低温低剂量电子显微镜下氢键有机框架的分子水平成像

IF 7.6 Q1 ENGINEERING, CHEMICAL
Yikuan Liu , Yanbin Chen , Liwei Xia , Shuo Zhang, Zhangnan Zhong, Liwei Wang, Yujie Huang, Xinru Jiang, Mengru Bu, Qunfeng Zhang, Xiaonian Li, Yihan Zhu
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引用次数: 0

摘要

与氢键有机框架(HOFs)结构不均质性相关的基本问题,如控制其功能和生长机制的表面末端和主客体异质结构,仍然是一个关键的知识缺口。这源于缺乏先进的具有分子精度的实空间结构表征工具。通过利用最先进的低温低剂量电子显微镜,这项工作克服了传统技术的光束损伤限制,并在分子水平上阐明了hof的晶体结构、表面末端和主客体结构。实空间观测证实了横向晶体生长符合梯田-边缘-扭结(TLK)模型,但偏离了经典的单体加成机制。相反,我们提出了一种非经典的合作多位点单体添加机制,其中在框架和客体位点同时添加单体最终驱动晶体饰面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular-level imaging of hydrogen-bonded organic frameworks by cryogenic low-dose electron microscopy

Molecular-level imaging of hydrogen-bonded organic frameworks by cryogenic low-dose electron microscopy
The fundamental problems associated with structural inhomogeneities of hydrogen-bonded organic frameworks (HOFs), such as surface terminations and host-guest heterostructures that govern their functionalities and growth mechanisms, remain a critical gap in knowledge. This arises from the lack of advanced real-space structural characterization tools with molecular precision. By leveraging state-of-the-art cryogenic low-dose electron microscopy, this work overcomes the beam damage limitations of traditional techniques and elucidates the crystal structures, surface terminations, and host-guest structures of HOFs at molecular-level. Real-space observations confirm lateral crystal growth consistent with the terrace-ledge-kink (TLK) model, but deviate from the classical monomer-addition mechanism. Instead, we propose a nonclassical cooperative multisite monomer-addition mechanism, where simultaneous monomer addition at both framework and guest sites eventually drives crystal faceting.
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来源期刊
Green Chemical Engineering
Green Chemical Engineering Process Chemistry and Technology, Catalysis, Filtration and Separation
CiteScore
11.60
自引率
0.00%
发文量
58
审稿时长
51 days
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