Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Iodine monochloride

From Wikipedia, the free encyclopedia
Iodine monochloride
I-Cl bond length = 232.07 pm
I-Cl bond length = 232.07 pm
Space-filling model
Space-filling model
A sample of Iodine monochloride reagent
A sample of Iodine monochloride reagent
Names
Preferred IUPAC name
Iodine monochloride
Iodine(I) chloride
Systematic IUPAC name
Chloroiodane
Other names
Iodine chloride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.029.306Edit this at Wikidata
EC Number
  • 232-236-7
MeSHIodine-monochloride
UNII
UN number1792
  • InChI=1S/ClI/c1-2 checkY
    Key: QZRGKCOWNLSUDK-UHFFFAOYSA-N checkY
  • InChI=1S/ClI/c1-2
    Key: QZRGKCOWNLSUDK-UHFFFAOYSA-N
  • InChI=1/ClI/c1-2
    Key: QZRGKCOWNLSUDK-UHFFFAOYAO
Properties
ICl
Molar mass162.35 g/mol
Appearancereddish-brown
Density3.10 g/cm3
Melting point27.2 °C (81.0 °F; 300.3 K) (α-form)
13.9 °C (β-form)
Boiling point97.4 °C (207.3 °F; 370.5 K)
Hydrolyzes
Solubilitysoluble inCS2
acetic acid
pyridine
alcohol,ether,HCl
−54.6×10−6 cm3/mol
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Corrosive, reacts with water to releaseHCl
Safety data sheet (SDS)https://chemicalsafety.com/sds1/sdsviewer.php?id=30683304
Related compounds
Related interhalogen compounds
Chlorine monofluoride
Bromine monochloride
Iodine monobromide
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Chemical compound

Iodine monochloride is aninterhalogen compound with theformulaICl. It is a red-brownchemical compound thatmelts nearroom temperature. Because of the difference in theelectronegativity ofiodine andchlorine, this molecule is highlypolar and behaves as a source of I+. Discovered in 1814 byGay-Lussac, iodine monochloride is the first interhalogen compound discovered.[1]

Preparation

[edit]

Iodine monochloride is produced simply by combining the halogens in a 1:1 molar ratio, according to the equation

I2 + Cl2 → 2 ICl

Whenchlorine gas is passed through iodine crystals, one observes the brown vapor of iodine monochloride. Dark brown iodine monochloride liquid is collected. Excess chlorine converts iodine monochloride intoiodine trichloride in a reversible reaction:

ICl + Cl2 ⇌ ICl3

Polymorphs

[edit]

ICl has twopolymorphs; α-ICl, which exists as black needles (red by transmitted light) with amelting point of 27.2 °C, and β-ICl, which exists as black platelets (red-brown by transmitted light) with a melting point 13.9 °C.[2]

In the crystal structures of both polymorphs the molecules are arranged in zigzag chains. β-ICl is monoclinic with thespace group P21/c.[3]

Reactions and uses

[edit]

Iodine monochloride is soluble in acids such asHF andHCl but reacts with pure water to form HCl, iodine, andiodic acid:

ICl + H2O → HCl + HI +12O2
2 ICl + H2O → 2 HCl + I2 +12O2
5 ICl + 3 H2O → 5 HCl + HIO3 + 2 I2

ICl is a usefulreagent inorganic synthesis.[2] It is used as a source ofelectrophilic iodine in the synthesis of certainaromatic iodides.[4] It also cleaves C–Si bonds.

ICl will also add to thedouble bond inalkenes to give chloro-iodoalkanes.

RCH=CHR′ + ICl → RCH(I)–CH(Cl)R′

When such reactions are conducted in the presence ofsodium azide, the iodo-azide RCH(I)–CH(N3)R′ is obtained.[5]

The Wijs solution, iodine monochloride dissolved in acetic acid, is used to determine theiodine value of a substance.

It can also be used to prepare iodates, by reaction with a chlorate. Chlorine is released as a byproduct.

Iodine monochloride is aLewis acid that forms 1:1adducts with Lewis bases such asdimethylacetamide andbenzene.

