ABSTRACT
The synthesis of cycloarenes in solution is challenging because of their low solubility and the often hindered cyclodehydrogenation reaction of their nonplanar precursors. Using an alternative on-surface synthesis protocol, we achieved an unprecedented double-stranded hexagonal cycloarene containing 108 sp2 carbon atoms. Its synthesis is based on hierarchical Ullmann coupling and cyclodehydrogenation of a specially designed precursor on a Au(111) surface. The structure and other properties of the cycloarene are investigated by scanning tunneling microscopy/spectroscopy, atomic force microscopy, and density functional theory calculations.
ABSTRACT
Control over the competition between an organometallic hexamer macrocycle and oligomer chains formed from the non-alternant aromatic 1,3-dibromoazulene (DBAz) precursor has been achieved in surface-assisted synthesis on a copper(111) surface. In contrast to kinetic reaction control via the high-dilution principle, the ring formation is achieved here by thermodynamic control, which is based on two-dimensional (2D) confinement and reversible bonds.