CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China , Hefei, Anhui 230026, China.
Acc Chem Res. 2014 Jul 15;47(7):2084-95. doi: 10.1021/ar5001007. Epub 2014 Apr 17.
All living organisms and soft matter are intrinsically responsive and adaptive to external stimuli. Inspired by this fact, tremendous effort aiming to emulate subtle responsive features exhibited by nature has spurred the invention of a diverse range of responsive polymeric materials. Conventional stimuli-responsive polymers are constructed via covalent bonds and can undergo reversible or irreversible changes in chemical structures, physicochemical properties, or both in response to a variety of external stimuli. They have been imparted with a variety of emerging applications including drug and gene delivery, optical sensing and imaging, diagnostics and therapies, smart coatings and textiles, and tissue engineering. On the other hand, in comparison with molecular chemistry held by covalent bonds, supramolecular chemistry built on weak and reversible noncovalent interactions has emerged as a powerful and versatile strategy for materials fabrication due to its facile accessibility, extraordinary reversibility and adaptivity, and potent applications in diverse fields. Typically involving more than one type of noncovalent interactions (e.g., hydrogen bonding, metal coordination, hydrophobic association, electrostatic interactions, van der Waals forces, and π-π stacking), host-guest recognition refers to the formation of supramolecular inclusion complexes between two or more entities connected together in a highly controlled and cooperative manner. The inherently reversible and adaptive nature of host-guest molecular recognition chemistry, stemming from multiple noncovalent interactions, has opened up a new platform to construct novel types of stimuli-responsive materials. The introduction of host-guest chemistry not only enriches the realm of responsive materials but also confers them with promising new applications. Most intriguingly, the integration of responsive polymer building blocks with host-guest recognition motifs will endow the former with further broadened responsiveness to external stimuli and accordingly more sophisticated functions. In this Account, we summarize recent progress in the field of responsive polymeric materials containing host-guest recognition motifs with selected examples and highlight their versatile functional applications, whereas small molecule-oriented host-guest supramolecular systems are excluded. We demonstrate how the introduction of host-guest chemistry into conventional polymer systems can modulate their responsive modes to external stimuli. Moreover, the responsive specificity and selectivity of polymeric systems can also be inherited from the host-guest recognition motifs, and these features provide extra advantages in terms of function integration. The following discussions are categorized in terms of design and functions, namely, host-guest chemistry toward the fabrication of responsive polymers and assemblies, optical sensing and imaging, drug and gene delivery, and self-healing materials. A concluding remark on future developments is also presented. We wish this prosperous field would incur more original and evolutionary ideas and benefit fundamental research and our daily life in a more convenient way.
所有生物和软物质本质上都是对外界刺激有响应和适应性的。受此启发,人们努力模仿自然界中微妙的响应特性,从而激发了各种响应型聚合物材料的发明。传统的刺激响应聚合物是通过共价键构建的,它们可以在化学结构、物理化学性质或两者方面发生可逆或不可逆的变化,以响应各种外部刺激。这些聚合物已经被赋予了各种新兴的应用,包括药物和基因传递、光学传感和成像、诊断和治疗、智能涂层和纺织品以及组织工程。另一方面,与由共价键控制的分子化学相比,基于弱且可逆的非共价相互作用的超分子化学因其易于获得、非凡的可逆性和适应性以及在多个领域的强大应用而成为一种制造材料的强大而通用的策略。超分子主体识别通常涉及两种或多种类型的非共价相互作用(例如氢键、金属配位、疏水缔合、静电相互作用、范德华力和π-π堆积),它是指两个或多个实体以高度受控和协同的方式连接在一起形成超分子包合物的过程。主体-客体分子识别化学的固有可逆性和适应性源于多种非共价相互作用,为构建新型刺激响应材料开辟了新的平台。主体-客体化学的引入不仅丰富了响应材料的领域,而且为其赋予了有前途的新应用。最有趣的是,将响应性聚合物构建块与主体-客体识别基序集成在一起,将使前者对外部刺激具有更广泛的响应性,并相应地具有更复杂的功能。在本综述中,我们总结了含有主体-客体识别基序的响应性聚合物材料的最新进展,并通过实例强调了它们在多功能应用方面的应用,而小分子导向的主体-客体超分子体系则被排除在外。我们展示了如何将主体-客体化学引入传统聚合物体系可以调节其对外界刺激的响应模式。此外,聚合物体系的响应特异性和选择性也可以从主体-客体识别基序继承,这些特性在功能集成方面提供了额外的优势。以下讨论按设计和功能分类,即主体-客体化学在响应聚合物和组装体的制备、光学传感和成像、药物和基因传递以及自修复材料方面的应用。最后还对未来的发展进行了总结。我们希望这个繁荣的领域能够产生更多原创和进化的思想,并以更方便的方式造福于基础研究和我们的日常生活。