An MD simulation study of Reichardt’s betaines in surfactant micelles: Unlike orientation and solvation of cationic, zwitterionic, and anionic dye species within the pseudophase

Keywords: solvatochromism, polarity, sodium dodecyl sulfate, cetyltrimethylammonium bromide, localization, orientation, hydration, molecular dynamics simulation

Abstract

Solvatochromic indicators of the pyridinium N-phenolate series, also known as Reichardt’s betaines, or Reichardt’s dyes, are often used for examining not only pure or mixed solvents, but also various colloidal aggregates, such as surfactant micelles, droplets of microemulsions etc. In order to disclose the locus of these molecular probes within the micellar pseudophase, we recently utilized the molecular dynamics (MD) simulations for the standard dye, i.e. 4-(2,4,6-triphenylpyridinium-1-yl)-2,6-diphenylphenolate, and three other dyes of this family of higher and lower hydrophobicity. Both zwitterionic (colored) and protonated (cationic, colorless) species were involved into the research, as these compounds are also used as acid-base indicators for micellar systems. In the present paper, we extended this investigation further. MD modeling was applied to another three dyes incorporated in sodium n-dodecyl sulfate and cetyltrimethylammonium bromide micelles. The following compounds were examined: (i) the most hydrophobic dye, bearing five tert-butyl groups, 4-[2,4,6-tri(4-tert-butylphenyl)pyridinium-1-yl]-2,6-di(4-tert-butylphenyl)phenolate, (ii) a dye with a hydrocarbon loop around the oxygen atom, 4-(2,4,6-triphenylpyridinium-1-yl)-n-(3,5-nonamethylene)phenolate, and (iii) the dye with additional carboxylate group attached to the phenyl group opposite to the phenol, 4-(4-carboxylatophenyl-2,6-diphenylpyridinium-1-yl)-2,6-diphenylphenol. The orientation and solvation of the cations, zwitterions (both colored and colorless), and the anion of the last-mentioned dye in micelles appeared to be dissimilar, depending on the molecular structure and ionization state. The results were compared with those obtained previously for the standard betaine dye. In some cases, the most probable orientation of the dyes in their colorless form was opposite to that of the standard Reichardt’s dye, i.e., their OH group is directed towards the center of the micelle.

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References

Nakagaki M. Physical Chemistry of Membranes (Russian transl.). Mir: Moscow, 1991.

Kedia N., Sarkar A., Purkayastha P., Bagchi S. An electronic spectroscopic study of micellisa-tion of surfactants and solvation of homomicelles formed by cationic or anionic surfactants us-ing a solvatochromic electron donor acceptor dye. // Spectrochim. Acta, Part A. 2014. Vol.131. P.398–406.

Maity A., Ghosh P., Das T., Dash J., Purkayastha P. Interaction of a new surface sensitive probe compound with anionic surfactants of varying hydrophobic chain length. // J. Colloid Interface Sci. 2011. Vol.364, No.2. P.395–399.

Abdel-Kadew M. H., Hamzah R. Y., Abdel-Halim S. T. Spectroscopic Characteristics of an Amphiphilic Merocyanine Dye: A Probe of Polarity in Micelles. // Colloids Surf. 1988. Vol.34, No.2. P.133-142.

Reichardt C., Welton T. Solvents and Solvent Effects in Organic Chemistry, 4th ed. Wiley-VCH: Weinheim, 2011.

Drummond C.J., Grieser F., Healy T. W. A single spectroscopic probe for the determination of both the interfacial solvent properties and electrostatic surface potential of model lipid membranes. // Faraday Discuss. Chem. Soc. 1986. Vol.81. P.95–106.

Mchedlov-Petrossyan N. O. Protolytic equilibrium in lyophilic nanosized dispersions: differ-entiating influence of the pseudophase and salt effects. // Pure Appl. Chem. 2008. Vol.80, No.7. P.1459–1510.

