Cubylamines and cubylmethylamines are of interest as antiviral agents. Reliable syntheses of some polyamides with cubane as the backbone of a polymer chain are described. Two monomers of cubane, cubane-1,4-dicarboxylic acid (CDA) and 1,4-diaminocubane (DAC), are used. Polymerizations of DAC, 1,6-hex
Synthesis and characterization of polyamides X 18
β Scribed by Xiaowen Cui; Weihua Li; Deyue Yan; Cuiming Yuan; Giuseppe Di Silvestro
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 108 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Step heating melt polycondensation was adopted in the preparation of polyamides based on 1,16βoctadecane diacid and Ξ±,Οο£Ώ(CH~2~)~2__n__~ diamines (n = 1β6). The structure was confirmed by various spectroscopic techniques (IR, Raman, ^1^HβNMR, and ^13^CβNMR). High molecular masses were obtained only in the presence of an excess of diamine and when the diamine possessed low volatility. The molecular masses were between (0.94 and 2.1) Γ 10^4^ Da for all polyamides under consideration. An excellent correlation between size exclusion chromatography and ^1^HβNMR data was demonstrated in the measurement of the degree of polymerization. The melting temperatures of the polyamides decreased from polyamide 12 18 to polyamide 2 18 as the amide density along the molecular chain declined. No significant variation was observed in the glassβtransition and decomposition temperatures of the polyamides that were obtained. Β© 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 1565β1571, 2005
π SIMILAR VOLUMES
A new diamine, 2,2-bis[4-(4-aminophenoxy)phenyl]norbornane (BAPN), containing both ether and norbornane cardo groups, was synthesized in three steps started from norcamphor. A series of cardo polyamides were obtained by the direct polycondensation of BAPN and various aromatic dicarboxylic acids in N
The synthesis is described of some aromatic polyamides based on unsubstituted, and methyl-, carboxy-, and sulfo-substituted diamines by interfacial polycondensation. Some of them are crosslinked and some of them contain heterocyclic aromatic rings. Their chemical structures are characterized by IR a