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Extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in glutamide-based molecular gels

Aggregation-induced chirality is potentially useful in sensor technology applications. Herein we show extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in molecular gels. The secondary chirality reflecting on enhancement of chiral signals (i.e...

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Autores principales: Takafuji, Makoto, Kawahara, Tomoki, Sultana, Nahid, Ryu, Naoya, Yoshida, Kyohei, Kuwahara, Yutaka, Oda, Reiko, Ihara, Hirotaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056163/
https://www.ncbi.nlm.nih.gov/pubmed/35518247
http://dx.doi.org/10.1039/d0ra05057a
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author Takafuji, Makoto
Kawahara, Tomoki
Sultana, Nahid
Ryu, Naoya
Yoshida, Kyohei
Kuwahara, Yutaka
Oda, Reiko
Ihara, Hirotaka
author_facet Takafuji, Makoto
Kawahara, Tomoki
Sultana, Nahid
Ryu, Naoya
Yoshida, Kyohei
Kuwahara, Yutaka
Oda, Reiko
Ihara, Hirotaka
author_sort Takafuji, Makoto
collection PubMed
description Aggregation-induced chirality is potentially useful in sensor technology applications. Herein we show extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in molecular gels. The secondary chirality reflecting on enhancement of chiral signals (i.e., circular dichroism (CD) and circularly polarised luminescence (CPL)) of the molecular gels formed from glutamide-attached terpyridine (G-tpy) is extremely enhanced by the coordination of its terpyridyl groups to metal ions such as Cu(2+), Zn(2+) and Ru(2+), which is due to dramatic changes in the stacked structure of the chromophore groups through the formation of metal ion complex. Metal-free terpyridine exists in a non-planar geometry, which suppress π–π stacking interactions among aggregates. The planarity of the terpyridyl group is improved through metal-ion complexation, which induces the metal-ion-coordinated terpyridyl groups to stack. The thermal stabilities of the CD signals are strongly affected by the metal-ion species. CPL signal is generated in the molecular gel formed from G-tpy–Zn(2+) complex accompanied by chelation-enhanced fluorescence. It is expected that large and sensitive coordination-driven secondary chirality signals (CD and CPL) are useful for sensing guest molecules and the surrounding environment.
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spelling pubmed-90561632022-05-04 Extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in glutamide-based molecular gels Takafuji, Makoto Kawahara, Tomoki Sultana, Nahid Ryu, Naoya Yoshida, Kyohei Kuwahara, Yutaka Oda, Reiko Ihara, Hirotaka RSC Adv Chemistry Aggregation-induced chirality is potentially useful in sensor technology applications. Herein we show extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in molecular gels. The secondary chirality reflecting on enhancement of chiral signals (i.e., circular dichroism (CD) and circularly polarised luminescence (CPL)) of the molecular gels formed from glutamide-attached terpyridine (G-tpy) is extremely enhanced by the coordination of its terpyridyl groups to metal ions such as Cu(2+), Zn(2+) and Ru(2+), which is due to dramatic changes in the stacked structure of the chromophore groups through the formation of metal ion complex. Metal-free terpyridine exists in a non-planar geometry, which suppress π–π stacking interactions among aggregates. The planarity of the terpyridyl group is improved through metal-ion complexation, which induces the metal-ion-coordinated terpyridyl groups to stack. The thermal stabilities of the CD signals are strongly affected by the metal-ion species. CPL signal is generated in the molecular gel formed from G-tpy–Zn(2+) complex accompanied by chelation-enhanced fluorescence. It is expected that large and sensitive coordination-driven secondary chirality signals (CD and CPL) are useful for sensing guest molecules and the surrounding environment. The Royal Society of Chemistry 2020-08-10 /pmc/articles/PMC9056163/ /pubmed/35518247 http://dx.doi.org/10.1039/d0ra05057a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Takafuji, Makoto
Kawahara, Tomoki
Sultana, Nahid
Ryu, Naoya
Yoshida, Kyohei
Kuwahara, Yutaka
Oda, Reiko
Ihara, Hirotaka
Extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in glutamide-based molecular gels
title Extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in glutamide-based molecular gels
title_full Extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in glutamide-based molecular gels
title_fullStr Extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in glutamide-based molecular gels
title_full_unstemmed Extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in glutamide-based molecular gels
title_short Extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in glutamide-based molecular gels
title_sort extreme enhancement of secondary chirality through coordination-driven steric changes of terpyridyl ligand in glutamide-based molecular gels
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056163/
https://www.ncbi.nlm.nih.gov/pubmed/35518247
http://dx.doi.org/10.1039/d0ra05057a
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