BODIPY类化合物的合成及其修饰方法概况

doi:10.12677/JOCR.2017.51003

期刊菜单

BODIPY类化合物的合成及其修饰方法概况
Synthesis of BODIPY Compounds and Their Modification Methods

DOI: 10.12677/JOCR.2017.51003, PDF, HTML, XML, 下载: 2,561 浏览: 7,088 科研立项经费支持
作者: 王南翔, 甄文：南京航空航天大学材料科学与技术学院，江苏南京
关键词: BODIPY；合成及修饰；方法概况；BODIPY； Synthesis and Modification； Method Summary

摘要: 近年来，氟硼二吡咯（BODIPY）类荧光化合物在生物标记、肿瘤光动力治疗（PDT）光敏剂、固态太阳能聚光器电致发光器件、荧光开光等不同领域中都成为了研究的焦点，特别是在传感器和生物探针方面。本文总结了BODIPY类化合物的多种合成及其修饰方法，希望对相关研究人员有所帮助。

Abstract: In recent years, BODIPY (Boron-dipyrromethene complex) compounds have been the focus of many studies in diverse areas. BODIPYs are fully recognized as excellent fluorescent materials in tunable laser, biological labeling, photosensitizers and photodynamic therapy of tumor (PDT), solid-state solar concentrators, electroluminescent devices, on-off fluorescent switches etc., and in particular the fluorophores in sensors and probes. This paper summarizes the synthesis of BODIPY compounds and its modification methods, hoping to help the relevant researchers.

文章引用：王南翔, 甄文. BODIPY类化合物的合成及其修饰方法概况[J]. 有机化学研究, 2017, 5(1): 15-20. https://doi.org/10.12677/JOCR.2017.51003

