Chloride substituents modify the physical properties of organic compounds in several ways. 12112-67-3, formula is C16H24Cl2Ir2, Name is Chloro(1,5-cyclooctadiene)iridium(I) dimer. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. Recommanded Product: Chloro(1,5-cyclooctadiene)iridium(I) dimer.
Hu, Fang;Zhang, Hua;Chu, Yunpeng;Hui, Xin-Ping research published ã?Efficient enantioselective synthesis of pyrazolines and isoxazolines enabled by an iridium-catalyzed intramolecular allylic substitution reactionã? the research content is summarized as follows. An efficient Ir-catalyzed enantioselective intramol. allylic substitution reaction of 2-tosylhydrazono or hydroxyimino carbonates for the synthesis of five-, six- and seven-membered heterocycles containing N-N and N-O bonds I [R1 = Ph, 3-MeC6H4, 2-thienyl, etc,; X = NTs, O; n = 1,2,3] was achieved.
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.
, Recommanded Product: Chloro(1,5-cyclooctadiene)iridium(I) dimer
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics