Journals / Turkish Journal of Chemistry / 2007 / Cilt: 31 - Sayı: 1

Studies on the Preparation of a,w -Telechelic Polymers by the Combination of Reverse Atom Transfer Radical Polymerization and Atom Transfer Radical Coupling Processes

Pages
1–10
Publication Date
2007-01-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

ATRC reactions of these polymers were efficient in obtaining telechelics and a maximum extent of coupling qmax = 0.99 can be attained under appropriate conditions.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Monofunctional polystyrenes with cyano, carboxylic acid, and hydroxyl terminal groups were synthesized by reverse atom transfer radical polymerization (RATRP) using corresponding azo initiators in conjunction with copper and iron complexes.
📊
Key Findings & Data:These functional polymers were further used in the atom transfer radical coupling (ATRC) reaction in the presence of Cu(I) and Cu(0) in order to obtain telechelic polystyrenes.
💡
Conclusion & Impact:ATRC reactions of these polymers were efficient in obtaining telechelics and a maximum extent of coupling qmax = 0.99 can be attained under appropriate conditions.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Reverse atom transfer radical polymerization (RATRP) · atom transfer radical coupling (ATRC) · azo-initiator

Abstract

Monofunctional polystyrenes with cyano, carboxylic acid, and hydroxyl terminal groups were synthesized by reverse atom transfer radical polymerization (RATRP) using corresponding azo initiators in conjunction with copper and iron complexes. These functional polymers were further used in the atom transfer radical coupling (ATRC) reaction in the presence of Cu(I) and Cu(0) in order to obtain telechelic polystyrenes. In the iron-mediated system, while RATRP experiments gave satisfactory results, the corresponding ATRC process yielded polymers with low functionality. The copper-mediated system, however, gave contrary results. In the RATRP step, initiation efficiency was rather low and polymers with relatively higher polydispersity were obtained. ATRC reactions of these polymers were efficient in obtaining telechelics and a maximum extent of coupling qmax = 0.99 can be attained under appropriate conditions.

Özet

Monofunctional polystyrenes with cyano, carboxylic acid, and hydroxyl terminal groups were synthesized by reverse atom transfer radical polymerization (RATRP) using corresponding azo initiators in conjunction with copper and iron complexes. These functional polymers were further used in the atom transfer radical coupling (ATRC) reaction in the presence of Cu(I) and Cu(0) in order to obtain telechelic polystyrenes. In the iron-mediated system, while RATRP experiments gave satisfactory results, the corresponding ATRC process yielded polymers with low functionality. The copper-mediated system, however, gave contrary results. In the RATRP step, initiation efficiency was rather low and polymers with relatively higher polydispersity were obtained. ATRC reactions of these polymers were efficient in obtaining telechelics and a maximum extent of coupling qmax = 0.99 can be attained under appropriate conditions.

🔖

Cite This Article

AYDOĞAN, B., YAĞCI, Y. (2007). Studies on the Preparation of a,w -Telechelic Polymers by the Combination of Reverse Atom Transfer Radical Polymerization and Atom Transfer Radical Coupling Processes. Turkish Journal of Chemistry, Cilt: 31 - Sayı: 1, 1–10. https://ajindex.com/articles/217984

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (24)

  1. V. Percec, C. Pugh, O. Nuyken, and S.D. Pask, “Macromonomers,Oligomers and Telechelics” in Comprehensive Polymer Science, Vol. 6, Eds.: G. Allen, J.C. Bevington, pp.281-357,
  2. Pergamon Press,
  3. Oxford, E.J. Goethals, “Telechelic Polymers: Synthesis and Applications” CRC Press,
  4. Boca Raton, FL, 1989.
  5. Y. Yagci, O. Nuyken and V. Graubner, “Telechelic Polymers” in Encyclopedia of Polymer Science and Technology, 3rdEd., vol. 12, Ed. J.I. Kroschwitz, pp. 57-130, John Wiley & Sons, Inc., New York, 2005. M. Fontanille, “Carbanion Polymerization: Termination and Functionalization” in Comprehensive Polymer Science, Eds.: G.C. Eastmond, A. Ledwith, S. Russo, and P. Sigwalt, Vol. 3, pp.425-432
  6. Pergamon Press, London, 1989. J.P. Kennedy and B. Ivan, “Designed Polymers by Carbocationic Macromolecular Engineering: Theory and Practice” Hanser Verlag, Munchen, 1992.
  7. E.J. Goethals, Makromol. Chem. Macromol. Symp. 6, 53-66 (1986).
  8. O.W. Webster, Makromol.Chem. Macromol. Symp. 70, 75-81 (1993).
  9. O.W. Webster, J. Polym. Sci.,Polym. Chem. Ed. 38, 2855-2860 (2000).
  10. J.C. Brosse, D. Depouet, F. Epaillard, J.C. Soatif, G. Legeay and K. Dusek, Adv. Polym. Sci. 81, 167-223 (1987).
  11. M.A. Hillmyer and R.H. Grubbs, Polym. Prepr. (Am. Chem. Soc. Div. Polym. Chem.) 34, 388 (1993).
  12. M.A. Hillmyer and R.H. Grubbs, Macromolecules 26, 872-874 (1993).
  13. C. Fraser, M. Hillmyer, E. Gutierrez and R.H. Grubbs, Macromolecules 28, 7256-7261 (1995).
  14. M.A. Hillmyer, S.T. Nguyen, R.H. Grubbs, Macromolecules 30, 718-721 (1997).
  15. B.R. Maughon, T. Morita, C.W. Bielawski and R.H. Grubbs, Macromolecules 33, 1929-1935 (2000).
  16. T. Morita, B.R. Maughan, C.W. Bielawski and R.H. Grubbs, Macromolecules 33, 6621-6623 (2000).
  17. C.W. Bielawski, O.A. Scherman and R.H. Grubbs, Polymer 42, 4939-4945 (2001).
  18. C.W. Bielawski, J.M. Jethmalani and R.H. Grubbs, Polymer 44, 3721-3726 (2003).
  19. S.A.F. Bon, F.A.C. Bergman, J.J.G.S. van Es, B. Klumperman and A.L. German, “Controlled radical polymerization: towards control of molecular weight” in Controlled Radical Polymerization, Ed., K. Matyjaszewski, pp. 236-255, ACS Symposium Series 685, 1998. M.K. Mishra and Y. Yagci, “Living Radical Polymerization” in Handbook of Radical Vinyl Polymeriza- tion”, pp. 233-274,
  20. Marcel Dekker, New York, 1998.
  21. J.S. Wang and K. Matyjaszewski, J. Am. Chem. Soc 117, 5614 (1995).
  22. S.G. Gaynor, S. Edelman and K. Matyjaszewski, Macromolecules 29, 1079 (1996).
  23. K. Matyjaszewski and J. Xia, Chem. Rev. 101, 2921 (2001).
  24. M.K. Geoges, R.P.N. Veregin, P.M. Kazmaier and G.K. Ha