毕业论文

打赏
当前位置: 毕业论文 > 文献综述 >

硝基控制的萘酰亚胺阴离子受体文献综述和参考文献(3)

时间:2020-10-06 09:47来源:毕业论文
检测CN的荧光传感器的开发,可以在含水介质中使用比只能在有机溶剂中检测的传感器更有意义。基于金属离子置换反应的传感器已发现适用于在含水介

    检测CN的荧光传感器的开发,可以在含水介质中使用比只能在有机溶剂中检测的传感器更有意义。基于金属离子置换反应的传感器已发现适用于在含水介质中检测CN。

    (3)  配体与CN反应

Schmittel等设计了两个钌络合物,以检测CN[56]。在乙腈中,此两个化合物472 nm和472 nm激发在732 nm处都有着微弱的发射。但在探针溶液中一旦加入2 eq CN,732 nm处的发射带消失,同时R17在624 nm,R18在614 nm处出现新的发射带。这些变化是因为CN与醛基发生亲核加成。此外,向含有R17和R18的溶液中加入CN,肉眼可以发现溶液颜色从橙红色变为黄色。

参考文献

[1] A. T. Wright and E. V. Anslyn, Chem. Soc. Rev., 2006, 35, 14.

[2]V. Amendola and L. Fabbrizzi, Chem. Commun., 2009, 513.

[3]L. Prodi, New J. Chem., 2005, 29, 20.

[4]J. Yoon, S. K. Kim, N. J. Singh and K. S. Kim, Chem. Soc. Rev.,2006, 35, 355.

[5]Fluorescent Chemosensors for Ion and Molecule Recognition,ed. A. W. Czarnik, American Chemical Society, Washington,D.C., 1992.

[6]B. C. Dickinson, D. Srikun and C. J. Chang, Curr. Opin. Chem.Biol., 2010, 14, 50.

[7]H. Kobayashi, M. Ogawa, R. Alford, P. L. Choyke and Y. Urano,Chem. Rev., 2010, 110, 2620.

[8]R. W. Sinkeldam, N. J. Greco and Y. Tor, Chem. Rev., 2010, 110,2579.

[9] C. Lodeiro, J. L. Capelo, J. C. Mejuto, E. Oliveira, H. M. Santos,B. Pedras and C. Nunez, Chem. Soc. Rev., 2010, 39, 2948.

[10] T. Gunnlaugsson, M. Glynn, G. M. Tocci, P. E. Kruger and F. M. Pfeffer, Coord. Chem. Rev., 2006, 250, 3094.

[11] P. J. Jiang and Z. J. Guo, Coord. Chem. Rev., 2004, 248, 205.

[12] T. W. Bell and N. M. Hext, Chem. Soc. Rev., 2004, 33, 589.

[13]K. W. Kulig, Cyanide Toxicity, U.S. Department of Health and Human Services, Atlanta, GA, 1991.

[14]Guidelines for Drinking-Water Quality, World Health Organization,Geneva, 1996.

[15] R. Takano, J. Exp. Med., 1916, 24, 207–211.

[16]S. I. Baskin and T. G. Brewer, in Medical Aspects of Chemical and Biological Warfare, ed. F. Sidell, E. T. Takafuji and D. R. Franz, TMM Publication, Washington, DC, 1997, ch.10, pp. 271–286.

[17] D. Shan, C. Mousty and S. Cosnier, Anal. Chem., 2004, 76,178–183.

[18] (a) Hudnall, T. W.; Gabbaı, F. P. J. Am. Chem. Soc. 2007, 129, 11978–11986. (b) Kim, Y.; Zhao, H.; Gabbaı , F P. Angew. Chem., Int. Ed.2009, 48, 4957–4960.

[19] Badugu, R.; Lakowicz, J R.; Geddes, C. D. J. Am. Chem. Soc. 2005,127, 3635–3641.

[20] Kim, Y.-H.; Hong, J.-I. Chem. Commun. 2002, 512–513.

[21] Chow, C -F.; Lam, M H W.; Wong, W –Y. Inorg. Chem. 2004, 43, 8387–8393.

[22] (a) Zelder, F. H. Inorg. Chem. 2008, 47, 1264–1266. (b) MannelCroise, C.; Zelder, F. Inorg. Chem. 2009, 48, 1272–1274.

[23]Lou, X.; Zhang, L.; Qin, J.; Li, Z. Chem. Commun. 2008, 5848–5850.

[24]Touceda-Varela, A.; Stevenson, E. I.; Galve-Gasio ´n, J. A.; Dryden, D. T. F.; Mareque-Rivas, J. C. Chem. Commun. 2008, 1998–2000.

[25] Zeng, Q.; Cai, P.; Li, Z.; Qin, J.; Tang, B. Z. Chem. Commun. 2008, 1094–1096.

[26] Li, Z. a.; Lou, X.; Yu, H.; Li, Z.; Qin, J. Macromolecules 2008, 41, 7433–7439.

[27] Shang, L.; Zhang, L.; Dong, S. Analyst 2009, 134, 107–113.

[28] Ros-Lis, J. V.; Martı ´nez-Ma ´n ˜ez, R.; Soto, J. Chem. Commun. 2002, 2248–2249.

[29] (a) Chung, Y. M.; Raman, B.; Kim, D.-S.; Ahn, K. H. Chem. Commun.2006, 186–188. (b) Chung, Y.; Lee, H.; Ahn, K. H. J. Org. Chem.2006, 71, 9470–9474. (c) Miyaji, H.; Kim, D.-S.; Chang, B.-Y.; Park, E.; Park, S.-M.; Ahn, K. H. Chem. Commun. 2008, 753–755. (d) Lee,H.; Chung, Y. M.; Ahn, K. H. Tetrahedron Lett. 2008, 49, 5544–5547. 硝基控制的萘酰亚胺阴离子受体文献综述和参考文献(3):http://www.751com.cn/wenxian/lunwen_62381.html

------分隔线----------------------------
推荐内容