Department of Chemistry , The University of Texas at Austin , 105 East 24th Street, Stop A5300 , Austin , Texas 78712 , United States.
School of Chemistry and Chemical Engineering , Jiangsu University , Zhenjiang , Jiangsu 212013 , China.
Acc Chem Res. 2019 Jul 16;52(7):1915-1927. doi: 10.1021/acs.accounts.9b00187. Epub 2019 Jun 11.
Soft materials have received considerable attention from supramolecular chemists and material scientists alike. This interest reflects the advantages provided by their soft, flexible nature and the convenience of the molecular self-assembly that underlies their preparation. Common soft supramolecular materials include polymeric gels, supramolecular polymers, nanoaggregates, and membranes. Polymeric gels are solidlike networks of cross-linked polymer chains. Supramolecular polymers contain repeat units connected through reversible non-covalent bonds. Nanoaggregates are formed as a result of hydrophobic interactions involving amphiphilic building blocks. Because of the presence of non-covalent interactions, supramolecular soft materials typically display stimuli-responsive or adaptive features. Various macrocyclic hosts, such as cyclodextrins, crown ethers, calixarenes, cucurbiturils, and pillararenes, and many classic non-covalent interactions have been harnessed to construct supramolecular soft materials. Only recently has anion binding been used as the underlying recognition motif. Anions are ubiquitous in the natural world. Their importance has inspired efforts to achieve good anion binding and to exploit anion recognition in a number of fields, including extraction, transport, sensing, and catalysis. Most of this effort has involved the use of stand-alone anion receptors. On the other hand, soft materials with anion recognition features could lead to new macromolecular systems of interest in the context of many application areas. In this Account, we summarize the latest efforts from our laboratory to prepare supramolecular soft materials, including polymeric gels, supramolecular polymers, and nanoaggregates, with bona fide anion recognition features. Two anion receptor systems, namely, calix[4]pyrroles (s) and a tetraimidazolium macrocycle known as the "Texas-sized" molecular box (), have been used for this purpose. To date, -based hydrogels have been utilized to capture anions from water and for coded information applications; -based organic polymeric gels have been used to extract dianions from aqueous source phases and for the on-site detection of chloride anions. Polymers containing and anion recognition subunits typically display responsive features and can be modified through application of appropriately chosen external stimuli. For instance, nanoaggregates may be formed as a result of the hydrophobic interactions of - and -based amphiphiles. The resulting aggregates were found to mimic the structural evolution of organelles and could be used as effective anion and ion pair extractants. This Account summarizes progress to date while underscoring potential opportunities associated with combining anion recognition and soft materials chemistry. The hope is to stimulate further advances in broad areas, including polymer science, supramolecular chemistry, biology, materials research, and information storage.
软物质受到超分子化学家与材料科学家的广泛关注。这种兴趣源于软物质灵活多变的特性,以及分子自组装所带来的便利性,这些特性为软物质的制备提供了便利。常见的软超分子材料包括聚合物凝胶、超分子聚合物、纳米聚集体和膜。聚合物凝胶是交联聚合物链形成的固态网络。超分子聚合物由通过可逆非共价键连接的重复单元组成。纳米聚集体是由涉及两亲性构筑块的疏水相互作用形成的。由于非共价相互作用的存在,超分子软物质通常具有刺激响应或自适应的特性。各种大环主体,如环糊精、冠醚、杯芳烃、葫芦脲和柱芳烃,以及许多经典的非共价相互作用,已被用于构建超分子软物质。直到最近,阴离子结合才被用作基础识别模式。阴离子在自然界中无处不在。它们的重要性激发了人们努力实现良好的阴离子结合,并在多个领域(包括提取、传输、传感和催化)中利用阴离子识别。这方面的大部分工作都涉及使用独立的阴离子受体。另一方面,具有阴离子识别功能的软物质可能会导致在许多应用领域中出现新的大分子系统。在本综述中,我们总结了我们实验室最近在制备具有真正阴离子识别功能的超分子软物质方面的努力,包括聚合物凝胶、超分子聚合物和纳米聚集体。为此,我们使用了两种阴离子受体系统,即杯[4]吡咯(s)和一种四咪唑大环,称为“德克萨斯大小”分子盒()。迄今为止,基于的水凝胶已被用于从水中捕获阴离子和用于编码信息应用;基于的有机聚合物凝胶已被用于从水相源中提取二价阴离子,并用于现场检测氯离子。含有阴离子识别单元的聚合物通常具有响应特性,并可以通过施加适当选择的外部刺激来进行修饰。例如,基于和的两亲分子的疏水相互作用可能会形成纳米聚集体。所得的聚集体被发现可以模拟细胞器的结构演变,并可用作有效的阴离子和离子对提取剂。本综述总结了迄今为止的进展,同时强调了将阴离子识别与软物质化学相结合的潜在机会。希望这能激发在包括聚合物科学、超分子化学、生物学、材料研究和信息存储在内的广泛领域的进一步进展。