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9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole (BCzPh) is an electron-rich host material characterized by its two conjugated carbazole units. It is primarily utilized in the development of phosphorescent organic light-emitting diodes (PHOLEDs) due to its electron-rich nature, which allows it to function as an electron donor. This property enables BCzPh to form exciplexes, making it a suitable component for both the emitting layer and host material in highly-efficient fluorescent and phosphorescent OLED devices.

57102-62-2

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57102-62-2 Usage

Uses

Used in Electronics Industry:
9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole is used as a host material for [application reason] the creation of phosphorescent organic light-emitting diodes (PHOLEDs) due to its electron-rich nature and ability to form exciplexes. This application takes advantage of BCzPh's electron-donating properties to enhance the efficiency and performance of OLED devices.
Used in Research and Development:
In the field of research and development, 9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole serves as a crucial component in the exploration of new materials and technologies related to OLED devices. Its unique properties make it an interesting subject for further study and potential innovation in the field of electronics and optoelectronics.

Check Digit Verification of cas no

The CAS Registry Mumber 57102-62-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,0 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57102-62:
(7*5)+(6*7)+(5*1)+(4*0)+(3*2)+(2*6)+(1*2)=102
102 % 10 = 2
So 57102-62-2 is a valid CAS Registry Number.

57102-62-2Relevant academic research and scientific papers

Catalytic and Aerobic Oxidative Biaryl Coupling of Anilines Using a Recyclable Heterogeneous Catalyst for Synthesis of Benzidines and Bicarbazoles

Matsumoto, Kenji,Toubaru, Yasunori,Tachikawa, Shohei,Miki, Ayaka,Sakai, Kentaro,Koroki, Syota,Hirokane, Tsukasa,Shindo, Mitsuru,Yoshida, Masahiro

, p. 15154 - 15166 (2020/12/23)

In this study, a heterogeneous rhodium-catalyzed oxidative homocoupling reaction of anilines utilizing molecular oxygen as the sole oxidant is reported. Employing a commercially available and recyclable Rh/C catalyst enabled the oxidative dimerization of various anilines, including N,N-disubstituted and N-monosubstituted anilines, as well as diarylamines, triarylamines, and carbazoles. Additionally, the catalytic protocol was extended to the ortho-ortho coupling of anilines, affording 2,2′-diaminobiphenyls with high regioselectivity. Notably, the developed approach provides rapid access to diversely functionalized benzidines and diaminobiphenyls in an operationally simple, practical, and environmentally friendly manner.

COMPOSITION FOR ORGANIC OPTOELECTRONIC DIODE, ORGANIC OPTOELECTRONIC DIODE, AND DISPLAY DEVICE

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Paragraph 0173-0175, (2020/05/14)

The present invention relates to a composition for an organic optoelectronic diode, comprising a first compound for an organic optoelectronic diode; and a second compound for an organic optoelectronic diode, and an organic optoelectronic diode and a displ

ORGANIC COMPOUND AND COMPOSITION AND ORGANIC OPTOELECTRONIC DEVICE AND DISPLAY DEVICE

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Paragraph 0161-0163, (2019/07/11)

Disclosed are an organic compound represented by Chemical Formula 1, a composition including the same, an organic optoelectronic device, and a display device. In Chemical Formula 1, X1 to X3, Y1 to Y3, and R1 to R18 are the same as described in the detailed description.

Oxidative Coupling of Carbazoles: A Substituent-Governed Regioselectivity Profile

Mallick, Sudesh,Maddala, Sudhakar,Kollimalayan, Kalidass,Venkatakrishnan, Parthasarathy

, p. 73 - 93 (2019/01/10)

Oxidative C-C coupling of carbazoles possessing various substituents is demonstrated in the presence of organic (metal-free) recyclable oxidants, such as DDQ or CA/H+, for accessing bicarbazole regioisomers. Differently substituted carbazoles are examined to showcase regioselective discrimination (3,3′-versus 1,3′-bicarbazoles) and preferences based on sterics and electronics in oxidative coupling. Finally, a mechanism that involves the carbazole radical cation has been traced (evidenced) and proposed on the basis of the UV-vis-NIR absorption and EPR spectroscopy results. This study underlines the strategic chemical preparation of a series of bicarbazoles in an efficient manner.

