The effects of intramolecular hydrogen bonding on the reactivity of phenoxyl radicals in model systems

• Published in: International journal of mass spectrometry 2015-11, Vol.390, p.124-131
• Main Authors: Lesslie, Michael, Piatkivskyi, Andrii, Lawler, John, Helgren, Travis R., Osburn, Sandra, O’Hair, Richard A.J., Ryzhov, Victor
• Format: Article
• Language: English
• Subjects: Density functional theory calculations; Hydrogen bonding; Ion-molecule reactions; Radical ions; Tyrosyl radicals
• ISSN: 1387-3806; 1873-2798
• DOI: 10.1016/j.ijms.2015.06.008

•Gas-phase reactivity of phenoxyl radical cations of aromatic nitrogen bases is studied.•Reactivity towards NO and C3H7SH decreases as N+-H⋯O distance decreases.•Reactivity decreases as spin density at the oxygen atom decreases.•LysTyr(O) radical cation is stabilized by hydrogen bonding at the radical site. The effects of hydrogen bonding and spin density at the oxygen atom on the gas-phase reactivity of phenoxyl radicals were investigated experimentally and theoretically in model systems and the dipeptide LysTyr. Gas-phase ion-molecule reactions were carried out between radical cations of several aromatic nitrogen bases with the neutrals nitric oxide and n-propyl thiol. Reactivity of radical cations 4–6 correlated with the spin density. The possibility of hydrogen bonding was explored in compounds which allowed four-, five-, and six-membered rings to be formed between the protonated nitrogen and the phenoxyl oxygen, while possessing similar spin density at the oxygen atom. The N+-H⋯O bond length was calculated to decrease in the series (1–3), consistent with the theoretical calculations finding weak hydrogen bonding in 2 and strong hydrogen bonding in 3. This coincided with the decrease in reaction rates of 1–3 with both nitric oxide and n-propyl thiol. DFT calculations found that the lowest energy structure of the distonic radical cation of the dipeptide [LysTyr(O)]+ has a short hydrogen bond between the protonated Lys side chain and the phenoxyl oxygen, 1.70Å, which is consistent with its low reactivity.