Article

Synthesis and Properties of Photochromic Dithienylethene Compounds with Triphenylamine Units

  • Wang Zhiqiang ,
  • Xiao Yin ,
  • Jin Huiyi ,
  • Tan Tingfeng ,
  • Wang Shirong ,
  • Li Xianggao
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  • a. School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072;
    b. The Co-Innovation Center of Chemistry and Chemical Engineering of Tianjin, Tianjin 300072;
    c. School of Science, Tianjin Chengjian University, Tianjin 300384

Received date: 2014-03-07

  Online published: 2014-05-14

Supported by

Project supported by the National Natural Science Foundation of China (No.21102098) and the National High Technology Research and Development Program of China (863 Program, No.2012AA030307).

Abstract

Combining dithienylethene photochromic unit with triphenylamine unit, three new photochromic dithienylethene compounds 1a1c were successfully synthesized using 5-chloro-2-methyl-3-acetylthiophene and diphenylaminobenzaldehydes as starting materials through Aldol condensation reaction, Michael addition reaction and McMurry coupling reaction, the structures of which were characterized by MS, 1H NMR and 13C NMR.Different from majority of previous studies that introduce different functional groups through thiophene rings, we bridged the triphenylamine unit with fluorescence property to the cyclopentene at β-position via C—C single bond, which will maintain the activation of photochromism and prevent other functional groups affecting the dithienylethene backbone.Their photochromic and fluorescence properties in solutions and polymethylmethacrylate films were investigated by UV-Vis and fluorescence spectra, respectively.The colorless solutions and films of 1a1c switch to yellow upon irradiation with 302 nm UV light and reach the photostationary state fast, while bleaching of the colored solutions happen upon irradiation with 450 nm blue light.When 1a1c are excited by UV light, the maximum fluorescence wavelengths of 1a1c increase along with the enhancement of the abilities of electron donating of substituent R, and 1a1c emit strong fluorescence in n-hexane, toluene and ethyl acetate, while weak in acetonitrile and none in chloroform.Moreover, upon irradiation at 302 nm, Förster resonance energy transfer occurs between triphenylamine unit and dithienylcyclopentene unit of 1a1c.Thus, the fluorescence intensities of 1a1c decrease along with the prolonging of irradiation time, which indicates the potential application of these compounds as fluorescence molecular switches.

Cite this article

Wang Zhiqiang , Xiao Yin , Jin Huiyi , Tan Tingfeng , Wang Shirong , Li Xianggao . Synthesis and Properties of Photochromic Dithienylethene Compounds with Triphenylamine Units[J]. Acta Chimica Sinica, 2014 , 72(6) : 731 -738 . DOI: 10.6023/A14030158

