Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/93068
Type: Artigo de periódico
Title: Nmr And Theoretical Study Of The (c=o)-n Rotational Barrier In The Isomers Cis- And Trans- 2-n,n-dimethylaminecyclohexyl 1-n′,n′- Dimethylcarbamate
Author: Basso E.A.
Oliveira P.R.
Wiectzycoski F.
Pontes R.M.
Fiorin B.C.
Abstract: Rotation around the conjugated C-N bond was investigated through dynamic NMR experiments, employing both 1H and 13C spectra, and theoretical calculations (HF and B3LYP with the 6-311+G** and 6-31G** basis sets). Theoretical results predicted slightly distinct gas-phase rotational barriers for the isomers, although inclusion of solvation effects causes the barriers to be essentially equal. Experiments corroborate with this result. 1H and 13C spectra provided somewhat different rate constants but the activation parameters (ΔS ‡, ΔH ‡ and ΔG ‡) are very similar for both. Additionally, we investigated the solvent effect through experiments in CDCl 3, CD 3OD, DMSO-d 6 and D 2O solutions and SCRF calculations. The results agree with previous studies that the rotational barrier in carbamates is solvent insensitive. © 2005 Elsevier B.V. All rights reserved.
Editor: 
Rights: fechado
Identifier DOI: 10.1016/j.molstruc.2005.06.001
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-26444517076&partnerID=40&md5=25bacd48aaba8e11f23aa64d068f1d01
Date Issue: 2005
Appears in Collections:Unicamp - Artigos e Outros Documentos

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