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Density Functional Theoretical Study on the Acid Dissociation Constant of an Emissive Analogue of Guanine

  • Lee, Yong-Jae (Department of Horticultural Bioscience, Pusan National University) ;
  • Jang, Yun Hee (Department of Materials Science and Engineering and Program for Integrated Molecular systems (PIMS), Gwangju Institute of Science and Technology) ;
  • Kim, Yongseong (Department of Science Education, Kyungnam University) ;
  • Hwang, Sungu (Department of Applied Nanoscience, Pusan National University)
  • 투고 : 2012.08.07
  • 심사 : 2012.09.21
  • 발행 : 2012.12.20

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참고문헌

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  3. Zhang, L.; Li, H.; Chen, X.; Cukier, R. I.; Bu, Y. J. Phys. Chem. B 2009, 113, 1173. https://doi.org/10.1021/jp8094648
  4. Shin, D.; Sinkeldam, R. W.; Tor, Y. J. Am. Chem. Soc. 2011, 133, 14912. https://doi.org/10.1021/ja206095a
  5. Hwang, S.; Jang, Y. H.; Cho, H.; Lee, Y.-J. Bull. Korean Chem. Soc. 2008, 29, 539. https://doi.org/10.5012/bkcs.2008.29.3.539
  6. Kim, Y.; Jang, Y. H.; Cho, H.; Hwang, S. Bull. Korean Chem. Soc. 2010, 31, 3013. https://doi.org/10.5012/bkcs.2010.31.10.3013
  7. Jang, Y. H.; Goddard, W. A., III; Noyes, K. T.; Sowers, L. C.; Hwang, S.; Chung, D. S. Chem. Res. Toxicol. 2002, 15, 1023. https://doi.org/10.1021/tx010146r
  8. Jang, Y. H.; Goddard, W. A., III; Noyes, K. T.; Sowers, L. C.; Hwang, S.; Chung, D. S. J. Phys. Chem. B 2003, 107, 344. https://doi.org/10.1021/jp020774x
  9. Rogstad, K. N.; Jang, Y. H.; Sowers, L. C.; Goddard, W. A., III Chem. Res. Toxicol. 2003, 16, 1455. https://doi.org/10.1021/tx034068e
  10. Hwang, S.; Jang, Y. H.; Cho, H.; Kim, Y. Bull. Korean Chem. Soc. 2010, 31, 168. https://doi.org/10.5012/bkcs.2010.31.01.168
  11. Jang, Y. H.; Hwang, S.; Chung, D. S. Chem. Lett. 2007, 36, 1496. https://doi.org/10.1246/cl.2007.1496
  12. Fox, J. J.; Wempen, I.; Hampton, A.; Doerr, I. L. J. Am. Chem. Soc. 1958, 80, 1669. https://doi.org/10.1021/ja01540a041

피인용 문헌

  1. Two-Photon-Induced Fluorescence of Isomorphic Nucleobase Analogs vol.15, pp.5, 2014, https://doi.org/10.1002/cphc.201400031
  2. Tautomers of a Fluorescent G Surrogate and Their Distinct Photophysics Provide Additional Information Channels vol.128, pp.28, 2016, https://doi.org/10.1002/ange.201601688
  3. Tautomers of a Fluorescent G Surrogate and Their Distinct Photophysics Provide Additional Information Channels vol.55, pp.28, 2016, https://doi.org/10.1002/anie.201601688
  4. Polymerase-Mediated Site-Specific Incorporation of a Synthetic Fluorescent Isomorphic G Surrogate into RNA vol.56, pp.5, 2016, https://doi.org/10.1002/anie.201609327
  5. , and NADPH vol.130, pp.4, 2017, https://doi.org/10.1002/ange.201711935
  6. , and NADPH vol.57, pp.4, 2017, https://doi.org/10.1002/anie.201711935
  7. Pulse-shaped two-photon excitation of a fluorescent base analogue approaches single-molecule sensitivity vol.20, pp.45, 2018, https://doi.org/10.1039/C8CP05496G
  8. Conformation/Tautomerization effect on the pKa values of lumazine and 6‐thienyllumazine vol.27, pp.8, 2014, https://doi.org/10.1002/poc.3320
  9. Polymerase‐Mediated Site‐Specific Incorporation of a Synthetic Fluorescent Isomorphic G Surrogate into RNA vol.129, pp.5, 2012, https://doi.org/10.1002/ange.201609327