Intramolecular dehydrofluorinative coupling of η6-arene and fluoroarylphosphine ligands in ruthenium complexes

McGibbon, Angela; Nieuwenhuyzen, Mark; Saunders, Graham C.

doi:10.1016/j.jfluchem.2011.05.004

Cited by 4 publications

(2 citation statements)

References 31 publications

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“…Saunders et al investigated intramolecular C–C bond formation reactions which lead to ligands with cyclopentadienyl phosphine moieties at rhodium and iridium centers as well as benzyl linked phosphines at ruthenium . An example for such a C–C coupling in the ligand sphere of a rhodium complex is shown in Scheme . ,,, The reaction is initiated by deprotonation of the Cp* ligand of 77 , which presumably results in the formation of the η 4 -fulvene complex 78 or the corresponding carbanion 79 .…”

Section: C–f Activation and C–c Bond Formationmentioning

confidence: 99%

Functionalization of Fluorinated Molecules by Transition-Metal-Mediated C–F Bond Activation To Access Fluorinated Building Blocks

et al. 2014

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Section: C–f Activation and C–c Bond Formationmentioning

confidence: 99%

Functionalization of Fluorinated Molecules by Transition-Metal-Mediated C–F Bond Activation To Access Fluorinated Building Blocks

et al. 2014

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“…As no resonance in the 31 P NMR spectrum was observed for a OP(C 6 F 5 ) 2 moiety associated with the degradation product 9, the P−O bond was presumed to have been cleaved, giving 9 the formula (3-OH-C 6 H 4 )PF 2 t Bu 2 . The fluorine atoms directly bound to the phosphorus are likely to have originated from the ortho or para positions of the pentafluorophenyl substituents on the phosphinite group, as these aromatic fluorines have been reported to be particularly susceptible to nucleophilic attack, [73][74][75] even from phosphorus nucleophiles. 76 However, the mechanism for the fluorination of the di-tert-butyl phosphine group is not known.…”

Section: Pcp Pincer Ligandsmentioning

confidence: 99%

Late Transition Metal Complexes of Pentafluorophenylphosphino-Pincer Ligands

Anderson¹

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<p>This thesis details the synthesis of new examples of electron-poor pincer ligands, featuring bis(pentafluorophenyl)phosphine donors attached to 1,3-substituted phenylene or 2,6-substituted pyridine backbones, to create tridentate PCP and PNP ligands. The effect of the ligands’ electronic nature on the coordination chemistry and ease of pincer complex synthesis with late transition metals is discussed, as is the catalytic activity of the resultant palladium pincer complexes in the Heck and Suzuki reactions. Symmetric PCP and PNP ligands possessing bis(pentafluorophenyl)phosphinite and bis(pentafluorophenyl)phosphoramine functionalities were synthesised by reaction of bis(pentafluorophenyl)phosphine bromide with resorcinol, 3-hydroxybenzyl-di- tert -butylphosphine, 2,6-diaminopyridine, or 2,6-dihydroxypyridine, affording 1,3- [(C6F5)2PO]2C6H4 (POCOPH, 1), 1-[(C6F5)2PO]-3-(tBu2PCH2)2C6H4 (POCCPH, 3), 2,6-[(C6F5)2PNH]2C6H3N (PNNNP, 10), and 2,6-[(C6F5)2PO]2C6H3N (PONOP, 11) respectively. The previously reported 1,3-[(C6F5)2PCH2]2C6H4 (PCCCPH, 2) was also synthesised, with the literature yield improved upon by the use of magnesium-anthracene to generate the required Grignard reagent. The coordination chemistry of the POCOPH ligand 1 with platinum(0) alkene and platinum(II) dimethyl precursors revealed an affinity for the formation of cis-bridged oligomeric structures. The dimer [(POCOPH)Pt(nb)]2 (14, nb = norbornene) was isolated and crystallographically characterised from the reaction between 1 and [Pt(nb)3]. The solid state structure revealed the presence of stabilising - interactions between the aromatic ligand backbones, which were also observed in solution by 1H NMR spectroscopy. Reactions of ligand 1 with platinum and palladium dichloride or chloromethyl starting materials led to rare examples of cis,trans-dimers of the type cis,trans-[(POCOPH)MClX]2 (M = Pd, Pt; X = Cl, Me). In part due to facile dimer formation with 1, metallation of the ligand backbone to form the tridentate pincer complex [(POCOP)PtCl] (25) required long reaction times and high temperatures. It was observed that platinum dichloride starting materials with more strongly binding ancillary ligands were less prone to oligomer formation, and could facilitate more rapid metallation to from 25. More facile pincer complex formation was also observed for more electron-rich ligands with both PCP and PNP pincer ligands. The electron poor platinum and palladium POCOP, PCCCP, and POCCP pincer complexes (where the free ligand had been deprotonated upon metallation) were synthesised and subsequently converted into the metal carbonyl species [(PCP)M(CO)]+. Analysis of C−O stretching frequencies by infrared spectroscopy confirmed complexes of POCOP ligand 1 were the most electron poor, while those of POCCP ligand 3 were the most electron rich. Decarbonylation of the palladium pincer complexes was observed in solution and in the solid state, and was more facile for complexes with a higher wavenumber C−O stretch. Reaction of the [(PCP)PtCl] pincer complexes with methyl nucleophiles revealed that treatment with methylmagnesium iodide resulted in halide exchange, while methyllithium promoted nucleophilic attack at phosphorus. Spectroscopic data indicated that in one instance this led to pentafluorophenyl migration to the metal centre to form a [(PCP)Pt(C6F5)] complex. Dimethylzinc was successful in methylating the platinum PCP complexes; however, it was observed to degrade the palladium PCP pincer complexes. Treatment of the rhodium PNP pincer complex [(PNNNP)RhCl] (49) with dimethylzinc also resulted in degradation, which spectroscopic evidence indicated proceeded via ligand deprotonation and the formation of a zinc adduct of 49. Low temperature protonolysis of the [(PCP)PtMe] species did not reveal any information about possible interactions between the metal and liberated methane. The catalytic activity of the electron-poor [(PCP)PdCl] complexes were assessed in the Heck and Suzuki cross-coupling reactions. The complexes of 1, 2, and 3 were all found to possess only modest activity in the Heck reaction, functioning as precatalysts which decomposed to give catalytically-active Pd(0) colloids. Under milder Suzuki reaction conditions, the most electron-poor complex, [(POCOP)PdCl] (28) proved to be one of the most active pincer catalysts known for this reaction, able to achieve a turnover number of 176,000 for the coupling of electronically-deactivated aryl bromides and phenylboronic acid. Mercury poisoning tests revealed that Suzuki reactions catalysed by 28 proceeded via a homogeneous active species.</p>

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Complex dependent regioselectivity in the nucleophilic substitution of fluorine of a coordinated tetrafluoropyridyl N-heterocycle carbene

Pachal¹,

Saunders²,

Weston³

2013

Inorganica Chimica Acta

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Intramolecular dehydrofluorinative coupling of η6-arene and fluoroarylphosphine ligands in ruthenium complexes

Cited by 4 publications

References 31 publications

Functionalization of Fluorinated Molecules by Transition-Metal-Mediated C–F Bond Activation To Access Fluorinated Building Blocks

Functionalization of Fluorinated Molecules by Transition-Metal-Mediated C–F Bond Activation To Access Fluorinated Building Blocks

Late Transition Metal Complexes of Pentafluorophenylphosphino-Pincer Ligands

Complex dependent regioselectivity in the nucleophilic substitution of fluorine of a coordinated tetrafluoropyridyl N-heterocycle carbene

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