Literature DB >> 15782267

The electron-poor phosphines P{C6H3(CF3)2-3,5}3 and P(C6F5)3 do not mimic phosphites as ligands for hydroformylation. A comparison of the coordination chemistry of P{C6H3(CF3)2-3,5}3 and P(C6F5)3 and the unexpectedly low hydroformylation activity of their rhodium complexes.

Matthew L Clarke1, Dianne Ellis, Kate L Mason, A Guy Orpen, Paul G Pringle, Richard L Wingad, Damien A Zaher, R Tom Baker.   

Abstract

The fluoroaryl phosphines P{C6H3(CF3)2-3,5}3 (La) and P(C6F5)3 (Lb) form the complexes trans-[MCl2(La)2] and trans-[MCl2(Lb)2](M = Pd or Pt) which have been isolated and fully characterised. 31P NMR studies of competition experiments show that the stability of trans-[PdCl2L2] is in the order L = Lb< La <PPh3. The crystal structure of trans-[PtCl2(La)2] is reported and reveals that the Pt-P bond lengths in trans-[PtCl2L2] are in the order L = Lb< La < PPh3. The equilibria established when [Pt(norbornene)3] is treated with or are investigated by 31P and 195Pt NMR spectroscopy and the species [PtLn(norbornene)3-n](n= 1-3) identified. Ligands and appear to have similar affinities for platinum(0). The complexes trans-[MCl(CO)(La)2] and trans-[MCl(CO)(Lb)2](M = Rh or Ir) have been synthesised and fully characterised; the values of nu(CO) are comparable with those for analogous phosphite complexes. The ligands La, Lb, P(C6H2F3-3,4,5)3 (Lc), P{C6H4(CF3)-2}3 (Ld), PPh3 and P(OPh)3 have been tested in rhodium-catalysed hydroformylation of 1-hexene and La, Lb, and PPh3 have been tested in rhodium-catalysed hydroformylation of 4-methoxystyrene. Ligands La, and Lb, have been shown to be stable under the hydroformylation catalysis conditions. For the 1-hexene reaction, the activity and selectivity for and are very similar to the PPh3 catalyst (TOF ca. 400 h(-1); n : iso 2.5-3.0) but for the sterically demanding and the activity and selectivity was much lower than with PPh3 (TOF ca. 15, n : iso ratio 0.6). Thus, the yield of heptanals obtained with the catalyst derived from La is 94% while under the same conditions with Lb only 6%. The TOF for the La/Rh catalyst was 5 times lower than for the P(OPh)3/Rh catalyst despite the superficially similar ligand electronic characteristics for La and P(OPh)3.

Entities:  

Year:  2005        PMID: 15782267     DOI: 10.1039/b418193j

Source DB:  PubMed          Journal:  Dalton Trans        ISSN: 1477-9226            Impact factor:   4.390


  6 in total

1.  P-C bond formation via P-H addition of a fluoroaryl phosphinic acid to ketones.

Authors:  Andreas Orthaber; Jörg H Albering; Ferdinand Belaj; Rudolf Pietschnig
Journal:  J Fluor Chem       Date:  2010-10       Impact factor: 2.050

2.  Hydrogenation of unactivated enamines to tertiary amines: rhodium complexes of fluorinated phosphines give marked improvements in catalytic activity.

Authors:  Sergey Tin; Tamara Fanjul; Matthew L Clarke
Journal:  Beilstein J Org Chem       Date:  2015-05-05       Impact factor: 2.883

3.  Efficient and Recyclable RuCl3 ⋅ 3H2O Catalyst Modified with Ionic Diphosphine for the Alkoxycarbonylation of Aryl Halides.

Authors:  Qing Zhou; Lei Liu; Wen-Di Guo; Wen-Yu Liang; Yong Lu; Ye Liu
Journal:  ChemistryOpen       Date:  2019-01-23       Impact factor: 2.911

4.  Fluorine-Substituted Arylphosphine for an NHC-Ni(I) System, Air-Stable in a Solid State but Catalytically Active in Solution.

Authors:  Kouki Matsubara; Takahiro Fujii; Rion Hosokawa; Takahiro Inatomi; Yuji Yamada; Yuji Koga
Journal:  Molecules       Date:  2019-09-04       Impact factor: 4.411

5.  A SF5 Derivative of Triphenylphosphine as an Electron-Poor Ligand Precursor for Rh and Ir Complexes.

Authors:  Maria Talavera; Silke Hinze; Thomas Braun; Reik Laubenstein; Roy Herrmann
Journal:  Molecules       Date:  2020-09-01       Impact factor: 4.411

6.  Development of highly efficient platinum catalysts for hydroalkoxylation and hydroamination of unactivated alkenes.

Authors:  Yali Zhou; Xingjun Xu; Hongwei Sun; Guanyu Tao; Xiao-Yong Chang; Xiangyou Xing; Bo Chen; Chen Xu
Journal:  Nat Commun       Date:  2021-03-29       Impact factor: 14.919

  6 in total

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