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Merck

663921

Sigma-Aldrich

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

98%

Synonym(e):

PTCDI-C5

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About This Item

Empirische Formel (Hill-System):
C34H30N2O4
CAS-Nummer:
Molekulargewicht:
530.61
MDL-Nummer:
UNSPSC-Code:
12352103
PubChem Substanz-ID:
NACRES:
NA.23

Assay

98%

Form

solid

mp (Schmelzpunkt)

>300 °C

λmax

527 nm

Fluoreszenz

λem ≤533 nm in chloroform

Halbleitereigenschaften

N-type (mobility~10−4 cm2/V·s)

SMILES String

CCCCCN1C(=O)c2ccc3c4ccc5C(=O)N(CCCCC)C(=O)c6ccc(c7ccc(C1=O)c2c37)c4c56

InChI

1S/C34H30N2O4/c1-3-5-7-17-35-31(37)23-13-9-19-21-11-15-25-30-26(34(40)36(33(25)39)18-8-6-4-2)16-12-22(28(21)30)20-10-14-24(32(35)38)29(23)27(19)20/h9-16H,3-8,17-18H2,1-2H3

InChIKey

JNZZCMNXYAOLTO-UHFFFAOYSA-N

Verwandte Kategorien

Allgemeine Beschreibung

N,N′-Dipentyl-3,4,9,10-perylenedicarboximide (PTCDI-C5) belongs to the class of perylene based semiconducting materials that can be used as active compounds in a variety of opto-electronic devices. Its properties include cost efficiency, high mobility of electrons, high molar absorption coefficient, reversible redox properties and good electrochemical properties.

Anwendung

Electron-transporting (n-type) organic semiconductor suitable for fabrication of n-channel organic field-effect transistors (OFETs). OFETs with electron mobilities με ~ 10-2 cm2/Vs and current on/off ratios on the order of 104 were made based on 1-dimensional nanowires prepared from N,N′-Dipentyl-3,4,9,10-perylenedicarboximide.
PTCDI-C5 can be used for a variety of applications which include liquid crystals, organic thin film transistors (OTFTs), solar cells, photovoltaics and sensors.

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


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Variable temperature film and contact resistance measurements on operating n-channel organic thin film transistors
Chesterfield RJ, et al.
Journal of Applied Physics, 95(11), 6396-6405 (2004)
Investigation of the spectral, optical and surface morphology properties of the N, N?-Dipentyl-3, 4, 9, 10-perylenedicarboximide small molecule for optoelectronic applications
Gunduz B
Polymers For Advanced Technologies, 27(2), 144-155 (2016)
Study of structural, optical properties and electronic structure of PTCDI-C5 organic nanostructure
Kurban M and Gunduz B
Chemical Physics Letters, 691(2), 14-21 (2018)
Sensing properties of the n, n?-dipentyl-3, 4, 9, 10-perylenedicarboximide small molecule for different concentrations and solvents for sensor applications
Gunduz B
Sensor Letters, 13(1), 52-63 (2015)
Frank Würthner
Chemical communications (Cambridge, England), (14), 1564-1579 (2004-07-21)
Perylene bisimide dyes and their organization into supramolecular architectures through hydrogen-bonding, metal ion coordination and pi-pi-stacking is discussed; further self-assembly leading to nano- and meso-scopic structures and liquid-crystalline compounds is also addressed.

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.

Organic materials in optoelectronic devices like LEDs and solar cells are of significant academic and commercial interest.

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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