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The Infrared Spectrum of HOOH+ Trapped in Solid Neon

Published

Author(s)

Warren E. Thompson, Catherine L. Lugez, Marilyn E. Jacox

Abstract

When a Ne:H2O2 mixture is codeposited at 4.3 K with a beam of neon atoms that have been excited in a microwave discharge, three new, photosensitive absorptions appear which can be assigned to the three infrared-active fundamentals of trans-HOOH+. When the Ne:H2O2 deposition system is pretreated with the vapors of D2O, the product absorptions include new peaks which can be attributed to vibrational fundamentals of trans-HOOD+ and trans-DOOD+. Density functional calculations of the vibrational fundamentals of the three hydrogen peroxide cation isotopologues support the proposed assignments. Broad, photosensitive product absorptions also appear near the positions of vibrational transitions of O3-, and may be contributed by a weakly bound complex of that species with H2O.
Citation
Journal of Chemical Physics
Volume
137
Issue
14

Keywords

HOOH, HOOH cation, infrared spectrum, isotopic substitution, neon matrix, O3 anion, photoionization

Citation

Thompson, W. , Lugez, C. and Jacox, M. (2012), The Infrared Spectrum of HOOH+ Trapped in Solid Neon, Journal of Chemical Physics, [online], https://doi.org/10.1063/1.4757389, https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=911738 (Accessed March 18, 2024)
Created October 11, 2012, Updated October 12, 2021