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 |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| 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 | ฿26,640.00 |
+
-
|
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.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :