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Merck
CN

792624

Sigma-Aldrich

6,12-Bis(2,3,4,5,6-pentafluorophenyl)indeno[1,2-b]fluorene

95%

Synonym(s):

di-C6F5-IF

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About This Item

Empirical Formula (Hill Notation):
C32H10F10
CAS Number:
1382350-89-1
Molecular Weight:
584.41
UNSPSC Code:
12352103
PubChem Substance ID:
329768351
NACRES:
NA.23

Key Documents

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Assay

95%

form

powder

mp

380-385 °C

SMILES string

FC1=C(F)C(F)=C(F)C(F)=C1C2=C3C=CC=CC3=C4C=C5C(C6=C(F)C(F)=C(F)C(F)=C6F)=C7C=CC=CC7=C5C=C42

InChI

1S/C32H10F10/c33-23-21(24(34)28(38)31(41)27(23)37)19-13-7-3-1-5-11(13)15-9-18-16(10-17(15)19)12-6-2-4-8-14(12)20(18)22-25(35)29(39)32(42)30(40)26(22)36/h1-10H

InChI key

OXAQTDQMTJVZOI-UHFFFAOYSA-N

General description

6,12-Bis(2,3,4,5,6-pentafluorophenyl)indeno[1,2-b]fluorene is a conjugated polycyclic hydrocarbon that has an indeno[1,2-b]fluorene as the base structure. It has potential application in the development of organic electronics.

Application

Ambipolar organic semiconductor for Organic Field Effect Transistor (OFET) applications.

The field-effect hole and electron mobilities extracted from its single crystal ambipolar transistor are 7 × 10^-4 and 3 × 10^-3 cm^2 V^-1 s^-1 in the saturation regime.

HOMO: -6.17 eV
LUMO: -4.00 eV

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKBS6729V

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Anomalous Paramagnetism in Closed-Shell Molecular Semiconductors.
Eyer GP, et al.
The Journal of Physical Chemistry C, 121(45), 24929-24935 (2017)
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

Articles

Soluble Pentacene Precursors

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

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