Cobalt-Mediated Synthesis of Angular [4]Phenylene: Structural Characterization of a Metallacyclopentadiene(Alkyne) Intermediate and Its Thermal and Photochemical Conversion
Organic Letters2002Vol. 4(12), pp. 2075–2078
Citations Over TimeTop 10% of 2002 papers
Abstract
[reaction: see text] The first X-ray crystal structure of a mononuclear metallacyclopentadiene(alkyne) complex has been obtained. This type of metallacycle is believed to be the key intermediate in the cobalt-mediated [2 + 2 + 2]cycloaddition of alkynes. Thermal treatment leads to the generation of angular [4]phenylene, the X-ray structural details of which are described. Under photochemical conditions, the cobaltacycle isomerizes to a highly strained (cyclobutadieno)dibenzocyclooctatrienyne complex.
Related Papers
- → Acetylene and Ethylene: Universal C2 Molecular Units in Cycloaddition Reactions(2021)27 cited
- → Strong coordination of cycloheptynes by gold(i) chloride: synthesis and structure of two complexes of the type [(alkyne)AuCl](1998)58 cited
- → Palladium-catalyzed desymmetric [2+2+2] cycloaddition of 1,6-enyne and alkyne(2020)8 cited
- → Evidence for Silica Surface Three- and Five-Membered Metallacycle Intermediates in the Catalytic Cycle of Hydroaminoalkylation of Olefins Using Single-Ti-Metal Catalysts(2020)5 cited
- → Addition Reactions: Cycloaddition(2014)