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Sigma-Aldrich

2,7-Diphenyl[1]benzothieno[3,2-b][1]benzothiophene

sublimed grade, 99%

Sinonimo/i:

2,7-Diphenylbenzo[b]benzo[4,5]thieno[2,3-d]thiophene, DPh-BTBT

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About This Item

Formula empirica (notazione di Hill):
C26H16S2
Peso molecolare:
392.54
Codice UNSPSC:
12352103
ID PubChem:
NACRES:
NA.23

Grado

sublimed grade

Saggio

99%

Forma fisica

powder or crystals

Punto di fusione

363-368 °C

Caratteristiche del semiconduttore

P-type (mobility=2 cm2/V·s)

Stringa SMILE

c1ccc(cc1)-c2ccc3c(c2)sc4c5ccc(cc5sc34)-c6ccccc6

InChI

1S/C26H16S2/c1-3-7-17(8-4-1)19-11-13-21-23(15-19)27-26-22-14-12-20(16-24(22)28-25(21)26)18-9-5-2-6-10-18/h1-16H
SBJIDUSVEICMRY-UHFFFAOYSA-N

Applicazioni

2,7-Diphenyl[1]benzothieno(3,2-b)[1]benzothiophene is an organic semiconductor material with high charge mobility. It finds application in the fabrication of organic thin film transistors (OFETs), photovoltaic cells and organic light emitting diodes (OLEDs).
Organic Field Effect Transistor (OFET) Materials; p-Type Organic Semiconductors; p-Type Small Molecules; sublimed grade materials

Note legali

Product of Nippon Kayaku

Pittogrammi

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Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Oral - Eye Irrit. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

247.1 °F

Punto d’infiammabilità (°C)

119.5 °C


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2, 7-Diphenyl (1) benzothieno (3, 2-b) benzothiophene, a new organic semiconductor for air-stable organic field-effect transistors with mobilities up to 2.0 cm2 V-1 s-1.
Takimiya K, et al.
Journal of the American Chemical Society, 128(39), 12604-12605 (2006)
Kazuo Takimiya et al.
Journal of the American Chemical Society, 128(39), 12604-12605 (2006-09-28)
Vapor-deposited thin films of a newly developed sulfur-containing heteroarene, 2,7-diphenyl[1]benzothieno[3,2-b][1]benzothiophene (DPh-BTBT), were used as an active layer of OFETs, which showed excellent FET characteristics in ambient conditions with mobilities of approximately 2.0 cm2 V-1 s-1 and Ion/Ioff of 107.
Alkylated Dinaphtho (2, 3-b: 2′ , 3′ -f) Thieno (3, 2-b) Thiophenes (Cn-DNTTs): Organic Semiconductors for High-Performance Thin-Film Transistors.
Kang MJ, et al.
Advanced Materials, 23(10), 1222-1225 (2011)
Takimiya, Kazuo; et al.
Science and Technology of Advanced Materials, 8, 273-276 (2007)
Facile synthesis of highly pi-extended heteroarenes, dinaphtho [2, 3-b: 2 `, 3 `-f] chalcogenopheno [3, 2-b] chalcogenophenes, and their application to field-effect transistors
Yamamoto T and Takimiya K
Journal of the American Chemical Society, 129(8), 2224-2225 (2007)

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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.

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