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Merck
CN

771503

Indeno[1,2-b]fluorene-6,12-dione

99%

别名:

trans-Fluorenacenedione, Indenofluorenedione

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关于此项目

经验公式(希尔记法):
C20H10O2
化学文摘社编号:
分子量:
282.29
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
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InChI

1S/C20H10O2/c21-19-13-7-3-1-5-11(13)15-9-18-16(10-17(15)19)12-6-2-4-8-14(12)20(18)22/h1-10H

SMILES string

O=C1c2ccccc2-c3cc4C(=O)c5ccccc5-c4cc13

InChI key

AAUHGKXJBZEARK-UHFFFAOYSA-N

assay

99%

form

powder

mp

350-354 °C

Application

Core unit affording n-type organic semiconductors for n-type FET
Indeno[1,2-b]fluorene-6,12-dione is a semiconducting polymer that can be used as an acceptor molecule in the fabrication of organic electronic devices such as organic light emitting diodes (OLEDs) and organic field effect transistors (OFETs).

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

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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High Performance n-Type Field-Effect Transistors Based on Indenofluorenedione and Diindenopyrazinedione Derivatives
Chemistry of Materials, 20, 2615-2617 (2008)
Preparation, physical properties and n-type FET characteristics of substituted diindenopyrazinediones and bis(dicyanomethylene) derivatives
Journal of Materials Chemistry, 22, 4483-4490 (2012)
An aromatic imine group enhances the EL efficiency and carrier transport properties of highly efficient blue emitter for OLEDs
Journal of Materials Chemistry, 20, 5930-5936 (2010)
Preparation, physical properties and n-type FET characteristics of substituted diindenopyrazinediones and bis (dicyanomethylene) derivatives
Nishida J, et al.
Journal of Materials Chemistry, 22(10), 4483-4490 (2012)
New 3pi-2Spiro Ladder-Type Phenylene Materials: Synthesis, Physicochemical Properties and Applications in OLEDs
Cocherel N, et al.
Chemistry?A European Journal , 14(36), 11328-11342 (2008)

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Fabrication procedure of organic field effect transistor device using a soluble pentacene precursor.

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