H2 activation using the first 1:1:1 hetero-tri(aryl)borane

Blagg, Robin J. and Wildgoose, Gregory G. (2016) H2 activation using the first 1:1:1 hetero-tri(aryl)borane. RSC Advances, 6 (48). pp. 42421-42427. ISSN 2046-2069

Preview	PDF (BW2016_SI) - Published Version Available under License Creative Commons Attribution. Download (1MB) | Preview
Preview	PDF (BW2016) - Published Version Available under License Creative Commons Attribution. Download (812kB) | Preview

Abstract

The novel 1:1:1 hetero-tri(aryl)borane (pentafluorophenyl){3,5-bis(trifluoromethyl)phenyl}(pentachlorophenyl)borane has been synthesised and structurally characterised. This has been show to act as the Lewis acidic component in FLPs for the heterolytic cleavage of H2 with three Lewis bases.

Item Type:	Article
Additional Information:	This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Faculty \ School:	Faculty of Science > School of Chemistry
Depositing User:	Pure Connector
Date Deposited:	29 Apr 2016 12:00
Last Modified:	22 Oct 2022 01:02
URI:	https://ueaeprints.uea.ac.uk/id/eprint/58501
DOI:	10.1039/C6RA07007H

Downloads

Actions (login required)

View Item