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Merck
CN

767611

Sigma-Aldrich

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

sublimed grade, 97%

别名:

DPh-BDT

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关于此项目

经验公式(希尔记法):
C22H14S2
化学文摘社编号:
分子量:
342.48
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.23
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等级

sublimed grade

方案

97%

表单

powder or crystals

mp

421-426 °C

半导体性质

P-type (mobility=4.6×10−3 cm2/V·s)

SMILES字符串

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

应用

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

法律信息

Product of Nippon Kayaku

象形图

Exclamation mark

警示用语:

Warning

危险声明

预防措施声明

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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

商品

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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