Oxidative aromatic coupling occupies a fundamental place in the modern chemistry of
aromatic compounds. It is a method of choice for the assembly of large and bewildering …

Die oxidative aromatische Kupplung nimmt einen grundlegenden Platz in der modernen
Arenchemie ein. Sie ist das Mittel der Wahl für den Aufbau großer, komplizierter …

Lateral furan‐expansion of polycyclic aromatics, which enables multiple O‐doping and
peripheral edge evolution of rylenes, is developed for the first time. Tetrafuranylperylene …

The π-magnetism of finite-sized nanoribbons occurring on the topological molecular
interfaces remains largely unexplored due to limited experimental examples. Herein, we …

Polycyclic aromatic hydrocarbons (PAHs) with a one‐dimensional (1D), ribbon‐like structure
have the potential to serve as both model compounds for corresponding graphene …

Conspectus Polycyclic (hetero) aromatic hydrocarbons (PAHs) have emerged as a focal
point in current interdisciplinary research, spanning the realms of chemistry, physics, and …

Via regioselective Ir-catalyzed C–H borylation and subsequent reactions (ie, viaBr4-Per or
(BF3K) 4-Per intermediates), we have introduced strong π-donors and acceptors at the 2, 5 …

We report an air-stable tetraradicaloid based on a rarely explored perylenequinonoid (PQ)
core, namely, tetrabenzo-annulated tetracyclopenta [b, e, k, n] perylene (TBCP), which has a …

The stable radical cation of large aromatic hydrocarbons remains a challenge, due to the
recessive aromatic character and high reactivity. Here we report the design, synthesis, and …

Two novel multiple B← N Lewis pair functionalized perylenes are reported. While OBN-Pery
shows a centrosymmetric and planar architecture, PBN-Pery displays an axisymmetric and …