[1]陶永新,杨学波.噻二唑类化合物的制备及其荧光性能[J].常州大学学报(自然科学版),2017,(06):1-7.[doi:10.3969/j.issn.2095-0411.2017.06.001]
 TAO Yongxin,YANG Xuebo.Synthesis and Fluorescent Properties of Thiadiazole-Based Compounds[J].Journal of Changzhou University(Natural Science Edition),2017,(06):1-7.[doi:10.3969/j.issn.2095-0411.2017.06.001]
点击复制

噻二唑类化合物的制备及其荧光性能()
分享到:

常州大学学报(自然科学版)[ISSN:2095-0411/CN:32-1822/N]

卷:
期数:
2017年06期
页码:
1-7
栏目:
化学化工
出版日期:
2017-12-10

文章信息/Info

Title:
Synthesis and Fluorescent Properties of Thiadiazole-Based Compounds
作者:
陶永新杨学波
常州大学 石油化工学院,江苏 常州 213164
Author(s):
TAO Yongxin YANG Xuebo
School of Petrochemical Engineering, Changzhou University, Changzhou 213164, China
关键词:
噻二唑 荧光 蓝光
Keywords:
thiadiazole fluorescence blue light
分类号:
O 626.2
DOI:
10.3969/j.issn.2095-0411.2017.06.001
文献标志码:
A
摘要:
设计并合成了化合物2-(4-甲氧基)苯基-5-苯基-1,3,4-噻二唑(MPPT),2-(4-羟基)苯基-5-苯基-1,3,4-噻二唑(HPPT)和含有共轭双键的2-(4-甲氧基)苯基-5-苯乙烯基-1,3,4-噻二唑(MPST)和2-(4-羟基)苯基-5-苯乙烯基-1,3,4-噻二唑(HPST)。荧光激发光谱显示,MPPT和HPPT激发峰重合,均呈现双峰,激发波长分别为240~280 nm和 355~380 nm; MPST和HPST激发峰也重合,亦呈现双峰,但第二激发峰相比MPPT和HPPT红移了28 nm,在390~410 nm范围内。荧光发射光谱显示,MPPT和HPPT都是单峰,发射范围都在360~500 nm; 而MPST和HPST也是单峰,但比MPPT和HPPT红移了26 nm,发射波长范围都在390~550 nm。结果表明分子结构中引入共轭双键的MPST和HPST比MPPT和HPPT更适合作为蓝光材料。研究显示可以利用分子共轭性来调整噻二唑类化合物的荧光发射区域,设计合成高纯的蓝光材料。
Abstract:
Compounds 2-(4-methoxyl)phenyl-5-phenyl-1,3,4-thiadiazole(MPPT), 2-(4-hydroxy)phenyl-5-phenyl-1,3,4-thiadiazole(HPPT)and 2-(4-methoxyl)phenyl-5-styryl-1,3,4-thiadiazole(MPST), 2-(4-hydroxyl)phenyl-5-styryl-1,3,4- thiadiazole(HPST)containing conjugated double bonds have been synthesized. Fluorescence excitation spectra show that the excitation peaks of MPPT and HPPT are congruent double peaks, which are from 240 nm to 280 nm and from 355 nm to 380 nm, MPST and HPST excitation peaks are also congruent double peaks. But the second one is red shift of 28 nm between 390 nm and 410 nm. Moreover, fluorescence emission spectra display that the MPPT and HPPT emission peaks are unimodal from 360 nm to 500 nm. Both MPST and HPST emission peaks are also unimodal, but it is red shift of 26 nm between 390 nm and 550 nm. The result of research shows that MPST and HPST containing conjugated double bonds are more suitable for material emitting blue light than MPPT and HPPT. The molecular conjugacy could be used to readjust fluorescence emission region of thiadiazole-based compounds for material emitting pure blue light.

参考文献/References:

