Selective <i>Para</i> ‐Functionalization of Aromatic C(sp <sup>2</sup> )─H Bonds via Atomically Dispersed Photocatalysis

J Jun Hu S Suman Pradhan (Department of Chemistry University of Bayreuth Bayreuth Germany) Y Yuman Qin (Department of Chemistry University of Bayreuth Bayreuth Germany) W Wenhao Su P Peng Ren L Lindsey Frederiksen (Institute of Chemical Sciences and Engineering) S Susanna Monti (CNR-ICCOM, Institute of Chemistry of Organometallic Compounds) G Giovanni Barcaro (CNR-IPCF, Institute of Chemical and Physical Processes) A Aleksander Jaworski (Department of Chemistry) A Anna Rokicińska (Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland) K Kaan Karaca (Department of Chemistry, Materials, and Chemical Engineering “Giulio Natta”, Politecnico di Milano, Piazza Leonardo Vinci 32, I-20133 Milan, Italy) P Piotr Kuśtrowski (Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland) G Gianvito Vilé (Department of Chemistry, Materials, and Chemical Engineering “Giulio Natta”, Politecnico di Milano, Piazza Leonardo Vinci 32, I-20133 Milan, Italy) D David Reyes (Interdisciplinary Center for Electron Microscopy) P Paul J. Dyson S Shoubhik Das (Department of Chemistry, University of Bayreuth, Universitätsstraße 30, 95447 Bayreuth, Germany)

Abstract

ABSTRACT Direct functionalization of aromatic C─H bonds is crucial in organic synthesis due to their wide applications in pharmaceutical chemistry and materials engineering, yet precise site selectivity remains challenging. Traditional methods often rely on electrophilic aromatic substitution or transition metal catalysis with directing group strategies, which can result in product mixtures or require pre‐installed functional groups. In this respect, recent advances using single‐atom catalysts (SACs) are promising due to their enhanced reactivity and selectivity. This study introduces a robust catalytic system for undirected para ‐C─H functionalization of electron‐rich arenes by using an atomically dispersed copper‐based photocatalyst. The method bypasses the requirement of pre‐installed directing groups, achieving site‐selective functionalization through an η 2 interaction with arenes under mild conditions, with a broad substrate scope, and excellent catalyst recyclability. Furthermore, this approach offers a novel method for incorporating functional groups into complex drug molecules, which is crucial in the synthesis of pharmaceuticals and natural products.

Article Details

Volume / Issue Vol. 65, Issue 24
Published June 08, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (16)

J

Jun Hu

S

Suman Pradhan

Department of Chemistry University of Bayreuth Bayreuth Germany

Y

Yuman Qin

Department of Chemistry University of Bayreuth Bayreuth Germany

W

Wenhao Su

P

Peng Ren

L

Lindsey Frederiksen

Institute of Chemical Sciences and Engineering

S

Susanna Monti

CNR-ICCOM, Institute of Chemistry of Organometallic Compounds

G

Giovanni Barcaro

CNR-IPCF, Institute of Chemical and Physical Processes

A

Aleksander Jaworski

Department of Chemistry

A

Anna Rokicińska

Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland

K

Kaan Karaca

Department of Chemistry, Materials, and Chemical Engineering “Giulio Natta”, Politecnico di Milano, Piazza Leonardo Vinci 32, I-20133 Milan, Italy

P

Piotr Kuśtrowski

Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland

G

Gianvito Vilé

Department of Chemistry, Materials, and Chemical Engineering “Giulio Natta”, Politecnico di Milano, Piazza Leonardo Vinci 32, I-20133 Milan, Italy

D

David Reyes

Interdisciplinary Center for Electron Microscopy

P

Paul J. Dyson

S

Shoubhik Das

Department of Chemistry, University of Bayreuth, Universitätsstraße 30, 95447 Bayreuth, Germany