Ir(pq)2acac

Base Information

Chemical Name:Ir(pq)2acac
CAS No.:337526-95-1
Molecular Formula:C35H27IrN2O2
Molecular Weight:701.83400
Hs Code.:

Synonyms:bis(2-phenylquinolyl-N,C(2'))iridium (acetylacetonate);(bt)2Ir(acac);Ir(2-phenylquinoline)2(acetylacetone);[Ir(2-phenylquinoline(1-))(acetylacetonate)];Ir(pq)2acac;PQ2Ir(acac);[Ir(pq)2(acac)];

Suppliers and Price of Ir(pq)2acac

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Sigma-Aldrich
(2,4-Pentanedionato)bis[2-(2-quinolinyl)phenyl]iridium(III) 98%
250mg
$ 211.00

Total 6 raw suppliers

Chemical Property of Ir(pq)2acac

Chemical Property:

Melting Point:306.1-314.5°C
PSA：41.90000
LogP:6.26690
Storage Temp.:?20°C

Purity/Quality:

98% ^*data from raw suppliers

(2,4-Pentanedionato)bis[2-(2-quinolinyl)phenyl]iridium(III) 98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Ir(pq)2acac may be used in the fabrication of phosphorescence polymer light emitting diodes (PhPLEDs).

Technology Process of Ir(pq)2acac

There total 8 articles about Ir(pq)2acac which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

: tetrakis(2-phenylquinoline-C2,N')(μ-dichloro)diiridium(III)

: 123-54-6,81235-32-7
acetylacetone

: 337526-95-1,1173886-71-9
bis(2-phenylquinoline)(acetylacetonate)iridium(III)

Guidance literature:: With sodum carbonate; In further solvent(s); ((pq)2IrCl)2, 2,4-pentanedione, and Na2CO3 were refluxed under inert gasatm. in 2-ethoxyethanol for 12-15 h; mixt. was cooled to room temp., ppt. was filtered off. washed with water, Et2O, and hexane, chromy. on silica using CH2Cl2 as eluent; elem. anal.;
DOI:10.1021/ic0008969