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Mercury chalcogenolates of a ligand having both sterically more bulkier and intramolecularly coordinating features: first isolation of a novel air stable mercury tellurolate
First isolation of air stable novel mercury tellurolate has been achieved using a ligand containing both steric and intramolecular coordinating features. Synthesis and characterization of stable monomeric mercury selenolate ( 9) and the novel air stable mercury tellurolate ( 10) incorporating [2-[1-...
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Published in: | Inorganica Chimica Acta 2005, Vol.358 (1), p.207-212 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | First isolation of air stable novel mercury tellurolate has been achieved using a ligand containing both steric and intramolecular coordinating features.
Synthesis and characterization of stable monomeric mercury selenolate (
9) and the novel air stable mercury tellurolate (
10) incorporating [2-[1-(3,5 dimethylphenyl)-2-naphthyl]-4,5-dihydro-4,4-dimethyloxazole], containing both sterically more demanding and intramolecularly coordinating groups have been described here. These complexes were prepared in good yields by oxidative addition of mercury metal to the corresponding dichalcogenides in methanol. FT-IR, multinuclear (
IH,
13C,
77Se and
125Te) NMR, thermal analysis and mass spectrometric techniques were used to characterize these complexes. The complex
9 was structurally characterized by single-crystal X-ray diffraction analysis. |
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ISSN: | 0020-1693 1873-3255 |
DOI: | 10.1016/j.ica.2004.08.020 |