CAS 104934-51-2 Poly(3-octylthiophene-2,5-diyl)

NAVIGATION

Poly(3-octylthiophene-2,5-diyl)

PRICE INQUIRY

Catalog Number

ACM104934512-8

CAS Number

104934-51-2

Product Name

Poly(3-octylthiophene-2,5-diyl)

Structure

Category

Bioelectronic Materials; Organic Field Effect Transistor (OFET) Materials; Organic Light-Emitting Diode (OLED) Materials; Organic Solar Cell (OPV) Materials

Synonyms

P3OT

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.

IUPAC Name

3-octylthiophene

Molecular Weight

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

Complexity

112

Covalently-Bonded Unit Count

Exact Mass

196.128572g/mol

Feature

Fluorescence: λex 442 nm; λem 562 nm in chloroform
Good processability, environmental stability and electroactivity.

Form

ITO/PEDOT:PSS/P3OT:PC61BM (1:2)/LiF/Al[10]• Short-circuit current density (Jsc): 5.55 mA/cm² • Open-circuit voltage (Voc): 0.5 V• Fill Factor (FF): 0.33• Power Conversion Efficiency (PCE): 0.91 %

Formal Charge

Heavy Atom Count

MDL Number

MFCD00241412

Monoisotopic Mass

196.128572g/mol

Packaging

1 g in glass bottle,Packaged in glass bottles

Rotatable Bond Count

Type

Polythiophene

XLogP3