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Merck
CN

768677

萘并[1,2-b:5,6-b′]二噻吩

97%

别名:

NDT

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经验公式(希尔记法):
C14H8S2
化学文摘社编号:
分子量:
240.34
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
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SMILES string

C1(C=CS2)=C2C(C=CC3=C4SC=C3)=C4C=C1

InChI

1S/C14H8S2/c1-3-11-12(13-9(1)5-7-15-13)4-2-10-6-8-16-14(10)11/h1-8H

InChI key

MOZTVOICZIVCFC-UHFFFAOYSA-N

assay

97%

form

solid

mp

153-160 °C

semiconductor properties

P-type (mobility>0.5 cm2/V·s)

General description

Naphtho[1,2-b:5,6-b′]dithiophene (NDT) is a π-conjugated naphthodithiophene derivative that has symmetrical planar structures. It is mainly utilized in the development of semiconductors due to its high charge mobility and high current on/off ratios.

Application

NDT has donor-acceptor copolymers which can be used in the fabrication of organic electronic devices such as organic light emitting diodes (OLEDs), organic solar cells (OSCs) and organic field effect transistors (OFETs).
This semiconducting material has been used in the synthesis of copolymers that show the highest mobility (>0.5 cm2 /Vs) in an NDT-based OFET device to date.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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分析证书(COA)

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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.

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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