Extension of oxygen-embedded polycyclic aromatic hydrocarbons (PAHs), in particular with a defined topology, is synthetically challenging primarily because of limited regio-specific methods and poor solubility of PAHs. We reported herein an efficient way to construct quinoidal pentacenes and nonacenes with regular zigzag O-inserted edges. These O-embedded backbones composed of benzene, pyranyl, and cyclohexa-1,4-diene moieties provided access to a new class of longitudinally conjugated acenes with superior stability. Their structures, confirmed by single-crystal XRD analysis, indicated that they possessed rich hydrogen/halogen-bonding interactions, which likely contribute to the strengthened aggregation. In contrast to many other O-annulated PAHs generally displaying short-absorption wavelengths due to partially interrupted electron communication, the O-embedded quinoidal acene exhibited highly red-shifted absorptions (up to ∼699 nm) and narrowed energy gaps (down to ∼1.5 eV). As with more O-containing rings and quinoidal subunits in the backbone, the conjugation size was enlarged, and the molar absorption coefficients (ε) of the λmax significantly increased further, in particular, a noticeable lower-energy peak at ∼790 nm for O-doping nonacenes N1-OH/OMe. By the thin-film-based organic field-effect transistor measurements, the relatively ordered O-doping pentacene P1-OMe possessed a hole transporting efficiency (μh) of 0.00406 cm–2 V–1 s–1 in in-air fabricated devices, while O-pentacene P1-PFB with two perfluorobutoxyl substituents witnessed an improved μh up to 0.0152 cm–2 V–1 s–1. In addition, one- or two-electron oxidation of O-pentacene/nonacene generated the corresponding radical cations or dications, in which electronic properties were dependent on the number of O-containing six-membered rings and quinoidal subunits. The study provided insights into the relationships between molecule structures and optoelectronic properties for the unique class of O-embedded PAHs.

AC u II -based metal-organic framework (MOF; 1), constructed withi midazole carboxylate ligands( 5-(1 H-imidazol-1-yl)isophthalic acid) and copper(II) ions was prepared and characterizedi nd etail by XRD, Brunauer-Emmett-Teller (BET), thermogravimetric analysis( TGA), and IR methods. Its catalytic performance for the directh ydroxylation of benzene to phenol has been investigated. Abenzene conversion of 29 %a sw ell as ah igh phenol selectivity above 95 %h as been obtained at 60 8Ci nw ater.T he cycling tests showed no significant decreasea fter five runs, indicatingg ood stability and reuse properties of the Cu II -based MOF (1). The effect of addingt he hydroxyl radicals cavenger,t hiourea,a nd the ESR spectra of the catalytic system have confirmed the existence of hydroxyl radicals, which indicates the catalytic mechanism follows aF enton-type route. This economically and environmentally friendly approachw ith Cu II -basedM OFs is expected to find applications in the hydroxylation of aromatics.

9-Ethynylfluorenyl radical derivatives were readily prepared in situ and underwent simultaneous intermolecular coupling reactions. Interestingly, the dimerization process took place in either a head-to-tail or a head-to-head mode between the acetylenic or the allenic resonance forms dependent on the terminal substituents, which could be well explained by their different spin distribution and steric hindrance effects. The structures of the products were confirmed by X-ray crystallographic and other spectroscopic analyses. It was also found that the newly generated dipropinyl dimers underwent a rearrangement and ring-cyclization reaction at room temperature, eventually giving unique difluorenylidene cyclobutene derivatives.

Open-shell diradicaloids have been intensively investigated recently due to their attractive and unique optical, electronic and magnetic properties. However, open-shell diradicaloids with non-planar conjugated frameworks are less studied, especially helical-shaped π systems. In this work, we synthesized tetraindeno-based singlet biradicals in a helical geometry, bridged by a curved cyclobutenyl o-quinodimethane molecule. Large diradical characters and extremely small singlet-triplet energy gaps, as well as unusual half-field transitions (forbidden ΔMs = 2) were revealed for these 3D diradicals.

C 3 symmetric hexa-peri-hexabenzocoronene carboxylic acid assembles into a rigid 2D honeycomb network at a solid–liquid interface.

Pentaarylated cyclopentcyclodienes have aggregation-induced emission (AIE) characteristics and can be easily derivatized, but are rarely studied. In order to examine the effect of the electronic properties and the position of the substituents on AIE properties, an expedient method for the synthesis of a series of pentaarylated cyclopentadiene derivatives was developed, and their UV-Vis, fluorescence spectra, fluorescence quantum yields as well as the XRD structures of single crystals were investigated. The AIE properties of pentaarylated cyclopentadiene derivatives were studied in detail.

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