Aromatic tetracarboxylic dianhydride having crank and twisted noncoplanar structure, 2,2 -bis(3,4-dicarboxyphenoxy)-1,1 -binaphthyl dianhydride, was synthesized by the reaction of 4-nitrophthalonitrile with 2,2 -dihydroxy-1,1 -binaphthyl, followed by alkaline hydrolysis of the intermediate bis(ether
Synthesis and characterization of optically active aromatic polyimides derived from 2,2′-bis(2-trifluoro- 4-aminophenoxy)-1,1′-binaphthyl and aromatic tetracarboxylic dianhydrides
✍ Scribed by Qiding Mi; Yu Ma; Lianxun Gao; Mengxian Ding
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 140 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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✦ Synopsis
Optically active 2,2Ј-bis(2-trifluoro-4-aminophenoxy)-1,1Ј-binaphthyl and its corresponding racemate were prepared by a nucleophilic substitution reaction of 1,1Ј-bi-2-naphthol with 2-chloro-5-nitrotrifluorotoluene and subsequently by the reduction of the resulting dinitro compounds. A series of optically active and optically inactive aromatic polyimides also were prepared therefrom. These polymers readily were soluble in common organic solvents such as pyridine, N,NЈ-dimethylacetamide, and m-cresol and had glass-transition temperatures of 256 ϳ 278 °C. The specific rotations of the chiral polymers ranged from 167 ϳ 258°, and their chiroptical properties also were studied.
📜 SIMILAR VOLUMES
A series of new optically active aromatic polyimides containing axially dissymmetric 1,1 -binaphthalene-2,2-diyl units were prepared from optically pure ( R)-(/)-or (S)-(0)-2,2-bis(3,4-dicarboxyphenoxy)-1,1 -binaphthalene dianhydrides and various aromatic diamines via a conventional two-step procedu
New polyarylates having benzopinacolone units were synthesized from 2,2-bis(4-hydroxyphenyl)-1,2-diphenylethanone and aromatic dicarboxylic acid chlorides. The polymers having an inherent viscosity of 0.71-0.94 dL/g were obtained by the two-phase method using toluene as an organic solvent. The polym
2,6-Bis(4-aminophenoxy)naphthalene (2,6-BAPON) was synthesized in two steps from the condensation of 2,6-dihydroxynaphthalene with p-chloronitrobenzene in the presence of potassium carbonate, giving 2,6-bis(4-nitrophenoxy)naphthalene, followed by hydrazine hydrate/Pd-C reduction. A series of new pol
A bis(ether amine) containing the ortho-substituted phenylene unit and pendant tert-butyl group, 1,2-bis(4-aminophenoxy)-4-tert-butylbenzene, was synthesized and used as a monomer to prepare polyimides with six commercial dianhydrides via a conventional two-stage procedure. The intermediate poly(ami