Dual roles for potassium hydride in haloarene reduction : CSNAr and SET reduction via organic electron donors formed in benzene
Barham, Joshua P. and Dalton, Samuel E. and Allison, Mark and Nocera, Giuseppe and Young, Allan and John, Matthew P. and McGuire, Thomas and Campos, Sébastien and Tuttle, Tell and Murphy, John A. (2018) Dual roles for potassium hydride in haloarene reduction : CSNAr and SET reduction via organic electron donors formed in benzene. Journal of the American Chemical Society, 140 (36). pp. 11510-11518. ISSN 1520-5126 (https://doi.org/10.1021/jacs.8b07632)
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Abstract
Potassium hydride behaves uniquely and differently than sodium hydride towards aryl halides. Its reactions with a range of haloarenes, including designed 2,6-dialkylhaloarenes, were studied in THF and in benzene. In THF, evidence supports concerted nucleophilic aromatic substitution, CSNAr, and the mechanism originally proposed by Pierre et al. is now validated through DFT studies. In benzene, besides this pathway, strong evidence for single electron transfer chemistry is reported. Experimental observations and DFT studies lead us to propose organic super electron donor generation to initiate BHAS (base-promoted homolytic aromatic substitution) cycles. Organic donor formation originates from deprotonation of benzene by KH; attack on benzene by the resulting phenylpotassium generates phenylcyclohexadienylpotassium that can undergo (i) deprotonation to form an organic super electron donor or (ii) hydride loss to afford biphenyl. Until now, BHAS reactions have been triggered by reaction of a base, MOtBu (M = K, Na), with many different types of organic additive, all containing heteroatoms (N or O or S) that enhance their acidity and place them within range of MOtBu as a base. This paper shows that with the stronger base, KH, even a hydrocarbon (benzene) can be converted into an electron-donating initiator.
ORCID iDs
Barham, Joshua P. ORCID: https://orcid.org/0000-0003-1675-9399, Dalton, Samuel E. ORCID: https://orcid.org/0000-0001-7806-247X, Allison, Mark ORCID: https://orcid.org/0000-0001-5597-7175, Nocera, Giuseppe ORCID: https://orcid.org/0000-0002-6640-7247, Young, Allan ORCID: https://orcid.org/0000-0002-1525-4703, John, Matthew P., McGuire, Thomas, Campos, Sébastien, Tuttle, Tell and Murphy, John A.;-
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Item type: Article ID code: 65217 Dates: DateEvent17 August 2018Published17 August 2018Published Online17 August 2018AcceptedSubjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry
Technology and Innovation Centre > BionanotechnologyDepositing user: Pure Administrator Date deposited: 21 Aug 2018 15:30 Last modified: 15 Dec 2024 01:26 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/65217