2007
DOI: 10.1002/pat.917
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Synthesis and characterization of a novel polytriazole resin with low‐temperature curing character

Abstract: A novel low-temperature curing polytriazole resin was prepared from a triazide and a tetraalkyne and characterized. The resin can be cured at 70-C. The glass transition temperature T g and thermal decomposition temperature T d5 of the cured resin with the molar ratio of azide to alkyne group [A]/ [B] ¼ 1.0:1.0 reached 324 and 355-C, respectively. The study on the curing kinetics of the resin shows that the apparent activation energy of the curing reaction is 93 kJ mol S1 . The flexural strength of the cured re… Show more

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Cited by 36 publications
(36 citation statements)
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“…[19][20][21][22][23][24] A new kind of thermosetting resin with terminal propargyl groups has recently been developed as a high-performance polymer owing to its good processability, advantageous dielectric and mechanical properties and excellent thermal stability, whether in air or in a nitrogen atmosphere. [25][26][27][28][29][30] This paper presents new modified BMI resins prepared from BMI, HSQ and dipropargyl aryl ethers. We investigated the processability, mechanical properties and heat resistance of the resins and their composites.…”
Section: Introductionmentioning
confidence: 99%
“…[19][20][21][22][23][24] A new kind of thermosetting resin with terminal propargyl groups has recently been developed as a high-performance polymer owing to its good processability, advantageous dielectric and mechanical properties and excellent thermal stability, whether in air or in a nitrogen atmosphere. [25][26][27][28][29][30] This paper presents new modified BMI resins prepared from BMI, HSQ and dipropargyl aryl ethers. We investigated the processability, mechanical properties and heat resistance of the resins and their composites.…”
Section: Introductionmentioning
confidence: 99%
“…12,13 The silicon-containing arylacetylene polymers composed of [ASiR 2 ACBCAArACBCA] (R ¼ alkyl or phenyl) units exhibit excellent thermal stabilities after curing. [14][15][16][17] There is high content of the ethynylene group in the backbone of the polymers.…”
Section: Introductionmentioning
confidence: 99%
“…[12][13][14][15][16][17][18][19][20][21][22][23][24][25][26] The classical (thermal) 1,3-dipolar cycloaddition can be performed between azides and terminal alkynes as well as internal triple bonds. Generally, the reactivity of alkynes for the click reaction is rather low due to its high electron density at the alkyne functionality.…”
Section: Introductionmentioning
confidence: 99%