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|Title: ||Synthesis and characterization of monomeric tellurolato complexes of zinc and cadmium: crystal and molecular structure of bis[2-(4,4-dimethyl-2-oxazolinyl)phenyl]ditelluride|
|Authors: ||MUGESH, G|
|Keywords: ||single-source precursors|
volatile cvd precursors
|Issue Date: ||1999|
|Publisher: ||ELSEVIER SCIENCE SA|
|Citation: ||JOURNAL OF ORGANOMETALLIC CHEMISTRY, 577(2), 243-248|
|Abstract: ||The synthesis and characterization of homoleptic zinc(II) and cadmium(II) tellurolates incorporating the intramolecularly chelating oxazoline ligand are described. The derivatives, M[Te(Ox)](2) [M = Zn (4) or Cd (5) and Ox = 2-(4,4-dimethyl-2-oxazolinyl)phenyl], are prepared in good yield via the metathesis reactions of MCl2 with lithium arenetellurolate, OxTe(-)Li(+) (2). Attempts to synthesise the mercury complex led to isolation of the corresponding ditelluride (3). Crystal structure of the ditelluride was determined by X-ray diffraction method. Of particular interest in the structure is the intramolecular interaction of the sp(2) nitrogen with the tellurium. The strength of the Te...N nonbonded interactions in this compound [Te(1)...N(1): 2.864(5), Te(2)...N(2): 2.694(5) Angstrom] is found to be stronger than the similar interactions found in related compounds. The zinc and cadmium complexes are quite stable in the solid state and highly soluble in common non-polar organic solvents. The variable temperature NMR spectra of Zn[Te(Ox)](2), (4) and Cd[Te(Ox)](2) (5) show the complexes to be chiral at low temperatures. (C) 1999 Elsevier Science S.A. .|
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