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Triethylgermyl triethylstannyl

Triethylgermyl triethylstannyl tellurium (b.p. 128°/1 torr) was similarly prepared in 62% yield5,6. [Pg.15]

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]

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

T ris(triethylgermyl)stibine, Ge-00219 T ris(triethylgermyl)thallium, Ge-00220 T ris(triethylstannyl)amine, Sn-00341... [Pg.153]

See other pages where Triethylgermyl triethylstannyl is mentioned: [Pg.8]    [Pg.17]    [Pg.17]    [Pg.150]    [Pg.174]    [Pg.174]   
See also in sourсe #XX -- [ Pg.15 , Pg.194 ]



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