171820-18-1Relevant articles and documents
Efficient Suzuki-Miyaura mono-arylation of symmetrical diiodo(hetero)arenes
Sapegin, Alexander,Krasavin, Mikhail
supporting information, p. 1948 - 1951 (2018/04/16)
A reliable protocol for converting 1,4-diiodo-2,3,5,6-tetrafluorobenzene into 1-(hetero)aryl-4-iodo-2,3,5,6-tetrafluorobenzene derivatives has been lacking in the literature. We have identified optimal conditions to achieve this conversion in good yields and have minimized formation of the bis-coupling product. The newly identified protocol involving the use of a syringe pump has been extended to other symmetrical diiodo(hetero)arenes.
Aryl 5-substitution of a phenyl-pyridine based ligand as a viable way to influence the opto-electronic properties of bis-cyclometalated Ir(iii) heteroleptic complexes
Grisorio, Roberto,Suranna, Gian Paolo,Mastrorilli, Piero,Mazzeo, Marco,Colella, Silvia,Carallo, Sonia,Gigli, Giuseppe
, p. 8939 - 8950 (2013/07/27)
This manuscript reports on the synthesis, the photophysical study and the electroluminescent properties of a series of heteroleptic cyclometalated iridium(iii) complexes based on 2,5-diaryl-pyridines as C^N cyclometalating ligands and acetylacetonate as ancillary ligand. The complexes were characterised by elemental analysis, ESI-MS, multinuclear NMR, TGA and electrochemistry. Their optical properties were investigated by UV-Vis and photoluminescence. DFT and TD-DFT calculations provided further insights into the effects of the 5-aryl substitution on the electronic and photophysical properties of the new complexes. The presence of suitable π-extended ligands exerts a beneficial effect on the performances of the corresponding solution-processed light-emitting diodes, leading to a maximum brightness of 10620 cd m-2 at a current efficiency of 10.0 cd A-1.