Skip to main content
Log in

Analytical micelles containing amphiphilic aminoanthraquinone solvatochromic reporter receptor

  • Published:
Colloid Journal Aims and scope Submit manuscript

Abstract

The feasibility of using an amphiphilic photoactive derivative of aminoanthraquinone (C18) as both a local solvatochromic probe reporting its position in a micelle and a component of an analytical supramolecular unit in mixed micelles based on a nonionic surfactant, Triton X100, has been considered. The solvatochromism of the 1,8-anthraquinone derivative (C18) has, for the first time, been investigated. Dipole moments of C18 molecules have been determined within the frameworks of the Lippert–Mataga, Kawski, and Reichardt approaches. It has been found that the Δμ values, as calculated with the help of the first two approaches and the Onsager radius, which is, for C18, equal to 5.8 Å, are markedly higher than the value obtained in terms of the Reichardt model. Possible reasons for discrepancies, which arise between experimental data and theoretical predictions when analyzing the solvatochromic properties of dyes, have been briefly discussed. C18 has been employed as an example to show that, for chromophores capable of donor–acceptor interactions, the use of protic solvents is more reasonable, because they ensure realization of a wider spectrum of interactions with a probe, among which the van der Waals interactions play an important role. Therewith, polarization effects, rather than charge separation, make a substantial contribution. In the case of amphiphilic chromophores, “enveloping” of polar groups with hydrocarbon chains decreases the local dielectric permittivity and the probability of intermolecular donor–acceptor interactions (hydrogen bonding). The character of the microenvironment of C18 reporter in micelles has been determined with the use of the “relative polarity parameter” proposed in this work. This parameter makes it possible to compare results obtained for different models of solvatochromism. It has been shown that the characteristics of C18 microenvironment in micelles correspond to those of water–alcohol solutions, with the chromophoric moieties of dye molecules located in the polar region of a micelle, this region being formed by hydrated ethylene-oxide chains of Triton X100. Polar receptor groups of C18, which face the aqueous phase, complete the hydrophilic shell of a micelle, while hydrocarbon chains of both components compose its hydrophobic core. This structure of the normal micelle and the markedly higher intensity of fluorescence of the micellar system than that of an aqueous C18 solution make possible the analytical determination of metal ions in aqueous media.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Tsien, R.Y., ACS Symp. Ser., 1993, vol. 538, p. 130.

    Article  CAS  Google Scholar 

  2. Valeur, B. and Berberan-Santos, M.N., Molecular Fluorescence: Principles and Applications, New York: Wiley, 2012.

    Book  Google Scholar 

  3. Cairo, C.W., Key, J.A., and Sadek, C.M., Curr. Opin. Chem. Biol., 2010, vol. 14, p. 57.

    Article  CAS  Google Scholar 

  4. Wysocki, L.M. and Lavis, L.D., Curr. Opin. Chem. Biol., 2011, vol. 15, p. 752.

    Article  CAS  Google Scholar 

  5. Demchenko, A.P., Mely, Y., Duportail, G., and Klymchenko, A.S., Biophys. J., 2009, vol. 96, p. 3461.

    Article  CAS  Google Scholar 

  6. Maier, O., Oberle, V., and Hoekstra, D., Chem. Phys. Lipids, 2002, vol. 116, p. 3.

    Article  CAS  Google Scholar 

  7. Yu, F., Han, X., and Chen, L., Chem. Commun., 2014, p. 12234.

    Google Scholar 

  8. Luo, M.-H. and Chen, K.-Y., Dyes Pigm., 2013, vol. 99, p. 456.

    Article  CAS  Google Scholar 

  9. Zamojc', K., Zdrowowicz, M., Jacewicz, D., Wyrzykowski, D., and Chmurzyn'ski, L., CRC Crit. Rev. Anal. Chem., 2016, vol. 46, p. 171.

    Article  CAS  Google Scholar 

  10. Park, H. and Chang, S.-K., Dyes Pigm., 2015, vol. 122, p. 324.

    Article  CAS  Google Scholar 

  11. Santin, L.R., Santos, S.C., Novo, D.L.R., Bianchini, D., Gerola, A.P., Braga, G., Caetano, W., Moreira, L.M., Bastos, E.L., and Romani, A.P., Dyes Pigm., 2015, vol. 119, p. 12.

    Article  CAS  Google Scholar 

  12. Wong, K.-F., Deng, J.-R., Wei, X.-Q., Shao, S.-P., Xiang, D.-P., and Wong, M.-K., Org. Biomol. Chem., 2015, vol. 13, p. 7408.

