{"title":"Synthesis and characterization of some non-symmetric iminic-thiadiazole derivatives and investigation of their mesomorphic behaviors","authors":"Hadeel Q.A. Habeeb, Ivan Hameed R. Tomi","doi":"10.1016/j.molstruc.2025.142066","DOIUrl":null,"url":null,"abstract":"<div><div>A series of new 1,3,4-thiadiazole mesogens have been synthesized, incorporating imine as an interconnection and alkoxy chain within their chemical structures. The synthesized precursors and compounds of series of N-(4-alkoxybenzylidene)-4-(5-(p-tolyl)-1,3,4-thiadiazol-2-yl)aniline (L6-n) derivatives were characterized using various analytical techniques to confirm their structure and purity. These techniques included: (FT-IR), both ¹H NMR and ¹³C NMR and mass spectroscopy, they provided comprehensive data, allowing the verification of the chemical structure and purity of the synthesized L6-n compounds. Differential Scanning Calorimetry (DSC) and Polarized Optical Microscopy (POM) have been employed as key techniques to examine the liquid crystalline behaviors of the synthesized compounds. All compounds in series (L6-n) display enantiotropic liquid crystalline properties. The first three mesogens in this series show only the nematic phase (N) while other homologs display both nematic and smectic C (SmC) phases in different thermal ranges. The mesomorphic properties were found to be dependent on the length of alkoxy chains attached at the end of the molecules. In this study, the mesomorphic properties of the synthesized compounds were compared with those of other compounds possessing similar chemical structures. The objective was to investigate the correlation between the chemical structure and the type of mesomorphic properties displayed by these compounds.</div></div>","PeriodicalId":16414,"journal":{"name":"Journal of Molecular Structure","volume":"1336 ","pages":"Article 142066"},"PeriodicalIF":4.0000,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Structure","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022286025007513","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
A series of new 1,3,4-thiadiazole mesogens have been synthesized, incorporating imine as an interconnection and alkoxy chain within their chemical structures. The synthesized precursors and compounds of series of N-(4-alkoxybenzylidene)-4-(5-(p-tolyl)-1,3,4-thiadiazol-2-yl)aniline (L6-n) derivatives were characterized using various analytical techniques to confirm their structure and purity. These techniques included: (FT-IR), both ¹H NMR and ¹³C NMR and mass spectroscopy, they provided comprehensive data, allowing the verification of the chemical structure and purity of the synthesized L6-n compounds. Differential Scanning Calorimetry (DSC) and Polarized Optical Microscopy (POM) have been employed as key techniques to examine the liquid crystalline behaviors of the synthesized compounds. All compounds in series (L6-n) display enantiotropic liquid crystalline properties. The first three mesogens in this series show only the nematic phase (N) while other homologs display both nematic and smectic C (SmC) phases in different thermal ranges. The mesomorphic properties were found to be dependent on the length of alkoxy chains attached at the end of the molecules. In this study, the mesomorphic properties of the synthesized compounds were compared with those of other compounds possessing similar chemical structures. The objective was to investigate the correlation between the chemical structure and the type of mesomorphic properties displayed by these compounds.
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