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The key to the process is the metal catalysts.
Other reducing agents have been used, such as hydrogen and a metal catalyst, but are much less common.
Typical examples use metal catalysts and H2 as the reagent.
The reaction is accelerated by light, metal catalysts, and aldehydes.
This process omitted the metal catalyst agent previously used.
The metal catalyst then breaks off from the ring, carrying away part of the organic molecule.
Systems for direct synthesis have been developed, most of which are based around finely dispersed metal catalysts.
This is augmented by metal catalysts such as copper.
Due to the use of metal catalysts, polymers inevitably have trace metals present.
In the presence of metal catalysts, sodium borohydride releases hydrogen.
They are capable of forming highly reactive metal catalysts.
For most practical purposes, hydrogenation requires a metal catalyst.
The reduction of O by metal catalysts is a key half-reaction in fuel cells.
The reaction requires a metal catalyst, often rhodium.
Typical metal catalysts involve gold, copper, nickel, and tin.
Since the use of precious metal catalysts is not required, this also decreases the total price of fuel production.
There are several requirements for the metal catalyst:
Investigators said the victims sometimes worked on the same experiments, researching polymers and heavy metal catalysts.
Many transition metal catalysts initiate catalysis in this manner.
Metal catalysts are necessary for auto oxidation of sporodesmin.
However, other metal catalysts yield mixtures of hydrocarbons suitable for various fuels.
The nitrobenzene is then hydrogenated (typically at 200-300 C) in the presence of metal catalysts.
Metal catalysts are required for such reactions.
Transition metal catalysts have also been used with hydrogen gas as the stoichiometric reductant.
Metal catalysts such as silver and manganese have been used to induce the fluorodecarboxylation.