Issue 50, 2020, Issue in Progress

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

Abstract

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 Cu2+, Zn2+ and Ru2+, 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–Zn2+ 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.

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

Supplementary files

Article information

Article type
Paper
Submitted
08 Jun 2020
Accepted
03 Aug 2020
First published
10 Aug 2020
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2020,10, 29627-29632

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

M. Takafuji, T. Kawahara, N. Sultana, N. Ryu, K. Yoshida, Y. Kuwahara, R. Oda and H. Ihara, RSC Adv., 2020, 10, 29627 DOI: 10.1039/D0RA05057A

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