4,7-Bis(5-bromo-4-hexylthiophen-2-yl)benzo[c][1,2,5]selenadiazole
98%
- Product Code: 59931
CAS:
1256447-82-1
| Molecular Weight: | 673.4299999999999 g./mol | Molecular Formula: | C₂₆H₃₀Br₂N₂S₂Se |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 642.4±65.0 °C(Predicted) | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in the development of organic electronic materials, particularly in the field of organic photovoltaics (OPVs). Its structure, featuring conjugated systems and electron-deficient selenadiazole units, makes it an excellent candidate for use as an electron acceptor in bulk heterojunction solar cells. The material helps improve the efficiency of light absorption and charge transport within the device, contributing to enhanced power conversion efficiency. Additionally, its incorporation into polymer blends or small-molecule systems can optimize the morphology of the active layer, further boosting device performance. Its brominated thiophene units also allow for further chemical modifications, enabling fine-tuning of its electronic properties for specific applications in organic electronics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿22,050.00 |
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4,7-Bis(5-bromo-4-hexylthiophen-2-yl)benzo[c][1,2,5]selenadiazole
This compound is primarily used in the development of organic electronic materials, particularly in the field of organic photovoltaics (OPVs). Its structure, featuring conjugated systems and electron-deficient selenadiazole units, makes it an excellent candidate for use as an electron acceptor in bulk heterojunction solar cells. The material helps improve the efficiency of light absorption and charge transport within the device, contributing to enhanced power conversion efficiency. Additionally, its incorporation into polymer blends or small-molecule systems can optimize the morphology of the active layer, further boosting device performance. Its brominated thiophene units also allow for further chemical modifications, enabling fine-tuning of its electronic properties for specific applications in organic electronics.
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