RELATIONSHIP BETWEEN SUBSTITUENT ELECTRONEGATIVITY AND FIELD PARAMETER IN THE ALIPHATIC SERIES - INTRODUCTION OF CHARGE SEPARATION PARAMETER (LAMBDA)

被引:4
作者
INAMOTO, N
MASUDA, S
NIWA, J
机构
[1] UNIV TOKYO,SPECTROCHEM RES CTR,TOKYO 113,JAPAN
[2] NAGOYA UNIV,COLL GEN EDUC,CHIKUSA KU,NAGOYA,AICHI 464,JAPAN
关键词
D O I
10.1002/poc.610030402
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The problem of non‐proportionality between the substituent field parameter (σF) and substituent electronegativity (Δι or σχ) was clarified by the introduction of the ‘charge‐separation parameter’ (λ), which is the component for the direction of the HX axis of the distance between positive and negative poles of the dipole in the HX molecule. Thus σF was correlated with Δι or σχ by the equation σF = aΔιλ (or σF = a′σχλ). The above proposal was further supported by performing an energy decomposition analysis for the isodesmic reaction in the isolated molecule system (\documentclass{article}\pagestyle{empty}\begin{document}${\rm X}\raise1pt\hbox{---} {\rm H} \cdots {\rm H}\mathop {\rm N}\limits^ + {\rm H}_3 $\end{document} or XH…HCO 2−) at shorter distances (2·0–4·5 Å). It was further shown that field parameters such as σi, F and σF(theor), and the pKa values in the series of aliphatic acids, and spectral data (UPS and 13C‐SCS) were also well correlated with Διλ or σχλ. It is concluded that λ and Δι or σχ are essential parameters for interpreting the electrostatic field effect in aliphatic substituent effects, and that the transmission due to the σ‐inductive effect is considered to be not as significant as the field effect after a few bonds away from the substituent. Copyright © 1990 John Wiley & Sons Ltd.
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页码:209 / 218
页数:10
相关论文
共 52 条
[1]   TRANSMISSION OF POLAR EFFECTS - PREDICTION BY KIRKWOOD-WESTHEIMER ELECTROSTATIC-FIELD EFFECT MODEL [J].
ACEVEDO, S ;
BOWDEN, K .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1977, (17) :608-609
[2]   TRANSMISSION OF ELECTRONIC SUBSTITUENT EFFECTS IN 4-SUBSTITUTED BICYCLO[2.2.2]OCTYL SYSTEMS [J].
ADCOCK, W ;
BUTT, G ;
KOK, GB ;
MARRIOTT, S ;
TOPSOM, RD .
JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (14) :2551-2557
[3]   DISSOCIATION CONSTANTS OF BICYCLO[2.2.2]OCT-2-ENE-1-CARBOXYLIC ACIDS DIBENZOBICYCLO[2.2.2]OCTA-2,5-DIENE-1-CARBOXYLIC ACIDS AND CUBANECARBOXYLIC ACIDS [J].
BAKER, FW ;
PARISH, RC ;
STOCK, LM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1967, 89 (22) :5677-&
[4]   INFLUENCE OF SUBSTITUENTS IN POSITION-4 ON IONIZATION-POTENTIAL OF QUINUCLIDINES [J].
BIERI, G ;
HEILBRON.E .
HELVETICA CHIMICA ACTA, 1974, 57 (03) :546-551
[5]  
BINKLEY JS, 1980, GAUSSIAN 80
[6]  
Bjerrum N, 1923, Z PHYS CHEM-STOCH VE, V106, P219
[7]   TRANSMISSION OF POLAR EFFECTS .V. KINETICS OF ESTERIFICATION WITH DIAZODIPHENYLMETHANE AND IONIZATION OF SUBSTITUTED ACETIC AND PROPIONIC ACIDS IN SEVERAL SOLVENTS [J].
BOWDEN, K ;
HARDY, M ;
PARKIN, DC .
CANADIAN JOURNAL OF CHEMISTRY, 1968, 46 (18) :2929-&
[8]  
BRANCH GEK, 1941, THEORY ORGANIC CHEM, pCH4
[9]  
BROWN HC, 1955, DETERMINATION ORG, V1, pCH14
[10]   NATURE OF SUBSTITUENT ELECTRONIC EFFECTS - EXISTENCE OF PI-INDUCTIVE EFFECT [J].
BROWNLEE, RTC ;
BUTT, G ;
CHAN, MP ;
TOPSOM, RD .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1976, (13) :1486-1490