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Cited by 3 publications
(3 citation statements)
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“…68 The replacement of 4,4´ DFBP with its 2,4´ isomer led to a decrease in the average weight molecular weight by more than a factor of 10 due, apparently, to the lower reactivity of the fluorine atom in the ortho position with respect to the carbon yl group.…”
Section: Synthesis Of Paek By the Nucleophilic Substitution Reactionmentioning
confidence: 99%
“…68 The replacement of 4,4´ DFBP with its 2,4´ isomer led to a decrease in the average weight molecular weight by more than a factor of 10 due, apparently, to the lower reactivity of the fluorine atom in the ortho position with respect to the carbon yl group.…”
Section: Synthesis Of Paek By the Nucleophilic Substitution Reactionmentioning
confidence: 99%
“…133 A series of crystallisable cardo copolyarylene ether ketones have been synthesised; their crystallisation is determined by the simultaneous presence of cardo bisphenols and hydroquinone (or 4,4 H -dihydroxybiphenyl) fragments. 135,136 The glass transition temperatures of these compounds reach 250 8C, whereas the melting temperatures lie in the range of 300 ± 350 8C.…”
Section: Variations Of Chemical Structures Of Monomersmentioning
confidence: 99%
“…Phthalide groups were also introduced into polyarylene ether ketones using an alternative procedure which employs a highly reactive difluoroderivative, viz., {3,3-bis[4-(4-fluorobenzoyl)phenyl]phthalide}. 133 This compound and various bisphenolates were used as starting materials in the synthesis of novel polyarylene ether ketones with softening temperatures up to 250 8C. It is noted that monolithic samples of cardo copolyarylene ether ketones containing 4,4 H -propane-2,2-diyldiphenol fragments manifest uniquely high impact strength with incision (up to 44 kJ m 72 ).…”
Section: A Ring ± Chain Polyheteroarylenesmentioning
confidence: 99%