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Journal of the Brazilian Chemical Society

Print version ISSN 0103-5053

Abstract

CAPIM, Saulo L et al. Revisiting the origin of the preferential π-π stacking conformation of the (+)-8-phenylmenthyl acrylate. J. Braz. Chem. Soc. [online]. 2010, vol.21, n.9, pp.1718-1726. ISSN 0103-5053.  http://dx.doi.org/10.1590/S0103-50532010000900018.

In this paper we report a theoretical study aiming to revisit the origin of the preferential π-π stacking conformation of the (+)-8-phenylmentyl acrylate (2). For this, we have applied several DFT and ab initio methods to calculate local minimum geometries, vibrational frequencies, thermochemical properties and 1H NMR chemical shifts for 2 and the model compound 3-phenylpropyl acrylate (3). We have observed that the MPW1B95 functional was the most suitable method to explain 1H NMR experimental data which show the stacking conformation of 2 (2S) is more stable that trans conformation (2T) and the stacking conformation of 3 (3S) is less stable that trans conformation (3T). After that, geometrical and energetic features of the intermolecular complex benzene...methylacrylate (4) have also been studied using MPW1B95 method. From our results, we have noticed that both steric and dispersion effects play a key role in the conformational equilibrium of 2.

Keywords : conformational analysis; intramolecular π-π stacking interactions; MPW1B95 functional; chiral auxiliaries; enantioselective synthesis.

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