2-(2-羟基苯基)苯并噻唑的合成及其光学性质
Synthesis and Spectroscopy of 2-(2-Hydroxyphenyl)benzothiazole
DOI: 10.12677/MC.2020.42002, PDF,   
作者: 徐浩斌:武汉工程大学化工与制药学院,湖北 武汉;北京神剑天军医学科学院京东祥鹄微波化学联合实验室,北京;邵开源:北京神剑天军医学科学院京东祥鹄微波化学联合实验室,北京;胡文祥*:武汉工程大学化工与制药学院,湖北 武汉;北京神剑天军医学科学院京东祥鹄微波化学联合实验室,北京;中国人民解放军战略支援部队航天系统部,北京
关键词: 苯并噻唑衍生物电致发光荧光微波或超声波合成Benzothiazole DerivativesElectroluminescence Fluorescence Microwave or Ultrasonic Synthesis
摘要: 2-(2-羟基苯基)苯并噻唑(BTZ)作为一类新型的有机电致发光材料,因其独特的性质而备受关注。它的光学性质已经得到了明确的阐述,由于其烯醇式激发态分子存在内质子转移的过程,从而表现出较大的斯托克斯位移。当BTZ存在于极性较小的溶剂中,有利于其酮式构型的稳定,使得激发态分子内质子转移(ESIPT)荧光强度增强,极性较大的溶剂会导致其正常荧光强度增加。此外,在羟基对位上接有吸电子基团时,苯环上电子云密度降低,同样有利于酮式构型的稳定,致使ESIPT荧光强度增强。BTZ可由多种方式合成,本文介绍了三条合成路线,实验室常利用水杨酸和邻氨基苯硫醇作为BTZ的合成原料,此法可一步得到产物,收率较高。2-(2-羟基苯基)苯并噻唑的衍生物,如锌、铍金属络合物,同样也表现出优良的光谱性质,是一类具有广阔开发前景的有机电致发光材料。
Abstract: The 2-(2-hydroxyphenyl)benzothiazole (BTZ) is a new kind of electroluminescent materials, which has attracted much attention because of its unique properties. Its optical properties have been clearly described, and due to the process of proton transfer in enol excited molecules, the Stokes displacement is relatively large. The presence of BTZ in a less polar solvent was conducive to the stability of its ketone configuration, which enhanced the fluorescence intensity of the excited intramoleculproton transfer (ESIPT), while the normal fluorescence intensity was increased in a more polar solvent. In addition, when the hydroxyl para is attached with electron-withdrawing groups, the electron cloud density on the benzene ring decreases, which is also conducive to the stability of the ketone configuration, resulting in the enhanced fluorescence intensity of ESIPT. Three synthetic routes of BTZ are introduced in this paper. In laboratory, salicylic acid and o-amino- benzmercaptan are often used as raw materials to synthesize BTZ, which can get good yield in one step. Derivatives of 2-(2-hydroxyphenyl)benzothiazole, such as zinc and beryllium metal complexes, also exhibit excellent spectral properties and are a kind of electroluminescent materials with broad development prospects.
文章引用:徐浩斌, 邵开源, 胡文祥. 2-(2-羟基苯基)苯并噻唑的合成及其光学性质[J]. 微波化学, 2020, 4(2): 13-21. https://doi.org/10.12677/MC.2020.42002

参考文献

[1] Belfield, K.D., Morales, A.R., Kang, B.S., et al. (2014) Synthesis, Characterization, Optical Properties of New Two- Photon-Absorbing Fluorene Derivatives. Chemistry of Materials, 16, 4634-4641. [Google Scholar] [CrossRef
[2] Haneda, S., Gan, Z.B., Eda, K., et al. (2007) Ligand Effects of 2-(2-pyridyl)benzazole-Pd Complexes on the X-Ray Crystallographic Structures, 1H NMR Spectra, and Catalytic Activities in Mizoroki-Heck Reactions. Organometallics, 26, 6551-6555. [Google Scholar] [CrossRef
[3] Troutman, R. (1997) Will OLED Displays Challenge Liquid Crystal Display in Notebook Computer Applications. Synthetic Metals, 91, 31-34. [Google Scholar] [CrossRef
[4] Charles, R.G. and Freiser, H. (1953) Synthesis of 2-(o-hydroxyphenyl)benzothiazole and of 2-(o -hydroxyphenyl) benzothiazoline. Journal of Organic Chemistry, 18, 422-425. [Google Scholar] [CrossRef
[5] 王任洁. 2-(2-羟基苯基)苯并噻唑衍生物的合成及性质研究[D]: [硕士论文]. 大连: 大连理工大学, 2008.
