Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Ratiometric Determination of Water Content in Acetonitrile by a Fluorescein Derivative Bearing Two Pyrene Subunits

  • Received : 2010.07.16
  • Accepted : 2010.08.10
  • Published : 2010.10.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Hisamoto, H.; Tohma, H.; Yamada, T.; Yamauchi, K.-I.; Siswanta, D.; Yoshioka, N.; Suzuki, K. Anal. Chim. Acta 1998, 373, 271. https://doi.org/10.1016/S0003-2670(98)00421-8
  2. Timm, R. A.; Falla, M. P. H.; Huila, M. F. G.; Peres, H. E. M.; Ramirez-Fernandez, F. J.; Araki, K.; Toma, H. E. Sens. Actuator B-Chem. 2010, 146, 61. https://doi.org/10.1016/j.snb.2010.01.045
  3. Vitha, M. F. J. Chem. Educ. 2001, 78, 370. https://doi.org/10.1021/ed078p370
  4. Wang, Q.; Li, X.; Wang, L.; Cheng, Y.; Xie, G. Ind. Eng. Chem. Res. 2005, 44, 4518. https://doi.org/10.1021/ie048755s
  5. Al-Zuhair, S.; Jayaraman, K. V.; Krishnan, S.; Chan, W.-H. Biochem. Eng. J. 2006, 30, 212. https://doi.org/10.1016/j.bej.2006.04.007
  6. O'Keefe, W. K.; Ng, F. T. T.; Rempel, G. L. J. Chromatogr. A 2008, 1182, 113. https://doi.org/10.1016/j.chroma.2007.12.044
  7. Nguyen, T. N. P.; Kim, K.-J. Ind. Eng. Chem. Res. 2010, 49, 4842. https://doi.org/10.1021/ie901677n
  8. Fischer, K. Angew. Chem. 1935, 48, 394. https://doi.org/10.1002/ange.19350482605
  9. Kestens, V.; Conneely, P.; Bernreuther, A. Food Chem. 2008, 106, 1454. https://doi.org/10.1016/j.foodchem.2007.01.079
  10. Desvergne, J. P.; Czarnik, A. W. Chemosensors of Ion and Molecule Recognition; Kluwer: Dordrecht, 1997.
  11. de Silva, A. P.; Gunaratne, H. Q. N.; Gunnlaugsson, T.; Huxley, A. J. M.; McCoy, C. P.; Rademacher, J. T.; Rice, T. E. Chem. Rev. 1997, 97, 1515. https://doi.org/10.1021/cr960386p
  12. Hisamoto, H.; Manabe, Y.; Yanai, H.; Tohma, H.; Yamada, T.; Suzuki, K. Anal. Chem. 1998, 70, 1255. https://doi.org/10.1021/ac970637+
  13. Citterio, D.; Kawada, T.; Yagi, J.; Ishigaki, T.; Hisamoto, H.; Sasaki, S. I.; Suzuki, K. Anal. Chim. Acta 2003, 482, 19. https://doi.org/10.1016/S0003-2670(03)00200-9
  14. Kumoi, S.; Kobayashi, H.; Ueno, K. Talanta 1972, 19, 505. https://doi.org/10.1016/0039-9140(72)80112-7
  15. Gruda, I.; Bolduc, F. J. Org. Chem. 1984, 49, 3300. https://doi.org/10.1021/jo00192a010
  16. Lu, H.; Rutan, S. C. Anal. Chem. 1996, 68, 1381. https://doi.org/10.1021/ac9507808
  17. Liu, W.; Wang, Y.; Jin, W.; Shen, G.; Yu, R. Anal. Chim. Acta 1999, 383, 299. https://doi.org/10.1016/S0003-2670(98)00789-2
  18. Niu, C. G.; Guan, A. L.; Zeng, G. M.; Liu, Y. G.; Li, Z. W. Anal. Chim. Acta 2006, 577, 264. https://doi.org/10.1016/j.aca.2006.06.046
