2,6-Dibromo-4-n-octyldithieno[3,2-b:2',3'-d]pyrrole
94%
- Product Code: 174418
CAS:
1346688-54-7
Molecular Weight: | 449.26 g./mol | Molecular Formula: | C₁₆H₁₉Br₂NS₂ |
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Density: | Storage Condition: | Room temperature |
Product Description:
Used primarily in organic electronics, this compound serves as a key building block in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its extended π-conjugated structure enhances charge carrier mobility, making it valuable in high-performance semiconductor materials. The bromine functional groups allow for efficient coupling reactions, such as Stille or Suzuki, enabling polymerization with various electron-rich or electron-deficient comonomers. Additionally, the alkyl side chain improves solubility in organic solvents, facilitating solution processing for thin-film device fabrication. Its incorporation into donor-acceptor type polymers helps fine-tune energy levels and optical properties, contributing to improved device efficiency and stability.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.050 | 10-20 days | €112.38 |
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2,6-Dibromo-4-n-octyldithieno[3,2-b:2',3'-d]pyrrole
Used primarily in organic electronics, this compound serves as a key building block in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its extended π-conjugated structure enhances charge carrier mobility, making it valuable in high-performance semiconductor materials. The bromine functional groups allow for efficient coupling reactions, such as Stille or Suzuki, enabling polymerization with various electron-rich or electron-deficient comonomers. Additionally, the alkyl side chain improves solubility in organic solvents, facilitating solution processing for thin-film device fabrication. Its incorporation into donor-acceptor type polymers helps fine-tune energy levels and optical properties, contributing to improved device efficiency and stability.
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