57103-21-6

Usage

Uses

Used in Organic Semiconductors:
3,6-Diiodo-9-phenyl-9H-carbazole is used as a key component in the synthesis of organic semiconductors for its ability to enhance the performance of these materials. Its unique structure contributes to improved charge transport and stability, making it suitable for various electronic applications.
Used in Photovoltaic Devices:
In the photovoltaic industry, 3,6-Diiodo-9-phenyl-9H-carbazole is utilized as a component in solar cells to improve their efficiency and durability. Its incorporation into the active layer of these devices can lead to better light absorption and charge separation, resulting in higher power conversion efficiencies.
Used in Medicinal Chemistry:
3,6-Diiodo-9-phenyl-9H-carbazole is employed as a starting material or intermediate in the synthesis of pharmaceutical compounds due to its interesting biological activities. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications in various medical fields.
Used in Optoelectronic Devices:
In the optoelectronics industry, 3,6-Diiodo-9-phenyl-9H-carbazole is used as a building block for the development of advanced materials with specific optical and electronic properties. Its incorporation into these devices can lead to improved performance, such as enhanced light emission or sensing capabilities.

Upstream product

• 1150-62-5 N-phenylcarbazole 
• 57103-20-5 3,6-dibromo-9-phenyl-9H-carbazole 
• 86-74-8 9H-carbazole 
• 591-50-4 iodobenzene 

Downstream Products

• 180507-24-8 N-phenylcarbazole-3,6-bis-[N,N,N'-tris-(trimethylsilyl)-carboxamidine] 
• 1092807-67-4 C₅₀H₄₃N₃O₄ 
• 1026033-48-6 3-(6-iodo-9-phenyl)carbazolyldiphenylamine 
• 211685-96-0 3,6-di(9H-carbazol-9-yl)-9-phenyl-9H-carbazole 
• 1401068-29-8 C₃₁H₂₀N₄ 
• 1401068-30-1 C₃₁H₁₉IN₄ 
• 1401067-94-4 C₄₄H₂₇N₇ 
• 918137-86-7 (9,9'-diphenyl-9H,9'H-[3,3'-biscarbazol]-6-yl)boronic acid 

Relevant academic research and scientific papers

Synthesis, crystal structures, and nonlinear optic and thermal properties of two diiodocarbazole derivatives

Two 3,6-diiodocarbazole derivatives were prepared from the iodination of the corresponding phenylcarbazole. 3,6-Diiodo-9-phenylcarbazole crystallises in the chiral space group P21 and shows good second-harmonic generation effects. Thermogravime

Heterocyclic compound and organic electroluminescence device including the same

Provided is a heterocyclic compound represented by Formula 1 below, and an organic electroluminescence device including the same in an emission layer. In Formula 1, X is a direct linkage or CR2R3 , Z1to Z8 are each independently CR4 or N, at least two of

Crystal structure of type-A 3,6-diiodo-N-phenylcarbazole and preparation method of crystal structure

The invention discloses a crystal structure of type-A 3,6-diiodo-N-phenylcarbazole and a preparation method of the crystal structure. The preparation method of the crystal structure comprises steps as follows: 0.1 g of 3,6-diiodo-N-phenylcarbazole is weig

3,6-Bis(indol-1-yl)-9-phenylcarbazoles as electroactive materials for electrophosphorescent diodes

Four derivatives of 3,6-bis(indol-1-yl)-9-phenylcarbazole were synthesized by Ullmann-type coupling including those having methoxy groups at the different positions. Thermal, optical and photophysical properties of the synthesized materials were studied.

N-PHENYL TRISCARBAZOLE

The present invention relates to a novel triscarbazole compound having substituent on N-phenyl, which can be represented by Formula (I). wherein R1 is selected from the group consisting of hydrogen, halogen or alkyl or alkoxy group having 1 to 20 carbon atoms wherein at least one hydrogen atom is optionally replaced by halogen; RA, RB, RC, RD and RE are any of substituents other than hydrogen wherein at least two of R1 and RA may further form a fused ring; and i, j, k, l and m are same or different at each occurrence and represent an integer from 0 to 4, with the proviso that when R1 is hydrogen, i is not 0. By introduction of the substituent on N-phenyl, the device efficiency, stability and lifetime can be increased while maintaining the solubility. These compounds can be used in various organic devices such as organic light emitting diodes, photovoltaic cells or organic semiconductor devices.

