Coordination‐Driven Terpyridine‐Based Twisted Prisms with Tunable Emissions and Hierarchical Self‐Assembly Properties. Issue 10 (26th March 2022)

• Record Type: Journal Article
• Authors: Zeng, Yunting; Jiang, Xin; Yu, Hao; Cao, Yan; Lai, Ziwei; Shi, Junjuan; Wang, Ming
• Is Part Of: Advanced optical materials. Volume 10:Issue 10(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-03-26
• Subjects: hierarchical self‐assembly -- supramolecular self‐assembly -- terpyridine -- tetraphenylethylene; Optical materials -- Periodicals; Photonics -- Periodicals; 620.11295
• DOI: 10.1002/adom.202102613
• Languages: English
• ISSNs: 2195-1071

Abstract

Abstract: Tunable fluorescence emission materials play a critical role in many fields such as biology and chemistry. With respect to metallo‐supramolecular assemblies, the construction of 3D tunable‐fluorescent supramolecular assemblies with 2, 2′:6′, 2″‐terpyridine (tpy) is still in its infancy. In this study, two luminous 3D supramolecular prisms self‐assembled with two terpyridine‐based tetraphenylethylene (TPE) ligands and metal Zn(II) are prepared, and the influence of hydrophobic alkyl chains on tunable fluorescence is further explored. By exploiting hydrophobic properties, the prism SA exhibits tunable visible‐light emission in the molecular‐aggregated state. Moreover, SA forms left‐hand and right‐hand helical nanofibers by hierarchical self‐assembly. However, the prism SB without hydrophobic chains does not exhibit tunable fluorescence emission, and only random spherical aggregates after hierarchical self‐assembly are formed. This study can aid to further strengthen the understanding about the effect of hydrophobic segments on photophysical properties and hierarchical self‐assembly of discrete supramolecular architectures. Abstract : Construction of 3D tunable‐fluorescent supramolecular assemblies with 2, 2′:6′, 2″‐terpyridine (tpy) is still in its infancy. In this study, the tunable visible‐light emission of terpyridine‐based supramolecular prism can be achieved by exploiting hydrophobic properties, and helical nanofibers are formed by hierarchical self‐assembly. This strategy offers an avenue for designing 3D tunable‐fluorescent supramolecular assemblies.