Jump to main content
Jump to site search
Access to RSC content Close the message box

Continue to access RSC content when you are not at your institution. Follow our step-by-step guide.


Issue 48, 2016, Issue in Progress
Previous Article Next Article

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

Author affiliations

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.

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

Back to tab navigation

Supplementary files

Article information


Submitted
16 Mar 2016
Accepted
20 Apr 2016
First published
28 Apr 2016

This article is Open Access

RSC Adv., 2016,6, 42421-42427
Article type
Paper

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

R. J. Blagg and G. G. Wildgoose, RSC Adv., 2016, 6, 42421
DOI: 10.1039/C6RA07007H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. Material from this article can be used in other publications provided that the correct acknowledgement is given with the reproduced material.

Reproduced material should be attributed as follows:

  • For reproduction of material from NJC:
    [Original citation] - Published by The Royal Society of Chemistry (RSC) on behalf of the Centre National de la Recherche Scientifique (CNRS) and the RSC.
  • For reproduction of material from PCCP:
    [Original citation] - Published by the PCCP Owner Societies.
  • For reproduction of material from PPS:
    [Original citation] - Published by The Royal Society of Chemistry (RSC) on behalf of the European Society for Photobiology, the European Photochemistry Association, and RSC.
  • For reproduction of material from all other RSC journals:
    [Original citation] - Published by The Royal Society of Chemistry.

Information about reproducing material from RSC articles with different licences is available on our Permission Requests page.


Social activity

Search articles by author

Spotlight

Advertisements