A hemicurcuminoid boron difluoride complex is used as an emitter in organic light-emitting diodes, showing far red/near-infrared electroluminescence with an external quantum efficiency as high as 2.1%. This dye blended in CBP thin films shows amplified spontaneous emission with a threshold of 22 μJ cm⁻² at 750 nm, making this compound attractive for organic semiconductor lasers operating in the near-infrared region.

Most commercially available CO detectors are based upon metal oxides or electrochemical cell technologies. None of these approaches use the selective adsorption of CO gas on a molecular complex. Conversely, cobalt(III) corroles can bind small gaseous molecules allowing them for an application as sensing components for gas detectors. Here we describe the ability of cobalt corroles to selectively coordinate carbon monoxide vs. dinitrogen and dioxygen. The coordination properties were determined in the solid state and the adsorption characteristics were compared to those of the reference compound (To-PivPP)Fe(1,2-Me₂Im), known for its remarkable CO binding properties. The adsorption data evidence that the selectivity, affinity and capacity of the cobalt(III) corroles for CO are larger than those of the porphyrin complex. However, from a chemical point of view, the selectivity of cobalt(III) corroles for CO vs. O₂ is infinite since these derivatives do not bind O₂ while (To-PivPP)Fe(1,2-Me₂Im) does with an M value (P_1/2 ^O₂/P_1/2 ^CO) equal to 51. In this manuscript we also show that the affinity of cobalt(III) corroles for CO is closely related to the Lewis acid character of the central cobalt(III) ion and therefore to the nature of the substituents at the periphery of the corrole macroring.