Preparation of P-and S-Containing UV-Cured Cardanol Polymers via Thiol-Ene Click Chemistry

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Abstract:

Tricardanolic phosphite was synthesized in 65% yield. This cardanol-derived small molecular compound was successfully transformed into UV-cured resin via thiol-ene click reaction, by using 4,4-di (mercaptomethyl) benzophenone as both a photoinitiator and a crosslinker. The fully bio-based P-and S-containing resin is expected to be flame-retardant materials.

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63-66

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September 2013

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© 2013 Trans Tech Publications Ltd. All Rights Reserved

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[1] Amorati R, Attanasi O, and Favi G, et al: Organic Biomolecular Chemistry, Vol 9 (2011), p.1352.

Google Scholar

[2] V.S. Balachandran, S.R. Jadhav, and P.K. Vemula, et al: Chemical Society Review, Vol. 42 (2013), p.427.

Google Scholar

[3] G. Mele and G. Vasapollo: Mini-Reviews of Organic Chemistry, Vol. 5 (2008), p.243.

Google Scholar

[4] C.J. Cheng, J.W. Zha, Z.B. Liu: Chinese Journal of Applied Chemistry, 2012, 29, 392.

Google Scholar

[5] J. Wang, Y.W. Wang, C.Q. Li, et al: Advanced Materials Research, Vols. 183-185 (2011), p.1534.

Google Scholar

[6] C.E. Hoyle and C.N. Bowman, Angewandte Chemie International Edition, Vol. 49 (2010), p.1540.

Google Scholar

[7] Z.B. Liu, C.J. Cheng, Y. Zheng, et al: Polymer Materials Science and Engineering, Vol. 28 (2012), p.156.

Google Scholar

[8] Y. Zheng, C.J. Cheng, H.Q. Huang, et al: Chinese Journal of Synthetic Chemistry, Vol. 19(2011), 376.

Google Scholar