Conclusions
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1.
The photoelectron spectra of seven methyl-substituted 1,3-dioxanes have been recorded and identified.
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2.
Empirical parameters have been found which characterize the magnitude of the inductive effect and the hyperconjugation between theσ C-C bonds of the substituents and the ne − and na + orbitals.
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3.
INDO quantum mechanical calculations have been carried out on the investigated compounds and qualitatively reproduce the pattern of the changes in the ionization potentials in the spectra.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2293–2295, October, 1983.
The authors express their gratitude to G. S. Lomakin for kindly making the programs for the CNDO/2 and INDO calculations available to them.
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Asfandiarov, N.L., Zykov, B.G. Photoelectron spectra of methyl-substituted 1,3-dioxanes. Russ Chem Bull 32, 2069–2072 (1983). https://doi.org/10.1007/BF00955773
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DOI: https://doi.org/10.1007/BF00955773