Complex Amphiphilic Networks Derived From Diamine-Terminated Poly(ethylene Glycol) and Benzylic Chloride-Functionalized Hyperbranched Fluoropolymers
Polymers and High Performance Materials
Amphiphilic copolymer networks were prepared from hyperbranched fluoropolymer (HBFP*, M-n = 38 kDa, by atom transfer radical-self condensing vinyl copolymerization) and linear diamine-terminated poly(ethylene glycol) (DA-PEG, M-n = 1,630 Da). Model studies found that the crosslinking mechanism occurred at ambient temperature as a result of reaction between DA-PEG and the benzylic chlorides of HBFP*. These networks underwent covalent attachment to glass microscope slides derivatized. with 3-aminopropyltriethoxysilane, whereupon gel percent studies at various weight percentages of DA-PEG to HBFP* found that curing could be achieved at lower temperatures and shortened time periods relative to the previously reported parent HBFP-PEG system. Thermogravimetric analysis revealed that the crosslinked materials gave no evident mass loss up to 250 degrees C. Differential scanning calorimetry of the complex amphiphilic networks showed a suppressed glass transition temperature, relative to that observed for neat HBFP*, and multiple melting DA-PEG endotherm(s) near 30 degrees C. The films possessed a topographically-complex surface with features that increased in tandem with an increase in the ratio of DA-PEG to HBFP*, as detected by atomic force microscopy and quantified by increased rms roughness values. Internal reflection infrared imaging revealed a heterogeneous surface composition and confirmed that the domain sizes increased as the weight percent of DA-PEG increased. (c) 2006 Wiley Periodicals, Inc.
Journal of Polymer Science Part A-Polymer Chemistry
Powell, K. T.,
Wooley, K. L.,
Urban, M. W.
(2006). Complex Amphiphilic Networks Derived From Diamine-Terminated Poly(ethylene Glycol) and Benzylic Chloride-Functionalized Hyperbranched Fluoropolymers. Journal of Polymer Science Part A-Polymer Chemistry, 44(16), 4782-4794.
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