DOI QR코드

DOI QR Code

First Hyperpolarizabilities of Nonlinear Optical Compounds: Susceptibility in Donor-Acceptor Stilbene Analogs

  • Park, Gyoo-Soon (Department of Chemistry, Kookmin University) ;
  • Jung, Woo-Sik (School of Chemical Engineering and Technology, Yeungnam University) ;
  • Ra, Choon-Sup (Department of Chemistry and Institute of Natural Science, Yeungnam University)
  • 발행 : 2004.09.20

초록

키워드

참고문헌

  1. Parasad, P. N.; Williams, D. J. Introduction to Nonlinear OpticalEffects in Molecules and Polymers; John Wiley & Sons: NewYork, 1991.
  2. Zyss, J. Molecular Nonlinear Optics: Materials, Physics andDevices; Academic Press: Boston, 1993.
  3. Nalwa, H. S., Miyata,S., Eds. Nonlinear Optics of Organic Molecules and Polymers;CRC Press: Boca Raton, FL, 1997.
  4. Marder, S. R.; Kippelen, B.; Jen, A. K.-Y.; Peyghambarian, N.Nature 1997, 388, 845. https://doi.org/10.1038/42190
  5. Shi, Y.; Zhang, C.; Bechtel, J. H.; Dalton, L. R.; Robinson, B. H.;Steier, W. H. Science 2000, 288, 119. https://doi.org/10.1126/science.288.5463.119
  6. Zhang, Y.; Burzynski, R.; Ghosal, S.; Casstsvens, M. K. Adv.Mater. 1996, 8, 111. https://doi.org/10.1002/adma.19960080203
  7. Dalton, L. R.; Steier, W. H.; Robinson, B.H.; Zhang, C.; Ren, A.; Garner, S.; Chen, A.; Londergan, T.;Irwin, L.; Carlson, B.; Fifield, L.; Phelan, G.; Kincaid, C.; Amend,J.; Jen, A. J. Mater. Chem. 1999, 9, 1905.
  8. Kajzar, F.; Lee, K.S.; Jen, A. K.-Y. Adv. Polym. Sci. 2003, 161, 1. https://doi.org/10.1007/3-540-45642-2_1
  9. Singer, K. D.; Sohn, J. E.; King, L. A.; Gorden, H. M.; Katz,H. E.; Dirk, C. W. J. Opt. Soc. Am. B 1989, 6, 1339. https://doi.org/10.1364/JOSAB.6.001339
  10. Cheng, L.-T.; Tam, W.; Stevenson, S. H.; Meredith, G. R.; Rikken, G.;Marder, S. R. J. Phys. Chem. 1991, 95, 10631. https://doi.org/10.1021/j100179a026
  11. Cheng, L. T.;Tam, W.; Marder, S. R.; Steigman, A. E.; Rikken, G.; Spangler, C.W. J. Phys. Chem. 1991, 95, 10643. https://doi.org/10.1021/j100179a027
  12. Rao, V. P.; Jen, A. K.-Y.; Wong, K. Y.; Drost, K. J. TetrahedronLett. 1993, 34, 1747. https://doi.org/10.1016/S0040-4039(00)60768-2
  13. Jen, A. K.-Y.; Cai, Y. M.; Bedworth, P. V.;Marder, S. R. Adv. Mater. 1997, 9, 132. https://doi.org/10.1002/adma.19970090207
  14. Cho, B. R.; Son, K. N.;Lee, S. J.; Kang, T. I.; Han, M. S.; Jeon, S..J.; Song, N. W.; Kim,D. Tetrahedron Lett. 1998, 39, 3167. https://doi.org/10.1016/S0040-4039(98)00450-X
  15. Song, S.; Lee, S. J.; Cho,B. R.; Shin, D.-H.; Park, K. H.; Lee, C. J.; Kim, N. Chem. Mater.1999, 11, 1406. https://doi.org/10.1021/cm9901313
  16. Shu, C.-F.; Wang, Y. K. J. Mater. Chem. 1998,8, 833. https://doi.org/10.1039/a708689j
  17. Brasselet, S.; Cherioux, F.; Audebert, P.; Zyss, J. Chem.Mater. 1999, 11, 1915. https://doi.org/10.1021/cm990093n
  18. Varanasi, P. R.; Jen, A. K.-Y.; Chandrasekhar, J.; Namboothiri, I.N. N.; Rathna, A. J. Am. Chem. Soc. 1996, 118, 12443. https://doi.org/10.1021/ja960136q
  19. Albert, I. D. L.; Marks, T. J.; Ratner, M. A. J. Am. Chem. Soc.1997, 119, 6575. https://doi.org/10.1021/ja962968u
  20. Breitung, E. M.; Shu, C.-F.; McMahon, R. J. J. Am. Chem. Soc.2000, 122, 1154. https://doi.org/10.1021/ja9930364
  21. Gaussian 98, Revision A.7, Frisch, M. J. et al., Gaussian, Inc.,Pittsburgh, PA, 2002.
  22. Whitaker, C. M.; Patterson, E. V.; Kott, K. L.;McMahon, R. J. J. Am. Chem. Soc. 1996, 118, 9966. https://doi.org/10.1021/ja960284g
  23. Park,G.; Ra, C. S.; Cho, B. R. Bull. Korean Chem. Soc. 2003, 24,1671. https://doi.org/10.5012/bkcs.2003.24.11.1671
  24. Mishima, M.;Mustanir, M. F.; Tsuno, Y. Bull. Chem. Soc. Jpn. 1996, 69, 2009. https://doi.org/10.1246/bcsj.69.2009
  25. Park, G.; Cho, B. R. J. Phy. Org. Chem. 2004, 17, 169. https://doi.org/10.1002/poc.709
  26. Park, G.; Ra, C. S. Bull. Korean. Chem. Soc. 2003, 24, 1051. https://doi.org/10.5012/bkcs.2003.24.8.1051
  27. Ra, C. S.; Kim, S. C.; Park, G. J. Mol. Struct. (Theochem)2004, 677, 173. https://doi.org/10.1016/j.theochem.2004.01.025

피인용 문헌

  1. Growth and nonlinear optical studies of N-acetyl-L-cysteine crystal vol.57, pp.1, 2012, https://doi.org/10.1051/epjap/2011110263
  2. -Pyran-4-ylidene Donor-Based Chromophores: The Relevance of the Location of a Thiophene Ring in the Spacer vol.77, pp.10, 2012, https://doi.org/10.1021/jo300373m
  3. Redetermination of 4-nitrostilbene vol.64, pp.12, 2008, https://doi.org/10.1107/S1600536808035459
  4. Physicochemical properties of highly efficient organic NLO crystal: 4-Aminobenzamide vol.128, pp.1, 2004, https://doi.org/10.1016/j.matchemphys.2011.02.043
  5. Monosubstituted acetonitriles: Structure, spectroscopic characterization and hyperpolarizabilities vol.35, pp.3, 2004, https://doi.org/10.1016/j.optmat.2012.09.001
  6. Theoretical study of borazine and substituted borazines using density functional theory method vol.193, pp.None, 2004, https://doi.org/10.1016/j.molliq.2013.12.011
  7. Spectroscopy and second hyperpolarizability of odd spin states of acetonitrile: Theoretical study vol.265, pp.None, 2004, https://doi.org/10.1016/j.saa.2021.120389