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Imaging an unsupported metal-metal bond in dirhenium molecules at the atomic scale.

作者信息

Cao Kecheng, Skowron Stephen T, Biskupek Johannes, Stoppiello Craig T, Leist Christopher, Besley Elena, Khlobystov Andrei N, Kaiser Ute

机构信息

Central Facility for Materials Science Electron Microscopy, Ulm University, Albert-Einstein-Allee 11, Ulm 89081, Germany.

School of Chemistry, University of Nottingham, University Park, Nottingham NG7 2RD, UK.

出版信息

Sci Adv. 2020 Jan 17;6(3):eaay5849. doi: 10.1126/sciadv.aay5849. eCollection 2020 Jan.

DOI:10.1126/sciadv.aay5849
PMID:32010771
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6968940/
Abstract

Metallic bonds remain one of the most important and least understood of the chemical bonds. In this study, we generated Re molecules in which the Re-Re core is unsupported by ligands. Real-time imaging of the atomic-scale dynamics of Re adsorbed on a graphitic lattice allows direct measurement of Re-Re bond lengths for individual molecules that changes in discrete steps correlating with bond order from one to four. Direct imaging of the Re-Re bond breaking process reveals a new bonding state with the bond order less than one and a high-amplitude vibrational stretch, preceding the bond dissociation. The methodology, based on aberration-corrected transmission electron microscopy imaging, is shown to be a powerful analytical tool for the investigation of dynamics of metallic bonding at the atomic level.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4194/6968940/9045062c8c6d/aay5849-F4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4194/6968940/2bc0c0e479e2/aay5849-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4194/6968940/12ab25c0ef00/aay5849-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4194/6968940/2efc6f47d93f/aay5849-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4194/6968940/9045062c8c6d/aay5849-F4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4194/6968940/2bc0c0e479e2/aay5849-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4194/6968940/12ab25c0ef00/aay5849-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4194/6968940/2efc6f47d93f/aay5849-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4194/6968940/9045062c8c6d/aay5849-F4.jpg

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本文引用的文献

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Direct Correlation of Carbon Nanotube Nucleation and Growth with the Atomic Structure of Rhenium Nanocatalysts Stimulated and Imaged by the Electron Beam.电子束刺激和成像的铼纳米催化剂原子结构与碳纳米管成核和生长的直接相关性。
Nano Lett. 2018 Oct 10;18(10):6334-6339. doi: 10.1021/acs.nanolett.8b02657. Epub 2018 Sep 13.
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Comparison of atomic scale dynamics for the middle and late transition metal nanocatalysts.中过渡金属和后过渡金属纳米催化剂原子尺度动力学的比较。
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Electron-Beam Manipulation of Silicon Dopants in Graphene.
电子束诱导形成开孔金属氮杂富勒烯的时间分辨成像与分析
Nat Chem. 2023 Oct;15(10):1444-1451. doi: 10.1038/s41557-023-01261-7. Epub 2023 Jun 29.
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Dynamic hetero-metallic bondings visualized by sequential atom imaging.通过连续原子成像可视化动态异金属键合
Nat Commun. 2022 May 27;13(1):2968. doi: 10.1038/s41467-022-30533-y.
电子束对石墨烯中硅掺杂剂的操控。
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Building one molecule from a reservoir of two atoms.从两个原子的储库中构建一个分子。
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Chemical Reactions of Molecules Promoted and Simultaneously Imaged by the Electron Beam in Transmission Electron Microscopy.电子束在透射电子显微镜中促进和同时成像的分子化学反应。
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