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Lanthanide complexes dithiophosphinates

Pinkerton and coworkers reported another method for separating the contact shifts and evaluating the hyperfine coupling constant A for P in NMR studies of a series of tetrakis lanthanide complexes derived from dithiophosphinates, [R S2P(CH3)2 4] (Spiliadis and Pinkerton 1982) and esters of dithiophosphoric acid, [R (XO)2PS2 4] ... [Pg.9]

Boehme, C., Wipff, G. 2001. The energetic and structural effects of steric crowding in phosphate and dithiophosphinate complexes of M3+ lanthanide cations. A computational study. Chem. Eur. J. 1 1398-1407. [Pg.45]

Cyanex 301 One of the solvent extraction processes, used together with UREX, for separating the components of used nuclear fuel. This process uses a complex phosphinic acid, [bis(2,4,4-trimethylpentyl)dithiophosphinic acid], made by Cytec Industries, Canada. Its purpose is to separate americium, curium, and lanthanide fission products from the other components. [Pg.93]

XAFS data for complexes of Cm with the HC301 extractant indicate only sulfur donation to the metal in the inner sphere of coordination. HC301 forms 3 1 complexes with the trivalent actinides and are coordinated in a bidentate mode as seen in Figure 91. Data indicates a hexacoordinate structure that resembles Z>3 symmetry in lanthanide dithiophosphinic acid complexes. [Pg.315]

Yttrium, Lanthanum and the Lanthanides. P NMR spectroscopy has been used to study complexation of La " by (4-02NC6H40)2P02H and (MeO)(4-02NC6H40)P02H. C and N NMR spectroscopy has been used to study complex formation between [SCN] andPr + and Nd. P chemical shifts of di(chlorophenyl)dithiophosphinic acid correlate quantitatively with the extrac-tability of Am and Eu ". ... [Pg.48]


See other pages where Lanthanide complexes dithiophosphinates is mentioned: [Pg.415]    [Pg.415]    [Pg.950]    [Pg.13]    [Pg.315]    [Pg.950]    [Pg.24]    [Pg.27]    [Pg.40]   
See also in sourсe #XX -- [ Pg.1087 ]




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