We
report a computational study of the little-studied neutral bisulfite,
bisulfate, dihydro-phosphite, and dihydro-phosphate radicals (HSO
x
•
, H
2
PO
x
•
,
x
=
3,4), calling special attention to their various tautomeric structures
together with p
K
a
values estimated from
the Gibbs free energies of their dissociations (at the G4 and CAM-B3LYP
levels of density functional theory). The energetics of microhydration
clusters with up to four water molecules for the S-based species and
up to eight water molecules for the P-based species were investigated.
The number of microhydrating water molecules needed to induce spontaneous
de-protonation is found to correlate the acid strength of each radical.
According to the computed Gibbs free reaction and activation energies,
S- and P-centered radicals preferentially add to the double bond of
propene (a lipid model), whereas the O-centered radical tautomers
prefer H-abstraction. The likely downstream reactions of these radicals
in biological media are discussed.