B-N-B Bond Embedded Phenalenyl and Its Anions.

Despite the great potential of heteroatom-containing polycyclic aromatic hydrocarbons in organic optoelectronics, there are very limited reports on heteroaromatics containing a B-N-B bond in the π-scaffold. Herein, stable 1,9-dibora-9a-azaphenalenyl (DBAP) derivatives, named BNB-embedded phenalenyls, are presented. The DBAP skeleton contains a three-center two-π-electron B-N-B moiety with 12 π-electrons and can be regarded as the isoelectronic structure of the phenalenyl cation. Chemical reduction of the phenyl derivative of DBAP by potassium generated the dianion containing 14 delocalized π-electrons, which can be regarded as the isoelectronic structure of the phenalenyl anion. The dianion is sandwiched and stabilized by two bulky [K([18]crown-6)]+ counterions according to its X-ray structure. However, its monoanion (an isoelectronic structure of the henalenyl radical) generated by mixing equal moles of neutral compound and dianion gave an unusual B-N-B-embedded benzo[cd]fluoranthene dianion, which again was confirmed by X-ray crystallographic analysis. The new dianion containing 20 π-electrons is highly aromatic and is further stabilized by [K([18]crown-6)]+ counterions. An aromaticity driven rearrangement mechanism was proposed for this unusual transformation. Based on X-ray structures and theoretical calculations, the B-N-B moiety in the neutral and anionic DBAP participates in the π-electron delocalization along the whole DBAP skeleton like their phenalenyl cation/radical/anion counterparts, but with more localized character. Therefore, our studies report the first synthesis and characterization of a B-N-B-embedded phenalenyl and its anionic species, which show unique electronic structure and unusual reactivity different from that of their all-carbon phenalenyl analogues.