188-73-8

Basic information

• Product Name: QUATERRYLENE
• Synonyms: QUATERRYLENE;4,5,6-c'd')diperylene;Benzo(1,2,3-cd;Benzo[10,5]anthra[9,1,2-cde]dibenzo[kl,rst]pentaphene;Benzo(1,2,3-cd:4,5,6-C'D')diperylene
• CAS NO: 188-73-8
• Molecular Formula: C40H20
• Molecular Weight: 500.59
• Mol File: 188-73-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.467±0.06 g/cm3(lit.)
• Refractive Index: 2.111
• CAS DataBase Reference: QUATERRYLENE(CAS DataBase Reference)
• NIST Chemistry Reference: QUATERRYLENE(188-73-8)
• EPA Substance Registry System: QUATERRYLENE(188-73-8)

Safety Data

• Hazardous Substances Data: 188-73-8(Hazardous Substances Data)

Usage

Description

QUATERRYLENE, a promising candidate for organic electronic applications, is characterized by its ability to absorb a broad spectrum of UV and visible light. It is known for its excellent thermal and oxidative stability, as well as a low HOMO-LUMO band gap, making it a versatile material for various applications.

Uses

Used in Organic Electronics:
QUATERRYLENE is used as a key component in organic electronics for its ability to absorb a broad spectrum of UV and visible light, contributing to improved performance and efficiency in electronic devices.
Used in Photovoltaic Components:
In the photovoltaic industry, QUATERRYLENE is used as a material for solar cells due to its light absorption properties and thermal stability, which can enhance the efficiency and durability of solar panels.
Used in Graphene Nanoribbons:
QUATERRYLENE is utilized as a component in the development of graphene nanoribbons, taking advantage of its thermal and oxidative stability to create high-performance nanomaterials for various applications.
Used in Electroactive Polymers:
The material is also used as a constituent in electroactive polymers, where its light absorption and stability properties contribute to the development of advanced materials for use in sensors, actuators, and other electronic devices.

InChI:InChI=1/C40H20/c1-5-21-6-2-10-24-28-14-18-32-34-20-16-30-26-12-4-8-22-7-3-11-25(36(22)26)29-15-19-33(40(34)38(29)30)31-17-13-27(37(28)39(31)32)23(9-1)35(21)24/h1-20H

Upstream product

• 198-55-0 PERYLENE 
• 126822-84-2 2,5,12,15-Tetra-tert-butylquaterrylen 

Related news

Growth and structural characterization of molecular superlattice of QUATERRYLENE (cas 188-73-8) and N,N′-dioctyl-3,4,9,10-perylenedicarboximide09/30/2019

A molecular superlattice consisting of alternate layers of N,N′-dioctyl-3,4,9,10-perylenedicarboximide (PTCDI-C 8 ) and quaterrylene was prepared by using an ultra-slow deposition technique. Film growth under equilibrium conditions with precise optimization of the substrate temperature ...detailed

Impact of surface modification by addition of self-assembled monolayer for carrier transport of QUATERRYLENE (cas 188-73-8) thin films09/29/2019

Quaterrylene field-effect transistors (FETs) were formed on a silicon oxide (SiO 2 ) layer and on an octadecyltrichlorosilane self-assembled monolayer (OTS-SAM). To elucidate the transport mechanisms in the respective devices, we examined the dependence of carrier mobility on film thickn...detailed

Ambipolar carrier transport in hetero-layered organic transistors consisting of QUATERRYLENE (cas 188-73-8) and N,N′-dioctyl-3,4,9,10-perylenedicarboximide09/28/2019

We examined the transistor properties of an N,N′-dioctyl-3,4,9,10-perylenedicarboximide (PTCDI-C 8 )/quaterrylene (QT) heteromolecular layer, in which the highly ordered molecular layers were stacked on the monolayer level. Ambipolar behavior was clearly observed when behaving as a fiel...detailed

Relevant articles and documents

Synthesis of Polycyclic Aromatic Hydrocarbons

The present invention relates to the synthesis of polycyclic aromatic compounds. Compounds such as terrylene or quaterrylene may now be prepared in relatively high yield by reaction of naphthalene or perylene via Scholl-type coupling in the presence of a superacid and an oxidant in an inert solvent.

Oligorylene als Modelle fuer "Poly(peri-naphthalin)"

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