Oxidation behavior of intramolecularly coordinated unsymmetrical diorganotellurides: isolation of novel tetraorganoditelluronic acids, [RR′Te(μ-O)(OH)2]2

The oxidation reaction of unsymmetrical diorganotellurides, namely, bis[2-{(dimethylamino)methyl}aryl]tellurides [aryl = phenyl (6), 2-methylphenyl (7), 2,6-dimethylphenyl (8) and 2,6-diisopropylphenyl (9)] with meta-chloroperbenzoic acid afforded the first examples of tetraorganoditelluronic acids, [RR ' Te(mu-O)(OH)(2)](2), where R = 2-NMe2CH2C6H4, R ' = C6H5 (10), 2-MeC6H4 (11), 2,6-MeC6H3 (12) and 2,6-(PrC6H3)-Pr-i (13). The structures of tetraorganoditelluronic acids 10-13 were authenticated by single crystal X-ray diffraction studies. From the molecular structures of 10-13, it was observed that the sp(3) N-donor atoms, which were initially involved in intramolecular TeMIDLINE HORIZONTAL ELLIPSISN bonding interactions in diorganotellurides 6-9, did not interact with the tellurium atoms in tetraorganoditelluronic acids 10-13. The Te-125 chemical shifts for 10-13 were considerably downfield shifted as compared with the values observed for the corresponding tellurides 6-9. The relative stabilities of the tetraorganoditelluronic acids 10-13 with respect to their lighter analogues (S and Se) have been assessed using DFT calculations.