Cloud point of poly(N-isopropylacrylamide) synthesized in the presence of cyclodextrin
✍ Scribed by Seung Jun Han; Mi Kyong Yoo; Yong Kiel Sung; Young Moo Lee; Chong Su Cho
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 406 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
Polymerization of N-isopropylacrylamide (NIPAAm) was performed in the presence of P-cyclodextrin (B-CD) [or hydroxypropyl-/3-cyclodextrin (HOP-P-CD)]. The formation of an inclusion complex between PNIPAAm and p-CD was confirmed by FT-IR, 'H N M R and 2D-NOESY NMR. It was found that the cloud point (CP) of poly(N-isopropylamide) (PNIPAAm) in the PNIPAAm/P-CD complex in aqueous solution increased up to about 57 "C whereas that in the PNIPAAm/P-CD blend is about 33 "C. The CP of PNIPAAm in the PNIPAAdP-CD complex is higher than that in the PNIPAAmMIOP-P-CD inclusion complex. E R and NMR results suggest that P ~P A A m chains are included in CD cavities.
📜 SIMILAR VOLUMES
## Abstract Time‐dependent phase separation/transition was observed in aqueous solutions of poly(__N__‐isopropylmethacrylamide) in the temperature range 38–42°C. The time before the second phase appears is a function of temperature and may reach up to several hours.
## Abstract **Summary:** Hydrophobically modified poly(__N__‐isopropylacrylamide) (PNIPAM) containing either an adamantyl or a dodecyl group were prepared and characterized. Self‐association in aqueous solutions was evidenced by fluorescence measurements using pyrene as a probe. The lower critical
Poly(N-isopropylacrylamide) (PNIPAM) is well known to exhibit reentrant behavior or cononsolvency in response to the composition of a mixed solvent consisting of water and a low-chain alcohol. Since the solvent structure plays an important role in this phenomenon, the presence of structure-breaking/
The radical polymerization of N-tert-butyl-N-allylacrylamide (t-BAA) was carried out in a dimethyl sulfoxide/H 2 O mixture in the presence of -cyclodextrin (-CD). The polymerization proceeded with the complete cyclization of the t-BAA unit and yielded optically active poly(t-BAA). The IR spectrum