2,2'-(9,9-bis(6-bromohexyl)-9H-fluorene-2,7-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
≥95%
- Product Code: 40450
CAS:
851775-62-7
| Molecular Weight: | 744.25226 g./mol | Molecular Formula: | C₃₇H₅₄B₂Br₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 736.5±50.0℃(Predicted) | |
| Density: | 1.25±0.1g/ml(Predicted) | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in the field of organic electronics, particularly in the synthesis of conjugated polymers. It serves as a key monomer in the preparation of organic semiconductors, which are essential components in organic light-emitting diodes (OLEDs) and organic photovoltaic (OPV) devices. The presence of the boronate ester groups enables efficient cross-coupling reactions, such as Suzuki-Miyaura coupling, facilitating the construction of extended π-conjugated systems. These systems are crucial for achieving desirable electronic properties, including charge transport and light absorption/emission. Additionally, the bromohexyl side chains enhance solubility and processability, making it easier to fabricate thin films for device applications. Its role in advancing flexible and lightweight electronic materials underscores its importance in modern technology.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white powder |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $292.36 |
+
-
|
| 1.000 | 10-20 days | $723.02 |
+
-
|
2,2'-(9,9-bis(6-bromohexyl)-9H-fluorene-2,7-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
This chemical is primarily utilized in the field of organic electronics, particularly in the synthesis of conjugated polymers. It serves as a key monomer in the preparation of organic semiconductors, which are essential components in organic light-emitting diodes (OLEDs) and organic photovoltaic (OPV) devices. The presence of the boronate ester groups enables efficient cross-coupling reactions, such as Suzuki-Miyaura coupling, facilitating the construction of extended π-conjugated systems. These systems are crucial for achieving desirable electronic properties, including charge transport and light absorption/emission. Additionally, the bromohexyl side chains enhance solubility and processability, making it easier to fabricate thin films for device applications. Its role in advancing flexible and lightweight electronic materials underscores its importance in modern technology.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
$0.00
$0.00
Total :