    Article  CAS  Google Scholar 

  13. Gilani, A.G., Moghadam, M., and Zakerhamidi, M., Dyes Pigm., 2012, vol. 92, p. 1052.

    Article  CAS  Google Scholar 

  14. Dong, Y., Wang, R., Li, G., Chen, C., Chi, Y., and Chen, G., Anal. Chem., 2012, vol. 84, p. 6220.

    Article  CAS  Google Scholar 

  15. Agnihotri, H., Mahalingavelar, P., Mande, H., Ghalsasi, P., and Kanvah, S., Dyes Pigm., 2015, vol. 123, p. 341.

    Article  CAS  Google Scholar 

  16. Kobayashi, H., Ogawa, M., Alford, R., Choyke, P.L., and Urano, Y., Chem. Rev., 2009, vol. 110, p. 2620.

    Article  CAS  Google Scholar 

  17. Shi, C., Zhang, C., Su, Y., and Cheng, T., Lancet Oncol., 2010, vol. 11, p. 815.

    Article  Google Scholar 

  18. Nesterov, E.E., Skoch, J., Hyman, B.T., Klunk, W.E., Bacskai, B.J., and Swager, T.M., Angew. Chem., Int. Ed. Engl., 2005, vol. 44, p. 5452.

    Article  CAS  Google Scholar 

  19. Lee, S., Park, K., Kim, K., Choi, K., and Kwon, I.C., Chem. Commun., 2008, p. 4250.

    Google Scholar 

  20. Kisin-Finfer, E., Ferber, S., Blau, R., Satchi-Fainaro, R., and Shabat, D., Bioorg. Med. Chem. Lett., 2014, vol. 24, p. 2453.

    Article  CAS  Google Scholar 

  21. Valeur, B. and Leray, I., Coord. Chem. Rev., 2000, vol. 205, p. 3.

    Article  CAS  Google Scholar 

  22. Carter, K.P., Young, A.M., and Palmer, A.E., Chem. Rev., 2014, vol. 114, p. 4564.

    Article  CAS  Google Scholar 

  23. Karakus,, E., Üçüncü, M., and Emrullahogğlu, M., Chem. Commun., 2014, p. 1119.

    Google Scholar 

  24. Choi, Y.W., Park, G.J., Na, Y.J., Jo, H.Y., Lee, S.A., You, G.R., and Kim, C., Sens. Actuators, 2014, vol. 194, p. 343.

    Article  CAS  Google Scholar 

  25. You, L., Zha, D., and Anslyn, E.V., Chem. Rev., 2015, vol. 115, p. 7840.

    Article  CAS  Google Scholar 

  26. Jia, L., Xu, L., Wang, Z., Xu, J., and Ji, J., Chin. J. Chem., 2014, vol. 32, p. 85.

    Article  CAS  Google Scholar 

  27. Chang, C.J., Gunnlaugsson, T., and James, T.D., Chem. Soc. Rev., 2015, vol. 44, p. 4176.

    Article  CAS  Google Scholar 

  28. Pinalli, R., Nachtigall, F.F., Ugozzoli, F., and Dalcanale, E., Angew. Chem., Int. Ed. Engl., 1999, vol. 38, p. 2377.

    Article  CAS  Google Scholar 

  29. Arslanov, V., Ermakova, E., Michalak, J., Bessmertnykh-Lemeune, A., Meyer, M., Raitman, O., Vysotskij, V., Guilard, R., and Tsivadze, A., Colloids Surf. A, 2015, vol. 483, p. 193.

    Article  CAS  Google Scholar 

  30. Ermakova, E., Raitman, O., Shokurov, A., Kalinina, M., Selector, S., Tsivadze, A., Arslanov, V., Meyer, M., Bessmertnykh-Lemeune, A., and Guilard, R., Analyst, 2016, vol. 141, p. 1912.

