5,6-Difluoro-4,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazole
97%
- Product Code: 48016
CAS:
1295502-63-4
| Molecular Weight: | 424.0780 g./mol | Molecular Formula: | C₁₈H₂₄B₂F₂N₂O₄S |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic electronics, particularly in the synthesis of conjugated polymers and small molecules for optoelectronic devices. Its structure, featuring boronate ester groups, makes it a valuable building block in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing π-conjugated systems. These systems are integral to the development of organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The difluoro substitution on the benzothiadiazole core enhances electron affinity and improves charge transport properties, making it suitable for high-performance electronic materials. Additionally, its incorporation into donor-acceptor copolymers can fine-tune bandgaps and optimize light absorption/emission characteristics, contributing to advancements in energy-efficient displays and renewable energy technologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £202.13 |
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5,6-Difluoro-4,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazole
This compound is primarily utilized in the field of organic electronics, particularly in the synthesis of conjugated polymers and small molecules for optoelectronic devices. Its structure, featuring boronate ester groups, makes it a valuable building block in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing π-conjugated systems. These systems are integral to the development of organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The difluoro substitution on the benzothiadiazole core enhances electron affinity and improves charge transport properties, making it suitable for high-performance electronic materials. Additionally, its incorporation into donor-acceptor copolymers can fine-tune bandgaps and optimize light absorption/emission characteristics, contributing to advancements in energy-efficient displays and renewable energy technologies.
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