Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Coumarin-Based Organogel Formed at Different Solvent Compositions and Their Luminescent Properties

  • Jung, Jin Hwan (Department of Chemistry and Research Institute of Natural Sciences, Gyeongsang National University) ;
  • Lee, Seon-Ae (Department of Chemistry and Research Institute of Natural Sciences, Gyeongsang National University) ;
  • Lee, Ji Ha (Department of Chemistry and Research Institute of Natural Sciences, Gyeongsang National University) ;
  • Choi, Heekyoung (Department of Chemistry and Research Institute of Natural Sciences, Gyeongsang National University) ;
  • Park, Jaehyeon (Department of Chemistry and Research Institute of Natural Sciences, Gyeongsang National University) ;
  • Kwon, Ki-Young (Department of Chemistry and Research Institute of Natural Sciences, Gyeongsang National University) ;
  • Choi, Myong Yong (Department of Chemistry and Research Institute of Natural Sciences, Gyeongsang National University) ;
  • Jung, Jong Hwa (Department of Chemistry and Research Institute of Natural Sciences, Gyeongsang National University)
  • Received : 2014.08.20
  • Accepted : 2014.09.01
  • Published : 2014.12.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Abdallah, D. J.; Weiss, R. G. Adv. Mater. 2000, 12, 1237. https://doi.org/10.1002/1521-4095(200009)12:17<1237::AID-ADMA1237>3.0.CO;2-B
  2. Oda, R.; Huc, I.; Candau, S. J. Angew. Chem., Int. Ed. 1998, 37, 2689. https://doi.org/10.1002/(SICI)1521-3773(19981016)37:19<2689::AID-ANIE2689>3.0.CO;2-Z
  3. Kitahara, T.; Shirakawa, M.; Kawano, S.-I.; Beginn, U.; Fujita, N.; Shinkai, S. J. Am. Chem. Soc. 2005, 127, 14980. https://doi.org/10.1021/ja0552038
  4. Shirakawa, M.; Fujita, N.; Shinkai, S. J. Am. Chem. Soc. 2005, 127, 4164. https://doi.org/10.1021/ja042869d
  5. Percec, V.; Glodde, M.; Bera, T. K.; Miura, Y.; Shiyanovskaya, I.; Singer, K. D.; Balagurusamy, V. S. K.; Heiney, P. A.; Schnell, I.; Rapp, A.; Spiess, H. W.; Hudson, S. D.; Duan, H. Nature 2002, 419, 384.
  6. Xiang, W.; Huang, W.; Bach, U.; Spiccia, L. Chem. Commun. 2013, 49, 8997, https://doi.org/10.1039/c3cc44555k
  7. Rodriguez-Llansola, F.; Escuder, B.; Miravet, J. F. J. Am. Chem. Soc. 2009, 131, 11478. https://doi.org/10.1021/ja902589f
  8. Xing, B.; Choi, M. F.; Xu, B. Chem. Eur. J. 2002, 8, 5028. https://doi.org/10.1002/1521-3765(20021104)8:21<5028::AID-CHEM5028>3.0.CO;2-1
  9. Reddy, T. T.; Lavenant, L.; Lefebvre, J.; Renard, D. Biomacromolecules 2006, 7, 323. https://doi.org/10.1021/bm050688d
  10. Jeong, B.; Kim, S. W.; Bae, Y. H. Adv. Drug Delivery Rev. 2002, 54, 37. https://doi.org/10.1016/S0169-409X(01)00242-3
  11. Jeong, B.; Bae, Y. H.; Kim, S. W. J. Controlled Release 2000, 63, 155. https://doi.org/10.1016/S0168-3659(99)00194-7
  12. Hirst, A. R.; Escuder, B.; Miravet, J. F.; Smith, D. K. Angew. Chem., Int. Ed. 2008, 47, 8002. https://doi.org/10.1002/anie.200800022
  13. Foster, J. A.; Steed, J. W. Angew. Chem., Int. Ed. 2010, 49, 6718. https://doi.org/10.1002/anie.201000070
  14. Park, J.; Lee, J. H.; Jaworski, J.; Shinkai, S.; Jung, J. H. Inorg. Chem. 2014, 53, 7181. https://doi.org/10.1021/ic500266f
  15. Tam, A. Y.; Yam, V. W. W. Chem. Soc. Rev. 2013, 42, 1540. https://doi.org/10.1039/c2cs35354g
  16. Moore, T. A.; Harter, M. L.; Song, P.-S. J. Mol. Spectrosc. 1971, 40, 144. https://doi.org/10.1016/0022-2852(71)90016-6
  17. Yuan, W. Z.; Lu, P.; Chen, S.; Lam, J. W. Y.; Wang, Z.; Liu, Y.; Kwok, H. S.; Ma, Y.; Tang, B. Z. Adv. Mater. 2010, 22, 2159. https://doi.org/10.1002/adma.200904056
  18. Ding, D.; Li, K.; Liu, B.; Tang, B. Z. Acc. Chem. Res. 2013, 46, 2441. https://doi.org/10.1021/ar3003464

Cited by

  1. Chiral Supramolecular Gels with Lanthanide Ions: Correlation between Luminescence and Helical Pitch vol.9, pp.4, 2017, https://doi.org/10.1021/acsami.6b13916