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Merck
모든 사진(1)

주요 문서

767611

Sigma-Aldrich

2,6-Diphenylbenzo[1,2-b:4,5-b′]dithiophene

sublimed grade, 97%

동의어(들):

DPh-BDT

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About This Item

실험식(Hill 표기법):
C22H14S2
CAS Number:
Molecular Weight:
342.48
MDL number:
UNSPSC 코드:
12352103
PubChem Substance ID:
NACRES:
NA.23

Grade

sublimed grade

분석

97%

양식

powder or crystals

mp

421-426 °C

반도체 특성

P-type (mobility=4.6×10−3 cm2/V·s)

SMILES string

c1ccc(cc1)-c2cc3cc4sc(cc4cc3s2)-c5ccccc5

InChI

1S/C22H14S2/c1-3-7-15(8-4-1)19-11-17-13-22-18(14-21(17)23-19)12-20(24-22)16-9-5-2-6-10-16/h1-14H

InChI key

WNNUVWFCGFUJFU-UHFFFAOYSA-N

애플리케이션

Organic Field Effect Transistor (OFET) Materials; p-Type Organic Semiconductors; p-Type Small Molecules; sublimed grade materials

법적 정보

Product of Nippon Kayaku

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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시험 성적서(COA)

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문서 라이브러리 방문

Juan Casado et al.
The journal of physical chemistry. A, 110(23), 7422-7430 (2006-06-09)
In this work, the interactions between heteroatoms (S, Se, and Te) and conjugated skeletons are analyzed. The study is carried out by using electronic absorption and fluorescence spectroscopies, electrochemistry, vibrational Raman spectroscopy, and theoretical calculations in the framework of DFT
Kazuo Takimiya et al.
Journal of the American Chemical Society, 126(16), 5084-5085 (2004-04-22)
2,6-Diphenylbenzo[1,2-b:4,5-b']dichalcogenophenes including thiophene, selenophene, and tellurophene analogues as organic semiconductors for field-effect transistors were effectively synthesized in three steps from commercially available 1,4-dibromobenzene. All three benzodichalcogenophenes acted as good p-type semiconductors, and particularly the selenophene analogue, 2,6-diphenylbenzo[1,2-b:4,5-b']diselenophene, showed high FET

문서

Sublimed materials for organic electronic devices such of OFETs and OTFTs allow the achievement of better electronic properties, and may help increase a device’s lifetime.

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

Solution-processed organic photovoltaic devices (OPVs) have emerged as a promising clean energy generating technology due to their ease of fabrication, potential to enable low-cost manufacturing via printing or coating techniques, and ability to be incorporated onto light weight, flexible substrates.

Thin, lightweight, and flexible electronic devices meet widespread demand for scalable, portable, and robust technology.

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