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Scandium trichloride tris

SCANDIUM TRICHLORIDE TRIS(TETRAHYDROFURAN) AND 0-DIKETIMINATE-SUPPORTED SCANDIUM CHLORIDE COMPLEXES... [Pg.20]

Solvates of the monohydroxylic alcohols have been extensively studied. The expected pattern of more solvent molecules per chloride molecule is reported for the lanthanide and yttrium trichlorides. For scandium trichloride, the existence of ScCl3-2EtOH and ScCl3-2C6H13OH compares unexpectedly with the tris-alcoholates reported for the n-C6... [Pg.75]

Finally some homoleptic alkyne complexes of scandium and some rare earths are known. Tris(phenylethynyl) scandium is formed as a dark brown product after treatment of phenylethyne with butyl lithium at — 78°C in hexane, followed by the addition of scandium trichloride at room temperature. The compound is inflammable in air (Hart and Saran, 1968 Hart et al., 1970). The reaction of the anionic... [Pg.509]

Taking into account the competitive hydrolysis of the silyl enol ether, this reaction is remarkable. The method was shown to be general and was extended to a variety of aldehydes and several a,j9-unsaturated carbonyl compounds giving uniformly 1,4-addition with aldehydes and a mixture of 1,4- and 1,2-adducts in the case of ketones [187]. Later, this aqueous version of the Mukaiya-ma reaction was shown to give near quantitative yields in the presence of a water-tolerant Lewis acid such as ytterbium triflate [188]. Keeping with the same concept,copper(II) triflate [189],indium(III) trichloride [190],tris(pentafluoro-phenyl)boron [191] and scandium(III) triflate in the presence of a surfactant [192] have proved to be active catalysts. [Pg.31]


See other pages where Scandium trichloride tris is mentioned: [Pg.20]    [Pg.21]    [Pg.23]    [Pg.20]    [Pg.21]    [Pg.23]    [Pg.32]   
See also in sourсe #XX -- [ Pg.20 , Pg.35 ]




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Scandium tris

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