Dielectric relaxation of nitroalkanes in dilute solutions

B. Singh, J.K. Vij
{"title":"Dielectric relaxation of nitroalkanes in dilute solutions","authors":"B. Singh,&nbsp;J.K. Vij","doi":"10.1016/0378-4487(82)80004-6","DOIUrl":null,"url":null,"abstract":"<div><p>The relative permittivity at frequencies of 10kHz and 10GHz and the refractive indices have been measured for dilute solutions of (a) nitroethane, (b) 1-nitropropane, (c) 2-nitropropane, and (d) 1-nitrobutane in cyclohexane at 10°, 20°, 30° and 40°C. Materials (b) and (c) together with (e)2-nitro 1-propanol and (f) 2-nitro-l-butanol, have also been studied in different nonpolar solvents. The electric dipole moments, the dielectric relaxation times, and the molar activation energy parameters have been calculated. The results for nitroalcohols show the existence of internal hydrogen bonding between the hydroxyl group and an oxygen atom of the nitro group. The plots of log τ versus log η for materials (b) and (c) are linear for the solvents n-heptane, cyclohexane and decalin. The possibility of interaction of these materials with p-xylene, carbon tetrachloride and p-dioxane are discussed. Activation enthalpy (ΔH<sub>ε</sub>) of these materials is observed to be higher in dilute solutions than in pure liquids, and also ΔH<sub>ε</sub> for nitrobutane is significantly lower than for the other materials.</p></div>","PeriodicalId":100049,"journal":{"name":"Advances in Molecular Relaxation and Interaction Processes","volume":"22 3","pages":"Pages 177-186"},"PeriodicalIF":0.0000,"publicationDate":"1982-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0378-4487(82)80004-6","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Molecular Relaxation and Interaction Processes","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0378448782800046","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4

Abstract

The relative permittivity at frequencies of 10kHz and 10GHz and the refractive indices have been measured for dilute solutions of (a) nitroethane, (b) 1-nitropropane, (c) 2-nitropropane, and (d) 1-nitrobutane in cyclohexane at 10°, 20°, 30° and 40°C. Materials (b) and (c) together with (e)2-nitro 1-propanol and (f) 2-nitro-l-butanol, have also been studied in different nonpolar solvents. The electric dipole moments, the dielectric relaxation times, and the molar activation energy parameters have been calculated. The results for nitroalcohols show the existence of internal hydrogen bonding between the hydroxyl group and an oxygen atom of the nitro group. The plots of log τ versus log η for materials (b) and (c) are linear for the solvents n-heptane, cyclohexane and decalin. The possibility of interaction of these materials with p-xylene, carbon tetrachloride and p-dioxane are discussed. Activation enthalpy (ΔHε) of these materials is observed to be higher in dilute solutions than in pure liquids, and also ΔHε for nitrobutane is significantly lower than for the other materials.

稀溶液中硝基烷烃的介电弛豫
测量了(a)硝基乙烷、(b) 1-硝基丙烷、(c) 2-硝基丙烷和(d) 1-硝基丁烷在环己烷中的稀溶液在10°、20°、30°和40°c下在10kHz和10GHz频率下的相对介电常数和折射率。材料(b)和(c)以及(e)2-硝基- 1-丙醇和(f) 2-硝基- 1-丁醇也在不同的非极性溶剂中进行了研究。计算了电偶极矩、介电弛豫时间和摩尔活化能参数。结果表明,在硝基醇的羟基和硝基的氧原子之间存在内部氢键。对于溶剂正庚烷、环己烷和十氢化萘,材料(b)和(c)的log τ与log η曲线呈线性关系。讨论了这些材料与对二甲苯、四氯化碳和对二恶烷相互作用的可能性。观察到这些材料的活化焓(ΔHε)在稀溶液中比在纯液体中高,并且硝化丁烷的活化焓(ΔHε)也明显低于其他材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信