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The Stereochemistry of Tellurium

Abstract

NEARLY ten years ago the late Mr. R. H. Vernon made a remarkable series of observations on the occurrence of isomerism in the alkyl derivatives of tellurium.1 The initial compound can be prepared by the direct action of metallic tellurium on methyl iodide, Te + 2CH3I-Te(CH3)2I2. Silver oxide then liberates from the iodide a weak ‘a’ base, TeMe2(OH)2, which when dehydrated undergoes a molecular rearrangement, and is converted into a rather stronger ‘/3’ base. From this ‘/3’ base a series of ‘/3’ salts can be obtained, which have the same composition as the ‘a’ salts derived from the ‘a’ base. Measurements of boiling-points of solutions in acetone, and of freezing-points of solutions in benzene and in nitrobenzene, indicated that the two chlorides had the same normal molecular weight, but that, whilst the a-dibromide and the a-di-iodide were also normal, the /3-compounds were partially polymerised thus:

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LOWRY, T. The Stereochemistry of Tellurium. Nature 123, 547–548 (1929). https://doi.org/10.1038/123547a0

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