67091-88-7Relevant academic research and scientific papers
Filling a Niche in “Ligand Space” with Bulky, Electron-Poor Phosphorus(III) Alkoxides
Hussein, Sharifa,Priester, Denis,Beet, Paul,Cottom, Jonathon,Hart, Sam J.,James, Tim,Thatcher, Robert J.,Whitwood, Adrian C.,Slattery, John M.
, p. 2262 - 2271 (2019)
The chemistry of phosphorus(III) ligands, which are of key importance in coordination chemistry, organometallic chemistry and catalysis, is dominated by relatively electron-rich species. Many of the electron-poor PIII ligands that are readily available have relatively small steric profiles. As such, there is a significant gap in “ligand space” where more sterically bulky, electron-poor PIII ligands are needed. This contribution discusses the coordination chemistry, steric and electronic properties of PIII ligands bearing highly fluorinated alkoxide groups of the general form PRn(ORF)3?n, where R=Ph, RF=C(H)(CF3)2 and C(CF3)3; n=1–3. These ligands are simple to synthesize and a range of experimental and theoretical methods suggest that their steric and electronic properties can be “tuned” by modification of their substituents, making them excellent candidates for large, electron-poor ligands.
Preparation and Nuclear Magnetic Resonance Studies of Pentacoordinated Phosphorus Compounds Containing Hexafluoroisopropoxy Groups
Denney, Donald, B.,Denney, Dorothy Z.,Hammond, Philip J.,Liu, Lun-Tsu,Wang, Yu-Pin
, p. 2159 - 2164 (2007/10/02)
The reaction of 1,1,1,3,3,3-hexafluoroisopropyl benzenesulfenate (7) with tris(1,1,1,3,3,3-hexafluoroisopropyl)phosphite (8) yielded tetrakis(1,1,1,3,3,3-hexafluoroisopropoxy)(phenylthio)phosphorane (9).Variable-temperature 19F NMR studies of 9 show that