N-phenyl triscarbazole

The present invention relates to a novel triscarbazole compound having substituent on N-phenyl, which can be represented by Formula (I). wherein R1 is selected from the group consisting of halogen or alkyl or alkoxy group having 1 to 20 carbon atoms wherein one or more hydrogen atom may be replaced by halogen; RA, RB, Rc, RD and RE are any of substituents; and i, j, k, l and m are same or different at each occurrence and represent an integer from 0 to 4. By introduction of the substituent on N-phenyl, the device efficiency, stability and lifetime can be increased while maintaining the solubility. These compounds can be used in various organic devices such as organic light emitting diodes, photovoltaic cells or organic semiconductor devices.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT ELEMENT

Provided are a long-lifetime organic electroluminescence device which can be fabricated in an improved yield owing to suppressed crystallization of molecules, and an aromatic amine derivative that realizes the device, i.e. , a novel aromatic amine derivative having a specific structure. Specifically provided are an organic electroluminescence device, including an organic thin film layer formed of one or more layers including at least a light emitting layer, the organic thin film layer being interposed between a cathode and an anode, and an aromatic amine derivative for at least one layer of the organic thin film layer, in particular, a hole transporting layer, the derivative having at least one such structure that a substituent in which two or more specific heterocycles are linked to each other, in particular, a substituent in which two or more specific heterocycles are linked through an aryl group is bonded to an amine through an aryl group.

NOVEL CARBAZOLE DERIVATIVE AND USE THEREOF

The invention discloses a novel carbazole derivative which has at least two carbazole structures in the molecule, can form a stable amorphous film by itself at normal temperature or higher, has a high glass transition temperature, and can be suitably used as an organo-electronic functional material. The following compound having the formula is mentioned as a representative example.

Novel Carbazole Compound, and Polymer Thereof

The present invention provides a carbazole compound represented by the following formula (I): wherein each Ar1 independently represents a substituted or unsubstituted monovalent aromatic group or an aromatic group containing a heteroring, and R1 and each R2 independently represent a hydrogen atom, an alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted aralkyl group.

Self-assembly of silver(I) coordination polymers from AgX (X = BF 4-, ClO4-, CF3COO -, and SO3CF3-) and a rigid bent 3,6-dicyano-9-phenylcarbazole ligand: The templating effect of anions

One rigid bent bridging ligand with highly planar π-conjugated spacers, 3,6-dicyano-9-phenylcarbazole (dcphcz), was designed and synthesized. The coordination reactions of dcphcz with a series of AgI salts with different counterions has been investigated. Four coordination polymers were obtained by solution reactions and characterized by IR, elemental analysis, and single-crystal X-ray diffraction. The solid-state structures of {[Ag(dcphcz)]BF4}n (1) and {[Ag(dcphcz)]ClO 4}n (2), exhibit similar 1D "zigzag" patterns. The complex {[Ag(dcphcz)][Ag2(dcphcz)(H2O) 2](SO3CF3)3·C 6H6·(H2O)2}n (3) includes two different one-dimensional (1D) chain units: one forms double-layer two-dimensional (2D) metal-organic frameworks (MOFs) through intermolecular Ag-O-Ag bridging interactions, the other features double-layer 2D supramolecular networks through C-H...O hydrogen-bonding interactions. The complex [Ag2(dcphcz)-(CF3COO)2]n (4) features a bundle of novel nanotubular structures, which contain silver chains formed by carboxylate spacers. Furthermore, all these complexes are connected by face-to-face π...π stacking interactions between carbazolyl planes, affording a series of three-dimensional (3D) architectures with different structural geometries. The structural diversities of these complexes demonstrated that counteranions and bridging ligands play essential roles in the construction of supramolecular frameworks. In addition, the luminescence properties of the free ligand dcphcz and complexes 1-4 were investigated. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.