Issue 27, 2007

Pentafluorophenyl copper: aggregation and complexation phenomena, photoluminescence properties, and applications as reagent in organometallic synthesis

Abstract

Recent advances in the chemistry of pentafluorophenyl copper are discussed, including the observation of strongly luminescent adducts with pyridine, the first successful structural characterization of an organocopper–arene complex, and the complexation with electron-rich transition metal complexes such as ferrocene derivatives. In addition, new applications in synthetic organometallic chemistry are discussed, which include the discovery of tin/copper exchange reactions for the preparation of organocopper compounds that are otherwise not readily accessible, and the selective transfer of the C6F5 groups to boron to form catalytically active and electronically interesting organoboron polymers.

Graphical abstract: Pentafluorophenyl copper: aggregation and complexation phenomena, photoluminescence properties, and applications as reagent in organometallic synthesis

Additions and corrections

Article information

Article type
Perspective
Submitted
22 Mar 2007
Accepted
10 May 2007
First published
30 May 2007

Dalton Trans., 2007, 2851-2858

Pentafluorophenyl copper: aggregation and complexation phenomena, photoluminescence properties, and applications as reagent in organometallic synthesis

F. Jäkle, Dalton Trans., 2007, 2851 DOI: 10.1039/B704372D

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