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663913

Sigma-Aldrich

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

98%

Sinonimo/i:

PTCDI-C8

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1 G
CHF 144.00

About This Item

Formula empirica (notazione di Hill):
C40H42N2O4
Numero CAS:
78151-58-3
Peso molecolare:
614.77
Numero MDL:
MFCD08276854
Codice UNSPSC:
12352103
ID PubChem:
24884668
NACRES:
NA.23

CHF 144.00

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Livello qualitativo

100

Saggio

98%

Stato

solid

Punto di fusione

>300 °C

λmax

526 nm

Fluorescenza

λem ≤533 nm in chloroform

Caratteristiche del semiconduttore

N-type (mobility=1.7 cm2/V·s)

Stringa SMILE

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
YFGMQDNQVFJKTR-UHFFFAOYSA-N

Categorie correlate

Applicazioni

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]

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
MKCR7447
MKCL8923
MKCG1408
MKBV5102V
MKBP9668V

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I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

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)
Lei Zhang et al.
Advanced materials (Deerfield Beach, Fla.), 30(28), e1801181-e1801181 (2018-05-22)
Self-standing nanostructures are of fundamental interest in materials science and nanoscience and are widely used in (opto-)electronic and photonic devices as well as in micro-electromechanical systems. To date, large-area and self-standing nanoelectrode arrays assembled on flexible substrates have not been
Wei Deng et al.
ACS applied materials & interfaces, 11(39), 36205-36212 (2019-08-31)
Highly ordered organic semiconductor single-crystal (OSSC) arrays are ideal building blocks for functional organic devices. However, most of the current methods are only applicable to fabricate OSSC arrays of a single component, which significantly hinders the application of OSSC arrays
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)
Visualizza tutti i documenti correlati

Articoli

Organic Materials for Thin Film Transistors

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.

Self-Assembled Nanodielectrics (SANDs) for Unconventional Electronics

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.

High Crystalline Organic Transistors

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

Polymer Semiconductors for Intrinsically Stretchable Organic Transistors

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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