Kang, Jisu team published research in Chemical Engineering Journal (Amsterdam, Netherlands) in 2022 | 12112-67-3

HPLC of Formula: 12112-67-3, Bis(1,5-cyclooctadiene)diiridium(I) is a useful research compound. Its molecular formula is C16H24Cl2Ir2-2 and its molecular weight is 671.7 g/mol. The purity is usually 95%.
Bis(1,5-cyclooctadiene)diiridium(I) Dichloride is a catalyst used in the iridium-catalyzed asymmetry hydrogenation of unfunctionalized exocyclic double carbon bonds. Also, it is used to test new NeoPHOX ligands derived from serine or threonine.
Bis(1,5-cyclooctadiene)diiridium(I) dichloride is an acid that can be prepared using a preparative method. It is an organometallic compound that can be used in the cross-coupling of activated terminal alkynes with aryl halides. Bis(1,5-cyclooctadiene)diiridium(I) dichloride has been synthesized by reacting furfural with chloride and acetonitrile. The ligand used was 2,2′-bipyridine. The reaction time to produce bis(1,5-cyclooctadiene)diiridium(I) dichloride is approximately three hours.
, 12112-67-3.

Chlorinated organic compounds are found in nearly every class of biomolecules. 12112-67-3, formula is C16H24Cl2Ir2, Name is Chloro(1,5-cyclooctadiene)iridium(I) dimer. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. HPLC of Formula: 12112-67-3.

Kang, Jisu;Zaen, Rena;Lee, Ji Hye;Hwang, Hyonseok;Park, Ki-Min;Kim, Seung Chan;Lee, Jun Yeob;Kang, Youngjin research published ã€?Effect of ancillary ligand on the photoluminescent and electroluminescent properties of blue Ir(III) complexes bearing main bipyridine ligandã€? the research content is summarized as follows. Homoleptic and heteroleptic cyclometalated blue iridium(III) complexes, namely, 1 and 2, incorporating 2â€?6â€?dimethoxy-5-trimethylsilyl-2,3â€?bipyridine (OMe2py-TMSpy) as the main ligand and acetylacetonate (acac) as the ancillary ligand, are developed for the comparison of their structure, photophys. properties, and electroluminescent characteristics. Both 1 and 2 exhibit distorted octahedral geometries around the iridium center, and the aspect ratios are 1.0 for 1 and 0.76 for 2, resp. The interat. contacts involving hydrogen bond interactions (H···N/O) in 1 are greater than those in 2, based on Hirshfeld surface anal. TD-DFT calculations reveal that the electronic transition for 1 may be attributed to intra-ligand charge transfer (ILCT, πbpy-π*bpy) mixed with metal-to-ligand charge transfer (MLCT, Ird-π*bpy), while for 2, it is attributed to the combination of ILCT/MLCT and addnl. ligand-to-ligand charge transfer (LLCT, πacac-π*bpy). Owing to the introduction of the ancillary ligand, the emission of complex 2 is red-shifted by only 6 nm compared to complex 1. However, the photoluminescent quantum efficiency of 2 is higher than that of 1 owing to the high radiative decay rate. Furthermore, phosphorescent organic light-emitting diodes (PhOLEDs) based on 2 achieve a high external quantum efficiency of 26.7%, which is one of the highest performances observed among reported blue PhOLEDs.

HPLC of Formula: 12112-67-3, Bis(1,5-cyclooctadiene)diiridium(I) is a useful research compound. Its molecular formula is C16H24Cl2Ir2-2 and its molecular weight is 671.7 g/mol. The purity is usually 95%.
Bis(1,5-cyclooctadiene)diiridium(I) Dichloride is a catalyst used in the iridium-catalyzed asymmetry hydrogenation of unfunctionalized exocyclic double carbon bonds. Also, it is used to test new NeoPHOX ligands derived from serine or threonine.
Bis(1,5-cyclooctadiene)diiridium(I) dichloride is an acid that can be prepared using a preparative method. It is an organometallic compound that can be used in the cross-coupling of activated terminal alkynes with aryl halides. Bis(1,5-cyclooctadiene)diiridium(I) dichloride has been synthesized by reacting furfural with chloride and acetonitrile. The ligand used was 2,2′-bipyridine. The reaction time to produce bis(1,5-cyclooctadiene)diiridium(I) dichloride is approximately three hours.
, 12112-67-3.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics