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Platinum dichlorobis!triphenylphosphine

Bis(dimethyl hydrogen phosphite-/ )bis(dimethyl phosphito-P)platinum(lI) (0.420 g, 0.66 mmole) and c/s-[dichlorobis(triphenylphosphine)platinum(ll)] (0.524 g, 0.66 mmole) are refluxed in toluene (25 mL) for 30 hours. The colorless reaction mixture is filtered while hot using vacuum to remove any unreacted c/s-[dichlorobis(triphenylphosphine)platinum(Il)]. The filtrate is transferred to a 100-mL, round-bottomed flask and evaporated to dryness on a rotary evaporator, using gentle heating if necessary. The cream-colored residue is dissolved in a mixture of dichloromethane (15 mL) and methanol (15 mL) and the solution is allowed to concentrate slowly under water aspirator vacuum on a rotary... [Pg.99]

The reaction of dichlorobis(triphenylphosphine)platinum(II) with Na[Co(CO)4] gives only the tetrametal cluster, Pt2Co2(PPh3)(CO)8, in a low yield.3 The corresponding trimetal cluster, PtCo2(PPh3)(CO)8,4 is obtained... [Pg.369]

Pinacolone, o-(diphenylphosphino)benzoyl-coordination chemistry, 401 Piperidine, IV-hydroxy-metal complexes, 797 pA a values azole ligands, 77 Plant roots amino acids, 962 carboxylic acids, 962 Plastocyanin copper binding site, 557 copper(II) complexes, 772 copper(II) site in, 770 Platinum, dichlorobis(benzonitrile)-IR spectrum, 264 Platinum, cis-dichlorodianunine-antitumor activity, 34, 979 Platinum, ethylenebis(triphenylphosphine)-reactions with 5,6-dimethyl-2,l,3-benzothiadiazole, 194 Platinum blue formation, 265 Platinum complexes acetylacetone reactions, 380 amides, 491 amidines... [Pg.1092]

Tetrakis(triphenylphosphine)platinum(0) is a pale yellow powder which decomposes in the air to a red liquid at 118-120° and melts in vacuo (1 mm.) to a yellow liquid at 159-160°. The infrared spectrum in Nujol show s absorption maxima at 700(vs), 737(vs), 837(w), 992(s), 1022(s), 1077(vs), 1147(m), 1162(m), 1302(w), and 1432(vs) cm. h The compound is soluble in benzene with dissociation by leaving the benzene solution in the air, a white pow der [the carbonatobis(triphenylphosphine)-platinum(II) formed by action of oxygen and carbon dioxide] separates slowly. The compound reacts wdth carbon tetrachloride, giving cfs-dichlorobis(triphenylphosphine)platinum(II). ... [Pg.106]

Tetrachloropalladate(II) ion catalyzes the interconversion of 1- and 2-butenes in aqueous solutions containing chloride and hydronium ions. Sodium tetrachloropalladate(II) catalyzes the conversion of allylbenzene to propenyl-benzene in acetic acid solutions. Tetrakis(ethylene))Lt,/x -dichlororhodium(l) catalyzes butene isomerization in methanolic hydrogen chloride solutions . Cyclooctadienes isomerize in benzene-methanol solutions of dichlorobis-(triphenylphosphine)platinum(11) and stannous chloride. Chloroplatinic acid-stannous chloride catalyzes the isomerization of pentenes. Coordination complexes of zero-valent nickel with tris(2-biphenylyl)phosphite or triphenyl-phosphine catalyze the isomerization of cis-1,2-divinylcyclobutane to a mixture of c/5,m-l, 5-cyclooctadiene and 4-vinylcyclohexene . Detailed discussions of reaction kinetics and mechanisms appear in the papers cited. [Pg.449]

The compound dissolves in benzene, with dissociation. By leaving the benzene solution in the air, (carbonato)bis(triphenylphosphine)platinum(II) separates slowly. It reacts easily with carbon tetrachloride giving cis-dichlorobis(triphenylphosphine)platinum(II). The complex is tricoordinated in the solid state, and shows a nearly pure sp hybridization of the platinum atom. ... [Pg.125]

R. W. Adams, G. E. Batley and J. C. Bailar, Jr., Homogeneous Catalytic Hydrogenation and Isomerization of Olefins with Dichlorobis(triphenylphosphine)platinum(II)-Tin Chloride Catalyst, Inorg. Nucl. Chem. Letters 4 455 (1968). [Pg.349]

The controlled-potential electrolyses were carried out in a cell with three separated compartments. The cathode was a reticulated carbon rod and the anode was a platinum wire. As reference electrode was used a modified SCE. The catholyte was prepared by dissolving 2-aminophenol in CH3CN, containing n-Bu NBF (0.2M) as well as an excess of base and dichlorobis(triphenylphosphine) palladium(II) or palladium(II) acetate as catalyst. Carbon monoxide was bubbled through a glass capillary into the cathodic solution that subsequently was kept under a CO pressure of 1 atm. The electrolyses were interrupted when the current dropped to the value of the background current. [Pg.94]


See other pages where Platinum dichlorobis!triphenylphosphine is mentioned: [Pg.114]    [Pg.115]    [Pg.505]    [Pg.313]    [Pg.1485]    [Pg.272]   


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