Abstract
Aryl tellurium trichlorides and tribromides undergo condensation reactions with acetone, acetophenone, N-dimethylaniline and resorcinol, giving rise to aryl tellurium dihalides. Aryl tellurium triiodides are not reactive. The dihalides derived from N-dimethylaniline and resorcinol undergo ionic interchange reactions with halide ions. When treated with reducing agents the dihalides derived from N-dimethylaniline are reduced to the corresponding tellurides, while the other dihalides are cleaved to the diaryl-ditellurides.
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