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Volumn 94, Issue 9, 1972, Pages 3153-3159

Chemiluminescence of Linear Hydrazides

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EID: 0009435230     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00764a044     Document Type: Article
Times cited : (26)

References (61)
  • 30
    • 0003835653 scopus 로고
    • E. Arnold, London
    • A. Albert, “The Acridines,” E. Arnold, London, 1951, p 148.
    • (1951) The Acridines , pp. 148
    • Albert, A.1
  • 32
    • 33947090328 scopus 로고
    • Light emission from electronically excited acridone is discussed in the following paper
    • Light emission from electronically excited acridone is discussed in the following paper: E. Rapaport, M. W. Cass, and E. H. White, J. Amer. Chem. Soc., 94, 3160 (1972).
    • (1972) J. Amer. Chem. Soc. , vol.94 , pp. 3160
    • Rapaport, E.1    Cass, M.W.2    White, E.H.3
  • 35
    • 0343013983 scopus 로고
    • For a recent review on base-catalyzed autoxidation see D. Swern, Ed., Wiley-Interscience, New York, N. Y.
    • For a recent review on base-catalyzed autoxidation see G. Sosnovsky and E. H. Zaret in “Organic Peroxides,” Vol. 1, D. Swern, Ed., Wiley-Interscience, New York, N. Y., 1970, p 517.
    • (1970) Organic Peroxides , vol.1 , pp. 517
    • Sosnovsky, G.1    Zaret, E.H.2
  • 47
    • 0007292795 scopus 로고
    • For an example of basic autoxidation of a resonance-stabilized carbanion, see
    • For an example of basic autoxidation of a resonance-stabilized carbanion, see: G. A. Russell, A. G. Bemis, E. J. Geels, E. G. Janzen, and A. J. Moye, Advan. Chem. Ser., No. 75, 195 (1968).
    • (1968) Advan. Chem. Ser. , Issue.75 , pp. 195
    • Russell, G.A.1    Bemis, A.G.2    Geels, E.J.3    Janzen, E.G.4    Moye, A.J.5
  • 54
    • 0004290166 scopus 로고
    • McGraw-Hill, New York, N. Y.
    • W. A. Pryor in “Free Radicals,” McGraw-Hill, New York, N. Y., 1966;
    • (1966) Free Radicals
    • Pryor, W.A.1
  • 57
    • 0001408035 scopus 로고
    • The reduction of triphenylmethyl radical under reversible conditions has been recorded at -0.83 V relative to a silver perchlorate electrode, which in turn has a potential of +0.32 V vs. a saturated calomel electrode The calculated value for the reverse process of oxidation of triphenylmethide ion (relative to the standard hydrogen electrode) is +0.18 V. The corresponding value for the oxidation of the anion of triphenylcyclopropene is +0.91 V
    • The reduction of triphenylmethyl radical under reversible conditions has been recorded at -0.83 V relative to a silver perchlorate electrode, which in turn has a potential of +0.32 V vs. a saturated calomel electrode (R. Breslow and K. Balasubramanian, J. Amer. Chem. Soc., 91, 5182 (1969)). The calculated value for the reverse process of oxidation of triphenylmethide ion (relative to the standard hydrogen electrode) is +0.18 V. The corresponding value for the oxidation of the anion of triphenylcyclopropene is +0.91 V.
    • (1969) J. Amer. Chem. Soc. , vol.91 , pp. 5182
    • Breslow, R.1    Balasubramanian, K.2
  • 61
    • 0002057239 scopus 로고
    • F. H. Johnson and Y. Haneda, Ed., Princeton University Press, Princeton, N. J.
    • J. Lee, A. S. Wesley, J. F. Ferguson, and H. H. Seliger in “Bioluminescence in Progress,” F. H. Johnson and Y. Haneda, Ed., Princeton University Press, Princeton, N. J., 1966, p 35.
    • (1966) Bioluminescence in Progress , pp. 35
    • Lee, J.1    Wesley, A.S.2    Ferguson, J.F.3    Seliger, H.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.