Control of Grafting Density and Distribution in Graft Polymers by Living Ring-Opening Metathesis. Copolymerization

被引:151
作者
Lin, Tzu-Pin [1 ]
Chang, Alice B. [1 ]
Chen, Hsiang-Yun [1 ]
Liberman-Martin, Allegra L. [1 ]
Bates, Christopher M. [2 ]
Voegtle, Matthew J. [3 ]
Bauer, Christina A. [3 ]
Grubbs, Robert H. [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
[2] Univ Calif Santa Barbara, Dept Chem Engn, Dept Mat, Santa Barbara, CA 93106 USA
[3] Whittier Coll, Dept Chem, Whittier, CA 90608 USA
基金
美国国家科学基金会;
关键词
MONTE-CARLO-SIMULATION; CYLINDRICAL MOLECULAR BRUSHES; SIDE-CHAIN LENGTH; ALT-B COPOLYMERS; BOTTLEBRUSH POLYMERS; BLOCK-COPOLYMERS; PERSISTENCE LENGTH; REACTIVITY RATIOS; POLYMERIZATION; CATALYST;
D O I
10.1021/jacs.7b00791
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Control over polymer sequence and architecture is crucial to both understanding structure property relationships and designing functional materials. In pursuit of these goals, we developed a new synthetic approach that enables facile manipulation of the density and distribution of grafts in polymers via living ring-opening metathesis polymerization (ROMP). Discrete endo,exo-norbornenyl dialkylesters (dimethyl DME, diethyl DEE, di-n-butyl DBE) were strategically designed to copolymerize with a norbornene-functionalized polystyrene (PS), polylactide (PLA), or polydimethylsiloxane (PDMS) macromonomer mediated by the third-generation metathesis catalyst (G3). The small molecule diesters act as diluents that increase the average distance between grafted side chains, generating polymers with variable grafting density. The grafting density (number of side chains/number of norbornene backbone repeats) could be straightforwardly controlled by the macromonomer/diluent feed ratio. To gain insight into the copolymer sequence and architecture, self-propagation and cross-propagation rate constants were determined according to a terminal copolymerization model. These kinetic analyses suggest that copolymerizing a macromonomer/diluent pair with evenly matched self -propagation rate constants favors randomly distributed side chains. As the disparity between macromonomer and diluent homopolymerization rates increases, the reactivity ratios depart from unity, leading to an increase in gradient tendency. To demonstrate the effectiveness of our method, an array of monodisperse polymers (PLA(x)-ran-DME1-x)(n) bearing variable grafting densities (x = 1.0, 0.75, 0.5, 0.25) and total backbone degrees of polymerization (n = 167, 133, 100, 67, 33) were synthesized. The approach disclosed in this work therefore constitutes a powerful strategy for the synthesis of polymers spanning the linear-to-bottlebrush regimes with controlled grafting density and side chain distribution, molecular attributes that dictate micro- and macroscopic properties.
引用
收藏
页码:3896 / 3903
页数:8
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