RAFT synthesis of triply responsive poly[-[2-(dialkylamino)ethyl]acrylamide]s and their -substitute determined response
The thermo- and pH/CO 2 -responsive poly[ N -[2-(dialkylamino)ethyl]acrylamide]s containing a polyacrylamide backbone but different N -substitutes of dialkylamine were synthesized and their solution properties were comparatively checked. A controllable RAFT synthesis of poly[ N -[2-(dialkylamino)eth...
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Veröffentlicht in: | Polymer chemistry 2016-05, Vol.7 (2), p.3423-3433 |
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Zusammenfassung: | The thermo- and pH/CO
2
-responsive poly[
N
-[2-(dialkylamino)ethyl]acrylamide]s containing a polyacrylamide backbone but different
N
-substitutes of dialkylamine were synthesized and their solution properties were comparatively checked. A controllable RAFT synthesis of poly[
N
-[2-(dialkylamino)ethyl]acrylamide]s was achieved when a typical trithiocarbonate containing an easily cleavable R group was employed. The RAFT polymerization rate decreases with the increasing C-number in the
N
-substitutes. The thermo- and pH/CO
2
-responsive property of poly[
N
-[2-(dialkylamino)ethyl]acrylamide]s is firmly correlative to the
N
-substitutes. With the C-number in the R-substitute increasing, the solution properties of poly(
N
-[2-(dialkylamino)ethyl]acrylamide)s undergo a soluble-to-thermoresponsive-to-insoluble evolution, and the critical pH of poly[
N
-[2-(dialkylamino)ethyl]acrylamide]s gradually decreases. The dialkylamine moieties in the poly[
N
-[2-(dialkylamino)ethyl]acrylamide]s lead to a characteristic CO
2
-response during CO
2
/N
2
bubbling. The present study reveals the structure-dependent solution properties of the thermo- and pH/CO
2
-responsive poly[
N
-[2-(dialkylamino)ethyl]acrylamide]s, and these multistimuli-responsive polymers are believed to be very useful due to the controllable RAFT synthesis and tunable solution properties.
The thermo- and pH/CO
2
-responsive poly[
N
-[2-(dialkylamino)ethyl]acrylamide]s containing a polyacrylamide backbone but different
N
-substitutes of dialkylamine were synthesized and their solution properties were comparatively checked. |
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ISSN: | 1759-9954 1759-9962 |
DOI: | 10.1039/c6py00526h |