Issue 26, 2023

Planar π-extended all-armchair edge topological cycloparaphenylenes

Abstract

It is important to reveal the optical properties and physical mechanisms of electron transitions within planar π-extended cycloparaphenylenes (CPPs) with full armchair edge topology in nanoscience and nanotechnology. The optical properties of the planar π-extended ring stripped from the Au(111) surface are theoretically studied, based on the latest experimental synthesis [Nat. Chem. 2022, 14, 871]. Our calculation results indicate that there is a blue-shift of absorption peaks in non-planar systems compared with planar systems. For non-planar systems, we proved that there is no fluorescence in the closed loop while the open loop exhibits fluorescence, using charge density differences and transition densities as evidence. And we realized the transition from the weak excited state to the strong excited state by the two photon absorption (TPA) method. The resonance Raman spectrum confirmed that the S1 excited state of the non-planar closed loop is a dark excited state. Moreover, there is a red-shift of absorption peaks in non-planar charged systems compared with non-planar uncharged systems. We also investigated the visualization of charge transfer using absorption and fluorescence spectroscopy. Our results can provide more insights into the optical properties and potential design of optical nanodevices.

Graphical abstract: Planar π-extended all-armchair edge topological cycloparaphenylenes

Article information

Article type
Paper
Submitted
19 Jan 2023
Accepted
07 Jun 2023
First published
07 Jun 2023

Phys. Chem. Chem. Phys., 2023,25, 17385-17396

Planar π-extended all-armchair edge topological cycloparaphenylenes

N. Li and M. Sun, Phys. Chem. Chem. Phys., 2023, 25, 17385 DOI: 10.1039/D3CP00299C

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