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C6(C6H5)4C5H4(C13H7(C6H13)2)N is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

908350-82-3

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908350-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 908350-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,3,5 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 908350-82:
(8*9)+(7*0)+(6*8)+(5*3)+(4*5)+(3*0)+(2*8)+(1*2)=173
173 % 10 = 3
So 908350-82-3 is a valid CAS Registry Number.

908350-82-3Downstream Products

908350-82-3Relevant academic research and scientific papers

High-efficiency solution processable electrophosphorescent iridium complexes bearing polyphenylphenyl dendron ligands

Huang, Chun,Zhen, Chang-Gua,Su, Siew Ping,Chen, Zhi-Kuan,Liu, Xiao,Zou, De-Chun,Shi, Yan-Rong,Loh, Kian Ping

experimental part, p. 1317 - 1324 (2009/09/06)

We report the synthesis and electrophosphorescent behavior of a series of novel iridium complex materials (Complexes A-F), which are composed of ligands bearing polyphenylphenyl dendron groups and acetylacetonate. Yellow to saturated red organic light-emitting diodes (OLEDs) based on these newly developed Ir complexes were fabricated through solution process by doping the complex materials into polyvinyl carbazole (PVK)/2-(4-biphenylyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole (PBD) matrices. The emission wavelengths of the materials could be effectively tuned from 549 nm to 640 nm by changing the conjugation of the ligands either through incorporating additional aromatic segment (e.g. phenyl or fluorenyl group) onto the basic dendron ligand or fusing two of the phenyl rings on the polyphenylphenyl dendron group. High performance devices with the configuration of ITO/poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) (PEDOT:PSS) (50 nm)/PVK:PBD (40%):Ir complex (6%) (70 nm)/2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) (12 nm)/Alq3 (20 nm)/Mg:Ag (150 nm) have been demonstrated. For example, when Complex B was used as the emissive layer, maximum current efficiency of 34.0 cd/A and external quantum efficiency of 10.3% have been achieved. When 1,3,5-tris(N-phenylbenzimidazol-2-yl) benzene (TPBI) was used as the block layer, the efficiencies can be further improved to 46.3 cd/A and 13.9%, respectively. These solution processed OLED devices demonstrated quite stable EL efficiencies over a large range of current density, which indicated that triplet-triplet annihilation in electrophosphorescence could be effectively suppressed by incorporation of the polyphenylphenyl dendron structure into iridium complexes.

SOLUTION PROCESSED ORGANOMETALLIC COMPLEXES AND THEIR USE IN ELECTROLUMINESCENT DEVICES

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Page/Page column 31-32, (2008/06/13)

The invention provides phosphorescent organometallic complexes. The complexes of the invention may be prepared as films further comprising a charge carrying host material may be used at an emissive layer in organic light emitting devices. In one embodiment, the complex is a hyper-branched organoiridium complex comprising a 2-phenylpuridine ligand wherein the phenyl ring or the pyridine ring contains 4 non-hydrogen substituents. In another embodiment, the complex is an organoiridium complex comprising a substituted 2-phenyl pyridine ligand, wherein at least one substituent contains a spiro group.

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