Skip to Content
Merck
CN
All Photos(2)

Documents

Safety Information

932361

Sigma-Aldrich

1,3,5-Tri[(3-pyridyl)-phen-3-yl]benzene

≥99% (HPLC)

Synonym(s):

TmPyPB

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C39H27N3
CAS Number:
921205-03-0
Molecular Weight:
537.65
MDL number:
MFCD16621131
UNSPSC Code:
12352005
NACRES:
NA.23

grade

sublimed grade

Quality Level

100

description

μe ≈ 1.0 x 10-3 cm2 V−1 s−1

Assay

≥99% (HPLC)

loss

0.5% TGA, > 310 °C (weight loss)

mp

195-200 °C

transition temp

Tg >310 °C ((0.5% weight loss))

solubility

chloroform: soluble
dichloromethane: soluble

fluorescence

λem 353 nm in dichloromethane (PL)

Orbital energy

HOMO 6.75 eV 
LUMO 2.75 eV 

λ

in dichloromethane

UV absorption

λ: 254 nm Amax

SMILES string

C1(C2=CC=CC(C3=CN=CC=C3)=C2)=CC(C4=CC=CC(C5=CN=CC=C5)=C4)=CC(C6=CC=CC(C7=CN=CC=C7)=C6)=C1

InChI

1S/C39H27N3/c1-7-28(34-13-4-16-40-25-34)19-31(10-1)37-22-38(32-11-2-8-29(20-32)35-14-5-17-41-26-35)24-39(23-37)33-12-3-9-30(21-33)36-15-6-18-42-27-36/h1-27H

InChI key

CINYXYWQPZSTOT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

1,3,5-Tri[(3-pyridyl)-phen-3-yl]benzene, also known as TmPyPB, is a solution-processable electron transport / hole blocking layer (ETL / HBL) material used in organic electronics. It has a μe around 1.0 x 10-3 cm2 V−1 s−1.
1,3,5-Tri[(3-pyridyl)phen-3-yl]benzene can be employed as a component in the synthesis of luminescent materials, including organic light-emitting diodes (OLEDs) or fluorescent dyes for sensing and imaging applications. It an be used as a building block or donor material in the active layer of Organic photovoltaics (OPV) devices.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

新产品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Wei Li et al.
Angewandte Chemie (International ed. in English), 58(2), 582-586 (2018-11-21)
To date, blue dual fluorescence emission (DFE) has not been realized because of the limited choice of chemical moieties and severe geometric deformation of the DFE emitters leading to strong intramolecular charge transfer (ICT) with a large Stokes shift in
Meng Li et al.
Angewandte Chemie (International ed. in English), 57(11), 2889-2893 (2018-01-23)
Aromatic-imide-based thermally activated delayed fluorescent (TADF) enantiomers, (+)-(S,S)-CAI-Cz and (-)-(R,R)-CAI-Cz, were efficiently synthesized by introducing a chiral 1,2-diaminocyclohexane to the achiral TADF unit. The TADF enantiomers exhibited high PLQYs of up to 98 %, small ΔEST  values of 0.06 eV, as well
Huijun Liu et al.
Angewandte Chemie (International ed. in English), 57(30), 9290-9294 (2018-06-02)
Non-doped organic light-emitting diodes (OLEDs) possess merits of higher stability and easier fabrication than doped devices. However, luminescent materials with high exciton use are generally unsuitable for non-doped OLEDs because of severe emission quenching and exciton annihilation in neat films.
Hui Wang et al.
Advanced materials (Deerfield Beach, Fla.), 26(30), 5198-5204 (2014-06-07)
Thermally activated delayed fluorescence emitters with small energy gap between the triplet and singlet (ΔEST ), TXO-PhCz and TXO-TPA, have been successfully synthesized by combining a hole-transporting TPA/PhCz moiety and an electron-transporting TXO moiety. Both compounds display efficient solid-state luminescence
Wei Li et al.
Angewandte Chemie (International ed. in English), 58(33), 11301-11305 (2019-06-14)
Blue thermally activated delayed fluorescence (TADF) emitters that can simultaneously achieve high efficiency in doped and nondoped organic light-emitting diodes (OLEDs) are rarely reported. Reported here is a strategy using a tri-spiral donor for such versatile blue TADF emitters. Impressively
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service