2007
DOI: 10.1177/0883911507076453
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Polymerization Kinetics of Poly(amidoamine)s in Different Solvents

Abstract: The polyaddition kinetics of 2-methylpiperazine to 1,4-bisacryloylpiperazine was determined in water, methanol, ethylene glycol, formamide, and dimethylformamide, respectively. In the protic solvents, the polyaddition proceeded through a two-step mechanism, each step involved one of the two different secondary amino groups; the difference in amine reactivity was ascribed to the different steric hindrance by the neighbouring groups. Each step followed pseudo-second-order kinetics; the kinetic constants included… Show more

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Cited by 17 publications
(17 citation statements)
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References 19 publications
(23 reference statements)
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“…are of a film with a very low ion concentration. No ions were present through an added salt and glycerol has an auto‐dissociation constant much lower than that of water thus auto‐disscociation of the solvent cannot contribute significantly to the concentration of cations and anions in the foam film . Figure shows that adding the salt NaI increases the amount of surfactant at the foam film surface as evident through the increase of the phosphorous concentration at the surface.…”
Section: Concentration Depth Profilesmentioning
confidence: 97%
“…are of a film with a very low ion concentration. No ions were present through an added salt and glycerol has an auto‐dissociation constant much lower than that of water thus auto‐disscociation of the solvent cannot contribute significantly to the concentration of cations and anions in the foam film . Figure shows that adding the salt NaI increases the amount of surfactant at the foam film surface as evident through the increase of the phosphorous concentration at the surface.…”
Section: Concentration Depth Profilesmentioning
confidence: 97%
“…Not surprisingly, the polyaddition reaction leading to PAAs is best performed, both in terms of attainable molecular weight and reaction rate, in water or, alternatively, alcohols whereas aprotic solvents are normally unsuitable [23]. The kinetics of the polymerization reaction of 2-methylpiperazine and 2,5-dimethylpiperazine with N,N′-bisacryloylpiperazine in water, methanol, ethylene glycol, formamide and dimethylformamide [23] demonstrated that in the protic solvents, 2-methylpiperazine polyaddition proceeded through a two-step mechanism, each of them involving one of the two sec-amine groups. The reaction rate constants related to these steps significantly differed because of the different steric hindrance induced by the neighboring groups.…”
Section: Synthetic Featuresmentioning
confidence: 99%
“…A source of protons is necessary to speed up the reaction and obtain high molecular weight products in reasonable time, whereas aprotic solvents are unsuitable as reaction media . A comparative kinetic study on the polyaddition kinetics of 2‐methylpiperazine and 2,5‐dimethylpiperazine with 1,4‐bisacryloylpiperazine, chosen as model PAA monomers, was performed in water, methanol, ethylene glycol, formamide, and dimethylformamide . In the protic solvents, the polyaddition involving 2‐methylpiperazine proceeded through a two‐step mechanism, each step involving one of the two different sec ‐amine groups, whose reaction constants were significantly different owing to the different steric hindrance by the neighboring groups.…”
Section: Synthetic Featuresmentioning
confidence: 99%