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Fluorinated [6]- and [9]cycloparaphenylene (CPP) derivatives, 8F-[6]CPP and 12F-[9]CPP, were synthesized based on the previous synthesis of the parent CPPs. While the reductive aromatization conditions used in the final step of the synthesis of the parent CPPs did not work for the fluorinated compounds, the use of PBr3 and SnCl2 in acetonitrile successfully accomplished the desired transformation. The structures of F-CPPs were determined by single-crystal X-ray analysis. Photo- and electrochemical analyses and host–guest chemistry revealed the effects of the introduction of fluorine atoms.

In this work, we achieved the triplet-energy control of polycyclic aromatic hydrocarbons (PAHs) by replacing the Carbon−Carbon (CC) unit with a Boron−Nitrogen (BN) unit. Time-dependent density functional theory calculations suggested that the insertion of the BN unit may cause localization of the singly occupied molecular orbitals 1 and 2 (SOMO1/SOMO2) in the triplet state, which in turn can reduce the exchange interaction and dramatically increase the high singlet–triplet excitation energy (ET). The PAH containing the BN unit, 4b-aza-12b-boradibenzo[g,p]chrysene, showed a large ET value and ambipolar carrier-transport abilities. The introduction of a phenyl substituent on 4b-aza-12b-boradibenzo[g,p]chrysene slightly reduced the ET values and the carrier-transport abilities, but increased the glass-transition temperatures. On the basis of these findings, we successfully built phosphorescent organic light-emitting diodes using the BN compounds as host materials, which exhibit a superior performance over th...

The triplet-energy control of polycyclic aromatic hydrocarbons (PAHs) was achieved by heteroatom incorporation. For instance, 4b-aza-12b-boradibenzo[g,p]chrysene showed a much larger ET value than the corresponding PAH, dibenzo[g,p]chrysene, and enable us to built phosphorescent organic light-emitting diodes (PHOLEDs) of high performance. We have also synthesized a variety of heteroatom-incorporated polycyclic aromatics with a large ET value, which improved not only efficiency of PHOLED but also lifetime.

The tandem phospha-Friedel-Crafts reaction transforms dichloro(m-teraryl)phosphine to the corresponding triarylphosphine derivatives containing curved π-conjugated frameworks with a phosphorus ring junction. The rigid molecular frameworks enable these unprecedented phosphine compounds to hold an extended π-conjugation spread over the whole molecule.

A P-fused double helicene consisting of a highly distorted benzene ring, with a bending angle of 23°, has been synthesized by a tandem intramolecular phospha-Friedel-Crafts reaction. Despite the distortion and reduced aromaticity, the double helicene shows thermal and chemical stability. These are important features that make these compounds attractive for applications as a new C2-symmetric bisphosphine ligand. The simple strategy proposed in this work can be used to prepare a diverse range of distorted molecules.

Combinations of N-heterocyclic carbenes (NHCs) and fluoride salts of the iron-group metals (Fe, Co, and Ni) have been shown to be excellent catalysts for the cross-coupling reactions of aryl Grignard reagents (Ar(1)MgBr) with aryl and heteroaryl halides (Ar(2)X) to give unsymmetrical biaryls (Ar(1)-Ar(2)). Iron fluorides in combination with SIPr, a saturated NHC ligand, catalyze the biaryl cross-coupling between various aryl chlorides and aryl Grignard reagents in high yield and high selectivity. On the other hand, cobalt and nickel fluorides in combination with IPr, an unsaturated NHC ligand, exhibit interesting complementary reactivity in the coupling of aryl bromides or iodides; in contrast, with these substrates the iron catalysts show a lower selectivity. The formation of homocoupling byproducts is suppressed markedly to less than 5% in most cases by choosing the appropriate metal fluoride/NHC combination. The present catalyst combinations offer several synthetic advantages over existing methods: practical synthesis of a broad range of unsymmetrical biaryls without the use of palladium catalysts and phosphine ligands. On the basis of stoichiometric control experiments and theoretical studies, the origin of the unique catalytic effect of the fluoride counterion can be ascribed to the formation of a higher-valent heteroleptic metalate [Ar(1)MF(2)]MgBr as the key intermediate in our proposed catalytic cycle. First, stoichiometric control experiments revealed the stark differences in chemical reactivity between the metal fluorides and metal chlorides. Second, DFT calculations indicate that the initial reduction of di- or trivalent metal fluoride in the wake of transmetalation with PhMgCl is energetically unfavorable and that formation of a divalent heteroleptic metalate complex, [PhMF(2)]MgCl (M = Fe, Co, Ni), is dominant in the metal fluoride system. The heteroleptic ate-complex serves as a key reactive intermediate, which undergoes oxidative addition with PhCl and releases the biaryl cross-coupling product Ph-Ph with reasonable energy barriers. The present cross-coupling reaction catalyzed by iron-group metal fluorides and an NHC ligand provides a highly selective and practical method for the synthesis of unsymmetrical biaryls as well as the opportunity to gain new mechanistic insights into the metal-catalyzed cross-coupling reactions.

Azaboradibenzo[6]helicene, a new semiconductor material possessing helical chirality, has been synthesized via a tandem bora-Friedel–Crafts-type reaction. Unprecedented carrier inversion between the racemate (displaying p-type semiconductivity) and the single enantiomer (displaying n-type semiconductivity) was observed and can be explained by changes in the molecular packing induced by helical homochirality.

A tandem intramolecular electrophilic arene borylation reaction has been developed for the synthesis of BN-fused polycyclic aromatic compounds such as 4b-aza-12b-boradibenzo[g,p]chrysene (A) and 8b,11b-diaza-19b,22b-diborahexabenzo[a,c,fg,j,l,op]tetracene. These compounds adopt a twisted conformation, which results in a tight and offset face-to-face stacking array in the solid state. Time-resolved microwave conductivity measurements prove that the intrinsic hole mobility of A is comparable to that of rubrene, one of the most commonly used organic semiconductors, indicating that BN-substituted PAHs are potential candidates for organic electronic materials.

m-Teraryl iodides are subjected to lithium—halogen exchange with subsequent trapping with PCl3 and tandem phospha-Friedel—Crafts reaction to afford the heptacyclic phosphine sulfudes (II).