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Hydrosilylation
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Hydrosilylation

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Hydrosilylation, also called catalytic hydrosilation, describes the addition of Si-H bonds across unsaturated bonds. Ordinarily the reaction is conducted catalytically and usually the substrates are unsaturated organic compounds. Alkenes and alkynes give alkyl and vinyl silanes; aldehydes and ketones give silyl ethers, while esters provide alkyl silyl mixed acetals. Hydrosilylation has been called the "most important application of platinum in homogeneous catalysis."

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Encyclopedic overview

6 sections
Contents
  • Scope and mechanism
  • Asymmetric hydrosilylation
  • Surface hydrosilylation
  • Catalysts
  • References
  • Further reading

Hydrosilylation, also called catalytic hydrosilation, describes the addition of Si-H bonds across unsaturated bonds. Ordinarily the reaction is conducted catalytically and usually the substrates are unsaturated organic compounds. Alkenes and alkynes give alkyl and vinyl silanes; aldehydes and ketones give silyl ethers, while esters provide alkyl silyl mixed acetals. Hydrosilylation has been called the "most important application of platinum in homogeneous catalysis."

==Scope and mechanism== thumb|350px|Idealized mechanism for metal-catalysed hydrosilylation of an alkene. Hydrosilylation of alkenes represents a commercially important method for preparing organosilicon compounds. The process is mechanistically similar to the hydrogenation of alkenes. In fact, similar catalysts are sometimes employed for the two catalytic processes.

Excerpted from Wikipedia’s “Hydrosilylation” article, available under the CC BY-SA 4.0 licence.

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