Malleable and Self-Healing Covalent Polymer Networks through Tunable Dynamic Boronic Ester Bonds

被引:834
作者
Cromwell, Olivia R. [1 ]
Chung, Jaeyoon [1 ]
Guan, Zhibin [1 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
基金
美国国家科学基金会;
关键词
MECHANICAL-PROPERTIES; HYDROGELS; METATHESIS; RECEPTORS; DESIGN;
D O I
10.1021/jacs.5b03551
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite numerous strategies involving dynamic covalent bond exchange for dynamic and self-healing materials, it remains a challenge to be able to tune the malleability and self-healing properties of bulk materials through simple small molecule perturbations. Here we describe the use of tunable rates of boronic ester transesterification to tune the malleability and self-healing efficiencies of bulk materials. Specifically, we used two telechelic diboronic ester small molecules with variable transesterification kinetics to dynamically cross-link 1,2-diol-containing polymer backbones. The sample cross-linked with fast-exchanging diboronic ester showed enhanced malleability and accelerated healing compared to the slow-exchanging variant under the same conditions. Our report demonstrates the possibility of transferring small molecule kinetics to dynamic properties of bulk solid material and may serve as a guide for the rational design of tunable dynamic materials.
引用
收藏
页码:6492 / 6495
页数:4
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