AM1 semiempirical molecular orbital calculations have been performed Ž . on the inclusion complexes of -cyclodextrin -CD with methylated benzoic acids in two orientations, the ''head-first'' and ''tail-first'' positions. In the former, the CO H 2 group points toward the primary hydroxyls of the CD
Theoretical and Experimental Studies of the Inclusion Phenomena of β-Cyclodextrin with Organic Amines
✍ Scribed by Le-Xin SONG; Hai-Ming WANG; Chuan-Feng TENG; Lei BAI; Peng XU; Xue-Qing GUO
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 198 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0256-7660
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A series of semiempirical molecular orbital calculations using the AM1 method were performed on the inclusion complexes of ␣and -cyclodextrin with benzoic acid and phenol in the ''head-first'' and ''tail-first'' positions. The AM1 results show that ␣-cyclodextrin complexes with both guest compounds
The complex formation between three structurally related sulfonamides (sulfadiazine (SDZ), sulfamerazine (SMR), and sulfamethazine (SMT)) and beta-cyclodextrin (beta-CD) was studied, by exploring its structure affinity relationship. In all the cases, 1:1 stoichiometries were determined with differen
## Abstract An inclusion compound comprising β‐cyclodextrin (β‐CD) and the trimetallic oligo(ferrocenylsilane) FcSiMe~2~[(η^5^‐C~5~H~4~)Fe(η^5^‐C~5~H~4~SiMe~2~)]Fc [Fc = (η^5^‐C~5~H~5~)Fe(η^5^‐C~5~H~4~)] has been prepared and characterised in the solid state by elemental analysis, powder X‐ray diff
Proton nuclear magnetic resonance spectroscopy showed that piroxicam sodium salt forms an inclusion complex with beta-cyclodextrin in aqueous solution. The 1:1 stoichiometry of the complex was determined by the continuous variation method. Significant nuclear Overhauser effects were observed between