3,9-Dibromo-5,11-dioctyl-5,11-dihydroindolo[3,2-b]carbazole
95%
- Product Code: 167392
CAS:
951307-27-0
| Molecular Weight: | 638.52 g./mol | Molecular Formula: | C₃₄H₄₂Br₂N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26743588 | |
| Melting Point: | Boiling Point: | 708.4±60.0 °C(Predicted) | |
| Density: | 1.32±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, seal, dry, light-proof |
Product Description:
Used as a high-performance organic semiconductor in organic field-effect transistors (OFETs) and organic photovoltaic (OPV) devices due to its excellent charge carrier mobility and thermal stability. Its planar molecular structure and strong intermolecular interactions enhance π-π stacking, improving electron delocalization and device efficiency. Commonly employed as a donor material in bulk heterojunction solar cells, where it contributes to higher power conversion efficiencies. Also explored in perovskite solar cells as a hole-transport layer owing to its suitable energy level alignment and film-forming properties. Its bromine substituents allow for further functionalization via cross-coupling reactions, enabling tailored modifications for specific electronic applications.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | ฿10,120.00 |
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| 250mg | 10-20 days | ฿29,100.00 |
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| 100mg | 10-20 days | ฿17,120.00 |
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3,9-Dibromo-5,11-dioctyl-5,11-dihydroindolo[3,2-b]carbazole
Used as a high-performance organic semiconductor in organic field-effect transistors (OFETs) and organic photovoltaic (OPV) devices due to its excellent charge carrier mobility and thermal stability. Its planar molecular structure and strong intermolecular interactions enhance π-π stacking, improving electron delocalization and device efficiency. Commonly employed as a donor material in bulk heterojunction solar cells, where it contributes to higher power conversion efficiencies. Also explored in perovskite solar cells as a hole-transport layer owing to its suitable energy level alignment and film-forming properties. Its bromine substituents allow for further functionalization via cross-coupling reactions, enabling tailored modifications for specific electronic applications.
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