Hydrophobically modified poly (acrylic acid) using calix[4]arene derivative. Ionophoric properties and extraction abilities toward alkali metal cations

Polymers for Advanced Technologies

Volumn 20, Issue 12, 2009, Pages 1050-1059

  Hajipour, A R ^a,b   Habibi, S ^a,b   Ruoho, A E ^a,b  

^a UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

^b ISFAHAN UNIVERSITY OF TECHNOLOGY   (Iran)

Author keywords

Calixarenes; Direct esterification; Grafting; Hydrophobic modification; Ionophores; Poly (acrylic acid)

Indexed keywords

ALKALI METAL CATIONS; BINDING ABILITIES; CALIX[4]ARENE DERIVATIVES; CALIX[4]ARENES; CALIXARENES; CHEMICAL COMPOSITIONS; DIRECT ESTERIFICATION; GRAFTING METHOD; GRAFTING YIELD; H NMR SPECTROSCOPY; HYDROPHOBIC MODIFICATION; MOLAR RATIO; N ,N-DIMETHYLFORMAMIDE; POLY(ACRYLIC ACID ); POLYACRYLIC ACIDS; QUARTZ MICROBALANCE; REACTION TIME; SEMI-PERMEABLE MEMBRANES; THERMAL PROPERTIES;

ALKALINITY; CARBOXYLIC ACIDS; CESIUM; CHLORINE COMPOUNDS; DIMETHYLFORMAMIDE; ESTERIFICATION; ESTERS; EXTRACTION; GRAFTING (CHEMICAL); HYDROPHOBICITY; ION SELECTIVE ELECTRODES; METAL RECOVERY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; ORGANIC ACIDS; OXIDE MINERALS; PHENOLS; POSITIVE IONS; QUARTZ; SCANNING ELECTRON MICROSCOPY; SENSORS; THERMODYNAMIC PROPERTIES;

ION SELECTIVE MEMBRANES;

CHEMICAL COMPOSITION; CHEMICAL MODIFICATION; GRAFTING; HYDROPHOBIC PROPERTY; POLYACRYLIC ACID; SOLUBILITY; TEMPERATURE; THERMAL PROPERTY;

EID: 75849152687     PISSN: 10427147     EISSN: 10991581     Source Type: Journal    
DOI: 10.1002/pat.1362     Document Type: Article

References (53)

