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化学进展 2011, Vol. 23 Issue (4): 739-749 前一篇   后一篇

• 综述与评论 •

方酸染料在离子识别中的研究

陈城, 王如勇, 傅南雁*   

  1. 福州大学 食品安全分析与检测教育部重点实验室 福建省食品安全分析与 检测技术重点实验室 福州 350108
  • 收稿日期:2010-07-01 修回日期:2010-10-01 出版日期:2011-04-24 发布日期:2011-02-25
  • 通讯作者: e-mail:nanyan_fu@fzu.edu.cn E-mail:nanyan_fu@fzu.edu.cn
  • 基金资助:

    国家自然科学基金项目(No.20702005)、福建省自然科学基金项目(No.2008J0148)和教育部留学回国人员科研启动基金项目(No.LXKQ0802)资助

Squaraine Dyes for Ion Recognition

Chen Cheng, Wang Ruyong, Fu Nanyan*   

  1. Key Laboratory of Analysis and Detection Technology for Food Safety, Ministry of Education, Fujian Provincial Key Laboratory of Analysis and Detection Technology for Food Safety, Fuzhou University, Fuzhou 350108, China
  • Received:2010-07-01 Revised:2010-10-01 Online:2011-04-24 Published:2011-02-25

作为一种新型的有机功能染料,方酸染料正引起化学界的极大兴趣。由于其特殊的D-A-D结构,方酸染料在可见-近红外区有强烈的吸收和荧光发射,因而越来越多地被应用在离子检测中。本文综述了近期方酸染料化学传感器的发展和应用,分别介绍了方酸染料在阳离子识别和阴离子识别中的分子设计、作用机理及应用,重点综述了方酸染料对汞、铜和锌等重金属离子的识别,以及对碱金属、碱土金属离子的识别作用,并展望了该领域的发展前景。

As a class of novel organic functional dye, squaraine dyes and their derivatives are gaining significant interest in the field of chemistry. Due to the unique D-A-D structure and the strong absorption and emission characters in the visible and near infrared region, squaraine has been used as the chemosensor in the ion recognition. This article covers the most recent studies in the development and application of squaraine dye-based chemosensors. The molecule design, recognition mechanism and application in both cation and anion recognition has been introduced. The recognizing process of heavy metal ions such as Hg2+、Cu2+ and Zn2+, as well as alkali metal ions and alkali earth metal ions, have been mainly reviewed. Moreover, the developing prospect for the further research has been expected.

