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Design, Synthesis and Self‐Assembly of Functional Amphiphilic Metallodendrimers

A new family of alkynylated, amphiphilic dendrimers consisting of amidoamine linkers connected to 5,5′‐functionalized 2,2′‐bipyridine cores has been developed and evaluated in the formation of metallodendrimers of different generations and in self‐assembly protocols. A convergent synthetic strategy...

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Detalles Bibliográficos
Autores principales: Neranon, Kitjanit, Alberch, Laura, Ramström, Olof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6948116/
https://www.ncbi.nlm.nih.gov/pubmed/31921545
http://dx.doi.org/10.1002/open.201900298
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author Neranon, Kitjanit
Alberch, Laura
Ramström, Olof
author_facet Neranon, Kitjanit
Alberch, Laura
Ramström, Olof
author_sort Neranon, Kitjanit
collection PubMed
description A new family of alkynylated, amphiphilic dendrimers consisting of amidoamine linkers connected to 5,5′‐functionalized 2,2′‐bipyridine cores has been developed and evaluated in the formation of metallodendrimers of different generations and in self‐assembly protocols. A convergent synthetic strategy was applied to provide dumbbell‐shaped amphiphilic dendrimers, where the 2,2′‐bipyridine cores could be coordinated to Fe(II) centers to afford corresponding metallodendrimers. The ability of the metallic‐ and non‐metallic dendritic structures to self‐assemble into functional supramolecular aggregates were furthermore evaluated in aqueous solution. Spherical aggregates with sizes of a few hundred nanometers were generally produced, where controlled disassembly of the metallodendrimers through decomplexation could be achieved.
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spelling pubmed-69481162020-01-09 Design, Synthesis and Self‐Assembly of Functional Amphiphilic Metallodendrimers Neranon, Kitjanit Alberch, Laura Ramström, Olof ChemistryOpen Full Papers A new family of alkynylated, amphiphilic dendrimers consisting of amidoamine linkers connected to 5,5′‐functionalized 2,2′‐bipyridine cores has been developed and evaluated in the formation of metallodendrimers of different generations and in self‐assembly protocols. A convergent synthetic strategy was applied to provide dumbbell‐shaped amphiphilic dendrimers, where the 2,2′‐bipyridine cores could be coordinated to Fe(II) centers to afford corresponding metallodendrimers. The ability of the metallic‐ and non‐metallic dendritic structures to self‐assemble into functional supramolecular aggregates were furthermore evaluated in aqueous solution. Spherical aggregates with sizes of a few hundred nanometers were generally produced, where controlled disassembly of the metallodendrimers through decomplexation could be achieved. John Wiley and Sons Inc. 2020-01-08 /pmc/articles/PMC6948116/ /pubmed/31921545 http://dx.doi.org/10.1002/open.201900298 Text en ©2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full Papers
Neranon, Kitjanit
Alberch, Laura
Ramström, Olof
Design, Synthesis and Self‐Assembly of Functional Amphiphilic Metallodendrimers
title Design, Synthesis and Self‐Assembly of Functional Amphiphilic Metallodendrimers
title_full Design, Synthesis and Self‐Assembly of Functional Amphiphilic Metallodendrimers
title_fullStr Design, Synthesis and Self‐Assembly of Functional Amphiphilic Metallodendrimers
title_full_unstemmed Design, Synthesis and Self‐Assembly of Functional Amphiphilic Metallodendrimers
title_short Design, Synthesis and Self‐Assembly of Functional Amphiphilic Metallodendrimers
title_sort design, synthesis and self‐assembly of functional amphiphilic metallodendrimers
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6948116/
https://www.ncbi.nlm.nih.gov/pubmed/31921545
http://dx.doi.org/10.1002/open.201900298
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