References

[edit]
  1. ^Greenwood, Norman N.; Earnshaw, Alan (1997).Chemistry of the Elements (2nd ed.).Butterworth-Heinemann. p. 790.doi:10.1016/C2009-0-30414-6.ISBN 978-0-08-037941-8.
  2. ^abBrisbois, Ronald G.; Wanke, Randall A.; Stubbs, Keith A.; Stick, Robert V. (2004). "Iodine Monochloride".Encyclopedia of Reagents for Organic Synthesis.doi:10.1002/047084289X.ri014.ISBN 0-471-93623-5.
  3. ^Carpenter, G. B.; Richards, S. M. (1 April 1962)."The crystal structure of β-iodine monochloride".Acta Crystallographica.15 (4):360–364.Bibcode:1962AcCry..15..360C.doi:10.1107/S0365110X62000882.
  4. ^Wallingford, V. H.; Krüger, P. A. (1943)."5-Iodo-anthranilic Acid".Organic Syntheses;Collected Volumes, vol. 2, p. 349.
  5. ^Padwa, A.; Blacklock, T.; Tremper, A."3-Phenyl-2H-Azirine-2-carboxaldehyde".Organic Syntheses;Collected Volumes, vol. 6, p. 893.
Iodine(−I)
Iodine(I)
Iodine(II)
Iodine(III)
Iodine(IV)
Iodine(V)
Iodine(VII)
Salts and covalent derivatives of thechloride ion
HClHe
LiClBeCl2B4Cl4
B12Cl12
BCl3
B2Cl4
+BO3
C2Cl2
C2Cl4
C2Cl6
CCl4
+C
+CO3
NCl3
ClN3
+N
+NO3
ClxOy
Cl2O
Cl2O2
ClO
ClO2
Cl2O4
Cl2O6
Cl2O7
ClO4
+O
ClF
ClF3
ClF5
Ne
NaClMgCl2AlCl
AlCl3
Si5Cl12
Si2Cl6
SiCl4
P2Cl4
PCl3
PCl5
+P
S2Cl2
SCl2
SCl4
+SO4
Cl2Ar
KClCaCl
CaCl2
ScCl3TiCl2
TiCl3
TiCl4
VCl2
VCl3
VCl4
VCl5
CrCl2
CrCl3
CrCl4
MnCl2
MnCl3
FeCl2
FeCl3
CoCl2
CoCl3
NiCl2CuCl
CuCl2
ZnCl2GaCl
GaCl3
GeCl2
GeCl4
AsCl3
AsCl5
+As
Se2Cl2
SeCl2
SeCl4
BrClKr
RbClSrCl2YCl3ZrCl2
ZrCl3
ZrCl4
NbCl3
NbCl4
NbCl5
MoCl2
MoCl3
MoCl4
MoCl5
MoCl6
TcCl3
TcCl4
RuCl2
RuCl3
RuCl4
RhCl3PdCl2AgClCdCl2InCl
InCl2
InCl3
SnCl2
SnCl4
SbCl3
SbCl5
Te3Cl2
TeCl2
TeCl4
ICl
ICl3
XeCl
XeCl2
XeCl4
CsClBaCl2*LuCl3
177LuCl3
HfCl4TaCl3
TaCl4
TaCl5
WCl2
WCl3
WCl4
WCl5
WCl6
ReCl3
ReCl4
ReCl5
ReCl6
OsCl2
OsCl3
OsCl4
OsCl5
IrCl2
IrCl3
IrCl4
PtCl2
PtCl4
PtCl2−6
AuCl
(Au[AuCl4])2
AuCl3
AuCl4
Hg2Cl2
HgCl2
TlCl
TlCl3
PbCl2
PbCl4
BiCl3PoCl2
PoCl4
AtClRn
FrClRaCl2**LrCl3RfCl4DbCl5SgO2Cl2BhO3ClHsMtDsRgCnNhFlMcLvTsOg
 
*LaCl3CeCl3PrCl3NdCl2
NdCl3
PmCl3SmCl2
SmCl3
EuCl2
EuCl3
GdCl3TbCl3DyCl2
DyCl3
HoCl3ErCl3TmCl2
TmCl3
YbCl2
YbCl3
**AcCl3ThCl3
ThCl4
PaCl4
PaCl5
UCl3
UCl4
UCl5
UCl6
NpCl3
NpCl4
PuCl3
PuCl4
PuCl2−6
AmCl2
AmCl3
CmCl3BkCl3CfCl3
CfCl2
EsCl2
EsCl3
FmCl2MdCl2NoCl2
Retrieved from "https://en.wikipedia.org/w/index.php?title=Iodine_monochloride&oldid=1328211861"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2026 Movatter.jp