Vm. Belyakova et Vl. Rapoport, LUMINESCENCE OF 2 HYDRATED FORMS OF ADENOSINE, Journal of photochemistry and photobiology.B, Biology, 19(2), 1993, pp. 105-109
The fluorescence excitation spectrum of dilute solutions of adenosine
(5 x 10(-5) M) mixtures of ethylene glycol and H2O at 77 K and pH 7.0
was found to be red shifted by 10 nm compared with the absorption spec
trum. This is explained by the existence of two monomeric species. The
major monomeric species has an absorption maximum at 260 nm and a flu
orescence quantum yield of less than 2 x 10(-4) and is assigned to the
adenosine molecules cyclically hydrogen bonded through the N7 atom an
d the amino group to water molecules. The minor monomeric species exhi
bits an absorption maximum at 270 nm and a fluorescence quantum yield
of greater than 2 x 10(-2) and is assigned to molecules without a cycl
ic hydrogen bond. The concentration dependence of the fluorescence exc
itation and emission spectra of adenosine also indicates the existence
of aggregates with fluorescence properties similar to those of adenyl
yl (3'-->5') adenine (ApA). A mechanism of S1 state quenching for ade
nosine molecules cyclically hydrogen bonded to water molecules is prop
osed.