Reductive Cleavage of Organic Peroxides by Iron Salts and Thiols

Andrew S. Olson, Abigail J. Jameson, Shiva K. Kyasa, Boone W. Evans, Patrick H Dussault

Research output: Contribution to journalArticle

Abstract

Despite the low bond strength of the oxygen-oxygen bond, organic peroxides are often surprisingly resistant to cleavage by nucleophiles and reductants. As a result, achieving decomposition under mild conditions can be challenging. Herein, we explore the reactivity of a selection of peroxides toward thiolates, phenyl selenide, Fe(II) salts, and iron thiolates. Peroxides activated by conjugation, strain, or stereoelectronics are rapidly cleaved at room temperature by thiolate anions, phenylselenide, or Fe(II) salts. Under the same conditions, unhindered dialkyl peroxides are only marginally reactive; hindered peroxides, including triacetone triperoxide and diacetone diperoxide (DADP), are inert. In contrast, all but the most hindered of peroxides are rapidly (<1 min at concentrations down to ∼40 mM) cleaved by mixtures of thiols and iron salts. Our observations suggest the possible intermediacy of strongly reducing complexes that are readily regenerated in the presence of stoichiometric thiolate or hydride. In the case of DADP, an easily prepared explosive of significant societal concern, catalytic amounts of iron and thiol are capable of promoting rapid and complete disproportionation. The availability of inexpensive and readily available catalysts for the mild reductive degradation of all but the most hindered of peroxides could have significant applications for controlled remediation of explosives or unwanted radical initiators.

Original languageEnglish (US)
Pages (from-to)14054-14063
Number of pages10
JournalACS Omega
Volume3
Issue number10
DOIs
StatePublished - Oct 25 2018

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Peroxides
Sulfhydryl Compounds
Iron
Salts
Oxygen
Nucleophiles
Reducing Agents
Remediation
Hydrides
Anions
Negative ions
Availability
Decomposition
Degradation
Catalysts

ASJC Scopus subject areas

  • Chemistry(all)
  • Chemical Engineering(all)

Cite this

Olson, A. S., Jameson, A. J., Kyasa, S. K., Evans, B. W., & Dussault, P. H. (2018). Reductive Cleavage of Organic Peroxides by Iron Salts and Thiols. ACS Omega, 3(10), 14054-14063. https://doi.org/10.1021/acsomega.8b01977

Reductive Cleavage of Organic Peroxides by Iron Salts and Thiols. / Olson, Andrew S.; Jameson, Abigail J.; Kyasa, Shiva K.; Evans, Boone W.; Dussault, Patrick H.

In: ACS Omega, Vol. 3, No. 10, 25.10.2018, p. 14054-14063.

Research output: Contribution to journalArticle

Olson, AS, Jameson, AJ, Kyasa, SK, Evans, BW & Dussault, PH 2018, 'Reductive Cleavage of Organic Peroxides by Iron Salts and Thiols', ACS Omega, vol. 3, no. 10, pp. 14054-14063. https://doi.org/10.1021/acsomega.8b01977
Olson, Andrew S. ; Jameson, Abigail J. ; Kyasa, Shiva K. ; Evans, Boone W. ; Dussault, Patrick H. / Reductive Cleavage of Organic Peroxides by Iron Salts and Thiols. In: ACS Omega. 2018 ; Vol. 3, No. 10. pp. 14054-14063.
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