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Ditertiary arsine oxides

There is an extensive chemistry of tertiary phosphine rhodium(III) complexes. However, there are comparatively few complexes of monodentate tertiary arsines, although the complexes of ditertiary arsines are more numerous. There are virtually no tertiary stibine complexes. The two main preparative routes to the complexes described in this section are (i) direct reaction pf the ligands with rhodium trichloride, which usually yields trichloro complexes and (ii) oxidative addition to rhodium(I) tertiary phosphine complexes, which gives rise to more diverse products of the type [RhXYZ(PRj) ], Metathetical reactions on the complexes prepared by either method (i) or (ii) have been used to prepare most of the remaining compounds. [Pg.1015]

Tetrafluoroborate,223 tetraphenylborate and iodide227 salts of a large range of rhodium(I) complex cations react oxidatively with dioxygen (equation 242). The physical properties of the dioxygen complexes are given in Table 80. The claim that a rhodium(I) species containing a ditertiary arsine... [Pg.1036]

The other hydrogen halides add oxidatively to rhodium(I) complexes of ditertiary phosphines or arsines giving rise to numerous monohydrido complexes, whose physical properties are also listed in Table 79. However, it is possible to prepare certain monohydrido complexes from rhodium(III) halides. One interesting reaction, carried out under an atmosphere of CO, gives rise to dicar-bonyldichlororhodate(I) salts (equation 241).226... [Pg.1036]


See other pages where Ditertiary arsine oxides is mentioned: [Pg.174]    [Pg.6052]    [Pg.174]    [Pg.6052]    [Pg.161]    [Pg.1234]    [Pg.1234]    [Pg.4688]    [Pg.5034]    [Pg.980]    [Pg.983]    [Pg.240]    [Pg.252]    [Pg.641]    [Pg.641]    [Pg.980]    [Pg.983]    [Pg.251]    [Pg.7125]    [Pg.7128]   
See also in sourсe #XX -- [ Pg.16 ]




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