journal article·2023-07-14

Synthesis of Low-Dielectric Polyureas by Incorporating Phenyl-Substituted Cage Silsesquioxanes in the Main Chain

Tasuku Kamitani, Masashi Nakamura, Seiji Watase, Tomoyuki Suzuki, Hiroaki Imoto, Kensuke Naka

ACS Applied Polymer Materials· Volume 5· Issue 7
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Abstract

Establishing a design concept for low-dielectric constant (ε r ) and low dissipation factor (tan δ) polymeric materials is vital to improve signal transmission rates. Polyurea-based polymers with strong dipole moments have been reported to achieve higher ε r (above 5.0) than most of the traditional polymer dielectrics. However, polyurea-based polymers with low ε r and tan δ values have not been reported yet. In this study, bis(3-aminopropyl)-double-decker-shaped phenyl-substituted silsesquioxane (DDSQ) ( 1 ) was polymerized with various diisocyanates, i.e., methylenediphenyl 4,4′-diisocyanate ( 2a ), 4,4′-diisocyanato-3,3′-dimethylbiphenyl diisocyanate ( 2b ), m -xylene diisocyanate ( 2c ), 1,3-bis(isocyanatomethyl)cyclohexane ( 2d ), 4,4′-methylenebis(cyclohexyl isocyanate) ( 2e ), and hexamethylene diisocyanate ( 2f ), to obtain the corresponding polyureas ( 3a – f ). Optically transparent, colorless, and flexible freestanding films were obtained by casting the polyurea solutions in tetrahydrofuran. Among the tested polymers, polyureas from 2a and 2e exhibited ε r less than 3.0. Incorporation of the DDSQ units produced free volume, resulting in low ε r . Polyureas from 2e and 2f exhibited the lowest tan δ of approx. 7 × 10 –3 . The polyurea from 2e had the lowest urea content and thus had the lowest density and lowest ε r . Additionally, strong hydrogen bonding in the polyurea from 2e inhibited local motion, resulting in a low tan δ even though the urea content was low. Water vapor permeability measurements revealed greater free volume content introduced by the co-oligomerization of polyhedral oligomeric silsesquioxanes (POSS), especially in the polyurea from 2e . Among the reported combinations, the combination of DDSQ and urea groups provides unique low ε r and low tan δ polymeric materials.
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Research context

OpenAlex topics: Silicone and Siloxane Chemistry · Synthesis and properties of polymers · Dielectric materials and actuators

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

Affiliations

Faculty of Molecular Chemistry and Engineering, Graduate School of Science and Technology, Kyoto Institute of Technology, Goshokaido-cho, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan

Morinomiya Center, Osaka Research Institute of Industrial Science and Technology, 1-6-50 Morinomiya, Joto-ku, Osaka 536-8553, Japan

Faculty of Materials Science and Engineering, Graduate School of Science and Technology, Kyoto Institute of Technology, Goshokaido-cho, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan

Materials Innovation Lab, Kyoto Institute of Technology, Goshokaido-cho, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan

Funding

Japan Society for the Promotion of Science

References (51)

Show source-provided references
1. 10.1021/cr900281910.1021/cr9002819 ↗
2. 10.3389/fmats.2021.77484310.3389/fmats.2021.774843 ↗
3. 10.1016/j.aiepr.2020.10.00110.1016/j.aiepr.2020.10.001 ↗
4. 10.1021/acsapm.0c0114110.1021/acsapm.0c01141 ↗
5. 10.1021/acsapm.1c0004310.1021/acsapm.1c00043 ↗
6. 10.1039/C7TC04220E10.1039/C7TC04220E ↗
7. 10.1021/acs.macromol.2c0128810.1021/acs.macromol.2c01288 ↗
8. 10.1039/C5RA20722C10.1039/C5RA20722C ↗
9. 10.1016/j.polymer.2003.11.02510.1016/j.polymer.2003.11.025 ↗
10. Oda H. · Trans. Mat. Res. Soc. Jpn. · 1994 · 14 · 1407
11. 10.1007/s00289-007-0775-810.1007/s00289-007-0775-8 ↗
12. 10.1177/095400830933756410.1177/0954008309337564 ↗
13. 10.1002/app.4782810.1002/app.47828 ↗
14. 10.1002/pola.2820810.1002/pola.28208 ↗
15. 10.1295/polymj.PJ200628010.1295/polymj.PJ2006280 ↗
16. 10.1002/macp.20030000210.1002/macp.200300002 ↗
17. 10.1021/acsapm.1c0133710.1021/acsapm.1c01337 ↗
18. 10.1557/PROC-476-16110.1557/PROC-476-161 ↗
19. 10.1557/PROC-381-17710.1557/PROC-381-177 ↗
20. 10.1021/acs.macromol.7b0200010.1021/acs.macromol.7b02000 ↗
21. 10.1021/cr900201r10.1021/cr900201r ↗
22. 10.1039/b506815k10.1039/b506815k ↗
23. 10.1246/bcsj.2015008110.1246/bcsj.20150081 ↗
24. Li G. · J. Inorg. Org. Polym. · 2001 · 11 · 12310.1023/A:1015287910502 ↗
25. 10.1002/pi.512110.1002/pi.5121 ↗
26. 10.1016/j.polymer.2004.10.00310.1016/j.polymer.2004.10.003 ↗
27. 10.1002/app.4229210.1002/app.42292 ↗
28. 10.1039/D0RA01122C10.1039/D0RA01122C ↗
29. 10.1021/ma034743r10.1021/ma034743r ↗
30. 10.1021/cm030393b10.1021/cm030393b ↗
31. 10.1021/ma702722710.1021/ma7027227 ↗
32. 10.1246/cl.2012.62210.1246/cl.2012.622 ↗
33. 10.1039/C5TC02432C10.1039/C5TC02432C ↗
34. 10.1039/D1PY00346A10.1039/D1PY00346A ↗
35. 10.1039/D2PY00980C10.1039/D2PY00980C ↗
36. 10.1002/adma.20120407210.1002/adma.201204072 ↗
37. 10.1038/ncomms421810.1038/ncomms4218 ↗
38. 10.1007/s11664-014-3374-010.1007/s11664-014-3374-0 ↗
39. 10.1063/1.314238810.1063/1.3142388 ↗
40. 10.1063/1.486593110.1063/1.4865931 ↗
41. 10.1021/acs.macromol.0c0027010.1021/acs.macromol.0c00270 ↗
42. 10.1038/s41428-021-00578-910.1038/s41428-021-00578-9 ↗
43. ISO 15106-5 (2015).
44. 10.1039/C8PY00758F10.1039/C8PY00758F ↗
45. 10.1002/macp.1997.02198011010.1002/macp.1997.021980110 ↗
46. 10.1021/ma062636210.1021/ma0626362 ↗
47. 10.1021/acs.chemmater.6b0453010.1021/acs.chemmater.6b04530 ↗
48. 10.1021/la300887p10.1021/la300887p ↗
49. 10.1016/j.cplett.2019.13704710.1016/j.cplett.2019.137047 ↗
50. 10.1002/masy.20035092710.1002/masy.200350927 ↗
51. 10.2494/photopolymer.8.31510.2494/photopolymer.8.315 ↗