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Supramolecular copolymerization driven by integrative self-sorting of hydrogen-bonded rosettes

Molecular recognition to preorganize noncovalently polymerizable supramolecular complexes is a characteristic process of natural supramolecular polymers, and such recognition processes allow for dynamic self-alteration, yielding complex polymer systems with extraordinarily high efficiency in their t...

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Autores principales: Aratsu, Keisuke, Takeya, Rika, Pauw, Brian R., Hollamby, Martin J., Kitamoto, Yuichi, Shimizu, Nobutaka, Takagi, Hideaki, Haruki, Rie, Adachi, Shin-ichi, Yagai, Shiki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113319/
https://www.ncbi.nlm.nih.gov/pubmed/32238806
http://dx.doi.org/10.1038/s41467-020-15422-6
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author Aratsu, Keisuke
Takeya, Rika
Pauw, Brian R.
Hollamby, Martin J.
Kitamoto, Yuichi
Shimizu, Nobutaka
Takagi, Hideaki
Haruki, Rie
Adachi, Shin-ichi
Yagai, Shiki
author_facet Aratsu, Keisuke
Takeya, Rika
Pauw, Brian R.
Hollamby, Martin J.
Kitamoto, Yuichi
Shimizu, Nobutaka
Takagi, Hideaki
Haruki, Rie
Adachi, Shin-ichi
Yagai, Shiki
author_sort Aratsu, Keisuke
collection PubMed
description Molecular recognition to preorganize noncovalently polymerizable supramolecular complexes is a characteristic process of natural supramolecular polymers, and such recognition processes allow for dynamic self-alteration, yielding complex polymer systems with extraordinarily high efficiency in their targeted function. We herein show an example of such molecular recognition-controlled kinetic assembly/disassembly processes within artificial supramolecular polymer systems using six-membered hydrogen-bonded supramolecular complexes (rosettes). Electron-rich and poor monomers are prepared that kinetically coassemble through a temperature-controlled protocol into amorphous coaggregates comprising a diverse mixture of rosettes. Over days, the electrostatic interaction between two monomers induces an integrative self-sorting of rosettes. While the electron-rich monomer inherently forms toroidal homopolymers, the additional electrostatic interaction that can also guide rosette association allows helicoidal growth of supramolecular copolymers that are comprised of an alternating array of two monomers. Upon heating, the helicoidal copolymers undergo a catastrophic transition into amorphous coaggregates via entropy-driven randomization of the monomers in the rosette.
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spelling pubmed-71133192020-04-03 Supramolecular copolymerization driven by integrative self-sorting of hydrogen-bonded rosettes Aratsu, Keisuke Takeya, Rika Pauw, Brian R. Hollamby, Martin J. Kitamoto, Yuichi Shimizu, Nobutaka Takagi, Hideaki Haruki, Rie Adachi, Shin-ichi Yagai, Shiki Nat Commun Article Molecular recognition to preorganize noncovalently polymerizable supramolecular complexes is a characteristic process of natural supramolecular polymers, and such recognition processes allow for dynamic self-alteration, yielding complex polymer systems with extraordinarily high efficiency in their targeted function. We herein show an example of such molecular recognition-controlled kinetic assembly/disassembly processes within artificial supramolecular polymer systems using six-membered hydrogen-bonded supramolecular complexes (rosettes). Electron-rich and poor monomers are prepared that kinetically coassemble through a temperature-controlled protocol into amorphous coaggregates comprising a diverse mixture of rosettes. Over days, the electrostatic interaction between two monomers induces an integrative self-sorting of rosettes. While the electron-rich monomer inherently forms toroidal homopolymers, the additional electrostatic interaction that can also guide rosette association allows helicoidal growth of supramolecular copolymers that are comprised of an alternating array of two monomers. Upon heating, the helicoidal copolymers undergo a catastrophic transition into amorphous coaggregates via entropy-driven randomization of the monomers in the rosette. Nature Publishing Group UK 2020-04-01 /pmc/articles/PMC7113319/ /pubmed/32238806 http://dx.doi.org/10.1038/s41467-020-15422-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Aratsu, Keisuke
Takeya, Rika
Pauw, Brian R.
Hollamby, Martin J.
Kitamoto, Yuichi
Shimizu, Nobutaka
Takagi, Hideaki
Haruki, Rie
Adachi, Shin-ichi
Yagai, Shiki
Supramolecular copolymerization driven by integrative self-sorting of hydrogen-bonded rosettes
title Supramolecular copolymerization driven by integrative self-sorting of hydrogen-bonded rosettes
title_full Supramolecular copolymerization driven by integrative self-sorting of hydrogen-bonded rosettes
title_fullStr Supramolecular copolymerization driven by integrative self-sorting of hydrogen-bonded rosettes
title_full_unstemmed Supramolecular copolymerization driven by integrative self-sorting of hydrogen-bonded rosettes
title_short Supramolecular copolymerization driven by integrative self-sorting of hydrogen-bonded rosettes
title_sort supramolecular copolymerization driven by integrative self-sorting of hydrogen-bonded rosettes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113319/
https://www.ncbi.nlm.nih.gov/pubmed/32238806
http://dx.doi.org/10.1038/s41467-020-15422-6
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