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9-(4-((2-ethylhexyl)oxy)phenyl)-9H-carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

946491-60-7

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946491-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 946491-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,6,4,9 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 946491-60:
(8*9)+(7*4)+(6*6)+(5*4)+(4*9)+(3*1)+(2*6)+(1*0)=207
207 % 10 = 7
So 946491-60-7 is a valid CAS Registry Number.

946491-60-7Relevant academic research and scientific papers

Architectural influence of carbazole push-pull-pull dyes on dye sensitized solar cells

Keerthi, Ashok,Sriramulu, Deepa,Liu, Yeru,Yuan Timothy, Chan Thuang,Wang, Qing,Valiyaveettil, Suresh

, p. 787 - 797 (2013)

Abstract Herein we report design, synthesis, characterization and application of a series of molecules with D-π-A structures that contain a push-pull-pull with substituted carbazole as the electron donor and cyanoacrylic acid as the electron acceptor bridged by a benzothiadiazole fragment. Theoretical, electrochemical and photophysical properties of the target molecules with respect to the chemical nature and position of substituent on the carbazole moiety were investigated in detail. The substituents on carbazole changed the solubility, packing and orientation of molecules on the TiO 2 surface of DSSCs. The dye sensitized solar cell performances of the molecules were studied and compared with respect to the position and substituent.

Synthesis and characterization of hole transporting materials containing bis(carbazole) groups for solid-state dye-sensitized solar cells

Jung, Suran,Kwon, Younghwan

, (2021/10/21)

In this study, bis(carbazole) derivatives, such as bis[N-(2-ethylhexyl)-carbazole-3-yl] (HTM_I) and bis[N-(2-ethylhexyloxylphenyl)-carbazole-3-yl] (HTM_II), were successfully synthesized for use as small-molecule organic hole-transporting materials (HTMs)

Red iridium coordination compound and preparation method thereof

-

Paragraph 0043; 0045, (2017/01/12)

The invention relates to a red iridium coordination compound and a preparation method thereof. The coordination compound consists of a main ligand of phenylquinoline-carbazole and an auxiliary ligand of modified phenylpyridine, wherein the phenylquinoline

Distinct phosphorescence enhancement of red-emitting iridium(III) complexes with formyl-functionalized phenylpyridine ligands

Cao, Sizhen,Hao, Lin,Lai, Wen-Yong,Zhang, Hao,Yu, Zhou,Zhang, Xinwen,Liu, Xu,Huang, Wei

, p. 4709 - 4718 (2016/06/09)

A new highly efficient red-emitting Ir(iii) complex, bis [9-(4-(2-ethylhexyloxy)phenyl)-3-(4-phenylquinolin-2-yl)-9H-carbazole] [3-(pyridin-2-yl) benzaldehyde]iridium(iii) (Ir-CHO), has been synthesized and characterized to investigate the impact of the e

Synthesis and characterization of poly(N-arylcarbazole-alt-aniline) copolymers as Blue-emitting host matrix for polymer light-emitting diodes

Wang, Hui,Ryu, Jeong-Tak,Han, Yoon Soo,Kim, Dae-Hwan,Choi, Byeong Dae,Park, Lee Soon,Teng, Dayong,Kwon, Younghwan

, p. 95/[375]-107/[387] (2007/10/03)

Thermally stable and solution-processable poly(N-arylcarbazole-alt-aniline) copolymers with high structural integrity were synthesized in good yields via palladium-catalyzed polycondensation of aniline with corresponding N-arylcarbazole monomers such as N-(2-ethylhexyloxyphenyl)-3,6-dibromocarbazole, bis[6-bromo-N-(2-ethylhexyloxyphenyl)carbazole-3-yl] and N-(4-(2-ethylhexyl)-3, 5-dibromomethylene-phenyl)carbazole, respectively. The optical and electrochemical properties of these copolymers were measured and compared with those of poly(N-alkylcarbazole-alt-aniline) copolymer. All synthesized poly(N-arylcarbazole-alt-aniline) copolymers showed maximum UV-Vis absorption peaks at around 300 nm in THF solution, and exhibited maximum photoluminescence peaks in the blue emission range from 430 to 460 nm. It was also found that poly(N-arylcarbazole-alt-aniline) copolymers had wider band gap energy than poly(N-alkylcarbazole-alt-aniline) copolymer.

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