Optically active 2,2ะ-bis(2-trifluoro-4-aminophenoxy)-1,1ะ-binaphthyl and its corresponding racemate were prepared by a nucleophilic substitution reaction of 1,1ะ-bi-2-naphthol with 2-chloro-5-nitrotrifluorotoluene and subsequently by the reduction of the resulting dinitro compounds. A series of opt
Synthesis and characterization of new aromatic polyesters and a polyether derived from 2,2-bis(4-hydroxyphenyl)-1,2-diphenylethanone
โ Scribed by Shinji Watanabe; Hitoshi Murayama; Miki Murata; Yuzuru Masuda; Masaru Tanabe; Yoshio Imai
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 128 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0887-624X
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โฆ Synopsis
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 polymers were easily soluble in various organic solvents and had high glass transition temperatures in the range of 200 -240ยฐC. An aromatic polyether having benzopinacolone unit was also prepared. However, its inherent viscosity was low because of the occurrence of a side reaction.
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A series of fluorine-containing aromatic homopolyacetals and copolyacetals with a wide range of unit ratios were synthesized by the solution polycondensation of 2,2-bis(4-hydroxyphenyl)-1,1,1,3,3,3-hexafluoropropane (bisphenol AF), 2,2-bis(4-hydroxyphenyl)propane (bisphenol A), or both with 2-(trifl
New aromatic diamines [(1) and ( 2)] containing polycycloalkane structures between two benzene rings were synthesized by HCl-catalyzed condensation reaction of aniline hydrochloride and corresponding polycycloalkanone derivatives. The structures of diamines were identified by 1 H-NMR, 13 C-NMR, FTIR