Richter M, Schellhammer KS, Machata P, Cuniberti G, Popov A, Ortmann F, Berger R, Muellen K, Feng X (2017)
Publication Type: Journal article
Publication year: 2017
Book Volume: 4
Pages Range: 847-852
Journal Issue: 5
DOI: 10.1039/c7qo00180k
By the combination of 9a-azaphenalene and a perpendicularly oriented acene, we have synthesized three derivatives of a series of novel, fully-conjugated nitrogen-containing polycyclic aromatic hydrocarbons (PAHs), namely [7,8]naphtho[2′,3′:1,2]indolizino[6,5,4,3-def]phenanthridine, with an acetylene triisopropylsilyl (TIPS), phenyl or benzothiophenyl substituent. Their optoelectronic properties were studied via UV-Vis-NIR absorption, fluorescence spectroscopy and cyclic voltammetry. In addition, in situ spectroelectrochemistry was performed to investigate the optical and magnetic properties of the mono-radical cation and anion by quasi-reversible oxidation and reduction of 11-(tert-butyl)-5,17-bis((triisopropylsilyl)ethynyl)[7,8]naphtho[2′,3′:1,2]indolizino[6,5,4,3-def]phenanthridine (1a). Theoretical modelling confirmed the predominately closed-shell electronic ground state with a weak diradical character depending on the geometry.
APA:
Richter, M., Schellhammer, K.S., Machata, P., Cuniberti, G., Popov, A., Ortmann, F.,... Feng, X. (2017). Polycyclic heteroaromatic hydrocarbons containing a benzoisoindole core. Organic Chemistry Frontiers, 4(5), 847-852. https://doi.org/10.1039/c7qo00180k
MLA:
Richter, Marcus, et al. "Polycyclic heteroaromatic hydrocarbons containing a benzoisoindole core." Organic Chemistry Frontiers 4.5 (2017): 847-852.
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