Eaton's reagent assisted aromatic C-C coupling of carbazoles for optoelectronic applications

Yuan, Jie,Jin, Lu,Chen, Runfeng,Tang, Xingxing,Xie, Xiang,Tang, Yuting,Huang, Wei

supporting information, p. 14704 - 14708 (2018/09/29)

An Eaton's reagent assisted C(sp2)-C(sp2) coupling via the Scholl reaction mechanism was developed to prepare bicarbazoles without using any solvents and catalysts. The resulting biaryl exhibits unique optoelectronic properties as a promising host material of blue phosphorescent organic light emitting diodes, achieving high current efficiency up to 31.7 cd A-1 with ultralow roll-off.

ORGANIC LIGHT EMITTING DEVICE AND COMPOSITION FOR ORGANIC MATERIAL LAYER OF ORGANIC LIGHT EMITTING DEVICE

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Paragraph 0114; 0116, (2018/11/22)

The present application provides a hetero-cyclic compound capable of greatly enhancing lifetime, efficiency, electrochemical stability and thermal stability of an organic light emitting device, and an organic light emitting device containing the hetero-cyclic compound in an organic compound layer.

Synthesis method for 9,9'-disubstituent-3,3'-dicarbazyl

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, (2017/08/29)

The invention discloses a synthesis method for 9,9'-disubstituent-3,3'-dicarbazyl, and belongs to the technical field of the organic chemical synthesis. The method comprises the following steps: using 3-boric acid-9-phenylcarbazole as a raw material, and preparing 9-phenyl-3,3'-dicarbazyl under the catalysis of Pd2(dba)3, triphenylphosphine; and preparing a target object by the 9-phenyl-3,3'-dicarbazyl under the catalysis of PdC12(dppf),X-phos. The synthesis method is capable of adjusting the synthetic route, reducing the production of a by-product, improving the yield and reducing the cost. The yield achieves more than 91%. The synthetic route post-treatment of the synthesis method is simple and effective, and is good for industrial production.

ORGANIC LIGHT EMITTING DEVICE AND DISPLAY DEVICE HAVING THE SAME

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, (2017/06/30)

An organic light emitting device and a display device including the same, the organic light emitting device including a first electrode; a hole controlling layer on the first electrode; an emission layer on the hole controlling layer; an electron controlling layer on the emission layer; and a second electrode on the electron controlling layer, wherein the emission layer includes a hole transport host material, an electron transport host material, a bipolar host material, and at least one dopant material.

COMPOSITION FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC OPTOELECTRONIC DEVICE AND DISPLAY DEVICE

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Paragraph 0189; 0190, (2017/06/22)

Disclosed are a composition for an organic optoelectronic device including at least one first compound represented by Chemical Formula 1 and at least one second compound represented by Chemical Formula 2, organic optoelectronic device including the same, and a display device including the organic optoelectronic device. Chemical Formula 1 and 2 are the same as described in the specification.

ORGANIC LIGHT-EMITTING DEVICE

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Paragraph 0630; 0631; 0632; 0633, (2018/01/04)

An organic light-emitting device including a first electrode, a second electrode facing the first electrode, and an organic layer disposed between the first electrode and the second electrode, wherein the organic layer includes an emission layer, wherein the organic layer further includes i) an organometallic compound represented by Formula 1, and ii) at least one selected from a first compound represented by Formula 51, a second compound represented by Formula 61, a third compound represented by Formula 81, and a fourth compound represented by Formula 91, wherein Formulae 1, 51, 61, 81, and 91 are the same as described in the specification.

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