protonated amine
protonated form
getting protonated
protonated species
strongly protonated
protonated state
was protonated
protonated nitrogen
now protonated
protonated ring
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.
protonated amine
protonated form
getting protonated
protonated species
strongly protonated
protonated state
was protonated
protonated nitrogen
now protonated
protonated ring
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.
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