5,6-Difluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole
99%
- Product Code: 94035
CAS:
1421762-30-2
Molecular Weight: | 662.023 g./mol | Molecular Formula: | C₂₀H₂₂F₂N₂S₃Sn₂ |
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EC Number: | MDL Number: | MFCD32856173 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, dark, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic electronics, particularly in the development of advanced materials for optoelectronic devices. Its structure, featuring thiophene and benzothiadiazole units, makes it highly suitable for applications in organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). The presence of trimethylstannyl groups facilitates efficient cross-coupling reactions, enabling precise tuning of the material's electronic properties. This chemical is often employed as a key building block in the synthesis of low-bandgap polymers, which are essential for enhancing the efficiency of solar cells by broadening the absorption spectrum. Additionally, its electron-deficient benzothiadiazole core contributes to improved charge transport characteristics, making it valuable in the design of high-performance organic semiconductors.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿3,627.00 |
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0.250 | 10-20 days | ฿6,237.00 |
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1.000 | 10-20 days | ฿16,362.00 |
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5,6-Difluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole
This compound is primarily utilized in the field of organic electronics, particularly in the development of advanced materials for optoelectronic devices. Its structure, featuring thiophene and benzothiadiazole units, makes it highly suitable for applications in organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). The presence of trimethylstannyl groups facilitates efficient cross-coupling reactions, enabling precise tuning of the material's electronic properties. This chemical is often employed as a key building block in the synthesis of low-bandgap polymers, which are essential for enhancing the efficiency of solar cells by broadening the absorption spectrum. Additionally, its electron-deficient benzothiadiazole core contributes to improved charge transport characteristics, making it valuable in the design of high-performance organic semiconductors.
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