Thiourea as a “Polar Hydrophobic” Hydrogen-Bonding Motif: Application to Highly Durable All-Underwater Adhesion

化学 氢键 硫脲 极地的 粘附 高分子化学 主题(音乐) 组合化学 纳米技术 立体化学 有机化学 分子 天文 声学 物理 材料科学
作者
Kohei Kikkawa,Yosuke Sumiya,Kazuki Okazawa,Kazunari Yoshizawa,Yoshimitsu Itoh,Takuzo Aida
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:146 (30): 21168-21175 被引量:54
标识
DOI:10.1021/jacs.4c07515
摘要

Here, we report that, in contrast to urea, thiourea functions as a "polar hydrophobic" hydrogen-bonding motif. Although thiourea is more acidic than urea, thiourea exchanges its N-H protons with water at a rate that is 160 times slower than that for urea at 70 °C. This suggests that thiourea is much less hydrated than urea in an aqueous environment. What led us to this interesting principle was the serendipitous finding that self-healable poly(ether thiourea) adhered strongly to wet glass surfaces. This discovery enabled us to develop an exceptionally durable all-underwater adhesive that can maintain large adhesive strength for over a year even in seawater, simply by mechanically mixing three water-insoluble liquid components on target surfaces. Because thiourea is hydrophobic, its hydrogen-bonding networks within the adhesive structure and at the adhesive-target interface are presumed to be dehydrated. For comparison, a reference adhesive using urea as a representative "polar hydrophilic" hydrogen-bonding motif was durable for less than 4 days in water. Highly durable all-underwater adhesives are needed in various fields of marine engineering and biomedical sciences, but their development has been a major challenge because a hydration layer that spontaneously forms in water always inhibits adhesion.
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