Conclusions
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1.
Unsubstituted 2-dialkylamino-1,3,2-dioxaphosphorinanes with three- and four-coordinated phosphorus exist as a mixture of two conformers in the liquid and solutions of polar solvents according to the vibration spectral data and calculations by the method of atomic-atomic potential functions; the conformers with an equatorial orientation of the dialkylamino group is energetically more advantageous and is realized in a crystal.
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2.
The cis-isomer of 2-diethylamino-2-thio-4-methyl-1,3,2-dioxaphosphorinane is conformationally homogeneous. Conformational equilibrium in which three conformers participate based on the results of the calculations: two chair and boat forms, is found for the less stable trans-isomer.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheksya, No. 11, pp. 2517–2524, November, 1984.
We would like to thank V. N. Nabiullin for participating in the synthesis of the compounds studied.
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Shagidullin, R.R., Shakirov, I.K., Plyamovatyi, A.K. et al. Vibration spectra and conformations of 1,3,2-dioxaphosphorinanes containing an exocyclic P-N bond. Russ Chem Bull 33, 2306–2312 (1984). https://doi.org/10.1007/BF00948843
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DOI: https://doi.org/10.1007/BF00948843