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Protonation and quaternization of 1, N 6 ‐ethenoadenosine: What are the species responsible for the fluorescence of 1, N 6 ‐ethenoadenosine?
Author(s) -
Inoue Yasuo,
Kuramochi Takao,
Imakubo Keiichi
Publication year - 1979
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.1979.360180908
Subject(s) - protonation , chemistry , fluorescence , aqueous solution , photochemistry , solvent , spectral line , absorption (acoustics) , medicinal chemistry , analytical chemistry (journal) , ion , organic chemistry , physics , quantum mechanics , acoustics , astronomy
Methylation of 1, N 6 ‐ethenoadenosine (εAdo) gives a mixture of N1‐ and N9‐quaternized methyl‐3‐β‐ D ‐ribofuranosylimidazo[2,1‐ i ] purinium salts (m 1 εAdo + and m 9 εAdo + , respectively). The ratio of the two forms of the protonated εAdo [H 1 εAdo + ]/[H 9 εAdo + ] has been estimated to be approximately 0.10 by comparing the uv absorption spectra of the protonated species of εAdo and the two nontautomerizable model compounds. In relation to a study on the protonation effect on the fluorescence of εAdo, we have now determined the effect of quaternization on the fluorescence spectra at 293 and 77 K. We have found that m 1 εAdo + and m 9 εAdo + are both fluorescent, and the high degree of coincidence between the fluorescence spectra of εAdo and m 1 εAdo + at pH 7 is noted. The m 1 εAdo + singlet form is a more efficient fluorescer than the m 9 εAdo + ion at room temperature (quantum yields of 0.43 and 0.11, respectively). All the results which are presented in this paper are consistent with the picture that there exist more than one species responsible for the fluorescence of εAdo, depending on the environment of the molecule in aqueous solution (temperature and pH of solvent).