    Article  CAS  Google Scholar 

  31. Kalyanasundaram, K. and Thomas, J., J. Am. Chem. Soc., 1977, vol. 99, p. 2039.

    Article  CAS  Google Scholar 

  32. Piñeiro, L., Novo, M., and Al-Soufi, W., Adv. Colloid Interface Sci., 2015, vol. 215, p. 1.

    Article  CAS  Google Scholar 

  33. Ray, G.B., Chakraborty, I., and Moulik, S.P., J. Colloid Interface Sci., 2006, vol. 294, p. 248.

    Article  CAS  Google Scholar 

  34. Dong, D.C. and Winnik, M.A., Photochem. Photobiol., 1982, vol. 35, p. 17.

    Article  CAS  Google Scholar 

  35. Sahoo, L., Sarangi, J., and Misra, P.K., Bull. Chem. Soc. Jpn., 2002, vol. 75, p. 859.

    Article  CAS  Google Scholar 

  36. Vitha, M.F., Weckwerth, J.D., Odland, K., Dema, V., and Carr, P.W., J. Phys. Chem., 1996, vol. 100, p. 18823.

    Article  CAS  Google Scholar 

  37. Fuguet, E., Ràfols, C., Bosch, E., and Rosés, M., Langmuir, 2003, vol. 19, p. 55.

    Article  CAS  Google Scholar 

  38. Shannigrahi, M. and Bagchi, S., J. Phys. Chem. B, 2005, vol. 109, p. 14567.

    Article  CAS  Google Scholar 

  39. Joshi, S. and Pant, D.D., J. Lumin., 2013, vol. 425, p. 59.

    CAS  Google Scholar 

  40. Vitha, M.F. and Carr, P.W., J. Phys. Chem. B, 1998, vol. 102, p. 1888.

    Article  CAS  Google Scholar 

  41. Mchedlov-Petrossyan, N.O., Vodolazkaya, N.A., Kornienko, A.A., Karyakina, E.L., and Reichardt, C., Langmuir, 2005, vol. 21, p. 7090.

    Article  CAS  Google Scholar 

  42. Deb, N., Shannigrahi, M., and Bagchi, S., J. Phys. Chem. B, 2008, vol. 112, p. 2868.

    Article  CAS  Google Scholar 

  43. Dash, N. and Krishnamoorthy, G., J. Fluoresc., 2010, vol. 20, p. 135.

    Article  CAS  Google Scholar 

  44. Shannigrahi, M. and Bagchi, S., J. Phys. Chem. B, 2004, vol. 108, p. 17703.

    Article  CAS  Google Scholar 

  45. Muthukumar, N., Ilangovan, A., Maruthamuthu, S., and Palaniswamy, N., Electrochim. Acta, 2007, vol. 52, p. 7183.

    Article  CAS  Google Scholar 

  46. Muthukumar, N., Ilangovan, A., Maruthamuthu, S., Palaniswamy, N., and Kimura, A., Mater. Chem. Phys., 2009, vol. 115, p. 444.

