Solvatochromic and Kinetic Response Models in (Ethyl Acetate + Chloroform or Methanol) Solvent Mixtures

P. Mancini; C. Adam; A. Del C. Pérez; L. R. Vottero

doi:10.3390/50300587

,

and

Área Química Orgánica, Dpto. de Química, Facultad de Ingeniería Química, Universidad Nacional del Litoral, Santiago del Estero 2829, (3000) Santa Fe, Argentina

^*

Author to whom correspondence should be addressed.

Molecules2000, 5(3), 587-588;https://doi.org/10.3390/50300587

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Abstract

The present work analyzes the solvent effects upon the solvatochromic response models for a set of chemical probes and the kinetic response models for an aromatic nucleophilic substitution reaction, in binary mixtures in which both pure components are able to form intersolvent complexes by hydrogen bonding.

Introduction

Recently, we analyzed the preferential solvation of a set of solvatochromic solutes 2,6-diphenyl-4- (2,4,6-triphenyl-1-pyridinio)phenolate (I), N,N-diethyl-4-nitroaniline (II), 4-nitroanisole (III), 4- nitroaniline (IV), 4-nitrophenol (V), and β-carotene (VI) (corresponding to the parameters E_T(30), π*, α, β y π₂*) by the application of preferential solvation models [1] (PSM), in mixtures of the following type: aprotic strong hydrogen-bond acceptor solvent and an aprotic cosolvent with hydrogen-bond do- nor capability [ethyl acetate (EAc) + chloroform] [2a,b].

On the other hand, we extended the preceding analysis to the kinetic data of an aromatic nucleophilic substitution (SNuAr) reaction between 1-fluoro-2,4-dinitrobenzene and morpholine carried out in the explored mixtures, relating the solvatochromic response model with the kinetic one.

Now, it is of interest to apply the preceding analysis to binary mixtures of EAc with a strong hydrogen-bond donor cosolvent (EAc + methanol), with the object to establish the influence of the acidity of the cosolvent.

Experimental

The experimental data were obtained by the methods reported previously [1]. The parameters of solvation were calculated by the application of the MATLAB 4.2 Program (The Mathworks, 0.1 inc.).

Results and Discussion

The preferential solvation models were applied to the solvatochromic data. The parameters of solvation f_2/1 and f_12/1, which measure the tendency of the solutes to be solvated by an individual component of the mixture or by the mixed solvent, indicate similar solvatochromic response model for (EAc + CHCl₃) [2a] and (EAc + MeOH) mixtures. The observed general trends are: (i) the solutes are preferentially solvated by the mixed solvent (donor acceptor complexes) and by the cosolvent, in preference to the EAc (f_2/1 and f_12/1 > 1); (ii) the preferential solvation order is complex > CoS > EAc (f_12/1 > f_2/1); (iii) the solute of reference β -carotene shows a tendency to ideality (f_12/1 and f_2/1 ≈ 1).

We extended the application of the PSM to the kinetic data. The analysis was performed at constant amine concentration and as a function of the solvent composition. The obtained results show a similar general tendency: preferential solvation by the cosolvent CHCl3 or MeOH in preference to the complex and EAc.

Both mixtures, which are capable to form complexes by hydrogen bonding between the EAc and the cosolvent, and also with self –association in the case of MeOH, reveal similar solvatochromic and kinetic response models.

Acknowledgements

We are indebted to the Universidad Nacional del Litoral (UNL), República Argentina. This work received financial support from the Science and Technology Secretariat, UNL, CAI+D Program (Projects 94-0858-007-054).

References and Notes

Ràfols, C.; Rosés, M.; Bosch, E. J. J. Chem. Soc., Perkin Trans. 1997, 2, 243. [CrossRef]
Mancini, P. M.; Terenzani, A.; Adam, C.; Vottero, L. R. J. Phys. Org. Chem. 1997, 10, 849. Mancini, P. M.; Terenzani, A.; Adam, C.; Vottero, L. R. J. Phys. Org. Chem. 1999, 12, 430. Mancini, P. M.; Terenzani, A.; Adam, C.; Pérez, A. del C.; Vottero, L. R. J. Phys. Org. Chem. 1999, 12, 713. [PubMed]