全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
化学进展  2015 

基于脲衍生物阴离子识别的电化学检测

DOI: 10.7536/PC141108, PP. 559-570

Keywords: 阴离子识别,,电化学传感器

Full-Text   Cite this paper   Add to My Lib

Abstract:

作为优良的氢键给予体,脲基(—NH—CO—NH—)是构筑阴离子识别受体的理想结构单元.而电化学方法因其方便快捷、灵敏度高等优点,近年来被广泛应用于阴离子的识别检测.本文对脲类受体的电化学阴离子识别进行了讨论,主要包括(i)归纳整理了电化学阴离子识别的机理,包括识别位点与阴离子结合之后对氧化还原中心的5种扰动机理和溶液中电化学测试受体和阴离子相互作用时常见现象的分析及对应结合常数的计算;(ii)电活性脲类阴离子受体的研究进展,包括受体分子的设计、识别和机理;(iii)探讨了该领域的后续发展方向.

References

[1]  Sessler J L, Gale P A, Cho W-S. Anion Receptor Chemistry. Cambridge: The Royal Society of Chemistry, 2006, 327.
[2]  Beer P D, Gale P A. Angew. Chem. Int. Ed., 2001, 40: 486.
[3]  Bianchi A, Bowman-James K, Garcia-Espaa E. Supramolecular Chemistry of Anions. New York: Wiley-VCH, 1997.
[4]  Nijhuis C A, Ravoo B J, Huskens J, Reinhoudt D N. Coord. Chem. Rev., 2007, 251: 1761.
[5]  Bu J, Lilienthal N D, Woods J E, Nohrden C E, Hoang K T, Truong D, Smith D K. J. Am. Chem. Soc., 2005, 127: 6423.
[6]  Beer P D, Gale P A, Chen Z. Adv. Phys. Org. Chem. Bethell D Ed. London: Academic Press, 1998. Vol. 31, 1.
[7]  胡京汉(Hu J H), 陈娟娟(Chen J J), 李建斌(Li J B), 祁京(Qi J). 无机化学学报(Chin. J. Inorg. Chem.), 2014, 30: 2544.
[8]  Duke R M, Veale E B, Pfeffer F M, Kruger P E, Gunnlaugsson T. Chem. Soc. Rev., 2010, 39: 3936.
[9]  Gunnlaugsson T, Glynn M, Tocci G M, Kruger P E, Pfeffer F M. Coord. Chem. Rev., 2006, 250: 3094.
[10]  Xu Z, Chen X, Kim H N, Yoon J. Chem. Soc. Rev., 2010, 39: 127.
[11]  曾振亚(Zeng Z Y), 何永炳(He Y B), 孟令芝(Meng L Z). 化学进展(Prog. Chem.), 2005, 17(2): 254.
[12]  吴芳英(Wu F Y), 张煊(Zhang X), 江云宝(Jiang Y B). 高等学校化学学报(Chem. Res. Chin. Univ.), 2003, 24(11): 1990.
[13]  Nishizawa S, Bühlmann P, Iwao M, Umezawa Y. Tetra. Lett., 1995, 36: 6483.
[14]  Fan E, Van Arman S A, Kincaid S, Hamilton A D. J. Am. Chem. Soc., 1993, 115: 369.
[15]  Beer P D, Bayly S R. Top. Curr. Chem., 2005, 255: 125.
[16]  钱小红(Qian X H), 金灿(Jin C), 张晓宁(Zhang X N), 姜艳(Jiang Y), 林晨(Lin C), 王乐勇(Wang L Y). 化学进展(Prog. Chem.), 2014, 26(10): 1701.
[17]  Smith P J, Reddington M V, Wilcox C S. Tetrahedron Lett., 1992, 33: 6085.
[18]  Nishizawa S, Bühlmann P, Iwao M, Umezawa Y. Tetrahedron Lett., 1995, 36: 6483.
[19]  Li A-F, Wang J H, Wang F, Jiang Y B. Chem. Soc. Rev., 2010, 39: 3729.
[20]  Jagessar R C, Shang M, Scheidt W R, Burns D H. J. Am. Chem. Soc., 1998, 120: 11684.
[21]  Custelcean R, Moyer B A, Bryantsev V S, Hay B P. Cryst. Growth Des., 2006, 6: 555.
[22]  Gale P A. Chem. Soc. Rev., 2010, 39: 3746.
[23]  Wenzel M, Hiscock J R, Gale P A. Chem. Soc. Rev., 2012, 41: 480.
