2-(4-nitrophenyl)-3,4,3',4'-bis(ethylenedioxy)-5,2'-bithiophene
- Product Code: 216071
CAS:
1350699-14-7
| Molecular Weight: | 403.436 g./mol | Molecular Formula: | C₁₈H₁₃NO₆S₂ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its extended π-conjugated system enhances charge carrier mobility, making it valuable for high-performance semiconductor materials. The electron-withdrawing nitro group improves electron affinity, which aids in n-type semiconductor behavior. It is also employed in the development of donor-acceptor type copolymers to tune bandgap and improve light absorption in solar cells. Due to its solubility and stability, it supports solution-processing techniques like spin coating and inkjet printing for flexible electronics.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿25,650.00 |
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2-(4-nitrophenyl)-3,4,3',4'-bis(ethylenedioxy)-5,2'-bithiophene
Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its extended π-conjugated system enhances charge carrier mobility, making it valuable for high-performance semiconductor materials. The electron-withdrawing nitro group improves electron affinity, which aids in n-type semiconductor behavior. It is also employed in the development of donor-acceptor type copolymers to tune bandgap and improve light absorption in solar cells. Due to its solubility and stability, it supports solution-processing techniques like spin coating and inkjet printing for flexible electronics.
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