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264229

Sigma-Aldrich

N,N′-Bis(2,5-di-tert-butylphenyl)-3,4,9,10-perylenedicarboximide

Dye content 97 %

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About This Item

Formule empirique (notation de Hill):
C52H50N2O4
Numéro CAS:
Poids moléculaire :
766.96
Numéro MDL:
Code UNSPSC :
12352103
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Pureté

97%

Forme

solid

Composition

Dye content, 97%

Pf

>300 °C (lit.)

λmax

528 nm

Propriétés du semi-conducteur

N-type (mobility=1.8x10−4 cm2/V·s)

Chaîne SMILES 

CC(C)(C)c1ccc(c(c1)N2C(=O)c3ccc4c5ccc6C(=O)N(C(=O)c7ccc(c8ccc(C2=O)c3c48)c5c67)c9cc(ccc9C(C)(C)C)C(C)(C)C)C(C)(C)C

InChI

1S/C52H50N2O4/c1-49(2,3)27-13-23-37(51(7,8)9)39(25-27)53-45(55)33-19-15-29-31-17-21-35-44-36(22-18-32(42(31)44)30-16-20-34(46(53)56)43(33)41(29)30)48(58)54(47(35)57)40-26-28(50(4,5)6)14-24-38(40)52(10,11)12/h13-26H,1-12H3

Clé InChI

BIYPCKKQAHLMHG-UHFFFAOYSA-N

Description générale

N,N′-Bis(2,5-di-tert-butylphenyl)-3,4,9,10-perylenedicarboximide (BTBP) is a fluorescence dye that can be used as an electron acceptor. It has an extinction coefficient of 7.4 x 104 cm-1 mol-1 dm3.

Application

An n-channel organic semiconductor.
BTBP is a dye that can be used in the development of organic electronic based devices which include organic light emitting diodes(OLED), electroluminescent device and organic solar cells(OSCs).

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

The cybotactic region surrounding fluorescent probes dissolved in 1-butyl-3-methylimidazolium hexafluorophosphate: effects of temperature and added carbon dioxide.
Baker SN, et al.
The Journal of Physical Chemistry B, 105(39), 9663-9668 (2001)
Effects of doping dyes on the electroluminescent characteristics of multilayer organic light-emitting diodes.
Suzuki H and Hoshino S
Journal of Applied Physics, 79(11), 8816-8822 (1996)
Insulated molecular wire with highly conductive pi-conjugated polymer core.
Terao J, et al.
Journal of the American Chemical Society, 131(50), 18046-18047 (2009)
Self-assembled gelators for organic electronics.
Babu SS, et al.
Angewandte Chemie (International Edition in English), 51(8), 1766-1776 (2012)
Three-layered multicolor organic electroluminescent device.
Yoshida M, et al.
Applied Physics Letters, 69(6), 734-736 (1996)

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Solution-processed organic photovoltaic devices (OPVs) have emerged as a promising clean energy generating technology due to their ease of fabrication, potential to enable low-cost manufacturing via printing or coating techniques, and ability to be incorporated onto light weight, flexible substrates.

Solution-processed organic photovoltaic devices (OPVs) have emerged as a promising clean energy generating technology due to their ease of fabrication, potential to enable low-cost manufacturing via printing or coating techniques, and ability to be incorporated onto light weight, flexible substrates.

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