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Group VII Donor Ligands

Silver(i).-Group VII Donor Ligands. AW-Dimethylthioformamide complexes AgCl,-2DMTF, AgBr,2DMTF, and AgI,DMTF have been characterized in solution and in the solid state, and the dissociation constant for reaction (26) was determined from conductivity measurements. Complex solubilities of AgX (X = Cl, Br, or I) have been determined in benzonitrile and trichloroacetonitrile mixtures with propylene-carbonate.The results were compared with previous work in acetonitrile and propionitrile. [Pg.387]

Treatment of AgBr with PPhj in refluxing MeCN yields the new dimer (60) and the tetramer [(PhaP)4 Ag4Br4], both of whose Jf-ray structures were also reported (see Table 7). Their stereochemistries were compared with the structurally analogous [Pg.387]

Danksagmuller, G. Gritzner, and V. Gutmann, Inorg. Chun. Acta, 1976,18,269. [Pg.387]

Ag3P309,H20 0.048 P3O9 cyclic anion has chair configuration h  [Pg.388]

A new ternary halide CaAg2H has been obtained as a black, diamagnetic compound either by hydriding CaAg2 alloy or by the solid state reaction between Ag and CaH2 in a H2 atmosphere.  [Pg.389]


Gold(lll).—Group VII Donor Ligands. The single-crystal polarized electronic spectra of NaAuCl4,2H20 have been measured at a number of temperatures. The bands... [Pg.393]

Ruthenium(ii).—Group VII Donors. Halide donor ligands. A study has shown that the blue complexes obtained by electrolytic reduction of H2[RuCl5H20] in acidic solution are further examples of mixed Ru"-Ru " complexes. They were previously assumed to contain only Ru . Dimers of the type Ru2Ch3Vi," (n = 0,1, or 2) were separated and isolated using ion-exchange chromatography. [Pg.351]

Osmium(n).—Group VII Donors. Hydrido- and halogeno-carbonyl complexes. Carbonylation of [OsHX(CO)(PCy3)2] has produced the novel dicarbonyl hydride [OsHX(CO)2(PCy3)2] (X = Cl or Br Cy = tricyclohexyl).17 I.r. and n.m.r. data indicate the geometry (17). Addition of other ligands to the five-co-ordinate... [Pg.346]

Clusters of the group V-VII metals in high formal oxidation states, stabilised by 7t-donor ligands such as oxide, sulphide, or halides. Examples here include [Nb6Cli2] +, [WeBrgJ +and [Re3Cl9] +. [Pg.138]

Little reliable data concerning the influence of the nature of ligands can be found in the literature. A recent study by Pretzer et at. covers the Group V triphenyl derivatives [25]. Use of triphenyl phosphine yields ethanol in high selectivity, whereas iriphcnyl arsine yields preponderantly acetaldehyde (c.f. Table VII). This finding is interpreted by correlating the o-donor ability of... [Pg.114]


See other pages where Group VII Donor Ligands is mentioned: [Pg.370]    [Pg.392]    [Pg.370]    [Pg.392]    [Pg.183]    [Pg.405]    [Pg.330]    [Pg.1297]    [Pg.3978]    [Pg.4751]    [Pg.349]    [Pg.363]    [Pg.380]    [Pg.393]    [Pg.439]    [Pg.276]    [Pg.384]    [Pg.2]    [Pg.385]    [Pg.622]    [Pg.147]    [Pg.150]    [Pg.2]    [Pg.95]    [Pg.3456]    [Pg.230]    [Pg.349]    [Pg.97]    [Pg.100]    [Pg.162]    [Pg.139]    [Pg.219]    [Pg.236]    [Pg.708]   


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Donor ligand

Group VII donors

Groups, vii

Ligand groups

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