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[1] Treibs A, Jacob K. Angew. Chem. Int. Ed. Engl., 1965, 4: 694
[2] Ajayagosh A. Acc. Chem. Res., 2005, 38: 449-459
[3] Hewage H S, Anslyn E V. J. Am. Chem. Soc., 2009, 131: 13099-13106
[4] 车庆林(Che Q L), 彭孝军(Peng X J). 染料工业(Dyestuffs and Coloration), 1999, 36: 8-14
[5] Law K Y, Bailey F C. US 4644082, 1987
[6] Liu L H, Nakatani K, Pansu R, Vachon J J, Tauc P, Ishow E. Adv. Mater., 2007, 19: 433-436
[7] Meiten K, Tetsuhiro K. JP 2007118254, 2007
[8] Merrit V Y, Hovel H J. App. Phys. Lett., 1976, 29: 414-415
[9] Ros-Lis J V, Marcos M D, Mártinez-Máez R, Rurack K, Soto J. Angew. Chem. Int. Ed., 2005, 44: 4405-4407
[10] Hsueh S, Lai C, Liu Y, Peng S, Chiu S. Angew. Chem. Int. Ed., 2007, 46: 2013-2017
[11] Volkova K D, Kovalska V B, Tatarets A L, Patsenker L D, Kryvorotenko D V, Yarmoluk S M. Dyes Pigm., 2007, 72: 285-292
[12] Wang B, Fan J, Sun S, Wang L, Song B, Peng X. Dyes Pigm., 2010, 85: 43-50
[13] Ajayaghosh A, Eldo J. Org. Lett., 2001, 3: 2595-2598
[14] de Silva A P, Gunaratne H Q N, Gunnlaugsson T, Huxley A J M, McCoy C P, Rademacher J T, Rice T E. Chem. Rev., 1997, 97: 1515-1566
[15] Ros-Lis J V, Mártinez-Má ez R, Sancenón F, Soto J, Spieles M, Rurack K. Chem. Eur. J., 2008, 14: 10101-10114
[16] Arunkumar E, Ajayaghosh A, Daub J. J. Am. Chem. Soc., 2005, 127: 3156-3164
[17] 冯新斌(Feng X B), 仇广乐(Qiu G L),付学吾(Fu X W), 何天容(He T R), 李平(Li P), 王少峰(Wang S F). 化学进展(Progress in Chemistry), 2009, 21: 436-457
[18] Ros-Lis J V, Martínez-Má ez R, Rurack K, Sancenón F, Soto J, Spieles M. Inorg. Chem., 2004, 43: 5183-5185
[19] Basheer M C, Thomas A K G, Suresh C H, Das S. Tetrahedron, 2006, 62: 605-610
[20] Avirah R R, Jyothish K, Ramaiah D. Org. Lett., 2007, 9: 121-124
[21] Lloris J M, Mártinez-Má ez R, Pardo T, Soto J, Padilla-Tosta M E. Chem.Commun., 1998, 837-838
[22] Guo X, Qian X, Jia L. J. Am. Chem. Soc., 2004, 126: 2272-2273
[23] Palomares E, Vilar R, Durrant J R. Chem.Commun., 2004, 362-363
[24] Casasús R, Marcos M D, Martínez-Má ez R, Ros-Lis J V, Soto J, Villaescusa L A, Amorós P, Beltrán D, Guillem C, Latorre J. J. Am. Chem. Soc., 2004, 126: 8612-8613
[25] Ros-Lis J V, Casasús R, Comes M, Coll C, Marcos M D, Martínez-Má ez R, Sancenón F, Soto J, Amorós P, Haskouri J E, Garró N, Rurack K. Chem. Eur. J., 2008, 14: 8267-8278
[26] Climent E, Marcos M D, Martínez-Má ez R, Sancenón F, Soto J, Rurack K, Amorós P. Angew. Chem. Int. Ed., 2009, 48: 8519-8522
[27] Chen C, Wang R, Guo L, Fu N , Dong H, Yuan Y. Org. Lett., 2011, 13: 1162-1165
[28] Georgopoulos P G, Roy A, Yonone-Lioy M J, Opiekun R E, Lioy P J. J. Toxicol. Environ. Health B, 2001, 4: 341-394
[29] Meng X M, Zhu M Z, Liu L, Guo Q X. Tetrahedron Lett., 2006, 47: 1559-1562
[30] Kim S H, Han S K, Kim J H, Lee M B, Koh K N, Kang S W. Dyes Pigm., 2000, 44: 55-61
[31] Wang W, Fu A, You J, Gao G, Lan J, Chen L. Tetrahedron, 2010, 66: 3695-3701
[32] 施锋(Shi F), 李宏洋(Li H Y), 彭孝军(Peng X J). 精细化工(Fine Chemicals), 2003, 20: 268-272
[33] Arunkumar E, Forbes C C, Noll B C, Smith B D. J. Am. Chem. Soc., 2005, 127: 3288-3289
[34] Johnson J R, Fu N, Arunkumar E, Leevy W M, Gammon S T, Piwinica-Worms D, Smith B D. Angew. Chem. Int. Ed., 2007, 46: 5528-5531
[35] Wallace K J, Gray M, Zhong Z, Lynch V M, Anslyn E V. Dalton Trans., 2005, 2436-2441
[36] Kim S H, Han S K, Jang G S, Koh K N, Kang S W, Keum S R, Yoon C M. Dyes Pigm., 2000, 44: 169-173
[37] Houk R J H, Wallace K J, Hewage H S, Anslyn E V. Tetrahedron, 2008, 64: 8271-8278
[38] Hirakawa H. Electronics and Communications in Japan (Part Ⅱ: Electronics), 1996, 79: 82-91
[39] Thomas Ⅲ S W, Joly G D, Swager T M.Chem. Rev., 2007, 107: 1339-1386
[40] Chenthamarakshan C R, Ajayaghosh A. Tetrahedron Lett., 1998, 39: 1795-1798
[41] Chenthamarakshan C R, Eldo J, Ajayaghosh A. Macromolecules, 1999, 32: 5846-5851
[42] Akkaya E U, Oguz U. Tetrahedron Lett., 1998, 39: 5857-5860
[43] Hsueh S Y, Lai C C, Liu Y H, Wang Y, Peng S M, Chiu S H.Org. Lett., 2007, 9: 4523-4526
[44] Hsueh S Y, Lai C C, Liu Y H, Wang Y, Peng S M, Chiu S H. Angew. Chem. Int. Ed., 2007, 46: 2013-2017
[45] Arunkumar E, Chithra P, Ajayaghosh A. J. Am. Chem. Soc., 2004, 126: 6590-6598
[46] Ajayaghosh A, Arunkumar E, Daub J. Angew. Chem. Int. Ed., 2002, 41: 1766-1769
[47] Ajayaghosh A, Chithra P, Varghese R. Angew. Chem. Int. Ed., 2007, 46: 230-233
[48] Ajayaghosh A, Chithra P, Varghese R, Divya K P. Chem. Commun., 2008, 969-971
[49] Ajayaghosh A, Arunkumar E. Org. Lett., 2005, 7: 3135-3138
[50] Gassensmith J J, Barr L, Baumes J M, Paek A, Nguyen A, Smith B D. Org. Lett., 2008, 10: 3343-3346
[51] Gassensmith J J, Matthys S, Lee J J, Wojcik A, Kamat P V, Smith B D. Chem. Eur. J., 2010, 16: 2916-2921
[52] Climent E, Casasús R, Marcos M D, Martínez-Má ez R, Sancenón F, Soto J. Dalton Trans., 2009, 4806-4814

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摘要

方酸染料在离子识别中的研究