Troadec, Thibault, Tan, Sze-yin, Wedge, Christopher J., Rourke, Jonathan P. ![]() ![]() |
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Abstract
Oxidation of zero‐valent phosphine complexes [M(PtBu3)2] (M=Pd, Pt) has been investigated in 1,2‐difluorobenzene solution using cyclic voltammetry and subsequently using the ferrocenium cation as a chemical redox agent. In the case of palladium, a mononuclear paramagnetic PdI derivative was readily isolated from solution and fully characterized (EPR, X‐ray crystallography). While in situ electrochemical measurements are consistent with initial one‐electron oxidation, the heavier congener undergoes C−H bond cyclometalation and ultimately affords the 14 valence‐electron PtII complex [Pt(κ2PC‐PtBu2CMe2CH2)(PtBu3)]+ with concomitant formation of [Pt(PtBu3)2H]+.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Chemistry |
Publisher: | Wiley |
ISSN: | 1433-7851 |
Date of First Compliant Deposit: | 16 January 2019 |
Date of Acceptance: | 16 February 2016 |
Last Modified: | 02 May 2023 18:22 |
URI: | https://orca.cardiff.ac.uk/id/eprint/118453 |
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