儿茶酚
共聚物
胶粘剂
生物粘附
聚合物
化学
异氰酸酯
高分子化学
苯酚
溶解
材料科学
有机化学
聚氨酯
图层(电子)
作者
Kan Zhan,Chaehoon Kim,Kyungmo Sung,Hirotaka Ejima,Naoko Yoshie
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2017-08-30
卷期号:18 (9): 2959-2966
被引量:212
标识
DOI:10.1021/acs.biomac.7b00921
摘要
Man-made glues often fail to stick in wet environments because of hydration-induced softening and dissolution. The wound healing process of a tunicate inspired the synthesis of gallol-functionalized copolymers as underwater adhesive. Copolymers bearing three types of phenolic groups, namely, phenol, catechol, and gallol, were synthesized via the methoxymethyl protection/deprotection route. Surprisingly, the newly synthesized copolymers bearing gallol groups exhibited stronger adhesive performances (typically 7× stronger in water) than the widely used catechol-functionalized copolymers under all tested conditions (in air, water, seawater, or phosphate-buffered saline solution). The higher binding strength was ascribed to the tridentate-related interfacial interaction and chemical cross-linking. Moreover, gallol-functionalized copolymers adhered to all tested surfaces including plastic, glass, metal, and biological material. In seawater, the performance of gallol-functionalized copolymer even exceeds the commercially available isocyanate-based glue. The insights from this study are expected to help in the design of biomimetic materials containing gallol groups that may be utilized as potential bioadhesives and for other applications. The results from such a kind of comparable study among phenol, catechol, and gallol suggests that tridentate structure should be better than bidentate structure for bonding to the surface.
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