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Ruthenium catalysts containing sulfonated

Itsimo [25] has also shown that polymer-supported OPEN monosulfonamides containing sulfonated pendent group (Scheme 16) are able to catalyze the HTR reduction of ketones in water with sodium formiate as hydrogen donor (S/C = 100). However, TsDPEN immobilized on polystyrene crosslinked or not, polymer 30 and 31 respectively, shrank in water. Sodium /j-styrene sulfonate was copolymerized with chiral A-(vinylbenzene-p-sulfonyl)-DPEN (20) imder radical polymerization conditions with or without DVB leading respectively to ligand 32 and 33. Control of the balance hydrophilicity/hydrophobieity of the polymer support is carried out by changing the salt from Na to quaternary ammonium. All of these polymers swelled in water, and their respective ruthenium, rhodium or iridium complexes were prepared. Compared to sodium salt polymer-supported catalyst from 32a and 33a, ammonium... [Pg.55]

Henbest and Trocha-Grimshaw have shown that sulfoxides may be oxidized to sulfones in the presence of iridium and rhodium complexes [139, 140]. Oxidations were studied by passing air through a solution of the sulfoxide in hot wopropanol containing 10% water in the presence of the catalyst. Sulfones were formed when chlorides of iridium or rhodium were used while chlorides of ruthenium, osmium and palladium were not effective. Under reaction conditions the chlorides should be converted wholly or partly to metal sulfoxide complexes. [Pg.40]


See other pages where Ruthenium catalysts containing sulfonated is mentioned: [Pg.107]    [Pg.1239]    [Pg.67]    [Pg.1354]    [Pg.97]    [Pg.187]    [Pg.275]    [Pg.207]    [Pg.61]    [Pg.273]    [Pg.57]   


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