Halogenation reactions of a ditelluride having bulky aryl groups leading to the formation of organotellurium halides

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  • Dedicated to Professor Kin-ya Akiba on the occasion of his 75th birthday.

Abstract

Halogenation reactions of BbtTe-TeBbt (Bbt; 2,6-bis[bis(trimethylsilyl)methyl]-4-[tris (trimethylsilyl)methyl]phenyl) with SO2Cl2, Br2, and I2 were examined. When 1 equiv of the reagents were used, the corresponding tellurium monohalides were obtained as stable crystalline compounds. Although iodination reaction of BbtTe-TeBbt using 3 equiv of I2 afforded BbtTeI, treatment of BbtTe-TeBbt with 3 equiv of SO2Cl2 and Br2 gave the corresponding tellurium trihalides, BbtTeX3(X = Cl, Br), as stable crystalline compounds. Characterization of the obtained tellurium mono- and trihalides was achieved by the spectroscopic and crystallographic analyses, together with theoretical calculations. © 2011 Wiley Periodicals, Inc. Heteroatom Chem 22:405–411, 2011; View this article online at wileyonlinelibrary.com. DOI 10.1002/hc.20698

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