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Key Documents

663913

Sigma-Aldrich

N,N′-Dioctyl-3,4,9,10-perylenedicarboximide

98%

Synonyme(s) :

PTCDI-C8

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About This Item

Formule empirique (notation de Hill):
C40H42N2O4
Numéro CAS:
Poids moléculaire :
614.77
Numéro MDL:
Code UNSPSC :
12352103
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Pureté

98%

Forme

solid

Pf

>300 °C

λmax

526 nm

Fluorescence

λem ≤533 nm in chloroform

Propriétés du semi-conducteur

N-type (mobility=1.7 cm2/V·s)

Chaîne SMILES 

CCCCCCCCN1C(=O)c2ccc3c4ccc5C(=O)N(CCCCCCCC)C(=O)c6ccc(c7ccc(C1=O)c2c37)c4c56

InChI

1S/C40H42N2O4/c1-3-5-7-9-11-13-23-41-37(43)29-19-15-25-27-17-21-31-36-32(40(46)42(39(31)45)24-14-12-10-8-6-4-2)22-18-28(34(27)36)26-16-20-30(38(41)44)35(29)33(25)26/h15-22H,3-14,23-24H2,1-2H3

Clé InChI

YFGMQDNQVFJKTR-UHFFFAOYSA-N

Application

PTCDI-C8 can be used as an organic semiconductor to fabricate a wide range of opto-electronic based devices such as light emitting diodes, photovoltaic cells, and field effect transistors.

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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Consulter la Bibliothèque de documents

Graphene-organic hybrid electronics.
Kim C and Kymissis I
Journal of Material Chemistry C, 5(19), 4598-4613 (2017)
Synthesis of PTCDI-C8 one dimensional nanostructures for photovoltaic applications.
IOP Conference Series: Materials Science and Engineering, 73(1), 012052-012052 (2015)
Three-dimensional molecular packing of thin organic films of PTCDI-C8 determined by surface X-ray diffraction.
Krauss TN, et al.
Langmuir, 24(22), 12742-12744 (2008)
Xiali Zhang et al.
Nanoscale horizons, 5(7), 1096-1105 (2020-05-20)
Ultrathin organic semiconductor (OSC) crystalline films hold the promise of achieving high-performance, flexible, and transparent organic electronic devices. However, fast and high-throughput solution deposition of uniform pinhole-free ultrathin OSC crystalline films over a large area remains a challenge. Here, we
N Hiroshiba et al.
Physical chemistry chemical physics : PCCP, 13(13), 6280-6285 (2011-03-02)
Photo-induced carrier processes at the heteromolecular interface of N,N'-dioctyl-3,4,9,10-perylenedicarboximide (PTCDI-C(8)) and quaterrylene (QT) on a molecular scale were examined by optical and photoelectron spectroscopy. The energy level alignments of the molecules were determined by X-ray photoelectron spectroscopy and the optical

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Flexible electronic circuits, displays, and sensors based on organic active materials will enable future generations of electronics products that may eventually enter the mainstream electronics market.

Flexible electronic circuits, displays, and sensors based on organic active materials will enable future generations of electronics products that may eventually enter the mainstream electronics market.

Flexible electronic circuits, displays, and sensors based on organic active materials will enable future generations of electronics products that may eventually enter the mainstream electronics market.

Flexible electronic circuits, displays, and sensors based on organic active materials will enable future generations of electronics products that may eventually enter the mainstream electronics market.

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