Bulletin of the Korean Chemical Society

  • 제32권8호
  • /
  • Pages.2795-2798
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  • 2011
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Anion Effects on Structure and Properties of Bis(3-methylimidazolium-1-yl) Salts

  • Noh, Tae-Hwan (Department of Chemistry and Chemistry Institute of Functional Materials, Pusan National University) ;
  • Ahn, Jung-Min (Department of Chemistry and Chemistry Institute of Functional Materials, Pusan National University) ;
  • Na, Young-Mee (Department of Chemistry and Chemistry Institute of Functional Materials, Pusan National University) ;
  • Jung, Ok-Sang (Department of Chemistry and Chemistry Institute of Functional Materials, Pusan National University)
  • 투고 : 2011.06.13
  • 심사 : 2011.06.20
  • 발행 : 2011.08.20
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참고문헌

  1. Hurley, F. H.; Wier, T. P. J. Electrochem. Soc. 1951, 98, 203. https://doi.org/10.1149/1.2778132
  2. Plechkova, N. V.; Seddon, K. R.; Tundo, P.; Perosa, A.; Zecchini, F. Methods and Reagents for Green Chemistry; Wiley: New York; 2007; pp 103-130.
  3. Toma, S.; Meeiarova, M.; Sebesta, R. Eur. J. Org. Chem. 2009, 321.
  4. Plechkova, N. V.; Seddon, K. R. Chem. Soc. Rev. 2008, 37, 123. https://doi.org/10.1039/b006677j
  5. Welton, T. Coord. Chem. Rev. 2004, 248, 2459. https://doi.org/10.1016/j.ccr.2004.04.015
  6. Wasserscheid, P.; Keim, W. Angew. Chem., Int. Ed. 2000, 39, 3772. https://doi.org/10.1002/1521-3773(20001103)39:21<3772::AID-ANIE3772>3.0.CO;2-5
  7. Han, X.; Armstrong, D. W. Acc. Chem. Res. 2007, 40, 1079. https://doi.org/10.1021/ar700044y
  8. Huddleston, J. G.; Rogers, R. D. Chem. Commun. 1998, 1765.
  9. MacFarlane, D.; Forsyth, M. The Handbook of Ionic Liquids: Electrochemistry; Wiley-VCH: Weinheim, 2008.
  10. Jin, C.; Ye, C.; Phillips, B. S.; Zabinski, J. S.; Liu, X.; Liu, W.; Shreeve, J. M. J. Mater. Chem. 2006, 16, 1529. https://doi.org/10.1039/b517888f
  11. Anderson, J. L.; Armstrong, D. W. Anal. Chem. 2005, 77, 6453. https://doi.org/10.1021/ac051006f
  12. Lambertus, G. R.; Crank, J. A.; McGuigan, M. E.; Kendler, S.; Armstrong, D. W.; Sacks, R. D. J. Chromatogr. A 2006, 1135, 230. https://doi.org/10.1016/j.chroma.2006.09.086
  13. Anderson, J. L.; Ding, R.; Ellern, A.; Armstrong, D. W. J. Am. Chem. Soc. 2005, 127, 593. https://doi.org/10.1021/ja046521u
  14. Gale, P. A. Coord. Chem. Rev. 2001, 213, 79. https://doi.org/10.1016/S0010-8545(00)00364-7
  15. Jung, O.-S.; Kim, Y. J.; Lee, Y.-A.; Park, K.-M.; Lee, S. S. Inorg. Chem. 2003, 42, 844. https://doi.org/10.1021/ic025935q
  16. Withersby, M. A.; Blake, A. J.; Champness, N. R.; Hubberstey, P.; Li, W.-S.; Schroder, M. Angew. Chem., Int. Ed. Engl. 1997, 36, 2327. https://doi.org/10.1002/anie.199723271
  17. Lee, J. W.; Kim, E. A.; Kim, Y. J.; Lee, Y.-A.; Pak, Y.; Jung, O.-S. Inorg. Chem. 2005, 44, 3151. https://doi.org/10.1021/ic048537r
  18. Janiak, C.; Uehlin, L.; Wu, H.-P.; Klufers, P.; Piotrowski, H.; Scharmann, T. G. J. Chem. Soc., Dalton Trans. 1999, 3121.
  19. Reed, C. A. Acc. Chem. Res. 1998, 31, 133. https://doi.org/10.1021/ar970230r
  20. Campos-Fernandez, C. S.; Clerac, R.; Dunbar, K. R. Angew. Chem., Int. Ed. 1999, 38, 3477. https://doi.org/10.1002/(SICI)1521-3773(19991203)38:23<3477::AID-ANIE3477>3.0.CO;2-P
  21. Turner, B.; Shterenberg, A.; Kapon, M.; Suwinska, K.; Eichen, Y. Chem. Commun. 2001, 13.
  22. Sharma, C. V. K.; Griffin, S. T.; Rogers, R. D. Chem. Commun. 1998, 215.
  23. Lee, B. S.; Chi, Y. S.; Lee, J. K.; Choi, I. S.; Song, C. E.; Namgoong, S. K.; Lee, S.-G. J. Am. Chem. Soc. 2004, 126, 480. https://doi.org/10.1021/ja038405h
  24. Schmidtchen, F. P.; Berger, M. Chem. Rev. 1997, 97, 1609. https://doi.org/10.1021/cr9603845
  25. Beer, P. D. Acc. Chem. Res. 1998, 31, 71. https://doi.org/10.1021/ar9601555
  26. Beer, P. D.; Smith, D. K. Prog. Inorg. Chem. 1997, 46, 1. https://doi.org/10.1002/9780470166475.ch1
  27. Bonhote, P.; Dias, A.-P.; Papageorgiou, N.; Kalyanasundaram, K.; Gratzel, M. Inorg. Chem. 2006, 35, 1168.
  28. Siegel, E. J. Phys. Status Solidi A 1972, 11, 45. https://doi.org/10.1002/pssa.2210110104
  29. Dearden, J. C. Sci. Total Environ. 1991, 59, 109.
  30. Sheldrick, G. M. SHELXS-97: A Program for Structure Determination; University of Gottingen, Germany, 1997
  31. Sheldrick, G. M. SHELXL-97: A Program for Structure Refinement; University of Gottingen, Germany, 1997.

