Metal‐Catalyzed Hydride Transfer from Alcohols to Photoexcited Dipyridophenazine†

Dipyridophenazine (dppz) is known to react with alcohols upon photoexcitation into an n-pi* transition at 378 nm to yield dihydrodipyridophenazine (dppzH(2)). This process occurs via H-atom abstraction from alcohols and subsequent disproportionation of the dppzH(center dot) radical species, to the final product. This reaction shows a primary kinetic isotope effect (KIE = 4.9) in methanol/perdeuteromethanol solvents, consistent with H-atom transfer processes. Addition of excess Zn(II) ions to the dppz solution not only accelerates the rate of photoreduction, but also lowers the KIE to 1.7, indicating a change in reaction mechanism. We postulate that the coordination of the alcoholic solvent to Zn(II) activates the alcohol alpha C-H bonds toward hydride transfer processes which would be consistent with the lowered KIE and faster overall reduction of the aromatic ligand. Interestingly, this appears to be an intramolecular process in which the Zn(II) is coordinated to both the dppz ligand and the reactive alcohol, as a sharp inflection in the overall rate increase is observed at a Zn:dppz ratio of 2:1. At this ratio, the dominant dppz species involves a Zn(II) bound to one dppz and several solvent molecules (methanol and water).