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Stability and structure of the inclusion complexes of alkyl-substituted hydroxyphenylazo derivatives of sulfanilic acid with .alpha.- and .beta.-cyclodextrins

✍ Scribed by Yoshida, Noboru.; Seiyama, Akitoshi.; Fujimoto, Masatoshi.

Book ID
120981545
Publisher
American Chemical Society
Year
1990
Tongue
English
Weight
624 KB
Volume
94
Category
Article
ISSN
0022-3654

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Quantitative structure–stability relatio
Quantitative structure–stability relationships among inclusion complexes of cyclodextrins I: Barbituric acid derivatives
✍ Antal Lopata; Ferenc Darvas; Ágnes Stadler-Szóke; József Szejtli 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 English ⚖ 295 KB

Quantitative structure-stability relationships (QSSRs) are formulated for the inclusion complexation of 17 barbituric acid derivatives with alpha- and beta-cyclodextrin. The variation in the complex stability constants K alpha and K beta is found to be partly accounted for by the molar refractivity