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Sugar-Functional Vinyl Addition Poly(norbornene)–Photopatternable Poly(norbornenyl gluconamide) Compositions Developed with Water
[Image: see text] The norbornenyl gluconamide (NBGA) monomer can be polymerized by a number of palladium catalysts to give water-soluble, vinyl addition poly(NBGA). Depending on the catalyst used, the reaction conditions, and the chain-transfer additives employed, high-molecular-weight polymers can...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641349/ https://www.ncbi.nlm.nih.gov/pubmed/31458562 http://dx.doi.org/10.1021/acsomega.8b00081 |
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author | Smith, Steven Paudel, Liladhar Cyrus, Crystal Burgoon, Hugh Fujita, Kazuyoshi Thoresen, Jennifer Thomas, Kim Langsdorf, Leah Rhodes, Larry F. |
author_facet | Smith, Steven Paudel, Liladhar Cyrus, Crystal Burgoon, Hugh Fujita, Kazuyoshi Thoresen, Jennifer Thomas, Kim Langsdorf, Leah Rhodes, Larry F. |
author_sort | Smith, Steven |
collection | PubMed |
description | [Image: see text] The norbornenyl gluconamide (NBGA) monomer can be polymerized by a number of palladium catalysts to give water-soluble, vinyl addition poly(NBGA). Depending on the catalyst used, the reaction conditions, and the chain-transfer additives employed, high-molecular-weight polymers can be obtained. These polymers can be thermally cross-linked at ca. 190 °C or at ca. 150 °C when the difunctional glutaraldehyde is added. A photopatternable composition is formed by the addition of a water-soluble diazide when the poly(NBGA) molecular weight is sufficiently high. After image-wise exposure, negative-tone patterns are revealed by water development. A detailed analysis of NBGA monomer structures by high-resolution nuclear magnetic resonance techniques including pure shift is reported showing that two diastereomers of each endo- and exo-isomer are formed from the reaction of norbornene methylamine and δ-gluconolactone. |
format | Online Article Text |
id | pubmed-6641349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66413492019-08-27 Sugar-Functional Vinyl Addition Poly(norbornene)–Photopatternable Poly(norbornenyl gluconamide) Compositions Developed with Water Smith, Steven Paudel, Liladhar Cyrus, Crystal Burgoon, Hugh Fujita, Kazuyoshi Thoresen, Jennifer Thomas, Kim Langsdorf, Leah Rhodes, Larry F. ACS Omega [Image: see text] The norbornenyl gluconamide (NBGA) monomer can be polymerized by a number of palladium catalysts to give water-soluble, vinyl addition poly(NBGA). Depending on the catalyst used, the reaction conditions, and the chain-transfer additives employed, high-molecular-weight polymers can be obtained. These polymers can be thermally cross-linked at ca. 190 °C or at ca. 150 °C when the difunctional glutaraldehyde is added. A photopatternable composition is formed by the addition of a water-soluble diazide when the poly(NBGA) molecular weight is sufficiently high. After image-wise exposure, negative-tone patterns are revealed by water development. A detailed analysis of NBGA monomer structures by high-resolution nuclear magnetic resonance techniques including pure shift is reported showing that two diastereomers of each endo- and exo-isomer are formed from the reaction of norbornene methylamine and δ-gluconolactone. American Chemical Society 2018-03-09 /pmc/articles/PMC6641349/ /pubmed/31458562 http://dx.doi.org/10.1021/acsomega.8b00081 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Smith, Steven Paudel, Liladhar Cyrus, Crystal Burgoon, Hugh Fujita, Kazuyoshi Thoresen, Jennifer Thomas, Kim Langsdorf, Leah Rhodes, Larry F. Sugar-Functional Vinyl Addition Poly(norbornene)–Photopatternable Poly(norbornenyl gluconamide) Compositions Developed with Water |
title | Sugar-Functional Vinyl Addition Poly(norbornene)–Photopatternable
Poly(norbornenyl gluconamide) Compositions Developed with Water |
title_full | Sugar-Functional Vinyl Addition Poly(norbornene)–Photopatternable
Poly(norbornenyl gluconamide) Compositions Developed with Water |
title_fullStr | Sugar-Functional Vinyl Addition Poly(norbornene)–Photopatternable
Poly(norbornenyl gluconamide) Compositions Developed with Water |
title_full_unstemmed | Sugar-Functional Vinyl Addition Poly(norbornene)–Photopatternable
Poly(norbornenyl gluconamide) Compositions Developed with Water |
title_short | Sugar-Functional Vinyl Addition Poly(norbornene)–Photopatternable
Poly(norbornenyl gluconamide) Compositions Developed with Water |
title_sort | sugar-functional vinyl addition poly(norbornene)–photopatternable
poly(norbornenyl gluconamide) compositions developed with water |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641349/ https://www.ncbi.nlm.nih.gov/pubmed/31458562 http://dx.doi.org/10.1021/acsomega.8b00081 |
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