Molecular Weight Dependence of Zero-Shear Viscosity in Atactic Polypropylene Bottlebrush Polymers

被引:126
作者
Dalsin, Samuel J. [1 ]
Hillmyer, Marc A. [2 ]
Bates, Frank S. [1 ]
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
关键词
OPENING-METATHESIS POLYMERIZATION; BRUSH BLOCK-COPOLYMERS; PHOTONIC CRYSTALS; BULK PROPERTIES; POLYSTYRENE; POLYMACROMONOMERS; MACROMONOMERS; DYNAMICS; SOFT;
D O I
10.1021/mz500082h
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
-A series of bottlebrush polymers with atactic polypropylene side chains were synthesized via ring-opening metathesis polymerization using Grubbs' third-generation catalyst (H(2)IMes)(3-BrPy)(2)(Cl)(2)Ru=CHPh. Polymers were prepared with fixed side chain length and variable backbone degree of polymerization (DP) ranging from 11 to 732 (M-w = 22-1500 kg/mol) and include the largest reported polyolefin-based bottlebrush polymers. The zero-shear viscosity of each polymer sample was measured using small-amplitude oscillatory shear measurements. Power law fits of zero-shear viscosity (eta(0)) versus weight-average molar mass (eta(0) similar to M-w(alpha)) revealed distinct regimes with differing molecular weight dependences. A weak dependence (alpha < 0.5) was observed at low molecular weight due to the increasingly compact nature of short bottlebrush polymers with the continued addition of side chains. The scaling transitioned to Rouse-like dynamics (alpha = 1.2) at high molecular weight as a consequence of a sphere-to-cylinder conformational change with increasing DP of the bottlebrush backbone.
引用
收藏
页码:423 / 427
页数:5
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