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Journal of Spectroscopy
Volume 2014 (2014), Article ID 970827, 10 pages
http://dx.doi.org/10.1155/2014/970827
Research Article

Characterization of Binary Organogels Based on Some Azobenzene Compounds and Alkyloxybenzoic Acids with Different Chain Lengths

1National Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, China
2Qinghuangdao Entry-Exit Inspection & Quarantine Bureau Coal Inspection Technique Center, Qinhuangdao 066000, China
3Hebei Key Laboratory of Applied Chemistry, School of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao 066004, China

Received 12 May 2014; Accepted 4 June 2014; Published 10 August 2014

Academic Editor: Xinqing Chen

Copyright © 2014 Yongmei Hu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. H. Yu and Q. Huang, “Improving the oral bioavailability of curcumin using novel organogel-based nanoemulsions,” Journal of Agricultural and Food Chemistry, vol. 60, no. 21, pp. 5373–5379, 2012. View at Publisher · View at Google Scholar · View at Scopus
  2. G. M. Newbloom, K. M. Weigandt, and D. C. Pozzo, “Electrical, mechanical, and structural characterization of self-assembly in poly(3-hexylthiophene) organogel networks,” Macromolecules, vol. 45, no. 8, pp. 3452–3462, 2012. View at Publisher · View at Google Scholar · View at Scopus
  3. D. Liu, D. Wang, M. Wang et al., “Supramolecular organogel based on crown ether and secondary ammoniumion functionalized glycidyl triazole polymers,” Macromolecules, vol. 46, no. 11, pp. 4617–4625, 2013. View at Publisher · View at Google Scholar · View at Scopus
  4. H. Sawalha, R. den Adel, P. Venema, A. Bot, E. Flöter, and E. van der Linden, “Organogel-emulsions with mixtures of β-sitosterol and γ-oryzanol: influence of water activity and type of oil phase on gelling capability,” Journal of Agricultural and Food Chemistry, vol. 60, no. 13, pp. 3462–3470, 2012. View at Publisher · View at Google Scholar · View at Scopus
  5. P. Rajamalli and E. Prasad, “Low molecular weight fluorescent organogel for fluoride ion detection,” Organic Letters, vol. 13, no. 14, pp. 3714–3717, 2011. View at Publisher · View at Google Scholar · View at Scopus
  6. S. Bouguet-Bonnet, M. Yemloul, and D. Canet, “New application of proton nuclear spin relaxation unraveling the intermolecular structural features of low-molecular-weight organogel fibers,” Journal of the American Chemical Society, vol. 134, no. 25, pp. 10621–10627, 2012. View at Publisher · View at Google Scholar · View at Scopus
  7. S. O'Sullivan and D. W. M. Arrigan, “Impact of a surfactant on the electroactivity of proteins at an aqueous-organogel microinterface array,” Analytical Chemistry, vol. 85, no. 3, pp. 1389–1394, 2013. View at Publisher · View at Google Scholar · View at Scopus
  8. H. Takeno, A. Maehara, D. Yamaguchi, and S. Koizumi, “A structural study of an organogel investigated by small-angle neutron scattering and synchrotron small-angle X-ray scattering,” Journal of Physical Chemistry B, vol. 116, no. 26, pp. 7739–7745, 2012. View at Publisher · View at Google Scholar · View at Scopus
  9. J. Lu, J. Hu, Y. Song, and Y. Ju, “A new dual-responsive organogel based on uracil-appended glycyrrhetinic acid,” Organic Letters, vol. 13, no. 13, pp. 3372–3375, 2011. View at Publisher · View at Google Scholar · View at Scopus
  10. M. Yemloul, E. Steiner, A. Robert et al., “Solvent dynamical behavior in an organogel phase as studied by NMR relaxation and diffusion experiments,” The Journal of Physical Chemistry B, vol. 115, no. 11, pp. 2511–2517, 2011. View at Publisher · View at Google Scholar · View at Scopus
  11. F. Xin, H. Zhang, B. Hao et al., “Controllable transformation from sensitive and reversible heat-set organogel to stable gel induced by sodium acetate,” Colloids and Surfaces A: Physicochemical and Engineering Aspects, vol. 410, pp. 18–22, 2012. View at Publisher · View at Google Scholar · View at Scopus
  12. F. S. Schoonbeek, J. H. van Esch, R. Hulst, R. M. Kellogg, and B. L. Feringa, “Geminal Bis-ureas as gelators for organic solvents: gelation properties and structural studies in solution and in the gel state,” Chemistry—A European Journal, vol. 6, no. 14, pp. 2633–2643, 2000. View at Publisher · View at Google Scholar · View at Scopus
  13. P. Anilkumar and M. Jayakannan, “A novel supramolecular organogel nanotubular template approach for conducting nanomaterials,” The Journal of Physical Chemistry B, vol. 114, no. 2, pp. 728–736, 2010. View at Publisher · View at Google Scholar · View at Scopus
  14. P. D. Wadhavane, R. E. Galian, M. A. Izquierdo et al., “Photoluminescence enhancement of CdSe quantum dots: a case of organogel-nanoparticle symbiosis,” Journal of the American Chemical Society, vol. 134, no. 50, pp. 20554–20563, 2012. View at Publisher · View at Google Scholar · View at Scopus
