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Indolo[3,2,1-jk]carbazole is a heterocyclic organic compound with a unique tricyclic structure, consisting of a carbazole fused to an indole ring. Indolo[3,2,1-jk]carbazole is known for its potential applications in various fields, such as pharmaceuticals, materials science, and organic synthesis. It exhibits interesting chemical properties, including a high degree of aromaticity and stability, which make it a subject of interest for researchers. The synthesis of indolo[3,2,1-jk]carbazole can be achieved through various methods, such as the Pictet-Spengler reaction and the Fischer indole synthesis, and it has been found to possess a range of biological activities, including anticancer and anti-inflammatory properties. The study of indolo[3,2,1-jk]carbazole and its derivatives continues to be an active area of research, with potential implications for the development of new drugs and materials.

205-95-8

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205-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 205-95-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,0 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 205-95:
(5*2)+(4*0)+(3*5)+(2*9)+(1*5)=48
48 % 10 = 8
So 205-95-8 is a valid CAS Registry Number.

205-95-8Related news

Indolo[3,2,1-jk]carbazole based planarized CBP derivatives as host materials for PhOLEDs with low efficiency roll-off09/28/2019

Three novel planarized CPB derivatives (ICzCz, ICzPCz, ICzICz) have been synthesized and characterized concerning applications as host materials for PhOLEDs. The incorporation of fully planar indolo[3,2,1-jk]carbazole (ICz) in the CBP scaffold has been systematically investigated, revealing a si...detailed

205-95-8Relevant academic research and scientific papers

Composition For Capping Layer of Organic Light Emitting Diode and Organic Light Emitting Diode Having The Same

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, (2021/02/16)

The present invention relates to an organic electroluminescent device, and more particularly, to an indolocarbazole derivative compound used as a material for a capping layer (CPL) of the organic electroluminescent device. More specifically, the present invention relates to an indolocarbazole derivative compound having an amine substituent, a composition for the CPL of the organic electroluminescent device comprising the same, and the organic electroluminescent device comprising the same.

Impact of the donor structure in new D-π-A systems based on indolo[3,2,1-jk]carbazoles on their thermal, electrochemical, optoelectronic and luminescence properties

Goriachiy, Dmitry,Ma?kowski, Sebastian,Schab-Balcerzak, Ewa,Siwy, Mariola,Slodek, Aneta,Sulowska, Karolina,Szafraniec-Gorol, Gra?yna,Taydakov, Ilya,Vasylieva, Marharyta,Zych, Dawid

, p. 7351 - 7362 (2021/06/22)

In this work, novel fluorophores with D-π-A architectures (ICz-1-ICz-6) were synthesized and investigated, where the indolo[3,2,1-jk]carbazole (ICz) framework is connected by an ethylene bridge with extensive donor moieties -e.g., fluorene, carbazole, phenothiazine, methoxyphenyl, bithiophene, and dibenzothiophene. The influences of the donor character of the substituents in the indolocarbazole derivatives on their thermal, optical and electrochemical properties were explored and compared with the quantum chemical calculations based on DFT and TD-DFT. AllICz-1-ICz-6compounds emit blue light with emission peaks between 390 and 430 nm in solution, except for compoundICz-5with a strong phenothiazine donor, which emits light at 463 nm. TheICz-6derivative with the dibenzothiophene unit features an exception to Kasha's rule. For the selected compoundsICz-2,ICz-4, andICz-5, preliminary electroluminescence tests were performed, both based on devices with a neat compound (ITO/PEDOT:PSS/ICz/Al) and with a guest-host configuration (ITO/PEDOT:PSS/PVK:PBD:ICz/Al), where two emission bands were detected covering the range from 400 to over 900 nm. Additionally, several multilayer OLED devices (ITO/PEDOT:PSS/poly-TPD/ICz-2-5/TPBi/LiF/Al) were prepared, and all diodes showed electroluminescence at 570 nm.

Efficient organic light-emitting diodes based on iridium(iii) complexes containing indolo[3,2,1-jk]carbazole derivatives with narrow emission bandwidths and low efficiency roll-offs

Liao, Xiang-Ji,Lu, Jun-Jian,Luo, Xu-Feng,Yan, Zhi-Ping,Yuan, Li,Zhang, Yi-Pin,Zheng, You-Xuan,Zhu, Jin-Jun

, p. 8226 - 8232 (2021/07/13)

