R. Wagemann et al., SPATIALLY FIXED OLIGOAMINES .3. PROTONATION OF MEANDER-TYPE HEXAMINESAND OCTAMINES, Journal of molecular structure, 372(2-3), 1995, pp. 195-202
Di- and tetraprotonation of oligoamines 1-3 pocessing bicyclo[3.1.O]he
xyl linking blocks were investigated by C-13 NMR spectroscopy and the
location of the protons in the resulting salts was determined via (1)J
(CH) coupling constants. The NMR spectroscopic prediction was confirme
d by X-ray structural analysis in the case of the diammonium salt 2 .
2 TFSA hexahydrate (TFSA, trifluoromethanesulfonic acid); intramolecul
ar hydrogen bonding was established in the solid state.