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多维光谱指纹图谱的新型相干分析光谱技术家族。

Multidimensional Spectral Fingerprints of a New Family of Coherent Analytical Spectroscopies.

机构信息

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

出版信息

Anal Chem. 2017 Dec 19;89(24):13182-13189. doi: 10.1021/acs.analchem.7b02917. Epub 2017 Nov 30.

DOI:10.1021/acs.analchem.7b02917
PMID:29135230
Abstract

Triply resonant sum frequency (TRSF) and doubly vibrationally enhanced (DOVE) spectroscopies are examples of a recently developed family of coherent multidimensional spectroscopies (CMDS) that are analogous to multidimensional NMR and current analytical spectroscopies. CMDS methods are particularly promising for analytical applications because their inherent selectivity makes them applicable to complex samples. Like NMR, they are based on creating quantum mechanical superposition states that are fully coherent and lack intermediate quantum state populations that cause quenching or other relaxation effects. Instead of the nuclear spin states of NMR, their multidimensional spectral fingerprints result from creating quantum mechanical mixtures of vibrational and electronic states. Vibrational states provide spectral selectivity, and electronic states provide large signal enhancements. This paper presents the first electronically resonant DOVE spectra and demonstrates the capabilities for analytical chemistry applications by comparing electronically resonant TRSF and DOVE spectra with each other and with infrared absorption and resonance Raman spectra using a Styryl 9 M dye as a model system. The methods each use two infrared absorption transitions and a resonant Raman transition to create a coherent output beam, but they differ in how they access the vibrational and electronic states and the frequency of their output signal. Just as FTIR, UV-vis, Raman, and resonance Raman are complementary methods, TRSF and DOVE methods are complementary to coherent Raman methods such as coherent anti-Stokes Raman spectroscopy (CARS).

摘要

三重共振和双重振动增强和光谱学是最近发展起来的一类相干多维光谱学(CMDS)的例子,类似于多维 NMR 和当前的分析光谱学。CMDS 方法在分析应用中特别有前途,因为它们固有的选择性使它们适用于复杂的样品。与 NMR 一样,它们基于创建完全相干的量子力学叠加态,而没有导致猝灭或其他弛豫效应的中间量子态。它们的多维光谱指纹不是来自 NMR 的核自旋态,而是来自于创建振动和电子态的量子力学混合物。振动态提供光谱选择性,电子态提供大的信号增强。本文介绍了第一个电子共振 DOVE 光谱,并通过比较电子共振 TRSF 和 DOVE 光谱与红外吸收和共振拉曼光谱,展示了用于分析化学应用的能力,使用 Styryl 9 M 染料作为模型系统。这些方法都使用两个红外吸收跃迁和一个共振拉曼跃迁来创建相干输出光束,但它们在访问振动和电子态的方式以及输出信号的频率上有所不同。就像傅里叶变换红外(FTIR)、紫外可见(UV-vis)、拉曼和共振拉曼一样,TRSF 和 DOVE 方法是互补的方法,与相干拉曼方法(如相干反斯托克斯拉曼光谱学(CARS))互补。

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