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Merck

771503

Sigma-Aldrich

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

99%

别名:

trans-Fluorenacenedione, Indenofluorenedione

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About This Item

经验公式(希尔记法):
C20H10O2
CAS号:
分子量:
282.29
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.23

化驗

99%

形狀

powder

mp

350-354 °C

SMILES 字串

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

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

InChI 密鑰

AAUHGKXJBZEARK-UHFFFAOYSA-N

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應用

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).

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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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)
Preparation, physical properties and n-type FET characteristics of substituted diindenopyrazinediones and bis(dicyanomethylene) derivatives
Journal of Materials Chemistry, 22, 4483-4490 (2012)
Synthesis and optoelectronic properties of indeno (1, 2-b) fluorene-6, 12-dione donor-acceptor-donor triads
Frederickson CK and Haley MM
The Journal of Organic Chemistry, 79(22), 11241-11245 (2014)
High performance n-type field-effect transistors based on indenofluorenedione and diindenopyrazinedione derivatives
Nakagawa T, et al.
Chemistry of Materials, 20(8), 2615-2617 (2008)
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)

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