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Conventional versus ultrasound and microwave assisted synthesis: Some new environmentally friendly functionalized picolinium-based ionic liquids with potential antibacterial activity Cover

Conventional versus ultrasound and microwave assisted synthesis: Some new environmentally friendly functionalized picolinium-based ionic liquids with potential antibacterial activity

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Open Access
|Sep 2015

References

  1. 1. J. H. Davis, Jr., Task-specific ionic liquids,.(2004) 1072–1079; DOI: 10.1246/cl.2004.1072.
  2. 2. J. H. Wang, D. H. Cheng, X. Y. Chen, Z. Du and Z. L. Fang, Direct extraction of double stranded DNA into ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate and its quantification,.(2007) 620–625; DOI: 10.1021/ac061145c.
  3. 3. F. Endres, Ionic liquids: solvents for the electrodeposition of metals and semiconductors,.(2002) 144–154; DOI: 10.1002/1439–7641(20020215)3:2.
  4. 4. Y. F. Lin and I. W. Sun, Electrodeposition of zinc from a Lewis acidic zinc chloride-1-ethyl-3-methylimidazolium chloride molten salt,(1999) 2771–2777; DOI: 10.1016/S0013-4686(99)00003-1.
  5. 5. M. A. M. Ibrahim, M. Messali, Z. Moussa, A. Y. Alzahrani, S. N. Alamry and B. Hammouti, Corrosion inhibition of carbon steel by imidazolium and pyridinium cations ionic liquids in acidic environment,(2013) 375–389; DOI: 10.4152/pea.201106375.
  6. 6. M. Messali, A green microwave-assisted synthesis, characterization and comparative study of new pyridazinium-based ionic liquids derivatives towards corrosion of mild steel in acidic environment,.(2011) 174–185.
  7. 7. M. Messali and M. A. M. Asiri, A green ultrasound-assisted access to some new 1-benzyl-3-(4-phenoxybutyl) imidazolium-based ionic liquids derivatives – potent agents inhibitors against corrosion of mild steel in acidic environment,(2013) 770–785.
  8. 8. A. Zarrouk, M. Messali, M. R. Aouad, H. Zarrok, R. Salghi, B. Hammouti, A. Chetouani and S. S. Al-Deyab, Some new ionic liquids derivatives: Synthesis, characterization and comparative study towards corrosion of C-steel in acidic media,.(2012) 3427–3436.
  9. 9. A. Zarrouk, M. Messali, H. Zarrok, R. Salghi, A. Al-Sheikh Ali, B. Hammouti, S. S. Al-Deyab and F. Bentiss, Synthesis, characterization and comparative study of new functionalized imidazolium-based ionic liquids derivatives towards corrosion of C38 steel in molar hydrochloric acid,.(2012) 6998–7015.
  10. 10. S. Takahashi, N. Koura, S. Kohara, M. L. Saboungi and L. A. Curtiss, Technological and scientific issues of room-temperature molten salts,(2009) 91–105; DOI: 10.1016/S1288-3255(99)00105-7.
  11. 11. J. F. Brennecke and E. J. Magin, Ionic liquids: innovative fluids for chemical processing,(2001) 2384–2389; DOI: 10.1002/aic.690471102.
  12. 12. F. Shi, Y. Gu, Q. Zhang and Y. Deng, Development of ionic liquids as green reaction media and catalysts,(2004) 179–186; DOI: 10.1023/B:CATS.0000038536.55980.
  13. 13. R. F. De Souza, J. C. Padilha, R. S. Goncalves and J. L. Rault-Berthelot, Dialkyl imidazolium ionic liquids as electrolytes for hydrogen production from water electrolysis,(2006) 211–216; DOI: 10.1016/j.elecom.2005.10.036.
  14. 14. P. Kubisa, Application of ionic liquids as solvents for polymerization processes,.(2004) 3–12; DOI: 10.1016/j.progpolymsci.2003.10.002.
