There are three possible isomers for hexa--hexabenzocoronene (HBC) with two extra K-regions, but only two of them have been reported, namely with the - and -configurations. Herein, we describe the synthesis of HBC with two extra K-regions in the -configuration, forming a longer zigzag edge compared with the other two isomers. The structure of was validated by laser desorption/ionization time-of-flight mass analysis and nuclear magnetic resonance spectra, as well as Raman and infrared spectroscopies supported by density functional theory calculations. The optical properties of were investigated by UV/vis absorption and ultrafast transient absorption spectroscopy. Together with the analysis of aromaticity, the influence of the zigzag edge on the π-conjugation pathway and HOMO-LUMO gaps of the three isomers were investigated.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163021 | PMC |
http://dx.doi.org/10.1039/d0sc04649c | DOI Listing |
J Am Chem Soc
April 2016
Max Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.
A multistep synthesis of hexa-peri-hexabenzocoronene (HBC) with four additional K-regions was developed through a precursor based on two benzotetraphene units bridged with p-phenylene, featuring preinstalled zigzag moieties. Characterization by laser desorption/ionization time-of-flight mass spectrometry, Raman and IR spectroscopy, and scanning tunneling microscopy unambiguously validated the successful formation of this novel zigzag edge-rich HBC derivative. STM imaging of its monolayers revealed large-area, defect-free adlayers.
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