References
- Wei, Y.; Chen, C.-T. J. Am. Chem. Soc. 2007, 129, 7478 https://doi.org/10.1021/ja070822x
- Balan, B.; Gopidas, K. R. Chem. Eur. J. 2007, 13, 5173 https://doi.org/10.1002/chem.200601756
- Hauser, P. C.; Liang, C. L. C.; Mueller, B. Meas. Sci. Technol. 1995, 6, 1081 https://doi.org/10.1088/0957-0233/6/8/001
- Kang, Y.; Moon, S.-T.; Park, S.; Kim, J.; Lee, S. S.; Park, K.-M. Bull. Kor. Chem. Soc. 2007, 28, 873 https://doi.org/10.5012/bkcs.2007.28.5.873
- An, B.-K.; Kwon, S.-K.; Park, S. Y. Bull. Korean Chem. Soc. 2005, 26, 1555 https://doi.org/10.5012/bkcs.2005.26.10.1555
- Mattoussi, H.; Murata, H.; Merritt, C. D.; Iizumi, Y.; Kido, J.; Kafafi, Z. H. J. Appl. Phys. 1999, 86, 2642 https://doi.org/10.1063/1.371104
- Choi, K.; Lee, C.; Lee, K. H.; Park, S. J.; Son, S. U.; Chung, Y. K.; Hong, J.-I. Bull. Korean Chem. Soc. 2006, 27, 1549 https://doi.org/10.5012/bkcs.2006.27.10.1549
- Tao, S.; Peng, Z.; Zhang, X.; Wang, P.; Lee, C.-S.; Lee, S.-T. Adv. Funct. Mater. 2005, 15, 1716 https://doi.org/10.1002/adfm.200500067
- Lim, S.-J.; An, B.-K.; Jung, S. D.; Chung, M.-A.; Park, S. Y. Angew. Chem. Int. Ed. 2004, 43, 6346 https://doi.org/10.1002/anie.200461172
- Lee, J. H.; Hwang, D. H. Chem. Commun. 2003, 2836
- Zeng, Q.; Li, Z.; Dong, Y.; Di, C.; Qin, A.; Hong, Y.; Ji, L.; Zhu, Z.; Jim, C. K. W.; Yu, G.; Li, Q.; Li, Z.; Liu, Y.; Qin, J.; Tang, B. Z. Chem. Commun. 2007, 1, 70
- Han, M.; Lee, S.; Jung, J.; Park, K.-M.; Kwon, S.-K.; Ko, J.; Lee, P. H.; Kang, Y. Tetrahedron 2006, 62, 9769 https://doi.org/10.1016/j.tet.2006.07.065
- Lakowicz, J. R. Principles of Fluorescence Spcetroscopy; Kluwer Academic: New York, 1996
- Williams, A. T. R.; Winfield, S. A.; Miller, J. N. Analyst 1983, 108, 1067 https://doi.org/10.1039/an9830801067
- Morrison, D. J.; Trefz, T. K.; Piers, W. E.; McDonald, R.; Parvez, M. J. Org. Chem. 2005, 70, 5309 https://doi.org/10.1021/jo0506231
- Liu, X.-M.; He, C.; Huang, J.; Xu, J. Chem. Mater. 2005, 17, 434. (references cited therein) https://doi.org/10.1021/cm048719j
- Yamada, S.; Ishii, E.; Konno, T.; Ishihara, T. Org. Biomol. Chem. 2007, 5, 1442 https://doi.org/10.1039/b701702b
- Bruker, SAINTPLUS NT Version 6.22. Software Reference Manual; Bruker AXS: Madison, Wisconsin, 2000
- Bruker, SHELXTL NT Version 6.10. Program for Solution and Refinement of Crystal Structures; Bruker AXS: Madison, Wisconsin, 2000
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