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三维三重共振和频光谱揭示钴胺素中的电子振动耦合:迈向反应坐标的探针

Three Dimensional Triply Resonant Sum Frequency Spectroscopy Revealing Vibronic Coupling in Cobalamins: Toward a Probe of Reaction Coordinates.

作者信息

Handali Jonathan D, Sunden Kyle F, Thompson Blaise J, Neff-Mallon Nathan A, Kaufman Emily M, Brunold Thomas C, Wright John C

机构信息

Department of Chemistry , University of Wisconsin-Madison , Madison Wisconsin 53706 , United States.

出版信息

J Phys Chem A. 2018 Nov 21;122(46):9031-9042. doi: 10.1021/acs.jpca.8b07678. Epub 2018 Nov 7.

DOI:10.1021/acs.jpca.8b07678
PMID:30365322
Abstract

Triply resonant sum frequency (TRSF) spectroscopy is a fully coherent mixed vibrational-electronic spectroscopic technique that is ideally suited for probing the vibrational-electronic couplings that become important in driving reactions. We have used cyanocobalamin (CNCbl) and deuterated aquacobalamin (DOCbl) as model systems for demonstrating the feasibility of using the selectivity of coherent multidimensional spectroscopy to resolve electronic states within the broad absorption spectra of transition metal complexes and identify the nature of the vibrational and electronic state couplings. We resolve three short and long axis vibrational modes in the vibrationally congested 1400-1750 cm region that are individually coupled to different electronic states in the 18 000-21 000 cm region but have minimal coupling to each other. Double resonance with the individual vibrational fundamentals and their overtones selectively enhances the corresponding electronic resonances and resolves features within the broad absorption spectrum. This work demonstrates the feasibility of identifying coupling between different pairs of vibrational states with different electronic states that together form the reaction coordinate surface of transition metal enzymes.

摘要

三重共振和频(TRSF)光谱是一种完全相干的混合振动 - 电子光谱技术,非常适合用于探测在驱动反应中变得重要的振动 - 电子耦合。我们使用氰钴胺(CNCbl)和氘代水合钴胺(DOCbl)作为模型系统,以证明利用相干多维光谱的选择性来解析过渡金属配合物宽吸收光谱内的电子态并确定振动和电子态耦合性质的可行性。我们在振动拥挤的1400 - 1750 cm区域分辨出三种短轴和长轴振动模式,它们分别与18000 - 21000 cm区域的不同电子态耦合,但相互之间的耦合极小。与各个振动基频及其泛音的双共振选择性地增强了相应的电子共振,并解析了宽吸收光谱内的特征。这项工作证明了识别不同对具有不同电子态的振动态之间耦合的可行性,这些振动态共同构成了过渡金属酶的反应坐标表面。

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