Generation and NMR studies of stable cations derived from monothia[3.2]- and dithia[3.3]metacyclophanes

Monothia[3.2]- and dithia[3.3]metacyclophanes 1-5 are S-protonated in FSO3H . SbF5 (4:1)-SO2 (or SO2ClF) superacids to give their corresponding acidic mono- and bis(sulfonium) cations. A detailed NMR study of the resulting ca tions and their precursors is provided; conformational aspects are also add ressed via NOE measurements. PM3 calculations are used in selected cases as a guiding tool to identify preferred conformations. A remarkable deactivat ion of the aryl rings occurs upon S-protonation, whereby further ring proto nation to form disulfoniomonoarenium trications does not occur, even though positive charge delocalization into the phenyl rings is limited.