## Abstract An inclusion complex of fenbufen with β‐cyclodextrin (β‐CD) in aqueous solution was characterized by ^1^H‐NMR spectroscopy. The [1:1] stoichiometry was determined and a stability constant of several 1000s (__M__^−1^) was calculated. The geometry of the inclusion complex was established
Studies of the Naproxen:β-Cyclodextrin Inclusion Complex
✍ Scribed by J. Wang; I.M. Warner
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 413 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0026-265X
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✦ Synopsis
The interaction of a nonsteroidal anti-inflammatory drug, naproxen, with (\beta)-CD has been studied by several analytical techniques, including 1-D and 2-D proton NMR, fluorescence spectroscopy, and FAB-MS. The negative ion FAB-MS confirmed the existence of a 1:1 inclusion complex of naproxen and (\beta-\mathrm{CD}). The formation constant of the complex was determined by use of I-D NMR and fluorescence measurement. In the 1-D NMR data, a modified Benesi-Hildebrand procedure was employed to calculate the formation constant. In order to estimate the structure of the inclusion complex, 2-D rotating-frame Overhauser enhancement spectroscopy (ROESY) NMR was used to determine the spatial interaction in this dynamic system. A spatial configuration of the complex has been proposed based on these data. 1993 Academic Press. Inc.
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The crystal structure of the inclusion complex of β-cyclodextrin (β-CD) synthesized with felbinac (4-biphenylacetic acid) was determined by single crystal X-ray diffraction at 150 K. The complex contains two β-CDs, two felbinac molecules, twenty-two water molecules in the asymmetric unit, and could
## Abstract [CpM(CO)__~n~__Cl] complexes with M = Fe (__n__ = 2) and Mo (__n__ = 3) have been immobilised in plain β‐cyclodextrin (β‐CD) and permethylated β‐CD (TRIMEB) by methods tailored according to the stabilities and solubilities of the individual components. Four adducts were obtained with a
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