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Volumn 72, Issue 26, 2007, Pages 10022-10028

Substituent and solvent effects on the β-heterolysis reaction of β-hydroxy arylethyl radicals

Author keywords

[No Author keywords available]

Indexed keywords

PHOTOLYSIS; RATE CONSTANTS; REACTION KINETICS; SEMICONDUCTOR LASERS; STYRENE; SUBSTITUTION REACTIONS;

EID: 37549069364     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo701874f     Document Type: Article
Times cited : (6)

References (53)
  • 1
    • 0000489779 scopus 로고
    • Frey, P. A. Chem. Rev. 1990, 90, 1343-1357.
    • (1990) Chem. Rev , vol.90 , pp. 1343-1357
    • Frey, P.A.1
  • 30
    • 0000900930 scopus 로고
    • Springer-Verlag: New York
    • Schmittel, M. In Electron Transfer 1; Springer-Verlag: New York, 1994; Vol. 169, pp 183-230.
    • (1994) Electron Transfer 1 , vol.169 , pp. 183-230
    • Schmittel, M.1
  • 43
  • 48
    • 37549043006 scopus 로고    scopus 로고
    • It is possible that the precursor is partially protonated in acidic HFIP. If so, the radical/protonated radical equilibrium state in eq 4 might be accessed from both the neutral radical and the protonated radical sides of the equilibrium. This situation does not affect the analysis for the elimination of water from the radical, since the radical/protonated radical pre-equilibrium state will still be established prior to the elimination step.
    • It is possible that the precursor is partially protonated in acidic HFIP. If so, the radical/protonated radical equilibrium state in eq 4 might be accessed from both the neutral radical and the protonated radical sides of the equilibrium. This situation does not affect the analysis for the elimination of water from the radical, since the radical/protonated radical pre-equilibrium state will still be established prior to the elimination step.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.