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Synthesis and Characterization of Hydroxy-telechelic Four-arm Star-shaped Oligo(tetrahydrofuran), Their Crosslinking, and Thermomechanical Investigation of the Poymer Network

Published online by Cambridge University Press:  01 March 2012

Ke-Ke Yang
Affiliation:
Center for Biomaterial Development and Berlin Brandenburg Center for Regenerative Therapies (BCRT), Institute of Polymer Research, Helmholtz-Zentrum Geesthacht, Kantstr.55, 14513 Teltow, Germany National Engineering Laboratory of Eco-Friendly Polymeric Materials (Sichuan), College of Chemistry, Sichuan University, Wangjiang Road 29, Chengdu 610064, P. R. China
J. Zotzmann
Affiliation:
Center for Biomaterial Development and Berlin Brandenburg Center for Regenerative Therapies (BCRT), Institute of Polymer Research, Helmholtz-Zentrum Geesthacht, Kantstr.55, 14513 Teltow, Germany
A. Lendlein
Affiliation:
Center for Biomaterial Development and Berlin Brandenburg Center for Regenerative Therapies (BCRT), Institute of Polymer Research, Helmholtz-Zentrum Geesthacht, Kantstr.55, 14513 Teltow, Germany Tianjin University-Helmholtz-Zentrum Geesthacht, Joint Laboratory for Biomaterials and Regenerative Medicine, Kantstr. 55, Teltow, Germany
M. Behl
Affiliation:
Center for Biomaterial Development and Berlin Brandenburg Center for Regenerative Therapies (BCRT), Institute of Polymer Research, Helmholtz-Zentrum Geesthacht, Kantstr.55, 14513 Teltow, Germany Tianjin University-Helmholtz-Zentrum Geesthacht, Joint Laboratory for Biomaterials and Regenerative Medicine, Kantstr. 55, Teltow, Germany
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Abstract

Here the synthesis of hydroxy-telechelic four-arm star-shaped oligotetrahydrofuran (4PTHF) with controllable molecular weight was explored, which was perfomed as living cationic ring-opening polymerization of THF using pentaerythritol and trifluoromethanesulfonicanhydride as initiation system. The molecular weights of the 4PTHF were a function of the reaction time. A polymer network was prepared from the hydroxy-telechelic 4PTHF precursor by crosslinking with diisocyanate and the shape-memory properties were determined. High values for Rf and Rr > 98% were obtained even at high programmed elongations, which suggest the 4PTHF-network as a promising shape-memory material. These materials might have a great potential, as the upscaling of synthesis could be successfully demonstrated.

Type
Research Article
Copyright
Copyright © Materials Research Society 2012

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References

REFERENCES

1. Behl, M., Zotzmann, J., and Lendlein, A., Adv. Polym. Sci., 226, 1 (2010).Google Scholar
2. Behl, M. and Lendlein, A., Soft Matter, 3, 58 (2007).Google Scholar
3. Li, J.H., et al. ., Macromolecules, 44, 5336 (2011).Google Scholar
4. Hsu, J.C., et al. ., Macromolecules, 44, 5168 (2011).Google Scholar
5. Leng, J.S., et al. ., Prog. Mater. Sci., 56, 1077 (2011).Google Scholar
6. Lendlein, A. and Langer, R., Science, 296, 1673 (2002).Google Scholar
7. Wischke, C., et al. ., Euro. J. Pharm. Sci., 41, 136 (2010).Google Scholar
8. Xue, L.A., Dai, S.Y., and Li, Z., Biomaterials, 31, 8132 (2010).Google Scholar
9. Takashima, K., Rossiter, J., and Mukai, T., Sensor. Actuat. A-Phys., 164, 116 (2010).Google Scholar
10. Filion, T.M., et al. ., Biomaterials, 32, 985 (2011).Google Scholar
11. Alteheld, A., et al. ., Angew. Chem. Int. Edit., 44, 1188 (2005).Google Scholar
12. Ahn, S.K., et al. ., ACS Nano, 5, 3085 (2011).Google Scholar
13. Behl, M., et al. ., Adv. Funct. Mater., 19, 102 (2009).Google Scholar
14. Zotzmann, J., et al. ., Adv. Mater., 22, 3424 (2010).Google Scholar
15. Zotzmann, J., et al. ., Adv. Funct. Mater., 20, 3583 (2010).Google Scholar
16. Lendlein, A., et al. ., Biomacromolecules, 10, 975 (2009).Google Scholar
17. VanCaeter, P., et al. ., Polymer Bull, 39, 589 (1997).Google Scholar
18. Zotzmann, J., et al. ., J. Mater. Sci. Mater. Med., 20, 1815 (2009).Google Scholar
19. Mah, S., Hwang, H.S., and Shin, J.H., J. Appl. Polym. Sci., 74, 2637 (1999).Google Scholar
20. Cai, G.F. and Yan, D.Y., Makromol. Chem., 187, 553 (1986).Google Scholar
21. Van Renterghem, L.M., Goethals, E.J., and Du Prez, F.E., Macromolecules, 39, 528 (2006).Google Scholar
22. Oike, H., et al. ., Macromol. Rapid Comm., 21, 1185 (2000).Google Scholar
23. Sugi, R., Yokoyama, A., and Yokozawa, T., Macromol. Rapid Comm., 24, 1085 (2003).Google Scholar
24. Arslan, H., et al. ., J. Appl. Polym. Sci., 102, 516 (2006).Google Scholar
25. Wagermaier, W., et al. ., Adv. Polym. Sci., 226, 97 (2010).Google Scholar