1. K.L. Gineste, C. Largueze, G. Pourcelly, J. Appl. Polym. Sci. 1994, 51, 63.
2. J.S. Roman, M.C. Escudero, A. Gallardo, R.S. Cruz, E. Jorge, J. Haro, L. Alvarez, I. Millan, J. Bujan, J.M. Bellon, J.L. Castillo-Olivares, Biomaterials 1994, 15, 759.
3. H. Arasawa, C. Odawara, R. Yokoyama, H. Saitoh, T. Yamauchi, N. Tsubokawa, React. Funct. Polym. 2004, 61, 153.
4. S. Liu, F. Zhou, S. Di D, Jiang, Colloids Surf. A 2004, 244, 87.
5. J.G. Heffernan, D.C. Sherrington, J. Appl. Polym. Sci. 1984, 29, 3013.
6. M. Chaimber, R. Parnas, Y. Cohen, J. Appl. Polym. Sci. 1989, 37, 2921.
7. G. Chen, A.S. Hoffman, Nature 1995, 375, 49.
8. S. Gupta, P. Uhlmann, M. Agrawal, V. Lesnyak, N. Gaponik, F. Simon, M. Stamm, A. Eychmüller, J. Mater. Chem. 2008, 18, 214.
9. G. Delaittre, J. Nicolas, C. Lefay, M. Save, B. Charleux, Chem. Commun. 2005, 614.
10. H. Zengin, B. Hu, J.A. Siddiqui, R.M. Ottenbrite, Polym. Adv. Technol. 2006, 17, 372.
11. F. Yang, H. Guo, X. Cai, X. Chen, React. Funct. Polym. 2005, 64, 163.
12. A.S. Shedge, A.K. Lele, P.P. Wadgaonkar, H. Hourdet, P. Perrin, C. Chassenieux, M.V. Badiger, Macromol. Chem. Phys. 2005, 206, 464.
13. O. Hormi, J. Heikkinen, J.P. Heiskanen, Polym. Adv. Technol. 2006, 17, 426.
14. Y.O. Park, Y. Ito, Y. Imanishi, Chem. Mater. 1997, 9, 2755.
15. Y. Ito, M. Inaba, D.-J. Chung, Y. Imanishi, Macromolecules 1992, 25, 7317.
16. C.D. Gutsche, Calixarenes, monographs in supramolecular chemistry, Vol 1 (Ed.: J. F Stoddart), The Royal Society of Chemistry, Cambridge, 1998.
17. C.D. Gutsche, M. Iqbal, D. Stewart, J. Org. Chem. 1986, 51, 742.
18. V. Bohmer, Angew. Chem. Int. Ed. Engl. 1995, 34, 713.
19. S. Shinkai, M. Takeshita, Bull. Chem. Soc. Jpn. 1995, 68, 1088.
20. D.M.W. Arrigan, G. Svehla, S.J. Harris, M.A. McKervey, Electroanalysis 1996, 6, 97.
21. H. Deligöz, Supramol. Chem. 2003, 15(5), 317.
22. M. Durmaz, S. Alpaydin, A. Sirit, M. Yilmaz, Tetrahedron: Asymmetry 2007, 18, 900.
23. E. Kocabas, A. Karakucuk, A. Sirit, M. Yilmaz, Tetrahedron: Asymmetry 2006, 17, 1514.
24. G.U. Jin-ying, H.E. Wan-ping, S.H.I. Xian-fa, J.I. Liang-nian, Chem. Res. Chinese Univ. 2008, 24(1), 106.
25. A. Pailleret, G.E. Herzog, D.W.M. Arrigan, Electrochem. Commun. 2003, 5, 68.
26. A. Oluyomi, J.L. Okunola, K.J. Seganish, P.Y. Salimian, T.D. Zavalij, Tetrahedron 2007, 63, 10743.
27. A. Yimaz, E. Yilmaz, M. Yilmaz, R.A. Bartsch, Dyes Pigments 2007, 74, 54.
28. W.F. Nijenhuis, A.R. Van Doorm, A.M. Reichwein, F. De Jong, D.N. Reinhoudt, J. Am. Chem. Soc. 1991, 113, 3607.
29. W.P. Zhu, J. Ling, Z.Q. Shen, Macromol. Chem. Phys. 2006, 207, 844.
30. L.P. Lou, L.M. Jiang, J.Z. Liu, W.L. Sun, Z.Q. Shen, Polym. Int. 2007, 56, 796.
31. S. Strandman, M. Luostarinen, S. Niemela, K. Rissanen, H. Tenhu, J. Polym. Sci. A Polym. Chem. 2004, 42, 4189.
32. S. Strandman, P. Pulkkinen, H. Tenhu, J. Polym. Sci. A Polym. Chem. 2005, 43, 3349.
33. W. Zhu, P. Gou, Z. Shen, Macromol. Symp. 2008, 261, 74.
34. S. Jacob, I. Majoros, J.P. Kennedy, Macromolecules 1996, 29, 8631.
35. O. Gungor, S. Memon, M. Yilmaz, D.M. Roundhill, React. Funct. Polym. 2005, 63,1.
36. M. Tabakci, S. Memon, M. Yilmaz, D.M. Roundhill, J. Polym. Sci. A. Polym. Chem. 2004, 42, 186.
37. A. Dondoni, A. Marra, M. Rossi, M. Scoponi, Polymer 2004, 45, 6195.
38. K.E. Koening, G.M. Lein, P. Stuckler, T. Kaneda, D.J. Cram, J. Am. Chem. Soc. 1979, 101, 3553.
39. R.C. Helgeso, G.R. Weisman, J.L. Toner, T.L. Tarnowski, L. Chau, J.M. Mayer, D.J. Cram, J. Am. Chem. Soc. 1979, 101, 4928.
40. G.M. Lein, D.J. Cram, J. Am. Chem. Soc. 1985, 107, 448.
41. E.M. Collins, M.A. McKervey, E. Madigan, M.B. Moran, M. Owens, G. Ferguson, S.J. Harris, J. Chem. Soc. Perkin Trans. 1991, 1, 3137.
42. A. Ikeda, H. Tsuzuki, S. Shinkai, J. Chem. Soc. Perkin Trans. 2, 1994, 2073.
43. A. Ikeda, S. Shinkai, J. Am. Chem. Soc. 1994, 116, 3102.
44. K.E. Koeing, G.M. Lein, P. Stuckler, T. Kaneda, D.J. Cram, J. Am. Chem. Soc. 1979, 101, 3553.
45. H. Deligöz, J. Inclusion Phenom. Macrocyclic Chem. 2006, 55, 197.
46. H. Deligöz, J. Inclusion Phenom. Macrocyclic Chem. 2000, 39, 123.
47. H. Deligöz, J. Polym. Sci. A. Polym. Chem. 1995, 33, 2851.
48. P.D. Beer, J.P. Martin, M.G.B. Drew, Tetrahedron 1992, 48, 9917.
49. D. Matt, C. Loeber, J. Vicenes, Z. Asfari, J. Chem. Soc. Chem. Commun. 1993, 604.
50. J.C. Ma, D.A. Dougherty, Chem. Rev. 1997, 97, 1303.
51. A. Ikeda, T. Nagasaki, K. Araki, S. Shinkai, Tetrahedron 1992, 48, 1059.
52. A. Ikeda, S. Shinkai, Chem. Rev. 1997, 97, 1713.
53. T. Nabeshima, T. Aoki, Y. Yano, Tetrahedron Lett. 1997, 38, 8323.