Machado V. G., Stock R. I., Reichardt C. Pyridinium N-phenolate betaine dyes. // Chem. Rev. 2014. Vol.114, No.20. P.10429–10475.

Farafonov V. S., Lebed A. V., Mchedlov-Petrossyan N. O. Character of localization and mi-croenvironment of the solvatochromic Reichardt’s betaine dye in SDS and CTAB micelles: MD simulation study. // Langmuir 2017. Vol.33, No.33. P.8342–8352.

Farafonov V. S., Lebed A. V., Mchedlov-Petrossyan N. O. Solvatochromic betaine dyes of different hydrophobicity in ionic surfactant micelles: Molecular dynamics modeling of loca-tion character. // Colloids. Surf. A 2018. Vol.538. P.583–592.

Farafonov V.S., Lebed A.V., Mchedlov-Petrossyan N.O. Solvatochromic Reichardt’s dye in micelles of sodium cetyl sulfate: MD modeling of location character and hydration. // Kharkov Univ. Bull., Chem. Ser. 2017. Vol.28, No.51. P.5–11.

Mchedlov-Petrossyan N. O., Vodolazkaya N. A., Kornienko A. A., Karyakina E. L., Reichardt C. Counterion-Induced Transformations of Cationic Surfactant Micelles Studied by using the Displacing Effect of Solvatochromic Pyridinium N-Phenolate Betaine Dyes // Langmuir 2005. Vol.21, No.16. P.7090–7096.

Grieser F., Drummond C. J. The Physicochemical Properties of Self-Assembled Surfactant Aggregates As Determined by Some Molecular Spectroscopic Probe Techniques. // J. Phys. Chem. 1988. Vol.92. P.5580−5593.

Pisárčik M., Devínsky A., Pupák A. Determination of Micelle Aggregation Numbers of Alkyl-trimethylammonium Bromide and Sodium Dodecyl Sulfate Surfactants Using Time-Resolved Fluorescence Quenching. // Open Chem. 2015. Vol.13, No.1. P.922−931.

Abraham M. J., Murtola T., Schulz R., Páll S., Smith J. C., Hess B., Lindahl E. GROMACS: High Performance Molecular Simulations Through Multi-Level Parallelism from Laptops to Supercomputers. SoftwareX 2015, 1–2, 19–25.

Breneman C. M., Wiberg K. B. Determining atom-centered monopoles from molecular elec-trostatic potentials. The need for high sampling density in formamide conformational analysis. // J. Comp. Chem. 1990. Vol.11, No.3. P.361–373.

Vanquelef E., Simon S., Marquant G., Garcia E., Klimerak G., Delepine J. C., Cieplak P., Dupradeau F.-Y. R.E.D. Server: a web service for deriving RESP and ESP charges and build-ing force field libraries for new molecules and molecular fragments. // Nucleic Acids Res. 2011. Vol.39. P.511–517.

Farafonov V. S., Lebed A. V. Developing and validating a set of all-atom potential models for sodium dodecyl sulfate. // J. Chem. Theory Comput. 2017. Vol.13, No.6. P.2742−2750

Farafonov V. S., Lebed A. V. Molecular dynamics simulation study of cetylpyridinum chlo-ride and cetyltrimethylammonium bromide micelles. // Kharkov Univ. Bull., Chem. Ser. 2016 Vol.27, No.50. P.25–30.

Citations

Nitroxyl spin probe in ionic micelles: A molecular dynamics study
(2020) Kharkov University Bulletin Chemical Series
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Published
2018-09-03
Cited
How to Cite
Farafonov, V. S., Lebed, A. V., & Mchedlov-Petrossyan, N. O. (2018). An MD simulation study of Reichardt’s betaines in surfactant micelles: Unlike orientation and solvation of cationic, zwitterionic, and anionic dye species within the pseudophase. Kharkiv University Bulletin. Chemical Series, (30), 27-35. https://doi.org/10.26565/2220-637X-2018-30-03

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