Azaacene Diradicals Based on Non-Kekulé Meta- Quinodimethane

03 April 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Non-Kekulé quinoidal azaacences m-A (1a,b) were synthesized and compared to their para- and ortho-quinodimethane analogues. m-A display high diradical characters (1b: y0 = 0.88) due to their meta-quinodimethane (m-QDM) topology. Electron paramagnetic (EPR), nuclear magnetic resonance (NMR) spectroscopies and supraquantum interference device (SQUID) measurements in combination with quantum-chemical calculations revealed singlet ground states for m-A with singlet-triplet gaps ΔEST (0.13-0.25 kcal mol-1) and thermally populated triplet states. These non-Kekulé structures are void of zwitterionic character and possess record high two-photon absorption cross sections over a broad spectral range in the near-infrared.

Keywords

aromaticity
azaacene
Clar sextets
non-Kekulé diradical
regioisomerism
two-photon absorption

Supplementary materials

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Description
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Supporting Information
Description
Experimental procedures, material characterization data and details regarding quantum chemical calculations.
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