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Smith, Dan A., Roşca, Dragoş-Adrian and Bochmann, Manfred 
ORCID: https://orcid.org/0000-0001-7736-5428
(2012)
Selective Au–C cleavage in (C∧N∧C)Au(III) aryl and alkyl pincer complexes.
Organometallics, 31 (17).
pp. 5998-6000.
ISSN 0276-7333
Abstract
Treatment of gold(III) pincer complexes (C∧N∧C)*AuX with trifluoroacetic acid (X = C6F5, thiophenyl, Me, Et) or of (C∧N∧C)*AuOAcF with AgOAcF/arylboronic acids leads to the selective cleavage of a C–Au bond under mild conditions to give the bidentate complexes (HC-C∧N)*Au(X)(OAcF) [(C∧N∧C)* = 2,6-(C6H3But)2pyridine]. Alkylation of (C∧N∧C)*Au(OAcF) with AlR3 (R = Me, Et) proved to be a high-yielding route to gold(III) alkyls. Au–C cleavage significantly influences reactivity, e.g., with boronic acids. The photoemission of the cleavage product (HC-C∧N)*Au(C6H4F)(OAcF) is about an order of magnitude more intense than that of its tridentate parent compound.
| Item Type: | Article |
|---|---|
| Faculty \ School: | Faculty of Science > School of Computing Sciences Faculty of Science > School of Chemistry |
| UEA Research Groups: | Faculty of Science > Research Groups > Smart Emerging Technologies Faculty of Science > Research Groups > Chemistry of Materials and Catalysis Faculty of Science > Research Groups > Chemistry of Light and Energy Faculty of Science > Research Groups > Synthetic Chemistry (former - to 2017) |
| Depositing User: | Users 2731 not found. |
| Date Deposited: | 21 Jan 2013 16:02 |
| Last Modified: | 10 Nov 2022 11:31 |
| URI: | https://ueaeprints.uea.ac.uk/id/eprint/40900 |
| DOI: | 10.1021/om300666j |
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