Copper(II) fluoride
This article includes a list of general references, but it lacks sufficient corresponding inline citations. (June 2021) |
Unit cell of the anhydrous form
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Ball-and-stick model of crystal packing in the anhydrous form
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Dihydrate
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Names | |
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IUPAC name
Copper difluoride
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Other names
Cupric fluoride; Copper fluoride; Copper (2+) Difluoride
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Identifiers | |
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3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.029.225 |
EC Number |
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PubChem CID
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UNII |
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CompTox Dashboard (EPA)
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Properties | |
CuF2 | |
Molar mass | 101.543 g/mol (anhydrous) 137.573 g/mol (dihydrate) |
Appearance | White crystalline powder When hydrated: Blue |
Density | 4.23 g/cm3 (anhydrous) 2.934 g/cm3 (dihydrate)[1] |
Melting point | 836 °C (1,537 °F; 1,109 K) (anhydrous) 130 °C (dihydrate, decomposes) |
Boiling point | 1,676 °C (3,049 °F; 1,949 K) (anhydrous) |
+1050.0·10−6 cm3/mol | |
Hazards | |
NIOSH (US health exposure limits): | |
PEL (Permissible)
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TWA 1 mg/m3 (as Cu)[2] |
REL (Recommended)
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TWA 1 mg/m3 (as Cu)[2] |
IDLH (Immediate danger)
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TWA 100 mg/m3 (as Cu)[2] |
Related compounds | |
Other anions
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Copper(II) bromide Copper(II) chloride |
Other cations
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Silver(II) fluoride Cobalt(II) fluoride |
Related compounds
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Copper(I) fluoride |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Copper(II) fluoride is an inorganic compound with the chemical formula CuF2. The anhydrous form is a white, ionic, crystalline, hygroscopic salt with a distorted rutile-type crystal structure, similar to other fluorides of chemical formulae MF2 (where M is a metal). The dihydrate, CuF2·2H2O, is blue in colour.[3]
Structure
[edit]Copper(II) fluoride has a monoclinic crystal structure[4] and cannot achieve a higher-symmetry structure. It forms rectangular prisms with a parallelogram base.[5] Each copper ion has four neighbouring fluoride ions at 1.93 Å separation and two further away at 2.27 Å.[3] This distorted octahedral [4+2] coordination is a consequence of the Jahn–Teller effect in d9 copper(II),[6] and leads to a distorted rutile structure similar to that of chromium(II) fluoride, CrF2, which is a d4 compound.[3]
Copper coordination | Fluorine coordination |
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Uses
[edit]Cupric fluoride catalyzes the decomposition of nitric oxides in emission control systems.[7]
Copper (II) fluoride can be used to make fluorinated aromatic hydrocarbons by reacting with aromatic hydrocarbons in an oxygen-containing atmosphere at temperatures above 450 °C (842 °F). This reaction is simpler than the Sandmeyer reaction, but is only effective in making compounds that can survive at the temperature used. A coupled reaction using oxygen and 2 HF regenerates the copper(II) fluoride, producing water.[8] This method has been proposed as a "greener" method of producing fluoroaromatics since it avoids producing toxic waste products such as ammonium fluoride.
Chemistry
[edit]Copper(II) fluoride can be synthesized from copper and fluorine at temperatures of 400 °C (752 °F). It occurs as a direct reaction.
- Cu + F2 → CuF2
It loses fluorine in the molten stage at temperatures above 950 °C (1742 °F).
- 2CuF2 → 2CuF + F2
- 2CuF → CuF2 + Cu
The complex anions of CuF3−, CuF42− and CuF64− are formed if CuF2 is exposed to substances containing fluoride ions F−.
Solubility
[edit]Copper(II) fluoride is slightly soluble in water, but starts to decompose when it is in hot water, producing basic F− and Cu(OH) ions.[citation needed]
Toxicity
[edit]There is little specific information on the toxicity of Copper(II) fluoride.
Copper toxicity can affect the skin, eyes, and respiratory tract. Serious conditions include metal fume fever, and hemolysis of red blood cells. Copper can also cause damage to the liver and other major organs.
