E. Barmatov, L. Stroganov, R. Talroze, V. Shibaev, N. Platé
{"title":"1 H NMR Spectroscopic Investigation of the Dynamics of Director Rotation in Comb-Shaped Liquid Crystal Polymers","authors":"E. Barmatov, L. Stroganov, R. Talroze, V. Shibaev, N. Platé","doi":"10.1142/9789814354271_0006","DOIUrl":null,"url":null,"abstract":"Wide-line 1 H NMR spectroscopy was used to investigate the kinetics of director rotation in the comb-shaped nematic polymer [CH 2 CH(COOR)] n (R= (CH 2 ) 4 OPhPhCN).The director rotation was found to conform to the following general features: the experimentally observed kinetics of director reorientation was interpreted in terms of the monodomain model; coefficients of rotational viscosity versus temperature plots were satisfactorily described by the Arrhenius equation with abnormally high activation energies; activation energy increased with an increase in polymer chain length; the rotational viscosity coefficient was related to polymer chain length via an exponential dependence; and an increase in temperature was accompanied by a linear increase of the exponent from 0.9 to 2.2","PeriodicalId":20346,"journal":{"name":"Polymer science","volume":"17 1","pages":"183-187"},"PeriodicalIF":0.0000,"publicationDate":"1993-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1142/9789814354271_0006","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
Wide-line 1 H NMR spectroscopy was used to investigate the kinetics of director rotation in the comb-shaped nematic polymer [CH 2 CH(COOR)] n (R= (CH 2 ) 4 OPhPhCN).The director rotation was found to conform to the following general features: the experimentally observed kinetics of director reorientation was interpreted in terms of the monodomain model; coefficients of rotational viscosity versus temperature plots were satisfactorily described by the Arrhenius equation with abnormally high activation energies; activation energy increased with an increase in polymer chain length; the rotational viscosity coefficient was related to polymer chain length via an exponential dependence; and an increase in temperature was accompanied by a linear increase of the exponent from 0.9 to 2.2