Synthesis, self-assembly behavior, and biological application of a new photochromic azo amphiphilic diblock copolymer

2011 ◽  
Vol 51 (8) ◽  
pp. 1662-1668 ◽  
Author(s):  
Han Ding ◽  
Zheng Wang ◽  
Lijiao Sheng ◽  
Gongwu Song
RSC Advances ◽  
2018 ◽  
Vol 8 (23) ◽  
pp. 12752-12759
Author(s):  
HuaQing Liang ◽  
QiHua Zhou ◽  
YongJiang Long ◽  
WanChu Wei ◽  
Shuo Feng ◽  
...  

Herein, a novel amphiphilic diblock copolymer consisting of isotactic polystyrene and 1,4-trans-polybutadiene-graft-poly(ethylene oxide) was synthesized and its self-assembly behavior was investigated.


2018 ◽  
Vol 34 (8) ◽  
pp. 945-951
Author(s):  
Xiaomeng CHENG ◽  
◽  
Dongxia JIAO ◽  
Zhihao LIANG ◽  
Jinjin WEI ◽  
...  

2020 ◽  
Vol 11 (2) ◽  
pp. 396-402 ◽  
Author(s):  
Sarah J. Byard ◽  
Cate T. O'Brien ◽  
Matthew J. Derry ◽  
Mark Williams ◽  
Oleksandr O. Mykhaylyk ◽  
...  

A new amphiphilic diblock copolymer prepared via polymerization-induced self-assembly forms spheres, worms, vesicles or lamellae in aqueous solution on adjusting the temperature.


e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Dong Chen ◽  
Ruixue Liu ◽  
Zhifeng Fu ◽  
Yan Shi

AbstractAmphiphilic diblock copolymer poly(methyl methacrylate)-b-poly(acrylic acid) (PMMA-b-PAA) was prepared by 1,1-diphenylethene (DPE) method. Firstly, free radical polymerization of methyl methacrylate was carried out with AIBN as initiator in the presence of DPE, giving a DPE-containing PMMA precursor with controlled molecular weight. tert-Butyl acrylate (tBA) was then polymerized in the presence of the PMMA precursor, and PMMA-b-PtBA diblock copolymer with controlled molecular weight was prepared. Finally, amphiphilic diblock copolymer PMMA-b-PAA was obtained by hydrolysis of PMMA-b-PtBA. The formation of PMMA-b-PAA was confirmed by 1H NMR spectrum and gel permeation chromatography. Transmission electron microscopy and dynamic light scattering were used to detect the self-assembly behavior of the amphiphilic diblock polymers in methanol.


2015 ◽  
Vol 4 (4) ◽  
pp. 381-386 ◽  
Author(s):  
Nghia P. Truong ◽  
John F. Quinn ◽  
Marion V. Dussert ◽  
Nikolle B. T. Sousa ◽  
Michael R. Whittaker ◽  
...  

Polymers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 2028
Author(s):  
Po-Chih Yang ◽  
Yueh-Han Chien ◽  
Shih-Hsuan Tseng ◽  
Chia-Chung Lin ◽  
Kai-Yu Huang

This paper gathered studies on multistimulus-responsive sensing and self-assembly behavior of a novel amphiphilic diblock copolymer through a two-step reverse addition-fragmentation transfer (RAFT) polymerization technique. N-Isopropylacrylamide (NIPAM) macromolecular chain transfer agent and diblock copolymer (poly(NIPAM-b-Azo)) were discovered to have moderate thermal decomposition temperatures of 351.8 and 370.8 °C, respectively, indicating that their thermal stability was enhanced because of the azobenzene segments incorporated into the block copolymer. The diblock copolymer was determined to exhibit a lower critical solution temperature of 34.4 °C. Poly(NIPAM-b-Azo) demonstrated a higher photoisomerization rate constant (kt = 0.1295 s−1) than the Azo monomer did (kt = 0.088 s−1). When ultraviolet (UV) irradiation was applied, the intensity of fluorescence gradually increased, suggesting that UV irradiation enhanced the fluorescence of self-assembled cis-isomers of azobenzene. Morphological aggregates before and after UV irradiation are shown in scanning electron microscopy (SEM) and dynamic light scattering (DLS) analyses of the diblock copolymer. We employed photoluminescence titrations to reveal that the diblock copolymer was highly sensitive toward Ru3+ and Ba2+, as was indicated by the crown ether acting as a recognition moiety between azobenzene units. Micellar aggregates were formed in the polymer aqueous solution through dissolution; their mean diameters were approximately 205.8 and 364.6 nm at temperatures of 25.0 and 40.0 °C, respectively. Our findings contribute to research on photoresponsive and chemosensory polymer material developments.


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