电化学
自愈水凝胶
组合化学
氧化还原
表面改性
材料科学
电极
共价键
纳米技术
化学
有机化学
高分子化学
物理化学
作者
Jinyang Li,Eunkyoung Kim,Kelsey M. Gray,Christina Conrad,Chen‐Yu Tsao,Sally P. Wang,Guanghui Zong,Giuliano Scarcelli,Kimberly M. Stroka,Lai‐Xi Wang,William E. Bentley,Gregory F. Payne
标识
DOI:10.1002/adfm.202001776
摘要
Abstract Biology uses diffusible oxidants to perform functions that range from signaling to matrix assembly, and these oxidation chemistries offer surprising selectivities. Here, it is reported that mediated electrochemistry can access the richness of such oxidation chemistries. Specifically, electrode‐imposed voltage inputs are used to locally generate oxidized mediators that can diffuse into polymer solutions and induce the formation of covalent bonds for the deposition and functionalization of hydrogels at the electrode surface. Depending on the mediator's redox potential ( E 0 ), it is possible to “gate” the voltage inputs to target specific residues (e.g., thiols or amines) and oxidation chemistries. Further, mediators of varying E 0 offer different reactivities and thus allow control of reaction‐diffusion rates to modulate the hydrogel's crosslink density and mechanical properties. Importantly, this mediated oxidation can be performed under physiologically relevant conditions to preserve labile biological functionalities (e.g., cell viability and protein function). Finally, it is demonstrated that protein fusion tags can be engineered to have “targetable” amino acid residues that enable protein function to be oxidatively conjugated to electrodeposited hydrogels. In summary, mediated electrochemistry can engage orthogonal oxidation chemistries to create functionalized matrices and thus mediated electrochemistry should add important capabilities to the electrofabrication toolbox.
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