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Synthesis of Hydrophobic Carbohydrate Polymers and Their Formation of Thermotropic Liquid Crystalline Phases
[Image: see text] The first synthesis of enantiopure glucose octyl ether polyamido-saccharides (GOE-PAS) with a defined molecular weight and narrow dispersity is reported using a controlled anionic ring-opening polymerization of a glucose-derived β-lactam sugar monomer possessing octyl ether chains....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999795/ https://www.ncbi.nlm.nih.gov/pubmed/24804154 http://dx.doi.org/10.1021/mz5000703 |
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author | Ghobril, Cynthia Heinrich, Benoît Dane, Eric L. Grinstaff, Mark W. |
author_facet | Ghobril, Cynthia Heinrich, Benoît Dane, Eric L. Grinstaff, Mark W. |
author_sort | Ghobril, Cynthia |
collection | PubMed |
description | [Image: see text] The first synthesis of enantiopure glucose octyl ether polyamido-saccharides (GOE-PAS) with a defined molecular weight and narrow dispersity is reported using a controlled anionic ring-opening polymerization of a glucose-derived β-lactam sugar monomer possessing octyl ether chains. This new polymer structure is characterized by NMR, infrared (IR), optical rotation, gel permeation chromatography (GPC), and thermogravimetric analysis (TGA). At room temperature, the polymers form lamellar (Lam) phases. Upon heating to mild temperatures (ca. 60 °C), the shortest polymer shows a direct transition to the isotropic (Iso) liquid state, while the longer polymers give rise to a hexagonal columnar (Col(h)) phase before becoming isotropic at higher temperatures (ca. 120 °C). |
format | Online Article Text |
id | pubmed-3999795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39997952015-03-27 Synthesis of Hydrophobic Carbohydrate Polymers and Their Formation of Thermotropic Liquid Crystalline Phases Ghobril, Cynthia Heinrich, Benoît Dane, Eric L. Grinstaff, Mark W. ACS Macro Lett [Image: see text] The first synthesis of enantiopure glucose octyl ether polyamido-saccharides (GOE-PAS) with a defined molecular weight and narrow dispersity is reported using a controlled anionic ring-opening polymerization of a glucose-derived β-lactam sugar monomer possessing octyl ether chains. This new polymer structure is characterized by NMR, infrared (IR), optical rotation, gel permeation chromatography (GPC), and thermogravimetric analysis (TGA). At room temperature, the polymers form lamellar (Lam) phases. Upon heating to mild temperatures (ca. 60 °C), the shortest polymer shows a direct transition to the isotropic (Iso) liquid state, while the longer polymers give rise to a hexagonal columnar (Col(h)) phase before becoming isotropic at higher temperatures (ca. 120 °C). American Chemical Society 2014-03-27 2014-04-15 /pmc/articles/PMC3999795/ /pubmed/24804154 http://dx.doi.org/10.1021/mz5000703 Text en Copyright © 2014 American Chemical Society |
spellingShingle | Ghobril, Cynthia Heinrich, Benoît Dane, Eric L. Grinstaff, Mark W. Synthesis of Hydrophobic Carbohydrate Polymers and Their Formation of Thermotropic Liquid Crystalline Phases |
title | Synthesis of Hydrophobic Carbohydrate Polymers and
Their Formation of Thermotropic Liquid Crystalline Phases |
title_full | Synthesis of Hydrophobic Carbohydrate Polymers and
Their Formation of Thermotropic Liquid Crystalline Phases |
title_fullStr | Synthesis of Hydrophobic Carbohydrate Polymers and
Their Formation of Thermotropic Liquid Crystalline Phases |
title_full_unstemmed | Synthesis of Hydrophobic Carbohydrate Polymers and
Their Formation of Thermotropic Liquid Crystalline Phases |
title_short | Synthesis of Hydrophobic Carbohydrate Polymers and
Their Formation of Thermotropic Liquid Crystalline Phases |
title_sort | synthesis of hydrophobic carbohydrate polymers and
their formation of thermotropic liquid crystalline phases |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999795/ https://www.ncbi.nlm.nih.gov/pubmed/24804154 http://dx.doi.org/10.1021/mz5000703 |
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