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Protactinium chloro complexes

Although protactinium(V) chloro complexes can also be prepared using methyl cyanide as the solvent (32) (cf. PaBrg" and Pale ), the use of thionyl chloride has several advantages. Thus, it means that one can start with protactinium(V) hydroxide and not the pentachloride, thionyl chloride itself affords protection against atmospheric moisture and dry-atmosphere boxes are not necessary for the preparations, and, in addition, protactinium(V) concentrations up to 0.5 M have been obtained by dissolving the hydroxide in thionyl chloride (75). Such solutions are quite stable in contrast to the hydrolytic condensation reactions which occur in concentrated hydrochloric acid at Pa(V) concentrations as low as 10 M. [Pg.29]

Salts of the analogous protactinium (V) (10) and uranium (V) (20) chloro complex ions, MClc, and MClg ", have been obtained from thionyl... [Pg.6]

CHLORO-COMPLEXES OF PENTAVALENT NIOBIUM, TANTALUM, PROTACTINIUM, TUNGSTEN AND URANIUM,... [Pg.437]

The results of solid state reactions of protactinium dioxide and pentoxide with other metal oxides (89, 93-96) support the view that the oxide systems of protactinium resemble those of other actinide elements rather than those of niobium and tantalum. However, when assessing results of this type one must always bear in mind the relative ionic radii of the respective M " and M + ions since they obviously play a large part in determining the structures of the complex phases. This comment applies equally well, of course, to the structural properties of other types of compound and in particular to the high coordination numbers exhibited by protactinium(V) in its chloro and nitrato complexes. [Pg.36]


See other pages where Protactinium chloro complexes is mentioned: [Pg.47]    [Pg.47]    [Pg.1182]    [Pg.1186]    [Pg.30]    [Pg.256]    [Pg.29]    [Pg.3021]    [Pg.3025]   
See also in sourсe #XX -- [ Pg.27 , Pg.28 ]

See also in sourсe #XX -- [ Pg.27 , Pg.28 ]




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Protactinium

Protactinium complexes

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