[{"date_created":"2022-09-08T11:46:45Z","citation":{"short":"L. Schmermund, S. Reischauer, S. Bierbaumer, C. Winkler, A. Diaz-Rodriguez, L.J. Edwards, S. Kara, T. Mielke, J. Cartwright, G. Grogan, B. Pieber, W. Kroutil, (n.d.).","ista":"Schmermund L, Reischauer S, Bierbaumer S, Winkler C, Diaz-Rodriguez A, Edwards LJ, Kara S, Mielke T, Cartwright J, Grogan G, Pieber B, Kroutil W. Switching between enantiomers by combining chromoselective photocatalysis and biocatalysis. <a href=\"https://doi.org/10.26434/chemrxiv.13521527\">10.26434/chemrxiv.13521527</a>.","ieee":"L. Schmermund <i>et al.</i>, “Switching between enantiomers by combining chromoselective photocatalysis and biocatalysis.” ChemRxiv.","ama":"Schmermund L, Reischauer S, Bierbaumer S, et al. Switching between enantiomers by combining chromoselective photocatalysis and biocatalysis. doi:<a href=\"https://doi.org/10.26434/chemrxiv.13521527\">10.26434/chemrxiv.13521527</a>","mla":"Schmermund, Luca, et al. <i>Switching between Enantiomers by Combining Chromoselective Photocatalysis and Biocatalysis</i>. ChemRxiv, doi:<a href=\"https://doi.org/10.26434/chemrxiv.13521527\">10.26434/chemrxiv.13521527</a>.","chicago":"Schmermund, Luca, Susanne Reischauer, Sarah Bierbaumer, Christoph Winkler, Alba Diaz-Rodriguez, Lee J. Edwards, Selin Kara, et al. “Switching between Enantiomers by Combining Chromoselective Photocatalysis and Biocatalysis.” ChemRxiv, n.d. <a href=\"https://doi.org/10.26434/chemrxiv.13521527\">https://doi.org/10.26434/chemrxiv.13521527</a>.","apa":"Schmermund, L., Reischauer, S., Bierbaumer, S., Winkler, C., Diaz-Rodriguez, A., Edwards, L. J., … Kroutil, W. (n.d.). Switching between enantiomers by combining chromoselective photocatalysis and biocatalysis. ChemRxiv. <a href=\"https://doi.org/10.26434/chemrxiv.13521527\">https://doi.org/10.26434/chemrxiv.13521527</a>"},"year":"2021","status":"public","doi":"10.26434/chemrxiv.13521527","day":"06","extern":"1","type":"preprint","language":[{"iso":"eng"}],"month":"01","main_file_link":[{"open_access":"1","url":"https://doi.org/10.26434/chemrxiv.13521527"}],"title":"Switching between enantiomers by combining chromoselective photocatalysis and biocatalysis","date_published":"2021-01-06T00:00:00Z","author":[{"first_name":"Luca","full_name":"Schmermund, Luca","last_name":"Schmermund"},{"last_name":"Reischauer","full_name":"Reischauer, Susanne","first_name":"Susanne"},{"first_name":"Sarah","full_name":"Bierbaumer, Sarah","last_name":"Bierbaumer"},{"last_name":"Winkler","full_name":"Winkler, Christoph","first_name":"Christoph"},{"last_name":"Diaz-Rodriguez","full_name":"Diaz-Rodriguez, Alba","first_name":"Alba"},{"last_name":"Edwards","first_name":"Lee J.","full_name":"Edwards, Lee J."},{"full_name":"Kara, Selin","first_name":"Selin","last_name":"Kara"},{"first_name":"Tamara","full_name":"Mielke, Tamara","last_name":"Mielke"},{"full_name":"Cartwright, Jared","first_name":"Jared","last_name":"Cartwright"},{"last_name":"Grogan","full_name":"Grogan, Gideon","first_name":"Gideon"},{"first_name":"Bartholomäus","full_name":"Pieber, Bartholomäus","last_name":"Pieber","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","orcid":"0000-0001-8689-388X"},{"first_name":"Wolfgang","full_name":"Kroutil, Wolfgang","last_name":"Kroutil"}],"publication_status":"submitted","abstract":[{"lang":"eng","text":"Controlling the selectivity of a chemical reaction with external stimuli is common in thermal processes, but rare in visible-light photocatalysis. Here we show that the redox potential of a carbon nitride photocatalyst (CN-OA-m) can be tuned by changing the irradiation wavelength to generate electron holes with different oxidation potentials. This tuning was the key to realizing photo-chemo-enzymatic cascades that give either the (S)- or the (R)-enantiomer of phenylethanol. In combination with an unspecific peroxygenase from Agrocybe aegerita, green light irradiation of CN-OA-m led to the enantioselective hydroxylation of ethylbenzene to (R)-1-phenylethanol (99% ee). In contrast, blue light irradiation triggered the photocatalytic oxidation of ethylbenzene to acetophenone, which in turn was enantioselectively reduced with an alcohol dehydrogenase from Rhodococcus ruber to form (S)-1-phenylethanol (93% ee)."}],"article_processing_charge":"No","publisher":"ChemRxiv","oa_version":"Preprint","oa":1,"date_updated":"2022-09-08T11:49:16Z","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"12070"}]