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https://locus.ufv.br//handle/123456789/22225
Tipo: | Artigo |
Título: | Influence of hydrogen bonds on the molecular structure and conformations of two (C30H48O2) pentacyclic triterpene isomers |
Autor(es): | Barbosa, L. C. A. Corrêa, R. S. Silva, S. R. Souza e Duarte, L. P. Silva, G. D. F. Ellena, J. Doriguetto, A. C. |
Abstract: | The structural study of two (C30H48O2) pentacyclic triterpene (PCTT) isomers is presented. These terpenes, known as 30-hydroxy-lup-20(29)-en-3-one (1) and (11α)-11-hydroxy-lup-20(29)-en-3-one (2), were isolated from Maytenus imbricata Mart. Ex Reissek (Celastraceae). The molecular structure of 1 and 2 differs in the position of the hydroxyl group. Both compounds crystallize in non-centrosymmetric space groups with two molecules in the asymmetric unit. The crystal structure of 1 shows a triclinic P1 space group (a = 9.5518(1) Å, b = 9.7083(1) Å, c = 14.4696(2) Å, α = 93.832(1)°, β = 102.833(1)°, and γ = 103.307(1)°), while compound 2 crystallizes in a monoclinic P21 one (a = 13.4439(16) Å, b = 14.4463(14) Å, c = 13.5224(9) Å and β = 99.703(8)°). The two molecules independent by symmetry of 1 differ slightly due to the presence of static disorder in oxygen atoms. In addition, the intermolecular geometries of 1 and 2 were analysed, and in each isomer the crystal packing is stabilized by O-H…O intermolecular hydrogen bonds and van der Waals forces. |
Palavras-chave: | Maytenus imbricata Pentacyclic triterpene Crystal structure Molecular conformation Static disorder Hydrogen bond |
Editor: | Journal of Structural Chemistry |
Tipo de Acesso: | P MAIK Nauka/Interperiodica |
URI: | https://doi.org/10.1134/S0022476612010210 http://www.locus.ufv.br/handle/123456789/22225 |
Data do documento: | Fev-2012 |
Aparece nas coleções: | Artigos |
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artigo.pdf Until 2100-12-31 | Texto completo | 192,82 kB | Adobe PDF | Visualizar/Abrir ACESSO RESTRITO |
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