[4,8-Bis[5-(dodecylthio)-2-thienyl]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl]bis[1,1,1-trimethylstannane]
98%
- Product Code: 93988
Alias:
1,1′-[4,8-Bis[5-(dodecylthio)-2-thienyl]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl]bis[1,1,1-trimethylstannane]
CAS:
1887135-97-8
| Molecular Weight: | 1080.91 g./mol | Molecular Formula: | C₄₈H₇₄S₆Sn₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 901.4℃ | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, sealed, dry, protected from light |
Product Description:
This chemical is primarily utilized in the field of organic electronics, particularly in the development of advanced materials for organic solar cells. Its structure is designed to enhance the efficiency of light absorption and charge transport, making it a valuable component in the active layer of photovoltaic devices. The compound's unique arrangement of thiophene and benzo[1,2-b:4,5-b′]dithiophene units, combined with the dodecylthio side chains, contributes to improved solubility and film-forming properties, which are crucial for the fabrication of thin-film solar cells. Additionally, the trimethylstannane groups facilitate cross-coupling reactions during the synthesis of conjugated polymers, enabling the creation of materials with tailored electronic properties. This chemical plays a significant role in advancing the performance and stability of next-generation organic photovoltaic systems.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | $466.78 |
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[4,8-Bis[5-(dodecylthio)-2-thienyl]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl]bis[1,1,1-trimethylstannane]
This chemical is primarily utilized in the field of organic electronics, particularly in the development of advanced materials for organic solar cells. Its structure is designed to enhance the efficiency of light absorption and charge transport, making it a valuable component in the active layer of photovoltaic devices. The compound's unique arrangement of thiophene and benzo[1,2-b:4,5-b′]dithiophene units, combined with the dodecylthio side chains, contributes to improved solubility and film-forming properties, which are crucial for the fabrication of thin-film solar cells. Additionally, the trimethylstannane groups facilitate cross-coupling reactions during the synthesis of conjugated polymers, enabling the creation of materials with tailored electronic properties. This chemical plays a significant role in advancing the performance and stability of next-generation organic photovoltaic systems.
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