Conformational changes of linear-dendrimer diblock copolymers in dilute solution

被引:13
|
作者
Passeno, LM
Mackay, ME [1 ]
Baker, GL
Vestberg, R
Hawker, CJ
机构
[1] Michigan State Univ, Dept Chem Engn & Mat Sci, E Lansing, MI 48823 USA
[2] Michigan State Univ, Dept Chem, E Lansing, MI 48823 USA
[3] Univ Calif Santa Barbara, Mat Res Lab, Santa Barbara, CA 93106 USA
关键词
D O I
10.1021/ma0517291
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The conformation of linear-dendrimer hybrid diblock copolymers in solution has been studied using both small-angle neutron scattering and dynamic light scattering. The diblock consisted of a fourth-generation benzyl ether dendrimer with different molecular weight polystyrene bonded to the focal point of the dendrimer; the total molecular weight ranged from 20 to 100 kDa. In agreement with previous studies, it was found that this dendron, without a linear chain attached, alters its size upon solvent change. The addition of a polystyrene chain to the focal point of a dendrimer was also found to have an effect on the dimensions and shape of the dendrimer block. A low-molecular-weight polystyrene chain swelled the dendrimer without perturbing its native spherelike conformation. However, at larger polystyrene molecular weights, the linear block manipulates a transition of the dendrimers' morphology form spherelike to an extended conformation. Control of this shape and size change has potential for these unique macromolecular architectures to function as a novel molecular building block.
引用
收藏
页码:740 / 746
页数:7
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