Tert-butyldioxophosphorane as metaphosphate analog

Authors

  • A.O. Kolodiazhna
  • E.V. Grishkun
  • A.O. Gudyma
  • O.O. Kolodiazhna
  • S.Yu. Sheiko
  • O.I. Kolodiazhnyi

DOI:

https://doi.org/10.15407/dopovidi2018.05.067

Keywords:

flesh-vacuum thermolysis, tert-butyldioxophosphorane, trimer of tert-butyldioxophosphorane

Abstract

The flash-vacuum thermolysis (FVT) of trimethylsilyl tert-butylhalogenophosphonates is performed in an attempt to generate tert-butyldioxophosphorane. The FVT proceeds with elimination of halogenotrimethylsilane to give unstable tert-butyldioxophosphorane readily transforming into a trimer. Tert-butylhalogenophoshonic acids form rather stable salts with trimethylamine, which eliminate triethytamine hydrohalohenide on the heating to afford a trimer.

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References

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Published

15.05.2024

How to Cite

Kolodiazhna, A., Grishkun, E., Gudyma, A., Kolodiazhna, O., Sheiko, S., & Kolodiazhnyi, O. (2024). Tert-butyldioxophosphorane as metaphosphate analog . Reports of the National Academy of Sciences of Ukraine, (5), 67–74. https://doi.org/10.15407/dopovidi2018.05.067

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