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Transient phenomena in the pulse radiolysis of retinyl polyenes. 2. Protonation kinetics

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00370a043· OSTI ID:5225259

The results of a study are presented concerning the kinetics of reactions of various retinyl derivatives with hydrogen ions released pulse radiolytically in aerated 2-propanol containing 0.5 M acetone and 0.2 M carbon tetrachloride. For retinal and polyene Schiff bases, their protonated forms absorb at much longer wavelengths than the unprotonated substrates and are monitored by kinetic spectrophotometry. In the cases of retinol and retinyl acetate, the initial H/sup +/ adduct undergoes loss of water and acetic acid, respectively, producing the retinyl carbonium ion (lambda/sub max/585 nm), which, in turn, decays with first-order kinetics (t/sub 1///sub 2/ = 10 +/- 3 ..mu..s). The rate constants for protonation are in the range 1 x 10/sup 7/ - 4 x 10/sup 9/ M/sup -1/ s/sup -1/. In the cases of polyene Schiff bases, the protonation rate constant increases slightly with increasing polyene chain length and is higher for 11-cis-retinal Schiff base than for its all-trans counterpart. The absorption spectral maxima of protonated polyene Schiff bases observed in the early stages of protonation in the pulse radiolysis are red-shifted by approx. 10 nm relative to those of the protonated forms obtained by adding dilute hydrochloric acid to Schiff base solutions in 2-propanol. This is explained by the lack of ion pairing in the protonated species seen in the pulse radiolysis.

Research Organization:
Univ. of Notre Dame, IN
OSTI ID:
5225259
Journal Information:
J. Am. Chem. Soc.; (United States), Journal Name: J. Am. Chem. Soc.; (United States) Vol. 104:6; ISSN JACSA
Country of Publication:
United States
Language:
English

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