Fluorinated Benzocyclobutene-Based Low-k Polymer at High Frequency
Source abstract
Abstract
Through the Heck reaction, a fluorinated monomer with cross-linkable substituted vinyl and benzocyclobutene groups has been successfully synthesized. Treating this monomer at elevated temperatures results in a cross-linked polymer, exhibiting favorable dielectric properties with a permittivity (Dk) of 2.53 and a dielectric loss (Df) of 2.18 × 10–3 at a frequency of 5 GHz. Such good dielectric properties are maintained, even when the polymer is immersed in boiling water for up to 96 h. The polymer also exhibits good thermal stability with a glass transition temperature (Tg) of 263 °C as well as a coefficient of thermal expansion (CTE) of 79 ppm/°C. These data manifest that the monomer is appropriate for its use as a precursor for encapsulation resins for the manufacture of devices used in the field of high-frequency communication.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Synthesis and properties of polymers · Silicone and Siloxane Chemistry · Dielectric materials and actuators
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Synthetic and Self-Assembly Chemistry for Organic Functional Molecules, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P.R. China
Funding
National Natural Science Foundation of China · Chinese Academy of Sciences
References (32)
Show source-provided references
1. 10.1002/app.1187410.1002/app.11874 ↗
2. 10.1021/cr900281910.1021/cr9002819 ↗
3. 10.1146/annurev-chembioeng-061010-11413710.1146/annurev-chembioeng-061010-114137 ↗
4. 10.1016/S0079-6700(00)00043-510.1016/S0079-6700(00)00043-5 ↗
5. 10.1021/acsapm.8b0008310.1021/acsapm.8b00083 ↗
6. 10.1002/marc.20200060010.1002/marc.202000600 ↗
7. 10.1039/C4TA05673F10.1039/C4TA05673F ↗
8. 10.1016/j.apsusc.2019.02.14110.1016/j.apsusc.2019.02.141 ↗
9. 10.1016/S0032-3861(02)00090-310.1016/S0032-3861(02)00090-3 ↗
10. 10.1002/aelm.20150048510.1002/aelm.201500485 ↗
11. 10.1016/j.eurpolymj.2012.03.01210.1016/j.eurpolymj.2012.03.012 ↗
12. 10.1039/c2py00528j10.1039/c2py00528j ↗
13. 10.1021/ma801253a10.1021/ma801253a ↗
14. 10.1021/acs.macromol.7b0088710.1021/acs.macromol.7b00887 ↗
15. 10.1007/s10854-017-7093-110.1007/s10854-017-7093-1 ↗
16. 10.1021/acs.chemrev.5b0049510.1021/acs.chemrev.5b00495 ↗
17. 10.1016/0079-6700(95)00026-710.1016/0079-6700(95)00026-7 ↗
18. 10.1021/ma052160710.1021/ma0521607 ↗
19. 10.1039/c3ra44991b10.1039/c3ra44991b ↗
20. 10.1021/ma501263c10.1021/ma501263c ↗
21. 10.1021/acs.macromol.6b0167810.1021/acs.macromol.6b01678 ↗
22. 10.1039/D0PY00909A10.1039/D0PY00909A ↗
23. 10.1021/ol049605g10.1021/ol049605g ↗
24. 10.1080/0022233910805408710.1080/00222339108054087 ↗
25. 10.1016/0079-6700(93)90004-V10.1016/0079-6700(93)90004-V ↗
26. 10.1021/acssuschemeng.8b0359410.1021/acssuschemeng.8b03594 ↗
27. 10.1021/acssuschemeng.6b0291910.1021/acssuschemeng.6b02919 ↗
28. 10.1039/C5PY00823A10.1039/C5PY00823A ↗
29. 10.1021/acs.macromol.7b0200010.1021/acs.macromol.7b02000 ↗
30. 10.1039/D1QM00635E10.1039/D1QM00635E ↗
31. 10.1021/acssuschemeng.0c0550310.1021/acssuschemeng.0c05503 ↗
32. 10.1039/D0PY01446J10.1039/D0PY01446J ↗