References
- Cho, D.-G.; Sessler, J. L. Chem. Soc. Rev. 2009, 38, 1647. https://doi.org/10.1039/b804436h
- Caltagirone, C.; Gale, P. A. Chem. Soc. Rev. 2009, 38, 520. https://doi.org/10.1039/b806422a
- Gale, P. A.; Garcia-Garrido, S. E.; Garric, J. Chem. Soc. Rev. 2008, 37, 151. https://doi.org/10.1039/b715825d
- Zimmermann-Dimer, L. M.; Machado, V. G. Quim. Nova 2008, 31, 2134. https://doi.org/10.1590/S0100-40422008000800038
- Anslyn, E. V. J. Org. Chem. 2007, 72, 687. https://doi.org/10.1021/jo0617971
- Nguyen, B. T.; Anslyn, E. V. Coord. Chem. Rev. 2006, 250, 3118. https://doi.org/10.1016/j.ccr.2006.04.009
- Gunnlaugsson, T.; Glynn, M.; Tocci, G. M.; Kruger, P. E.; Pfeffer, F. M. Coord. Chem. Rev. 2006, 250, 3094. https://doi.org/10.1016/j.ccr.2006.08.017
- Kubik, S.; Reyheller, C.; Stuwe, S. J. Inclusion Phenom. Macrocyclic Chem. 2005, 52, 137. https://doi.org/10.1007/s10847-005-0601-6
- Suksai, C.; Tuntulani, T. Chem. Soc. Rev. 2003, 32, 192. https://doi.org/10.1039/b209598j
- Martinez-Manez, R.; Sancenon, F. Chem. Rev. 2003, 103, 4419. https://doi.org/10.1021/cr010421e
- Xu, Z.; Chen, X.; Kim, H. N.; Yoon, J. Chem. Soc. Rev. 2010, 39, 127. https://doi.org/10.1039/b907368j
- World Health Organization, Concise International Chemical Assessment Document 61, Hydrogen Cyanide and Cyanides: Human Health Aspects; Geneva, 2004; pp 4-5. http:// www.who.int/ipcs/publications/cicad/en/cicad61.pdf (accessed January 09, 2009).
- Baskin, S. I.; Brewer, T. G. In Medical Aspects of Chemical and Biological Warfare; Sidell, F., Takafuji, E. T., Franz, D. R., Eds.; TMM Publications: Washington, DC, 1997; pp 271-286. Chapter 10.
- Vennesland, B.; Comm, E. E.; Knownles, C. J.; Westly, J.; Wissing, F. Cyanide in Biology; Academic Press: London, 1981.
- Ryall, B.; Davies, J. C.; Wilson, R.; Shoemark, A.; Williams, H. D. Eur. Respir. J. 2008, 32, 740. https://doi.org/10.1183/09031936.00159607
- Govan, J. R. W.; Deretic, V. Microbiol. Rev. 1996, 60, 539.
- The Agency for Toxic Substances and Disease Registry, Toxicological profile for cyanide, Atlanta, GA, US Department of Health and Human Services, pp 1-2, http://www.atsdr.cdc.gov/ toxprofiles/tp8-c1.pdf (accessed January 9, 2010).
- Young, C.; Tidwell, L.; Anderson, C. Cyanide: Social, Industrial, and Economic Aspects; Minerals, Metals, and Materials Society: Warrendale, 2001.
- Mak, K. K. W.; Yanase, H.; Renneberg, R. Biosens. Bioelectron. 2005, 20, 2581. https://doi.org/10.1016/j.bios.2004.09.015
- Xu, Z.; Pan, J.; Spring, D. R.; Cui, J.; Yoon, J. Tetrahedron 2010, 66, 1678. https://doi.org/10.1016/j.tet.2010.01.008
- Wang, J.; Ha, C.-S. Tetrahedron 2010, 66, 1846. https://doi.org/10.1016/j.tet.2010.01.031
- Lee, J. H.; Jeong, A. R.; Shin, I.-S.; Kim, H.-J.; Hong, J.- I. Org. Lett. 2010, 12, 764. https://doi.org/10.1021/ol902852g
- Lee, G. W.; Kim, N.-K.; Jeong, K.- S. Org. Lett. 2010, 12, 2634. https://doi.org/10.1021/ol100830b
- Saha, S.; Ghosh, A.; Mahato, P.; Mishra, S.; Mishra, S. K.; Suresh, E.; Das, S.; Das, A. Org. Lett. 2010, 12, 3406. https://doi.org/10.1021/ol101281x
- Hong, S.-J.; Yoo, J.; Kim, S.-H.; Kim, J. S.; Yoon, J.; Lee, C.-H. Chem. Commun. 2009, 189.
