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Trivalent uranium coordination chemistry

Coordination Chemistry. The coordination chemistry of trivalent uranium is certainly characterized by the large atomic dimensions as appearing in series of compounds featuring C-, N-, S-, and O-donor based ligand complexes. [Pg.323]

This is a convenient, facile, and high-yield preparative route for quantitative preparation of the complexes above no special equipment is required. UI3(THF)4 crystallizes in a P2x/c space group. It is mononuclear with pentagonal-pyramidal coordination geometry around the central uranium atom. This compound is stable until 75°C, then THF molecules are removed by steps, forming UI3 at 162°C. Lewis base adducts of uranium tri-iodide, such as UI3(THF)4 above, are synthetically useful precursors for trivalent uranium chemistry (see Sec. 5.3.2) [360]. [Pg.440]


See other pages where Trivalent uranium coordination chemistry is mentioned: [Pg.329]    [Pg.329]    [Pg.323]    [Pg.328]    [Pg.336]    [Pg.339]    [Pg.70]    [Pg.19]    [Pg.20]    [Pg.853]    [Pg.385]    [Pg.341]    [Pg.195]   
See also in sourсe #XX -- [ Pg.336 , Pg.337 , Pg.338 , Pg.339 , Pg.340 , Pg.341 ]




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