Adams' catalyst, also known as platinum dioxide, is usually represented as

platinum Platinum is a chemical element with the symbol Pt and atomic number 78. It is a dense, malleable, ductile, highly unreactive, precious, silverish-white transition metal. Its name originates from Spanish , a diminutive of "silver". Platin ...

(IV) oxide hydrate, PtO₂•H₂O. It is a catalyst for

hydrogenation Hydrogenation is a chemical reaction between molecular hydrogen (H2) and another compound or element, usually in the presence of a catalyst such as nickel, palladium or platinum. The process is commonly employed to reduce or saturate organic c ...

and hydrogenolysis in

organic synthesis Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional construction of organic compounds. Organic molecules are often more complex than inorganic compounds, and their synthesis has developed into one o ...

. This dark brown powder is commercially available. The oxide itself is not an active catalyst, but it becomes active after exposure to hydrogen whereupon it converts to platinum black, which is responsible for reactions.

Preparation

Adams' catalyst is prepared from chloroplatinic acid H₂PtCl₆ or ammonium chloroplatinate, (NH₄)₂PtCl₆, by fusion with

sodium nitrate Sodium nitrate is the chemical compound with the formula . This alkali metal nitrate salt is also known as Chile saltpeter (large deposits of which were historically mined in Chile) to distinguish it from ordinary saltpeter, potassium nitrate. ...

. The first published preparation was reported by V. Voorhees and Roger Adams. The procedure involves first preparing a platinum nitrate which is then heated to expel nitrogen oxides. :H₂PtCl₆ + 6 NaNO₃ → Pt(NO₃)₄ + 6 NaCl _(aq) + 2 HNO₃ :Pt(NO₃)₄ → PtO₂ + 4 NO₂ + O₂ The resulting brown cake is washed with water to free it from nitrates. The catalyst can either be used as is or dried and stored in a desiccator for later use. Platinum can be recovered from spent catalyst by conversion to ammonium chloroplatinate using aqua regia followed by

ammonia Ammonia is an inorganic compound of nitrogen and hydrogen with the formula . A stable binary hydride, and the simplest pnictogen hydride, ammonia is a colourless gas with a distinct pungent smell. Biologically, it is a common nitrogenous ...

Uses

Adams' catalyst is used for many applications. It has shown to be valuable for

, hydrogenolysis,

dehydrogenation In chemistry, dehydrogenation is a chemical reaction that involves the removal of hydrogen, usually from an organic molecule. It is the reverse of hydrogenation. Dehydrogenation is important, both as a useful reaction and a serious problem. A ...

, and

oxidation Redox (reduction–oxidation, , ) is a type of chemical reaction in which the oxidation states of substrate change. Oxidation is the loss of electrons or an increase in the oxidation state, while reduction is the gain of electrons or ...

reactions. During the reaction, platinum metal ( platinum black) is formed which has been cited to be the active catalyst. Hydrogenation occurs with syn stereochemistry when used on an alkyne resulting in a cis-alkene. Some of the most important transformations include the hydrogenation of ketones to alcohols or

ether In organic chemistry, ethers are a class of compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. They have the general formula , where R and R′ represent the alkyl or aryl groups. Ethers can again ...

s (the latter product forming in the presence of alcohols and acids) and the reduction of nitro compounds to amines. However, reductions of

alkene In organic chemistry, an alkene is a hydrocarbon containing a carbon–carbon double bond. Alkene is often used as synonym of olefin, that is, any hydrocarbon containing one or more double bonds.H. Stephen Stoker (2015): General, Organic ...

s can be performed with Adam's catalyst in the presence of nitro groups without reducing the nitro group. When reducing nitro compounds to amines, platinum catalysts are preferred over palladium catalysts to minimize hydrogenolysis. The catalyst is also used for the hydrogenolysis of phenyl phosphate esters, a reaction that does not occur with palladium catalysts. The pH of the solvent significantly affects the reaction course, and reactions of the catalyst are often enhanced by conducting the reduction in neat acetic acid, or solutions of acetic acid in other solvents.

Development

Before development of Adams' catalyst, organic reductions were carried out using colloidal platinum or platinum black. The colloidal catalysts were more active but posed difficulties in isolating reaction products. This led to more widespread use of platinum black. In Adams' own words:

"...Several of the problems I assigned my students involved catalytic reduction. For this purpose we were using as a catalyst platinum black made by the generally accepted best method known at the time. The students had much trouble with the catalyst they obtained in that frequently it proved to be inactive even though prepared by the same detailed procedure which resulted occasionally in an active product. I therefore initiated a research to find conditions for preparing this catalyst with uniform activity."

Safety

Little precaution is necessary with the oxide but, after exposure to H₂, the resulting platinum black can be

pyrophoric A substance is pyrophoric (from grc-gre, πυροφόρος, , 'fire-bearing') if it ignites spontaneously in air at or below (for gases) or within 5 minutes after coming into contact with air (for liquids and solids). Examples are organolith ...

. Therefore, it should not be allowed to dry and all exposure to oxygen should be minimized.

References

External links