Synthesis and Self‐Assembly Behavior of Organic–Inorganic Poly(ethylene oxide)‐block‐Poly(MA POSS)‐block‐Poly(N‐isopropylacrylamide) Triblock Copolymers

Macromolecular Chemistry and Physics - Tập 213 Số 4 - Trang 458-469 - 2012
Yaochen Zheng1, Lei Wang1, Rentong Yu1, Sixun Zheng1
1Department of Polymer Science and Engineering and State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai 200240, P. R. China

Tóm tắt

AbstractIn this work, the synthesis of 3‐methacryloxypropylheptaphenyl POSS, a new POSS macromer (denoted MA‐POSS) is reported. The POSS macromer is used to synthesize PEO‐b‐P(MA‐POSS)‐b‐PNIPAAm triblock copolymers via sequential atom transfer radical polymerization (ATRP). The organic‐inorganic, amphiphilic and thermoresponsive ABC triblock copolymers are characterized by means of nuclear magnetic resonance spectroscopy (NMR) and gel permeation chromatography (GPC). Differential scanning calorimetry (DSC) and atomic force microscopy (AFM) show that the hybrid ABC triblock copolymers are microphase‐separated in bulk. Cloud point measurements show that the effect of the hydrophiphilic block (i.e. PEO) on the LCSTs is more pronounced than the hydrophobic block (i.e. P(MA‐POSS)). Both transmission electron microscopy (TEM) and dynamic light scattering (DLS) show that all the triblock copolymers can be self‐organized into micellar aggregates in aqueous solutions. The sizes of the micellar aggregates can be modulated by changing the temperature. The temperature‐tunable self‐assembly behavior is interpreted using a combination of the highly hydrophobicity of P(MA‐POSS), the water‐solubility of PEO and the thermoresponsive property of PNIPAAm in the triblock copolymers.

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Tài liệu tham khảo

10.1021/cr00037a012

10.1002/(SICI)1099-0739(199810/11)12:10/11<707::AID-AOC776>3.0.CO;2-1

10.1023/A:1015287910502

10.1016/j.progpolymsci.2003.08.003

10.1080/15583720802656237

10.1021/ma102360t

10.1016/j.progpolymsci.2011.05.002

10.1021/ma020226h

10.1021/ma062069i

10.1016/j.polymer.2006.06.050

10.1021/ma0618171

10.1021/jp9043623

10.1016/j.polymer.2008.11.024

10.1021/ma902830f

10.1021/am101258k

10.1017/CBO9780511801280

10.1021/ma960609d

10.1021/ma960846g

10.1021/ma9800764

10.1002/(SICI)1097-0126(200005)49:5<453::AID-PI332>3.0.CO;2-H

10.1021/ma00128a067

10.1021/ma9910787

10.1016/S0032-3861(03)00027-2

10.1016/j.polymer.2005.12.025

10.1002/adma.200900518

10.1021/ma101276d

10.1021/ma9018944

10.1021/ma800872v

10.1021/la101686q

10.1021/ma102510u

10.1080/10601326808051910

10.1016/0079-6700(92)90023-R

10.1021/ma960499a

10.1021/ma002082h

10.1021/ma0600254

10.1021/jp061055b

10.1002/pola.23461

10.1021/ic50035a010

10.1021/ma048877w

10.1002/pola.21893

10.1021/ma980725b

10.1021/ma050261z

10.1016/B978-0-08-054819-7.00001-7

10.1021/ma062538g

10.1021/jp075891c

Feast W. J., 1993, Polymer Surface and Interface, II

10.1021/ma950900d

10.1021/ma9903456

10.1021/ma020463k

10.1021/ma0203187

10.1021/ma021623v

10.1002/polb.20157