1996
DOI: 10.1007/bf01435391
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General features of the reaction of 4,4?-difluorobenzophenone with potassium diphenoxide of 2,2-bis (4-hydroxyphenyl)propane

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Cited by 18 publications
(11 citation statements)
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“…It has been previously shown that the BC method is more accurate, as it discriminates the bonds between the main chain and side groups that contribute significantly to polymer rigidity [ 59 ]. We can observe the same picture in Table 7 , as follows: MAPEs and MPEs are mainly lower for BC, except for the C2 polymer.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…It has been previously shown that the BC method is more accurate, as it discriminates the bonds between the main chain and side groups that contribute significantly to polymer rigidity [ 59 ]. We can observe the same picture in Table 7 , as follows: MAPEs and MPEs are mainly lower for BC, except for the C2 polymer.…”
Section: Resultsmentioning
confidence: 99%
“…The synthesis of poly(arylene ether ketone)s (PAEKs: C1–C3, Figure 1 ) was carried out by polycondensation method according to the mechanism of the reaction of nucleophilic substitution of activated halogen in arylene dihalide, by the interaction of 4,4′-difluorobenzophenone with dipotassium phenolates of bisphenols (bisphenol A, bisphenol AF, phenolphthalein), similar to the method described in [ 59 ] ( Figure 1 ). Further, 4,4′-Difluorobenzophenone (0.0988 mol), bi-sphenol(2,2-bis(4′-hydroxyphenyl)propane or 2,2-bis(4′-hydroxyphenyl)hexafluoropropane or 3,3-bis(4′-hydroxyphenyl) phthalide) (0.1 mol), 4-fluorobenzophenone (0.0024 mol), pre-milled freshly calcined K2CO3 (0.13 mol), N,N-dimethylacetamide (200 mL), and chlorobenzene (100 mL) were loaded in an argon-blown four-necked flask equipped with a stirrer, an argon supply tube, and a system for azeotropic removal of water.…”
Section: Methodsmentioning
confidence: 99%
“…The co-PAEKs shown in Figure 1 were synthesized by polycondensation of 4,4difluorobenzophenone with dipotassium bisphenolates proceeding from the mechanism of nucleophilic substitution of activated halogen in the aryl dihalide, analogously to the earlier described preparation of homopolymers [13]. The concentration of the bisphenols mixture was 0.5 mol per 1 L of the solvent, with a 30% excess of K 2 CO 3 .…”
Section: Methodsmentioning
confidence: 99%
“…Fig. 1 were synthesized by polycondensation of 4,4'difluorobenzophenone with dipotassium bisphenolates proceeding by the mechanism of nucleophilic substitution of activated halogen in the aryl dihalide analogously to the earlier described preparation of homopolymers [13]. The concentration of the bisphenols mixture was 0.5 mol per 1 liter of the solvent with K2CO3 being in the 30% excess.…”
Section: Introductionmentioning
confidence: 99%