| Catalog Number | ACM104934512 |
|---|---|
| Product Name | Poly(3-octylthiophene-2,5-diyl) |
| CAS Number | 104934-51-2 |
| Structure |  |
| Synonyms | P3OT |
| IUPAC Name | 3-octylthiophene |
| MW (10³) | average Mn ~34,000 |
| Molecular Formula | (C12H18S)n |
| Canonical SMILES | CCCCCCCCC1=CSC=C1 |
| InChI | InChI=1S/C12H20S/c1-2-3-4-5-6-7-8-12-9-10-13-11-12/h9-11H,2-8H2,1H3 |
| InChI Key | WQYWXQCOYRZFAV-UHFFFAOYSA-N |
| Melting Point | 190 °C |
| Solubility | chloroform, methylene chloride, toluene, and THF: soluble |
| Appearance | black |
| Application | P3OT forms a nanocomposite with carbon nanotubes (CNTs) for devising a high performance semiconducting material. It can also be used as a π-conjugating polymer for the fabrication of organic electronic based devices which include polymeric diodes, solar cells and photovoltaic modules. Rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, microelectrical amplifiers, field-effect transistors and non-linear optical materials. Rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, microelectrical amplifiers, field-effect transistors and non-linear optical materials. Poly (3-octylthiophene-2,5-diyl) (P3OT)-single walled carbon nanotubes composites were prepared., 3 Doped P3OT may be used in NO2 sensing applications. 2 For the characterization and solid-state properties of this polymer, see J. Am. Chem. Soc. . Used in organic field-effect transistors and in polymer-based solar cells. Conducting polymer. Rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, microelectrical amplifiers, field-effect transistors and non-linear optical materials. |
| Storage | room temp |
| Description | Greater than 98.5% head-to-tail regiospecific conformation. Poly(3-octylthiophene-2,5-diyl) (P3OT) is an alkylthiophene based conductive polymer with high electroluminescence, which is soluble in most of the organic solvents. It can be prepared by the electrochemical polymerization of 3-octylthiophene (3OT). It is hydrophobic and can be used as a transducer for ion selective electrodes. |
| Complexity | 112 |
| Covalently-Bonded Unit Count | 1 |
| Exact Mass | 196.128572g/mol |
| Formal Charge | 0 |
| Heavy Atom Count | 13 |
| Linear Formula | (C12H18S)n |
| Monoisotopic Mass | 196.128572g/mol |
| Type | Polythiophene |
| Rotatable Bond Count | 7 |
| XLogP3 | 6.1 |
| Catalog | Fluorescence | MW (10³) | Mn (10³) | Orbital Energy |
|---|---|---|---|---|
| ACM104934512A | λex 442 nm; λem 562 nm in chloroform | ~34 | ||
| ACM104934512B | ~25 | HOMO 5.25 eV LUMO 3.55 eV |
||
| ACM104934512C | λex 419 nm; λem 550 nm in chloroform | 36.6 | 22 |
※ Please kindly note that our products are for research use only.
Privacy Policy | Cookie Policy | Copyright © 2025 Alfa Chemistry. All rights reserved.
