## Abstract A family of amphiphilic cyclodextrins (**6, 7**) has been prepared through 6β__S__βalkylation (alkyl=__nβ__dodecyl and __nβ__hexadecyl) of the primary side and 2β__O__βPEGylation of the secondary side of Ξ±β, Ξ²β, and Ξ³βcyclodextrins (PEG=poly(ethylene glycol)). These cyclodextrins form n
Bilayer membranes of fluorocarbon amphiphiles
β Scribed by Kunitake, Toyoki ;Higashi, Nobuyuki
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1985
- Weight
- 376 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0025-116X
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The molecular motion in the synthetic bilayer membranes formed from a series of single-chain ammonium amphiphiles with The synthetic routes of the 15 C n SBC m N / amphiphiles and their elemena rigid Schiff base segment, the diphenylazomethine chromophore, tary analysis were reported by Liang et al.
mimetic chemistry, amplification of biomolecular recogni-Isotherms for adsorption of bilayer-forming synthetic amphition, and design of biosensors. However, the assembly of philes or phospholipids from vesicles onto hydrophilic silica partibilayer-forming molecules at interfaces is not yet well cles