Self-assembly of polypeptide/π-conjugated polymer/polypeptide triblock copolymers in rod-rod-rod and coll-rod-coil conformations

被引:70
|
作者
Rubatat, Laurent [1 ,2 ]
Kong, Xiangxing [3 ]
Jenekhe, Samson A. [3 ]
Ruokolainen, Janne [4 ]
Hojeij, Mohamad [5 ]
Mezzenga, Raffaele [1 ,2 ,6 ]
机构
[1] Univ Fribourg, Dept Phys, CH-1700 Fribourg, Switzerland
[2] Univ Fribourg, Fribourg Ctr Nanomat, CH-1700 Fribourg, Switzerland
[3] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
[4] Aalto Univ, FIN-02150 Espoo, Finland
[5] Ecole Polytech Fed Lausanne, Lab Electrochim Phys & Analyt, CH-1015 Lausanne, Switzerland
[6] Nestle Res Ctr, CH-1000 Lausanne 26, Switzerland
关键词
D O I
10.1021/ma702278a
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Self-assembly in the bulk of a series of hybrid triblock copolymers formed by a poly(9,9-dihexylfluorene-2,7-diyl) (PHF) middle block and two poly(gamma-benzyl-L-glutamate) (PBLG) end blocks has been studied. Since the alpha-helical secondary structure of the PBLG block may be either maintained or suppressed depending on the solvent casting history, the PBLG-PHF-PBLG copolymers exhibit two different conformations: a rod-rod-rod or coil-rod-coil configuration, respectively. In order to provide insight into the influence of conformation on self-aggregation of these systems, three copolymers with different block ratio were investigated in both conformations using small- and wide-angle scattering techniques and transmission electron microscopy. Time-resolved photoluminescence measurements were performed on the same samples to explore the effect of morphology on photophysical properties. The observed photoluminescence spectra and dominant excited lifetimes of the poly(9,9-dihexylfluorene-2,7-diyl) block were found to differ markedly in rod-rod-rod and coil-rodcoil configurations and were correlated to the morphology of the self-assembled triblock copolymers.
引用
收藏
页码:1846 / 1852
页数:7
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