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103136

Sigma-Aldrich

Iodopentafluorobenzene

99%

Synonym(s):

2,3,4,5,6-Pentafluoroiodobenzene, Pentafluoroiodobenzene

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About This Item

Empirical Formula (Hill Notation):
C6F5I
CAS Number:
827-15-6
Molecular Weight:
293.96
EC Number:
212-565-2
MDL number:
MFCD00001032
UNSPSC Code:
12352100
PubChem Substance ID:
24846596
NACRES:
NA.22

Quality Level

200

assay

99%

refractive index

n20/D 1.496 (lit.)

bp

161 °C (lit.)

density

2.204 g/mL at 25 °C (lit.)

SMILES string

Fc1c(F)c(F)c(I)c(F)c1F

InChI

1S/C6F5I/c7-1-2(8)4(10)6(12)5(11)3(1)9

InChI key

OPYHNLNYCRZOGY-UHFFFAOYSA-N

Related Categories

General description

Iodopentafluorobenzene forms supramolecular complexes with aromatic electron donors by forming halogen bonds to form discrete heterodimeric aggregates.

Application

  • Iodopentafluorobenzene was used to study the formation of radical ions of iodopentafluorobenzene in aqueous solution.
  • It was used as solvent in a study to determine singlet oxgen lifetimes from phosphorescence decays in halogen substituted perfluorinated solvents by infrared emission spectrometery.
  • It has potential applications in plasma processing industry and in preparation of catalysts.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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’.

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Formation and redox properties of radical ions of iodopentafluorobenzene in aqueous solution: a pulse radiolysis study
Mohan H and Mittal JP
The Journal of Physical Chemistry, 99(33), 12559-12564 (1995)
Iodopentafluorobenzene: Electronic state spectroscopy by high-resolution vacuum ultraviolet photoabsorption and photoelectron spectroscopy.
Eden S, et al.
Chemical Physics, 359(1), 111-117 (2009)
Chenxin Ran et al.
Chemical Society reviews, 47(12), 4581-4610 (2018-04-24)
The rapid development of solar cells (SCs) based on organic-inorganic hybrid metal triiodide perovskite (MTP) materials holds great promise for next-generation photovoltaic devices. The demonstrated power conversion efficiency of the SCs based on MTP (PSCs for short) has reached over
Co-crystals of iodopentafluorobenzene with nitrogen donors: 2-D molecular assemblies through halogen bonding and aryl-perfluoroaryl interactions.
Wasilewska A, et al.
CrystEngComm, 9(3), 203-206 (2007)
Influence of heavy atoms on the deactivation of singlet oxygen (1. DELTA. g) in solution
Schmidt R
Journal of the American Chemical Society, 111(18), 6983-6987 (1989)

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