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Pyrene, 1-(3-bromophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

918654-99-6

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918654-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918654-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,6,5 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 918654-99:
(8*9)+(7*1)+(6*8)+(5*6)+(4*5)+(3*4)+(2*9)+(1*9)=216
216 % 10 = 6
So 918654-99-6 is a valid CAS Registry Number.

918654-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-bromophenyl)pyrene

1.2 Other means of identification

Product number -
Other names 3-pyrenylbromobenzene

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:918654-99-6 SDS

918654-99-6Relevant academic research and scientific papers

Semiconducting Material Comprising a Phosphine Oxide Matrix and Metal Salt

-

, (2018/05/03)

The present invention is directed to a semiconducting material comprising: i) a compound according to formula (I) wherein R1, R2 and R3 are independently selected from C1-C30-alkyl, C3-C30 cycloalkyl, C2-C30-heteroalkyl, C6-C30-aryl, C2-C30-heteroaryl, C1-C30-alkoxy, C3-C30-cycloalkyloxy, C6-C30 aryloxy, and from structural unit having general formula E-A-, wherein—A is a C6-C30 phenylene spacer unit, and—E is an electron transporting unit that is selected from C10-C60 aryl and C6-C60 heteroaryl comprising up to 6 heteroatoms independently selected from O, S, P, Si and B and that comprises a conjugated system of at least 10 delocalized electrons, and—at least one group selected from R1, R2 and R3 has the general formula E-A-; and ii) at least one complex of a monovalent metal having formula (II) wherein—M+ is a positive metal ion bearing a single elementary charge, and each of A1, A2, A3 and A4 is independently selected from H, substituted or unsubstituted C6-C20 aryl and substituted or unsubstituted C2-C20 heteroaryl, wherein a heteroaryl ring of at least 5 ring-forming atoms of the substituted or unsubstituted C2-C20 heteroaryl comprises at least one hetero atom selected from O, S and N.

Phosphine oxide functionalized pyrenes as efficient blue light emitting multifunctional materials for organic light emitting diodes

Mallesham, Godumala,Swetha, Chidirala,Niveditha, Surukonti,Mohanty, Maneesha Esther,Babu, Nanubolu Jagadeesh,Kumar, Arunandan,Bhanuprakash, Kotamarthi,Rao, Vaidya Jayathirtha

, p. 1208 - 1224 (2015/02/19)

In a search for blue light emitting multifunctional materials, the electron transport enhancing diphenyl phosphine-oxide (Ph2PO) group has been appended to blue light emitting pyrene derivatives. This design, we observe, leads to highly efficient electron transporting blue-emitters for non-doped organic light emitting devices (OLEDs) with good film formation characteristics. The superior performance is attributed to enhanced charge transport and formation of pyrene excimers assisted by thermally activated delayed fluorescence (TADF) in the device. We report the synthesis and characterization using experimental and computational methods of six such pyrene derivatives. Although three of these derivatives show quenching of luminescence in solvents at higher concentrations, in the thin film invariably all six of them exhibit typical pyrene excimer emission. X-ray crystal analysis reveals π-π stacking and the C-H...O interactions in the solid due to the PO group. The measured electron mobilities for all the compounds are higher in comparison to the standard electron transport material, Alq3. Non-doped OLEDs with the pyrene derivatives as emitters (multi-layer configuration) as well as electron transport cum emitters (bilayer configuration) exhibit excellent efficiencies. The derivatives as emitters display a performance with current efficiencies (ηc) in the range 21.1-30.1 cd A-1, power efficiencies (ηp) 11.0-15.76 lm W-1, external quantum efficiencies (EQE) 7.2-9.1% and brightness 28500-42750 cd m-2. In addition, the derivatives as electron transporting emitters demonstrate very good external quantum efficiencies in the range of 3.0-4.0%. These results demonstrate a successful strategy to obtain blue light emitting multifunctional materials for OLED applications.

INDENOTRIPHENYLENE DERIVATIVES AND ORGANIC LIGHT EMITTING DEVICE USING THE SAME

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, (2014/05/20)

The present invention discloses a new indenotriphenylene derivatives and organic light emitting device using the derivatives. The organic light emitting device employing new indenotriphenylene derivatives as host material can lower driving voltage, prolong half-lifetime, increasing efficiency. The new indenotriphenylene derivatives are represented by the following formula (A): Wherein A1, A2 are substituted or unsubstituted fused ring hydrocarbon units with one to five rings. Preferably A1, A2 are phenyl group, naphthyl group, anthracenyl group, pyrenyl group, chrysenyl group. Perylenyl group. R1 to R4 are identical or different. R1 to R4 are independently selected from the group consisting of a hydrogen atom, a halide, alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 30 carbon atoms, a substituted or unsubstituted heteroaryl group having 6 to 30 carbon atoms. X is selected from carbon atom or nitrogen atom.

PYRENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENCE DEVICE MAKING USE OF THE SAME

-

Page/Page column 41-42, (2008/06/13)

A pyrene derivative of specified structure; and an organic electroluminescence device comprising a negative electrode and a positive electrode and, interposed therebetween, one or two or more organic thin film layers including at least a light emitting la

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