473863
Octafluoro-1,4-diiodobutane
98%
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About This Item
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assay
98%
refractive index
n20/D 1.429 (lit.)
bp
150 °C (lit.)
mp
−9 °C (lit.)
density
2.474 g/mL at 25 °C (lit.)
SMILES string
FC(F)(I)C(F)(F)C(F)(F)C(F)(F)I
InChI
1S/C4F8I2/c5-1(6,3(9,10)13)2(7,8)4(11,12)14
InChI key
JILAKKYYZPDQBE-UHFFFAOYSA-N
Categorías relacionadas
General description
Octafluoro-1,4-diiodobutane (ofib, C4F8I2) is also referred to as 1,1,2,2,3,3,4,4-octafluoro-1,4-diiodobutane. It acts as a halogen bond donor compound and its cocrystallization with methyldiphenylphosphine oxide (mdppo) has been investigated. In combination with a calixcrown compound ofib forms a ′binary host′ system, which is employed for the isolation of cesium iodide from aqueous to fluorous phase.
Application
Octafluoro-1,4-diiodobutane may be used as a guest molecule to prepare a chiral bidentate inclusion complex with pyridyl moieties of a pyridoallenoacetylenic host. It may be employed in the synthesis of three-component supramolecular complexes.
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Organic letters, 16(4), 1136-1139 (2014-02-12)
A chiral bidentate inclusion complex has been formed by halogen-bond interaction between the pyridyl moieties of a pyridoallenoacetylenic host and octafluorodiiodobutane. X-ray crystallography showed that the guest adopts a chiral conformation inside the molecular channels formed by stacking of the
Switching between halogen-and hydrogen-bonding in stoichiometric variations of a cocrystal of a phosphine oxide.
CrystEngComm, 14(19), 6110-6114 (2012)
Dipyridinocalixcrown/diiodoperfluorocarbon binary host systems for CsI: structural studies and fluorous phase extraction of caesium.
Tetrahedron, 63(23), 4951-4958 (2007)
Metric engineering of supramolecular Borromean rings.
Chemical Communications (Cambridge, England), 17, 1819-1821 (2006)
Journal of applied toxicology : JAT, 39(7), 945-954 (2019-03-06)
Fluorinated diiodine alkanes (FDIAs), important industrial intermediates in the synthesis of various perfluorinated compounds, which are distributed widely in wildlife and humans. Recent studies showed that FDIAs had in vitro estrogenic effects. However, to date, little information is available regarding
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