Ab initio modeling of the solvent influence on the azo-hydrazone tautomerism

被引:54
|
作者
Antonov, L
Kawauchi, S
Satoh, M
Komiyama, J
机构
[1] Natl Foresty Univ, Dept Ecol, Sofia 1756, Bulgaria
[2] Tokyo Inst Technol, Dept Polymer Sci, Meguro Ku, Tokyo 152, Japan
关键词
tautomerism; azo dyes; hydrogen bonding; solvent effect;
D O I
10.1016/S0143-7208(98)00044-8
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The solvent effect on the azo (A) -hydrazone (H) tautomeric equilibrium of 1-phenylazo-4-naphthol is modeled by using ab initio quantum-chemical calculations. It was found that in methanol, methylene chloride and water there exists a strong hydrogen bonding between the particular tautomer and solvent, as well as dipole-dipole dye-solvent interactions. The results show that the H-form is more stable in water and methylene chloride, while methanol and i-octane stabilize the A-form. The calculational results obtained are in very good agreement with the experimental data in these solvents published previously. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:163 / 170
页数:8
相关论文
共 50 条
  • [31] Cyclization of thiohydrazonate esters and azo-hydrazone tautomerism of 2-arylhydrazono-3-oxo-1,4-benzothiazines
    Shawali, AS
    Elsheikh, S
    Párkányi, C
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2003, 40 (02) : 207 - 212
  • [32] Solvatochromism, halochromism, and azo-hydrazone tautomerism in novel V-shaped azo-azine colorants - consolidated experimental and computational approach
    Choudhari, Amol S.
    Patil, Sharad R.
    Sekar, Nagaiyan
    COLORATION TECHNOLOGY, 2016, 132 (05) : 387 - 398
  • [33] Ab initio calculations of solvent effects on guanine and thioguanine tautomerism
    Yekeler, H
    INDIAN JOURNAL OF CHEMISTRY SECTION A-INORGANIC BIO-INORGANIC PHYSICAL THEORETICAL & ANALYTICAL CHEMISTRY, 2000, 39 (12): : 1231 - 1240
  • [34] STUDY OF THE MIXED-SOLUTIONS OF AN ANIONIC AND A NON-IONIC SURFACTANT BY USING THE AZO-HYDRAZONE TAUTOMERISM OF AN ACIDIC DYE
    MEGURO, K
    TABATA, Y
    FUJIMOTO, N
    ESUMI, K
    BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1983, 56 (02) : 627 - 628
  • [35] Azo-hydrazone molecular switches: Synthesis and NMR conformational investigation
    Kurutos, Atanas
    Kamounah, Fadhil S.
    Dobrikov, Georgi M.
    Pittelkow, Michael
    Sauer, Stephan P. A.
    Hansen, Poul Erik
    MAGNETIC RESONANCE IN CHEMISTRY, 2021, 59 (11) : 1116 - 1125
  • [37] An analysis of azo-hydrazone tautomerism of reactive azobenzene and pyrazolinyl-azo dyes using the semiempirical molecular orbital PM5 method
    Hihara, T
    Okada, Y
    Morita, Z
    DYES AND PIGMENTS, 2004, 61 (03) : 199 - 225
  • [38] Spectroscopic and quantum chemical investigations of substituent effects on the azo-hydrazone tautomerism and acid-base properties of arylazo pyridone dyes
    Dostanic, J.
    Mijin, D.
    Uscumlic, G.
    Jovanovic, D. M.
    Zlatar, M.
    Loncarevic, D.
    SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2014, 123 : 37 - 45
  • [39] LASER FLASH-PHOTOLYSIS OF AROMATIC AZO-HYDRAZONE SYSTEMS
    MCVIE, J
    MITCHELL, AD
    SINCLAIR, RS
    TRUSCOTT, TG
    JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1980, (02): : 286 - 290
  • [40] AZO-HYDRAZONE CONVERSION .3. AUTOXIDATION OF BENZALDEHYDE PHENYLHYDRAZONES
    YAO, HC
    RESNICK, P
    JOURNAL OF ORGANIC CHEMISTRY, 1965, 30 (08): : 2832 - &