    Article  CAS  Google Scholar 

  47. Choi, J.R., Jeoung, S.C., and Cho, D.W., Chem. Phys. Lett., 2004, vol. 385, p. 384.

    Article  CAS  Google Scholar 

  48. Del Giacco, T., Latterini, L., and Elisei, F., Photochem. Photobiol. Sci., 2003, vol. 2, p. 681.

    Article  CAS  Google Scholar 

  49. Israelachvili, J.N., Mitchell, D.J., and Ninham, B.W., J. Chem. Soc., Faraday Trans., 1976, vol. 72, p. 1525.

    Article  Google Scholar 

  50. Reichardt, C., Solvents and Solvent Effects in Organic Chemistry, New York: Wiley, 2004.

    Google Scholar 

  51. Lippert, E., Ber. Bunsen-Ges. Phys. Chem., 1957, vol. 61, p. 962.

    CAS  Google Scholar 

  52. Mataga, N., Kaifu, Y., and Koizumi, M., Bull. Chem. Soc. Jpn., 1956, vol. 29, p. 465.

    Article  CAS  Google Scholar 

  53. Bakhshiev, N.G., Opt. Spektrosk., 1964, vol. 16, p. 821.

    CAS  Google Scholar 

  54. Kosower, E.M. and Dodiuk, H., J. Am. Chem. Soc., 1974, vol. 96, p. 6195.

    Article  CAS  Google Scholar 

  55. Kawski, A., Kuklinski, B., and Bojarski, P., Z. Naturforsch. A: Phys. Sci., 2002, vol. 57, p. 716.

    Article  CAS  Google Scholar 

  56. Kamlet, M.J., Abboud, J.L., and Taft, R., J. Am. Chem. Soc., 1977, vol. 99, p. 6027.

    Article  CAS  Google Scholar 

  57. Kamlet, M.J., Abboud, J.L.M., Abraham, M.H., and Taft, R., Org. Chem., 1983, vol. 48, p. 2877.

    Article  CAS  Google Scholar 

  58. Mancini, P.M., Adam, C.G., Fortunato, G.G., and Vottero, L.R., Arkivoc, 2007, vol. 2007, no. 16, p. 266.

    Google Scholar 

  59. Catalán, J., J. Phys. Chem. B, 2009, vol. 113, p. 5951.

    Article  CAS  Google Scholar 

  60. Katritzky, A.R., Fara, D.C., Yang, H., Tamm, K., Tämm, T., and Karelson, M., Chem. Rev., 2004, vol. 104, p. 175.

    Article  CAS  Google Scholar 

  61. Sinkeldam, R.W. and Tor, Y., Org. Biomol. Chem., 2007, vol. 5, p. 2523.

    Article  CAS  Google Scholar 

  62. Catalan, J., Org. Chem., 1997, vol. 62, p. 8231.

    Article  CAS  Google Scholar 

  63. Paul, B.K., Samanta, A., Kar, S., and Guchhait, N., J. Lumin., 2010, vol. 130, p. 1258.

    Article  CAS  Google Scholar 

  64. Dhar, S., Rana, D.K., Roy, S.S., Roy, S., Bhattacharya, S., and Bhattacharya, S.C., J. Lumin., 2012, vol. 132, p. 957.

    Article  CAS  Google Scholar 

  65. Airinei, A., Homocianu, M., and Dorohoi, D.O., J. Mol. Liq., 2010, vol. 157, p. 13.

    Article  CAS  Google Scholar 

  66. Sasirekha, V. and Ramakrishnan, V., Spectrochim. Acta, Part A, 2008, vol. 70, p. 626.

    Article  CAS  Google Scholar 

  67. Dahiya, P., Choudhury, S.D., Maity, D., Mukherjee, T., and Pal, H., Spectrochim. Acta, Part A, 2008, vol. 69, p. 134.

    Article  CAS  Google Scholar 

  68. Siddlingeshwar, B. and Hanagodimath, S., Spectrochim. Acta, Part A, 2009, vol. 72, p. 490.

    Article  CAS  Google Scholar 

  69. He, L., Freeman, H.S., Lu, L., and Zhang, S., Dyes Pigm., 2011, vol. 91, p. 389.

    Article  CAS  Google Scholar 

  70. Zakerhamidi, M., Ghanadzadeh, A., and Moghadam, M., Spectrochim. Acta, Part A, 2011, vol. 79, p. 74.

    Article  CAS  Google Scholar 

  71. Olivares, S.P., Risso, S., and Gutierrez, M.I., Spectrochim. Acta, Part A, 2008, vol. 71, p. 336.

    Article  CAS  Google Scholar 

  72. Vázquez, M.E., Blanco, J.B., and Imperiali, B., J. Am. Chem. Soc., 2005, vol. 127, p. 1300.

    Article  CAS  Google Scholar 

  73. Samanta, A., Paul, B.K., Mahanta, S., Singh, R.B., Kar, S., and Guchhait, N., J. Photochem. Photobiol. A, 2010, vol. 212, p. 161.

