Polycyclic aromatic hydrocarbons consisting of three fused anthracene units were designed as new π‐conjugated compounds having helical structures. These expanded helicenes were synthesized by Pt‐catalyzed cycloisomerization of the corresponding ethynyl‐substituted precursors. The nonplanar and helical structure was confirmed by X‐ray analysis and DFT calculations, and the barrier to helical inversion was estimated to be 34 kJ mol−1. The enantiomers of the diphenyl derivative were successfully resolved by chiral HPLC. Enantiopure samples showed good chiroptical performance in the CD (|Δϵ| 1380 L mol−1cm−1) and CPL (|glum| 0.013) spectra, and these values were considerably large for simple organic molecules. The unique chiroptical properties are discussed on the basis of the molecular structure and the electronic state with the aid of time‐dependent DFT calculations.

Polycyclic aromatic compounds consisting of four or five fused anthracene units were synthesized by PtCl2‐catalyzed cycloisomerization as novel long expanded helicenes. These compounds have helical structures with significant stacking of the terminal anthracene moieties at 0.33 nm interlayer distance. In the UV‐vis and fluorescence spectra, the absorption and emission bands were red‐shifted as the number of fused anthracene units was increased. The characteristic broad and long‐lived emission bands of the long analogues are explained by the excimer‐like stabilization of the excited state. These photophysical data as well as their cyclic voltammetric data are discussed on the basis of the π‐conjugation and interlayer π⋅⋅⋅π interactions in the molecular structures and the molecular orbitals. The barrier and mechanism of helical inversion are also reported.

Invited for the cover of this issue is Shinji Toyota and co‐workers at Tokyo Institute of Technology and Okayama University of Science. The image depicts a spirally rising dragon to represent the helical molecular structures in the manuscript. Read the full text of the article at 10.1002/chem.202004720.

Oligomers consisting of 10-mesitylanthracene-1,8-diyl units were synthesized by Ni-mediated coupling of the corresponding dibromide as new oligoarene compounds. The structures and properties of these oligomers were investigated by NMR and electronic spectroscopy. Conformational analyses with the aid of DFT calculations revealed that each biaryl axis adopted a nearly perpendicular conformation, and the trimers and tetramers existed as a mixture of diastereomeric conformers.

One of the helical anthracenes, [4]HA in which two fused anthracene ends are spatially arranged upper and lower, exhibits a ratiometric fluorescence response due to the hydrostatic pressure-dependent intramolecular [4+4]...