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有机二维纳米结构的可控合成:反应驱动的协同超分子聚合

Controlled synthesis of organic two-dimensional nanostructures reaction-driven, cooperative supramolecular polymerization.

作者信息

Dhiman Shikha, Ghosh Rita, Sarkar Souvik, George Subi J

机构信息

Supramolecular Chemistry Laboratory, New Chemistry Unit, School of Advanced Materials (SAMat), Jawaharlal Nehru Centre of Advanced Scientific Research (JNCASR) Jakkur Bangalore 560064 India

出版信息

Chem Sci. 2020 Jul 21;11(47):12701-12709. doi: 10.1039/d0sc02670k.

Abstract

The bottom-up approach of supramolecular polymerization is an effective synthetic method for functional organic nanostructures. However, the uncontrolled growth and polydisperse structural outcome often lead to low functional efficiency. Thus, precise control over the structural characteristics of supramolecular polymers is the current scientific hurdle. Research so far has tended to focus on systems with inherent kinetic control by the presence of metastable state monomers either through conformational molecular design or by exploring pathway complexity. The need of the hour is to create generic strategies for dormant states of monomers that can be extended to different molecules and various structural organizations and dimensions. Here we venture to demonstrate chemical reaction-driven cooperative supramolecular polymerization as an alternative strategy for the controlled synthesis of organic two-dimensional nanostructures. In our approach, the dynamic imine bond is exploited to convert a non-assembling dormant monomer to an activated amphiphilic structure in a kinetically controlled manner. The chemical reaction governed retarded nucleation-elongation growth provides control over dispersity and size.

摘要

超分子聚合的自下而上方法是制备功能性有机纳米结构的一种有效合成方法。然而,不受控制的生长和多分散的结构结果常常导致功能效率低下。因此,精确控制超分子聚合物的结构特征是当前的科学难题。迄今为止的研究倾向于聚焦通过构象分子设计或探索途径复杂性,利用亚稳态单体的存在实现固有动力学控制的体系。当务之急是为单体的休眠状态创建通用策略,该策略可扩展到不同分子以及各种结构组织和维度。在此,我们尝试展示化学反应驱动的协同超分子聚合,作为有机二维纳米结构可控合成的替代策略。在我们的方法中,利用动态亚胺键以动力学控制的方式将非组装休眠单体转化为活化的两亲结构。化学反应控制的延迟成核-伸长生长实现了对分散性和尺寸的控制。

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