Correlation analysis of substituent effects on the acidity of benzoic acids by the AM1 method

Tomoko Sotomatsu, Yoshiyuki Murata, Toshio Fujita

Research output: Contribution to journalArticle

62 Citations (Scopus)

Abstract

Theoretical analysis of the electronic effect of aromatic substituents was done with the use of the AM1 computational procedure. The gas‐phase acidity of substituted benzoic acids was linear with the difference in the heat of formation between corresponding benzoic acids and benzoate anions, the energy of the highest occupied molecular orbital, and the net charge on the acidic oxygen atoms of the corresponding benzoate anions. The Hammett σ constant was linearly correlated with the net charge on the atoms of the acid moiety of substituted benzoic acids. The AM1 computational procedure satisfactorily reproduced the electronic properties of a wide variety of substituents.

Original languageEnglish
Pages (from-to)94-98
Number of pages5
JournalJournal of Computational Chemistry
Volume10
Issue number1
DOIs
Publication statusPublished - 1989
Externally publishedYes

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Benzoic acid
Benzoates
Correlation Analysis
Acidity
Charge
Electronic Properties
Negative ions
Oxygen
Atoms
Theoretical Analysis
Heat
Linearly
Electronics
Anions
Molecular orbitals
Electronic properties
Energy
Acids

ASJC Scopus subject areas

  • Chemistry(all)
  • Computational Mathematics

Cite this

Correlation analysis of substituent effects on the acidity of benzoic acids by the AM1 method. / Sotomatsu, Tomoko; Murata, Yoshiyuki; Fujita, Toshio.

In: Journal of Computational Chemistry, Vol. 10, No. 1, 1989, p. 94-98.

Research output: Contribution to journalArticle

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