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747092

Sigma-Aldrich

C8-BTBT

≥99% (HPLC)

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C30H40S2
CAS Number:
Molecular Weight:
464.77
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Assay

≥99% (HPLC)

form

powder

mp

108-112 °C

semiconductor properties

P-type (mobility=5.5 cm2/V·s)

SMILES string

CCCCCCCCC1=CC2=C(C=C1)C3=C(C(C=CC(CCCCCCCC)=C4)=C4S3)S2

InChI

1S/C30H40S2/c1-3-5-7-9-11-13-15-23-17-19-25-27(21-23)31-30-26-20-18-24(22-28(26)32-29(25)30)16-14-12-10-8-6-4-2/h17-22H,3-16H2,1-2H3

InChI key

YWIGIVGUASXDPK-UHFFFAOYSA-N

General description

C8-BTBT is a conducting polymer with [1]benzothieno[3,2-b][1]- benzothiophene (BTBT) as the base material for the development of air-stable semiconductors. It can form a spin coated thin film that can be used as a p-type semiconductor with charge mobility of 43 cm2V-1s-1. It exhibits highly ordered self-assembled monolayer (SAM) on graphene and hexagonal boron nitride (hBN) with sheet resistance: <1,000 ohm/sq

Application

C8-BTBT is a conjugating polymer that can be used in a variety of organic electronics based applications which includes organic photovoltaic cells (OPV), organic light emitting diodes (OLEDs) and organic thin film transistors (OTFTs).
High field-effect mobility of 5.5-5.7 cm2/Vs and high On/Off ratio of 109 ; solution-processed (solubility of 80 mg/mL) OFETs

Legal Information

Product of Nippon Kayaku

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Solution-processable organic single crystals with bandlike transport in field-effect transistors.
Liu C, et al.
Advanced Materials, 23(4), 523-526 (2011)
Orientation-dependent energy level alignment and film growth of 2, 7-diocty [1] benzothieno [3, 2-b] benzothiophene (C8-BTBT) on HOPG.
Lyu L, et al.
J. Chem. Phys., 144(3), 034701-034701 (2016)
Hideaki Ebata et al.
Journal of the American Chemical Society, 129(51), 15732-15733 (2007-11-30)
2,7-Dialkyl[1]benzothieno[3,2-b]benzothiophenes were tested as solution-processible molecular semiconductors. Thin films of the organic semiconductors deposited on Si/SiO2 substrates by spin coating have well-ordered structures as confirmed by XRD analysis. Evaluations of the devices under ambient conditions showed typical p-channel FET responses
Molecular ordering of high-performance soluble molecular semiconductors and re-evaluation of their field-effect transistor characteristics.
Izawa T, et al.
Advanced Materials, 20(18), 3388-3392 (2008)
Zhimin Chai et al.
ACS applied materials & interfaces, 10(21), 18123-18130 (2018-05-09)
Assembly of organic semiconductors with ordered crystal structure has been actively pursued for electronics applications such as organic field-effect transistors (OFETs). Among various film deposition methods, solution-based film growth from small molecule semiconductors is preferable because of its low material

Articles

Dr. Chan and researchers highlight flexible transistors are the building blocks of next-generation soft electronics. Among all the reported material systems that can be fabricated by researchers, such as circuits, biosensors, stretchable displays, and others,1–5 small molecular weight organic semiconductors are among the most promising candidates for flexible transistor applications. For these small molecular weight organic semiconductors, the semiconductor forming the conductive channel dominates the device performance.

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

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