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663905

Sigma-Aldrich

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

98%

Sinonimo/i:

PTCDI-Ph

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About This Item

Formula empirica (notazione di Hill):
C36H18N2O4
Numero CAS:
128-65-4
Peso molecolare:
542.54
Numero CE:
204-902-7
Numero MDL:
MFCD00151605
Codice UNSPSC:
12352103
ID PubChem:
24884667
NACRES:
NA.23

Saggio

98%

Forma fisica

solid

Punto di fusione

>300 °C

λmax

527 nm

Fluorescenza

λem ≤534 nm in chloroform

Caratteristiche del semiconduttore

N-type (mobility=10−5 cm2/V·s)

Stringa SMILE

O=C1N(c2ccccc2)C(=O)c3ccc4c5ccc6C(=O)N(c7ccccc7)C(=O)c8ccc(c9ccc1c3c49)c5c68

InChI

1S/C36H18N2O4/c39-33-25-15-11-21-23-13-17-27-32-28(36(42)38(35(27)41)20-9-5-2-6-10-20)18-14-24(30(23)32)22-12-16-26(31(25)29(21)22)34(40)37(33)19-7-3-1-4-8-19/h1-18H
OGEZSLXPCKHGKO-UHFFFAOYSA-N

Descrizione generale

N,N′-Diphenyl-3,4,9,10-perylenedicarboximide (PTCDI-Ph) is an asphaltene based conducting polymer that has an archipelago model. It is a perylene diimide derivative that has a high electron affinity and shows good chemical stability. It can be used as an active layer in the development of organic electronic devices.

Applicazioni

PTCDI-Ph is a conjugating polymer that forms an ultrathin film that can be used in the fabrication of organic field effect transistors (OFETs) for nitrogen dioxide sensor based applications.

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
04103PD

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The influence of CO2 on the structure of confined asphaltenes in calcite nanopores.
Mohammed S and Gadikota G
Fuel: The Science and Technology of Fuel and Energy, 236, 769-777 (2019)
Response enhancement mechanism of NO2 gas sensing in ultrathin pentacene field-effect transistors.
Mirza M, et al.
Organic Electronics, 24(9), 96-100 (2015)
High performance nitrogen dioxide sensor based on organic field-effect transistor utilizing ultrathin CuPc/PTCDI-C8 heterojunction.
Fan H, et al.
Synthetic Metals, 211(9), 161-166 (2016)
Electronic structure of the conduction band of the interface region of ultrathin films of substituted perylenedicarboximides and the germanium oxide surface.
Komolov AS, et al.
Physics of the Solid State, 58(9), 1901-1905 (2016)
Heteroepitaxy growth high performance films of perylene diimide derivatives.
Huang L, et al.
Organic Electronics, 11(2), 195-201 (2010)

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.

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.

Soluble Pentacene Precursors

Fabrication procedure of organic field effect transistor device using a soluble pentacene precursor.

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