Novel 2,5-dimethylene-2,5-dihydrothieno[3,2-b] thiophene derivatives such as 2,5-bis[di(ethylthio)methylene]-2,5-dihydrothieno[3,2-b]thiophene (4b) and 2,5bis[cyano(ethylthio)methylene]-2,5-dihydrothieno[3,2-b]thiophene (4c) were successfully synthesized as isolable crystals. Polymerization behavio
The synthesis of monomers that expand on polymerization. Synthesis and polymerization of 8,10,19,20-tetraoxatrispiro[5.2.2.5.2.2]heneicosane
β Scribed by Endo, Takeshi ;Katsuki, Hirokazu ;Bailey, William J.
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1976
- Weight
- 173 KB
- Volume
- 177
- Category
- Article
- ISSN
- 0025-116X
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β¦ Synopsis
Abstract
A spiro orthocarbonate containing two cyclohexyl groups, 8,10,19,20βtetraoxatrispiro[5.2.2.5.2.2]heneicosane (1), was prepared. The monomer was polymerized with Lewis acids such as boron trifluoride etherate or stannic chloride as catalysts. The IR and NMR spectra indicated that the polymer was an alternating copolymer with ether and carbonate linkages. This monomer underwent expansion on polymerization.
π SIMILAR VOLUMES
The new cyclic carbonate monomer 2,4,8,10-tetraoxaspiro [5,5]undecane-3one (DOXTC) was prepared in ΓΊ 80% yield by the reaction of 1,3-dioxane-5,5-dimethanol with ethyl chloroformate in tetrahydrofuran (THF). DOXTC homopolymerization and copolymerizations with trimethylene carbonate (TMC) were carrie