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Photoracemization-Based Viedma Ripening of a BINOL Derivative
Authors:Giuseppe Belletti  Carola Tortora  Indradevi D. Mellema  Dr. Paul Tinnemans  Dr. Hugo Meekes  Prof. Dr. Floris P. J. T. Rutjes  Prof. Dr. Svetlana B. Tsogoeva  Prof. Dr. Elias Vlieg
Affiliation:1. Radboud University, Institute for Molecules and Materials, Heyendaalseweg 135, 6525 AJ, Nijmegen, The Netherlands;2. Chair of Organic Chemistry I, Department of Chemistry and Pharmacy, Friedrich-Alexander-Universität Erlangen-Nürnberg, Nikolaus-Fiebiger-Str. 10, 91058 Erlangen, Germany
Abstract:Viedma ripening is a deracemization process that has been used to deracemize a range of chiral molecules. The method has two major requirements: the compound needs to crystallize as a conglomerate and it needs to be racemizable under the crystallization conditions. Although conglomerate formation can be induced in different ways, the number of racemization methods is still rather limited. To extend the scope of Viedma ripening, in the present research we applied UV-light-induced racemization in a Viedma ripening process, and report the successful deracemization of a BINOL derivative crystallizing as a conglomerate. Irradiation by UV light activates the target compound in combination with an organic base, required to promote the excited-state proton transfer (ESPT), leading thereafter to racemization. This offers a new tool towards the development of Viedma ripening processes, by using a cheap and “green” catalytic source like UV light to racemize suitable chiral compounds.
Keywords:chirality  crystal growth  deracemization  photoracemization  Viedma ripening
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