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Palladium(II) oxide


slightly soluble in aqua regia | NFPA-H = | NFPA-F = | NFPA-R = | NFPA-S = Palladium(II) oxide is the inorganic compound of formula PdO. It is the only well characterised oxide of palladium. It is prepared by treating the metal with oxygen. Above about 900 °C, the oxide reverts to palladium metal and oxygen gas. It is not attacked by acids.

Structure

The structure of PdO is tetragonal (P42/mmc) a = 3.044, c = 5.328 Å. The Pd atoms are square planar as expected for a d8 metal ion and the oxygen atoms are approximately tetrahedral. The closest Pd–Pd distance is 3.044 Å and is almost within the range which can be considered a bonding distance.

Preparation

PdO is often obtained as a poorly defined material that is generated for applications as a catalyst. Palladium oxide is prepared by heating palladium sponge metal in oxygen at 350 °C.

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The oxide is obtained as a black powder. The oxide also may be prepared specially for catalytic use by heating variously a mixture of palladium(II) chloride and potassium nitrate,

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or the product of dissolving palladium in aqua regia, followed by the addition of sodium nitrate at 600 °C. A hydrated form of the oxide (which dissolves in acid) can be prepared by precipitation from solution, for example, by hydrolysis of palladium nitrate or reaction of a soluble palladium compound with a strong base. The brown hydrated oxide converts to black anhydrous oxide on heating. Its susceptibility to attack by acids decreases at lower water content.

The hydrated oxide, PdO.nH2O can be produced as a dark-yellow precipitate by adding alkali to a solution of palladium nitrate, Pd(NO3)2.

Applications

Materials called palladium oxide are useful catalysts for catalytic hydrogenation in organic synthesis.

References

References

  1. {{Greenwood&Earnshaw1st
  2. (1990). "Preparation and Properties of the System CuxPd1-xO (0<=x<=0.175)". J. Solid State Chem..
  3. Donald Starr and R. M. Hixon. (1943). "Tetrahydrofuran".
  4. Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1965, NY. Vol. 2. p. 1583.
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