70351-89-2

Basic information

• Product Name: 2,3,6,7,10,11-Hexakis[decyloxy]triphenylene
• Synonyms: 2,3,6,7,10,11-Hexakis[decyloxy]triphenylene
• CAS NO: 70351-89-2
• Molecular Formula: C78H132O6
• Molecular Weight: 1165.87908
• Mol File: 70351-89-2.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,3,6,7,10,11-Hexakis[decyloxy]triphenylene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,6,7,10,11-Hexakis[decyloxy]triphenylene(70351-89-2)
• EPA Substance Registry System: 2,3,6,7,10,11-Hexakis[decyloxy]triphenylene(70351-89-2)

Safety Data

• Hazardous Substances Data: 70351-89-2(Hazardous Substances Data)

Usage

Molecular structure

2,3,6,7,10,11-Hexakis[decyloxy]triphenylene consists of six decyloxy (C10H21O) groups attached to a central triphenylene core.

Type of compound

It is a complex chemical compound.

Family

It is a member of the triphenylene family.

Type of hydrocarbon

It is a polycyclic aromatic hydrocarbon.

Known for

Triphenylene compounds are known for their rigid and planar structures.

Enhanced properties

The addition of decyloxy groups to the triphenylene core enhances its solubility and processability.

Applications

2,3,6,7,10,11-Hexakis[decyloxy]triphenylene is useful in various organic electronic applications such as organic semiconductors and liquid crystal materials.

Suitability

The specific arrangement of the decyloxy groups and the rigid core of the molecule make it suitable for use in the fabrication of organic light-emitting diodes, organic field-effect transistors, and other optoelectronic devices.

Versatility

2,3,6,7,10,11-Hexakis[decyloxy]triphenylene is a versatile compound with potential applications in the field of organic electronics.

Upstream product

• 25934-47-8 1,2-bis-decyloxy-benzene 
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• 120-80-9 benzene-1,2-diol 

Relevant articles and documents

Oxidative cyclotrimerization of unsaturated compounds with DDQ and triflic acid: An efficient synthetic route to triply-fused benzene rings

Intermolecular oxidative cyclotrimerization reactions of alkenes and aromatic compounds with DDQ and trifluoromethanesulfonic acid are described. Scholl-type oxidation reactions involving alkenes have not previously been demonstrated. Moreover, the DDQ/acid system has never been used for intermolecular oxidative cyclization reactions. This convenient, metal-free reagent system (DDQ/TfOH) is advantageous with respect to metal-based Scholl-type oxidants because it eliminates the possibility of halogenation of aromatic compounds as a competing side reaction.

Synthesis and specific features of mesomorphic behavior of new polysubstituted triphenylenes

Previously unknown 2,3,6,7,10,11-hexakis(dodecyloxy)triphenylene and -(tetradecyloxy)triphenylene were synthesized. The structures of the synthesized compounds were proved by elemental analysis and spectral methods. Polymesomorphism was found for the first time and studied for substances of the hexaalkoxytriphenylene homologic series, as well as liotropic mesomorphism in a series of organic solvents.

Synthesis and investigation of polysubstituted triphenylenes with a predictable type of mesomorphism

This paper reports on synthesis and investigation of columnar mesophases of the new members of the homologous series of nitro and amino derivatives of hexaalkoxytriphenylenes, whose mesomorphism was predicted earlier. The forecast is in good agreement with the experimental data. The effect of the introduction of the donor and acceptor groups into the central fragment of triphenylene on the phase transition temperature, texture, and range of existence of columnar mesophases is examined. The predicting ability of the molecular parameters suggested previously for the series under analysis is discussed. It is found that introduction of a nitro group, which is a strong electron acceptor, into the central fragment of triphenylene lowers the melting temperature of the compound versus its analog and does not promote columnar mesomorphism in the lower nonmesomorphous homologs. At the same time, this slightly expands the range of existence of the mesophase in higher homologs.