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Attempted hydrogen-deuterium exchange of trimethyloxonium ion, (CH3)3O+ with excess of 1:1 (2)HF/SbF5 superacid at -30 degreesC over a period of 30 days showed no exchange. Theoretical calculations at the MP2/6-31G** level are in accord with the lack of hydrogen-deuterium exchange in the methyl group of the (CH3)3O+ cation as protonation (protosolvation) prefers the oxygen lone pair of electrons, instead of a C---H bond. Methylation of aromatics with the (CH3)3O+CF3SO3- in CF3SO3H and 2CF3SO3H:B(O3SCF3)3 was also studied. Whereas in triflic acid no alkylation was observed, in triflatoboric acid, a powerful superacid, alkylation takes place, indicating protolytic activation of the trimethyloxonium ion.

proceedings of the national academy of sciences of the united states of america

Attempted hydrogen–deuterium exchange of the protio -trimethyloxonium dication (CH 3 ) 3 OH 2+ , study of methylating ability of (CH 3 ) 3 O + in superacids and theoretical investigations