4.8 Review

Dynamic Covalent Polymer Networks: A Molecular Platform for Designing Functions beyond Chemical Recycling and Self-Healing

期刊

CHEMICAL REVIEWS
卷 121, 期 3, 页码 1716-1745

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrev.0c00938

关键词

-

资金

  1. National Natural Science Foundation of China [52033009, 52003232, 21625402, 51822307]
  2. Postdoctoral Innovation Support Program [BX20190294]

向作者/读者索取更多资源

Dynamic covalent polymer networks have shown unique roles in chemical recycling and self-healing, with recent advancements in dynamic chemistry and material concepts leading to promising applications in energy, electronics, and beyond. The design versatility and functional properties offered by DCPN have gained traction, with opportunities in shape-shifting materials, artificial muscles, and network topologies manipulation. Additionally, molecular design strategies for exploiting functional material properties have been a focus, showing potential for shaping the future alongside classical thermoplastic and thermoset polymers.
Dynamic covalent polymer networks (DCPN) have historically attracted attention for their unique roles in chemical recycling and self-healing, which are both relevant for sustainable societal development. Efforts in these directions have intensified in the past decade with notable progress in newly discovered dynamic covalent chemistry, fundamental material concepts, and extension toward emerging applications including energy and electronic devices. Beyond that, the values of DCPN in discovering/designing functional properties not offered by classical thermoplastic and thermoset polymers have recently gained traction. In particular, the dynamic bond exchangeability of DCPN has shown unparalleled design versatility in various areas including shape-shifting materials/devices, artificial muscles, and microfabrication. Going beyond this basic bond exchangeability, various molecular mechanisms to manipulate network topologies (topological transformation) have led to opportunities to program polymers, with notable concepts such as living networks and topological isomerization. In this review, we provide an overview of the above progress with particular focuses on molecular design strategies for the exploitation of functional material properties. Based on this, we point out the remaining issues and offer perspectives on how this class of materials can shape the future in ways that are complementary with classical thermoplastic and thermoset polymers.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据