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Side-Chain Supramolecular Polymers Employing Conformer Independent Triple Hydrogen Bonding Arrays

[Image: see text] Derivatives of thymine have been extensively used to promote supramolecular materials assembly. Such derivatives can be synthetically challenging to access and may be susceptible to degradation. The current article uses a conformer-independent acceptor–donor–acceptor array (ureidop...

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Autores principales: Gooch, Adam, Murphy, Natasha S., Thomson, Neil H., Wilson, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3903092/
https://www.ncbi.nlm.nih.gov/pubmed/24478529
http://dx.doi.org/10.1021/ma402069b
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author Gooch, Adam
Murphy, Natasha S.
Thomson, Neil H.
Wilson, Andrew J.
author_facet Gooch, Adam
Murphy, Natasha S.
Thomson, Neil H.
Wilson, Andrew J.
author_sort Gooch, Adam
collection PubMed
description [Image: see text] Derivatives of thymine have been extensively used to promote supramolecular materials assembly. Such derivatives can be synthetically challenging to access and may be susceptible to degradation. The current article uses a conformer-independent acceptor–donor–acceptor array (ureidopyrimidine) which forms moderate affinity interactions with diamidopyridine derivatives to effect supramolecular blend formation between polystyrene and poly(methyl methacrylate) polymers obtained by RAFT which have been functionalized with the hydrogen bonding motifs.
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spelling pubmed-39030922014-01-27 Side-Chain Supramolecular Polymers Employing Conformer Independent Triple Hydrogen Bonding Arrays Gooch, Adam Murphy, Natasha S. Thomson, Neil H. Wilson, Andrew J. Macromolecules [Image: see text] Derivatives of thymine have been extensively used to promote supramolecular materials assembly. Such derivatives can be synthetically challenging to access and may be susceptible to degradation. The current article uses a conformer-independent acceptor–donor–acceptor array (ureidopyrimidine) which forms moderate affinity interactions with diamidopyridine derivatives to effect supramolecular blend formation between polystyrene and poly(methyl methacrylate) polymers obtained by RAFT which have been functionalized with the hydrogen bonding motifs. American Chemical Society 2013-12-11 2013-12-23 /pmc/articles/PMC3903092/ /pubmed/24478529 http://dx.doi.org/10.1021/ma402069b Text en Copyright © 2013 American Chemical Society Terms of Use CC-BY (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html)
spellingShingle Gooch, Adam
Murphy, Natasha S.
Thomson, Neil H.
Wilson, Andrew J.
Side-Chain Supramolecular Polymers Employing Conformer Independent Triple Hydrogen Bonding Arrays
title Side-Chain Supramolecular Polymers Employing Conformer Independent Triple Hydrogen Bonding Arrays
title_full Side-Chain Supramolecular Polymers Employing Conformer Independent Triple Hydrogen Bonding Arrays
title_fullStr Side-Chain Supramolecular Polymers Employing Conformer Independent Triple Hydrogen Bonding Arrays
title_full_unstemmed Side-Chain Supramolecular Polymers Employing Conformer Independent Triple Hydrogen Bonding Arrays
title_short Side-Chain Supramolecular Polymers Employing Conformer Independent Triple Hydrogen Bonding Arrays
title_sort side-chain supramolecular polymers employing conformer independent triple hydrogen bonding arrays
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3903092/
https://www.ncbi.nlm.nih.gov/pubmed/24478529
http://dx.doi.org/10.1021/ma402069b
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