Abstract In this work we report the synthesis, structure, and electronic properties of carbon‐rich compounds dehydrobiphenyleno[12]annulenes (DBP[12]As) comprising antiaromatic four‐membered rings (4MR) and 12‐membered ring (12MR). Ultraviolet–visible absorption spectra and electrochemical behaviors of DBP[12]As confirmed their relatively narrow highest occupied molecular orbital (HOMO)–lowest unoccupied molecular orbital (LUMO) gap values and high HOMO energy levels, which were supported by density functional theory simulations. Parent DBP[12]A adopts a slipped herringbone structure in a crystalline state, with the molecules forming 1D stacks via π–π interactions. The experimentally derived bond lengths, bonding analyses using the Wiberg bond indices, and localized orbital locator calculation support a stronger double bond character for the 12MR bonds than the 4MR bonds in the inner six‐membered ring. The chemical shifts of hydrogens in1H NMR spectra, as well as magnetically induced ring current analyses using quantum chemical calculations, indicate that the 4MRs have stronger antiaromatic character than the 12MR. The present information is useful for a fundamental understanding of carbon‐rich compounds with different antiaromatic units as well as designing novel molecules with unique electronic properties.
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Towards a taxonomy of topology for polynuclear aromatic hydrocarbons: linking electronic and molecular structure
Trends linking the topological characteristics of polynuclear aromatic hydrocarbons (PAH) to their electronic properties are reported. TD-DFT electronic spectra computations, using the 6-31G* basis set and B3LYP exchange correlation functional, were calculated for a series of PAH, allowing for the HOMO–LUMO gaps to be reported. Clar structures provide an avenue to link the physical structure and the aromaticity of the molecule; which, when extended by bond length and harmonic oscillator model of aromaticity analysis, provide powerful tools to understand the link between electronic and physical structure. These results lead to the conclusion that all PAH structures show a decrease in HOMO–LUMO gap as a function of size, but the rate of that decrease is directly related to the topology of the molecules. A PAH taxonomy was developed that categorizes PAH into categories with similar topological properties, which allows for modelling of changes in the HOMO–LUMO gap with PAH size. An atom-pair minimization algorithm was used to calculate the binding energy (BE) of homogeneous dimers of the studied PAH. The BE per carbon atom increases with the overall size of the structure to an asymptotic limit, but as with the HOMO–LUMO gap, topology plays a critical secondary factor. Previously published, experimentally determined optical band gaps (OBG) from Tauc/Davis–Mott analysis of extinction spectra in various laminar, non-premixed flames produced a correlation between the HOMO–LUMO gaps of high-symmetry, nearly circular D 2h symmetry molecules to molecular size. The work presented here provides a much more nuanced and predictive evaluation of how OBG depends on structure and size.
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- Award ID(s):
- 1706757
- PAR ID:
- 10075459
- Date Published:
- Journal Name:
- Phys. Chem. Chem. Phys.
- Volume:
- 19
- Issue:
- 41
- ISSN:
- 1463-9076
- Page Range / eLocation ID:
- 28458 to 28469
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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