2001
DOI: 10.1016/s0032-3861(00)00352-9
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Synthesis of functional polymers by chemical modification of PECH and PECH–PEO with substituted phenolates

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Cited by 24 publications
(14 citation statements)
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“…Since we obtained good modification degrees and detected no dehydrochlorination side reactions in the chemical modification of PECH [12,13], we were encouraged to use the same strategy and reaction conditions also for poly(epichlorohydrin-co-ethylene oxide) [P(ECH-co-EO)]. In a very recent paper [14], we have reported the preparation of a new family of liquid crystalline columnar polyethers by chemically modifying P(ECH-co-EO) with the dendron 3,4,5-tris[4-(n-dodecan-1-yloxy) benzyloxy]benzoate under different conditions.…”
Section: Introductionmentioning
confidence: 78%
“…Since we obtained good modification degrees and detected no dehydrochlorination side reactions in the chemical modification of PECH [12,13], we were encouraged to use the same strategy and reaction conditions also for poly(epichlorohydrin-co-ethylene oxide) [P(ECH-co-EO)]. In a very recent paper [14], we have reported the preparation of a new family of liquid crystalline columnar polyethers by chemically modifying P(ECH-co-EO) with the dendron 3,4,5-tris[4-(n-dodecan-1-yloxy) benzyloxy]benzoate under different conditions.…”
Section: Introductionmentioning
confidence: 78%
“…This can be supported further by elemental analysis data and the calculations of the reaction yield mentioned below. Also, 13 C NMR spectra were free from any of the signals corresponding to unsaturated vinyl ether units 22,23 in a detectable amount indicating the absence of dehydrohalogenation reaction under our experimental conditions and excluding the possibility of side product formation.…”
Section: Methodsmentioning
confidence: 75%
“…[7][8][9][10][11] Much attention has been paid to the modification of PECH with a large number of nucleophiles such as azides, 12 carbazole, 13 carboxylates, 14,15 sulphur compounds 12,[16][17][18] and phenolates [19][20][21] either under conventional conditions or under phase transfer catalysis (PTC) conditions. [22][23][24] On this basis, the present work deals with the preparation of PECH through cationic ring opening polymerization followed by nucleophilic displacement of chlorine functionality with heterocyclic amines using Mghnite-H + catalyst, a new non-toxic cationic initiator, heterocyclic monomers 25,26 and vinyl monomers. 27,28 The catalyst can be easily separated later from the polymer product and regenerated by heating at a temperature above 100 ℃.…”
Section: Introductionmentioning
confidence: 99%
“…Much attention has been paid to the modification of polyepichlorohydrine (PECH) with a large number of nucleophiles such as carboxylates, phenolates, heterocyclic amines [2][3][4][5][6].…”
Section: Introductionmentioning
confidence: 99%
“…In cationic polymerization, the traditional catalysts, namely BF3, FSO3H, HClO4, are not always effective and require the presence, in great quantity, of a promoter [1][2][3][4][5][6][7][8] such as olefin oxide, acetyl, chloride, or acetic anhydride.…”
Section: Introductionmentioning
confidence: 99%