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Rhodium complexes sulfur dioxide

Apart from anion exchange reactions the complexes are inert. One of the few reagents to bring about a change in the coordination sphere is sulfur dioxide which coordinates to rhodium without displacement of a bidentate ligand. However, the product is not well characterized and the crystals contain clathrated sulfur dioxide.250... [Pg.928]

However, not all bidentate ligands form complexes of this stoichiometry. Although sulfur dioxide displaces CO from a binuclear rhodium(I) complex, the product (97) retains a rhodium-rhodium bond.1048 The complexes of (98) form primarily fac products when allowed to react with rhodium trichloride.1049 The strength of the rhodium-sulfur bond is also shown in the failure of diphos or... [Pg.1039]

Reaction with sulfur dioxide yields a o--allylic rhodium-sulfur dioxide complex (1). [Pg.245]

The [Rh(NH3)5(OH)] cation, and its chromium(III) analog, react very rapidly with sulfur dioxide in aqueous solution, to give O-sulfito complexes, which lose sulfur dioxide on addition of acid. Rate constants for reaction of the rhodium(III), chromium(III), and cobalt(III) complexes [M(NH3)5(OH)] with sulfur dioxide are 1.8 x 10, 2.9 x 10, and 4.7 x 10 dm mol" s", respectively. This great similarity of rates contrasts with the situation in respect of formation of carbonato complexes, where formation rate constants show a marked dependence on the p a of the aquo form of the hydroxo substrate. [Pg.186]


See other pages where Rhodium complexes sulfur dioxide is mentioned: [Pg.212]    [Pg.252]    [Pg.176]    [Pg.249]    [Pg.809]    [Pg.405]    [Pg.139]    [Pg.1041]    [Pg.1042]    [Pg.4079]    [Pg.809]    [Pg.100]    [Pg.220]    [Pg.1372]    [Pg.4078]    [Pg.1041]    [Pg.1042]    [Pg.1302]    [Pg.4495]    [Pg.4496]    [Pg.4756]    [Pg.6954]    [Pg.261]    [Pg.264]    [Pg.215]    [Pg.115]   
See also in sourсe #XX -- [ Pg.907 ]




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