Synthesis and Physical Properties of Polyfluorinated Cycloparaphenylenes.

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.

Shortest Double-Walled Carbon Nanotubes Composed of Cycloparaphenylenes.

Invited for this month's cover is the group of Prof. Dr. Shigeru Yamago at the Kyoto University (Japan). The image shows the host-guest possibilities of cycloparaphenylenes (CPPs) of different sizes. Size selective interaction between [n]CPP and [n+5]CPP affords a host-guest complex, [n+5]CPP⊃[n]CPP, which is the shortest double-walled armchair carbon nanotube. The size-selective complex formation illustrates the importance of van der Waals interactions. A ternary complex, [15]CPP⊃[10]CPP⊃C60 , also forms from [15]CPP, [10]CPP, and C60 . Read the full text of the article at 10.1002/cplu.201700097.

Shortest Double-Walled Carbon Nanotubes Composed of Cycloparaphenylenes.

The host-guest chemistry of cycloparaphenylenes (CPPs) of different sizes is described. [n]CPPs (n=5, 6, 7, 8, and 10) selectively interact with [n+5]CPPs, forming complexes [n+5]CPP⊃[n]CPP, which are the shortest double-walled armchair carbon nanotubes. The size selectivity is dictated by the difference in diameters of the CPPs (that is, 0.34-0.35 nm), which maximizes attractive van der Waals interactions. Theoretical calculations suggest that the orbital energies of the CPPs become perturbed upon complex formation, and orbital mixing between the two CPPs is predicted for large CPP pairs. The association constants in 1,1,2,2-[D2 ]tetrachloroethane, estimated by 1 H NMR titration, are approximately 103  mol L-1 at 50 °C. Van't Hoff plot analysis reveals that complexation is driven mainly by entropy owing to desolvation of the CPPs. [13]CPP also forms a complex with [4]cyclo-2,7-pyrenylene ([4]CPY), which is a π-extended [8]CPP. Theoretical calculations suggest that the formation of [13]CPP⊃[4]CPY is more exothermic than that of [13]CPP⊃[8]CPP. A ternary complex, [15]CPP⊃[10]CPP⊃C60 , is also formed by mixing [15]CPP and [10]CPP⊃C60 .

Construction of a highly distorted benzene ring in a double helicene.

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.

Azaboradibenzo[6]helicene: carrier inversion induced by helical homochirality.

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.

Synthesis of BN-fused polycyclic aromatics via tandem intramolecular electrophilic arene borylation.

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.

Tandem phospha-Friedel-Crafts reaction toward curved π-conjugated frameworks with a phosphorus ring junction.

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.

Highly selective biaryl cross-coupling reactions between aryl halides and aryl Grignard reagents: a new catalyst combination of N-heterocyclic carbenes and iron, cobalt, and nickel fluorides.

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.