1993
DOI: 10.1002/app.1993.070470211
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Arylidene polymers. XVIII. Synthesis and thermal behavior of organometallic arylidene polyesters containing ferrocene derivatives in the main chain

Abstract: Egypt 71 51 6 SYNOPSIS A new interesting category of organometallic polyesters based on diarylidenecycloalkanones containing ferrocene derivatives in the polymer main chain has been prepared by interfacial polycondensation of 1,1 '-dichlorocarbonyl ferrocene or 1,1 '-dichlorocarbonyl-4,4'-diiodoferrocene with 2,5-bis ( p -hydroxybenzylidene ) cyclopentanone, 2,5-divanillylidenecyclopentanone, 2,6-bis ( p -hydroxybenzylidene ) cyclohexanone, 2,6-divanillylidenecyclohexanone, and 2,7-bis ( p -hydroxybenzylidene)… Show more

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Cited by 40 publications
(23 citation statements)
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“…Abd-Alla et al [34] synthesized a new interesting category of organometallic polyesters 5a-e based on dibenzylidene-cycloalkanones containing ferrocene derivatives in the main chain by interfacial polycondensation of 1,1 -dichlorocarbonyl ferrocene or 1,1 -dichlorocarbonyl-4,4 -diiodoferrocene with 2,5-bis(4-hydroxybenzylidene)cyclopentanone, 2,5-bis(4-hydroxy-3-methoxybenzylidene)cyclopentanone, 2,6-bis(4-hydroxybenzylidene)cyclohexanone, 2,6-bis(4-hydroxy-3-methoxybenzylidene)cyclohexanone and 2,7-bis(4-hydroxybenzylidene)cycloheptanone at ambient temperature (Fig. 3).…”
Section: Ferrocene Polymersmentioning
confidence: 99%
“…Abd-Alla et al [34] synthesized a new interesting category of organometallic polyesters 5a-e based on dibenzylidene-cycloalkanones containing ferrocene derivatives in the main chain by interfacial polycondensation of 1,1 -dichlorocarbonyl ferrocene or 1,1 -dichlorocarbonyl-4,4 -diiodoferrocene with 2,5-bis(4-hydroxybenzylidene)cyclopentanone, 2,5-bis(4-hydroxy-3-methoxybenzylidene)cyclopentanone, 2,6-bis(4-hydroxybenzylidene)cyclohexanone, 2,6-bis(4-hydroxy-3-methoxybenzylidene)cyclohexanone and 2,7-bis(4-hydroxybenzylidene)cycloheptanone at ambient temperature (Fig. 3).…”
Section: Ferrocene Polymersmentioning
confidence: 99%
“…Moreover, it should be noted that the presence of methoxyl groups as substituent in the phenyl ring caused some hindering between the repeating units and inforced its to the unsymmetrical orienation in the polymer chains and reduced the close packed structure and hence these copolyesters exhibit only a low degree of crystallinity [30]. Moreover, in copolyesters (IVe, Ve, Vie) the presence of -N=N-as a polar group in addition to -C=C-bonds induces some order between two adjacent chains in the polymer towards some extent of crystallinity [36][37] …”
Section: X-ray Analysismentioning
confidence: 99%
“…The thermal stabilities of selected examples of copolyesters were evaluated by thermogravimeteric analysis (TGA), Differential thermal analysis (DTA) in air at a heating rate of 10°C min high hindrances to internal rotation about primary valance bonds, and hence raises T g [32].…”
Section: Thermal Analysismentioning
confidence: 99%