Light-induced cross-linking and post-cross-linking modification of polyglycidol

The photoinduced radical generation process has received renewed interest due to its economic and ecological appeal. Herein the light-induced cross-linking of functional polyglycidol and its post-cross-linking modification are presented. Linear polyglycidol was first functionalized with a tertiary a...

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Published inChemical communications (Cambridge, England) Vol. 54; no. 13; pp. 1647 - 1650
Main Authors Marquardt, F, Bruns, M, Keul, H, Yagci, Y, Möller, M
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 2018
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Summary:The photoinduced radical generation process has received renewed interest due to its economic and ecological appeal. Herein the light-induced cross-linking of functional polyglycidol and its post-cross-linking modification are presented. Linear polyglycidol was first functionalized with a tertiary amine in a two-step reaction. Dimethylaminopropyl functional polyglycidol was cross-linked in a UV-light mediated reaction with camphorquinone as a type II photoinitiator. The cross-linked polyglycidol was further functionalized by quaternization with various organoiodine compounds. Aqueous dispersions of the cross-linked polymers were investigated by means of DLS and zeta potential measurements. Polymer films were evaluated by DSC and XPS.
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ISSN:1359-7345
1364-548X
DOI:10.1039/c7cc09498a