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用于阴离子识别的二茂铁基偶氮苯化合物的合成(英文) 被引量:1

Synthesis of ferrocene-and azobenzene-based compounds for anion recognition
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摘要 目的:研究二茂铁基偶氮苯化合物的光电响应性能及离子识别性能,并研究取代基对其离子识别性能的影响。创新点:考察取代基对于二茂铁基偶氮苯化合物的影响,并提出可能的机理。方法:循环伏安(CV)法和紫外可见吸收光谱(UV-vis)法。结论:通过CV法和UV-vis法研究二茂铁基偶氮苯化合物的离子识别性能,发现硝基取代的化合物对于F^-和H_2PO_4^-具有选择性离子识别作用,而氨基取代的化合物则识别作用不明显。 A series of ferrocene- and azobenzene-based compounds with acyl amine groups attached were designed and synthesized to explore their potential application in anion recognition. Their electro- and photo-properties, and the effect of nitro and amine substituents of the benzene ring on anion recognition were studied by UV-vis absorption spectroscopy (UV) and cyclic voltammetry (CV). The results showed that a nitro group substituent has a positive effect on the binding affinity and sensitivity, which might be due to the strong hydrogen bonding interaction between the receptor and the guest, while an amino group substituent has a negative effect on the sensitivity. Furthermore, the shift in the UV-vis absorption spectra was observed as a color change, which can be used for the naked-eye detection ofF- and H2PO4 .
出处 《Journal of Zhejiang University-Science A(Applied Physics & Engineering)》 SCIE EI CAS CSCD 2016年第2期144-154,共11页 浙江大学学报(英文版)A辑(应用物理与工程)
基金 supported by the National Natural Science Foundation of China(Nos.21272210,21472168,21372200,and 21411130187) the International Science and Technology Cooperation of the Ministry of Science and Technology of China(No.2009DFR40640) the Science and Technology Program of Zhejiang Province(Nos.2013C24001 and 2013C31146) the Science and Technology Innovation Team of Ningbo City(No.2011B82002),China
关键词 二茂铁 偶氮苯 光电响应 离子识别 Ferrocene, Azobenzene, Hydrogen bonding, High density information storage, Anion recognition
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  • 1Amer, W.A., Yu, H.J., Wang, L., et al., 2013. Synthesis, characterization and properties of some main-chain ferrocene-based polymers containing aromatic units. Journal of Inorganic and Organometallic Polymers and Materials, 23(6): 1431-1444. http://dx.doi.org/10.1007/s 10904-013-9946-2.
  • 2Apreutesei, D., Mehl, G.H., Scutaru, D., 2007. Ferrocene- containing liquid crystals bearing a cholesteryl unit. Liquid Crystals, 34(7):819-831. http://dx.doi.org/l 0.1080/02678290701478715.
  • 3Beer, ED., Graydon, A.R., Johnson, A., et al., 1997. Neutral ferrocenoyl receptors for the selective recognition and sensing of anionic guests. Inorganic Chemistry, 36(10): 2112-2118. http://dx.doi.org/10.1021/ic961401b.
  • 4Carlescu, I., Scutaru, A.M., Apreutesei, D., et al., 2007. The liquid crystalline behaviour of ferrocene derivatives containing azo and imine linking groups. Liquid Crystals, 34(7):775-785. http://dx.doi.org/10.1080/02678290701343190.
  • 5Deng, L.B., Wang, L., Huo, J., et al., 2008. Preparation of N,N'-bisethoxyethane[12]amideferrocenophane and its application in anion recognition. Journal of Physical Chemistry B, 112(17):5333-5337. http://dx.doi.org/10.1021/jp710824a.
  • 6Ikeda, T., Tsutsumi, O., 1995. Optical switching and image storage by means of azobenzene liquid-crystal films. Science, 268(5219):1873-1875. http://dx.doi.org/10.1126/science.268.5219.1873.
  • 7Kumar, G.S., Neckers, D.C., 1989. Photochemistry of azobenzene-containing polymers. Chemical Reviews, 89(8):1915-1925. http ://dx.doi.org/10.1021/cr00098a012.
  • 8Kuo, L.J., Liao, J.H., Chen, C.T., et al., 2003. Two-arm fer- rocene amide compounds: synclinal conformations for selective sensing of dihydrogen phosphate ion. Organic Letters, 5( 11): 1821-1824. http://dx.doi.org/10.1021/o1034364i.
  • 9Kurihara, M., Hirooka, A., Kume, S., et al., 2002. Redox- conjugated reversible isomerization of ferrocenyl- azobenzene with a single green light. Journal of the American Chemical Society, 124(30):8800-8801. http://dx.doi.org/10.1021/ja026625+.
  • 10Kurosawa, M., Takuya, N., Takayuki, M., et al., 1999. Syn- thesis of azo-bridged ferrocene oligomers and a polymer and electrochemical and optical analysis of internuclear electronic interactions in their mixed-valence states. In- organic Chemistry, 38(22):5113-5123. http://dx, doi.org/10.1021/ic990646w.

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