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通过分子晶体剥离制备的独立手性二维单层膜。

Free-standing homochiral 2D monolayers by exfoliation of molecular crystals.

作者信息

Dong Jinqiao, Liu Lingmei, Tan Chunxia, Xu Qisong, Zhang Jiachen, Qiao Zhiwei, Chu Dandan, Liu Yan, Zhang Qun, Jiang Jianwen, Han Yu, Davis Anthony P, Cui Yong

机构信息

School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules and State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai, P. R. China.

School of Chemistry, University of Bristol, Bristol, UK.

出版信息

Nature. 2022 Feb;602(7898):606-611. doi: 10.1038/s41586-022-04407-8. Epub 2022 Feb 23.

Abstract

Two-dimensional materials with monolayer thickness and extreme aspect ratios are sought for their high surface areas and unusual physicochemical properties. Liquid exfoliation is a straightforward and scalable means of accessing such materials, but has been restricted to sheets maintained by strong covalent, coordination or ionic interactions. The exfoliation of molecular crystals, in which repeat units are held together by weak non-covalent bonding, could generate a greatly expanded range of two-dimensional crystalline materials with diverse surfaces and structural features. However, at first sight, these weak forces would seem incapable of supporting such intrinsically fragile morphologies. Against this expectation, we show here that crystals composed of discrete supramolecular coordination complexes can be exfoliated by sonication to give free-standing monolayers approximately 2.3 nanometres thick with aspect ratios up to approximately 2,500:1, sustained purely by apolar intermolecular interactions. These nanosheets are characterized by atomic force microscopy and high-resolution transmission electron microscopy, confirming their crystallinity. The monolayers possess complex chiral surfaces derived partly from individual supramolecular coordination complex components but also from interactions with neighbours. In this respect, they represent a distinct type of material in which molecular components are all equally exposed to their environment, as if in solution, yet with properties arising from cooperation between molecules, because of crystallinity. This unusual nature is reflected in the molecular recognition properties of the materials, which bind carbohydrates with strongly enhanced enantiodiscrimination relative to individual molecules or bulk three-dimensional crystals.

摘要

具有单层厚度和极高纵横比的二维材料因其高表面积和独特的物理化学性质而备受关注。液体剥离是获取此类材料的一种直接且可扩展的方法,但一直局限于由强共价、配位或离子相互作用维持的薄片。分子晶体中重复单元通过弱非共价键结合在一起,其剥离可以产生范围更广的具有不同表面和结构特征的二维晶体材料。然而,乍一看,这些弱作用力似乎无法支撑这种本质上脆弱的形态。与这种预期相反,我们在此表明,由离散的超分子配位络合物组成的晶体可以通过超声处理剥离,得到厚度约为2.3纳米、纵横比高达约2500:1的独立单层,完全由非极性分子间相互作用维持。这些纳米片通过原子力显微镜和高分辨率透射电子显微镜进行表征,证实了它们的结晶性。这些单层具有复杂的手性表面,部分源自单个超分子配位络合物组分,也源自与相邻分子的相互作用。在这方面,它们代表了一种独特类型 的材料,其中分子组分都同样暴露于其环境中,就好像在溶液中一样,但由于结晶性,其性质源于分子间的协同作用。这种不寻常的性质反映在材料的分子识别特性中,与单个分子或块状三维晶体相比,它们与碳水化合物结合时对映体识别能力大大增强。

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