A synthesis of amphiphilic per(2,3-di-O-alkyl)-a-and b-cyclodextrins and hexakis(6-deoxy-6-thio-2,3di-O-pentyl)-a-cyclodextrin and their monolayer behavior on a water surface is presented. Long alkyl chains were introduced by a treatment of the per(6-O-tert-butyldimethylsilyl) derivatives with an ap
Catalytic Au Electrodes Based on SAMs of per(6-deoxy-6-thio-2,3-di-O-methyl)-β-cyclodextrin
✍ Scribed by Kazimierz Chmurski; Anna Koralewska; Andrzej Temeriusz; Renata Bilewicz
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 318 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1040-0397
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Heptakis(2,6-di-O-methyl-3-O-pentyl)-b-cyclodextrin was monofunctionalized by the regioselective introduction of exactly one x-epoxyoctyl group at the primary site of the cyclodextrin. The site-specifically substituted cyclodextrin was immobilized to commercially available aminopropyl silica by nucl
## Abstract As a continuation of previous studies on the use of cyclodextrin derivatives (CD) for the separation of volatile compounds by capillary GC, the influence of diluting phases other than OV‐1701 or OV‐1701‐OH has been investigated. 2,6‐Di‐__O__‐methyl‐3‐__O__‐pentyl‐β‐cyclodextrin (2,6‐Di