Citation

BibTex format

@article{Parkin:2026:10.1021/acsomega.6c06786,
author = {Parkin, LA and White, AJP and Ashley, AE and Britovsek, GJP},
doi = {10.1021/acsomega.6c06786},
journal = {ACS Omega},
pages = {50417--50422},
title = {Insights into Electrophilic Methane Activation with High-Valent Lead in Trifluoroacetic Acid and Trifluoromethanesulfonic Acid.},
url = {http://dx.doi.org/10.1021/acsomega.6c06786},
volume = {11},
year = {2026}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - The formation of high-valent lead compounds has been investigated in trifluoroacetic acid (HTFA) and trifluoromethyl sulfonic acid (HOTf). Pb-(IV) species are formed in these acids, starting from Pb3O4 or other Pb-(IV) precursors (Pb-(OAc)4, PbPh4). Attempts to isolate Pb-(IV) compounds resulted in the isolation of the Pb-(II) salts Pb-(TFA)2(HTFA)2 and Pb-(OTf)2(HOTf), which have been structurally characterized. Pb-(TFA)4 and Pb-(OTf)4 can undergo reductive elimination in solution to give their respective Pb-(II) compounds and formation of CF3TFA and CF3OTf, together with loss of CO2 and SO3, respectively. A solution of Pb-(OTf)4 in HOTf/Tf2O activates methane at 5 bar at 60 °C to give MeTf, MeOTf and HOTf. The formation of PbMe-(OTf)3 is believed to be a key intermediate in these reactions, which reacts with Tf2O to form MeTf and Pb-(OTf)4, and undergoes reductive elimination to form MeOTf and Pb-(OTf)2.
AU - Parkin,LA
AU - White,AJP
AU - Ashley,AE
AU - Britovsek,GJP
DO - 10.1021/acsomega.6c06786
EP - 50422
PY - 2026///
SP - 50417
TI - Insights into Electrophilic Methane Activation with High-Valent Lead in Trifluoroacetic Acid and Trifluoromethanesulfonic Acid.
T2 - ACS Omega
UR - http://dx.doi.org/10.1021/acsomega.6c06786
UR - https://www.ncbi.nlm.nih.gov/pubmed/42662590
VL - 11
ER -

Contact

Prof. Dr. George Britovsek FRSC

Director MRes Catalysis & Engineering

Tel: +44 (0)20 7594 5863

Email: g.britovsek@imperial.ac.uk

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