Benzo[1'',2'':4,54'',5'':4',5']bissilolo[3,2-b:3',2'-b']dithiophene, 4,4,9,9-tetrahexyl-4,9-dihydro-2,7-bis(trimethylstannyl)-
98%
- Product Code: 59869
CAS:
1569453-45-7
| Molecular Weight: | 960.79 g./mol | Molecular Formula: | C₄₄H₇₄S₂Si₂Sn₂ |
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| Density: | Storage Condition: | room temperature |
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 well-suited for use as a building block in the synthesis of conjugated polymers, which are critical for efficient light absorption and charge transport in photovoltaic devices. The presence of trimethylstannyl groups facilitates cross-coupling reactions, enabling the creation of high-performance donor-acceptor copolymers. These copolymers are essential for enhancing the power conversion efficiency of organic solar cells, making it a valuable component in renewable energy research. Additionally, its tetrahexyl side chains contribute to improved solubility and processability, which are crucial for solution-based fabrication techniques.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,338.02 |
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Benzo[1'',2'':4,54'',5'':4',5']bissilolo[3,2-b:3',2'-b']dithiophene, 4,4,9,9-tetrahexyl-4,9-dihydro-2,7-bis(trimethylstannyl)-
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 well-suited for use as a building block in the synthesis of conjugated polymers, which are critical for efficient light absorption and charge transport in photovoltaic devices. The presence of trimethylstannyl groups facilitates cross-coupling reactions, enabling the creation of high-performance donor-acceptor copolymers. These copolymers are essential for enhancing the power conversion efficiency of organic solar cells, making it a valuable component in renewable energy research. Additionally, its tetrahexyl side chains contribute to improved solubility and processability, which are crucial for solution-based fabrication techniques.
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