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RESEARCH PRODUCT

Do the Intramolecular π Interactions Improve the Stability of Ionic, Pyridine-Carbene-Based Iridium(III) Complexes?

Joan CanoRubén CasillasRubén D. Costa

subject

ChemistryLigandStackingchemistry.chemical_elementIonic bondingPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergyIntramolecular forcePolymer chemistryPyridineIridiumPhysical and Theoretical ChemistryCarbeneDiimine

description

Throughout the last years one of the most intensive research topics in light-emitting electrochemical cells (LECs) focused on the design of blue-emitting, ionic iridium(III) complexes. To this end, the most recent strategy is the use of carbene-based ancillary ligands. Although blue LECs have been successfully fabricated, the stability has been noted as the main drawback. To overcome this problem, Zhang et al. have recently explored the use of π interactions to enhance the strength of pyridine-carbene-based complexes. The authors suggested that the use of intramolecular π–π stacking interactions by means of pendant phenyl rings to improve the stability of LECs is not as effective as in devices with diimine-based complexes. To interpret this phenomenon clearly, the features of a family of pyridine-carbene-based iridium(III) complexes, in which phenyl groups are sequentially attached to the carbene and the pyridine rings of the ancillary ligand, have been thoroughly studied by using a theoretical approach. ...

https://doi.org/10.1021/jp401380b