F1506
9-芴酮
98%
别名:
9H-芴-9-酮, 芴-9-酮（8CI）
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关于此项目
经验公式（希尔记法）:
C13H8O
化学文摘社编号:
分子量:
180.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-630-7
Beilstein/REAXYS Number:
1636531
MDL number:
Assay:
98%
产品名称
9-芴酮, 98%
InChI key
YLQWCDOCJODRMT-UHFFFAOYSA-N
InChI
1S/C13H8O/c14-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)13/h1-8H
SMILES string
O=C1c2ccccc2-c3ccccc13
assay
98%
bp
342 °C (lit.)
mp
80-83 °C (lit.)
Quality Level
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Application
9-芴酮已被广泛用作合成各种有机电子材料的前体。一些一般的例子是：
- 蓝色和绿色磷光有机发光二极管（PHOLEDs）的主体的合成。
- 芴基分子马达的合成。
- 开壳 Chichibabin 碳氢化合物作为潜在的有机自旋电子材料的合成。
- 通过 1，2-二（1-萘基）乙烷的光敏化作用，它也可以作为一种敏化剂来形成二萘品苯。
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
325.4 °F
flash_point_c
163 °C
ppe
Eyeshields, Gloves, type N95 (US)
Novel carbazole/fluorene hybrids: Host materials for blue phosphorescent OLEDs.
Shih P I, et al.
Organic Letters, 8(13), 2799-2802 (2006)
Yufang Liu et al.
Journal of computational chemistry, 30(16), 2723-2727 (2009-04-29)
The geometric structures and infrared (IR) spectra in the electronically excited state of a novel doubly hydrogen-bonded complex formed by fluorenone and alcohols, which has been observed by IR spectra in experimental study, are investigated by the time-dependent density functional
Facile synthesis of picene from 1, 2-di (1-naphthyl) ethane by 9-fluorenone-sensitized photolysis.
Okamoto H, et al.
Organic Letters, 13(10), 2758-2761 (2011)
Stable Tetrabenzo-Chichibabin?s hydrocarbons: tunable ground state and unusual transition between their closed-shell and open-shell resonance forms.
Zeng Z, et al.
Journal of the American Chemical Society, 134(35), 14513-14525 (2012)
Marek Józefowicz et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 67(2), 316-320 (2006-09-15)
Electronic absorption, excitation and fluorescence spectra of fluorenone and 4-hydroxyfluorenone were recorded at room temperature in several aprotic solvent of varying polarities. The ground (mu(g)) and excited (mu(e)) state dipole moments of both molecules were estimated from solvatochromic shifts of
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