protonated

the protonated amine readily accepted a chloride ion.

mass spectrometry revealed a significant peak for the protonated molecule.

the nitrogen atom became protonated under acidic conditions.

we observed a shift in the spectrum due to protonated species.

the protonated form of the amino acid is positively charged.

the reaction favored the formation of a protonated intermediate.

the protonated histidine exhibited altered binding properties.

the solvent strongly solvated the protonated substrate.

the protonated peptide was identified by tandem mass spectrometry.

the protonated base readily undergoes deprotonation.

the protonated adduct was stable at room temperature.