  15. 15. R. Kawano, H. Matsui, C. Matsuyama, A. Sato, M. A. B. H. Susan, N. Tanabe and M. Watanabe, High performance dye-sensitized solar cells using ionic liquids as their electrolytes,(2004) 87–92; DOI: 10.1016/j.jphotochem.2003.12.019.
  16. 16. G. Zbancioc, A. M. Zbancioc and I. I. Mangalagiu, Ultrasound and microwave assisted synthesis of dihydroxyacetophenone derivatives with or without 1,2-diazine skeleton,(2014) 802–811; DOI: 10.1016/j.ultsonch.2013.09.012.
  17. 17. D. Garella, S. Tagliapietra, V. P. Mehta, E. Van Der Eycken and G. Cravotto, Straightforward functionalization of 3,5-dichloro-2-pyrazinones under simultaneous microwave and ultrasound irradiation,, 136–140; DOI: 10.1055/s-0029-1217065.
  18. 18. V. Bejan, D. Mantu and I. I. Mangalagiu, Ultrasound and microwave assisted synthesis of isoindolo-1,2-diazine: A comparative study,.(2012) 999–1002; DOI: 10.1016/j.ultsonch.2012.02.012.
  19. 19. I. I. Mangalagiu, Recent achievements in the chemistry of 1,2-diazines,.(2011) 730–752; DOI: 10.2174/138527211794519050.
  20. 20. G. Zbancioc and I. I. Mangalagiu, Pyrrolopyridazine derivatives as blue organic luminophores: synthesis and properties. Part 2,(2010) 278–282; DOI: 10.1016/j.tet.2009.10.110.
  21. 21. A. Loupy, A. Petit, J. Hamelin, F. Texier-Boulier, P. Jacquault and D. Mathe, New solvent free organic synthesis using focused microwaves,, 1213–1234; DOI: 10.1055/s-1998–6083.
  22. 22. M. Messali, An efficient and green sonochemical synthesis of some new eco-friendly functionalized ionic liquids,.(2014) 63–70; DOI: 10.1016/j.arabjc.2013.08.023.
  23. 23. M. Messali and S. A. Ahmed, A green microwave-assisted synthesis of new pyridazinium-based ionic liquids as an environmentally friendly alternative,.(2011) 70–75; DOI: 10.4236/gsc.2011.13012.
  24. 24. M. Messali, A facile and green microwave-assisted synthesis of new functionalized picolinium-based ionic liquids (in press); DOI: 10.1016/j.arabjc.2011.06.030.
  25. 25. J. R. Carreon, K. M. Stewart, K. P. Mahon, S. Shin and S. O. Kelley, Cyanine dye conjugates as probes for live cell imaging,(2007) 5182–5185; DOI: 10.1016/j.bmcl.2007.06.097.
  26. 26. M. Messali, Z. Moussa, A. Y. Alzahrani, M. Y. El-Naggar, A. S. El Douhaibi, Z. M. A. Judeh and B. Hammouti, Synthesis, characterization, antimicrobial activity of new green-chemistry-friendly ionic liquids,(2013) 1627–1634; DOI: 10.1016/j.chemosphere.2012.12.062.
  27. 27. M. Messali, M. R. Aouad, A. A. Ali, N. Rezki, T. Ben Hadda and B. Hammouti, Synthesis, characterization, and POM analyses of novel bioactive imidazolium-based ionic liquids,(2015) 1387–1395; DOI: 10.1007/s00044-014-1211-x.
  28. 28. Clinical and Laboratory Standards Institute (CLSI),, Wayne (PA) 1999.
  29. 29. H. Nomura, Y. Isshiki, K. Sakuda, K. Sakuma and S. Kondo, The antibacterial activity of compounds isolated from Oakmoss againstand other(2012) 1560–1567; DOI: 10.1007/s11064-012-0751-z.
  30. 30. Clinical and Laboratory Standards Institute (CLSI),. Approved standard, 5th ed., Wayne (PA) 2000.
DOI: https://doi.org/10.1515/acph-2015-0028 | Journal eISSN: 1846-9558 | Journal ISSN: 1330-0075
Language: English
Page range: 253 - 270
Accepted on: Jun 19, 2015
Published on: Sep 30, 2015
Published by: Croatian Pharmaceutical Society
In partnership with: Paradigm Publishing Services
Related subjects:

© 2015 Mouslim Messali, published by Croatian Pharmaceutical Society
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.