9,9-Dihexylfluorene-2,7-diboronic acid bis(1,3-propanediol) ester
97%
- Product Code: 60419
CAS:
250597-29-6
| Molecular Weight: | 502.31 g./mol | Molecular Formula: | C₃₁H₄₄B₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 121-125 °C(lit.) | Boiling Point: | 662.1±48.0 °C |
| Density: | 1.07±0.1 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the field of organic electronics, particularly in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). It serves as a key intermediate in the synthesis of conjugated polymers, which are essential for creating efficient light-emitting and energy-harvesting devices. The boronic ester groups in the molecule facilitate Suzuki coupling reactions, enabling the formation of high-performance polymeric materials with tailored electronic properties. Its incorporation into polymer backbones enhances charge transport and stability, making it valuable for advanced optoelectronic applications. Additionally, its solubility in organic solvents simplifies processing during device fabrication.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿5,800.00 |
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9,9-Dihexylfluorene-2,7-diboronic acid bis(1,3-propanediol) ester
This chemical is primarily used in the field of organic electronics, particularly in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). It serves as a key intermediate in the synthesis of conjugated polymers, which are essential for creating efficient light-emitting and energy-harvesting devices. The boronic ester groups in the molecule facilitate Suzuki coupling reactions, enabling the formation of high-performance polymeric materials with tailored electronic properties. Its incorporation into polymer backbones enhances charge transport and stability, making it valuable for advanced optoelectronic applications. Additionally, its solubility in organic solvents simplifies processing during device fabrication.
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