pH-Responsive Supramolecular Self-Assembly of Well-Defined Zwitterionic ABC Miktoarm Star Terpolymers

被引:94
作者
Liu, Hao [1 ]
Li, Changhua [1 ]
Liu, Hewen [1 ]
Liu, Shiyong [1 ]
机构
[1] Univ Sci & Technol China, CAS Key Lab Soft Matter Chem, Dept Polymer Sci & Engn, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China
关键词
HYDROPHILIC BLOCK-COPOLYMERS; TRANSFER RADICAL POLYMERIZATION; RING-OPENING POLYMERIZATION; DOUBLE-GRAFT-COPOLYMERS; CROSS-LINKED MICELLES; GRAIN-GROWTH KINETICS; STOPPED-FLOW PH; DIBLOCK COPOLYMER; MICELLIZATION KINETICS; AQUEOUS-SOLUTION;
D O I
10.1021/la803813r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the first example of the synthesis and pH-responsive supramolecular self-assembly of double hydrophilic ABC miktoarm star terpolymers. Well-defined ABC miktoarm star terpolymers consisting of poly(ethylene glycol), poly(tert-butyl methacrylate), and poly(2-(diethylamino)ethyl methacrylate) arms [PEG (-b-PtBMA)-b-PDEA] were synthesized via the combination of consecutive click reactions and atom transfer radical polymerization (ATRP), starting from a trifunctional core molecule, 1-azido-3-chloro-2-propanol (ACP). The click reaction of monoalkynyl-terminated PEG with an excess of ACP afforded difunctional PEG bearing a chlorine and a secondary hydroxyl moiety at the chain end, PEG(113)(-Cl)-OH (1). After azidation with NaN3, PEG-based macroinitiator PEG(113)(-N-3)-Br (3) was prepared by the esterification of PEG(113)(-N-3)-OH (2) with 2-bromoisobutyryl bromide and then employed in the ATRP of tert-butyl methacrylate (tBMA). The obtained PEG(-N-3)-b-PtBMA copolymers (4) possessed an azido moiety at the diblock junction point. The preparation of PEG(-b-PtBMA)-b-PDEA miktoarm star terpolymers was then achieved via the click reaction of 4 with an excess of monoalkynyl-terminated PDEA. The obtained miktoarm, star terpolymers were successfully converted into PEG(-b-PMAA)-b-PDEA, where PMAA is poly(methacrylic acid). In aqueous solution, PEG(-bPMAA)-b-PDEA zwitterionic ABC miktoarm star terpolymers can self-assemble into three types of micellar aggregates by simply adjusting solution pH at room temperature. Above pH 8, PDEA-core micelles stabilized by PEG/ionized PMAA hybrid coronas were formed due to the insolubility of PDEA block. In the range of pH 5-7, micelles possessing polyion complex cores formed as a result of charge compensation between partially ionized PMAA and partially protonated PDEA sequences. At pH < 4, hydrogen bonding interactions between fully protonated PMAA and PEG led to the formation of another type of micellar aggregates possessing hydrogen-bonded complex cores stabilized by protonated PDEA coronas. The fully reversible pH-responsive formation of three types of aggregates were characterized by H-1 NMR, dynamic and static laser light scattering (LLS), and transmission electron microscopy (TEM).
引用
收藏
页码:4724 / 4734
页数:11
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