Switching the Mechanism of NADH Photooxidation by Supramolecular Interactions
Alexander K. Mengele, Dominik Weixler, Avinash Chettri, Maite Maurer, F. Huber, Gerd M. Seibold, Benjamin Dietzek, Bernhard J. Eikmanns, Sven Rau
Abstract
Abstract A series of three Ru(II) polypyridine complexes was investigated for the selective photocatalytic oxidation of NAD(P)H to NAD(P) + in water. A combination of (time‐resolved) spectroscopic studies and photocatalysis experiments revealed that ligand design can be used to control the mechanism of the photooxidation: For prototypical Ru(II) complexes a 1 O 2 pathway was found. Rudppz ([(tbbpy) 2 Ru(dppz)]Cl 2 , tbbpy=4,4'‐di‐ tert ‐butyl‐2,2'‐bipyridine, dppz=dipyrido[3,2‐ a :2′,3′‐ c ]phenazine), instead, initiated the cofactor oxidation by electron transfer from NAD(P)H enabled by supramolecular binding between substrate and catalyst. Expulsion of the photoproduct NAD(P) + from the supramolecular binding site in Rudppz allowed very efficient turnover. Therefore, Rudppz permits repetitive selective assembly and oxidative conversion of reduced naturally occurring nicotinamides by recognizing the redox state of the cofactor under formation of H 2 O 2 as additional product. This photocatalytic process can fuel discontinuous photobiocatalysis.