ABSTRACT
Sulfur-containing compounds, particularly derivatives of thiophene, are well studied for organic optoelectronic applications. Incorporating selenium or tellurium in place of sulfur imparts different physical properties due to the fundamental differences of these atoms relative to their lighter analogues. This has a profound influence on the properties of molecules and materials that incorporate chalcogens that may ultimately lead to new opportunities and applications. This mini-review will focus on the quantitative and qualitative photophysical characteristics of organic materials containing selenium and tellurium as well as their emerging applications as molecular photoactive species, including light-emitting sensors, triplet sensitizers, and beyond.
ABSTRACT
The monoanion of dihydrogenated corannulene isolated in the form of its potassium salt, namely tris(diglyme-κ(3)O,O',O'')potassium hexacyclo[11.5.2.0(4,17).0(7,16).0(10,15).0(14,18)]icosa-1,3,5,7(16),8,10(15),11,13,17-nonaenide, [K(C6H14O3)3](C20H12), has been structurally characterized for the first time. The X-ray study confirms the previous NMR spectroscopic prediction that the two H atoms are attached to the same six-membered ring to form 1,2-dihydrocorannulene, thus destroying the aromaticity of only one arene ring of the corannulene core. The direct comparison of (C20H12)(-) with the parent corannulene anion, (C20H10)(-), is provided to illustrate the geometry perturbations caused by rim hydrogenation.