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Volumn 69, Issue 5, 2004, Pages 984-995

Attenuation of the substituent effects along the aliphatic chain

Author keywords

Ab initio calculations; Aliphatic compounds; Bicyclooctane derivatives; DFT; Inductive effect; Isodesmic reaction; Methylene groups; Reaction energy; Substituent effect

Indexed keywords

ALIPHATIC COMPOUND; BICYCLO[2.2.2]OCTANE DERIVATIVE; CARBENE; CARBENOID;

EID: 3242769876     PISSN: 00100765     EISSN: None     Source Type: Journal    
DOI: 10.1135/cccc20040984     Document Type: Article
Times cited : (4)

References (41)
  • 19
    • 0001895041 scopus 로고
    • N. B. Chapman and J. Shorter, Eds, Plenum Press, London
    • a) Exner O. in: Advances in Linear Free Energy Relationships (N. B. Chapman and J. Shorter, Eds), pp. 1-69. Plenum Press, London 1972;
    • (1972) Advances in Linear Free Energy Relationships , pp. 1-69
    • Exner, O.1
  • 37
    • 3242810033 scopus 로고    scopus 로고
    • Personal communication
    • For instance, attempts were unsuccessful to determine the gas-phase acidity of 2-chloroethanol: Gal J.-F., Maria P.-C.: Personal communication.
    • Gal, J.-F.1    Maria, P.-C.2
  • 41
    • 0003956918 scopus 로고
    • McGraw-Hill, New York
    • An almost identical opinion was offered by Hammett already in 1970: "Both the inductive effect and the electric field effect should be recognized as methods of mathematical approximation... The temptation to treat them as distinct physical phenomena should, however, be firmly resisted". Hammett L. P.: Physical Organic Chemistry, 2nd ed., p. 376. McGraw-Hill, New York 1970.
    • (1970) Physical Organic Chemistry, 2nd Ed. , pp. 376
    • Hammett, L.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.