Karstedt's catalyst is an organoplatinum compound derived from divinyl-containing disiloxane. This coordination complex is widely used in hydrosilylation catalysis. It is a colorless solid that is generally assumed to be a mixture of related Pt(0) alkene complexes. The catalyst is named after Bruce D. Karstedt, who developed it in the early 1970s while working for General Electric.
Carbon-silicon bonds are often generated via hydrosilylation of alkenes. This reaction has very important applications to industry. While it is favorable thermodynamically, hydrosilylation does not proceed in the absence of a catalyst, such as Karstedt's catalyst. The catalyst is produced by treatment of chloroplatinic acid by the divinyltetramethyldisiloxane.
The catalyst can also be used in a reductive amination reaction between a carboxylic acid and an amine with phenylsilane as the reducing agent.
The oxidation state of the platinum is 0. Using X-ray crystallography, the structure of Pt<sub>2</sub>[(Me<sub>2</sub>SiCH=CH<sub>2</sub>)<sub>2</sub>O]<sub>3</sub> has been confirmed. Each Pt(0) center is surrounded by three alkene ligands provided by three 1,1,3,3-tetramethyl-1,3-divinyldisiloxane ligands. The Pt center and six coordinated carbon atoms are approximately coplanar, as found for simpler complexes such as Pt(C<sub>2</sub>H<sub>4</sub>)<sub>3</sub>.