English
新闻公告
More
化学进展 2007, Vol. 19 Issue (9): 1258-1266 前一篇   后一篇

• 综述与评论 •

香豆素类荧光传感器*

马文辉1,2 彭孝军1** 徐群2 宋波1,2   

  1. 1.大连理工大学精细化工国家重点实验室 大连 116012;
    2.齐齐哈尔大学化学与化学工程学院 齐齐哈尔 161006
  • 收稿日期:2006-10-16 修回日期:2006-11-15 出版日期:2007-09-24 发布日期:2007-09-25
  • 通讯作者: 彭孝军

Coumarin-Based Fluorescent Sensors

Ma Wenhui1,2;Peng Xiaojun1**;Xu Qun2;Song Bo1,2   

  1. 1. State Key Laboratory of Fine Chemicals, Dalian University of Technology,Dalian 116012,China;
    2. College of Chemistry and Chemical Engineering , Qiqihar University,Qiqihar 161006, China
  • Received:2006-10-16 Revised:2006-11-15 Online:2007-09-24 Published:2007-09-25
  • Contact: Peng Xiaojun
荧光传感器能够将分子识别的信息转换成荧光信号,荧光法在灵敏度、选择性和实时原位检测等方面优势突出。实时检测被分析物的水平已引起包括化学家、生物学家、临床生物化学家和环境学家的极大兴趣。以香豆素为基础的荧光传感器近年来已成为一个新兴的研究热点。本文综述了香豆素类荧光传感器在阳离子、阴离子、中性分子识别检测中的分子设计、作用机理和应用效果,展望了该领域的发展方向。
Fluorescent sensors can transfer molecular recognition events into fluorescent signals。Of the various kinds of chemosensors,fluorescent sensors offer distinct advantages in terms of sensitivity , selectivity , response time and in situ observation.Monitoring in real-time and real-space the level of analytes is of great interest to many scientists, including chemists, biologists, clinical biochemists and environmentalists. Fluorescent sensors based on coumarin have drawn much attention in recent years .In this paper,the molecular design、mechanism and application of coumarin-based fluorescent sensors for cations、anions and neutral molecules are reviewed. The developing orientation for further research is presented.

中图分类号: 

()

