Reactions of Strained Hydrocarbons with Alkene and Alkyne Metathesis Catalysts
Matthew E. Carnes, D. Buccella, Theo Siegrist, Michael L. Steigerwald, Colin Nuckolls
Abstract
Matthew E. Carnes, D. Buccella, Theo Siegrist, Michael L. Steigerwald, Colin Nuckolls
Abstract
Here we describe the metathesis reactions of a strained eight-membered ring that contains both alkene and alkyne functionality. We find that the alkyne metathesis catalyst produces polymer through a ring-opening alkyne metathesis reaction that is driven by the strain release from the monomer. The strained monomer provides unusual reactivity with ruthenium-based alkene metathesis catalysts. We isolate a discrete trimeric species a Dewar benzene derivative that is locked in this form through an unsaturated cyclophane strap.
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Here we describe the metathesis reactions of a strained eight-membered ring that contains both alkene and alkyne functionality. We find that the alkyne metathesis catalyst produces polymer through a ring-opening alkyne metathesis reaction that is driven by the strain release from the monomer. The strained monomer provides unusual reactivity with ruthenium-based alkene metathesis catalysts. We isolate a discrete trimeric species a Dewar benzene derivative that is locked in this form through an unsaturated cyclophane strap.
Key concepts: Alkene, Alkyne, Metathesis, Chemistry, Acyclic diene metathesis, Monomer, Ruthenium, Catalysis