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Volumn 5, Issue 2, 2003, Pages 163-169

3-Methylimidazolium bromohydrogenates(I): A room-temperature ionic liquid for ether cleavage

Author keywords

[No Author keywords available]

Indexed keywords

1 METHYLIMIDAZOLE; ALCOHOL DERIVATIVE; ALKYL ETHER; BROMINE DERIVATIVE; ETHER DERIVATIVE; HYDROBROMIC ACID; IMIDAZOLE DERIVATIVE; IONIC LIQUID; PHENOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0344392733     PISSN: 14639262     EISSN: None     Source Type: Journal    
DOI: 10.1039/b211548d     Document Type: Article
Times cited : (89)

References (46)
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    • (a) J. Shabtai, W. Zmierczak, S. Kadangode, E. Chornet and D. K. Johnson, Lignin conversion to high-octane fuel additives, Biomass: A Growth Opportunity in Green Energy and Value-Added Products, Proceedings of the Biomass Conference of the Americas, 4th, Oakland, California, Aug. 29-Sept. 2, 1999;
    • (1999) Lignin Conversion to High- Octane Fuel Additives
    • Shabtai, J.1    Zmierczak, W.2    Kadangode, S.3    Chornet, E.4    Johnson, D.K.5
  • 8
    • 84988785050 scopus 로고
    • ed. E. Yeager and A. J. Salkind, John Wiley & Sons, New York
    • D. F. Evans and Sister M. A. Matesich, Techniques of Electrochemistry, ed. E. Yeager and A. J. Salkind, John Wiley & Sons, New York, 1973, vol. 2, p. 49.
    • (1973) Techniques of Electrochemistry , vol.2 , pp. 49
    • Evans, D.F.1    Matesich, S.M.A.2
  • 12
    • 0004306024 scopus 로고
    • ed. A. T. Blomquist and H. Wasserman, Academic Press Inc., New York
    • J. B. Stothers, Carbon-13 NMR Spectroscopy, ed. A. T. Blomquist and H. Wasserman, Academic Press Inc., New York, 1972, vol. 24, p. 128.
    • (1972) Carbon-13 NMR Spectroscopy , vol.24 , pp. 128
    • Stothers, J.B.1
  • 14
    • 0001593270 scopus 로고
    • ed. F. A. Cotton, John Wiley & Sons, New York
    • D. G. Tuck, Progress in Inorganic Chemistry, ed. F. A. Cotton, John Wiley & Sons, New York, 1968, vol. 9, pp. 161-194.
    • (1968) Progress in Inorganic Chemistry , vol.9 , pp. 161-194
    • Tuck, D.G.1
  • 23
    • 84988752584 scopus 로고    scopus 로고
    • note
    • It has become obvious through the course of this work that perhaps a cautionary comment regarding the 'solvent' effect on relative orders of acid or base strength is warranted. It seems as though the relative order of acid or base strength determined from aqueous studies has become generalized to a point where it has replaced the order determined from gas phase studies. That 1-methylimidazole could possibly retain its nitrogenic proton as the 3-methylimidazolium cation in the melt is not precluded by the fact that it does not do so in water or any other solvent because 1-methylimidazole is intrinsically a strong base.
  • 27
    • 84988741309 scopus 로고    scopus 로고
    • See ref. 11, p. 818
    • See ref. 11, p. 818.
  • 28
    • 0004182966 scopus 로고
    • Saunders College Publishing, New York, 2nd edn.
    • R. S. Drago, Physical Methods For Chemists, Saunders College Publishing, New York, 2nd edn., 1992, p. 270.
    • (1992) Physical Methods for Chemists , pp. 270
    • Drago, R.S.1
  • 31
  • 36
    • 84988747163 scopus 로고    scopus 로고
    • see ref. 5
    • (d) see ref. 5.
  • 37
    • 84988740870 scopus 로고    scopus 로고
    • note
    • Certain high melting alcohols may require a work up scheme if they can not be distilled or sublimed out of solution.
  • 41
    • 84988744088 scopus 로고    scopus 로고
    • see ref. 5
    • (d) see ref. 5.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.