1,6-Bis(5-(trimethylstannyl)thiophen-2-yl)hexane
98%
- Product Code: 94000
CAS:
1884354-21-5
| Molecular Weight: | 576.03 g./mol | Molecular Formula: | C₂₀H₃₄S₂Sn₂ |
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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 synthesis of conjugated polymers and small molecules. Its structure, featuring thiophene units linked by a hexane chain, makes it a valuable building block for creating materials with desirable electronic properties. It is often employed in the development of organic semiconductors, which are essential components in organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The trimethylstannyl groups facilitate cross-coupling reactions, such as Stille coupling, enabling the formation of extended π-conjugated systems. These systems are crucial for achieving high charge carrier mobility and efficient light absorption or emission in electronic devices. Additionally, its application in thin-film technologies allows for the fabrication of flexible and lightweight electronic components, contributing to advancements in wearable technology and renewable energy solutions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,700.00 |
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1,6-Bis(5-(trimethylstannyl)thiophen-2-yl)hexane
This chemical is primarily utilized in the field of organic electronics, particularly in the synthesis of conjugated polymers and small molecules. Its structure, featuring thiophene units linked by a hexane chain, makes it a valuable building block for creating materials with desirable electronic properties. It is often employed in the development of organic semiconductors, which are essential components in organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The trimethylstannyl groups facilitate cross-coupling reactions, such as Stille coupling, enabling the formation of extended π-conjugated systems. These systems are crucial for achieving high charge carrier mobility and efficient light absorption or emission in electronic devices. Additionally, its application in thin-film technologies allows for the fabrication of flexible and lightweight electronic components, contributing to advancements in wearable technology and renewable energy solutions.
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