CaltechAUTHORS
  A Caltech Library Service

Negative-Ion Photoelectron Spectroscopy, Gas-Phase Acidity, and Thermochemistry of the Peroxyl Radicals CH_3OO and CH_3CH_2OO

Blanksby, Stephen J. and Ramond, Tanya M. and Davico, Gustavo E. and Nimlos, Mark R. and Kato, Shuji and Bierbaum, Veronica M. and Lineberger, W. Carl and Ellison, G. Barney and Okumura, Mitchio (2001) Negative-Ion Photoelectron Spectroscopy, Gas-Phase Acidity, and Thermochemistry of the Peroxyl Radicals CH_3OO and CH_3CH_2OO. Journal of the American Chemical Society, 123 (39). pp. 9585-9596. ISSN 0002-7863. https://resolver.caltech.edu/CaltechAUTHORS:20170407-064628878

[img] PDF - Supplemental Material
See Usage Policy.

85Kb

Use this Persistent URL to link to this item: https://resolver.caltech.edu/CaltechAUTHORS:20170407-064628878

Abstract

Methyl, methyl-d3, and ethyl hydroperoxide anions (CH_3OO-, CD_3OO-, and CH_3CH_2OO-) have been prepared by deprotonation of their respective hydroperoxides in a stream of helium buffer gas. Photodetachment with 364 nm (3.408 eV) radiation was used to measure the adiabatic electron affinities:  EA[CH_3OO, X̃^2A‘‘] = 1.161 ± 0.005 eV, EA[CD_3OO, X̃^2A‘‘] = 1.154 ± 0.004 eV, and EA[CH_3CH_2OO, X̃^2A‘‘] = 1.186 ± 0.004 eV. The photoelectron spectra yield values for the term energies:  ΔE(X̃^2A‘‘−Ã^2A‘)[CH_3OO] = 0.914 ± 0.005 eV, ΔE(X̃^2A‘‘−Ã^2A‘)[CD_3OO] = 0.913 ± 0.004 eV, and ΔE(X̃^2A‘‘−Ã^2A‘)[CH_3CH_2OO] = 0.938 ± 0.004 eV. A localized RO−O stretching mode was observed near 1100 cm^(-1) for the ground state of all three radicals, and low-frequency R−O−O bending modes are also reported. Proton-transfer kinetics of the hydroperoxides have been measured in a tandem flowing afterglow−selected ion flow tube (FA-SIFT) to determine the gas-phase acidity of the parent hydroperoxides: Δ_(acid)G_(298)(CH_3OOH) = 367.6 ± 0.7 kcal mol^(-1), Δ_(acid)G_(298)(CD_3OOH) = 367.9 ± 0.9 kcal mol^(-1), and Δ_(acid)G_(298)(CH_3CH_2OOH) = 363.9 ± 2.0 kcal mol^(-1). From these acidities we have derived the enthalpies of deprotonation: Δ_(acid)H_(298)(CH_3OOH) = 374.6 ± 1.0 kcal mol^(-1), Δ_(acid)H_(298)(CD_3OOH) = 374.9 ± 1.1 kcal mol^(-1), and Δ_(acid)H_(298)(CH_3CH_2OOH) = 371.0 ± 2.2 kcal mol^(-1). Use of the negative-ion acidity/EA cycle provides the ROO−H bond enthalpies: DH_(298)(CH_3OO−H) = 87.8 ± 1.0 kcal mol^(-1), DH_(298)(CD_3OO−H) = 87.9 ± 1.1 kcal mol^(-1), and DH_(298)(CH_3CH_2OO−H) = 84.8 ± 2.2 kcal mol^(-1). We review the thermochemistry of the peroxyl radicals, CH_3OO and CH_3CH_2OO. Using experimental bond enthalpies, DH_(298)(ROO−H), and CBS/APNO ab initio electronic structure calculations for the energies of the corresponding hydroperoxides, we derive the heats of formation of the peroxyl radicals. The “electron affinity/acidity/CBS” cycle yields Δ_fH_(298)[CH_3OO] = 4.8 ± 1.2 kcal mol^(-1) and Δ_fH_(298)[CH_3CH_2OO] = −6.8 ± 2.3 kcal mol^(-1).


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1021/ja010942jDOIArticle
http://pubs.acs.org/doi/abs/10.1021/ja010942jPublisherArticle
http://pubs.acs.org/doi/suppl/10.1021/ja010942jRelated ItemSupporting Information
ORCID:
AuthorORCID
Okumura, Mitchio0000-0001-6874-1137
Additional Information:© 2001 American Chemical Society. Received 12 April 2001. Published online 7 September 2001. Published in print 1 October 2001. S.J.B., M.R.N., and G.B.E. are pleased to acknowledge support by the Chemical Physics Program, United States Department of Energy (DE-FG02-87ER13695); G.B.E. is a Fellow of the J. S. Guggenheim Foundation. W.C.L. is pleased to ackowledge support from the National Science Foundation (CHE 9703486). V.M.B. and S.K. gratefully acknowledge support from the National Science Foundation (CHE 9734867). M.O. is pleased to acknowledge JILA for the award of a Visiting Fellowship and the National Science Foundation (grant CHE 9700610). The GAUSSIAN98 calculations were carried out in part with a cluster of RSC-6000 digital computers supported by NSF (CHE 9412767) and in part using the facilities of the National Center for Supercomputing Application (CE980028N). We thank Prof. Tarek Sammakia for advice and assistance with the preparation of the methyl and ethyl hydroperoxides and Prof. Chuck DePuy for useful discussions.
Funders:
Funding AgencyGrant Number
Department of Energy (DOE)DE-FG02-87ER13695
NSFCHE-9703486
NSFCHE-9734867
NSFCHE-9700610
NSFCHE-9412767
Issue or Number:39
Record Number:CaltechAUTHORS:20170407-064628878
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20170407-064628878
Official Citation:Negative-Ion Photoelectron Spectroscopy, Gas-Phase Acidity, and Thermochemistry of the Peroxyl Radicals CH3OO and CH3CH2OO Stephen J. Blanksby, Tanya M. Ramond, Gustavo E. Davico, Mark R. Nimlos, Shuji Kato, Veronica M. Bierbaum, W. Carl Lineberger, G. Barney Ellison, and Mitchio Okumura Journal of the American Chemical Society 2001 123 (39), 9585-9596 DOI: 10.1021/ja010942j
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:75817
Collection:CaltechAUTHORS
Deposited By: Ruth Sustaita
Deposited On:07 Apr 2017 14:17
Last Modified:03 Oct 2019 16:54

Repository Staff Only: item control page