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Merck
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주요 문서

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495336

Sigma-Aldrich

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

regioregular

동의어(들):

P3BT

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모든 사진(2)

About This Item

CAS Number:
98837-51-5
MDL number:
MFCD00677712
UNSPSC 코드:
12352103
NACRES:
NA.23

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.

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).
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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시험 성적서(COA)

Lot/Batch Number
MKCQ4100
MKCN7087
MKBD6215
MKAA0709
11314CE

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COA 검색

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이미 열람한 고객

Slide 1 of 2

1 of 2

Poly(3-hexylthiophene-2,5-diyl) regioregular, average Mw 20,000-45,000

Sigma-Aldrich

900563

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

Poly(3-hexylthiophene-2,5-diyl) regioregular, average Mw 50,000-75,000

Sigma-Aldrich

900550

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

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)
Nanofiber preparation by whisker method using solvent-soluble conducting polymers
Samitsu S, et al.
Thin Solid Films, 516(9), 2478-2486 (2008)
All-organic thin-film transistors patterned by means of selective electropolymerization
Becker E, et al.
Applied Physics Letters, 83(19), 4044-4046 (2003)
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)
Journal of the American Chemical Society, 117, 233-233 (1994)

문서

Conducting Polymer Device Applications

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

Polymer Semiconductors for Intrinsically Stretchable Organic Transistors

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

Nanoparticle-based Zinc Oxide Electron Transport Layers for Printed Organic Photodetectors

Recent progress in the area of solution-processed functional materials has led to the development of a variety of thin-film optoelectronic devices with significant promise in the industrial and consumer electronics fields.

자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..

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