We describe the first coronoid nanographene C216-molecule. As an extended polycyclic aromatic hydrocarbon containing a defined cavity, our molecule can be seen as a model system to study the influence of holes on the physical and chemical properties of graphene. Along the pathway of an eight-step synthesis including Yamamoto-type cyclization followed by 6-fold Diels-Alder cycloaddition, C216 was obtained by oxidative cyclodehydrogenation in the final step. The defined molecular structure with a cavity was unambiguously validated by MALDI-TOF mass spectrometry and FTIR, Raman, and UV-vis absorption spectroscopy coupled with DFT simulations.
We have studied the Raman spectra of C 78 H 26 , a polycyclic aromatic hydrocarbon with D 2h symmetry point group resembling a longitudinally confined graphene ribbon (or a graphene island) with armchair edge. The experimental spectra recorded with several excitation laser lines have been compared with the results from a theoretical analysis of the resonant Raman response based on density functional theory calculations. Compared to previous investigation the spectra show better signal-to-noise ratio, which allows determining previously unresolved weak spectroscopic features. We have extended our analysis to the overtone and combination region (i.e. above 2000 cm À1 ) demonstrating the presence of signals attributable to 2G, G + D, 2D, D j + D k and G + acoustic-like modes. Moreover, we have measured the temperature dependence of the G peak position, which turns out to show a similar behavior with respect to that of graphene/graphite.
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. The optical properties of the modified HBC were investigated by UV/visible absorption spectroscopy.
Graphene nanoribbons (GNRs) with an unprecedented "necklace-like" structure were synthesized through a bottom-up chemical approach, based on the oxidative cyclodehydrogenation of tailor-made polyphenylene precursors. A polycyclic aromatic hydrocarbon consisting of 84 sp(2) carbons (C84) was also synthesized and characterized as a model compound. Characterizations by a combination of MALDI-TOF MS and FTIR, Raman, and UV/Vis absorption spectroscopy validated the formation of the necklace-like GNRs. The absorption spectrum and DFT calculations revealed a bandgap of approximately 1.4 eV for this novel GNR system, which has not been attained with other GNR structures, enabling further fine-tuning of GNR bandgaps by structural modulation.
The molecular structure and vibrational properties of perchlorinated HBC and the parent HBC have been investigated by density functional theory calculations and vibrational spectroscopy.
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