Abstract
Two series of novel intrinsically microporous polyimides were synthesized from 9,9′-spirobifluorene-2,2′-diamine (SBF) and its bromine-substituted analogue 3,3′-dibromo-9,9′-spirobifluorene-2, 2′-diamine (BSBF) with three different dianhydrides (6FDA, PMDA, and SPDA). All polymers exhibited high molecular weight, good solubility in common organic solvents, and high thermal stability. Bromine-substituted polyimides showed significantly increased gas permeabilities but slightly lower selectivities than the SBF-based polyimides. The CO2 permeability of PMDA-BSBF (693 Barrer) was 3.5 times as high as that of PMDA-SBF (197 Barrer), while its CO2/CH4 selectivity was similar (19 vs 22). Molecular simulations of PMDA-SBF and PMDA-BSBF repeat units indicate that the twist angle between the PMDA and fluorene plane changes from 0 in PMDA-SBF to 77.8 in PMDA-BSBF, which decreases the ability of the polymer to pack efficiently due to severe steric hindrance induced by the bromine side groups. © 2013 American Chemical Society.
Original language | English (US) |
---|---|
Pages (from-to) | 9618-9624 |
Number of pages | 7 |
Journal | Macromolecules |
Volume | 46 |
Issue number | 24 |
DOIs | |
State | Published - Dec 3 2013 |
Bibliographical note
KAUST Repository Item: Exported on 2020-10-01ASJC Scopus subject areas
- Materials Chemistry
- Organic Chemistry
- Polymers and Plastics
- Inorganic Chemistry