[ 1 ] De Silva A P , Gunaratne H Q N , Gunnlaugsson T , et al . Chem.Rev. , 1997 , 97 : 1515 —1566
[ 2 ] Valeur B. Molecular Fluorescence : Principles and Applications.Weinheim: Wiley-VCH Verlag Gmb H , 2001. 273 —350
[ 3 ] Callan J F , De Silva A P , Magri D C. Tetrahedron , 2005 , 61 :8551 —8588
[ 4 ] Haupt K, Mosbach K. Chem. Rev. , 2000 , 100 (7) : 2495 —2504
[ 5 ] Nolan E M, Racine M E , Lippard S J . Inorg. Chem. , 2006 , 45 :2742 —2749
[ 6 ] Nolan E M, Jaworski J , Okamoto K I. J . Am. Chem. Soc. ,2005 , 127 (48) : 16812 —16823
[ 7 ] Zhong H , Qian Z H , Xu L. Organic Letters , 2006 , 8(5) : 859 —861
[ 8 ] Xiang Y, Tong A J . Organic Letters , 2006 , 8(8) : 1549 —1552
[ 9 ] Kiyose K, Kojima H , Urano Y. J . Am. Chem. Soc. , 2006 , 128 (20) : 6548 —6549
[10] Sasaki E , Kojima H , Nishimatsu H. J . Am. Chem. Soc. , 2005 ,127(11) : 3684 —3685
[11] Qi X, Jun E J , Xu L. J . Org. Chem. , 2006 , 71 (7) : 2881 —2884
[12] Wu Y K, Peng X J , Guo B C. Org. Biomol . Chem. , 2005 , 8 :1387 —1392
[13] Wang J B , Qian X H. Chem. Commun. , 2006 , 109 —111
[14] Fan J L , Wu Y K, Peng X J . Chemistry Letters , 2004 , 33(10) :1392 —1393
[15] Rurack K. Spectrochimica Acta Part A , 2001 , 57 :2161 —2195
[16] Valeur B , Leray I. Coordination Chemistry Reviews ,2000 , 205 :3 —40
[17] Prodi L , Bolletta F , Montalti M. Coordination Chemistry Reviews ,2000 , 205 : 59 —83
[18] Jiang P J , Guo Z J . Coordination Chemistry Reviews , 2004 , 248 :205 —229
[19] Blackburn C , Bai M Q , Lecompte K A , et al . Tetrahedron Letters , 1994 , 35(43) : 7915 —7918
[20] Golchini K, Mackovic-Basic M, Gharib S A , et al . Am. J .Physiol . , 1990 , 258 : F438 —F443
[21] Kastenholz F , Grell E , Bats J W, et al . J . Fluoresc. , 1994 , 4(3) :243 —246
[22] Doludda M, Kastenholz F , Lewitzki E ,et al . J . Fluoresc. , 1996 ,6 (3) : 159 —163
[23] Crossley R , Goolamali Z , Sammes P G. J . Chem. Soc. , Perkin Trans. 2 ,1994 , 7 : 1615 —1623
[24] Crossley R , Goolamali Z , Gosper J J , et al . J . Chem. Soc. ,Perkin Trans. 2 , 1994 , 3 : 513 —520
[25] Leray I , Asfari Z , Vicens J , et al . J . Fluoresc. , 2004 , 14(4) :451 —458
[26] Leray I , Asfari Z , Vicens J , et al . J . Chem. Soc. , Perkin Trans. 2 , 2002 , 1429 —1434
[27] Valeur B , Leray I. Inorganica Chimica Acta , 2007 , 360 (3) :765 —774
[28] Brunet E , Alonso M T , Juannes O , et al . Tetrahedron Letters ,1997 , 38(25) : 4459 —4462
[29] Suzuki Y, Komatsu H , Iked T , et al . Anal . Chem. , 2002 , 74 :1423 —1428
[30] Maton L , Taziaux D , Soumillion J P , et al . J . Mater. Chem. ,2005 , 15 : 2928 —2937
[31] Brunet E , Garcia-Losada P , Rodríguez-Ubis J C , et al . Can. J .Chem. , 2002 , 80 : 169 —174
[32] Komatsu H , Miki T , Citterio D , et al . J . Am. Chem. Soc. ,2005 , 127 (31) : 10798 —10799
[33] KarslíN , Erk μ. Dyes and Pigments , 1996 , 32(2) : 85 —92
[34] Erk μ, Gê?men A , Bulut M. Journal of Inclusion Phenomena and Molecular Recognition in Chemistry , 1998 , 31 : 319 —331
[35] Bourson J , Borrel M N , Valeur B. Analytica Chimica Acta ,1992 , 257 : 189 —193
[36] Li L D , Wei Y, Tong A J . Analytica Chimica Acta , 2001 , 427 :29 —37
[37] Bourson J , Pouget J , Valeur B. J . Phys. Chem. , 1993 , 97 :4552 —4557
[38] Habib J L H , Branger C , Soumillion J P , et al . Journal of Photochemistry and Photobiology A : Chemistry , 1998 , 116 :127 —133
[39] Taziaux D , Soumillion J P , Habib J L H. Journal of Photochemistry and Photobiology A : Chemistry , 2004 , 162 :599 —607
[40] Leray I , Habib J L H , Branger C , et al . Journal of Photochemistry and Photobiology A: Chemistry , 2000 ,135 : 163 —169
[41] Erk μ, Bulut M, Gê?men A. Journal of Inclusion Phenomena and Macrocyclic Chemistry , 2000 , 37 : 441 —450
[42] Ma Y M , Luo W, Quinn P J , et al . J . Med. Chem. , 2004 , 47 :6349 —6362
[43] Jang Y J , Moon B S , Park M S , et al . Tetrahedron Letters ,2006 ,47 : 2707 —2710
[44] Lim N C , Yao L L , Freake H C , et al . Bioorganic &Medicinal Chemistry Letters , 2003 , 13 : 2251 —2254
[45] Lim N C , Brückner C. Chem. Commun. , 2004 , 1094 —1095
[46] Kulatilleke C P , Silva S A , Eliav Y. Polyhedron , 2006 , 25(13) :2593 —2596
[47] Dakanali M, Roussakis E , Kay A R , et al . Tetrahedron Letters ,2005 , 46(24) : 4193 —4196
[48] Chatterjee M, Chatterjee S , Roy M B , et al . Journal of Luminescence , 2002 , 99 : 175 —183
[49] Wang J B , Qian X H , Cui J N. J . Org. Chem. , 2006 , 71 :4308 —4311
[50] Valeur B , Pouget J , Bouson J , et al . J . Phys. Chem. , 1992 ,96 : 6545 —6549
[51] Chen C T , Huang W P. J . Am. Chem. Soc. , 2002 , 124 :6246 —6247
[52] Khatri V K, Upreti S , Pandey P S. Organic Letters , 2006 , 8(9) :1755 —1758
[53] Ramón M M, Félix S. Chem. Rev. , 2003 , 103 : 4419 —4476
[54] Mizukami S , Nagano T , Urano Y, et al . J . Am. Chem. Soc. ,2002 , 124 : 3920 —3925
[55] Samankumara K R A , Sandanayake , Imazu S , et al . Chemistry Letters , 1995 ,139 —140
[56] Burdette S C , Lippard S J . Coordination Chemistry Reviews ,2001 , 216/217 : 333 —361
[57] Plater M J , Greig I , Helfrich M H , et al . J . Chem. Soc. , Perkin Trans. 1 , 2001 , (20) : 2553 —2559
[58] Soh N , Sakawaki O , Makihara K, et al . Bioorganic &Medicinal Chemistry , 2005 , 13 : 1131 —1139
[59] Prodi L. New J . Chem. , 2005 , 29 : 20 —31
[60] Toal S J , Jones K A , Magde D. J . Am. Chem. Soc. , 2005 , 127(33) : 11661 —11665

