<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Troadec T</submitter><funding>Advantage West Midlands</funding><funding>Leverhulme Trust</funding><funding>Royal Society</funding><funding>European Regional Development Fund</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>3754-7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4797707</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>55(11)</volume><pubmed_abstract>Oxidation of zero-valent phosphine complexes [M(P(t) Bu3 )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 Pd(I) 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 Pt(II) complex [Pt(κ(2) PC -P(t) Bu2 CMe2 CH2 )(P(t) Bu3 )](+) with concomitant formation of [Pt(P(t) Bu3 )2 H](+) .</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>One-Electron Oxidation of [M(P(t) Bu3 )2 ] (M=Pd, Pt): Isolation of Monomeric [Pd(P(t) Bu3 )2 ](+) and Redox-Promoted C-H Bond Cyclometalation.</pubmed_title><pmcid>PMC4797707</pmcid><funding_grant_id>RPG-2012-718</funding_grant_id><funding_grant_id>EP/L027100/1</funding_grant_id><pubmed_authors>Troadec T</pubmed_authors><pubmed_authors>Rourke JP</pubmed_authors><pubmed_authors>Unwin PR</pubmed_authors><pubmed_authors>Chaplin AB</pubmed_authors><pubmed_authors>Tan SY</pubmed_authors><pubmed_authors>Wedge CJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>One-Electron Oxidation of [M(P(t) Bu3 )2 ] (M=Pd, Pt): Isolation of Monomeric [Pd(P(t) Bu3 )2 ](+) and Redox-Promoted C-H Bond Cyclometalation.</name><description>Oxidation of zero-valent phosphine complexes [M(P(t) Bu3 )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 Pd(I) 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 Pt(II) complex [Pt(κ(2) PC -P(t) Bu2 CMe2 CH2 )(P(t) Bu3 )](+) with concomitant formation of [Pt(P(t) Bu3 )2 H](+) .</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2026-05-05T11:41:48.615Z</modification><creation>2019-03-27T02:11:25Z</creation></dates><accession>S-EPMC4797707</accession><cross_references><pubmed>26879233</pubmed><doi>10.1002/anie.201511467</doi></cross_references></HashMap>