2H-Benzotriazole, 5,6-difluoro-2-(2-hexyldecyl)-4,7-bis[5-(trimethylstannyl)-2-thienyl]-
98%
- Product Code: 94032
CAS:
2365391-00-8
| Molecular Weight: | 869.39 g./mol | Molecular Formula: | C₃₆H₅₅F₂N₃S₂Sn₂ |
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| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily used in the development of advanced organic electronic materials, particularly in the field of organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). Its unique structure, incorporating fluorine and thienyl groups, enhances the efficiency of charge transport and light absorption in these devices. The compound is often employed as a key component in the active layer of OPVs, where it contributes to improved energy conversion efficiency by optimizing the morphology and electronic properties of the blend. In OLEDs, it serves as an electron transport material, facilitating better device performance and stability. Additionally, its trimethylstannyl groups make it a valuable intermediate in cross-coupling reactions, enabling the synthesis of complex conjugated polymers and small molecules for high-performance optoelectronic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿7,272.00 |
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2H-Benzotriazole, 5,6-difluoro-2-(2-hexyldecyl)-4,7-bis[5-(trimethylstannyl)-2-thienyl]-
This chemical is primarily used in the development of advanced organic electronic materials, particularly in the field of organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). Its unique structure, incorporating fluorine and thienyl groups, enhances the efficiency of charge transport and light absorption in these devices. The compound is often employed as a key component in the active layer of OPVs, where it contributes to improved energy conversion efficiency by optimizing the morphology and electronic properties of the blend. In OLEDs, it serves as an electron transport material, facilitating better device performance and stability. Additionally, its trimethylstannyl groups make it a valuable intermediate in cross-coupling reactions, enabling the synthesis of complex conjugated polymers and small molecules for high-performance optoelectronic applications.
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