Complex formation of native and hydroxypropylated cyclodextrins with benzoic acid in aqueous solution: Volumetric and 1H NMR study
✍ Scribed by Irina Terekhova; Malgorzata Koźbiał; Roman Kumeev; Paweł Gierycz
- Book ID
- 113555110
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 470 KB
- Volume
- 514
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## 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 complex formation of alpha-cyclodextrin (alpha-CyD), beta-cyclodextrin (beta-CyD), and 2-hydroxylpropyl-beta-cyclodextrin (HP-beta-CyD) with an angiotensin converting enzyme inhibitor, captopril, in aqueous solution was studied by (1)H- and (13)C-nuclear magnetic resonance spectroscopi
Complex formation between cyclodextrins and 1 ,d-dihydroxyanthraquinone in buffer solution has been investigated using absorption, its second derivative (D'), and fluorescence spectroscopy. The results showed that whereas the self-association process was found for 1,8-dihydroxyanthraquinone alone, t