Journal
ORGANOMETALLICS
Volume 31, Issue 14, Pages 4971-4979Publisher
AMER CHEMICAL SOC
DOI: 10.1021/om300209a
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Funding
- EPSRC
- Spanish Ministerio de Ciencia e Innovacion
- Royal Society
- EPSRC [EP/F000650/1, EP/D04779X/1, EP/F003285/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/F003285/1, EP/F000650/1, EP/D04779X/1] Funding Source: researchfish
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UV irradiation of Cp'Mn(CO)(3) (Cp' = eta(5)-C5H4Me) in the presence of the free N-heterocyclic carbenes IEt2Me2, (IPr2Me2)-Pr-i, IMes, and IPr affords the NHC dicarbonyl complexes Cp'Mn(CO)(2)(NHC) (1-4). Time-resolved infrared spectroscopy in alkane solution reveals that 1-4 photodissociate CO to generate Cp'Mn(CO)(NHC) (1-CO, 2-CO, 3-CO, 4-CO), which exhibit solvent-independent second-order rate constants (k(CO)) for reaction with CO. These observations are consistent with 1-CO to 4-CO being stabilized by intramolecular agostic interactions with the NHCs rather than intermolecular alkane coordination. Density functional theory calculations provide support for this hypothesis and locate a series of agostic structures varying from delta-agostic (1-CO, 2-CO), to epsilon-agostic (3-CO), to phi-agostic (4-CO). The atoms-in-molecules approach is used to characterize these species, along with the gamma-agostic interaction seen in the CpMn(CO)(PPh3) analogue (5-CO), and shows that these species are distinguished primarily by the magnitude of the electron density at the agostic ring critical point.
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