Phenyl platinum 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... 

Phenyl, platinum complex, 26 136 QH,N, Pyridine, osmium complex, 26 291 OH,NO, 4-Pyridinecarboxylic acid, rhodium complex, 27 292... 

CgH, Phenyl, platinum complex, 26 136 CgHjCI, Benzene, chloro-, chromium complex, 28 139... 

Molecules having only a sulfoxide function and no other acidic or basic site have been resolved through the intermediacy of metal complex formation. In 1934 Backer and Keuning resolved the cobalt complex of sulfoxide 5 using d-camphorsulfonic acid. More recently Cope and Caress applied the same technique to the resolution of ethyl p-tolyl sulfoxide (6). Sulfoxide 6 and optically active 1-phenylethylamine were used to form diastereomeric complexes i.e., (-1-)- and ( —)-trans-dichloro(ethyl p-tolyl sulfoxide) (1-phenylethylamine) platinum(II). Both enantiomers of 6 were obtained in optically pure form. Diastereomeric platinum complexes formed from racemic methyl phenyl (and three para-substituted phenyl) sulfoxides and d-N, N-dimethyl phenylglycine have been separated chromatographically on an analytical column L A nonaromatic example, cyclohexyl methyl sulfoxide, did not resolve. 

The reaction of cyclic nitrone with phenyl isothiocyanate <2003MI253>, isocyanate <1974JOC568>, or cyano-esters <1995JP11417> has been reported. The beneficial effect of activation of the dipolarophile by coordination on a platinum complex and focused microwave irradiation has been described (Scheme 15) <2003JCD2540>. 

The most common route to alkyl or aryl complexes of the type [AuRL] is by the treatment of a halide complex with an alkyl- or aryllithium reagent. The first reactions of this type were performed (15) in 1959 [Eq. (5)], and the methyl and phenyl compounds were found to have chemical and thermal stabilities intermediate between those of the previously known organopalladium and -platinum complexes. 

F-Cyclooctene is chiral, and it was resolved into enantiomers by Cope and coworkers100 by separation of diasteromeric platinum complexes containing 20 and (+)-phenyl-2-aminopropane as ligands. Thermal racemization occurred around 150 °C with a rate... 

The platinum complex 171 easily reacts with excess of phenylacetylene with the formation of a 1 1 mixture of 1,4-digermacyclohexa-2,5-diene and (//-ace ty I ene)bis(tri phenyl phosphine (platinum in quantitative yields (Equation 4)... 

---