction in sc-ethane and exhibits minima near the compressibility maxima. The rate constants for electron detachment change little with pressure but increase with temperature. Activation volumes for detachment are small. To explain the small volume change observed for this reaction, it is proposed that at the higher pressures clustering around the neutral pyrazine is comparable to that around the ion; i.e., the partial molar volumes are comparable. The free energy change (DeltaGr) of this reaction decreases between 40 and 60 bar and then is fairly constant at higher pressures. The dependence of DeltaGr on pressure is consistent with clustering around the neutral pyrazine at higher pressure. Also, the electron affinity of the clusters, pyrazineXen, increases with n to a few tenths of an eV.
Related Concept Videos
Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control
π Electron Effects on Chemical Shift: Overview
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.
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds
Thermal and Photochemical Electrocyclic Reactions: Overview
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation

