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Well-defined aqueous nanoassemblies from amphiphilic meta-terphenyls and their guest incorporation

Spherical molecular assemblies with diameters of ∼2 nm were quantitatively formed in water from new amphiphilic meta-terphenyls with two hydrophilic pendants at the central benzene ring. Whereas intermolecular interactions between small aromatic rings are typically weak, the obtained nanoassemblies...

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Detalles Bibliográficos
Autores principales: Okazawa, Yusuke, Kondo, Kei, Akita, Munetaka, Yoshizawa, Michito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499508/
https://www.ncbi.nlm.nih.gov/pubmed/28717497
http://dx.doi.org/10.1039/c5sc01545f
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author Okazawa, Yusuke
Kondo, Kei
Akita, Munetaka
Yoshizawa, Michito
author_facet Okazawa, Yusuke
Kondo, Kei
Akita, Munetaka
Yoshizawa, Michito
author_sort Okazawa, Yusuke
collection PubMed
description Spherical molecular assemblies with diameters of ∼2 nm were quantitatively formed in water from new amphiphilic meta-terphenyls with two hydrophilic pendants at the central benzene ring. Whereas intermolecular interactions between small aromatic rings are typically weak, the obtained nanoassemblies are stable enough at wide-ranging concentrations and mostly remain intact even in the presence of similar nanoassemblies with polyaromatic frameworks. The nanoassembly with pentamethyl-substituted terminal benzene rings provides superior host capability for fluorescent dyes in water.
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spelling pubmed-54995082017-07-17 Well-defined aqueous nanoassemblies from amphiphilic meta-terphenyls and their guest incorporation Okazawa, Yusuke Kondo, Kei Akita, Munetaka Yoshizawa, Michito Chem Sci Chemistry Spherical molecular assemblies with diameters of ∼2 nm were quantitatively formed in water from new amphiphilic meta-terphenyls with two hydrophilic pendants at the central benzene ring. Whereas intermolecular interactions between small aromatic rings are typically weak, the obtained nanoassemblies are stable enough at wide-ranging concentrations and mostly remain intact even in the presence of similar nanoassemblies with polyaromatic frameworks. The nanoassembly with pentamethyl-substituted terminal benzene rings provides superior host capability for fluorescent dyes in water. Royal Society of Chemistry 2015-08-01 2015-06-09 /pmc/articles/PMC5499508/ /pubmed/28717497 http://dx.doi.org/10.1039/c5sc01545f Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Okazawa, Yusuke
Kondo, Kei
Akita, Munetaka
Yoshizawa, Michito
Well-defined aqueous nanoassemblies from amphiphilic meta-terphenyls and their guest incorporation
title Well-defined aqueous nanoassemblies from amphiphilic meta-terphenyls and their guest incorporation
title_full Well-defined aqueous nanoassemblies from amphiphilic meta-terphenyls and their guest incorporation
title_fullStr Well-defined aqueous nanoassemblies from amphiphilic meta-terphenyls and their guest incorporation
title_full_unstemmed Well-defined aqueous nanoassemblies from amphiphilic meta-terphenyls and their guest incorporation
title_short Well-defined aqueous nanoassemblies from amphiphilic meta-terphenyls and their guest incorporation
title_sort well-defined aqueous nanoassemblies from amphiphilic meta-terphenyls and their guest incorporation
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499508/
https://www.ncbi.nlm.nih.gov/pubmed/28717497
http://dx.doi.org/10.1039/c5sc01545f
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