journal article·2012-10

Synthesis of Aromatic Polyhedral Oligomeric SilSesquioxane (POSS) Dianilines for Use in High-Temperature Polyimides

Vandana Vij, Timothy S. Haddad, Gregory R. Yandek, Sean M. Ramirez, Joseph M. Mabry

Silicon· Volume 4· Issue 4
Publisher page

Abstract

A series of novel aromatic Polyhedral Oligomeric SilSesquioxane (POSS) dianiline molecules has been synthesized for use in the preparation of high temperature aromatic polyimides. A general synthetic strategy was devised to improve the structure, yield, and utility of POSS dianilines over those currently available. Peripheral aromatic functionality was specifically incorporated in order to improve thermal properties and to increase compatibility with aromatic polymers. Silyloxy and/or aromatic functional groups were used to link the aniline groups to the POSS cage in order to ensure that this linkage was not a thermal weak point. Additionally, the stereochemistry of the aniline functionality has been varied to produce both meta- and para- isomers. The new dianiline monomers can be used to produce high molecular weight polyimide polymers. These dianilines have been incorporated both as pendants to the polymer backbone, and in a “bead-on-a-string” fashion by insertion into the polymer main-chain. In addition to producing POSS polyimides with superior thermal stability, these new monomers will allow full characterization and comparison of POSS-polyimides with differing structures in order to delineate the structure-property relationships of POSS and polymer architectures.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Silicone and Siloxane Chemistry · Synthesis and properties of polymers · Advanced ceramic materials synthesis

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References (40)

