Journals / Turkish Journal of Chemistry / 2009 / Cilt: 33 - Sayı: 5

Synthesis and physical studies of polycarbonate of p-tert-butylcalix[4]arena: a highly selective receptor for $Na^+$

Pages
647–656
Publication Date
2022-11-05
DOI
—
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⚡ TL;DR(Too Long; Didn't Read)

The experimental results indicate that the polycarbonate was successfully synthesized with average molecular weight Mw , (2.328 × 104 g/mol), which was determined by static light scattering method using a Berry plot.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The synthesis and characterization of a polycarbonate of p-tert-butylcalix[4]arene 4 are reported.
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Key Findings & Data:It was synthesized by condensation of p-tert-butylcalix[4]arenetetraol derivative 3 with ethyl chloroformate.
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Conclusion & Impact:The experimental results indicate that the polycarbonate was successfully synthesized with average molecular weight Mw , (2.328 × 104 g/mol), which was determined by static light scattering method using a Berry plot.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

The synthesis and characterization of a polycarbonate of p-tert-butylcalix[4]arene 4 are reported. It was synthesized by condensation of p-tert-butylcalix[4]arenetetraol derivative 3 with ethyl chloroformate. This new polymer possesses a hydrolyzable backbone and tunable hydrophobic/hydrophilic properties. The experimental results indicate that the polycarbonate was successfully synthesized with average molecular weight Mw , (2.328 × 104 g/mol), which was determined by static light scattering method using a Berry plot. The structure of this polymer was determined by IR spectroscopy. The thermal properties were investigated using differential scanning calorimetry (DSC). The degree of crystallinity was measured by means of XRD. The extraction ability of compounds 3 and 4 toward alkali metal cations was studied using conductometry. It was observed that compound 4 had the highest extractability and selectivity toward Na+.

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Cite This Article

ASMAN, G., ASHRAM, M., AL-GHEZAWI, N., AWAAD, I. A. (2022). Synthesis and physical studies of polycarbonate of p-tert-butylcalix[4]arena: a highly selective receptor for $Na^+$. Turkish Journal of Chemistry, Cilt: 33 - Sayı: 5, 647–656. https://ajindex.com/articles/602138

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References (27)

  1. Vicens, J.; B¨ohmer, V. Calixarenes: A Versatile Class of Macrocyclic Compounds; Kluwer: Dordrecht, 1991
  2. Asfari, Z.; B¨ohmer, V.; Harroweld, J.; Vicens, J. (Eds.), Calixarenes 2001, Kluwer Academic Publishers, Dordrecht
  3. Kim, J. S.; Shon, O. J.; Sim, W. B.; Kim, S. K.; Cho, M. H.; Kim, J. G.; Suh, I. H.; Kim, D. W. J. Chem. Soc., Perkin Trans. 1, 2001, 31-36
  4. Kim, J. S.; Thuery, P.; Nierlich, M.; Rim, J. A.; Yang, S. H.; Lee, J. K.; Cho, K. H., Lee, J. H.; Vicens, J. Bull. Korean Chem. Soc. 2001, 22, 321-324
  5. Vicens, J.; B¨ohmer, V.; Calixarenes: A Versatile Class of Macrocyclic Compounds Topics in Inclusion Science, Kluwer Academic Publishers, Dordrecht, 1991
  6. Mathieu, M.; Asfari, Z.; Vicens, J.; Tetrahedron Lett. 2002, 43, 1225-1229
  7. Kim, J. S.; Yu, S. H.; Cho, M. H.; Shon, O. J.; Rim, J. A.; Yang, H.; Lee, J. K.; Lee, S. J. Bull. Korean Chem. Soc. 2001, 22, 519-522
  8. Sugiura, M. Sep. Sci. Tech. 1990, 25, 1189-1199
  9. Blanda, M. T.; Adou, E. Chem. Commun. 1998, 139-140
  10. Dondoni, A.; Ghiglione, C.; Marra, A.; Scoponi, M. Chem. Commun. 1997, 673-674
  11. Harris, S. J.; Barrett, G.; McKervey, M. A. J. Chem. Commun. 1991, 1224-1225
  12. Delig¨oz, H. and Yilmaz, M. J. Polym. Sci. Part A: Polym. Chem. 1995, 33, 2851-2853
  13. Yilmaz, M. React. Funct. Polym. 1999, 40, 129-133
  14. Gravett, D.;.; Guillet, J. E. Macromolecules 1996, 29, 617-624
  15. Lanza, R. P.; Langer, R.; Chick, W. L. Principles of Tissue Engineering, R.G. Landes/Academic Press: San Diego, CA, 1997
  16. Ratner, B. D.; Hoffman, A. S.; Schoen, F. J.; Lemons, J. E. Biomaterials Science: An Introduction to Material in Medicine, Academic Press: San Diego, 2000
  17. Griffith, L. G.; Naughton, G. Science, 2002, 295, 1009-1014
  18. Zhou, Q. J.; Kohn, K. Macromolecules 1990, 23, 3399-3406
  19. Gelbin, M. E.; Kohn, J. J. Am. Chem. Soc. 1992, 114, 3962-3965
  20. Kimura, Y.; Shirotani, K.; Yamane, H.; Kitao, T. Macromolecules 1988, 21, 3338-3340
  21. Tian, D.; Dubois, P.; Grandfils, C. J´erˆome, R. Macromolecules 1997, 30, 406-409
  22. Barrera, D. A.; Zylstra, E.; Lansbury, P. T.; Langer, R. J. Am. Chem. Soc. 1993, 115, 11010-11011
  23. Barrera, D. A.; Zylstra, E.; Lansbury, P. T.; Langer, R. Macromolecules 1995, 28, 425-432
  24. Elisseeff, J.; Anseth, K.; Langer, R.; Hrkach, J. S. Macromolecules 1997, 30, 2182-2184
  25. Carnahan, M. A.; Grinstaff, M. W. J. Am. Chem. Soc. 2001, 123, 2905-2906
  26. Carnahan, M. A.; Grinstaff, M. W. Macromolecules 2001, 34, 7648-7655
  27. Carnah