Synthesis and properties of cationic multiblock polyaramides and polyimides

被引:5
作者
Biery, Alison R. [1 ]
Knauss, Daniel M. [1 ]
机构
[1] Colorado Sch Mines, Dept Chem, Golden, CO 80401 USA
关键词
cationic polymer; diallyldimethylammonium; multiblock copolymer; polyaramide; polyimide; DIRECT POLYCONDENSATION REACTION; RADICAL POLYMERIZATION; GENE DELIVERY; POLYELECTROLYTES; POLYAMIDES; STABILITY; MEMBRANES; BEHAVIOR; CHLORIDE;
D O I
10.1002/pol.20220447
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(diallyldimethylammonium chloride) (PDADMAC) is a useful material due to its high charge density and alkaline stability, but its hydrophilic nature limits applications to those where the dissolved polymer is appropriate. To make polymers suitable for applications as films and membranes containing the diallyldimethylammonium moiety, multiblock copolymers of polyaramides (PA) and polyimides (PI), materials known for their excellent physical properties and stabilities, were synthesized. Aminophenyl difunctionalized PDADMAC oligomers were synthesized using a disulfide iniferter then counterion exchanged to the hexafluorophosphate anion to produce telechelic oligomers with good solubility in polar aprotic solvents. The oligomers were reacted in situ with the proper difunctional monomers to produce PA, polyetheraramides, PI, and polyetherimides. All the classes of copolymers were synthesized over a range of compositions at high yield and material properties were demonstrated to be a result of both the backbone chemistry and the composition. Several of the synthesized copolymers formed films with good clarity, strength, and flexibility. The copolymers containing ether linkages had increased backbone flexibility and demonstrated better film-forming properties. The multiblock copolyaramides and copolyimides demonstrate a method to produce materials with excellent thermal stability and good strength and flexibility, making them uniquely capable of serving as water insoluble, cationic films, and membranes.
引用
收藏
页码:197 / 210
页数:14
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