Hydroxyl radical piggybacking on hydrogen carbonate

Svend J Knak Jensen, I. Csizmadia

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

The reaction of the hydroxyl radical and the hydrogen carbonate anion is studied computationally. The most stable product is the hydrate of the carbonate radical. Theoretical estimates of the involved thermodynamical functions and activation energies suggest the hydrogen carbonate anion may play a role as a transporter of the hydroxyl radical and a mediator leading to lowering of the oxidative stress.

Original languageEnglish
Pages (from-to)633-637
Number of pages5
JournalChemical Physics Letters
Volume341
Issue number5-6
DOIs
Publication statusPublished - Jun 29 2001

Fingerprint

hydroxyl radicals
Bicarbonates
Hydroxyl Radical
Anions
carbonates
Oxidative stress
Carbonates
hydrogen
Hydrates
anions
transporter
Activation energy
hydrates
activation energy
estimates
products
energy

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Spectroscopy
  • Atomic and Molecular Physics, and Optics

Cite this

Hydroxyl radical piggybacking on hydrogen carbonate. / Jensen, Svend J Knak; Csizmadia, I.

In: Chemical Physics Letters, Vol. 341, No. 5-6, 29.06.2001, p. 633-637.

Research output: Contribution to journalArticle

Jensen, Svend J Knak ; Csizmadia, I. / Hydroxyl radical piggybacking on hydrogen carbonate. In: Chemical Physics Letters. 2001 ; Vol. 341, No. 5-6. pp. 633-637.
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