{"title":"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","authors":"Konstantin Meletov","doi":"10.1002/jrs.6713","DOIUrl":null,"url":null,"abstract":"<p>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 D<sub>5d</sub> and D<sub>5h</sub> 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 D<sub>5d</sub> conformation.</p>","PeriodicalId":16926,"journal":{"name":"Journal of Raman Spectroscopy","volume":null,"pages":null},"PeriodicalIF":2.4000,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Raman study of the conformational instability of a ferrocene molecule at high pressure: Influence of a crystal field\",\"authors\":\"Konstantin Meletov\",\"doi\":\"10.1002/jrs.6713\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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 D<sub>5d</sub> and D<sub>5h</sub> 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 D<sub>5d</sub> conformation.</p>\",\"PeriodicalId\":16926,\"journal\":{\"name\":\"Journal of Raman Spectroscopy\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2024-06-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Raman Spectroscopy\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jrs.6713\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"SPECTROSCOPY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Raman Spectroscopy","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jrs.6713","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"SPECTROSCOPY","Score":null,"Total":0}
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.
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.