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Synthesis of a resin monomer-soluble polyrotaxane crosslinker containing cleavable end groups
A resin monomer-soluble polyrotaxane (PRX) crosslinker with cleavable end groups was synthesized to develop degradable photosetting composite resins. The PRX containing 50 α-cyclodextrins (α-CDs) with disulfide end groups was initially modified with n-butylamine to obtain a resin monomer-soluble PRX...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273235/ https://www.ncbi.nlm.nih.gov/pubmed/25550723 http://dx.doi.org/10.3762/bjoc.10.274 |
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author | Seo, Ji-Hun Nakagawa, Shino Hirata, Koichiro Yui, Nobuhiko |
author_facet | Seo, Ji-Hun Nakagawa, Shino Hirata, Koichiro Yui, Nobuhiko |
author_sort | Seo, Ji-Hun |
collection | PubMed |
description | A resin monomer-soluble polyrotaxane (PRX) crosslinker with cleavable end groups was synthesized to develop degradable photosetting composite resins. The PRX containing 50 α-cyclodextrins (α-CDs) with disulfide end groups was initially modified with n-butylamine to obtain a resin monomer-soluble PRX. The PRX containing 13 n-butyl groups per α-CD molecule was completely soluble in conventional resin monomers such as 2-hydroxyethyl methacrylate (HEMA) and urethane dimethacrylate (UDMA). The synthesized n-butyl-containing PRX was further modified with 2-aminoethyl methacrylate to provide crosslinkable acrylic groups onto PRX. The prepared resin monomer-soluble PRX crosslinker was successfully polymerized with a mixture of HEMA and UDMA to provide photosetting plastic. It was confirmed that the Vickers hardness of the prepared plastic was greatly decreased after treatment with dithiothreitol. This indicates that the resin monomer-soluble PRX crosslinker can be applied to design degradable photosetting plastics potentially used in the industrial or biomedical field. |
format | Online Article Text |
id | pubmed-4273235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-42732352014-12-30 Synthesis of a resin monomer-soluble polyrotaxane crosslinker containing cleavable end groups Seo, Ji-Hun Nakagawa, Shino Hirata, Koichiro Yui, Nobuhiko Beilstein J Org Chem Full Research Paper A resin monomer-soluble polyrotaxane (PRX) crosslinker with cleavable end groups was synthesized to develop degradable photosetting composite resins. The PRX containing 50 α-cyclodextrins (α-CDs) with disulfide end groups was initially modified with n-butylamine to obtain a resin monomer-soluble PRX. The PRX containing 13 n-butyl groups per α-CD molecule was completely soluble in conventional resin monomers such as 2-hydroxyethyl methacrylate (HEMA) and urethane dimethacrylate (UDMA). The synthesized n-butyl-containing PRX was further modified with 2-aminoethyl methacrylate to provide crosslinkable acrylic groups onto PRX. The prepared resin monomer-soluble PRX crosslinker was successfully polymerized with a mixture of HEMA and UDMA to provide photosetting plastic. It was confirmed that the Vickers hardness of the prepared plastic was greatly decreased after treatment with dithiothreitol. This indicates that the resin monomer-soluble PRX crosslinker can be applied to design degradable photosetting plastics potentially used in the industrial or biomedical field. Beilstein-Institut 2014-11-10 /pmc/articles/PMC4273235/ /pubmed/25550723 http://dx.doi.org/10.3762/bjoc.10.274 Text en Copyright © 2014, Seo et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Seo, Ji-Hun Nakagawa, Shino Hirata, Koichiro Yui, Nobuhiko Synthesis of a resin monomer-soluble polyrotaxane crosslinker containing cleavable end groups |
title | Synthesis of a resin monomer-soluble polyrotaxane crosslinker containing cleavable end groups |
title_full | Synthesis of a resin monomer-soluble polyrotaxane crosslinker containing cleavable end groups |
title_fullStr | Synthesis of a resin monomer-soluble polyrotaxane crosslinker containing cleavable end groups |
title_full_unstemmed | Synthesis of a resin monomer-soluble polyrotaxane crosslinker containing cleavable end groups |
title_short | Synthesis of a resin monomer-soluble polyrotaxane crosslinker containing cleavable end groups |
title_sort | synthesis of a resin monomer-soluble polyrotaxane crosslinker containing cleavable end groups |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273235/ https://www.ncbi.nlm.nih.gov/pubmed/25550723 http://dx.doi.org/10.3762/bjoc.10.274 |
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