Triphenylphosphine mediated Ir/Ni Dual Photoredox Catalyzed C(sp2)-C(sp3) coupling of alkyl alcohol and aryl bromide

Abstract

Herein, we present a mild C(sp2)-C(sp3) coupling methodology from alkyl alcohol and aryl bromide under blue light irradiation. The triphenylphosphine mediated alkyl radical generated under photochemical condition was coupled with the aryl bromide in the presence of Ni/dtbpy as catalyst system to provide the C-C coupled product in moderate to good yields. The substrate scope optimization under this condition showed a range of aryl and hetero aryl bromide could be coupled successfully with functionalized benzyl alcohols and other aliphatic alcohols under this condition.

Supplementary files

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Communication
Submitted
31 Oct 2025
Accepted
01 Jan 2026
First published
02 Jan 2026

New J. Chem., 2026, Accepted Manuscript

Triphenylphosphine mediated Ir/Ni Dual Photoredox Catalyzed C(sp2)-C(sp3) coupling of alkyl alcohol and aryl bromide

K. Inamke, A. Kharat, P. Kamath and S. Das, New J. Chem., 2026, Accepted Manuscript , DOI: 10.1039/D5NJ04281J

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements