Amphiphilic polymers for micellar networks

2020 ◽  
pp. 1-14
Author(s):  
Ralf Weberskirch ◽  
Oskar Nuyken
Keyword(s):  
Polymers ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 460
Author(s):  
Daisuke Kugimoto ◽  
Aoi Taniguchi ◽  
Masaki Kinoshita ◽  
Isamu Akiba

Associating behavior of star-like amphiphilic polymers consisting of two or three poly(ethylene oxide) (PEO) chains and one stearyl chain (C18) was investigated. Although the aggregation number (Nagg) of linear analogue of amphiphilic polymers monotonically decreased with increasing number-average molecular weight of PEO (Mn,PEO), the Nagg of micelles of star-like amphiphilic polymers with Mn,PEO = 550 g/mol was smaller than that with Mn,PEO = 750 g/mol, whereas that with Mn,PEO ≥ 750 g/mol showed general Mn,PEO dependence. Small-angle X-ray scattering analyses revealed that the occupied area of one PEO chain on the interface between hydrophobic core and corona layer in the micelles of star-like polymers was much narrower than that in the linear amphiphilic polymers. This result indica ted the PEO chains of star-like polymers partially took unfavorable conformation near the core–corona interface in polymer micelles. The effect of local conformation of PEO chains near the interface on the associating behavior became significant as Mn,PEO decreased. Therefore, in polymer micelles of star-like amphiphilic polymers containing PEO with Mn,PEO = 550 g/mol, the enlargement of occupied area of PEO on the core–corona interface should be caused to avoid the formation of unfavorable conformations of partial PEO chains, resulting in a decrease in Naggs.


2017 ◽  
Vol 35 (11) ◽  
pp. 1180-1187 ◽  
Author(s):  
Wanli Kang ◽  
Jiatong Jiang ◽  
Yao Lu ◽  
Derong Xu ◽  
Hairong Wu ◽  
...  

2020 ◽  
Vol 320 ◽  
pp. 114440
Author(s):  
Boris A. Noskov ◽  
Kirill A. Timoshen ◽  
Alexey G. Bykov

2014 ◽  
Vol 5 (22) ◽  
pp. 6461-6471 ◽  
Author(s):  
Sarah Decato ◽  
Troy Bemis ◽  
Eric Madsen ◽  
Sandro Mecozzi

Semifluorinated polymer surfactants containing one, two, or three perfluoro-tert-butyl groups were synthesized and fully characterized. Theranostic applications are discussed.


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