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246883

Sigma-Aldrich

6,13-Pentacenequinone

99%

Sinónimos:

6,13-Pentacenedione

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About This Item

Fórmula empírica (notación de Hill):
C22H12O2
Número de CAS:
3029-32-1
Peso molecular:
308.33
MDL number:
MFCD00003709
UNSPSC Code:
12352100
PubChem Substance ID:
24854833
NACRES:
NA.22

assay

99%

form

solid

SMILES string

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 key

UFCVADNIXDUEFZ-UHFFFAOYSA-N

General description

Electronic structure of the lowest excited triplet state of 6,13-pentacenequinone has been studied by continuous-wave time-resolved electron paramagnetic resonance and pulsed electron nuclear double resonance.

Application

6,13-Pentacenequinone has been used in:
  • deposition of 6,13-pentacenequinone thin films on n-Si substrates by thermal evaporation
  • as precursor to diarylpentacenes, potential organic field-effect transitors

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

Tetrahedron, 63, 9699-9699 (2007)
Structural and optical properties of 6, 13-pentacenequinone thin films.
Hwang DK, et al.
Applied Physics Letters, 85(23), 5568-5570 (2004)
Tsugunosuke Masubuchi et al.
The Journal of chemical physics, 145(24), 244306-244306 (2017-01-05)
Pentacene (C
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

Artículos

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.

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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