ELECTRONIC AND SPATIAL STRUCTURE OF PIPERIDINE AND ITS SUBSTITUTED DERIVATIVES FROM THE RESULTS OF <i>ab initio</i> CALCULATIONS

Abstract

The results of non empirical quantum-chemical  calculations using the RHF/6-31G(d) and MP2/6-31G(d) methods do not agree with proposals for the axial position of the H atom on the N atom in the piperidine molecule. According to RHF/6-31G(d) calculations for the N-methylpiperidine molecule and its chloro-substituted derivatives an equatorially placed methyl group is energetically more favored than an axial. The axial C–Cl and  C–H bonds in these molecules are longer than the equatorial. The  35Cl NQR frequencies for the axial Cl atoms are lower than the equatorial. The  35Cl NQR frequency of the axial chlorine atom in 2-chloro-1-methylpiperidine is anomalously low. This is chiefly due to the high population density of its pσ-orbital and this is a result of the polarization of the C–Cl bond via the N atom unshared electron pair directly through the field. The effect of a similar unshared electron pair on the parameters of the C–Cl bond in the ClCH2NH2 molecule has been studied by the RHF/6-31(g) method for different angles of rotation of the ClCH2 group around the C–N bond.

How to Cite
Feshina, E. V.; Zhizhina, L. I.; Feshin, V. P.  Chem. Heterocycl. Compd. 2005, 41, 883. [Khim. Geterotsikl. Soedin. 2005, 1044.]

For this article in the English edition, see DOI 10.1007/s10593-005-0243-z