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化学进展  2013 

基于有机硅化合物的反应型氟离子荧光化学传感器

DOI: 10.7536/PC120730, PP. 288-295

Keywords: 荧光传感器,氟离子,反应型传感器,有机硅化合物

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Abstract:

作为半径最小的阴离子,氟离子(F-)表现出高电负性和强碱性,因而具有特殊的化学性质。由于F-与人类健康和环境安全密切相关,因此它的识别与检测已引起了人们极大的关注。到目前为止,用于选择性检测F-的荧光化学传感器已有大量报道,这些传感器主要是基于有机硼化合物和氢键质子给体。与这些传感器相比,反应型传感器具有更高的选择性,并且更容易在水环境中实现F-检测。本文根据有机硅化合物的结构不同,分别综述了近年来基于硅醚、硅炔及其他有机硅化合物的反应型氟离子荧光化学传感器的合成研究进展,其中包括本课题组的一些研究工作。

References

[1]  Gale P A. Coord. Chem. Rev., 2001, 213: 79-128
[2]  Sessler J L, Davis J M. Acc. Chem. Res., 2001, 34: 989-997
[3]  Beer P D, Gale P A. Angew. Chem. Int. Ed., 2001, 40: 486-516
[4]  Martinez-Má?ez R, Sancenón F. Chem. Rev., 2003, 103: 4419-4476
[5]  Horowitz H S. J. Public Health Dent., 2003, 63: 3-10
[6]  Cametti M, Rissanen K. Chem. Commun., 2009, 2809-2829
[7]  Martinez-Má?ez R, Sancenón F. J. Fluoresc., 2005, 15: 267-285
[8]  Wade C R, Broomsgrove A E J, Aldridge S, Gabba? F P. Chem. Rev., 2010, 110: 3958-3984
[9]  Yamaguchi S, Akiyama S, Tamao K. J. Am. Chem. Soc., 2001, 123: 11372-11375
[10]  Liu X, Bai D, Wang S. Angew. Chem. Int. Ed., 2006, 45: 5475-5478
[11]  Boiocchi M, Boca L D, Gómez D E, Fabbrizzi L, Licchelli M, Monzani E. J. Am. Chem. Soc., 2004, 126: 16507-16514
[12]  Anzenbacher P Jr, Jursíková K, Sessler J L. J. Am. Chem. Soc., 2000, 122: 9350-9351
[13]  Mizuno T, Wei W H, Eller L R, Sessler J L. J. Am. Chem. Soc., 2002, 124: 1134-1135
[14]  Maeda H, Haketa Y, Nakanishi T. J. Am. Chem. Soc., 2007, 129: 13661-13674
[15]  Shimshock S J, Waitermire R E, Deshong P. J. Am. Chem. Soc., 1991, 113: 8791-8796
[16]  Zhang W, Robins M J. Tetrahedron Lett., 1992, 33: 1177-1180
[17]  Corey E J, Yi K Y. Tetrahedron Lett., 1992, 33: 2289-2290
[18]  Yamaguchi S, Akiyama S, Tamao K. J. Am. Chem. Soc., 2000, 122: 6793-6794
[19]  Kim T H, Swager T M. Angew. Chem. Int. Ed., 2003, 42: 4803-4806
[20]  Kim S Y, Park J, Koh M, Park S B, Hong J I. Chem. Commun., 2009, 4735-4737
[21]  Yang X, Ye S, Bai Q, Wang X. J. Fluoresc., 2007, 17: 81-87
[22]  Jiang X, Vieweger M C, Bollinger J C, Dragnea B, Lee D. Org. Lett., 2007, 9: 3579-3582
[23]  Bozdemir O A, Sozmen F, Buyukcakir O, Guliyev R, Cakmak Y, Akkaya E U. Org. Lett., 2010, 12: 1400-1403
[24]  Hu R, Feng J, Hu D, Wang S, Li S, Li Y, Yang G. Angew. Chem. Int. Ed., 2010, 49: 4915-4918