    Article  CAS  Google Scholar 

  74. Lackowicz, J.R., Principles of Fluorescence Spectroscopy, New York: Plenum, 1983.

    Book  Google Scholar 

  75. Onsager, L., J. Am. Chem. Soc., 1936, vol. 58, p. 1486.

    Article  CAS  Google Scholar 

  76. Kirkwood, J.G., J. Chem. Phys., 1934, vol. 2, p. 351.

    Article  CAS  Google Scholar 

  77. Mataga, N., Kaifu, Y., and Koizumi, M., Bull. Chem. Soc. Jpn., 1955, vol. 28, p. 690.

    Article  CAS  Google Scholar 

  78. Lippert, E., Z. Naturforsch. A: Phys. Sci., 1955, vol. 10, p. 541.

    Article  Google Scholar 

  79. Misra, R. and Kar, S., Chem. Phys., 2012, vol. 397, p. 65.

    Article  CAS  Google Scholar 

  80. Reichardt, C., Pure Appl. Chem., 2004, vol. 76, p. 1903.

    Article  CAS  Google Scholar 

  81. Ravi, M., Soujanya, T., Samanta, A., and Radhakrishnan, T., J. Chem. Soc., Faraday Trans., 1995, vol. 91, p. 2739.

    Article  Google Scholar 

  82. Patra, D. and Barakat, C., Spectrochim. Acta, Part A, 2011, vol. 79, p. 1034.

    Article  CAS  Google Scholar 

  83. Jana, S., Ghosh, S., Dalapati, S., Kar, S., and Guchhait, N., Spectrochim. Acta, Part A, 2011, vol. 78, p. 463.

    Article  CAS  Google Scholar 

  84. Fukuda, K., Nakahara, H., and Kato, T., J. Colloid Interface Sci., 1976, vol. 54, p. 430.

    Article  CAS  Google Scholar 

  85. Koutek, B., Collect. Czech. Chem. Commun., 1978, p. 2368.

    Google Scholar 

  86. Mukherjee, S., Chattopadhyay, A., Samanta, A., and Soujanya, T., J. Phys. Chem., 1994, vol. 98, p. 2809.

    Article  CAS  Google Scholar 

  87. Jacques, P., Graff, B., Diemer, V., Ay, E., Chaumeil, H., Carre, C., and Malval, J.-P., Chem. Phys. Lett., 2012, vol. 531, p. 242.

    Article  CAS  Google Scholar 

  88. Bilot, L. and Kawski, A., Z. Naturforsch. A: Phys. Sci., 1962, vol. 17, p. 621.

    Article  Google Scholar 

  89. Bilot, L. and Kawski, A., Z. Naturforsch. A: Phys. Sci., 1963, vol. 18, p. 10.

    Google Scholar 

  90. Kawski, A. and Bojarski, P., Spectrochim. Acta, Part A, 2011, vol. 82, p. 527.

    Article  CAS  Google Scholar 

  91. Kawski, A., Kuklinski, B., and Bojarski, P., Chem. Phys., 2006, vol. 320, p. 188.

    Article  CAS  Google Scholar 

  92. Kawski, A. and Kolakowski, W., Acta Phys. Pol., A, 1966, vol. 29, p. 507.

    CAS  Google Scholar 

  93. Homocianu, M., Airinei, A., and Dorohoi, D.O., J. Adv. Res. Phys., 2011, vol. 2, no. 1, p. 011105.

    Google Scholar 

  94. Rudrappa, T.J., Int. J. Sci. Technol. Res., 2014, vol. 3, p. 107.

    Google Scholar 

  95. Stepanov, N.F., Sorosovskii Obrazovat. Zh., 2001, p. 28.

    Google Scholar 

  96. Sokolov, N.D., Usp. Fiz. Nauk, 1955, vol. 57, p. 205.

    Article  CAS  Google Scholar 

  97. Gregory, J., Clary, D., Liu, K., Brown, M., and Saykally, R., Science (Washington, D.C.), 1997, vol. 275, p. 814.

    Article  CAS  Google Scholar 

  98. Srividya, N., Sinha, A., and Rao, T.P., J. Solution Chem., 2000, vol. 29, p. 847.

    Article  CAS  Google Scholar 

  99. Choi, J.-Y., Park, E.-J., Chang, S.-H., and Kang, T.-J., Bull. Korean Chem. Soc., 2009, vol. 30, p. 1452.

    Article  CAS  Google Scholar 

  100. Shivraj, B.S. and Hanagodimatha, S., Indian J. Pure Appl. Phys., 2015, vol. 53, p. 18.

    Google Scholar 

  101. Bauer, M., Rollberg, A., Barth, A., and Spange, S., Eur. J. Org. Chem., 2008, vol. 2008, p. 4475.

    Article  CAS  Google Scholar 

  102. Lan, Y., Corradini, M.G., Liu, X., May, T.E., Borondics, F., Weiss, R.G., and Rogers, M.A., Langmuir, 2014, vol. 30, p. 14128.

    Article  CAS  Google Scholar 

  103. Vitha, M.F., Weckwerth, J.D., Odland, K., Dema, V., and Carr, P.W., Anal. Chem., 1997, vol. 69, p. 2268.

    Article  CAS  Google Scholar 

  104. Bashford, C.L., Chance, B., Smith, J.C., and Yoshida, T., Biophys. J., 1979, vol. 25, p. 63.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to V. V. Arslanov.

Additional information

Original Russian Text © E.V. Ermakova, V.V. Arslanov, 2017, published in Kolloidnyi Zhurnal, 2017, Vol. 79, No. 6, pp. 713–727.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ermakova, E.V., Arslanov, V.V. Analytical micelles containing amphiphilic aminoanthraquinone solvatochromic reporter receptor. Colloid J 79, 748–761 (2017). https://doi.org/10.1134/S1061933X17060060

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1061933X17060060

Navigation