- Lee, K.-S.; Lee, J. T.; Hong, J.-I.; Kim, H.-J. Chem. Lett. 2007, 36, 816. https://doi.org/10.1246/cl.2007.816
- Chen, C.-L.; Chen, Y.-H.; Chen, C.-Y.; Sun, S.-S. Org. Lett. 2006, 8, 5053. https://doi.org/10.1021/ol061969g
- Kim, Y. H.; Hong, J. I. Chem. Commun. 2002, 512.
- Anzenbacher, P. Jr.; Tyson, D. S.; Jursikova, K.; Castellano, F. N. J. Am. Chem. Soc. 2002, 124, 6232. https://doi.org/10.1021/ja0259180
- Chow, C. F.; Lam, M. H. W.; Wong, W. Y. Inorg. Chem. 2004, 43, 8387. https://doi.org/10.1021/ic0492587
- Badugu, R., Lakowicz, J. R.; Geddes, C. D. J. Am. Chem. Soc. 2005, 127, 3635. https://doi.org/10.1021/ja044421i
- Ros-Lis, J. V.; Martinez-Manez, R.; Soto, J. Chem. Commun. 2005, 5260.
- Sun, S. S.; Lees, A. J. Chem. Commun. 2000, 1687.
- Miyaji, H.; Sessler, J. L. Angew. Chem. Int. Ed. 2001, 40, 154. https://doi.org/10.1002/1521-3773(20010105)40:1<154::AID-ANIE154>3.0.CO;2-G
- Ganesh, V.; Sanz, M. P. C.; Mareque-Rivas, J. C. Chem. Commun. 2007, 5010.
- Zeng, Q.; Cai, P.; Li, Z.; Qin, J.; Tang, B. Z. Chem. Commun. 2008, 1094.
- Lou, X. D.; Zhang, L.; Qin, J.; Li, Z. Chem. Commun. 2008, 5848.
- Li, Z. A.; Lou, X. D.; Yu, H. B.; Li, Z.; Qin, J. Macromolecules 2008, 41, 7433. https://doi.org/10.1021/ma8013096
- Chung, S. Y.; Nam, S. W.; Lim, J.; Park, S.; Yoon, J. Chem. Commun. 2009, 2866.
- Tomasulo, M.; Sortino, S.; White, A. J. P.; Raymo, F. M. J. Org. Chem. 2006, 71, 744. https://doi.org/10.1021/jo052096r
- Ren, J. Q.; Zhu, W. H.; Tian, H. Talanta 2008, 75, 760. https://doi.org/10.1016/j.talanta.2007.12.024
- Garcia, F.; Garcia, J. M.; Garcia- Acosta, B.; Martinez-Manez, R.; Sancenon, F.; Soto, J. Chem. Commun. 2005, 2790.
- Ros-Lis, J. V.; Martinez-Manez, R.; Soto, J. Chem. Commun. 2002, 2248.
- Chung, Y.; Lee, H.; Ahn, K. H. J. Org. Chem. 2006, 71, 9470. https://doi.org/10.1021/jo061798t
- Yang, Y. K.; Tae, J. Org. Lett. 2006, 8, 5721. https://doi.org/10.1021/ol062323r
- Lee, K. S.; Kim, H. J.; Kim, G. H.; Shin, I.; Hong, J. I. Org. Lett. 2008, 10, 49. https://doi.org/10.1021/ol7025763
- Kwon, S. K.; Kou, S.; Kim, H. N.; Chen, X. Q.; Wang, H.; Nam, S. W.; Kim, S. H.; Swamy, K. M. K.; Park, S.; Yoon, J. Tetrahedron Lett. 2008, 49, 4102. https://doi.org/10.1016/j.tetlet.2008.04.139
- Park, S.; Kim, H. J. Chem. Commun. 2010, 9197.
- Chung, Y. M.; Raman, B.; Kim, D. S.; Ahn, K. H. Chem. Commun. 2006, 186.
