Electrophilic substitution of acetyltrimethylsilane with tellurium(IV) halides: A synthetic route to 3-methyl-5-(trimethylsilyl)-1,2-oxatellurol-1-ium halides

The reaction of tellurium tetrahalides, TeX<inf>4</inf> (XCl. Br) with acetyltrimethylsilane in CCl<inf>4</inf> at ambient temperature, unlike that of the aryltellurium trichlorides, ArTeCl<inf>3</inf> that give the expected electrophilic substitution products, Ar(Me<inf>3</inf>SiCOCH<inf>2</inf>)TeCl<inf>2</inf>, (Ar = 1-C<inf>10</inf>H<inf>7</inf>, 2; 2,4,6-Me<inf>3</inf>C<inf>6</inf>H<inf>2</inf>, 3), afforded novel silylated heterocycles, 3-methyl-5-(trimethylsilyl)-1,2-oxatellurol-1-ium halides 1a and 1b. These Te(II) heterocyclic compounds undergo halide exchange with sodium iodide and also add dihalogens oxidatively to afford the corresponding iodide, 1c and the Te(IV) trihalides, 5a and 5b respectively. A large lowering of ν(CO) is indicative of strong Te⋯OC interactions among these heterocycles, and is also substantiated by single-crystal X-ray diffraction data for 3-methyl-5-(trimethylsilyl)-1,2-oxatellurol-1-ium chloride. The ¹²⁵Te chemical shifts for the new 10-Te-3 telluranes and 12-Te-5 pertelluranes that involve tellurium bound to two highly electronegative atoms (O, X) are among the highest (downfield) reported for organotellurium(II) and (IV) compounds.