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246883

Sigma-Aldrich

6,13-五并苯醌

99%

别名:

6,13-并五苯二酮

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About This Item

经验公式（希尔记法）:
C22H12O2
CAS号:
3029-32-1
分子量:
308.33
MDL號碼:
MFCD00003709
分類程式碼代碼:
12352100
PubChem物質ID:
24854833
NACRES:
NA.22

化驗

99%

形狀

solid

官能基

ketone

SMILES 字串

O=C1c2cc3ccccc3cc2C(=O)c4cc5ccccc5cc14

InChI

1S/C22H12O2/c23-21-17-9-13-5-1-2-6-14(13)10-18(17)22(24)20-12-16-8-4-3-7-15(16)11-19(20)21/h1-12H

InChI 密鑰

UFCVADNIXDUEFZ-UHFFFAOYSA-N

相关类别

一般說明

6,13-并五苯醌的最低激发三重态的电子结构已通过连续波时间分辨电子顺磁共振和脉冲电子核双共振进行了研究。

應用

6,13-并五苯醌已被用于：
  • 通过热蒸发在n-Si基底上沉积6,13-并五苯醌薄膜
  • 作为二芳基戊二烯的前体，潜在的有机场效应晶体管

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

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

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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分析证书(COA)

Lot/Batch Number
0000303210
0000303211
0000271889
0000282159
0000297582

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Tsugunosuke Masubuchi et al.
The Journal of chemical physics, 145(24), 244306-244306 (2017-01-05)
Pentacene (C
Tetrahedron, 63, 9699-9699 (2007)
Takuji Shimokage et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 58(6), 1201-1208 (2002-05-08)
Continuous-wave time-resolved EPR (cw-TREPR) and pulsed electron nuclear double resonance (ENDOR) studies have been carried out to clarify the electronic structure of the lowest excited triplet (Tl) state of 5,12-naphthacenequinone (5,12-NpQ) as well as 1,4-anthraquinone (1,4-AQ) and 6,13-pentacenequinone (6,13-PeQ). The
Structural and optical properties of 6, 13-pentacenequinone thin films.
Hwang DK, et al.
Applied Physics Letters, 85(23), 5568-5570 (2004)

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Silylethyne-substituted Pentacenes

Silylethyne substitution offers an opportunity to tune solubility for application-specific needs and self-assembly for electronic performance and has yielded semiconductors with excellent device performance.

Silylethyne-substituted Pentacenes

Silylethyne substitution offers an opportunity to tune solubility for application-specific needs and self-assembly for electronic performance and has yielded semiconductors with excellent device performance.

Silylethyne-substituted Pentacenes

Silylethyne substitution offers an opportunity to tune solubility for application-specific needs and self-assembly for electronic performance and has yielded semiconductors with excellent device performance.

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