- Ryu, D.; Park, E.; Kim, D. S.; Yan, S.; Lee, J. Y.; Chang, B. Y.; Ahn, K. H. J. Am. Chem. Soc. 2008, 130, 2394. https://doi.org/10.1021/ja078308e
- Niu, H. T.; Jiang, X. L.; He, J. Q.; Cheng, J. P. Tetrahedron Lett. 2008, 49, 6521. https://doi.org/10.1016/j.tetlet.2008.08.115
- Niu, H. T.; Su, D.; Jiang, X.; Yang, W.; Yin, Z.; He, J.; Cheng, J. P. Org. Biomol. Chem. 2008, 6, 3038. https://doi.org/10.1039/b808589g
- Ekmekci, Z.; Yilmaz, M. D.; Akkaya, E. U. Org. Lett. 2008, 10, 461. https://doi.org/10.1021/ol702823u
- Yoon, S.; Albers, A. E.; Wong, A. P.; Chang, C. J. J. Am. Chem. Soc. 2005, 127, 16030. https://doi.org/10.1021/ja0557987
- Helal, A.; Thao, N. T. T.; Lee, S.; Kim, H.-S. J. Inclusion Phenom. Macrocyclic Chem. 2010, 66, 87. https://doi.org/10.1007/s10847-009-9648-0
- Helal, A.; Kim, H.-S. Tetrahedron Lett. 2009, 50, 5510. https://doi.org/10.1016/j.tetlet.2009.07.078
- Helal, A.; Lee, S. H.; Kim, S. H.; Kim, H.-S. Tetrahedron Lett. 2010, 51, 3531. https://doi.org/10.1016/j.tetlet.2010.04.126
- Helal, A.; Rashid, M. H. O.; Choi, C.-H.; Kim, H.-S. Tetrahedron 2011, 67, 2794. https://doi.org/10.1016/j.tet.2011.01.093
- Kramer, R. Angew. Chem. Int. Ed. 1998, 37, 772. https://doi.org/10.1002/(SICI)1521-3773(19980403)37:6<772::AID-ANIE772>3.0.CO;2-Z
- Xiang, Y.; Tong, A.; Jin, P.; Ju, Y. Org. Lett. 2006, 8, 2863. https://doi.org/10.1021/ol0610340
- Chen, X.; Li, Z.; Xiang, Y.; Tong, A. Tetrahedron Lett. 2008, 49, 4697. https://doi.org/10.1016/j.tetlet.2008.05.137
- Keck, J.; Kramer, H. E. A.; Port, H.; Hirsch, T.; Fischer, P.; Rytz, G. J. Phys. Chem. 1996, 100, 14468. https://doi.org/10.1021/jp961081h
- Henary, M. M.; Fahrni, C. J. J. Phys. Chem. A 2002, 106, 5210. https://doi.org/10.1021/jp014634j
- Santra, S.; Krishnamoorthy, G.; Dogra, S. K. J. Phys. Chem. A 2000, 104, 476. https://doi.org/10.1021/jp992678a
- Mosquera, M.; Penedo, J. C.; Rios Rodriguez, M. C.; Rodriguez-Prieto, F. J. Phys. Chem. 1996, 100, 5398. https://doi.org/10.1021/jp9533638
- Das, K.; Sarkar, N.; Majumdar, D.; Bhattacharyya, K. Chem. Phys. Lett. 1992, 198, 443. https://doi.org/10.1016/0009-2614(92)80025-7
- Connors, K. A. Binding Constants: the Measurement of Molecular Complex Stability; New York: Wiley, 1987; pp 21-101; 339-343.
- Forgues, S. F.; LeBris, M. T.; Gutte, J. P.; Valuer, B. J. Phys. Chem. 1988, 92, 6233. https://doi.org/10.1021/j100333a013
- Thordarson, P. Chem. Soc. Rev. 2011, 40, 1305. https://doi.org/10.1039/c0cs00062k
- Fabbrizzi, L.; Licchelli, M.; Pallavicini, P.; Parodi, L.; Taglietti, A. In Transition Metals in Supramolecuar Chemistry; Sauvage, J. P., Ed.; Fluorescent Sensors for and with Transition Metals; John Wiley & Sons Ltd: Chichester, 1999.
- Ci, Y. X.; Zhou, T. Z. The Coordinated Complexes in Analytical Chemistry; Peking University Press: Beijing, 1984.
- Shortreed, M.; Kopelman, R.; Kuhn, M.; Hoyland, B. Anal. Chem. 1996, 68, 1414. https://doi.org/10.1021/ac950944k
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