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Affecting the Tellurium Atom

Tellurophene and substituted tellurophenes react with bromine to give Te,Te-dibromides, as do dialkyl and diaryl telluriums. Tetrachlorotellurophene and chlorine combined to produce tetrachlorotellurophene Te.Te-dichloride in quantitative yield . The corresponding reactions with iodine have not been investigated. The dibromides are reduced to tellurophenes by aqueous sodium hydrogen sulfite or zinc powder in glacial acetic acid.  [Pg.747]

Tetraphenyltellurophene did not react with methyl iodide to give a telluronium iodide. Whether or not other tellurophenes react with methyl iodide or other alkyl halides has not been explored. [Pg.747]


Ethoxycarbonyl)-ethen-l-yl aryl telluriums were similarly hydrolyzed without affecting the tellurium atom or the carbon-carbon double bond6,7. The free acids were isolated as sharp-melting solids in yields ranging from 60 to 95%. Examples of compounds prepared in this manner are ... [Pg.451]


See other pages where Affecting the Tellurium Atom is mentioned: [Pg.747]    [Pg.762]    [Pg.771]    [Pg.781]    [Pg.803]    [Pg.809]    [Pg.817]    [Pg.836]    [Pg.839]    [Pg.843]    [Pg.854]    [Pg.747]    [Pg.762]    [Pg.771]    [Pg.781]    [Pg.803]    [Pg.809]    [Pg.817]    [Pg.836]    [Pg.839]    [Pg.843]    [Pg.854]   


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Reactions Affecting the Tellurium Atom

Tellurium atoms

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