[6] 陈明强. 2-(2-羟基苯基)苯并噻唑的合成及荧光性能研究[J]. 中国矿业大学学报, 2002, 31(3): 319-323.
[7] Zhou, J., Shi, R., Liu, J., et al. (2015) An ESIPT-Based Fluorescent Probe for Sensitive Detection of Hydrazine in Aqueous Solution. Organic & Biomolecular Chemistry, 13, 5344-5348. [Google Scholar] [CrossRef
[8] 赵春柳, 张桂兰, 袁中香, 等. 激发态分子内质子转移有机分子的研究进展[J]. 光电子激光, 1999, 10(4): 380-384.
[9] Weller, A. (1956) Intramolecular Proton Transfer in Excited States. Zeitschriftfuer Elek-trochemie und Angewandte Physikalische Chemie, 60, 1144-1147.
[10] Kwon, J.E. and Park, S.Y. (2011) Advanced Organic Optoelectronic Materials: Harnessing Excited-State Intramolecular Proton Transfer (ESIPT) Process. Advanced Materials, 23, 3615-3642. [Google Scholar] [CrossRef] [PubMed]
[11] 钱妍, 蔡敏敏, 解令海, 等. 基于2-(2’-羟基苯基)苯并噻唑的激发态分子内质子转移化合物的光物理行为研究[J]. 化学学报, 2010, 68(22): 2285-2289.
[12] Wang, A.H., et al. (2003) Femtosecond Fluorescence Upconversion Studies of Excited-State Proton Transfer Dynamics in 2-(2’-hydroxyphenyl)benzoxazole (HBO) in Liquid Solution and DNA. Chemical Physics Letters, 367, 599-608. [Google Scholar] [CrossRef
[13] 郑加金, 张桂兰, 吴峰, 等. 激发态质子转移分子2-(2’-羟基苯基)苯并噻唑在不同溶剂中的光谱特性[J]. 光谱学与光谱分析, 2008, 28(5): 970-973.
[14] Stefan, L., Alexander, J.W., Eberhard, R., et al. (2003) Microscopic Mechanism of Ultrafast Excited-State Intramolecular Proton Transfer: A 30-Fs Study of 2-(2’-hydroxyphenyl)benzothiazole. Journal of Physical Chemistry A, 107, 10580-10590. [Google Scholar] [CrossRef
[15] Regina, D.V., Vincent, D.W., Lukas, K., et al. (2003) Ultrafast Excited-State Proton Transfer of 2-(2’-hydroxyphenyl) benzothiazole: Theoretical Analysis of the Skeletal Deformations and the Active Vibrational Modes. The Journal of Physical Chemistry A, 107, 10591-10599. [Google Scholar] [CrossRef
[16] 张志于, 李洋洋, 李庆, 等. 2-(2-羟基苯基)苯并噻唑及其衍生物光谱性质的研究[C]//中国化学会第十二届全国物理有机化学学术会议论文摘要集. 武汉: 武汉大学, 2017: 1.
[17] 张志宇. 2-(2-羟基苯基)苯并噻唑系及其与卟啉二元化合物的合成和光物理行为的研究[D]: [硕士论文]. 湘潭: 湖南科技大学, 2019.
[18] Hamada, Y., Sano, T., Fujii, H., Nishio, Y. and Shibata, K. (1996) White-Light-Emitting Material for Organic Electroluminescent Devices. Japanese Journal of Applied Physics, 35, 1339-1341. [Google Scholar] [CrossRef
[19] 许慧侠, 陈柳青, 王华, 等. 2-(2-羟基苯基)苯并噻唑铍的制备与性能研究[J]. 功能材料, 2006(37): 79-82.
[20] Takami, S., Kawai, T. and Irie, M. (2010) Photochromism of Dithiazolylethenes Having Methoxy Groups at the Reaction Centers. European Journal of Organic Chemistry, 2002, 3796-3800. [Google Scholar] [CrossRef