Fig. 1: Traditional chemistry of transition-metal carbonyls with nucleophiles and main-group metallomimetic analogues based on boron. | Nature Communications

Fig. 1: Traditional chemistry of transition-metal carbonyls with nucleophiles and main-group metallomimetic analogues based on boron.

From: A step-for-step main-group replica of the Fischer carbene synthesis at a borylene carbonyl

Fig. 1: Traditional chemistry of transition-metal carbonyls with nucleophiles and main-group metallomimetic analogues based on boron.The alternative text for this image may have been generated using AI.

a Fischer carbene synthesis and a variant thereof. Strong nucleophiles generally attack TM carbonyls at the carbon atom of a carbonyl ligand, leading to TM acylate complexes, which, when treated a cationic electrophile, provide either a Fischer carbene complex or a TM acyl complex, depending on a range of factors. b Fischer carbene synthesis at boron. The Fischer carbene synthesis can by replicated with metallomimetic borylene carbonyls, leading to bora-Fischer carbenes or acylborane Lewis adducts, main-group analogues of the traditional TM counterparts.

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