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1 January 2001 Studies of All-trans-retinal as a Photooxidizing Agent
Willa S. Harper, Elizabeth R. Gaillard
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The photophysical properties of all-trans-retinal (RAL) have been extensively studied because of the importance of the retinoids in the visual process. However, little information is available regarding the participation of RAL in photochemical transformations such as photooxidation. RAL is one of several native chromophores that have been suggested to act as photosensitizers of damage in the human retina, and this damage would likely occur through oxidative pathways. Time-resolved and steady state techniques have been used to examine the photoreactivity of RAL toward several suitable substrates. The lifetime of the RAL triplet excited state is observed to decrease with increasing concentration of the well-known electron and hydrogen atom donors, 2,3,5,6-tetramethyl-1,4-phenylenediamine (DAD), hydroquinone (HQ), methylhydroquinone (MHQ), 2,3-dimethylhydroquinone (DMHQ) and trimethylhydroquinone (TMHQ), although the bimolecular rate constants for the reaction are much less than that of diffusion controlled (2.9 × 107 M−1 s−1, 1.2 × 105 M−1 s−1, 1.2 × 105 M−1 s−1, 1.5 × 105 M−1 s−1 and 1.6 × 106 M−1 s−1, for DAD, HQ, MHQ, DMHQ and TMHQ, respectively). In the presence of the donors, new absorptions grow concomitant with the decay of the triplet excited state, and for DAD and TMHQ, the observed spectra are similar to the spectra of p-phenylenediamine and TMHQ radicals. Irradiation of RAL in argon-saturated methanol results in fairly efficient photobleaching of RAL and in the formation of two new compounds having absorption spectra that are shifted below 300 nm. Irradiation of RAL in argon-saturated acetonitrile also results in photobleaching of RAL, but the reaction proceeds at a slower rate.

Willa S. Harper and Elizabeth R. Gaillard "Studies of All-trans-retinal as a Photooxidizing Agent," Photochemistry and Photobiology 73(1), 71-76, (1 January 2001).<0071:SOATRA>2.0.CO;2
Received: 8 September 2000; Accepted: 1 September 2000; Published: 1 January 2001

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