  15. W. Liu, P. Xing, F. Xin et al., “Novel double phase transforming organogel based on β-cyclodextrin in 1,2-propylene glycol,” The Journal of Physical Chemistry B, vol. 116, no. 43, pp. 13106–13113, 2012. View at Publisher · View at Google Scholar · View at Scopus
  16. M. Bielejewski and J. Tritt-Goc, “Evidence of solvent-gelator interaction in sugar-based organogel studied by field-cycling NMR relaxometry,” Langmuir, vol. 26, no. 22, pp. 17459–17464, 2010. View at Publisher · View at Google Scholar · View at Scopus
  17. Y. Li, J. Liu, G. Du et al., “Reversible heat-set organogel based on supramolecular interactions of β-Cyclodextrin in N, N -dimethylformamide,” The Journal of Physical Chemistry B, vol. 114, no. 32, pp. 10321–10326, 2010. View at Publisher · View at Google Scholar · View at Scopus
  18. Y. Marui, A. Kikuzawa, T. Kida, and M. Akashi, “Unique organogel formation with macroporous materials constructed by the freeze-drying of aqueous cyclodextrin solutions,” Langmuir, vol. 26, no. 13, pp. 11441–11445, 2010. View at Publisher · View at Google Scholar · View at Scopus
  19. A. R. Hirst, D. K. Smith, and J. P. Harrington, “Unique nanoscale morphologies underpinning organic gel-phase materials,” Chemistry—A European Journal, vol. 11, no. 22, pp. 6552–6559, 2005. View at Publisher · View at Google Scholar · View at Scopus
  20. M. Moniruzzaman and P. R. Sundararajan, “Low molecular weight organogels based on long-chain carbamates,” Langmuir, vol. 21, no. 9, pp. 3802–3807, 2005. View at Publisher · View at Google Scholar · View at Scopus
  21. T. Jiao, Y. Wang, F. Gao, and J. Zhou, “Photoresponsive organogel and organized nanostructures of cholesterol imide derivatives with azobenzene substituent groups,” Progress in Natural Science: Materials International, vol. 22, no. 1, pp. 64–70, 2012. View at Publisher · View at Google Scholar · View at Scopus
  22. T. Jiao, F. Gao, Y. Wang, J. Zhou, F. Gao, and X. Luo, “Supramolecular gel and nanostructures of bolaform and trigonal cholesteryl derivatives with different aromatic spacers,” Current Nanoscience, vol. 8, no. 1, pp. 111–116, 2012. View at Publisher · View at Google Scholar · View at Scopus
  23. P. Mukhopadhyay, Y. Iwashita, M. Shirakawa, S. Kawano, N. Fujita, and S. Shinkai, “Spontaneous colorimetric sensing of the positional isomers of dihydroxynaphthalene in a 1D organogel matrix,” Angewandte Chemie: International Edition, vol. 45, no. 10, pp. 1592–1595, 2006. View at Publisher · View at Google Scholar · View at Scopus
  24. T. Jiao, Y. Wang, Q. Zhang, J. Zhou, and F. Gao, “Regulation of substituent groups on morphologies and self-assembly of organogels based on some azobenzene imide derivatives,” Nanoscale Research Letters, vol. 8, no. 1, article 160, 8 pages, 2013. View at Publisher · View at Google Scholar · View at Scopus
  25. J. L. Gurav, I. Jung, H. Park, E. S. Kang, and D. Y. Nadargi, “Silica aerogel: synthesis and applications,” Journal of Nanomaterials, vol. 2010, Article ID 409310, 11 pages, 2010. View at Publisher · View at Google Scholar · View at Scopus
  26. A. S. Al Dwayyan, M. N. Khan, and M. S. Al Salhi, “Optical characterization of chemically etched nanoporous silicon embedded in sol-gel matrix,” Journal of Nanomaterials, vol. 2012, Article ID 713203, 7 pages, 2012. View at Publisher · View at Google Scholar · View at Scopus
  27. H. Guo, T. Jiao, X. Shen et al., “Binary organogels based on glutamic acid derivatives and different acids: solvent effect and molecular skeletons on self-assembly and nanostructures,” Colloids and Surfaces A: Physicochemical and Engineering Aspects, vol. 447, pp. 88–96, 2014. View at Google Scholar
  28. M. Žinić, F. Vögtle, and F. Fages, “Cholesterol-based gelators,” Topics in Current Chemistry, vol. 256, pp. 39–76, 2005. View at Publisher · View at Google Scholar · View at Scopus
  29. T. Wang, Y. Li, and M. Liu, “Gelation and self-assembly of glutamate bolaamphiphiles with hybrid linkers: effect of the aromatic ring and alkyl spacers,” Soft Matter, vol. 5, no. 5, pp. 1066–1073, 2009. View at Publisher · View at Google Scholar · View at Scopus
  30. T. Jiao, Q. Huang, Q. Zhang, D. Xiao, J. Zhou, and F. Gao, “Self-assembly of organogels via new luminol imide derivatives: diverse nanostructures and substituent chain effect,” Nanoscale Research Letters, vol. 8, no. 1, pp. 1–8, 2013. View at Publisher · View at Google Scholar · View at Scopus
  31. Y. G. Li, T. Y. Wang, and M. H. Liu, “Ultrasound induced formation of organogel from a glutamic dendron,” Tetrahedron, vol. 63, no. 31, pp. 7468–7473, 2007. View at Publisher · View at Google Scholar · View at Scopus