中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Inhomogeneous-collapse driven micelle-vesicle transition of amphiphilic block copolymers

文献类型:期刊论文

作者Liu, Biaolan; Ru, Geying; Feng, Jiwen; Wu, Shuaishuai; Zhang, Yu; Wang, Jian
刊名SOFT MATTER
出版日期2017-10-21
卷号13期号:39页码:7106-7111
DOI10.1039/c7sm01540b
文献子类Article
英文摘要Understanding the morphological transition dynamics related to the hydrophilic-hydrophobic interface has been a challenge due to the lack of an effective evaluation method. Herein, nuclear magnetic resonance spectroscopy was employed to study the morphological transition related chain collapse of poly(N, N '-diethylaminoethylmethacrylate)- b-poly(N-isopropylacrylamide) (PDEAEMA133-b-PNIPA322) and poly(N, N '-dimethylaminoethylmethacrylate)- b-poly(N-isopropylacrylamide) (PDMAEMA95-b-PNIPA228) and was proved to be a powerful technique in morphological transition mechanism studies once combined with dynamic light scattering and transmission electron microscopy. Unlike the cooperative coil collapse of two blocks in the PDMAEMA95-b-PNIPA228 alkaline solution upon heating which induces the assembly of a nanostructure (similar to 200 nm) with a hydrophobic core containing both collapsed PDMAEMA and PNIPA segments and a hydrophilic surface part consisting of un-shrunk PDMAEMA and PNIPA segments, PDEAEMA133-b-PNIPA322 with a low-temperature core-shell micelle structure showed a micelle-vesicle transition due to temperature-induced inhomogeneous-collapse of PNIPA. The PNIPA segments in the shell sequentially collapse outside (starting at the core-shell interface), accompanied by a gradual decrease in micelle size. Above the critical temperature, the residual hydrophilic PNIPA segments become too short to stabilize the micelle structure, the micelles then transform into vesicles of a slightly larger size, instead of micelle aggregation and precipitation as normally expected.
WOS关键词POLY N-ISOPROPYLACRYLAMIDE ; DIBLOCK COPOLYMERS ; RAFT POLYMERIZATION ; PHASE-TRANSITION ; MORPHOLOGICAL TRANSITION ; TRIBLOCK COPOLYMERS ; DRUG-DELIVERY ; END-GROUPS ; NMR ; METHACRYLATE
WOS研究方向Chemistry ; Materials Science ; Physics ; Polymer Science
语种英语
WOS记录号WOS:000412778600015
资助机构National Natural Science Foundation of China(21204099 ; National Natural Science Foundation of China(21204099 ; 11274347 ; 11274347 ; 21221064) ; 21221064) ; National Natural Science Foundation of China(21204099 ; National Natural Science Foundation of China(21204099 ; 11274347 ; 11274347 ; 21221064) ; 21221064)
源URL[http://ir.wipm.ac.cn/handle/112942/11419]  
专题武汉物理与数学研究所_磁共振基础研究部
作者单位Chinese Acad Sci, State Key Lab Magnet Resonance & Atom & Mol Phys, Natl Ctr Magnet Resonance Wuhan, Wuhan Inst Phys & Math, Wuhan 430071, Hubei, Peoples R China
推荐引用方式
GB/T 7714
Liu, Biaolan,Ru, Geying,Feng, Jiwen,et al. Inhomogeneous-collapse driven micelle-vesicle transition of amphiphilic block copolymers[J]. SOFT MATTER,2017,13(39):7106-7111.
APA Liu, Biaolan,Ru, Geying,Feng, Jiwen,Wu, Shuaishuai,Zhang, Yu,&Wang, Jian.(2017).Inhomogeneous-collapse driven micelle-vesicle transition of amphiphilic block copolymers.SOFT MATTER,13(39),7106-7111.
MLA Liu, Biaolan,et al."Inhomogeneous-collapse driven micelle-vesicle transition of amphiphilic block copolymers".SOFT MATTER 13.39(2017):7106-7111.

入库方式: OAI收割

来源:武汉物理与数学研究所

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