Synthesis, characterization, and rheological behavior of polyethylene glycols end-capped with fluorocarbon hydrophobes

被引:132
作者
Xu, B
Li, L
Yekta, A
Masoumi, Z
Kanagalingam, S
Winnik, MA
Zhang, KW
Macdonald, PM
机构
[1] PERKIN ELMER CORP,APPL BIOSYST DIV,FOSTER CITY,CA 94404
[2] UNIV TORONTO,DEPT CHEM,TORONTO,ON M5S 3H6,CANADA
[3] UNIV TORONTO,ERINDALE COLL,TORONTO,ON M5S 3H6,CANADA
关键词
D O I
10.1021/la960799l
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two polyethylene glycols (PEG, M = 35 000) end-capped with short fluorocarbon tails were synthesized and characterized. In aqueous solution, the fluorocarbon portions associate strongly to form micelle-like structures which are bridged by PEG chains to form a three-dimensional network. As a result, these polymers in solution exhibit unusual rheological properties as a function of fluorocarbon length, polymer concentration, and shear rate (frequency). Their zero-shear viscosity increases with concentration, a common behavior of associating polymers. The viscosity is dramatically enhanced by replacing the end hydrophobe C6F13 with C8F17, a consequence of the stronger association interaction of C8F17 in aqueous solution. The polymer with the longer end group exhibits strong shear thinning once a critical shear rate is reached, whereas for the C6F13 end-capped polymer, we cannot with our equipment reach the shear-thinning regime. Our data indicate that between 2 and 6 wt %, and perhaps over a wider range of concentrations, both systems can be characterized in terms of identical values of the plateau modulus G(N) degrees, implying a similar concentration of chains bridging micelles in each system. The G(N) degrees values increase strongly with polymer concentration, consistent with a larger fraction of bridging chains and a smaller fraction of looping chains at elevated concentration. The viscosity difference between the two polymers can be explained in terms of a slower exit rate of the longer fluorocarbon from its micelle.
引用
收藏
页码:2447 / 2456
页数:10
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