Stabilization of Semiquinone Intermediates in the Photoreduction of Phenanthrenequinone by Complex Formation

Rennert, J.; Mayer, Mariya; Levy, Jéssica; Kaplan, Joel A.

doi:10.1111/j.1751-1097.1969.tb05690.x

Cited by 4 publications

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“…This latter effect may be due to paramagnetic triplet quenching. It is interesting to note that Rennert et al [42] have found that group I1 metal ions complex and stabilize the semiquinone radical of phenanthroquinone in degassed ethanol.…”

Section: )mentioning

confidence: 99%

Chlorophyll One‐electron Photochemistry: Light‐induced Absorbance Changes and Esr Signals for Various Porphyrin‐quinone and Hydroquinone Systems in Alcohol Solvents*

White

Tollin

1971

Photochem & Photobiology

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Light-dark optical difference spectra of degassed ethanol or pyridine solutions of chlorophyll and benzoquinone or hydroquinone at temperatures above -50°C show only the semiquinone absorbance band. Decay of the signals is second order, with a rate constant in agreement with earlier ESR results.Light-induced optical changes due to chlorophyll can be elicited by lowering the temperature of ethanol solutions of chlorophyll and benzoquinone to a region of high viscosity. Hydroquinone is not effective in producing these optical changes.Similar results are achieved at room temperature by using as solvent a degassed mixture of the alcohols: cyclohexanol, rert-butanol, and ethanol (CBE). Difference spectra show bleaching of the chlorophyll bands and increased absorbance in the intermediate wavelength region (460-580 nm). Decay kinetics are first order, while the rise is complicated (probably biphasic).ESR signals have no hyperfine structure and also decay by first order kinetics, at a rate which is faster than that of the optical changes. The ESR signals reach a steady state more rapidly than the optical signals, without biphasic kinetics. These results demonstrate that at least two species are generated.Addition of acid increases the amount of bleaching in CBE, while small amounts of base decrease it. Larger amounts of base cause chlorophyll bleaching to completely disappear and only the semiquinone anion is observed. Activation energies for the chlorophyll a-benzoquinone photoreaction in CBE are 10-14 kcal/mole. Lower potential quinones give lower activation energies. The rate constant for quenching of the triplet state of chlorophyll a by p-carotene in CBE is 7.5 &0.5 X 108 (M set)-'. p-carotene also quenches photoproduct formation. The bimolecular rate constant for formation of the photoproduct with benzoquinone was calculated to be 7 X 108 (M sec)-I.The redox potential of the quinone affects both the magnitude of the shlorophyll absorbance changes and the rate of decay. The higher the potential, the larger the changes and the slower the decay. Other porphyrin systems show similar photoreactions only if they are chelated with a group I1 metal, such as MgZ+, Cd+*, or Zn+z.The results are interpreted in terms of the formation, by a triplet-sensitized one-electron transfer from solvent to quinone, of a chlorophyll-semiquinone complex which is stabilized via coordination with the chelated metal.

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Section: )mentioning

confidence: 99%