超分子化学
粘附
化学
超分子聚合物
聚苯乙烯
胶粘剂
氢键
聚合物
微尺度化学
纳米技术
纳米尺度
碱基对
非共价相互作用
超分子组装
背景(考古学)
DNA
分子
材料科学
有机化学
古生物学
图层(电子)
数学教育
生物
生物化学
数学
作者
Cyrus A. Anderson,Amanda Jones,Ellen M. Briggs,Eric J. Novitsky,Darrell W. Kuykendall,Nancy R. Sottos,Steven C. Zimmerman
摘要
Adhesion phenomena are essential to many biological processes and to synthetic adhesives and manufactured coatings and composites. Supramolecular interactions are often implicated in various adhesion mechanisms. Recently, supramolecular building blocks, such as synthetic DNA base-pair mimics, have drawn attention in the context of molecular recognition, self-assembly, and supramolecular polymers. These reversible, hydrogen-bonding interactions have been studied extensively for their adhesive capabilities at the nano- and microscale, however, much less is known about their utility for practical adhesion in macroscopic systems. Herein, we report the preparation and evaluation of supramolecular coupling agents based on high-affinity, high-fidelity quadruple hydrogen-bonding units (e.g., DAN·DeUG, Kassoc = 10(8) M(-1) in chloroform). Macroscopic adhesion between polystyrene films and glass surfaces modified with 2,7-diamidonaphthyridine (DAN) and ureido-7-deazaguanine (DeUG) units was evaluated by mechanical testing. Structure-property relationships indicate that the designed supramolecular interaction at the nanoscale plays a key role in the observed macroscopic adhesive response. Experiments probing reversible adhesion or self-healing properties of bulk samples indicate that significant recovery of initial strength can be realized after failure but that the designed noncovalent interaction does not lead to healing during the process of adhesion loss.
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