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Temperature and pH dual-responsive behavior of polyhedral oligomeric silsesquioxane-based star-block copolymer with poly(acrylic acid-block-N-isopropylacrylamide) as arms
被引:16
作者:
Bai, Yu
[1
]
Wei, Jia
[1
]
Yang, Liping
[1
]
He, Chaobin
[2
]
Lu, Xuehong
[1
]
机构:
[1] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[2] Inst Mat Res & Engn, Singapore 117602, Singapore
关键词:
Poly(N-isopropylacrylamide) (PNIPAm);
Polyhedral oligomeric silsesquioxane (POSS);
Temperature responsive;
pH responsive;
Critical temperature (T-c);
TRANSFER RADICAL POLYMERIZATION;
POLY N-ISOPROPYLACRYLAMIDE;
RAFT POLYMERIZATION;
MOLECULAR-WEIGHT;
PHASE-TRANSITION;
THERMAL RESPONSE;
AQUEOUS-SOLUTION;
POLY(N-ISOPROPYLACRYLAMIDE);
HYDROGELS;
ACID);
D O I:
10.1007/s00396-011-2562-1
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Poly(acrylic acid-block-N-isopropylacrylamide) (PAAc-b-PNIPAm)-tethered octafunctional polyhedral oligomeric silsesquioxane (POSS) were synthesized via POSS-initialized atom transfer radical polymerization. When very short PAAc blocks are placed between the POSS core and PNIPAm short chains, the critical temperature (T-c) of POSS-PAAc-b-PNIPAm determined by cloud point measurements varies in a wide temperature range with pH, and its T-c is even lower than that of POSS-PNIPAm with similar chain length at pH=5.0, indicating a synergic effect between high local chain density and intramolecular interaction between PAAc and PNIPAm. When the PAAc blocks are relatively long, the pH response of POSS-PAAc-b-PNIPAm diminishes owing to the reduced local PNIPAm chain density.
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页码:507 / 515
页数:9
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