2015
DOI: 10.1007/s13369-015-1860-1
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Green Polymerization of 4-(Oxiran-2-ylmethyl)morpholine

Abstract: Synthesis and cationic polymerization of a new monomer 4-(oxiran-2-ylmethyl)morpholine (OMM) is reported. The monomer was prepared by the reaction of morpholine with epichlorohydrine followed by treatment with sodium hydroxide. The green polymerization of OMM was performed in bulk under suitable condition at temperature 40 • C using an activated smectite clay catalyst, known as Maghnite-H + (Mag-H + ) as proton source. The products are proven by infrared spectroscopy (IR) as well as by nuclear magnetic resonan… Show more

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Cited by 5 publications
(1 citation statement)
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“…Many modifications have been done on PECH by different nucleophiles such as potassium 3,4,5-tris[4-(n-dodecan-1-yloxy)benzyloxy]benzoate [12], aliphatic potassium carboxylates [2], phenolate [4,13], amine [14], biphenyl carboxylic and naphthalene carboxylic acid derivatives [15], sodium methoxide [16], sodium azide [17], vinyl-terminated aromatic potassium carboxylate [18], aromatic and aliphatic thiol compounds [19], imidazolium groups [20], morpholine [21].…”
Section: Introductionmentioning
confidence: 99%
“…Many modifications have been done on PECH by different nucleophiles such as potassium 3,4,5-tris[4-(n-dodecan-1-yloxy)benzyloxy]benzoate [12], aliphatic potassium carboxylates [2], phenolate [4,13], amine [14], biphenyl carboxylic and naphthalene carboxylic acid derivatives [15], sodium methoxide [16], sodium azide [17], vinyl-terminated aromatic potassium carboxylate [18], aromatic and aliphatic thiol compounds [19], imidazolium groups [20], morpholine [21].…”
Section: Introductionmentioning
confidence: 99%