Synthesis, Mesogenic and Spectroscopic Properties of 2,5-Disubstituted Thiophene Derivatives  

Synthesis, Mesogenic and Spectroscopic Properties of 2,5-Disubstituted Thiophene Derivatives

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作  者:韩杰 王彦美 王晓光 

机构地区:[1]Department of Chemistry, Nankai University, Tianjin 300071, China

出  处:《Chinese Journal of Chemistry》2006年第11期1594-1598,共5页中国化学(英文版)

基  金:Project supported by the National Natural Science Foundation of China (No. 20402009) and the Personnel Unit of Nankai University.

摘  要:Two series of 2,5-disubstituted thiophene derivatives (series 1: 2,5-bis(p-alkoxyphenylethynyl)thiophene and series 2: 2,5-bis[p-(p-alkoxyphenylethynyl)(phenylethynyl)]thiophene) were synthesized and characterized by ^1H NMR, ^13C NMR, HRMS and elemental analysis. The relationship between the structure and the mesogenic and spectroscopic properties has been discussed. The results show that compounds 1a-1f all exhibited an enantiotropic nematic mesophase, which was confirmed by the polarized optical microscopy (POM), differential scanning calorimeter (DSC) and variable temperature powder X-ray diffraction (PXRD). In contrast, the extended conjugated analogues 2a-2b had no liquid crystal properties. As for the spectroscopic properties, incorporating more phenylethynyl units results in red-shifted absorption and emission spectra, greatly enhanced quantum efficiency.Two series of 2,5-disubstituted thiophene derivatives (series 1: 2,5-bis(p-alkoxyphenylethynyl)thiophene and series 2: 2,5-bis[p-(p-alkoxyphenylethynyl)(phenylethynyl)]thiophene) were synthesized and characterized by ^1H NMR, ^13C NMR, HRMS and elemental analysis. The relationship between the structure and the mesogenic and spectroscopic properties has been discussed. The results show that compounds 1a-1f all exhibited an enantiotropic nematic mesophase, which was confirmed by the polarized optical microscopy (POM), differential scanning calorimeter (DSC) and variable temperature powder X-ray diffraction (PXRD). In contrast, the extended conjugated analogues 2a-2b had no liquid crystal properties. As for the spectroscopic properties, incorporating more phenylethynyl units results in red-shifted absorption and emission spectra, greatly enhanced quantum efficiency.

关 键 词:THIOPHENE liquid crystal property spectroscopic property 

分 类 号:O626.4[理学—有机化学]

 

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