[1]邢程远,黄华,杨鹏辉,等. 含吡啶环的N-(1,3,4-噻二唑-2-基)苯甲酰胺类化合物的合成及其抑菌活性[J].化学通报,2017,80(9):868-872.
[2]宋春雪,刘汉壮,朱凯歌,等. 1,3,4-噻二唑衍生物的合成及抗腐蚀性能研究[J]. 润滑油,2016,31(5):47-50.
[3]商永嘉,陆友梅,何勇,等. 新型噻二唑类液晶的合成与研究[J].有机化学,2000,20(3):372-376.
[4]SATO M,TAKEUCHI S,HINO R. Preparation and properties of new wholly aromatic polyesters containing a terphenyl analogue of 1,3,4-thiadiazole in the main chain[J]. Macromolecular Rapid Communications,1999,20:373-377.
[5]SATO M,TADA Y,NAKASHIMA S,et al. Synthesis and optical and electrochemical properties of thermotropic, liquid-crystalline, semirigid copolyesters based on 2,5-diphenyl-1,3,4-thiadiazole units[J]. Journal of Polymer Science Part A: Polymer Chemistry,2005,43:1511-1525.
[6]NAKASHIMA S,SATO M,YAMAGUCHI I. Synthesis and properties of liquid crystalline triblock copolymers by ATRP, having electron-transporting thiadiazole unit[J]. Polymer International,2008,57:39-49.
[7]SATO M,MIZOI M,UEMOTO Y. Synthesis and properties of liquid-crystalline semi-rigid polyesters based on isophthalates of nitro or methoxyazobenzene and dioxydiundecanols of biphenyl or 2,5-diphenyl-1,3,4-thiadiazole[J]. Macromolecular Chemistry and Physics,2001,202:3634-3641.
[8]SATO M,YAMAUCHI K,HANDA M,et al. Synthesis and optical properties of new conjugated polymers composed of 1,3,4-thiadiazole and 2,5-dialk-oxybenzene rings[J]. Macromolecular Rapid Communications,2000, 21:1234-1237.
[9]TAKUMA Y,IMASE T,SASAKI S,et al. Synthesis,solid structure,and optical properties of new thiophene-based alternating π-conjugated copolymers containing 4-alkyl-1,2,4-triazole or 1,3,4-thiadiazole unit as the partner unit[J]. Macromolecules,2005,38:1500-1503.
[10]BROCKS G,TOL A. Electronic structure of heterocyclic ring chain polymers[J]. Synthetic Metals,1999,11:516-517.
[11]JANSSON E,JHA P C,?GREN H. Density functional study of triazole and thiadiazole systems as electron transporting materials[J].Chemical Physics,2006,330: 166-171.
[12]种国双,路建美,陶永新.末端含1,3,4-噻二唑聚苯乙烯的ATRP合成及其荧光性能研究[J].江苏工业学院学报,2007,19(4):1-4.
[13]陶永新,杨学波,路建美. 侧链含2,5-二苯基-1,3,4-噻二唑的聚苯乙烯制备及其性能. [J].江苏工业学院学报, 2009, 21(4):16-19.
[14]TAO Y X,XU Q F,LU J M,et al. The synthesis, electrochemical and fluorescent properties of monomers and polymers containing 2,5-diphenyl- 1,3,4-thiadiazole[J].Dyes and Pigments,2010,84: 153-158.
[15]SILVERSTEIN R M. 有机化合物的波谱分析[M].药明康德新药开发有限公司分析部,译.上海:华东理工大学出版社,2007:198.

相似文献/References:

[1]赖梨芳,陈林提,程美令,等.基于3,4-吡唑二甲酸的锌配合物的合成、晶体结构和荧光性质[J].常州大学学报(自然科学版),2017,(05):16.[doi:10.3969/j.issn.2095-0411.2017.05.003]
 LAI Lifang,CHEN Linti,CHENG Meiling,et al.Synthesis, Crystal Structure and Luminescent Property of Zinc Complex Based on 3,4-Pyrazoledicarboxylic Acid Ligand[J].Journal of Changzhou University(Natural Science Edition),2017,(06):16.[doi:10.3969/j.issn.2095-0411.2017.05.003]
[2]盛 扬,李 帅,段宗权,等.Ag-In-Zn-S四元量子点的制备及其表面修饰[J].常州大学学报(自然科学版),2019,31(06):39.
 SHENG Yang,LI Shuai,DUAN Zongquan,et al.Synthesis and Surface Modification of Ag-In-Zn-S Quaternary Quantum Dots[J].Journal of Changzhou University(Natural Science Edition),2019,31(06):39.
[3]马 骁,李继鹏,薛 阳,等.高量子产率吡啶嗡盐可逆机械变色荧光性质[J].常州大学学报(自然科学版),2020,32(04):19.[doi:10.3969/j.issn.2095-0411.2020.04.003]
 MA Xiao,LI Jipeng,XUE Yang,et al.Study of Reversible Mechanochromic Fluorescence Property of Pyridinium Salt with High Quantum Yield[J].Journal of Changzhou University(Natural Science Edition),2020,32(06):19.[doi:10.3969/j.issn.2095-0411.2020.04.003]
[4]张艳秋,孙旻睿,杜尔登,等.Eu3+修饰配位聚合物的构筑及对水中Pb2+的荧光检测[J].常州大学学报(自然科学版),2022,34(05):39.[doi:10.3969/j.issn.2095-0411.2022.05.006]
 ZHANG Yanqiu,SUN Minrui,DU Erdeng,et al.Fluorescent Detection of Pb2+ in Water Environment by a Eu3+ Functionalized Coordination Polymer[J].Journal of Changzhou University(Natural Science Edition),2022,34(06):39.[doi:10.3969/j.issn.2095-0411.2022.05.006]

备注/Memo

备注/Memo:
收稿日期:2017-07-10。
基金项目:国家自然科学基金资助项目(21775013)。
作者简介:陶永新(1971—),男,安徽安庆人,博士,副教授,主要从事功能材料制备及应用研究。
更新日期/Last Update: 1900-01-01