Chemometrical Analysis of Substituent Effects. V. ortho Effect

取代基 化学 药物化学 分子内力 位阻效应 乙腈 反应速率常数 二甲基甲酰胺 计算化学 立体化学 有机化学 溶剂 物理 量子力学 动力学
作者
Oldřich Pytela,Josef Liška
出处
期刊:ChemPlusChem [Wiley-VCH]
卷期号:59 (9): 2005-2021 被引量:27
标识
DOI:10.1135/cccc19942005
摘要

The dissociation constants of nineteen ortho substituted benzoic acids have been determined in eight organic solvents (methanol, ethanol, acetone, dimethyl sulfoxide, dimethylformamide, acetonitrile, pyridine, 1,2-dichloroethane). The correlation between the σ I , σ R , and υ constants were unsuccessful due to neglecting the description of intramolecular hydrogen bond effect. The method of conjugated deviations has been applied to the results obtained and to those given in literature for ortho substituted benzoic acids (the dissociation constants, the reaction with diphenyldiazomethane, 33 sets), and values of three types of substituent constants have been determined for 29 substituents. The first of these substituent constants, σ o i , describes the electronic effects and was adjusted with the application of the isoparameter relation (σ o i as a function of σ m i ) suggested in previous communications. This constant (after excluding the substituents NHCOCH 3 and OCOCH 3 ) correlates very well ( R = 0.993) with the σ I and σ R constants. The second substituent constant, σ HG i , describes the interaction of the reaction centre (the oxygen atom of carboxylate anion) with the substituent, and it has non-zero values for the substituents OH, SH, NH 2 , NHCH 3 , NHCOCH 3 , COOH, CONH 2 , and SO 2 NH 2 . The third substituent constant, σ S i , describes the steric effects and is not significantly related to any of the known quantities of this type. The set given was tested together with the triad of σ I , σ R , and υ on the definition set and on a set extended by other 28 sets of processes with ortho substituted compounds. On the whole, the set of substituent constants suggested explains 94.6% of variability of data, whereas only 66.0% are explained with the use of σ I , σ R , and u constants. Moreover, the tests have shown that the σ o i constant is not suitable for interpretations of processes involving direct conjugation between the reaction centre and substituent.

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