1065-80-1

Usage

Uses

Used in Organic Electronic Materials:
Hexabenzo[a,d,g,j,m,p]coronene is utilized as a key component in organic electronic materials due to its excellent thermal and chemical stability, as well as its highly conjugated structure. This makes it suitable for enhancing the performance and reliability of electronic devices.
Used in Semiconductors:
In the semiconductor industry, Hexabenzo[a,d,g,j,m,p]coronene is employed as a material with potential applications in the development of advanced semiconductor devices. Its unique properties contribute to improving the efficiency and performance of these devices.
Used in Molecular Electronics and Optoelectronic Devices:
Hexabenzo[a,d,g,j,m,p]coronene is used as a promising candidate in molecular electronics and optoelectronic devices owing to its strong fluorescence and highly conjugated structure. This allows for its potential use in creating innovative devices with improved functionality and efficiency.
Used in Organic Light-Emitting Diodes (OLEDs):
In the field of organic light-emitting diodes, Hexabenzo[a,d,g,j,m,p]coronene is employed for its strong fluorescence properties, which can be harnessed to improve the brightness, color, and efficiency of OLEDs.
Used in Organic Photovoltaics:
Hexabenzo[a,d,g,j,m,p]coronene is also studied for its potential use in organic photovoltaics, where its unique properties can contribute to the development of more efficient and cost-effective solar cells.
Used as a Model for Studying Larger Polycyclic Aromatic Hydrocarbons:
Furthermore, Hexabenzo[a,d,g,j,m,p]coronene serves as an important model compound for studying the properties and behavior of larger polycyclic aromatic hydrocarbons, aiding in the understanding of their structure-property relationships and potential applications in various industries.

InChI:InChI=1/C48H24/c1-2-14-26-25(13-1)37-27-15-3-4-16-28(27)39-31-19-7-8-20-32(31)41-34-22-10-12-24-36(34)42-35-23-11-9-21-33(35)40-30-18-6-5-17-29(30)38(26)44-43(37)45(39)47(41)48(42)46(40)44/h1-24H

Upstream product

• 16322-10-4 3,5-di(2-biphenylyl)-o-terphenyl 
• 954097-67-7 6,13-bis(diphenylmethylidene)-6,13-dihydropentacene 
• 1643-10-3 5,7,12,14-Tetraphenyl-5,7,12,14-tetrahydroxy-5,7,12,14-tetrahydro-6,13-dimethyl-pentacen 

Relevant academic research and scientific papers

Polysubstituted Hexa-cata-hexabenzocoronenes: Syntheses, Characterization, and Their Potential as Semiconducting Materials in Transistor Applications

A series of tetra- and octa-substituted hexa-cata-hexabenzocoronenes (cata-HBCs) were synthesized from tetraryl olefins via iodine- and iron chloride-catalyzed oxidative cyclodehydrogenation reactions. The substitutions on the periphery of the parent HBC serve to modify the photophysical properties, highest occupied molecular orbital-lowest unoccupied molecular orbital gaps, and thermal stabilities of the respective derivatives. The crystal structures were determined to display multiple twists in the framework, resulting in different packing motifs depending on the position, type, and number of functional groups on the hexabenzocoronene framework. Nearly perfect co-facial packing to marginally or extensively shifted co-facial stacks were obtained due to substitution. The single crystals of parent HBC were used to fabricate single-crystal field-effect transistors, from which the highest p-channel mobility of 0.51 cm2 V-1 s-1 was measured. Thin-film transistors of selected HBCs were also prepared, and 0.61 cm2 V-1 s-1 was obtained for MeHBC-2. These results attest the potential of these materials as semiconducting materials.

Triple condensation of aryl methyl ketones catalyzed by amine and trifluoroacetic acid: Straightforward access to 1,3,5-triarylbenzenes under mild conditions

An efficient triple condensation reaction of aryl methyl ketones catalyzed by ethylenediamine and trifluoroacetic acid was reported. A broad scope of 1,3,5-triarylbenzenes was obtained in good to excellent yields. The reaction provides a novel and practical approach to access organic materials of polycyclic aromatic hydrocarbons under mild conditions.

Molecular wires from contorted aromatic compounds

(Figure Presented) In a twist: A design strategy for molecule-based electronic materials using aromatic compounds with a nonplanar core is presented. A new class of hexabenzocoronene is put forth that has its core severely distorted out of planarity into a corrugated structure. When substituted with four alkoxy side chains, this material self-assembles into infinitely long columns through stacking (see picture) and acts as an active layer in field-effect transistors.