In this work, two cyclometalated ligands 2-(pyridin-2-yl)indolo[3,2,1-jk]carbazole (pyidcz) and 2-(4-(trifluoromethyl)pyridin-2-yl)indolo[3,2,1-jk]carbazole (tfpyidcz) containing an indolo[3,2,1-jk]carbazole unit were synthesized for achieving highly efficient iridium(iii) complexes (pyidcz)2Ir(tmd) and (tfpyidcz)2Ir(tmd) (tmd = 2,2,6,6-tetramethyl-3,5-heptanedione). The two Ir(iii) complexes exhibit emissions peaking at 499 and 554 nm, respectively, with narrow full width at half maximum (FWHM) values of 35 and 53 nm, respectively, short phosphorescence lifetimes less than 1 μs and high photoluminescence quantum yields of up to 90% in CH2Cl2solution. The organic light-emitting diodes (OLEDs) with (pyidcz)2Ir(tmd) and (tfpyidcz)2Ir(tmd) emitters show good performances. The (pyidcz)2Ir(tmd)-based device shows a turn-on voltage (Von) of 3.6 V with a maximum brightness (Lmax) of 39123 cd m?2, a maximum current efficiency (ηc,max) of 69.2 cd A?1, a maximum power efficiency (ηp,max) of 36.8 lm W?1and a maximum external quantum efficiency (EQEmax) of 21.2%. In particular, the FWHM bandwidth of the electroluminescence spectrum is only 33 nm, which was rarely reported for Ir(iii) complex-based OLEDs. The performance of the (tfpyidcz)2Ir(tmd)-based device is slightly better with aVonof 3.3 V, aLmaxof 31714 cd m?2, aηc,maxof 78.4 cd A?1, aηp,maxof 54.7 lm W?1and an EQEmaxof 24.0%. Furthermore, the efficiency roll-offs of both devices are small, and theηcvalues at 10?000 cd m?2brightness are still maintained at 60.0 and 71.4 cd A?1, respectively, which provide a powerful reference for developing indolo[3,2,1-jk]carbazole-based Ir(iii) complexes for efficient OLEDs.

Novel indolo[3,2,1-jk]carbazole-based bipolar host material for highly efficient thermally activated delayed-fluorescence organic light-emitting diodes

Hiraga, Yasuhide,Kuwahara, Rempei,Hatta, Taizo

, (2021/07/28)

A novel bipolar material (ICzPyr) composed of electron-donating indolo[3,2,1-jk]carbazole and electron-withdrawing pyridmidine was developed and its use as a host material in thermally activated delayed-fluorescence (TADF) organic light-emitting diode (OL

Organic Light Emitting Material and Organic Light Emitting Diode Having The Same

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, (2021/11/02)

The present invention relates to a compound derivative for an organic electroluminescent device and an organic electroluminescent device using the same. The present invention relates to an aromatic compound including an indolocarbazolyl group and a spirobifluorenyl group, and more particularly, to an aromatic compound including an indolocarbazolyl group and a spirobifluorenyl group.

Organic Light Emitting Material and Organic Light Emitting Diode Having The Same

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, (2020/09/16)

The present invention relates to a compound derivative used in an organic electroluminescent device, and an organic electroluminescent device using the same. More particularly, the present invention relates to an indolocarbazole derivative compound having an amine substituent. When using the indolocarbazole derivative compound as a light emitting material for an organic layer of an organic electroluminescent device, an effect of deriving high luminous efficiency even with a low driving voltage can be provided.(AA) Negative electrode(BB) Electron injection layer(CC) Electron transport layer 2(DD) Electron transport layer 1(EE) Light emission layer(FF) Electron suppression layer(GG) Hole transport layer(HH) Hole injection layer(II) Positive electrode(JJ) SubstrateCOPYRIGHT KIPO 2021

Indolo[3, 2, 1-jk]carbazole derivative, preparation method and application thereof, and electronic device

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, (2019/10/04)

The invention relates to an indolo[3, 2, 1-jk]carbazole derivative, a preparation method and application thereof, and an electronic device. The indolo[3, 2, 1-jk]carbazole derivative has a hole mobility up to 6.5*10cmVS, also can be applied as a hole transport material in solar cell devices, and can effectively inhibit energy consumption and improve the energy conversion efficiency, device life, electric current density, filling factor, threshold voltage and other performance of solar cell devices.

COMPOUND AND ORGANIC ELECTRONIC DEVICE COMPRISING THE SAME

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Paragraph 0289-0292, (2018/05/03)

The present invention relates to compounds represented by chemical formula I, and organic electronic devices comprising the same. The compound according to one embodiment of the present invention is used in an organic electronic device including an organic light emitting device, to lower the driving voltage of the organic electronic device, improve the light efficiency, and improve the lifetime characteristics of the device by the thermal stability of the compound.COPYRIGHT KIPO 2018

Delay fluorescent compound and using the same and display device having the organic light-emitting diode (by machine translation)

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, (2016/10/09)

The present invention relates to delay fluorescent compound and the use of the compound of the organic light-emitting diode and the display device. Fluorescent compounds of the present invention is shown as delay 1 is shown, wherein n is 1 or 0, A is selected from the following formula 2, D is selected from the following formula 3, L 1 and L 2 each independently is selected from the following formula 4, wherein type 2 of in R 1 is selected from hydrogen or phenyl, X, Y and Z each independently selected from the group consisting of carbon and nitrogen, and the X, Y and Z for at least two of the nitrogen, type 4 of in R 2 is selected from hydrogen or C1-C10 alkyl. (by machine translation)

DELAYED FLUORESCENCE COMPOUND, AND ORGANIC LIGHT EMITTING DIODE AND DISPLAY DEVICE USING THE SAME

-

, (2016/10/09)

Discussed is a delayed fluorescence compound including a first electron donor moiety of indolo-[3,2,1-j,k]carbazole; a second electron donor moiety selected from indolo-[3,2,1-j,k]carbazole, carbazole or triphenylamine; and an electron acceptor moiety selected from dibenzothiophene sulfone or diphenyl sulfone, wherein the first and second electron donor moieties are combined to the electron acceptor moiety, and the electron acceptor moiety is combined to a first position or a para-position of the first electron donor moiety.

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