One-Pot Synthesis of a Polyrotaxane via Selective Threading of a PEI-b-PEG-b-PEI Copolymer
✍ Scribed by Hak Soo Choi; Tooru Ooya; Nobuhiko Yui
- Book ID
- 102470847
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 218 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1616-5187
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✦ Synopsis
Abstract
Summary: A functional polyrotaxane of a PEI‐b‐PEG‐b‐PEI copolymer is synthesized in aqueous solution in a one‐pot sequence. To obtain a polyrotaxane with PEG‐block‐selective inclusion complexes, the solution pH of the polypseudorotaxane is lowered to 4.4 in the presence of 9‐anthraldehyde (AN), which triggers the expulsion of the α‐cyclodextrins (α‐CDs) from the flank PEI chains.
Synthetic strategy of a block‐selective polyrotaxane between a PEI‐b‐PEG‐b‐PEI copolymer and α‐cyclodextrins.
magnified imageSynthetic strategy of a block‐selective polyrotaxane between a PEI‐b‐PEG‐b‐PEI copolymer and α‐cyclodextrins.
📜 SIMILAR VOLUMES
## Abstract An improved and simple method for the preparation of pyrazolo[3,4‐__b__][1,5]benzoxazepine, ‐benzothiazepine and ‐benzodiazepine derivatives was established by the reaction of 5‐chloro‐1‐phenylpyrazole‐4‐carbaldehydes, ethyl 3‐(5‐chloro‐1,3‐diphenylpyrazol‐4‐yl)‐2‐cyanoacrylate and 1,4‐