Backbone Reactivity of Manganese(I) NacNac Complexes

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Authors: Antonia Reisenhofer, Michael Johann Jöbstl, Antoine Dupé, Nadia C. Mösch‐Zanetti
Cited by: 1
References: 42

Abstract

High Resolution Image Download MS PowerPoint Slide The reactivity of manganese(I) NacNac complexes was investigated toward various substrates for potential catalytic applications. The reaction of the five-coordinate β-diketiminate complex [Mn(La)(CO) 3 ] (La: MeC(NAr)CRC(NAr)Me, Ar = 2,6-Me 2 Ph, R = H 2a ) with formaldehyde allowed the isolation of complex [Mn(La–H 2 CO)(CO) 3 ] ( 3a ), where the aldehyde had added with the formation of a C–C and Mn–O bond. Similarly, reactions of the β-diketiminate complexes with acetylene and phenylacetylene resulted in [Mn(Lx–R′C 2 H)(CO) 3 ] (x = a Ar = 2,6-Me 2 Ph R′ = H, 4a, R′ = Ph 5a; x = b Ar = Ph, R′ Ph 4b ). In contrast, the β-diketiminate Mn(I) complex 2a reacted with the labile coordination of acetonitrile which could be removed via vacuum. However, nitrile insertion was observed with the β-diketimine complexes of the type [MnBr(CO) 3 (HLx)]. The nitrile moiety was inserted into the α–C-H bond of the LxH ligand via the formation of a C–C and Mn–N bond, giving [Mn(Lx–R″CNH)(CO) 3 ] (x = a Ar = 2,6-Me 2 Ph R″ = Me 6a, R″ = Ph 7a; x = c Ar = Ph, R″ = Me 6c ). This versatile reactivity of β-diketiminate and β-diketimine manganese(I) complexes delivers important knowledge for future investigations of their catalytic properties.

Fields of Study & Subjects

Organometallic Complex Synthesis and Catalysis Metal-Catalyzed Oxygenation Mechanisms Magnetism in coordination complexes

Publication details

Journal / source
Organometallics
Publisher
American Chemical Society (ACS)
Volume
45
Issue
13
Pages
1626–1634
Publication date
3 July 2026
Language
EN