Introduction：Basic information about Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine) CAS 220797-16-0, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine) Basic informationClassification Applications
| Product Name: | Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine) |
| Synonyms: | Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine);TFB AldrichCPR;s-TFB,Poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-(4,4’-(N-(4-sec-butyl- phenyl)diphenylamine);P-200 Poly(9,9-dioctylfluorene-co-N-(4-(1-methylpropyl)phenyl)diphenylamine);Polyimino]-1,4-phenylene(9,9-dioctyl-9H-fluorene-2,7-diyl)-1,4-phenylene];4-(sec-Butyl)-N-(4-(9,9-dioctyl-7-phenyl-9H-fluoren-2-yl)phenyl)aniline(poly);Poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-(4,4'-(N-(4-sec-butylphenyl) diphenylamine)];N-(4-(sec-butyl)phenyl)-N-(4-(9,9-dioctyl-7-phenyl-9H-fluoren-2-yl)phenyl)-[1,1'-biphenyl]-4-amine |
| CAS: | 220797-16-0 |
| MF: | C51H63N |
| MW: | 690.05262 |
| EINECS: | |
| Product Categories: | |
| Mol File: | 220797-16-0.mol |
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Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine) Chemical Properties
| Melting point | 166.2℃ |
| form | powder |
| color | yellow |
| InChIKey | RBFSUOVKQODUII-UHFFFAOYSA-N |
| SMILES | N(C1=CC=C(C(CC)C)C=C1)C1=CC=C(C2C=CC3C4=C(C(CCCCCCCC)(CCCCCCCC)C=3C=2)C=C(C2=CC=CC=C2)C=C4)C=C1 |
| Solvent | THF, Toluene and Chloroform |
| Absorption | λmax?390 nm (in THF) |
Safety Information
| Storage Class | 13 - Non Combustible Solids |
Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine) Usage And Synthesis
| Classification | Hole transport material (HTL), Hole injection material (HIL), Electron blocking material (EBL), OLEDs, Perovskite solar cells, Organic and printed electronics. |
| Applications | Poly(9,9-dioctylfluorene-alt-N-(4-sec-butylphenyl)-diphenylamine) (TFB) is a triarylamine based semiconductor with a band gap of 3 eV (HOMO and LUMO levels of 5.3 and 2.3 eV, respectively) and a relatively high hole mobility of 2 ×10-3 cm2 V-1 s-1.
Due to its low ionisation potential and high hole mobility, TFB serves primarily as hole transport layer (HTL), hole-injection layer (HIL) and electron-blocking layer (EBL) material in organic electronic devices. When built into device as an interface material, TFB as an electron blocking layer will not only reduce the chance of electron leakage, but also reduce the possibility of exciton quenching between the interface of the active layer and charge transport layer (F8BT/MoOx for example). |
| Description | Poly(9,9-dioctylfluorene-alt-N-(4-sec-butylphenyl)-diphenylamine) (TFB) is a triarylamine based semiconductor with a band gap of 3 eV (HOMO and LUMO levels of 5.3 and 2.3 eV, respectively) and a relatively high hole mobility of 2 ×10-3 cm2 V-1 s-1. |
| Uses | TFB can be used in the formation of multilayer quantum dot-based light-emitting diodes (LEDs). It can also be used in the fabrication of highly responsive gas sensors for breath analysis. |
| Uses | TFB can be used for a variety of optoelectronic applications such as organic light emitting diodes (OLEDs), quantum dot displays (QDs) and solar cells. |
| General Description | TFB, a hole transporting material and an electron-blocking layer, has high hole mobility, low electron affinity, and high ionic potential. Its electron blocking nature results in effective confinement of injected charge carriers in the perovskite layers. |
| References | [1] Hwang, Jaehyung and A. Kahn. “Interface energetics of polyfluorene and fluorene-arylamine copolymers.” SPIE Optics + Photonics 5 1 (2006): 0.
[2] Yajun Xia, R. Friend. “Polymer bilayer structure via inkjet printing.” Applied Physics Letters 88 1 (2006): 163508.
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Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine) Preparation Products And Raw materials