Metal fluorides are generally safe at low levels and are added to water in many countries to protect against tooth decay. At higher levels they can cause toxic effects ranging from nausea and vomiting to tremors, breathing problems, serious convulsions and even coma. Brain and kidney damage can result. Chronic exposure can cause losses in bone density, weight loss and anorexia.
Hazards
[edit]Experiments using copper(II) fluoride should be conducted in a fume hood because metal oxide fumes can occur. The combination of acids with copper(II) fluoride may lead to the production of hydrogen fluoride, which is highly toxic and corrosive.
References
[edit]- ^ Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, ISBN 0-07-049439-8
- ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0150". National Institute for Occupational Safety and Health (NIOSH).
- ^ a b c d Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 1184–1185. ISBN 978-0-08-037941-8.
- ^ a b Fischer, P.; Hälg, W.; Schwarzenbach, D.; Gamsjäger, H. (1974). "Magnetic and crystal structure of copper(II) fluoride". J. Phys. Chem. Solids. 35 (12): 1683–1689. doi:10.1016/S0022-3697(74)80182-4.
- ^ C. Billy; H. M. Haendler (1957). "The Crystal Structure of Copper(II) Fluoride". Journal of the American Chemical Society. 79 (5): 1049–51. doi:10.1021/ja01562a011.
- ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 1190–1191. ISBN 978-0-08-037941-8.
- ^ Meshri, Dayal T. (2000), "Fluorine compounds, inorganic, copper", Kirk-Othmer Encyclopedia of Chemical Technology, New York: John Wiley, doi:10.1002/0471238961.0315161613051908.a01, ISBN 9780471238966
- ^ M. A. Subramanian; L. E. Manzer (2002). "A "Greener" Synthetic Route for Fluoroaromatics via Copper (II) Fluoride". Science. 297 (5587): 1665. doi:10.1126/science.1076397. PMID 12215637. S2CID 32697750.
- P. C. de Mello; M. Hehenberg; S. Larson; M. Zerner (1980). "Studies of the electronic structure of copper fluorides and copper chlorides". Journal of the American Chemical Society. 102 (4): 1278–1288. doi:10.1021/ja00524a010.
- H. M. Haendler; L. H. Towle; E. F. Bennett; W. L. Patterson (1954). "The Reaction of Fluorine with Copper and Some of its Compounds. Some Properties of Copper(II) Fluoride". Journal of the American Chemical Society. 76 (8): 2178–2179. doi:10.1021/ja01637a039.
- T. C. Ehlert; J. S. Wang (1977). "Thermochemistry of the copper fluorides". Journal of Physical Chemistry. 81 (22): 2069–2073. doi:10.1021/j100537a005.
- Dierks, S. "Copper Fluoride". http://www.espimetals.com/index.php/msds/537-copper-fluoride (accessed October 9).
- Subramanian, M. A.; Manzer, L. E. (2002). "A 'Greener' Synthetic Route for Fluoroaromantics via Copper (II) Fluoride". Science. 297 (5587): 1665. doi:10.1126/science.1076397. PMID 12215637. S2CID 32697750.
- Olejniczak, I.; Wolak, J.; Barszcz, B.; Schlueter, J.; Manson, J. (2010). "CuF2 Structural Changes in Two-Dimensional Quantum Magnet (H2O)2(pyz) Under Pressure: Raman Study". AIP Conference Proceedings. 1267 (1): 597–598. Bibcode:2010AIPC.1267..597O. doi:10.1063/1.3482697.
- Kent, R. A.; Mcdonald, J. D.; Margrave, J. L. (1966). "Mass Spectrometric Studies at High Temperatures. IX. The Sublimation Pressure of Copper(II) Fluoride". Journal of Physical Chemistry. 70 (3): 874–877. doi:10.1021/j100875a042.
- Shashkin, S. Y.; Goddard III, W. A. (1986). "Electron Correlation effects in ligand field parameters and other properties of copper II fluoride". Journal of Physical Chemistry. 90 (2): 250–255. doi:10.1021/j100274a010.