Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Customising excitation properties of polycyclic aromatic hydrocarbons by rational positional heteroatom doping: the peri-xanthenoxanthene (PXX) case

Valentini, Cataldo, Gowland, Duncan, Bezzu, C. Grazia, Romito, Deborah, Demitri, Nicola, Bonini, Nicola and Bonifazi, Davide ORCID: https://orcid.org/0000-0001-5717-0121 2022. Customising excitation properties of polycyclic aromatic hydrocarbons by rational positional heteroatom doping: the peri-xanthenoxanthene (PXX) case. Chemical Science 13 (21) , pp. 6335-6347. 10.1039/D2SC01038K

[thumbnail of d2sc01038k.pdf] PDF - Published Version
Available under License Creative Commons Attribution Non-commercial.

Download (2MB)

Abstract

In this paper we tackle the challenge of gaining control of the photophysical properties of PAHs through a site-specific N-doping within the structural aromatic framework. By developing a simple predictive tool that identifies C(sp2)-positions that if substituted with a heteroatom would tailor the changes in the absorption and emission spectral envelopes, we predict optimal substitutional patterns for the model peri-xanthenoxanthene (PXX) PAH. Specifically, TDDFT calculations of the electron density difference between the S1 excited state and S0 ground state of PXX allowed us to identify the subtleties in the role of sites i.e., electron donating or withdrawing character on excitation. The replacement of two C(sp2)-atoms with two N-atoms, in either electron donating or withdrawing positions, shifts the electronic transitions either to low or high energy, respectively. This consequently shifts the PXX absorption spectral envelop bathochromically or hypsochromically, as demonstrated by steady-state absorption spectroscopic measurements. Within the series of synthesised N-doped PXX, we tune the optical band gap within an interval of ∼0.4 eV, in full agreement with the theoretical predictions. Relatedly, measurements show the more blueshifted the absorption/emission energies, the greater the fluorescence quantum yield value (from ∼45% to ∼75%). On the other hand, electrochemical investigations suggested that the N-pattern has a limited influence on the redox properties. Lastly, depending on the N-pattern, different supramolecular organisations could be obtained at the solid-state, with the 1,7-pattern PXX molecule forming multi-layered, graphene-like, supramolecular sheets through a combination of weak H-bonding and π–π stacking interactions. Supramolecular striped patterned sheets could also be formed with the 3,9- and 4,10-congeners when co-crystallized with a halogen-bond donor molecule.

Item Type: Article
Date Type: Published Online
Status: Published
Schools: Chemistry
Additional Information: Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)
Publisher: Royal Society of Chemistry
ISSN: 2041-6520
Date of First Compliant Deposit: 4 July 2022
Date of Acceptance: 27 April 2022
Last Modified: 10 Nov 2022 11:33
URI: https://orca.cardiff.ac.uk/id/eprint/150967

Actions (repository staff only)

Edit Item Edit Item

Downloads

Downloads per month over past year

View more statistics