References

[1] Myles, A.J.; Branda, N.R.Adv.Funct.Mater.2002, 12, 167.
[2] Wen, G.-T.; Ding, X.-Y.; Liu, L.; Guo, Q.-X.Prog.Chem.2005, 17, 826.(文国涛, 丁晓媛, 刘磊, 郭庆祥, 化学进展, 2005, 17, 826.)
[3] Li, C.; Gong, W.-L.; Hu, Z.; Aldred, M.P.; Zhang, G.-F.; Chen, T.; Huang, Z.-L.; Zhu, M.-Q.RSC Adv.2013, 3, 8967.
[4] Irie, M.Chem.Rev.2000, 100, 1685.
[5] Lucas, L.N.; Jong, J.J.D.D.; Esch, J.H.V.; Kellogg, R.M.; Feringa, B.L.Eur.J.Org.Chem.2003, 2003, 155.
[6] Golovkova, T.A.; Kozlov, D.V.; Neckers, D.C.J.Org.Chem.2005, 70, 5545.
[7] Zou, Q.; Zhang, J.-J.; Tian, H.Prog.Chem.2012, 24, 1632.(邹祺, 张隽佶, 田禾, 化学进展, 2012, 24, 1632.)
[8] Zhang, J.-Q.; Jin, J.-Y.; Zhang, J.-J.; Zou, L.Chin.J.Chem.2012, 30, 1741.
[9] Areephong, J.; Hurenkamp, J.H.; Milder, M.; Meetsma, A.; Herek, J.L.; Browne, W.R.; Feringa, B.L.Org.Lett.2009, 11, 721.
[10] Tanaka, Y.; Ishisaka, T.; Inagaki, A.; Koike, T.; Lapinte, C.; Akita, M.Chem.-Eur.J.2010, 16, 4762.
[11] Göstl, R.; Kobin, B.; Grubert, L.; Pätzel, M.; Hecht, S.Chem.-Eur.J.2012, 18, 14282.
[12] Li, X.; Tian, H.Macromol.Chem.Phys.2005, 206, 1769.
[13] He, Z.; Wong, W.-Y.; Yu, X.; Kwok, H.-S.; Lin, Z.Inorg.Chem.2006, 45, 10922.
[14] Tao, S.; Zhou, Y.-C.; Lee, C.-S.; Lee, S.-T.; Huang, D.; Zhang, X.-H.J.Phys.Chem.C 2008, 112, 14603.
[15] Tao, Y.-T.; Wang, Q.; Shang, Y.; Yang, C.-L.; Ao, L.; Qin, J.-G.; Ma, D.-G.; Shuai, Z.-G.Chem.Commun.2009, 77.
[16] Tian, H.; Yang, X.; Chen, R.; Zhang, R.; Hagfeldt, A.; Sun, L.J.Phys.Chem.C 2008, 112, 11023.
[17] Ning, Z.-J.; Tian, H.Chem.Commun.2009, 5483.
[18] Liang, Y.-L.; Peng, B.; Liang, J.; Tao, Z.-L.; Chen, J.Org.Lett.2010, 12, 1204.
[19] Chen, J.; Wang, M.Chem.Res.Chin.Univ.2013, 29, 584.
[20] Cheng, S.-H.; Hsiao, S.-H.; Su, T.-H.; Liou, G.-S.Macromolecules 2005, 38, 307.
[21] Chen, W.-H.; Wang, K.-L.; Liaw, D.-J.; Lee, K.-R.; Lai, J.-Y.Macromolecules 2010, 43, 2236.
[22] Yen, H.-J.; Lin, H.-Y.; Liou, G.-S.Chem.Mater.2011, 23, 1874.
[23] Chen, M.; Yang, S.-W.; Zheng, J.-M.; Xu, C.-Y.Acta Chim.Sinica 2013, 71, 713.(陈梅, 杨树威, 郑建明, 徐春叶, 化学学报, 2013, 71, 713.)
[24] Fang, Z.; Chellappan, V.; Webster, R.-D.; Ke, L.; Zhang, T.; Liu, B.; Lai, Y.J.Mater.Chem.2012, 22, 15397.
[25] Ohsumi, M.; Hazama, M.; Fukaminato, T.; Irie, M.Chem.Commun.2008, 3281.
[26] Zheng, C.-M.; Wang, T.-T.; Zeng, H.-P.Chin.J.Org.Chem.2012, 32, 719.(郑春梅, 王婷婷, 曾和平, 有机化学, 2012, 32, 719.)
[27] Xu, J.-G.; Wang, Z.-B.The Methods of Fluorescence Spectroscopy Analysis, Science Press, Beijing, 2006, pp.26, 49~51, 57~58.(许金钩, 王尊本, 荧光分析法, 科学出版社, 北京, 2006, pp.26, 49~51, 57~58.)
[28] Reichardt, C.Chem.Rev.1994, 94, 2319.
[29] Giordano, L.; Jovin, T.M.; Irie, M.; Jares-Erijman, E.A.J.Am.Chem.Soc.2002, 124, 7481.
[30] Chai, C.; Armarego, W.L.F.Purification of Laboratory Chemicals, Butterworth-Heinemann, Burlington, MA, 2009, p.434.
[31] Danko, M.; Andics, A.; Kosa, C.; Hrdlovic, P.; Vegh, D.Dyes Pigm.2012, 92, 1257.
[32] Shao, Q.M.S.Thesis, South China University of Technology, Guangzhou, 2011.(邵强, 硕士论文, 华南理工大学, 广州, 2011.)

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