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CAS RN: 110134-47-9 | Product Number: P2513
Poly(3-hexylthiophene-2,5-diyl) (regioregular) [for organic electronics]
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Purity:
Synonyms:
- P3HT (regioregular)
Product Documents:
| Size | Unit Price | Saitama (Kawaguchi) | Hyogo (Amagasaki) | Stock in other WH |
Shipping Information
|
|---|---|---|---|---|---|
| 100MG |
¥16,800
|
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| 500MG |
¥58,800
|
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* The displayed price is the unit price and does not include consumption tax. The unit prices displayed are the latest and are subject to change without notice.
* To send your quote request for bulk quantities, please click on the "Request Bulk Quote" button. Please note that we cannot offer bulk quantities for some products.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
| Product Number | P2513 |
| Physical State (20 deg.C) | Solid |
Storage Temperature 
|
Room Temperature (Recommended in a cool and dark place, <15°C) |
| Condition to Avoid | Light Sensitive |
| CAS RN | 110134-47-9 |
| Related CAS RN
|
156074-98-5&104934-50-1&125321-66-6 |
| Reaxys Registry Number | 8828732 |
Specifications
| Hole Mobility(mu FET) | min 0.10cm2/Vs (OTS Si/SiO2 substrate) |
| Palladium | max. 100 ppm |
| Molecular weight of number average | 27000 to 45000 |
| Stereoregularity | min. 99.0 % |
| NMR | confirm to structure |
Properties (reference)
| HOMO Level | -4.8 eV |
GHS
Related Laws:
Transport Information:
Application
High-Regioregular P3HT-Based Transistor Realizing Hole Mobility of Over 20 cm2/Vs
References
- Electric-double-layer field-effect transistors with ionic liquids
- High-Performance Organic Field-Effect Transistors Gated by Imidazolium-Based Ionic Liquids
Application
Highly Regioselective Organic Semiconducting Polymer: P3HT
P3HT was synthesized by a direct arylation polymerization (DArP)1,2) and features a highly regioselective structure with a consistent average molecular weight and polydispersity index. In addition, P3HT is useful for solution process-able organic solar cells,3,4) perovskite solar cells,5) and organic transistor research,6) due in part to its high solubility.
Figure 1. Organic Photovoltaics (OPV)
Figure 2. Perovskite Solar Cell (PSC)
Figure 3. Organic Transistor (OFET)
This material was produced by collaboration with Prof. Fumiyuki Ozawa
at Institute for Chemical Research, Kyoto University.
References
- 1)Palladium-catalyzed dehydrohalogenative polycondensation of 2-bromo-3-hexylthiophene: An efficient approach to head-to-tail poly(3-hexylthiophene)
- 2)Structural analysis of poly(3-hexylthiophene) prepared via direct heteroarylation polymerization
- 3)A review of recent plasmonic nanoparticles incorporated P3HT: PCBM Organic thin film solar cells
- 4)Poly(3-hexylthiophene): Synthetic methodologies and properties in bulk heterojunction solar cells
- 5)Hole-transport materials for perovskite solar cells
- 6)25th Anniversary article: Organic field-effect transistors: The path beyond amorphous silicon
Documents
Product Articles
[TCIMAIL No.176] Highly Regioselective Organic Semiconducting Polymer: P3HT[Product Highlights] High-Regioregular P3HT-Based Transistor Realizing Hole Mobility of Over 20 cm2/Vs
[Product Highlights] High Regioregular p-type Organic Semiconducting Polymer
[Organic Transistor] Performance evaluation of highly regioregular “P3HT”
[Organic Transistor] Fabrication and Evaluation of Organic Field-Effect Transistors (OFETs) : P3HT
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