Intramolecular Excited State Proton Transfer of 2-(2'-Hydroxyphenyl)benzimidazole in Nonionic Micelles: Tweens
Related Experiment Video
Updated: Oct 28, 2026

Isotopic Effect in Double Proton Transfer Process of Porphycene Investigated by Enhanced QM/MM Method
Published on: July 19, 2019
Spectral characteristics and prototropic reactions of 2-(2'-hydroxyphenyl)benzimidazole (HPBI) in Tween-20, Tween-40, Tween-60, Tween-80, and dioxane-water mixtures of different compositions have been studied. Comparison of the fluorescence band maxima of the tautomer band in nonionic micelles with the correlation diagram, drawn between the fluorescence band maxima and the dielectric constants of the dioxane-water mixtures, have shown that the effective dielectric constant (epsiloneff) at the binding site of HPBI is 18 +/- 2 for all the Tweens. Fluorescence lifetimes (tauf) and fluorescence quantum yields (phifl) have shown that the hydrophobicity of these micelles is maximum for Tween-80 and at a minimum for Tween-20. Similar results have also been observed from the pKa values for the deprotonation of HPBI, whereas the protonation reaction of HPBI occurs at the site in nonionic micelles which is more hydrophilic than that where the deprotonation reaction takes place. The protonation reaction in 2-(2'-methoxyphenyl)benzimidazole (MPBI) has shown that the value of epsiloneff in Tweens where this reaction occurs is less hydrophobic than the site where the same reaction occurs in HPBI. Copyright 1998 Academic Press.
Spectral characteristics and prototropic reactions of 2-(2'-hydroxyphenyl)benzimidazole (HPBI) in Tween-20, Tween-40, Tween-60, Tween-80, and dioxane-water mixtures of different compositions have been studied. Comparison of the fluorescence band maxima of the tautomer band in nonionic micelles with the correlation diagram, drawn between the fluorescence band maxima and the dielectric constants of the dioxane-water mixtures, have shown that the effective dielectric constant (epsiloneff) at the binding site of HPBI is 18 +/- 2 for all the Tweens. Fluorescence lifetimes (tauf) and fluorescence quantum yields (phifl) have shown that the hydrophobicity of these micelles is maximum for Tween-80 and at a minimum for Tween-20. Similar results have also been observed from the pKa values for the deprotonation of HPBI, whereas the protonation reaction of HPBI occurs at the site in nonionic micelles which is more hydrophilic than that where the deprotonation reaction takes place. The protonation reaction in 2-(2'-methoxyphenyl)benzimidazole (MPBI) has shown that the value of epsiloneff in Tweens where this reaction occurs is less hydrophobic than the site where the same reaction occurs in HPBI. Copyright 1998 Academic Press.
Related Concept Videos
¹H NMR: Complex Splitting
Splitting diagrams or splitting tree diagrams are routinely used to depict such complex couplings. While drawing splitting diagrams, the splitting with the larger coupling constant is usually applied first.
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group with both...
Nucleophilic Aromatic Substitution: Elimination–Addition
Intermolecular Forces
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation

