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Chlorine Monofluoride
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image
[7790‐89‐8]
ClF
(MW 54.45)
InChI =
1S/ClF/c1‐2
InChIKey =
OMRRUNXAWXNVFW‐UHFFFAOYSA‐N
(reagent used as a source of electrophilic chlorine and nucleophilic fluoride; formation of hypochlorites; synthesis of chloramines: dihalogenation of alkenes; oxidative fluorination of sulfur derivatives)
Physical Data:
Colorless gas at room temperature; colorless solid, mp −155.6 °C; pale yellow liquid, bp −100.1 °C;
d
1.62 g cm
−3
.
Form Supplied in:
pressurized container.
Preparative Methods:
gaseous chlorine monofluoride can be obtained by heating equimolar amounts of F
2
and Cl
2
at 230 °C in copper tubes,
1
or at 250 °C in nickel tubes using a 5% excess of Cl
2
.
2
Preparations involving silver salts or alkali metal fluorides upon heating have also been reported in addition with a method at low temperature using SbF
5
at 35 °C.
3
Other procedures have been described using ClF
3
with Cl
2
and CsF upon heating or with HgCl
2
at 25 °C.
4
ClF can also be prepared and used
in situ
by mixing
N
‐chlorosuccinimide and HF.
5,6
Purification:
depending on the preparative method, the major impurities are ClF
3
, HF, F
2
, and/or Cl
2
. Fractional condensation with a trap at –142 °C to retain impurities and a trap at –196 °C to condense pure ClF can be used.
4
Handling, Storage, and Precautions:
chlorine fluorides are strong oxidizing agents and are toxic. Hydrolysis can produce shock‐sensitive chlorine oxides and toxic by‐products (ClO
2
F, Cl
2
, HF). ClF
3
is also a decomposition product and is highly pyrophoric. Protect from sunlight. Do not expose to temperatures above 50 °C. Keep the container closed when not in use. Reacts violently with metals and reducing agents. Appropriate shielding is required for high‐pressure work. Wear protective clothing and a face mask at all times.
Title: Chlorine Monofluoride
Description:
image
[7790‐89‐8]
ClF
(MW 54.
45)
InChI =
1S/ClF/c1‐2
InChIKey =
OMRRUNXAWXNVFW‐UHFFFAOYSA‐N
(reagent used as a source of electrophilic chlorine and nucleophilic fluoride; formation of hypochlorites; synthesis of chloramines: dihalogenation of alkenes; oxidative fluorination of sulfur derivatives)
Physical Data:
Colorless gas at room temperature; colorless solid, mp −155.
6 °C; pale yellow liquid, bp −100.
1 °C;
d
1.
62 g cm
−3
.
Form Supplied in:
pressurized container.
Preparative Methods:
gaseous chlorine monofluoride can be obtained by heating equimolar amounts of F
2
and Cl
2
at 230 °C in copper tubes,
1
or at 250 °C in nickel tubes using a 5% excess of Cl
2
.
2
Preparations involving silver salts or alkali metal fluorides upon heating have also been reported in addition with a method at low temperature using SbF
5
at 35 °C.
3
Other procedures have been described using ClF
3
with Cl
2
and CsF upon heating or with HgCl
2
at 25 °C.
4
ClF can also be prepared and used
in situ
by mixing
N
‐chlorosuccinimide and HF.
5,6
Purification:
depending on the preparative method, the major impurities are ClF
3
, HF, F
2
, and/or Cl
2
.
Fractional condensation with a trap at –142 °C to retain impurities and a trap at –196 °C to condense pure ClF can be used.
4
Handling, Storage, and Precautions:
chlorine fluorides are strong oxidizing agents and are toxic.
Hydrolysis can produce shock‐sensitive chlorine oxides and toxic by‐products (ClO
2
F, Cl
2
, HF).
ClF
3
is also a decomposition product and is highly pyrophoric.
Protect from sunlight.
Do not expose to temperatures above 50 °C.
Keep the container closed when not in use.
Reacts violently with metals and reducing agents.
Appropriate shielding is required for high‐pressure work.
Wear protective clothing and a face mask at all times.
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