Copper(II) nitrate

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Copper(II) nitrate
General
Systematic name Copper(II) nitrate
Other names Cupric nitrate
Molecular formula N2CuO6 (anhydrous)
Molar mass 187.56 g/mol,
241.60 (Cu(NO3)2.3(H2O),
232.59 (Cu(NO3)2.2.5H2O
Appearance blue crystals
CAS number [3251-23-8] (anhydrous),
[10031-43-3] (Cu(NO3)2.3(H2O),

[19004-19-4] (Cu(NO3)2.2.5(H2O)

Properties
Density and phase 2.32 g/cm3 (anhydrous)
Solubility in water 138 g/100 mL (0 °C) trihydrate
Melting point 210 °C sublimes (anhydrous)
Boiling point decomp
Structure
Molecular shape  ?
Coordination
geometry
 ?
Crystal structure  ?
Dipole moment  ? D
Hazards
MSDS External MSDS
Main hazards Toxic, irritant
NFPA 704

0
3
0
 
R/S statement R: R22 R36/37/38 R48/20/21/22 R66
S: ?
RTECS number GL7875000
Supplementary data page
Structure and
properties
n, εr, etc.
Thermodynamic
data
Phase behaviour
Solid, liquid, gas
Spectral data UV, IR, NMR, MS
Related compounds
Other anions  ?
Other cations  ?
Related compounds CuNO3,
copper(II) sulfate
Except where noted otherwise, data are given for
materials in their standard state (at 25°C, 100 kPa)
Infobox disclaimer and references

Copper(II) nitrate is the chemical compound with the formula Cu(NO3)2. Commonly referred to simply as copper nitrate, the anhydrous form is a blue, crystalline solid. Hydrated forms of copper nitrate, also blue, are commonly used in school laboratories to demonstrate chemical voltaic cell reactions. The hydrated and anhydrous species have remarkably different properties, illustrating the effect of water of crystallization.

The Roman numeral sign is to specify that the copper has an oxidation state of +2.

Contents

[edit] Properties

Hydrated and anhydrous copper nitrates behave differently.

[edit] Anhydrous form

The bright blue anhydrous material, Cu(NO3)2, is a volatile solid, subliming in a vacuum. In the gas-phase, Cu(NO3)2 is square planar, each Cu center being surrounded by four oxygen atoms. Upon condensation, this monomer polymerizes.[1]

[edit] Hydrated copper nitrate

Crystalline Cu(NO3)2(H2O)2.5 features octahedral Cu centers surrounded by water and the nitrate anions.[1] This hydrate decomposes at ca. 170 °C into copper(II) oxide, nitrogen dioxide and oxygen:

2Cu(NO3)2(s) → 2CuO(s) + 4NO2(g) + O2(g)

Copper nitrate can be used to generate nitric acid by heating it until decomposition and passing the fumes directly into water. This method is similar to the last step in the Ostwald process. The equations are as follows:

2Cu(NO3)2 → 2CuO + 4NO2 + O2
NO2 + H2O → 2 HNO3 + NO

Copper nitrate soaked splints of wood burn with an emerald green flame. Addition of Magnesium nitrate gives a lime green color.

[edit] Synthesis

Cu(NO3)2 forms when copper metal is treated with N2O4:[2]

Cu + 2 N2O4 → Cu(NO3)2 + 2 NO

[edit] Use in organic synthesis

Copper nitrate, in combination with acetic anhydride, is an effective reagent for nitration of aromatic compounds, under what are known as "Menke conditions", in honor of the Dutch chemist who discovered that metal nitrates are effective reagents for nitration. [3] Hydrated copper nitrate absorbed onto clay affords a reagent called "claycop". The resulting blue clay is used as a slurry, for example for the oxidation of thiols to disulfides. Claycop is also used to convert dithioacetals to carbonyls.[4] A related reagent based on Montmorillonite has proven useful for the nitration of aromatic compounds.[5]

[edit] External links

[edit] References

  1. ^ a b Wells, A.F. Structural Inorganic Chemistry, Oxford: Clarendon Press (1984). ISBN 0-19-855370-6.
  2. ^ Jolly, W. L. "The Synthesis and Characterization of Inorganic Compounds" Prentice Hall, London, 1970
  3. ^ Menke J.B. (1925). "Nitration with nitrates". Recueil des Travaux Chimiques des Payes-Bas 44: 141.
  4. ^ Balogh, M. "Copper(II) Nitrate–K10 Bentonite Clay" in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. DOI: 10.1002/047084289.
  5. ^ Collet, C.; Delville, A.; Laszlo, P. “Clays Direct Aromatic Nitration” Angewandte Chemie International Edition in English, 2003, Volume 29, Issue 5 , Pages 535 - 536. DOI 10.1002/anie.199005351.
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