Optically active poly(amide–imide)s containing axially dissymmetric 1,1′-binaphthyl moieties
✍ Scribed by Naiheng Song; Lianxun Gao; Mengxian Ding
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 184 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
No coin nor oath required. For personal study only.
✦ Synopsis
Novel optically active aromatic poly(amide-imide)s (PAIs) were prepared from newly synthesized 2,2Ј-bis(3,4-dicarboxybenzamido)-1,1Ј-binaphthyl dianhydride ((ϩ)-, (S)-, and (R)-BNDADA). PAIs based on dianhydride monomers with different ee % were investigated with respect to their structures and chiroptical properties. These polymers were highly soluble in polar aprotic solvents such as N,N-dimethylacetamide, N-methyl-2-pyrrolidone, pyridine, etc., and showed high glass transition temperatures of 287-290°C and 5% weight loss temperatures of 450 -465°C in nitrogen. Optically active PAIs exhibited high specific rotations, excellent optical stabilities, and a dependence of optical activities on temperature. Investigations on chiroptical properties indicated that chiral conformation was possessed by optically active PAIs.
📜 SIMILAR VOLUMES
## Abstract EPICLON [3a,4,5,7a‐Tetrahydro‐7‐methyl‐5‐(tetrahydro‐2,5‐dioxo‐3‐furanyl)‐1,3‐isobenzofurandione] or [5‐(2,5‐dioxotetrahydrofurfuryl)‐3‐methyl‐3‐cyclohexyl‐1,2‐dicarboxylic acid anhydride] (**1**) was reacted with L‐phenylalanine (**2**) in acetic acid, and the resulting amic acid was r
Distributions of A 2 A 4 , A 2 I 4 , I 2 A 4 and I 2 I 4 % of tolylene 2,4 (D9) units in ternary poly(imide-amide)s -obtained with [1 commercial tolylene diisocyanate (D) + t trimellic anhydride (T) + p terephthalic acid (P), t + p = 1, molar ratios] monomer mixtures -versus acid (COOH) or anhydride