journal article·2014-09

Synthesis and Thermal Stability of Crosslinked Carbazole-Substituted Poly(Dimethylsiloxane) for Led Encapsulation

Norhuda Hidayah Nordin, Mohamad Riduwan Ramli, Nadras Othmanand, Zulkifli Ahmad

Polymers and Polymer Composites· Volume 22· Issue 7
Publisher page

Abstract

A series of carbazole substituted poly(dimethylsiloxane) (PDMS) was synthesized by hydrosilylation reaction of 9-vinyl carbazole into PDMS structure. It was then crosslinked with vinyl trimethoxysilane by condensation reaction. The fabricated product increased in refractive index with increasing carbazole content. The higher carbazole content also produced high thermal stability with an increase in Tg and degradation temperature. This behaviour owe much to the carbazole moiety as well as the formation of crosslink network These features contribute to potential use as electronic devices encapsulants and coatings.
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Research context

OpenAlex topics: Silicone and Siloxane Chemistry · Synthesis and properties of polymers · Photopolymerization techniques and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang, Malaysia

References (26)

Show source-provided references
1. 10.1002/app.2318910.1002/app.23189 ↗
2. 10.1016/S0003-2670(03)00575-010.1016/S0003-2670(03)00575-0 ↗
3. CareyJ.A., CollinsW.D.III, and PosseltJ.L. High stability optical encapsulation and packaging for light-emitting diodes in the green, blue, and near UV range, U.S. Patent 6,204,523. (2003).
4. 10.1002/1097-4628(20010124)79:4<652::AID-APP90>3.0.CO;2-U10.1002/1097-4628(20010124)79:4<652::AID-APP90>3.0.CO;2-U ↗
5. Chojnowski J. · 2000
6. 10.1007/s10971-009-2117-910.1007/s10971-009-2117-9 ↗
7. 10.1007/BF0324581310.1007/BF03245813 ↗
8. 10.1016/S0014-3057(02)00374-910.1016/S0014-3057(02)00374-9 ↗
9. Xie K. · J. Fiber Bioeng. Informatics · 2008 · 1 · 71
10. 10.1016/j.polymer.2006.02.03010.1016/j.polymer.2006.02.030 ↗
11. 10.1016/j.polymdegradstab.2011.10.00110.1016/j.polymdegradstab.2011.10.001 ↗
12. 10.1002/047175712810.1002/0471757128 ↗
13. 10.1021/ie50559a03410.1021/ie50559a034 ↗
14. Thomas V. · Journal of Biomedical Materials Research Part A · 2009 · 89 · 19210.1002/jbm.a.31937 ↗
15. 10.1016/j.eurpolymj.2008.09.00110.1016/j.eurpolymj.2008.09.001 ↗
16. 10.1201/978142001252110.1201/9781420012521 ↗
17. 10.1002/0470025107.ch610.1002/0470025107.ch6 ↗
18. 10.1016/j.jphotochem.2007.08.03310.1016/j.jphotochem.2007.08.033 ↗
19. 10.1016/S0022-3093(05)80486-710.1016/S0022-3093(05)80486-7 ↗
20. 10.1007/BF0058769910.1007/BF00587699 ↗
21. Nielsen L. · J. Macromol. Sci. Rev. Macromol. Chem. C3 · 1969 · 399 · 699
22. 10.1016/j.polymdegradstab.2009.12.00210.1016/j.polymdegradstab.2009.12.002 ↗
23. 10.1016/0032-3861(96)82909-010.1016/0032-3861(96)82909-0 ↗
24. 10.1002/pi.431510.1002/pi.4315 ↗
25. 10.1016/S0141-3910(01)00261-010.1016/S0141-3910(01)00261-0 ↗
26. 10.1002/pola.2167910.1002/pola.21679 ↗