851576-76-6Relevant academic research and scientific papers
The coordination chemistry of pentafluorophenylphosphino pincer ligands to platinum and palladium
Anderson, Bradley G.,Spencer, John L.
, p. 6421 - 6432 (2014/06/09)
The synthesis of electron-poor PCP pincer ligands 1,3-((C6F 5)2PO)2C6H4, 1,3-((C 6F5)2PCH2)2C 6H4, and 1-((C6F5) 2PO)-3-(tBu2PCH2)C6H4, and their coordination chemistry to platinum and palladium is described. The most electron-poor ligand 1,3-((C6F5)2PO) 2C6H4 (POCOPH) reacts with Group10 metal chloride precursors to form a range of unusual cis, trans-dimers of the type κ2-P,P-[(POCOPH)MCl(L)]2 (M=Pt, Pd; L=Cl, Me), which undergo metallation to form [(POCOP)MCl] pincer complexes only under prolonged thermolysis. The formation of such cis,trans-dimers during pincer complex formation can be mitigated through the use of starting materials with more strongly binding ancillary ligands, improving the overall rate of ligand metallation. Carbonyl complexes of the type [(PCP)M(CO)]+ were synthesised from the pincer chloride complexes by halide abstraction, and displayed large ν(C-O) values, from 2170-2111cm-1, confirming the electron-poor nature of the compounds. The [(PCP)Pd(CO)]+ complexes also demonstrated the ability to reversibly bind carbon monoxide both in solution and the solid state, with the rate of decarbonylation increasing with increasing wavenumber for the C-O stretch. Back and forth: The electron-poor P(C6F5)2 donor group was incorporated into the PCP pincer ligand motif to generate a range of poorly donating ligands. Palladium carbonyl complexes of these ligands demonstrated the ability to reversibly bind CO, with the ease of CO displacement increasing with increasing ν(CO) values (see figure). These ligands also displayed a reluctance to undergo metallation on Pt or Pd, which led to the formation of rare examples of cis,trans-dimers.
Electron-poor pentafluorophenyl-substituted PCP - Palladium pincer complexes
Chase, Preston A.,Gagliardo, Marcella,Lutz, Martin,Spek, Anthony L.,Van Klink, Gerard P. M.,Van Koten, Gerard
, p. 2016 - 2019 (2008/10/09)
A novel fluoroaryl-substituted PCP ligand has been synthesized and used to generate the corresponding Pd complexes. The bonding of the fluoroaryl phosphine has been investigated by X-ray crystallography, NMR spectroscopy, and a competition experiment, which indicate that the ligand is sterically comparable to its well-known phenyl analogue but clearly imparts significant electronic differences to the metal center.
