Affiliation:
1. Dipartimento di Chimica “Giacomo Ciamician” Alma Mater Studiorum – Università di Bologna Via Gobetti 85 40129 Bologna Italy
2. Center for Chemical Catalysis – C3 Alma Mater Studiorum – Università di Bologna Via Selmi 2 40126 Bologna Italy
3. Department of Pharmacy – Drug Sciences University of Bari “A. Moro” Via E. Orabona 4 70125 Bari Italy
Abstract
AbstractDual photoredox catalysis is modifying the approach to sustainable metal catalysis based on metals in low oxidation state, as the use of stoichiometric metal as reductants are avoided. In this study, we showcase the potential use of vanadium in a dual photoredox process, allowing us to effectively control the formation of V(II) and its corresponding chemical reactions. A diastereoselective pinacol coupling with aromatic aldehydes is described. The process shows broad scope, and interestingly, unprotected salicylic aldehydes are compatible with the reaction protocol. Additionally, among all the ligands investigated we found that inexpensive bipyridines control the diastereoselection of the reaction favoring the d,l chiral compound (dr>20:1 for most of the aldehydes investigated). To promote the reaction and avoid an unproductive and not stereoselective radical coupling of the generated ketyl radical, the use of [DMQA]+, a stable organic dye, was found crucial. Furthermore, this dye possesses the remarkable capability of efficiently capturing light in the red segment of the visible spectrum, effectively raising efficiency of the protocol. The utilization of red light carries notable advantages in terms of penetration and safety, making it particularly significant. Moreover, careful photophysical investigations were able to give indications about the mechanism of the reaction.