Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

Safety Information

792144

Sigma-Aldrich

6,12-Bis(2,4,6-trimethylphenyl)indeno[1,2-b]fluorene

97% (HPLC)

Synonym(s):

6,12-Dimesitylindeno[1,2-b]fluorene

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C38H32
CAS Number:
1374154-86-5
Molecular Weight:
488.66
UNSPSC Code:
12352103
PubChem Substance ID:
329768315

Assay

97% (HPLC)

form

powder

Orbital energy

HOMO -5.78 eV 
LUMO -3.56 eV 

SMILES string

CC(C=C1C)=CC(C)=C1C2=C3C(C=CC=C3)=C(C2=C4)C=C5C4=C(C=CC=C6)C6=C5C7=C(C)C=C(C)C=C7C

InChI

1S/C38H32/c1-21-15-23(3)35(24(4)16-21)37-29-13-9-7-11-27(29)31-20-34-32(19-33(31)37)28-12-8-10-14-30(28)38(34)36-25(5)17-22(2)18-26(36)6/h7-20H,1-6H3

InChI key

RVYZMPWWAUBURT-UHFFFAOYSA-N

General description

6,12-Bis(2,4,6-trimethylphenyl)indeno[1,2-b]fluorene is a conjugated polycyclic hydrocarbon which has indeno[1,2-b]fluorene as the skeleton. It has a 6−5−6−5−6 fused ring system with small band gap absorption and biradicaloid properties. It can be potentially used in organic electronics based applications.

Application

6,12-Bis(2,4,6-trimethylphenyl)indeno[1,2-b]fluorene can be potentially used in the fabrication of ambipolar semiconductors, organic light emitting diodes (OLEDs), organic field effect transistors (OFETs), and organic photovoltaic (OPV) devices.
n-type electron-accepting organic semiconductor for Organic Field Effect Transistor (OFET) applications

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

792144-VAR:
792144-BULK:
792144-1G:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support.

Already Own This Product?

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

Visit the Document Library

Isomeric indacenedibenzothiophenes: synthesis, photoelectric properties and ambipolar semiconductivity.
Ren L, et al.
Journal of Material Chemistry C, 4(23), 5202-5206 (2016)
Toward tetraradicaloid: The effect of fusion mode on radical character and chemical reactivity.
Hu P, et al.
Journal of the American Chemical Society, 138(3), 1065-1077 (2016)
Indeno [1, 2-b] fluorenes: Fully Conjugated Antiaromatic Analogues of Acenes.
Chase DT, et al.
Angewandte Chemie (International Edition in English), 123(5), 1159-1162 (2011)
Daniel T Chase et al.
Journal of the American Chemical Society, 134(25), 10349-10352 (2012-06-16)
Herein we report the synthesis and characterization of a series of 6,12-diarylindeno[1,2-b]fluorenes (IFs). Functionalization with electron donor and acceptor groups influences the ability of the IF scaffold to undergo two-electron oxidation and reduction to yield the corresponding 18- and 22-π-electron
Electron-accepting 6, 12-diethynylindeno [1, 2-b] fluorenes: synthesis, crystal structures, and photophysical properties.
Chase DT, et al.
Angewandte Chemie (International Edition in English), 50(47), 11103-11106 (2011)

Articles

Soluble Pentacene Precursors

Fabrication procedure of organic field effect transistor device using a soluble pentacene precursor.

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