{"title":"某些热致液晶聚酯酰胺的合成、表征及光交联性研究","authors":"Kavitha Erra Kalappa, S. Antony, N. Ramalakshmi","doi":"10.30799/JACS.187.18040202","DOIUrl":null,"url":null,"abstract":"Article history: Received 15 June 2018 Accepted 27 June 2018 Available online 22 July 2018 Five thermotropic liquid crystalline poly(ester-amides) were synthesized by polycondensation method using varying dicarboxylic acids with a common diamine namely 4,4'-diaminodiphenyl and a common diol namely 2,6-bis(4-hydroxy-3-methoxybenzylidene)cyclohexanone (CHBV). The solubility data and viscosity measurements of these synthesized poly(ester-amides) were used for qualitative characterization. The spectroscopic techniques such as FT-IR, 1H NMR, 13C NMR were performed for investigating micro structural features. By differential scanning calorimetry (DSC), the thermal phase transition behavior of these poly(ester-amides) was studied. Scanning electron microscopy (SEM) technique was used to investigate the morphology of these poly(ester-amides). By using UV-visible spectroscopic technique, the photocrosslinkability of these poly(ester-amides) were studied by irradiating these poly(ester-amides) under a 160 W medium pressure mercury lamp. SEM analysis of these UV irradiated poly(ester-amides) showed the changes in morphology. Thus, the poly(esteramides) containing arylidene keto moiety in the main chain exhibited nematic mesophase and were photocrosslinked upon UV irradiation. X-ray diffraction (XRD) patterns of these poly(ester-amides) were taken to assess the degree of crystallinity.","PeriodicalId":14902,"journal":{"name":"Journal of Advanced Chemical Sciences","volume":"27 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Synthesis, Characterization and Photocrosslinkable Studies of Certain Thermotropic Liquid Crystalline Poly(ester-amides)\",\"authors\":\"Kavitha Erra Kalappa, S. Antony, N. Ramalakshmi\",\"doi\":\"10.30799/JACS.187.18040202\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Article history: Received 15 June 2018 Accepted 27 June 2018 Available online 22 July 2018 Five thermotropic liquid crystalline poly(ester-amides) were synthesized by polycondensation method using varying dicarboxylic acids with a common diamine namely 4,4'-diaminodiphenyl and a common diol namely 2,6-bis(4-hydroxy-3-methoxybenzylidene)cyclohexanone (CHBV). The solubility data and viscosity measurements of these synthesized poly(ester-amides) were used for qualitative characterization. The spectroscopic techniques such as FT-IR, 1H NMR, 13C NMR were performed for investigating micro structural features. By differential scanning calorimetry (DSC), the thermal phase transition behavior of these poly(ester-amides) was studied. Scanning electron microscopy (SEM) technique was used to investigate the morphology of these poly(ester-amides). By using UV-visible spectroscopic technique, the photocrosslinkability of these poly(ester-amides) were studied by irradiating these poly(ester-amides) under a 160 W medium pressure mercury lamp. SEM analysis of these UV irradiated poly(ester-amides) showed the changes in morphology. Thus, the poly(esteramides) containing arylidene keto moiety in the main chain exhibited nematic mesophase and were photocrosslinked upon UV irradiation. X-ray diffraction (XRD) patterns of these poly(ester-amides) were taken to assess the degree of crystallinity.\",\"PeriodicalId\":14902,\"journal\":{\"name\":\"Journal of Advanced Chemical Sciences\",\"volume\":\"27 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-07-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Advanced Chemical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.30799/JACS.187.18040202\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Advanced Chemical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30799/JACS.187.18040202","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis, Characterization and Photocrosslinkable Studies of Certain Thermotropic Liquid Crystalline Poly(ester-amides)
Article history: Received 15 June 2018 Accepted 27 June 2018 Available online 22 July 2018 Five thermotropic liquid crystalline poly(ester-amides) were synthesized by polycondensation method using varying dicarboxylic acids with a common diamine namely 4,4'-diaminodiphenyl and a common diol namely 2,6-bis(4-hydroxy-3-methoxybenzylidene)cyclohexanone (CHBV). The solubility data and viscosity measurements of these synthesized poly(ester-amides) were used for qualitative characterization. The spectroscopic techniques such as FT-IR, 1H NMR, 13C NMR were performed for investigating micro structural features. By differential scanning calorimetry (DSC), the thermal phase transition behavior of these poly(ester-amides) was studied. Scanning electron microscopy (SEM) technique was used to investigate the morphology of these poly(ester-amides). By using UV-visible spectroscopic technique, the photocrosslinkability of these poly(ester-amides) were studied by irradiating these poly(ester-amides) under a 160 W medium pressure mercury lamp. SEM analysis of these UV irradiated poly(ester-amides) showed the changes in morphology. Thus, the poly(esteramides) containing arylidene keto moiety in the main chain exhibited nematic mesophase and were photocrosslinked upon UV irradiation. X-ray diffraction (XRD) patterns of these poly(ester-amides) were taken to assess the degree of crystallinity.