Photochemical Manganese-Catalyzed [2 + 2 + 2] Cycloaddition Reactions.

We report the cyclotrimerization reactions of triynes using Mn(I) complexes derived from MnBr(CO) and phosphine ligands, such as 1,1-bis(diphenylphosphino)methane (dppm). These reactions are driven by irradiation under mild conditions (30-80 °C) without the need of additional photoinitiators. Our catalytic screening revealed that counteranions and ligands significantly influence the process. This method accommodates a broad range of functionalities in the substrates, including alkyl, aryl, Bpin, SiMe, GeEt, PPh, pyridyl, and thienyl moieties, without notable interference in the transformation. Additionally, this method enables reactions with oligoalkynes-like (un)substituted hexaynes, producing 2-fold cyclization products in very good yields. Under stoichiometric conditions, the cyclization of diynes with phosphaalkynes results in the unique photochemical synthesis of phosphinines. Experimental and theoretical mechanistic studies indicate that the dissociation of the diphosphine ligand precedes the involvement of the Mn carbonyl species in the catalytic cycle. The ligand plays a crucial role in stabilizing the catalyst during the catalytic transformation and preventing the formation of unreactive cluster species.