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Merck
모든 사진(2)

주요 문서

495336

Sigma-Aldrich

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

regioregular

동의어(들):

P3BT

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1 G
₩897,362

₩897,362


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1 G
₩897,362

About This Item

CAS Number:
MDL number:
UNSPSC 코드:
12352103
NACRES:
NA.23

₩897,362


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분자량

Mw 54,000 (typical)

색상

black

solubility

chlorinated solvents: soluble (partially soluble in THF, diethylether)

형광

λex 440 nm; λem 567 nm in chloroform

Mw/Mn

2.3 (typical)

SMILES string

[s]1c(c(cc1C)CCCC)C

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

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일반 설명

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.[1][2]

애플리케이션

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).[3][4]
Rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, microelectrical amplifiers, field-effect transistors and non-linear optical materials.

포장

Packaged in glass bottles

법적 정보

Product 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

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

이미 열람한 고객

Effect of alkyl side-chain length and solvent on the luminescent characteristics of poly (3-n-alkylthiophene)
Shin C and Lee H
Synthetic Metals, 140(2-3), 177-181 (2004)
High molecular weights, polydispersities, and annealing temperatures in the optimization of bulk-heterojunction photovoltaic cells based on poly (3-hexylthiophene) or poly (3-butylthiophene)
Hiorns RC, et al.
Advances in Functional Materials, 16(17), 2263-2273 (2006)
All-organic thin-film transistors patterned by means of selective electropolymerization
Becker E, et al.
Applied Physics Letters, 83(19), 4044-4046 (2003)
Nanofiber preparation by whisker method using solvent-soluble conducting polymers
Samitsu S, et al.
Thin Solid Films, 516(9), 2478-2486 (2008)
Journal of the American Chemical Society, 117, 233-233 (1994)

문서

The application of conducting polymers at the interface with biology is an exciting new trend in organic electronics research.

Intrinsically stretchable active layers for organic field-effect transistors (OFET) are discussed. Polymer structural modification & post-polymerization modifications are 2 methods to achieve this.

Novel Graphene‑Based Nanostructures Production, Functionalization, and Engineering

Progress in solution-processed functional materials leads to thin-film optoelectronic devices for industrial and consumer electronics.

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