There are three possible isomers for hexa-peri-hexabenzocoronene (HBC) with two extra K-regions, but only two of them have been reported, namely with the meta- and para-configurations. Herein, we describe the synthesis of HBC 4 with two extra K-regions in the ortho-configuration, forming a longer zigzag edge compared with the other two isomers. The structure of 4 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 4 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.
Hexa-peri-benzocoronene with two extra K-regions in an ortho-configuration / Dumslaff, T.; Gu, Y.; Paterno, G. M.; Qiu, Z.; Maghsoumi, A.; Tommasini, M.; Feng, X.; Scotognella, F.; Narita, A.; Mullen, K.. - In: CHEMICAL SCIENCE. - ISSN 2041-6520. - 11:47(2020), pp. 12816-12821. [10.1039/d0sc04649c]
Hexa-peri-benzocoronene with two extra K-regions in an ortho-configuration
Scotognella F.;
2020
Abstract
There are three possible isomers for hexa-peri-hexabenzocoronene (HBC) with two extra K-regions, but only two of them have been reported, namely with the meta- and para-configurations. Herein, we describe the synthesis of HBC 4 with two extra K-regions in the ortho-configuration, forming a longer zigzag edge compared with the other two isomers. The structure of 4 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 4 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.File | Dimensione | Formato | |
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https://hdl.handle.net/11583/2985602