参考文献

[1]	Boens, N., Leen, V. and Dehaen, W. (2012) Fluorescent Indicators Based on Bodipy. Chemical Society Reviews, 41, 1130-1172. https://doi.org/10.1039/C1CS15132K
[2]	Liu, Q., Yin, B., Yang, T., et al. (2013) A General Strategy for Biocompatible, High-Effective up Conversion Nanocapsules Based on Triplet-Triplet Annihilation. Journal of the American Chemical Society, 135, 5029-5037. https://doi.org/10.1021/ja3104268
[3]	Huang, L. and Zhao, J. (2013) C60-Bodipy Dyad Triplet Photo Sensitizers as Organic Photo Catalysts for Photo Catalytic Tandem Oxidation/[3+2] Cycloaddition Reactions to Prepare Pyr-rolo[2,1-a]isoquinoline. Chemical Communications, 49, 3751-3753. https://doi.org/10.1039/c3cc41494a
[4]	Benstead, M., Mehl, G.H. and Boyle, R.W. (2011) 4,4’-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as Components of Novel Light Active Materials. Tetrahedron, 67, 3573-3601. https://doi.org/10.1016/j.tet.2011.03.028
[5]	Olivier, J.-H., Barbera, J., Bahaidarah, E., et al. (2012) Self-Assembly of Charged Bodipy Dyes To Form Cassettes That Display Intracomplex Electronic Energy Transfer and Accrete into Liquid Crystals. Journal of the American Chemical Society, 134, 6100-6103. https://doi.org/10.1021/ja3007935
[6]	Nepomnyashchii, A.B. and Bard, A.J. (2012) Electrochemistry and Elec-trogenerated Chemiluminescence of Bodipy Dyes. Accounts of Chemical Research, 45, 1844-1853. https://doi.org/10.1021/ar200278b
[7]	Kamkaew, A., Lim, S.H., Lee, H.B., et al. (2013) Bodipy Dyes in Photo-dynamic Therapy. Chemical Society Reviews, 42, 77-88. https://doi.org/10.1039/C2CS35216H
[8]	He, H., Si, L., Zhong, Y., et al. (2012) Iodized Bodipy as a Long Wavelength Light Sensitizer for the Near-Infrared Emission of Yt-terbium(iii) Ion. Chemical Communications, 48, 1886-1888. https://doi.org/10.1039/c2cc17037j
[9]	Huang, L., Yu, X., Wu, W., et al. (2012) Styryl Bodipy-C60 Dyads as Efficient Heavy-Atom-Free Organic Triplet Photosensitizers. Organic Letters, 14, 2594-2597. https://doi.org/10.1021/ol3008843
[10]	Hepp, A., Ulrich, G., Schmechel, R., et al. (2004) Highly Efficient Energy Transfer to a Novel Organic Dye in OLED Devices. Synthetic Metals, 146, 11-15.
[11]	Shi, W.-J., Liu, J.-Y. and Ng, D.K.P. (2012) A Highly Selective Colorimetric and Fluorescent Probe for Cu2+ and Hg2+ Ions Based on a Distyryl BODIPY with Two Bis(1,2,3-triazole)amino Receptors. Chemistry—An Asian Journal, 7, 196-200. https://doi.org/10.1002/asia.201100598
[12]	Bonaccorsi, P., Aversa, M.C., Barattucci, A., et al. (2012) Artificial Light-Harvesting Antenna Systems Grafted on a Carbohyate Drdrate Platform. Chemical Commu-nications, 48, 10550-10552. https://doi.org/10.1039/c2cc35555h
[13]	Chan, L., Tritsch, J.R. and Zhu, X.Y. (2012) Harvesting Singlet Fission for Solar Energy Conversion: One- versus Two-Electron Transfer from the Quantum Me-chanical Superposition. Journal of the American Chemical Society, 134, 18295-18302.
[14]	Ziessel, R., Ulrich, G. and Harriman, A. (2007) The Chemistry of Bodipy: A New El Dorado for Fluorescence Tools. New Journal of Chemistry, 31, 496-501. https://doi.org/10.1039/b617972j
[15]	Ulrich, G., Ziessel, R. and Harriman, A. (2008) The Chemistry of Fluorescent Bodipy Dyes: Versatility Unsurpassed. Angewandte Chemie International Edition, 47, 1184-1201. https://doi.org/10.1002/anie.200702070
[16]	Lee, S., Park, K., Kim, K.W., et al. (2008) Activatable Imaging Probes with Amplified Fluorescent Signals. Chemical Communications, 36, 4250-4260. https://doi.org/10.1039/b806854m
[17]	Shane, O.M., Michael, J.H., Lorcan, T.A., et al. (2005) Supramolecular Photonic Therapeutic Agents. Journal of the American Chemical Society, 127, 16360-16361. https://doi.org/10.1021/ja0553497
[18]	Li, Z., Mintzer, E. and Bittman, R. (2006) First Synthesis of Free Choles-terol-BODIPY Conjugates. Journal of Organic Chemistry, 71, 1718-1721. https://doi.org/10.1021/jo052029x
[19]	Boyer, J.H., Haag, A.M., Sathyamoorthi, G., et al. (1993) Pyrrome-thene-BF2 Complexes as Laser Dyes. Heteroatom Chemistry, 4, 39-49. https://doi.org/10.1002/hc.520040107
[20]	Loudet, A. and Burgess, K. (2007) BODIPY Dyes and Their Deriva-tives: Syntheses and Spectroscopic Properties. Chemical Reviews, 107, 4891-4932. https://doi.org/10.1021/cr078381n
[21]	刘汉壮. 基于硼—二吡咯亚甲基荧光探针的合成和性质研究[D]: [博士学位论文]. 南京: 南京大学, 2011.
[22]	Loudet, A., Bandichhor, R., Wu, L.X. and Burgess, K. (2008) Function-alized BF2 Chelated Azadipyrromethene Dyes. Tetrahedron, 64, 3642-3654. https://doi.org/10.1016/j.tet.2008.01.117
[23]	Ulrich, G. and Ziessel, R. (2008) The Chemistry of Fluorescent BODIPY Dyes: Versatility Unsurpassed. Angewandte Chemie International Edition, 47, 1184-1201. https://doi.org/10.1002/anie.200702070

为你推荐

友情链接