## Abstract Heptakis(2,6‐di‐__O__‐methyl‐3‐__O__‐pentyl) (2‐__O__‐methyl‐6‐__O__‐oct‐1‐enyl‐3‐O‐pentyl)‐γ‐cyclodextrin was immobilized to narrow‐bore fused silica capillaries after selective modification. One __tert__‐butyldimethylsilyl group was introduced into octakis‐(2‐__O__‐methyl‐3‐__O__‐pent
Cyclodextrin derivatives for GC separation of racemic mixtures of volatile compounds. Part VIII: 2,6-di-O-methyl-3-O-pentyl-γ-cyclodextrin and 2,6-di-O-methyl-3-O-(4-oxo-pentyl)- and 2,6-di-O-pentyl-3-O-(4-oxo-pentyl)-β-and -γ-cyclodextrins
✍ Scribed by Bicchi, Carlo ;D'amato, Angela ;Manzin, Valeria ;Galli, Anna ;Galli, Mario
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 309 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0935-6304
No coin nor oath required. For personal study only.
✦ Synopsis
In previous papers, 2,6-di-O-methyl-3-O-pentyl-~-cyclodextrin (CD) was demonstrated to be successful in separating volatile compounds, while avoiding the drawbacks of 2,3,6-tri-O-methyl-P-CD in terms of column stability and operating temperature. Since a CD chiral selector of universal use has not yet been found, and at least two (or more) columns coated with different CD derivatives are therefore necessary for routine work, the performance of 2,6-di-O-methyI-3-0-pentyl-y-C D, 2'6d i -O-methyl-3-0-(4-0~0-penty1)-y-CD, 2,6-di-O-pentyl-3-0-(4-oxo-pentyl)-P-CD, and 2 4di-O-penty1-3-0-(-4-oxo-pentyl)-y-CD diluted in polysiloxanes for the separation of volatile compounds in aromas and essential oils will be illustrated; each column coated with each of the newly synthesized CD derivatives was evaluated by analyzing more than 150 different racemates with different structures.
📜 SIMILAR VOLUMES
## 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
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 This paper describes an evaluation of the chromatographic performance of columns coated with amorphous cyclodextrin (CD) derivatives, in particular 2,3,6‐tripentyl‐β‐CD (2,3,6‐TriPe‐β‐CD), 2,6‐dipentyl‐3‐methyl‐β‐CD (2,6‐DiPe‐3‐Me‐β‐CD), and 2,6‐dimethyl‐3‐pentyl‐β‐CD (2,6‐DiMe‐3‐Pe‐β‐C