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76727-11-2

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76727-11-2 Usage

Description

6,13-diphenylpentacene is an organic compound that possesses unique electronic properties, making it a versatile material for various applications in the field of organic electronics.

Uses

Used in Organic Solar Cells:
6,13-diphenylpentacene is used as a small molecule electron donor or p-type semiconductor in solution-processed organic solar cells. Its ability to efficiently transport charge and absorb light makes it a promising candidate for improving the performance and efficiency of solar cells.
Used in Organic Light Emitting Diodes (OLEDs):
In the display industry, 6,13-diphenylpentacene is used as a red-emitting dopant in organic light-emitting diodes (OLEDs). Its high photoluminescence efficiency and excellent color purity contribute to the development of high-quality and energy-efficient OLED displays.
Used in Organic Thin Film Transistors (OTFTs):
6,13-diphenylpentacene is also utilized as a high mobility charge transport material in organic thin-film transistors (OTFTs). Its high charge carrier mobility and stability make it suitable for various electronic applications, including sensors, flexible electronics, and integrated circuits.

Check Digit Verification of cas no

The CAS Registry Mumber 76727-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,2 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76727-11:
(7*7)+(6*6)+(5*7)+(4*2)+(3*7)+(2*1)+(1*1)=152
152 % 10 = 2
So 76727-11-2 is a valid CAS Registry Number.

76727-11-2 Well-known Company Product Price

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  • Aldrich

  • (760641)  6,13-Diphenylpentacene  98%

  • 76727-11-2

  • 760641-1G

  • 3,363.75CNY

  • Detail

76727-11-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,13-diphenylpentacene

1.2 Other means of identification

Product number -
Other names 6,13-diphenylpentancene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76727-11-2 SDS

76727-11-2Relevant articles and documents

Organization of acenes with a cruciform assembly motif

Miao, Qian,Chi, Xiaoliu,Xiao, Shengxiong,Zeis, Roswitha,Lefenfeld, Michael,Siegrist, Theo,Steigerwald, Michael L.,Nuckolls, Colin

, p. 1340 - 1345 (2006)

This study explores the assembly in the crystalline state of a class of pentacenes that are substituted along their long edges with aromatic rings forming rigid, cruciform molecules. The crystals were grown from the gas phase, and their structures were co

Exciton Isolation in Cross-Pentacene Architecture

Lijina,Benny, Alfy,Ramakrishnan, Remya,Nair, Nanditha G.,Hariharan, Mahesh

, p. 17393 - 17402 (2020)

Null aggregates are an elusive, emergent class of molecular assembly categorized as spectroscopically uncoupled molecules. Orthogonally stacked chromophoric arrays are considered as a highlighted architecture for null aggregates. Herein, we unveil the nul

Substituent effects in pentacenes: Gaining control over HOMO-LUMO gaps and photooxidative resistances

Kaur, Irvinder,Jia, Wenling,Kopreski, Ryan P.,Selvarasah, Selvapraba,Dokmeci, Mehmet R.,Pramanik, Chandrani,McGruer, Nicol E.,Miller, Glen P.

supporting information; experimental part, p. 16274 - 16286 (2009/05/08)

A combined experimental and computational study of a series of substituted pentacenes including halogenated, phenylated, silylethynylated and thiolated derivatives is presented. Experimental studies include the synthesis and characterization of six new and six known pentacene derivatives and a kinetic study of each derivative under identical photooxidative conditions. Structures, HOMO-LUMO energies and associated gaps were calculated at the B3LYP/6-311+G**//PM3 level while optical and electrochemical HOMO-LUMO gaps were measured experimentally. The combined results provide for the first time a quantitative assessment of HOMO-LUMO gaps and photooxidative resistances for a large series of pentacene derivatives as a function of substituents. The persistence of each pentacene derivative is impacted by a combination of steric resistance and electronic effects as well as the positional location of each substituent. Silylethynyl-substituted pentacenes like TIPS-pentacene possess small HOMO-LUMO gaps but are not the longest lived species under photooxidative conditions, contrary to popular perception. A pentacene derivative with both chlorine substituents in the 2,3,9,10 positions and o-alkylphenyl substituents in the 6,13 positions is longer lived than TIPS-pentacene. Of all the derivatives studied, alkylthio- and arylthio-substituted pentacenes are most resistant to photooxidation, possess relatively small HOMO-LUMO gaps and are highly soluble in a variety of organic solvents. These results have broad implications for the field of organic molecular electronics where OFET, OLED, and other applications can benefit from highly persistent, solution processable pentacene derivatives.

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