OLED Material
CAS.1242056-42-3 HTL
9H-Fluoren-2-aMine, N-[1,1'-biphenyl]-4-yl-9,9-diMethyl-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]-
  
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| 9H-Fluoren-2-aMine, N-[1,1'-biphenyl]-4-yl-9,9-diMethyl-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]- Basic information | 
| Product Name: | 9H-Fluoren-2-aMine, N-[1,1'-biphenyl]-4-yl-9,9-diMethyl-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]- | 
| Synonyms: | 9H-Fluoren-2-aMine, N-[1,1'-biphenyl]-4-yl-9,9-diMethyl-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]-;N-[1,1'-Diphenyl]-4-yl-9,9-dimethyl-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]-9H-fluoren-2-amine;N-(biphenyl-4-yl)-9,9-dimethyl-N-(4-(9-phenyl-9H-carbazol-3-yl)phenyl)-9H-fiuoren-2-amine;9H-Fluoren-2-Amine,N-[1,1'-biphenyl]-4-yl-9,9-diMethyl-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl, 99.5%;Biphenyl-4-yl-(9,9-dimethyl-9H-fluoren-2-yl)-[4-(9-phenyl-8a,9-dihydro-4bH-carbazol-3-yl)-phenyl]-amine;N-(4-Biphenylyl)-9,9-dimethyl-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]-9H-fluoren-2-amine;N-[[1,1′-biphenyl]-3-yl]-9,9-dimethyl-N-[4-[9-phenyl-9H-carbazol-3-yl]phenyl]-9H-fluoren-2-amine;N-[1,1'-Diphenyl]-4-yl-9,9-dimethyl-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]-9H-fluorene-2-amine | 
| CAS: | 1242056-42-3 | 
| MF: | C51H38N2 | 
| MW: | 678.86 | 
| EINECS: | |
| Product Categories: | |
| Mol File: | 1242056-42-3.mol | 
| ![9H-Fluoren-2-aMine, N-[1,1'-biphenyl]-4-yl-9,9-diMethyl-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]- Structure](https://www.chemicalbook.com/CAS/GIF/1242056-42-3.gif) | |
| 9H-Fluoren-2-aMine, N-[1,1'-biphenyl]-4-yl-9,9-diMethyl-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]- Chemical Properties | 
| density | 1.14 | 
| storage temp. | Keep in dark place,Sealed in dry,Room Temperature | 
| form | powder | 
| pka | -2.80±0.40(Predicted) | 
| color | white to yellow | 
| Safety Information | 
| 9H-Fluoren-2-aMine, N-[1,1'-biphenyl]-4-yl-9,9-diMethyl-N-[4-(9-phenyl-9H-carbazol-3-yl)phenyl]- Usage And Synthesis | 
| Chemical Properties | Off-white powder | 
| Uses | N-([1,1μ-biphenyl]-4-yl)-9,9-dimethyl-N-(4-(9-phenyl-9H-carbazol-3-yl)phenyl)-9H-fluoren-2-amine (BCFN) is an electron-rich material, with the HOMO energy level of 5.3 eV, the LUMO energy level of 2.2 eV and high hole mobility of 5.43 * 10-5 cm2V-1s-1. As a result, it is used as a hole-transport and hole-injection material in organic light-emitting diodes. BCFN has shown its advantages in improving the hole mobility of polymer-based hole transport layer; lower driving voltage of device, better efficiency, and higher EQE due to exciplex formation by utilizing in EML; and better device lifetimes in the combination of Ir(piq)2(acac) to act as an electron scavenger layer for an reported device. BCFN is a good morphologically stable material with Tg of 125 °C and Td of 375 °C. With a ET of 2.58 eV, BCFN is also a very good charge transporting layer material due to its large band gap (Eg = 3.1 eV) 2 for green, red and white phosphorescent organic light-emitting diodes (PhOLEDs). OLED Device Performance: BCFN increase the hole transport mobility of PVK (pure PVK: 2.09*10-9 V cm-1 S-1; 30% of BCFN in PVK: 9.86*10-7 V cm-1 S-1; 50% of BCFN in PVK: 1.15*10-5 V cm-1 S-1): 1. ITO/PEDOT:PSS (40 nm)/PVK:BCFN (3:7, 20 nm)/BCFN:PFO (x:1-x, 80 nm)/CsF (1.5 nm)/Al (120 nm) Color: Blue BCFN in combination of ET1 to act as EML in forming exciplex and improve device performance: 2. ITO/HIL/HTL/(ET1+P1) or (ET1+BCFN+P1(doped)/ETL/ LiF/Al Color: red Device emission area of 81cm2, and at 1000 cd m-2, the efficiency exceeds 200 lm/W and the EQE exceeds 50 %. lifespan@95: from 71h to 133h BCFN in combination with Ir(piq)2(acac) as electron scavenger layer: 3. ITO/NDP series in BCFN (3wt.%, 10nm)/BCFN(160nm) or BCFN(130nm)+BCFN:Ir(piq)2(acac)(2wt.%, 10nm)+BCFN(20)/ [Ir(TMSBppy)ppy2]:BPTZBC (10 wt.%, 40nm))/ TPBi:Liq (1:1 wt. % ratio, 36nm)/ Liq (0.1nm)/Al (60 nm) Color: yellow Efficiencies are not affected. lifespan@95: from 71h to 133h', 'N-([1,1μ-Biphenyl]-4-yl)-9,9-dimethyl-N-(4-(9-phenyl-9H-carbazol-3-yl)phenyl)-9H-fluoren-2-amine can be used in different application areas as an emissive layer or hole transport layer due the presence of π-conjugated structure and electron-donating/accepting groups. It is suitable to be used in R&D studies such as organic field-effect transistors (OFETs), molecular electronics, sensors, organic photovoltaics (OPVs), and organic light-emitting diodes (OLEDs). | 
          
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