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Tellurium Dicyanates

Heating bis[2-broraoethyl] tellurium diacetate in acetic acid under a nitrogen atmosphere yielded 1,2-dibromoethane, 1,2-diacetoxyethane, and l-acetoxy-2-bromoethane  [Pg.617]

Diaryl tellurium dichlorides and the sodium salts of ketoximes reacted in benzene at 20° to give diaryl tellurium dioximates. These oximates are white, crystalline solids. [Pg.617]

Diphenyl Tellurium Bis[diphenyl kctoximate] A mixture of 0.352 g (1 mmol) of diphenyl tellurium dichloride, 0.438 g (2 mmol) sodium diphenyl ketoximatc, and 60 ml benzene is stirred at 20° for 3 h. The sodium chloride is removed by filtration. The filtrate is concentrated under reduced pressure. The solid residue is dissolved in 20/ /benzene and reprecipitated by addition of 20/ /petroleum ether (60-80°). The crystals are dried under vacuum yield 80% m.p. 148°. [Pg.617]

diorgano tellurium dicyanates are treated as diorgano dinitrogen compounds (p. 637), however, it must be emphasized that this treatment is not intended to give information on the bonding mode. [Pg.617]

Irgolic Organo Tellurium Compounds with 2 Te —C Bonds or 1 Te = C Bond [Pg.618]


Diary] Tellurium Dioximales Diorgano Tellurium Dicyanates... [Pg.617]

Diorgano tellurium dicyanates are formed when diorgano tellurium dihalides are stirred with silver cyanate in chloroform, acetone, or toluene. [Pg.637]


See other pages where Tellurium Dicyanates is mentioned: [Pg.617]    [Pg.636]    [Pg.637]    [Pg.617]    [Pg.636]    [Pg.637]    [Pg.617]    [Pg.636]    [Pg.637]    [Pg.617]    [Pg.636]    [Pg.637]   


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Dicyanates

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