[24]  Gale P A, Busschaert N, Haynes C J E, Karagiannidis L E, Kirby I L. Chem. Soc. Rev., 2014, 43: 205.
[25]  魏梅莹(Wei M Y), 李少光(Li S G), 贾传东(Jia C D), 吴彪(Wu B). 高等学校化学学报(Chem. Res. Chin. Univ.), 2011, 32(9): 1939.
[26]  陈政(Chen Z). 科学(Science), 1995, 47(1): 40.
[27]  Miller S R, Gustowski D A, Chen Z H, Gokel G W, Echegoyen L, Kaifer A E. Anal. Chem., 1988, 60: 2021.
[28]  Amendola V, Fabbrizzi L, Mosca L. Chem. Soc. Rev., 2010, 39: 3889.
[29]  Pratt M D, Beer P D. Polyhedron, 2003, 22: 649.
[30]  Otón F, Tárraga A, Espinosa A, Velasco M D, Molina P. J. Org. Chem., 2006, 71: 4590.
[31]  Laurent P, Miyaji H, Collinson S R, Proke? I, Moody C J, Tucker J H R, Slawin A M Z. Org. Lett., 2002, 4: 4037.
[32]  Willener Y, Joly K M, Moody C J, Tucker J H R. J. Org. Chem., 2008, 73: 1225.
[33]  Otón X X, Tarraga A, Espinosa A, Velasco M D, Bautista D, Molina P. J. Org. Chem., 2005, 70: 6603.
[34]  Bard A J, Faulkner L R. Electrochemical Methods. New York: John Wiley & Sons, 1980, p29.
[35]  Evans A J, Matthews S E, Cowley A R, Beer P D. Dalton Trans., 2003: 4644.
[36]  Moon K, Kaifer A E. J. Am. Chem. Soc., 2004, 126: 15016.
[37]  Li M, Wu B, Jia C, Huang X, Zhao Q, Shao S, Yang X J. Chem. Eur. J., 2011, 17: 2272.
[38]  Li M, Hao Y, Wu B, Jia C, Huang X, Yang X J. Org. Biomol. Chem., 2011, 9: 5637.
[39]  Evans N H, Beer P D. Org. Bio. Chem., 2011, 9: 92.
[40]  Li M, Wu B, Cui F, Hao Y, Huang X, Yang X J. Z. Anorg. Allg. Chem., 2011, 637: 2306.
[41]  Huang X, Wu B, Jia C, Hay B P, Li M, Yang X J. Chem. Eur. J., 2013, 19: 9034.
[42]  Alonso B, Casado C M, Cuadrado I, Morána M, Kaifer A E. Chem. Commun., 2002, 1778.
[43]  王建军(Wang J J), 王立(Wang L), 王学杰(Wang X J). 化学进展(Prog. Chem.), 2003, 15(5): 409.
[44]  Valério C, Fillaut J L, Ruiz J, Guittard J, Blais J C, Astruc D. J. Am. Chem. Soc., 1997, 119: 2588.
[45]  Beer P D, Davis J J, Drillsma-Milgrom D A, Szemes F. Chem. Commun., 2002: 1716.
[46]  Cormode D P, Evans A J, Davis J J, Beer P D. Dalton Trans., 2010, 39: 6532.
[47]  Ito A, Sakamaki D, Ino H, Taniguchi A, Hirao Y, Tanaka K, Kanemoto K, Kato T. Eur. J. Org. Chem., 2009: 4441.
[48]  Clare J P, Statnikov A, Lynch V, Sargent A L, Sibert J W. J. Org. Chem., 2009, 74: 6637.
[49]  Mahmoud K, Long Y T, Schatte G, Kraatz H B. J. Organomet. Chem., 2004, 689: 2250.
[50]  Bu J, Lilienthal N D, Woods J E, Nohrden C E, Hoang K P, Truong D, Smith D K. J. Am. Chem. Soc., 2005, 127: 6423.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133