简介概要

Synthesis and Characterization of Soluble Aromatic Azopolyamides Containing Sulfone and Ether Units

来源期刊:Journal Of Wuhan University Of Technology Materials Science Edition2009年第4期

论文作者:董丽杰 熊传溪

文章页码:594 - 598

摘    要:A series of new polyamides 3a-d containing aryl-azo, ether and sulfone groups in the main chain were synthesized from bis[4-(4-aminophenoxy)phenyl sulfone] 1 and several azo aromatic diacyl chlorides 2a-d by the low temperature solution polycondensation technique. FTIR spectroscopy, nuclear magnetic resonance (NMR) and elemental analyses confirmed the structure of these polymers. Owing to the aryl and amide groups in the main chain, these polymers exhibit photochromic properties as well as excellent thermal stabilities. The transition temperatures (Tg) are between 242 and 265 ℃, and the char yields at 800 ℃ in nitrogen atmosphere were above 39%. Based on incorporation of flexible ether linkages and polar sulfone groups, the polyamides show desirable solubility in organic solvents such as DMAc, N,N-dimethylformamide (DMF), N-methyl-2-pyrroidinone (NMP) and dimethylsulfoxide (DMSO). And it is exemplified that polyamide containing 2 and 2′ substitutes performed better solubility.

详情信息展示

Synthesis and Characterization of Soluble Aromatic Azopolyamides Containing Sulfone and Ether Units

董丽杰1,2,熊传溪1,2

1. School of Materials Science and Engineering,Wuhan University of Technology2. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing,Wuhan University of Technology

摘 要:A series of new polyamides 3a-d containing aryl-azo, ether and sulfone groups in the main chain were synthesized from bis[4-(4-aminophenoxy)phenyl sulfone] 1 and several azo aromatic diacyl chlorides 2a-d by the low temperature solution polycondensation technique. FTIR spectroscopy, nuclear magnetic resonance (NMR) and elemental analyses confirmed the structure of these polymers. Owing to the aryl and amide groups in the main chain, these polymers exhibit photochromic properties as well as excellent thermal stabilities. The transition temperatures (Tg) are between 242 and 265 ℃, and the char yields at 800 ℃ in nitrogen atmosphere were above 39%. Based on incorporation of flexible ether linkages and polar sulfone groups, the polyamides show desirable solubility in organic solvents such as DMAc, N,N-dimethylformamide (DMF), N-methyl-2-pyrroidinone (NMP) and dimethylsulfoxide (DMSO). And it is exemplified that polyamide containing 2 and 2′ substitutes performed better solubility.

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