Issue 43, 2023

Tellurolate: an effective Te-atom transfer reagent to prepare the triad of group 5 metal bis(tellurides)

Abstract

We show in this work how lithium tellurolate Li(X)nTeCH2SiMe3 (X = THF, n = 1, 1; X = 12-crown-4, n = 2, 2), can serve as an effective Te-atom transfer reagent to all group 5 transition metal halide precursors irrespective of the oxidation state. Mononuclear and bis(telluride) complexes, namely (PNP)M(Te)2 (M = V; Nb, 3; Ta, 4; PNP = N[2-PiPr2-4-methylphenyl]2), are reported herein including structural and spectroscopic data. Whereas the known complex (PNP)V(Te)2 can be readily prepared from the trivalent precursor (PNP)VCl2, two equiv. of tellurolate, and elemental Te partially solubilized with PMe3, complex 3 can also be similarly obtained following the same procedure but with or without a reductant, Na/NaCl. Complex 4 on the other hand is formed from the addition of four equiv. of tellurolate to (PNP)TaF4. Having access to a triad of (PNP)M(Te)2 systems for group 5 metals has allowed us to compare them using a combination of theory and spectroscopy including Te-L1 edge XANES data.

Graphical abstract: Tellurolate: an effective Te-atom transfer reagent to prepare the triad of group 5 metal bis(tellurides)

Supplementary files

Article information

Article type
Edge Article
Submitted
07 Jul 2023
Accepted
04 Oct 2023
First published
05 Oct 2023
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2023,14, 12277-12282

Tellurolate: an effective Te-atom transfer reagent to prepare the triad of group 5 metal bis(tellurides)

S. Senthil, S. Kwon, R. Y. Kong, S. N. MacMillan, P. Zatsepin, M. R. Gau, P. J. Carroll, M. Baik, K. M. Lancaster and D. J. Mindiola, Chem. Sci., 2023, 14, 12277 DOI: 10.1039/D3SC03470D

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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