1H NMR study of complexation of α- and β-cyclodextrins with some biologically active acids
✍ Scribed by I. V. Terekhova; O. V. Kulikov; R. S. Kumeev; M. Yu. Nikiforov; G. A. Al’per
- Publisher
- SP MAIK Nauka/Interperiodica
- Year
- 2005
- Tongue
- English
- Weight
- 51 KB
- Volume
- 31
- Category
- Article
- ISSN
- 1070-3284
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## Abstract ^1^H NMR spectroscopic study of citalopram (CT) in the absence as well as in the presence of β‐cyclodextrin (β‐CD) in aqueous solution revealed the formation of four 1:1 β‐CD–CT inclusion complexes. The stoichiometry of the complexes was determined by the continuous variation (Job) meth
The inclusion complexes of 2-, 3-, and 4-hydroxypyridines with @cyclodextrin in aqueous solution have been studied by high field 'H NMR. All complexes showed a 1: 1 stoichiometry and the apparent association constants reflected the polarity of the guest compounds in a qualitative fashion. The inclus