4.8 Article

Accurate Single-Molecule Kinetic Isotope Effects

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 144, 期 7, 页码 3146-3153

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c12490

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资金

  1. National Key R&D Program of China [2017YFA0204901, 2021YFA1200101]
  2. National Natural Science Foundation of China [21727806, 21933001, 22150013, 22173050, 21933012]
  3. Tencent Foundation through the XPLORER PRIZE
  4. Beijing National Laboratory for Molecular Sciences [BNLM202010]
  5. Frontiers Science Center for New Organic Matter at Nankai University [63181206]
  6. High-Performance Computing Platform of the Center for Life Science at Peking University

向作者/读者索取更多资源

An accurate single-molecule kinetic isotope effect (sm-KIE) has been used to overcome the limitations of conventional ensemble KIE and provide a more accurate and sensitive determination method. This method has demonstrated high detection sensitivity and accuracy in observing the TS structures and multidimensional regulation of Claissen rearrangement.
An accurate single-molecule kinetic isotope effect (sm-KIE) was applied to circumvent the inherent limitation of conventional ensemble KIE by using graphene-molecule-graphene single-molecule junctions. In situ monitoring of the single-molecule reaction trajectories in real time with high temporal resolution has the capability to characterize the deeper information brought by KIE. The C-O bond cleavage and the C-C bond formation of the transition state (TS) were observed in the Claisen rearrangement through the secondary kinetic isotope effect, demonstrating the high detection sensitivity and accuracy of this method. More interestingly, this sm-KIE can be used to determine TS structures under different electric fields, revealing the multidimensional regulation of the TS. The detection and manipulation of the TS provide a broad perspective to understand and optimize chemical reactions and biomimetic progress.

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