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CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity†‡
Fabian Fischer,Tobias Pientka,Haijun Jiao,Anke Spannenberg
Catalysis Science & Technology Pub Date : 10/02/2020 00:00:00 , DOI:10.1039/D0CY00876A
Abstract

The efficient synthesis and structural characterisation of a series of novel CpCo(I)–olefin–phosphite/phosphoramidite complexes and their evaluation in catalytic cyclotrimerisation reactions are reported. The protocol for precatalyst synthesis is widely applicable to different P-containing ligands, especially phosphites and phosphoramidites, as well as acyclic and cyclic olefins. A selection of the prepared complexes was investigated towards their catalytic performance in [2 + 2 + 2] cycloaddition reactions of diynes and nitriles, as well as triynes. While revealing significant differences in reactivity, the most reactive precatalysts work even already at 75 °C. One of these precatalysts also proved its potential in exemplary (co)cyclotrimerisations towards functionalised pyridines and benzenes. The energetics of complex formation and exemplary ligand exchange with a substrate diyne were elucidated by theoretical calculations and compared with the catalytic reactivity.

Graphical abstract: CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
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