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Triethylgermyl triethylsilyl

Pentane solutions of this compound decompose at 20° with loss of mercury to form triethylgermyl triethylsilyl tellurium4. [Pg.14]

Triethylgermyl triethylsilyltelluro mercury decomposed in hexane to triethylgermyl triethylsilyl tellurium5. [Pg.17]

Ethyl triethylsilyl and ethyl triethylgermyl tellurium reacted with triethylstannane at 20° to produce triethylsilyl(-germyl) triethylstannyl tellurium5 6. [Pg.15]

When diethyl tellurium was heated with triethylsilane at 200° for seven hours, or with triethylgermane at 140° for seven hours, the Te — C bond was cleaved, ethane liberated, and mixtures of ethyl triethylsilyl tellurium/bis[triethylsilyl] tellurium or ethyl triethylgermyl telluriumlbis[triethylgermyl] tellurium were formed6. However, triethylstannane and diethyl tellurium yieled only bis[triethylstannyl] tellurium even at 20° 5 6. [Pg.15]

Bis[triethylsilyl] tellurium reacted with triethylgermane with liberation of triethylsilane and formation of bis[triethylgermyl] tellurium6 1. Bis[triethylgermyl] tellurium and triethyl-stannane reacted similarly6,7. [Pg.16]

Ethyl triethyhilyl tellurium (11% b.p. 53°/l torr) was similarly prepared by heating the reactants at 200°. Bis[triethylsilyl] tellurium and bis[triethylgermyl] tellurium are also formed in these reactions3,4. [Pg.192]

Ethyl triethylgermyl tellurium and ethyl triethylsilyl tellurium reacted with trieth-ylstannane at 20c forming diethyl tellurium and triethylstannyl triethylsilyl (or -germylj tellurium4... [Pg.194]

Triethylsilanetellurol, prepared from bis[triethylsilyl] tellurium and trifluoroacetic acid (s.p. 18), and bis[triethylgermyl] mercury yielded, depending on reaction conditions, mercury bis[triethylsilanetellurolate or triethylgermylmercury triethylsilanetellurolate. ... [Pg.14]

Bis[triethylsilyl] tellurium or bis[triethylgermyl] tellurium were heated with trisfpenta-fluorophenyl]bromostannane in toluene at 100° for two hours. Evaporation of the solvent, dissolution of the residue in petroleum ether, and chilling the solution to —10°, precipitated crystals of bis[tns(pentafluorophenyl)stannyl] tellurium (m.p. 118°) in 51% yield". ... [Pg.16]


See other pages where Triethylgermyl triethylsilyl is mentioned: [Pg.769]    [Pg.17]    [Pg.287]    [Pg.17]    [Pg.209]   
See also in sourсe #XX -- [ Pg.14 , Pg.17 ]

See also in sourсe #XX -- [ Pg.14 , Pg.17 ]




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Triethylsilyl

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