Affiliation:
1. Departement für Chemie, Biochemie und Pharmazie Universität Bern Freiestrasse 3 3012 Bern Switzerland
2. Department of Pure and Applied Chemistry University of Strathclyde 295 Cathedral Street G1 1XL Glasgow UK
3. Department of Chemistry University of Bath Claverton Down, BA2 7AY Bath UK
Abstract
AbstractExploiting bimetallic cooperation alkali‐metal manganate (II) complexes can efficiently promote oxidative homocoupling of terminal alkynes furnishing an array of conjugated 1,3‐diynes. The influence of the alkali‐metal on these C−C bond forming processes has been studied by preparing and structurally characterizing the alkali‐metal tetra(alkyl) manganates [(TMEDA)2Na2Mn(CH2SiMe3)4] and [(PMDETA)2K2Mn(CH2SiMe3)4]. Reactivity studies using phenylacetylene as a model substrate have revealed that for the homocoupling to take place initial metalation of the alkyne is required. In this regard, the lack of basicity of neutral Mn(CH2SiMe3)2 precludes the formation of the diyne. Contrastingly, the tetra(alkyl) alkali‐metal manganates behave as polybasic reagents, being able to easily deprotonate phenylacetylene yielding [{(THF)4Na2Mn(C≡CPh)4}∞] and [(THF)4Li2Mn(C≡CPh)4]. Controlled exposure of [{(THF)4Na2Mn(C≡CPh)4}∞] and [(THF)4Li2Mn(C≡CPh)4] to dry air confirmed their intermediary in formation of 1,4‐diphenyl‐1,3‐butadiyne in excellent yields. While the Na/Mn(II) partnership proved to be the most efficient in stoichiometric transformations, under catalytic regimes, the combination of MC≡CAr (M= Li, Na) and MnCl2 (6 mol %) only works for lithium, most likely due to the degradation of alkynylsodiums under the aerobic reaction conditions.
Funder
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Royal Society
Subject
General Chemistry,Catalysis,Organic Chemistry