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Tris pentafluorophenyl

Xenon difluoride has been used to oxidize a number of antimony compounds [102, 109] in yields ranging from 73 to 98%. Elemental fluorine oxidized tris(pen-tafluorophenyl)stibine to tris(pentafluorophenyl)stibine difluoride in 98% yield [706]. Oxidative fluonnation of stibines has also been accomplished with iodine pentafluoride [707]. [Pg.46]

Imidazole reacts with dimethylzirconocene in the presence of a strong Lewis base, tris(pentafluorophenyl)borane, to yield the betaine species 22 (96JOM(518)17), which when exposed to the atmosphere is hydrolyzed to 23. [Pg.123]

Octaethyl and tris(pentafluorophenyl) corroles, known as oec and tpfc, respectively, are also efficient for the stabilization of P(VI) phosphorus [53,54]. The electron-rich oec reacts with PCI3 to form (oec)P=0 40 that can be further derived into dihydrido 41a, dimethyl 41b and diphenyl 41c compounds by reduction with LiAlH4 and reactions with methyl and phenyl Grignard reagents. [Pg.13]

Vaughan, L.G. and Sheppard, W.A. (1970) Organogold chemistry. II. Tris (pentafluorophenyl)gold(I II). Journal... [Pg.164]

Mono- and binuclear gold(I) and gold(III) complexes with S2C-PR3 ligands. X-ray crystal structures of tris (pentafluorophenyl)... [Pg.168]

III) and m-(triethylphosphoniodithio-formate-S,S )bis[tris (pentafluorophenyl) gold(III)] dichloromethane (1/1). [Pg.168]

Uson, R., Laguna, A., Laguna, M., Fernandez, F., Jones, P.G. and Sheldrick, G.M. (1982) Tris(pentafluorophenyl)gold (III) complexes. Journal of the Chemical Society, Dalton Transactions, (10), 1971-1976. [Pg.175]

Jones, P.G., Terroba, R., Fernandez, E. and Laguna, M. (2002) Tris (pentafluorophenyl) [2-(diphenylphosphino)thiophenol-kPjgold (III) dichloromethane solvate. Acta Crystallographica, Section E Structure Reports Online, E58(3), m90-m92... [Pg.175]

Jones, P.G. (1992) [(Methyldiphenylphosphonio)methanide] tris(pentafluorophenyl)gold(III) acetone solvate. Acta Cr/staUographica, Section C Crystal Structure Communications, C48(7), 1209-1211. [Pg.177]

In the tris-pentafluorophenyl analog (TFPC), in contrast to other Co corroles, aromatic amines can substitute PPh3 to form six-coordinate trivalent bis(amine) complexes.788 Bis-chlorosulfon-ation of TFPC occurs regioselectively to give the 2,17-(pyrrole)-bis-chlorosulfonated derivative fully characterized as its triphenylphosphinecobalt(III) complex.789 The amphiphilic bis-sulfonic acid was also obtained. [Pg.69]

MRH values calculated for 14 combinations, largely with oxidants, are given. Tris(pentafluorophenyl)boron... [Pg.833]

Figure 36 Anion bridging in (a) solid tris(pentafluorophenyl) telluronium chloride and (b) dimesityl(pentafluorophenylseleno) telluronium hexafluoroantimonate... Figure 36 Anion bridging in (a) solid tris(pentafluorophenyl) telluronium chloride and (b) dimesityl(pentafluorophenylseleno) telluronium hexafluoroantimonate...

See other pages where Tris pentafluorophenyl is mentioned: [Pg.650]    [Pg.63]    [Pg.155]    [Pg.144]    [Pg.176]    [Pg.177]    [Pg.437]    [Pg.1006]    [Pg.1006]    [Pg.1241]    [Pg.1241]    [Pg.1275]    [Pg.260]    [Pg.11]    [Pg.125]    [Pg.126]    [Pg.126]    [Pg.127]    [Pg.132]    [Pg.747]    [Pg.748]    [Pg.748]    [Pg.750]    [Pg.750]    [Pg.751]    [Pg.752]    [Pg.753]    [Pg.756]    [Pg.22]    [Pg.164]    [Pg.351]    [Pg.837]   
See also in sourсe #XX -- [ Pg.689 ]




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Pentafluorophenylation

Tris(pentafluorophenyl) Borane

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