  19. Ercelen, S.; Klymchenko, A. S.; Demchenko, A. P. Anal. Chim. Acta 2002, 464, 273. https://doi.org/10.1016/S0003-2670(02)00493-2
  20. Niu, C. G.; Qin, P. Z.; Zeng, G. M.; Gui, X. Q.; Guan, A. L. Anal. Bioanal. Chem. 2007, 387, 1067. https://doi.org/10.1007/s00216-006-1016-y
  21. Kim, K. N.; Song, K. C.; Noh, J. H.; Chang, S.-K. Bull. Korean Chem. Soc. 2009, 30, 197. https://doi.org/10.5012/bkcs.2009.30.1.197
  22. Lavis, L. D.; Raines, R. T. ACS Chem. Biol. 2008, 3, 142. https://doi.org/10.1021/cb700248m
  23. Choi, M. G.; Kim, M. H.; Kim, H. J.; Park, J. E.; Chang, S.-K. Bull. Korean Chem. Soc. 2007, 28, 1818. https://doi.org/10.5012/bkcs.2007.28.10.1818
  24. Valeur, B.; Leray, I. Coord. Chem. Rev. 2000, 205, 3. https://doi.org/10.1016/S0010-8545(00)00246-0
  25. Winnik, F. M. Chem. Rev. 1993, 93, 587. https://doi.org/10.1021/cr00018a001
  26. Margulies, D.; Felder, C. E.; Melman, G.; Shanzer, A. J. Am. Chem. Soc. 2007, 129, 347. https://doi.org/10.1021/ja065317z
  27. Xu, L.-W.; Xia, C.-G.; Li, L. J. Org. Chem. 2004, 69, 8482. https://doi.org/10.1021/jo048778g
  28. Arimori, S.; Consiglio, G. A.; Phillips, M. D.; James, T. D. Tetrahedron Lett. 2003, 44, 4789. https://doi.org/10.1016/S0040-4039(03)00942-0
  29. Marcus, E.; Fitzpatrick, J. T. J. Org. Chem. 1960, 25, 199. https://doi.org/10.1021/jo01072a012
  30. Dale, T. J.; Rebek, J., Jr. J. Am. Chem. Soc. 2006, 128, 4500. https://doi.org/10.1021/ja057449i
  31. Lakowick, J. R. Principles of Fluorescence Spectroscopy, 2nd ed.; Kluwer: New York, 1999; pp 185-194.
  32. Gawley, R. E.; Zhang, Q.; Higgs, P. I.; Wang, S.; Leblanc, R. M. Tetrahedron Lett. 1999, 40, 5461. https://doi.org/10.1016/S0040-4039(99)01066-7
  33. Pohlers, G.; Scaiano, J. C.; Sinta, R. Chem. Mater. 1997, 9, 3222. https://doi.org/10.1021/cm970587p
  34. Shao, N.; Wang, H.; Gao, X. D.; Yang, R. H.; Chan, W. H. Anal. Chem. 2010, 82, 4628. https://doi.org/10.1021/ac1008089
  35. Demerseman, P.; Tric, B.; Strapélias, H.; Royer, R. J. Heterocyclic Chem. 1985, 22, 1337. https://doi.org/10.1002/jhet.5570220539

Cited by

  1. Intramolecular Excimer Formation for Covalently Linked Boron Dipyrromethene Dyes vol.115, pp.44, 2011, https://doi.org/10.1021/jp2070419
  2. Highly sensitive fluorescent sensing for water based on poly(m-aminobenzoic acid) vol.48, pp.24, 2012, https://doi.org/10.1039/c2cc17856g
  3. Optode Membrane for Detecting a Wide Range of Water Content in Organic Solvents vol.36, pp.1, 2015, https://doi.org/10.1002/bkcs.10042
  4. 4-Amino-Benzo[F]Isoindole-1,3-Dione Derivatives As Turn-On Fluorescent Indicators For Water Determination In Acetonitrile vol.4, pp.None, 2018, https://doi.org/10.17721/moca.2018.183-191