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Phosphine, iridium complex ruthenium complexes

CsHuN, Ethanamine, A-ethyl-A-methyl-tungsten complex, 26 40, 42 C6HF5, Benzene, pentafluoro-gold complexes, 26 86-90 C H4I2, Benzene, 1,2-diido-iridium complex, 26 125 CJT, Phenyl platinum complex, 26 136 C,H,N, Pyridine osmium complex, 26 291 OHtS, Benzenethiol osmium complex, 26 304 QH7P, Phosphine, phenyl-cobalt-iron complex, 26 353 QH 1-Butyne, 3,3-dimethyl-mercury-molybdenum-ruthenium complex, 26 329-335 C6H 4P, Phosphine, triethyl-platinum complex, 26 126 platinum complexes, 26 135-140 CsHisPO, Triethyl phosphite iron complex, 26 61... [Pg.414]

C2H,N, Pyridine, 3,5-dimethyl-palladium complex, 26 210 CbHsNO, Benzoyl isocyanide chromium com-C HbO, Ethanone, 1-phenyl-manganese complex, 26 156-158 CBH, 02, Methyl benzoate chromium complex, 26 32 C H i, o-Xylylene magnesium complex, 26 147 ChH P, Phosphine, dimethylphenyl-iron complex, 26 61 ruthenium complex, 26 273 ChH12, 1,5-Cyclooctadiene iridium complex, 26 122 ruthenium complexes, 26 69-72, 253-256 ChH OjPS, 2-Butenedioic acid, 2-(dimethylphosphinothioyl)-dimethyl ester, manganese complex, 26 163... [Pg.415]

C1bHi5As, Arsine, triphenyl-iron complex, 26 61 C H 5OjP, Triphenyl phosphite ruthenium complex, 26 178 CuHijP, Phosphine, triphenyl-cobalt complex, 26 190—197 cobalt-gold-ruthenium, 26 327 gold complex, 26 90, 325, 326 gold-manganese complex, 26 229 iridium complexes, 26 117-120, 122-125, 201, 202... [Pg.416]

PC8HM, Phosphine, dimethylphenyl-, 22 133 iridium complex, 21 97 PC 2H27, Phosphine, tributyl-, chromium complexes, 23 38 PC18H1S, Phosphine, triphenyl-, 21 78 23 38 cobalt complexes, 23 24-25 cobalt, iridium, and rhodium complexes, 22 171, 173, 174 iridium complex, 21 104 palladium complex, 22 169 palladium and platinum complexes, 21 10 ruthenium complex, 21 29 PNOC 2Hl2, Phosphinic amide, diphenyl-, lanthanoid complexes, 23 180 PNAH.2, Propionitrilc, 3,3, 3 -phosphinidy-netri-,... [Pg.251]

Complexes of other metals are used to sensitize emulsions, and some are used to sensitize even further (supersensitize) gold-sensitized emulsions. " Among these are (NH4)2[PtCl4], (NH4)2[PdCl4], (NH4)2[PdCy, K2[IrCl6] and similar compounds with ruthenium and the other halides. Sensitization by iridium salts and complex ions has been reviewed recently. Mechanisms of action of palladium(II) salts and complex ions on gold-sensitized emulsions have been studied. Several phosphine complexes of palladium and platinum, for example (2), are reported to be effective sensitizers, as are many macrocyclic polyamine compounds and their metal complexes,for example the Cu", Ni", Fe " and Rh " chelates of the cyclen ligand, 1,4,7,10-tetraazacyclododecane (3). [Pg.6242]

Stimulating results achieved in hydrogenation of C=C double bonds with phosphinerhodium complexes led to the application of these compounds for the catalytic reduction of C=0 and C=N double bonds. The present review summarizes the results in this area reported up until now. To give a more complete picture of the subject, some reports on iridium and ruthenium phosphine complex catalysts have been included as well. [Pg.317]

Fig. 9 a ruthenium(Il)-arene complexes b rhodium and ruthenium carbene complexes c rhodium, iridium and ruthenium tripodal phosphine complexes d gold [1,3-(dimesitylmeth)dimidazolinium)] chloride complexes e metal carboxamide derivatives... [Pg.194]

Reductive eliminations of methane, toluene, and cyclohexane (Equations 8.11-8.13) occur from (PPh3)jPt(Me)(H), -> (PMe3),Ru(H)(CHjPh),> and Cp Lr(PMe)3(C,H )H without prior dissociation of ligand. The absence of ligand dissociation prior to reductive elimination was shown in these cases by a zero-order dependence of the reaction rates on the concentration of added phosphine. The rates for these elimination reactions vary dramatically. The platinum complex reacts at -25 °C, the ruthenium complex at 85 °C, and the iridium complex at 135 °C. Although one could rationalize these relative rates in many ways, the platinum compound likely reacts faster than the iridium complex because it is less electron rich, while the ruthenium complex likely reacts faster than the iridium complex because it contains a second-row metal center. [Pg.326]


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See also in sourсe #XX -- [ Pg.21 , Pg.29 , Pg.78 ]




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Iridium Phosphines

Phosphine iridium complex

Phosphine, dimethylphenyl-, ruthenium iridium complexes

Ruthenium phosphines

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