Issue 43, 2020

A theoretical mechanistic study of IrIII/CuI-metallaphotoredox catalyzed asymmetric radical decarboxylative cyanation

Abstract

Visible-light-induced asymmetric metallaphotoredox catalysis has become a powerful strategy in synthetic organic chemistry. IrIII/CuI dual asymmetric catalysis has been developed to achieve enantioselective decarboxylative cyanation. However, detailed mechanisms, such as catalytic cycles for dual catalysts and the role of a chiral ligand, remain obscure in these reactions. In this study, the catalytic cycle of this reaction is systematically investigated by DFT calculations to clarify the quenching mechanism of the photocatalyst and the origin of the excellent enantioselectivity. Interestingly, the radical mechanism merging oxidative quenching (IrIII–*IrIII–IrIV–IrIII) and copper catalytic cycles (CuI–CuII–CuIII–CuI) is favourable. It consists of five major processes: single-electron oxidation of *IrIII by N-hydroxy-phthalimide (NHP) esters followed by decarboxylation to generate benzyl radical, oxidation of CuI by IrIVvia a single-electron transfer (SET) process, cyanide exchange, radical capture by CuII, and C–CN reductive elimination from CuIII. The cyanide exchange is the rate-determining step, whereas the C–CN reductive elimination is the enantio-determining step of the reaction. In addition, the origin of the high enantioselectivity was analyzed from the steric and electronic effects. This study will hopefully benefit the future understanding of such photoredox-mediated dual catalyzed asymmetric synthesis.

Graphical abstract: A theoretical mechanistic study of IrIII/CuI-metallaphotoredox catalyzed asymmetric radical decarboxylative cyanation

Supplementary files

Article information

Article type
Paper
Submitted
26 Goue. 2020
Accepted
07 Here 2020
First published
08 Here 2020

Dalton Trans., 2020,49, 15276-15286

A theoretical mechanistic study of IrIII/CuI-metallaphotoredox catalyzed asymmetric radical decarboxylative cyanation

Y. Liang, G. Sun, Z. Su and W. Guan, Dalton Trans., 2020, 49, 15276 DOI: 10.1039/D0DT02630A

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