Show source-provided references
1. Voronkov MG, Lavrent’yev VI (1982) Top Curr Chem 102:19910.1007/3-540-11345-2_12 ↗
2. Baney RH, Itoh M, Sakakibara A, Suzuki T (1995) Chem Rev 95:140910.1021/cr00037a012 ↗
3. Cordes DB, Lickiss PD, Rataboul F (2010) Chem Rev 110:208110.1021/cr900201r ↗
4. Lickiss PD, Rataboul F (2008) Adv Organomet Chem 57:110.1016/S0065-3055(08)00001-4 ↗
5. Provatas A, Matisons JG (1997) Trends Polym Sci 5:327
6. Hartmann-Thompson C (2011) Applications of polyhedral oligomeric silsesquioxanes. Springer, New York10.1007/978-90-481-3787-9 ↗
7. Phillips SH, Haddad TS, Tomczak SJ (2004) Curr Opin Solid State Mater Sci 8:2110.1016/j.cossms.2004.03.002 ↗
8. Li G, Wang L, Ni H, Pittman CU, Jr (2002) J Inorg Organmet Polym 11:12310.1023/A:1015287910502 ↗
9. Pittman CU, Jr, Li G-Z, Ni H (2003) Macromol Symp 196:30110.1002/masy.200390170 ↗
10. Joshi M, Butola BS (2004) J Macromol Sci Polym Rev C44:38910.1081/MC-200033687 ↗
11. Pielichowski K, Njuguna J, Janowski B, Pielichowski J (2006) Adv Polym Sci 201:22510.1007/12_077 ↗
12. Gushikem Y, Benvenutti EV, Kholin YV (2008) Pure Appl Chem 80:159310.1351/pac200880071593 ↗
13. Kuo S-W, Chang F-C (2011) Prog Polym Sci 36:164910.1016/j.progpolymsci.2011.05.002 ↗
14. Laine RM, Roll MF (2011) Macromolecules 44: 107310.1021/ma102360t ↗
15. Choi J, Tamaki R, Kim SG, Laine RM (2003) Chem Mater 15:336510.1021/cm030286h ↗
16. Ni Y, Zheng S (2004) Chem Mater 16:514110.1021/cm049463k ↗
17. Chen G-X, Si L, Lu P, Li Q (2012) J Appl Polym Sci 125:392910.1002/app.36400 ↗
18. Liang K, Toghiani H, Li G, Pittman CU, Jr (2005) J Polym Sci Part A Polym Chem 43:388710.1002/pola.20861 ↗
19. Liu H, Zheng S (2005) Macromol Rapid Commun 26:19610.1002/marc.200400465 ↗
20. Zhang ZP, Pei JZ, Chen SF, Du HZ, Wen Y (2011) Adv Mater Res 216:63510.4028/www.scientific.net/AMR.216.635 ↗
21. Zhang Z, Liang G, Wang J, Ren P (2007) Polym Compos 28:17510.1002/pc.20281 ↗
22. Wright ME, Schorzman DA, Feher FJ, Jin R-Z (2003) Chem Mater 15:26410.1021/cm020238h ↗
23. Gonzalez RI, Tomczak SJ, Minton TK, Brunsvold AL, Hoflund GB (2003) Eur Space Agency Spec Pub SP-540:113
24. Minton TK, Wright ME, Tomczak SJ, Marquez SA, Shen L, Brunsvold AL, Cooper R, Zhang J, Vij V, Guenthner AJ, Petteys BJ (2012) ACS Appl Mater Interfaces 4:49210.1021/am201509n ↗
25. Tomczak SJ, Vij V, Minton TK, Brunsvold AL, Marchant D, Wright ME, Petteys BJ, Guenthner AJ, Yandek GR, Mabry JM (2008) ACS Symp Ser 978:14010.1021/bk-2007-0978.ch013 ↗
26. Leu CM, Chang YT, Wei KH (2003). Macromolecules 36:912210.1021/ma034743r ↗
27. Leu CM, Reddy GM, Wei KH, Shu CF (2003) Chem Mater 15:226110.1021/cm0208408 ↗
28. Wright ME, Petteys BJ, Guenthner AJ, Fallis S, Yandek GR, Tomczak SJ, Minton TK, Brunsvold A (2006) Macromolecules 39:471010.1021/ma060372d ↗
29. Tomczak SJ, Vij V, Marchant D, Minton TK, Brunsvold AL, Wright ME, Petteys BJ, Guenthner AJ, Yandek GR, Mabry J (2006) Proc SPIE-Int Soc Opt Eng 6308:630804/630801
30. Hoque MA, Kakihana Y, Shinke S, Kawakami Y (2009) Macromolecules 42:330910.1021/ma900124x ↗
31. Wu S, Hayakawa T, Kikuchi R, Grunzinger SJ, Kakimoto M, Oikawa H (2007) Macromolecules 40:569810.1021/ma070547z ↗
32. Wu S, Hayakawa T, Kakimoto M-A, Oikawa H (2008) Macromolecules 41:348110.1021/ma7027227 ↗
33. Katoh T, Kikukawa T, Ito K, Yoshida K, Yamamoto Y (2006) US Pat Appl 20060194068 A1
34. Fina A, Tabuani D, Carniato F, Frache A, Boccaleri E, Camino G (2006) Thermochim Acta 440:3610.1016/j.tca.2005.10.006 ↗
35. Moore BM, Ramirez SM, Yandek GR, Haddad TS, Mabry JM (2011) J Organomet Chem 696:267610.1016/j.jorganchem.2011.03.035 ↗
36. Moore BM, Yandek GR, Ramirez SM, Mabry JM (2012) J Phys Chem C 116:in press10.1021/jp3039708 ↗
37. Yang Z, Han S, Zhang R, Feng S, Zhang C, Zhang S (2011) Polym Degrad Stab 96:214510.1016/j.polymdegradstab.2011.09.014 ↗
38. Pangborn AB, Giardello MA, Grubbs RH, Rosen RK, Timmers FJ (1996) Organometallics 15:151810.1021/om9503712 ↗
39. Shriver DF (1969) The manipulation of air-sensitive compounds. McGraw-Hill, New York
40. Seurer B, Vij V, Haddad T, Mabry JM, Lee A (2010) Macromolecules 43:933710.1021/ma101640q ↗