Bismuth Bound to Transition Metals: Visible‐Light‐Induced Olefin Coordination, Reductive Elimination, and Oxidative Addition.

A series of dibenzobismepinyl (C14H10Bi) substituted transition metal complexes of the type [(C14H10Bi)M(CO)x(L)] (M=Mn, Co, Fe) was prepared in salt elimination reactions from a halobismepine and sodium metallates. Irradiation of these complexes with visible light has been investigated, aiming at the elimination of one carbonyl ligand and the concomitant coordination of the bismepine's olefin moiety to the transition metal center. The resulting complexes of the type [{κ2<italic>C</italic>,κ1<italic>Bi</italic>‐(C14H10)Bi}M(CO)x−1(L)] (M=Co, Fe) have been isolated and fully characterized. When two dibenzobismepinyl units are positioned in the coordination sphere of an iron carbonyl complex fragment, reductive elimination/oxidative addition events of the dibismuthane (C14H10Bi)2 have been shown to be relevant. The analytical techniques applied in this work include (heteronuclear) NMR spectroscopy, elemental analysis, single‐crystal X‐ray diffraction analysis, UV/Vis spectroscopy, IR spectroscopy and (TD)‐DFT calculations. [ABSTRACT FROM AUTHOR]