Issue 10, 2019

Hydroxyl-functionalized triazolylidene-based PEPPSI complexes: metallacycle formation effect on the Suzuki coupling reaction

Abstract

We report the preparation and full characterization of a series of hydroxyl functionalized 1,2,3-triazolylidene-based PEPPSI complexes 2a–c and their catalytic application in the Suzuki cross coupling reaction of aryl chlorides/amides with boronic acids. Under basic reaction conditions, complexes 2a–c show a notable increase in their catalytic efficiency compared with two ether-wingtip functionalized PEPPSI analogues (3 and 4) and a commercially available NHC-Pd complex (5). The catalytic results suggest that deprotonation of the hydroxyl group in complexes 2a–c plays an important role in the overall process. Deprotonation of the alcohol moiety of complexes 2a–b with sodium tert-butoxide allows for the isolation of metallacycles 6a–b, which are proposed as the active species of cross coupling reactions.

Graphical abstract: Hydroxyl-functionalized triazolylidene-based PEPPSI complexes: metallacycle formation effect on the Suzuki coupling reaction

Supplementary files

Article information

Article type
Paper
Submitted
07 Nov. 2018
Accepted
10 Janv. 2019
First published
11 Janv. 2019

Dalton Trans., 2019,48, 3214-3222

Hydroxyl-functionalized triazolylidene-based PEPPSI complexes: metallacycle formation effect on the Suzuki coupling reaction

D. Rendón-Nava, A. Álvarez-Hernández, A. L. Rheingold, O. R. Suárez-Castillo and D. Mendoza-Espinosa, Dalton Trans., 2019, 48, 3214 DOI: 10.1039/C8DT04432E

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