2,2'-((2,6-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[1,2-b:4,5-b']dithiophene-4,8-diyl)bis(thiophene-5,2-diyl))bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane
97%
- Product Code: 59851
CAS:
1942110-76-0
| Molecular Weight: | 858.38 g./mol | Molecular Formula: | C₄₂H₅₄B₄O₈S₄ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the development of organic electronic materials, particularly in the synthesis of conjugated polymers and small molecules for organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). Its structure, featuring multiple dioxaborolane groups, makes it a valuable monomer for polymerization reactions, enabling the creation of materials with tailored electronic properties. The compound is often employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to construct π-conjugated systems with high charge carrier mobility. These systems are essential for efficient energy conversion and light emission in next-generation electronic devices. Additionally, its use in organic semiconductors contributes to advancements in flexible and lightweight electronics, offering potential applications in wearable technology and renewable energy solutions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $644.16 |
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2,2'-((2,6-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[1,2-b:4,5-b']dithiophene-4,8-diyl)bis(thiophene-5,2-diyl))bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily utilized in the development of organic electronic materials, particularly in the synthesis of conjugated polymers and small molecules for organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). Its structure, featuring multiple dioxaborolane groups, makes it a valuable monomer for polymerization reactions, enabling the creation of materials with tailored electronic properties. The compound is often employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to construct π-conjugated systems with high charge carrier mobility. These systems are essential for efficient energy conversion and light emission in next-generation electronic devices. Additionally, its use in organic semiconductors contributes to advancements in flexible and lightweight electronics, offering potential applications in wearable technology and renewable energy solutions.
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