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Merck

663913

Sigma-Aldrich

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

98%

Synonym(e):

PTCDI-C8

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About This Item

Empirische Formel (Hill-System):
C40H42N2O4
CAS-Nummer:
Molekulargewicht:
614.77
MDL-Nummer:
UNSPSC-Code:
12352103
PubChem Substanz-ID:
NACRES:
NA.23

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Qualitätsniveau

Assay

98%

Form

solid

mp (Schmelzpunkt)

>300 °C

λmax

526 nm

Fluoreszenz

λem ≤533 nm in chloroform

Halbleitereigenschaften

N-type (mobility=1.7 cm2/V·s)

SMILES String

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

InChIKey

YFGMQDNQVFJKTR-UHFFFAOYSA-N

Anwendung

PTCDI-C8 can be used as an organic semiconductor to fabricate a wide range of opto-electronic based devices such as light emitting diodes,[1] photovoltaic cells,[2] and field effect transistors.[3]

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Die Dokumentenbibliothek aufrufen

Synthesis of PTCDI-C8 one dimensional nanostructures for photovoltaic applications.
IOP Conference Series: Materials Science and Engineering, 73(1), 012052-012052 (2015)
Graphene-organic hybrid electronics.
Kim C and Kymissis I
Journal of Material Chemistry C, 5(19), 4598-4613 (2017)
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)
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
Control over Patterning of Organic Semiconductors: Step-Edge-Induced Area-Selective Growth.
Wang W, et al.
Advanced Materials, 21(46), 4721-4725 (2009)

Artikel

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.

Review the potential of self-assembled multilayer gate dielectric films fabricated from silane precursors for organic, inorganic, and transparent TFT and for TFT circuitry and OLED displays.

Small molecular weight organic semiconductors are promising for flexible transistor applications in next-gen soft electronics.

Intrinsically stretchable active layers for organic field-effect transistors (OFET) are discussed. Polymer structural modification & post-polymerization modifications are 2 methods to achieve this.

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