## 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
Crystal Structure of β-Cyclodextrin-Felbinac Inclusion Complex
✍ Scribed by Enju Wang; Guangying Chen; Hong Liu
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 109 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0256-7660
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✦ Synopsis
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 be formulated as
In the crystal lattice, the two β-CD moieties form a head-to-head dimer jointed through hydrogen bonds, and the felbinacs that interact by face-to-face π-π stacking are included in the β-CD dimer cavity with their carboxyl groups protruding out from cavity opening. In crystals the dimer units of β-CD are stacked in an intermediate type (IM) that consists of closely packed β-CD dimer layers.
📜 SIMILAR VOLUMES
## 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