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Volumn 131, Issue 44, 2009, Pages 16162-16170

Steric and solvation effects in ionic SN2 reactions

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL ALCOHOLS; CHLORIDE IONS; CURRENT SYSTEM; GASPHASE; IONIC SOLVATION; IONIC SYSTEMS; MODEL SYSTEM; POLARIZABLE CONTINUUM MODEL; SHARP CONTRAST; SHIELDING EFFECT; SIZE DEPENDENCE; SOLVATION EFFECT; SOLVATION ENERGY; STERIC EFFECT; STERIC HINDRANCE EFFECTS; TRANSITION STATE;

EID: 70450195860     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9053459     Document Type: Article
Times cited : (72)

References (67)
  • 1
    • 0004028219 scopus 로고
    • Newman, M. S., Ed.; John Wiley and Sons: New York
    • Steric Effects in Organic Chemistry; Newman, M. S., Ed.; John Wiley and Sons: New York, 1956.
    • (1956) Steric Effects in Organic Chemistry
  • 2
    • 70450218615 scopus 로고
    • Ingold, C. K
    • 2nd ed.; Cornell University Press: Ithaca
    • Ingold, C. K. Structure and Mechanism in Organic Chemistry, 2nd ed.; Cornell University Press: Ithaca, 1969.
    • (1969) Structure and Mechanism in Organic Chemistry
  • 7
    • 70450220944 scopus 로고    scopus 로고
    • They may also be called ethyl, n-propyl, iso-butyl, neo-pentyl groups if the center carbon is also counted
    • They may also be called ethyl, n-propyl, iso-butyl, neo-pentyl groups if the center carbon is also counted.
  • 8
    • 70450217994 scopus 로고    scopus 로고
    • 3Cl, into this series. However, this is less appropriate because the difference between the parent reaction and methyl substituted one is an α-methyl group while the difference between the rest of the series is a β-methyl group
    • 3Cl, into this series. However, this is less appropriate because the difference between the parent reaction and methyl substituted one is an α-methyl group while the difference between the rest of the series is a β-methyl group.
  • 63
    • 70450215933 scopus 로고    scopus 로고
    • NIST Webbook http://webbook.nist.gov.
  • 64
    • 70450217215 scopus 로고    scopus 로고
    • There are several exceptions to the general trends we have discussed; most involve isopropyl. The isopropyl transition state is asymmetric, with the two methyl groups pointing to one chloride, which is pushed away further than the other chloride. It may not be a good intermediate between methyl and tert-butyl
    • There are several exceptions to the general trends we have discussed; most involve isopropyl. The isopropyl transition state is asymmetric, with the two methyl groups pointing to one chloride, which is pushed away further than the other chloride. It may not be a good intermediate between methyl and tert-butyl.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.