I. Rossi, C. Brodbeck, Nguyen-van-Thanh, H. Strapelias , A. Ruoff, H. Burger, R. Eujen
{"title":"Raman bandwidths and molecular motion in liquid HSiCℓ3 and DSiCℓ3","authors":"I. Rossi, C. Brodbeck, Nguyen-van-Thanh, H. Strapelias , A. Ruoff, H. Burger, R. Eujen","doi":"10.1016/0378-4487(81)80058-1","DOIUrl":null,"url":null,"abstract":"<div><p>The three Raman A<sub>l</sub>-bands of trichloromonosilanes HSiCℓ<sub>3</sub>, DSiCℓ<sub>3</sub> are studied in the neat liquid state and in solution (isotopic dilution and inert solvent SiCℓ<sub>4</sub>). The depolarization ratio ϱ is measured from the integrated strengths. The relaxation times τ<sub>v</sub> and τ<sub>2R</sub> are deduced from the corresponding correlation functions G<sub>v</sub>(t) and G<sub>2R</sub>(t).</p><p>Pure dephasing relaxation is predominant for the vibrational modes; the rotational relaxation appears to be of the diffusional type in SiCℓ4 and nearly free for the neat liquids at room temperature.</p></div>","PeriodicalId":100049,"journal":{"name":"Advances in Molecular Relaxation and Interaction Processes","volume":"21 3","pages":"Pages 181-188"},"PeriodicalIF":0.0000,"publicationDate":"1981-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0378-4487(81)80058-1","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Molecular Relaxation and Interaction Processes","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0378448781800581","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The three Raman Al-bands of trichloromonosilanes HSiCℓ3, DSiCℓ3 are studied in the neat liquid state and in solution (isotopic dilution and inert solvent SiCℓ4). The depolarization ratio ϱ is measured from the integrated strengths. The relaxation times τv and τ2R are deduced from the corresponding correlation functions Gv(t) and G2R(t).
Pure dephasing relaxation is predominant for the vibrational modes; the rotational relaxation appears to be of the diffusional type in SiCℓ4 and nearly free for the neat liquids at room temperature.