Allyl phthalazinone synthesis,polymerization and polymer properties  

Allyl phthalazinone synthesis,polymerization and polymer properties

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作  者:Li-Ming Dong Xi-Gao Jian 

机构地区:[1]School of Chemistry & Chemical Engineering,Xuzhou Institute of Technology [2]Department of Polymer Science & Materials,Dalian University of Technology

出  处:《Chinese Chemical Letters》2014年第4期605-608,共4页中国化学快报(英文版)

基  金:supported by the Natural Science Foundation of Jiangsu Province(No.BK2012142);the Natural Science Foundation of the Jiangsu Higher Education Institutions of China(No.11KJD150005)

摘  要:A phthalazinone monomer with an allyl group, i.e. 4-(3-allyl-4-hydroxyphenyl)phthalazin-1(2H)-one, was synthesized and then copolymerized with 4-(4-hydroxylphenyl)(2H)-phthalazin-1-one and 2,6- diflurobenzonitrile by means of aromatic nucleophilic polycondensation to provide a series of crosslinkable poly(aryl ether nitrile)s. The virgin copolymers exhibited good solubility in polar organic solvents with relative high molecular weights (Mw: 45,130-58,403, inherent viscosities: 0.58-0.75 dL/ g). After cross-linking, the thermal stability and solvent resistance of the polymer increased.A phthalazinone monomer with an allyl group, i.e. 4-(3-allyl-4-hydroxyphenyl)phthalazin-1(2H)-one, was synthesized and then copolymerized with 4-(4-hydroxylphenyl)(2H)-phthalazin-1-one and 2,6- diflurobenzonitrile by means of aromatic nucleophilic polycondensation to provide a series of crosslinkable poly(aryl ether nitrile)s. The virgin copolymers exhibited good solubility in polar organic solvents with relative high molecular weights (Mw: 45,130-58,403, inherent viscosities: 0.58-0.75 dL/ g). After cross-linking, the thermal stability and solvent resistance of the polymer increased.

关 键 词:Poly(aryl ether nitrile) Crosslinking Phthalazinone 

分 类 号:O631.3[理学—高分子化学]

 

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