高压下二茂铁分子构象不稳定性的拉曼研究:晶体场的影响

IF 2.4 3区 化学 Q2 SPECTROSCOPY Journal of Raman Spectroscopy Pub Date : 2024-06-25 DOI:10.1002/jrs.6713
Konstantin Meletov
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引用次数: 0

摘要

在高达 20 GPa 的压力下测量了二茂铁晶体的拉曼光谱,发现在环境压力下分子间声子的带宽异常大。随着压力的增加,带宽在 ~2 GPa 时增加到最大值,然后在 ~4 GPa 时减小到最小值,这与分子内声子与压力无关的带宽相等。带宽的不寻常行为与二茂铁分子在其 D5d 和 D5h 构象之间的跃迁引起的不稳定性有关。将构象间的跃迁时间缩短至晶格振动周期,会导致分子间声子带失去一致性并变宽。据测定,在环境条件下,构象间的能量势垒约为 17.6 meV/分子,而在 4.9 GPa 条件下则为 80 meV/分子。能垒随压力的增加而增大,这是由于晶体场的增强抑制了跃迁,并使分子稳定在 D5d 构象上。
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Raman study of the conformational instability of a ferrocene molecule at high pressure: Influence of a crystal field

The Raman spectra of ferrocene crystals were measured at pressures up to 20 GPa, and an abnormally large bandwidth of intermolecular phonons at ambient pressure was found. With an increase in the pressure, the bandwidth increased to a maximum at ~2 GPa and then decreased to a minimum at ~4 GPa, which was equal to the pressure-independent bandwidth of intramolecular phonons. The unusual behavior of the bandwidth was related to the instability of a ferrocene molecule caused by jumps between its D5d and D5h conformations. A decrease in the time of jumps between the conformations to the period of crystal lattice vibrations led to a loss of coherence and broadening of intermolecular phonon bands. The energy barrier between the conformations was determined to be ~17.6 meV/molecule under ambient conditions and 80 meV/molecule at 4.9 GPa. An increase in the barrier with pressure was due to the enhancement of the crystal field, which resulted in the inhibition of the jumps and the stabilization of the molecule in the D5d conformation.

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来源期刊
CiteScore
5.40
自引率
8.00%
发文量
185
审稿时长
3.0 months
期刊介绍: The Journal of Raman Spectroscopy is an international journal dedicated to the publication of original research at the cutting edge of all areas of science and technology related to Raman spectroscopy. The journal seeks to be the central forum for documenting the evolution of the broadly-defined field of Raman spectroscopy that includes an increasing number of rapidly developing techniques and an ever-widening array of interdisciplinary applications. Such topics include time-resolved, coherent and non-linear Raman spectroscopies, nanostructure-based surface-enhanced and tip-enhanced Raman spectroscopies of molecules, resonance Raman to investigate the structure-function relationships and dynamics of biological molecules, linear and nonlinear Raman imaging and microscopy, biomedical applications of Raman, theoretical formalism and advances in quantum computational methodology of all forms of Raman scattering, Raman spectroscopy in archaeology and art, advances in remote Raman sensing and industrial applications, and Raman optical activity of all classes of chiral molecules.
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