Two superaromatic terpyridine ligands (1 and 2) incorporating a corannulene unit at the 4'-position are reported. The optical and metal sensing properties of both ligands were investigated by the naked eye, and UV-vis and fluorescence spectroscopy in this work. In 1, the corannulene motif is directly connected to the 4'-phenylterpyridine domain, while in 2, the corannulene motif and the 4'-phen...

The gas-phase infrared spectra of radical cationic and protonated corannulene were recorded by infrared multiple-photon dissociation (IRMPD) spectroscopy using the IR free electron laser for infrared experiments. Electrospray ionization was used to generate protonated corannulene and an IRMPD spectrum was recorded in a Fourier-transform ion cyclotron resonance mass spectrometer monitoring H-los...

A phase transition between two-dimensional polymorphs of the buckybowl corannulene on a Cu(111) surface can be suppressed by spatial confinement, allowing stabilisation of the metastable polymorph over the stable one.

The first ferrocene-fused organometallic compounds derived from the buckybowl sumanene (C21H12) are presented. Both compounds, sumanenylferrocene and 1,1'-disumanenylferrocene, have been synthesized by Negishi-type cross-coupling of iodosumanene and were studied crystallographically. Sumanenylferrocenes form unique packing motifs, which are both different from those of their corannulene congene...

The on-surface synthesis of corannulene-based non-planar nanographenes was studied with the aid bond-resolving scanning tunneling microscopy.

Key words polycyclic aromatic hydrocarbons - corannulenes dibenzobistetracene

The smallest and most strained member of a family of π-conjugated cyclic porphyrin oligomers was synthesized by using pentapyridyl templates based on ferrocene and corannulene. Both templates are effective for directing the synthesis of the butadiyne-linked cyclic pentamer, despite the fact that the radii of their N5 donor sets are too small by 0.5 Å and 0.9 Å, respectively (from DFT calculatio...