Oligomeric epoxide–amine adducts based on 2-amino-N-isopropylacetamide and α-amino-ε-caprolactam: Solubility in presence of cyclodextrin and curing properties
2-Amino-N-isopropylacetamide and α-amino-ε-caprolactam were reacted with glycerol diglycidyl ether to give novel oligomeric thermoresponsive epoxide–amine adducts. These oligomers exhibit a lower critical solution temperature (LCST) behavior in water. The solubility properties were influenced with r...
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doaj-875e97e50b4148468b1848a7bdbc94de2021-02-02T00:12:42ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972013-12-01912803281110.3762/bjoc.9.3151860-5397-9-315Oligomeric epoxide–amine adducts based on 2-amino-N-isopropylacetamide and α-amino-ε-caprolactam: Solubility in presence of cyclodextrin and curing propertiesJulian Fischer0Helmut Ritter1Institute of Organic Chemistry and Macromolecular Chemistry, Heinrich-Heine-University Düsseldorf, Universitätsstraße 1, D-40225 Düsseldorf, GermanyInstitute of Organic Chemistry and Macromolecular Chemistry, Heinrich-Heine-University Düsseldorf, Universitätsstraße 1, D-40225 Düsseldorf, Germany2-Amino-N-isopropylacetamide and α-amino-ε-caprolactam were reacted with glycerol diglycidyl ether to give novel oligomeric thermoresponsive epoxide–amine adducts. These oligomers exhibit a lower critical solution temperature (LCST) behavior in water. The solubility properties were influenced with randomly methylated β-cyclodextrin (RAMEB-CD) and the curing properties of the amine–epoxide mixtures were analyzed by oscillatory rheology and differential scanning calorimetry, whereby significant differences in setting time, viscosity, and stiffness were observed.https://doi.org/10.3762/bjoc.9.315amino acidscuring propertiescyclodextrinepoxide–amine oligomersLCST |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Julian Fischer Helmut Ritter |
spellingShingle |
Julian Fischer Helmut Ritter Oligomeric epoxide–amine adducts based on 2-amino-N-isopropylacetamide and α-amino-ε-caprolactam: Solubility in presence of cyclodextrin and curing properties Beilstein Journal of Organic Chemistry amino acids curing properties cyclodextrin epoxide–amine oligomers LCST |
author_facet |
Julian Fischer Helmut Ritter |
author_sort |
Julian Fischer |
title |
Oligomeric epoxide–amine adducts based on 2-amino-N-isopropylacetamide and α-amino-ε-caprolactam: Solubility in presence of cyclodextrin and curing properties |
title_short |
Oligomeric epoxide–amine adducts based on 2-amino-N-isopropylacetamide and α-amino-ε-caprolactam: Solubility in presence of cyclodextrin and curing properties |
title_full |
Oligomeric epoxide–amine adducts based on 2-amino-N-isopropylacetamide and α-amino-ε-caprolactam: Solubility in presence of cyclodextrin and curing properties |
title_fullStr |
Oligomeric epoxide–amine adducts based on 2-amino-N-isopropylacetamide and α-amino-ε-caprolactam: Solubility in presence of cyclodextrin and curing properties |
title_full_unstemmed |
Oligomeric epoxide–amine adducts based on 2-amino-N-isopropylacetamide and α-amino-ε-caprolactam: Solubility in presence of cyclodextrin and curing properties |
title_sort |
oligomeric epoxide–amine adducts based on 2-amino-n-isopropylacetamide and α-amino-ε-caprolactam: solubility in presence of cyclodextrin and curing properties |
publisher |
Beilstein-Institut |
series |
Beilstein Journal of Organic Chemistry |
issn |
1860-5397 |
publishDate |
2013-12-01 |
description |
2-Amino-N-isopropylacetamide and α-amino-ε-caprolactam were reacted with glycerol diglycidyl ether to give novel oligomeric thermoresponsive epoxide–amine adducts. These oligomers exhibit a lower critical solution temperature (LCST) behavior in water. The solubility properties were influenced with randomly methylated β-cyclodextrin (RAMEB-CD) and the curing properties of the amine–epoxide mixtures were analyzed by oscillatory rheology and differential scanning calorimetry, whereby significant differences in setting time, viscosity, and stiffness were observed. |
topic |
amino acids curing properties cyclodextrin epoxide–amine oligomers LCST |
url |
https://doi.org/10.3762/bjoc.9.315 |
work_keys_str_mv |
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1724314300132098048 |