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Isolation of the novel example of a monomeric organotellurinic acid

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Abstract

The stoichiometrically controlled alkaline hydrolysis of 4, (ppy)TeCl3, [ppy = 2-(2′-pyridyl)phenyl] afforded the partially hydrolyzed μ-oxo-bridged dinuclear telluroxane 5, [(ppyTeCl2)2(μ-O)] and a novel example of an Intramolecular Chalcogen Bonding (IChB) stabilized, monomeric organotellurinic acid 6, (ppy)Te(O)OH. The oxidation of diaryl ditelluride 7, (ppyTe)2 using H2O2 resulted in the isolation of μ-oxo-bridged dimethyl ester 8, [(ppy)Te(O)(OH)(OMe)]2(O). The molecular structures of 4–6 and 8 are unambiguously authenticated by single crystal X-ray diffraction studies. The electronic structure of monomeric tellurinic acid 6 is investigated using DFT calculations. The Natural Bond Order (NBO) analysis, in corroboration with Atoms in Molecules (AIM) analysis reveals that tellurinic acid 6 is stabilized by σ-hole participation of the tellurium atom with the pyridyl N-atom resulting in strong electrostatic interactions between the N and Te atoms.

Graphical abstract: Isolation of the novel example of a monomeric organotellurinic acid

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Submitted
12 Oct 2019
Accepted
20 Dec 2019
First published
21 Dec 2019

Dalton Trans., 2020, Advance Article
Article type
Paper

Isolation of the novel example of a monomeric organotellurinic acid

R. Deka, A. Sarkar, R. J. Butcher, P. C. Junk, D. R. Turner, G. B. Deacon and H. B. Singh, Dalton Trans., 2020, Advance Article , DOI: 10.1039/C9DT04013G

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