Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/56502
Type: Artigo de periódico
Title: Conformational analysis in N-methylfluoroamides. A theoretical, NMR and IR investigation
Author: Tormena, CF
Amadeu, NS
Ritter, R
Abraham, RJ
Abstract: Theoretical calculations plus the solvent dependence of the H-1, C-13 NMR and IR spectra were used to determine the conformational equilibrium in N-methyl-2-fluoroacetamide (NMFA) and N-methyl-2-fluoropropionamide (NMFP). Ab initio calculations were used to identify the stable rotamers and obtain their geometries and the application of solvation theory on the (1)J(CF) coupling constant gave the conformer populations in the solvents studied. In NMFA ab initio calculations at the CBS-Q level yielded only two stable rotamers, the cis and trans, with DeltaE(cis-trans) = 19.7 kJ mol(-1). The presence of two conformers was confirmed by the FTIR spectra. Assuming these forms, the observed couplings when analysed by solvation theory gave DeltaE = 21.3 kJ mol(-1) in the vapour phase, decreasing to 8.9 kJ mol(-1) in CDCl3 and to 0.8 kJ mol(-1) in DMSO. For NMFP the B3LYP calculations at the 6-311++g(2df,2p) level gave only the trans rotamer as stable, while the gauche form was a plateau in the potential energy surface. However the FTIR spectra clearly showed the presence of two conformers. A minimum for the gauche rotamer was only found when the SCRF (self consistent reaction field) routine was included in the theoretical calculations. The equilibrium in NMFP was therefore analysed by solvation theory in terms of the trans and gauche rotamers to give DeltaE(gauche-trans) = 15.9 kJ mol(-1) in the vapour phase, decreasing to 10.8 kJ mol(-1) in CCl4 and to 0.5 kJ mol(-1) in DMSO.
Country: Inglaterra
Editor: Royal Soc Chemistry
Rights: aberto
Identifier DOI: 10.1039/b111048a
Date Issue: 2002
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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