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  1. Specific Counterion Repercussions on the Thermal, pH-Response, and Electrochemical Properties of Side-Chain Leucine Based Chiral Polyelectrolytes vol.30, pp.44, 2014, https://doi.org/10.1021/la503452f
  2. Crystal structure of 1,1′-(pentane-1,5-diyl)bis(3-methyl-1H-imidazol-3-ium)bis(hexafluorophosphate), C13H22F12N4P2 vol.233, pp.4, 2018, https://doi.org/10.1515/ncrs-2018-0027
  3. Crystal structure of 1,1′-(hexane-1,6-diyl)bis(3-methyl-1H-imidazol-3-ium) bis(hexafluoro phosphate), C14H24F12N4P2 vol.232, pp.1, 2011, https://doi.org/10.1515/ncrs-2016-0153
  4. Crystal structure of 1,1′-(hexane-1,6-diyl)bis(3-methyl-1H-imidazol-3-ium) bis(hexafluoro phosphate), C14H24F12N4P2 vol.232, pp.1, 2011, https://doi.org/10.1515/ncrs-2016-0153
  5. Crystal structure of 1,1′-butanebis(3-methyl-1H-imidazol-3-ium)bis(hexafluorophosphate), C12H20F12N4P2 vol.232, pp.6, 2011, https://doi.org/10.1515/ncrs-2017-0135
  6. Crystal structure of 1,1′-butanebis(3-methyl-1H-imidazol-3-ium)bis(hexafluorophosphate), C12H20F12N4P2 vol.232, pp.6, 2011, https://doi.org/10.1515/ncrs-2017-0135