Autor(es):
Gil, Francisco P. S. C. 
; Costa, A. M. Amorim da ; Teixeira-Dias, J. J. C.
Data: 1995
Identificador Persistente: http://hdl.handle.net/10316/10482
Origem: Estudo Geral - Universidade de Coimbra
Detalhes do Documento
Conformational Analysis of CmH2m+1OCH2CH2OH (m = 1-4): The Role of CH.cntdot..c...
Descrição
Structures and energies of the more stable conformations of C ~ H ~ ~ + I O C H ~ C(HCm~EOl, Hm = 1-4) have been determined by gradient geometry refinement at ab initio level. For m = 3 (C~EIa)n d m = 4 (C~EI )t,h e results show that attractive CH-O intramolecular interactions associated with the formation of five-membered rings in the alkylic fragments of these molecules lead to the stabilization of gauche arrangements in the CC-CO axes. Since these CH-O interactions compete, in energy terms, with conformational effects, they are found to have important structural consequences. In addition, the formation of five-membered rings closed by CH-O and OH-O contacts gives rise to vibrational couplings in the C(H2)tO!C(H2) moieties and to conformationally sensitive vibrations. http://dx.doi.org/10.1021/j100020a033
Structures and energies of the more stable conformations of C ~ H ~ ~ + I O C H ~ C(HCm~EOl, Hm = 1-4) have been determined by gradient geometry refinement at ab initio level. For m = 3 (C~EIa)n d m = 4 (C~EI )t,h e results show that attractive CH-O intramolecular interactions associated with the formation of five-membered rings in the alkylic fragments of these molecules lead to the stabilization of gauche arrangements in the CC-CO axes. Since these CH-O interactions compete, in energy terms, with conformational effects, they are found to have important structural consequences. In addition, the formation of five-membered rings closed by CH-O and OH-O contacts gives rise to vibrational couplings in the C(H2)tO!C(H2) moieties and to conformationally sensitive vibrations. http://dx.doi.org/10.1021/j100020a033
Tipo de Documento
Artigo
Idioma Inglês
Idioma Inglês
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