[1] 陈戈慧, 马楠, 于帅兵, 王娇, 孔金明, 张学记. 可卡因免疫及适配体生物传感器[J]. 化学进展, 2023, 35(5): 757-770.
[2] 鲍艳, 许佳琛, 郭茹月, 马建中. 基于微纳结构的高灵敏度柔性压力传感器[J]. 化学进展, 2023, 35(5): 709-720.
[3] 赵京龙, 沈文锋, 吕大伍, 尹嘉琦, 梁彤祥, 宋伟杰. 基于人体呼气检测应用的气体传感器[J]. 化学进展, 2023, 35(2): 302-317.
[4] 钟衍裕, 王正运, 刘宏芳. 抗坏血酸电化学传感研究进展[J]. 化学进展, 2023, 35(2): 219-232.
[5] 傅安辰, 毛彦佳, 王宏博, 曹志娟. 基于二氧杂环丁烷骨架的化学发光探针发展和应用研究[J]. 化学进展, 2023, 35(2): 189-205.
[6] 赖燕琴, 谢振达, 付曼琳, 陈暄, 周戚, 胡金锋. 基于1,8-萘酰亚胺的多分析物荧光探针的构建和应用[J]. 化学进展, 2022, 34(9): 2024-2034.
[7] 卢继洋, 汪田田, 李湘湘, 邬福明, 杨辉, 胡文平. 电喷印刷柔性传感器[J]. 化学进展, 2022, 34(9): 1982-1995.
[8] 于兰, 薛沛然, 李欢欢, 陶冶, 陈润锋, 黄维. 圆偏振发光性质的热活化延迟荧光材料及电致发光器件[J]. 化学进展, 2022, 34(9): 1996-2011.
[9] 李立清, 郑明豪, 江丹丹, 曹舒心, 刘昆明, 刘晋彪. 基于邻苯二胺氧化反应的生物分子比色/荧光探针[J]. 化学进展, 2022, 34(8): 1815-1830.
[10] 周宇航, 丁莎, 夏勇, 刘跃军. 荧光探针在半胱氨酸检测的应用[J]. 化学进展, 2022, 34(8): 1831-1862.
[11] 乔瑶雨, 张学辉, 赵晓竹, 李超, 何乃普. 石墨烯/金属-有机框架复合材料制备及其应用[J]. 化学进展, 2022, 34(5): 1181-1190.
[12] 姜鸿基, 王美丽, 卢志炜, 叶尚辉, 董晓臣. 石墨烯基人工智能柔性传感器[J]. 化学进展, 2022, 34(5): 1166-1180.
[13] 颜范勇, 臧悦言, 章宇扬, 李想, 王瑞杰, 卢贞彤. 检测谷胱甘肽的荧光探针[J]. 化学进展, 2022, 34(5): 1136-1152.
[14] 林瑜, 谭学才, 吴叶宇, 韦富存, 吴佳雯, 欧盼盼. 二维纳米材料g-C3N4在电化学发光中的应用研究[J]. 化学进展, 2022, 34(4): 898-908.
[15] 赵惠, 胡文博, 范曲立. 双光子荧光探针在生物传感中的应用[J]. 化学进展, 2022, 34(4): 815-823.
阅读次数
全文


摘要

香豆素类荧光传感器*