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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...

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Autores principales: Smith, Steven, Paudel, Liladhar, Cyrus, Crystal, Burgoon, Hugh, Fujita, Kazuyoshi, Thoresen, Jennifer, Thomas, Kim, Langsdorf, Leah, Rhodes, Larry F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
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.
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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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