[25]  Bao Y, Liu B, Du F, Wang H, Tian J, Bai R. J. Mater. Chem., 2012, 22: 5291-5294
[26]  Cao J, Zhao C, Feng P, Zhang Y, Zhu W. RSC Adv., 2012, 2: 418-420
[27]  Rao M R, Mobin S M, Ravikanth M. Tetrahedron, 2010, 66: 1728-1734
[28]  Buckland D, Bhosale S V, Langford S J. Tetrahedron Lett., 2011, 52: 1990-1992
[29]  Descalzo A B, Jiménez D, Haskouri J E, Beltrán D, Amorós P, Marcos M D, Martínez-Má?ez R, Sotoa J. Chem. Commun., 2002, 562-563
[30]  肖文香(Xiao W X), 肖丹(Xiao D). 化学研究与应用(Chemical Research and Application), 2009, 21: 1320-1322
[31]  Zhu C Q, Chen J L, Zheng H, Wu Y Q, Xu J G. Anal. Chim. Acta, 2005, 539: 311-316
[32]  Gunnlaugsson T, Glynn M, Tocci G M, Kruger P E, Pfeffer F M. Coord. Chem. Rev., 2006, 250: 3094-3117
[33]  Farley J R, Wergedal J E, Baylink D J. Science, 1983, 222: 330-332
[34]  Kleerekoper M. Endocrinol. Metab. Clin. North Am., 1998, 27: 441-452
[35]  Weatherall J A. Pharmacology of Fluorides. in Handbook of Experimental Pharmacology XX/1. Berlin: Springer-Verlag, 1969. Part 1. 141-172
[36]  Cittanova M L, Lelongt B, Verpont M C. Anesthesiology, 1996, 84: 428-435
[37]  Singh P P, Barjatiya M K, Dhing S, Bhatnagar R, Kothari S, Dhar V. Urol. Res., 2001, 29: 238-244
[38]  Cho E J, Moon J W, Ko S W, Lee J Y, Kim S K, Yoon J, Nam K C. J. Am. Chem. Soc., 2003, 125: 12376-12377
[39]  Corey E J, Venkateswarlu A. J. Am. Chem. Soc., 1972, 94: 6190-6191
[40]  Collington E W, Finch H, Smith I J. Tetrahedron Lett., 1985, 26: 681-684
[41]  Kim S Y, Hong J I. Org. Lett., 2007, 9: 3109-3112
[42]  Yang X. Spectrochim. Acta Part A, 2007, 67: 321-326
[43]  Yang X, Qi H, Wang L, Su Z, Wang G. Talanta, 2009, 80: 92-97
[44]  Bhalla V, Singh H, Kumar M. Org. Lett., 2010, 12: 628-631
[45]  Bao Y, Liu B, Wang H, Tian J, Bai R. Chem. Commun., 2011, 47: 3957-3959
[46]  Zhang J F, Lim C S, Bhuniya S, Cho B R, Kim J S. Org. Lett., 2011, 13: 1190-1193
[47]  Cao X, Lin W, Yu Q, Wang J. Org. Lett., 2011, 13: 6098-6101
[48]  Sokkalingam P, Lee C H. J. Org. Chem., 2011, 76: 3820-3828
[49]  Zhu B, Yuan F, Li R, Li Y, Wei Q, Ma Z, Du B, Zhang X. Chem. Commun., 2011, 47: 7098-7100
[50]  Jiang Y, Hu X, Hu J, Liu H, Zhong H, Liu S. Macromolecules, 2011, 44: 8780-8790
[51]  Fu L, Jiang F, Fortin D, Harvey P D, Liu Y. Chem. Commun., 2011, 47: 5503-5505
[52]  Lu H, Wang Q, Li Z, Lai G, Jiang J, Shen Z. Org. Biomol. Chem., 2011, 9: 4558-4562

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