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Merck

282286

Sigma-Aldrich

1,4-Diiodotetrafluorobenzene

98%

Sinónimos:

1,2,4,5-Tetrafluoro-3,6-diiodobenzene, 1,4-Diiodo-2,3,5,6-tetrafluorobenzene, 3,6-Diiodo-1,2,4,5-tetrafluorobenzene, Tetrafluoro-1,4-diiodobenzene, p-Diiodoperfluorobenzene

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About This Item

Fórmula empírica (notación de Hill):
C6F4I2
Número de CAS:
Peso molecular:
401.87
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

mp

108-110 °C (lit.)

functional group

fluoro
iodo

SMILES string

Fc1c(F)c(I)c(F)c(F)c1I

InChI

1S/C6F4I2/c7-1-2(8)6(12)4(10)3(9)5(1)11

InChI key

VIXRAZODEODOJF-UHFFFAOYSA-N

General description

1,4-Diiodotetrafluorobenzene forms trimeric complexes as new, halogen-bonded mesogens with two molecules of alkoxystilbazole. The electron density study of the halogen-bonded complex of 4,4′-dipyridyl-N,N′-dioxide with 1,4-diiodotetrafluorobenzene at 90K has been reported.

1,4-Diiodotetrafluorobenzene is a ditopic perfluorinated iodobenzene used for cocrystallization of halopyridinium salts.

Application

1,4-Diiodotetrafluorobenzene has been used as the halogen bonding donor during the preparation of phosphorescent cocrystal with polycyclic aromatic hydrocarbons.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Mesogenic, trimeric, halogen-bonded complexes from alkoxystilbazoles and 1, 4-diiodotetrafluorobenzene.
<BIG>Bruce DW, et al. </BIG>
New. J. Chem., 32(3), 477-482 (2008)
Halogen and hydrogen bond motifs in ionic cocrystals derived from 3-halopyridinium halogenides and perfluorinated iodobenzenes
Lidija P et al.
Crystal Growth & Design, 21, 6044-6050 (2021)
Jiehao Fu et al.
iScience, 23(3), 100965-100965 (2020-03-22)
Here we introduce a σ-hole-containing volatile solid additive, 1, 4-diiodotetrafluorobenzene (A3), in PM6:Y6-based OSCs. Aside from the appropriate volatility of A3 additive, the synergetic halogen interactions between A3 and photoactive matrix contribute to more condensed and ordered molecular arrangement in
Jay Quentin et al.
Molecules (Basel, Switzerland), 25(4) (2020-02-23)
The halogen-bond (X-bond) donors 1,3- and 1,4-diiodotetrafluorobenzene (1,3-di-I-tFb and 1,4-di-I-tFb, respectively) form cocrystals with trans-1,2-bis(2-pyridyl)ethylene (2,2'-bpe) assembled by N···I X-bonds. In each cocrystal, 2(1,3-di-I-tFb)·2(2,2'-bpe) and (1,4-di-I-tFb)·(2,2'-bpe), the donor molecules support the C=C bonds of 2,2'-bpe to undergo an intermolecular [2+2]
Phosphorescent co-crystal assembled by 1, 4-diiodotetrafluorobenzene with carbazole based on C-Ip halogen bonding.
<BIG>Gao HY, et al. </BIG>
Journal of Materials Chemistry, 22(12), 5336-5343 (2012)

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