추천 제품
Quality Level
분석
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.)
작용기
fluoro
iodo
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
일반 설명
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.
애플리케이션
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 Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
이미 열람한 고객
Switching between halogen-and hydrogen-bonding in stoichiometric variations of a cocrystal of a phosphine oxide.
CrystEngComm, 14(19), 6110-6114 (2012)
Metric engineering of supramolecular Borromean rings.
Chemical Communications (Cambridge, England), 17, 1819-1821 (2006)
Dipyridinocalixcrown/diiodoperfluorocarbon binary host systems for CsI: structural studies and fluorous phase extraction of caesium.
Tetrahedron, 63(23), 4951-4958 (2007)
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
Environmental health perspectives, 120(1), 119-125 (2011-10-13)
Polyfluorinated iodine alkanes (PFIs) are important intermediates in the synthesis of organic fluoride products. Recently, PFIs have been detected in fluoropolymers as residual raw materials, as well as in the ambient environment. High production volumes and potential environmental releases of
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