495336
Poly(3-butylthiophene-2,5-diyl)
regioregular
Synonym(s):
P3BT
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Recommended Products
mol wt
Mw 54,000 (typical)
color
black
solubility
chlorinated solvents: soluble (partially soluble in THF, diethylether)
fluorescence
λex 440 nm; λem 567 nm in chloroform
Mw/Mn
2.3 (typical)
InChI
1S/C10H16S/c1-4-5-6-10-7-8(2)11-9(10)3/h7H,4-6H2,1-3H3
InChI key
DUOSBQJOYVIVOR-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
Conducting polymer, 80-90% head-to-tail regiospecific conformation.
Poly(3-butylthiophene-2,5-diyl) (P3BT) is an alkylthiophene based conducting polymer that can be used as a donor molecule in the development of organic electronics. It is a π-conjugating polymer with a π-π stacking distance of 0.395 nm.
Application
P3BT can act as a hole transporting layer (HTL) which can potentially be used in the fabrication of organic field effect transistors (OFETs), chemical sensors, rechargeable batteries and polymeric solar cells (PSCs).
Rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, microelectrical amplifiers, field-effect transistors and non-linear optical materials.
Packaging
Packaged in glass bottles
Citation
For solid state properties see J. Am. Chem. Soc. .
Legal Information
Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Effect of alkyl side-chain length and solvent on the luminescent characteristics of poly (3-n-alkylthiophene)
Synthetic Metals, 140(2-3), 177-181 (2004)
All-organic thin-film transistors patterned by means of selective electropolymerization
Applied Physics Letters, 83(19), 4044-4046 (2003)
Nanofiber preparation by whisker method using solvent-soluble conducting polymers
Thin Solid Films, 516(9), 2478-2486 (2008)
High molecular weights, polydispersities, and annealing temperatures in the optimization of bulk-heterojunction photovoltaic cells based on poly (3-hexylthiophene) or poly (3-butylthiophene)
Advances in Functional Materials, 16(17), 2263-2273 (2006)
Journal of the American Chemical Society, 117, 233-233 (1994)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service