自愈水凝胶
自催化
材料科学
盐变质反应
瞬态(计算机编程)
复分解
级联
水解
耗散系统
化学工程
聚合物
化学
高分子化学
计算机科学
有机化学
催化作用
热力学
复合材料
物理
工程类
聚合
操作系统
作者
Jingyi Zhang,Jian Liu,Huizeng Li,Xiaohe Li,Yuanfeng Zhao,Peng Zhao,Jiaxi Cui,Bo Yang,Yanlin Song,Yijun Zheng
标识
DOI:10.1021/acsami.2c03177
摘要
It is challenging to design complex synthetic life-like systems that can show both autoevolution and fuel-driven transient behaviors. Here, we report a new class of chemical reaction networks (CRNs) to construct life-like polymer hydrogels. The CRNs are constituted of autocatalytic cascade reactions and fuel-driven reaction networks. The reactions start with only two compounds, that is, thiol of 4-arm-PEG-SH and thiuram disulfides, and undergo thiol oxidation (k1), disulfide metathesis (k2), and thionate hydrolysis-coupling reactions (k3) subsequently, leading to a four-state autonomous transition of sol(I) → soft gel → sol(II) → stiff gel. Moreover, thiuram disulfides can be applied as a fuel to drive the repeated occurrence of metathesis and hydrolysis-coupling reactions, generating dissipative stiff gel → sol(II) → stiff gel cycles. Systematic kinetics studies reveal that the event and lifetime of every transient state could be delicately tailored-up by varying the thiuram disulfide concentration, pH of the system, and thiuram structures. Since the consecutive transient behaviors are precisely predictable, we envision the strategy's potential in guiding the molecular designs of autonomous and adaptive materials for many fields.
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