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Key Documents

264229

Sigma-Aldrich

N,N'-双(2,5-二叔丁基苯基)-3,4,9,10-苝二甲酰亚胺

Dye content 97 %

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About This Item

經驗公式(希爾表示法):
C52H50N2O4
CAS號碼:
分子量::
766.96
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.23

化驗

97%

形狀

solid

成份

Dye content, 97%

mp

>300 °C (lit.)

λmax

528 nm

半導體屬性

N-type (mobility=1.8x10−4 cm2/V·s)

SMILES 字串

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

InChI 密鑰

BIYPCKKQAHLMHG-UHFFFAOYSA-N

一般說明

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.

應用

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).

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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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)

文章

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

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

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.

There is widespread demand for thin, lightweight, and flexible electronic devices such as displays, sensors, actuators, and radio-frequency identification tags (RFIDs). Flexibility is necessary for scalability, portability, and mechanical robustness.

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