INCLUSION COMPOUNDS OF α-CYCLODEXTRIN WITH ALKYLTHIOLS

We report the formation of á-cyclodextrin (áCD) inclusion compounds with octanethiol (OT), decanethiol (DT) and dodecanethiol (DDT). Elemental Microanalysis, ¹H-NMR solution, Scanning Electronic Microscopy (SEM) and Powder X-ray Diffraction analysis (PXRD) confirm the inclusion process of the alkylt...

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Autores principales: JARA,PAUL, BARRIENTOS,LORENA, HERRERA,BARBARA, SOBRADOS,ISABEL
Lenguaje:English
Publicado: Sociedad Chilena de Química 2008
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072008000200005
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Sumario:We report the formation of á-cyclodextrin (áCD) inclusion compounds with octanethiol (OT), decanethiol (DT) and dodecanethiol (DDT). Elemental Microanalysis, ¹H-NMR solution, Scanning Electronic Microscopy (SEM) and Powder X-ray Diffraction analysis (PXRD) confirm the inclusion process of the alkylthiols in to the á-cyclodextrin molecules. The basic host structure of the products is similar to that of typical channel type structure cyclodextrin inclusion compounds. The guest presents extended linear (zig-zag) conformation. The presence of the -SH groups located in the (001) plane of the á-cyclodextrins-alkylthiol crystal, is evidenced by Energy dispersive X-ray (EDX) analysis. 13C CP-MAS NMR spectra of new á-cyclodextrin host-guest inclusion compounds are described.