Novel aromatic polyimides containing symmetric, bulky di-tert-butyl substituents unit were synthesized from 1,4-bis(4-aminophenoxy)2,5-di-tert-butylbenzene (BADTB) and various aromatic tetracarboxylic dianhydrides by the conventional twostage procedure that included ring-opening polyaddition in a po
Synthesis and properties of novel aromatic polyimides derived from bis(p-aminophenoxy)methylphenylsilane
โ Scribed by Der-Jang Liaw; Wen-Chung Ou Yang; Lain-Jong Li; Mei-Hui Yang
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 500 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
A novel siloxane-containing diamine, bis(p-aminophenoxy )methylphenylsilane (BAMPS), was synthesized from the condensation of dichloromethylpheny lsilane with p-aminophenol in the presence of triethylamine. A series of BAMPS-based aromatic polyamides were prepared from BAMPS and various aromatic tetracarboxylic dianhydrides by the usual twostep procedure including ring-opening polyaddition to poly(amic acid)s and subsequent cvclodehydration to polyamides. The inherent viscosities of poly(amic acid)s IIIa-IIIf ranged from 0.09 to 0.36 dL g ' in N, N-dimethylacetamide at a concentration of 0.5 g dL ' at 300('. The inherent viscosities of polyamides were between 0.06 and 0.32 dL g-' in various solvents at 30ยฐC. Polyamides, especially IV= and IV~, were soluble in a wide range of organic solvents such as IV-methyl -2-pyrrolidinone, concentrated HzSOi, N, N-dimethylacetamide, N, N-dimet hy]formamide, and dimethyl sulfoxide. The polyamides were characterized by elementary analysis, IR spectra, TGA, and DSC. They also had glass transition temperatures ranging from 128 to 181 "C. The 10% mass loss temperature was recorded in the range of 404-44; \0C in nitrogen and of 315-339ยฐC in oxygen.
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## Abstract Novel aromatic polyimides were synthesized from 9,10โdihydroโ9,10โ__o__โbenzenoanthraceneโ1,5โdiamine (2,7โtriptycenediamine) and aromatic tetracarboxylic dianhydrides. The polymerization was carried out in a twoโstep procedure including ringโopening polyโaddition giving polyamic acids,
A new silane-containing diamine, bis(p-aminophenoxy)diphenylsilane (BAPPS) (I), was prepared by the condensation of p-aminophenol with dichlorodiphenylsilane. A series of silane-containing aromatic polyamides was prepared by the direct polycondensation of BAPPS with various aromatic dicarboxylic aci
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
## SYNOPSIS A series of novel bis(phen0xy)naphthalene-containing polyamides having inherent viscosity up to 2.02 dL/g were synthesized by the direct polycondensation of the diamine 1,7bis(4-aminophenoxy)naphthalene with various aromatic dicarboxylic acids in N-methyl-8-pyrrolidone (NMP) using trip