Ultrafast infrared transient absorption spectroscopy of gas-phase Ni(CO)4 photodissociation at 261 nm

Ultrafast infrared transient absorption spectroscopy of gas-phase Ni(CO)4 photodissociation at 261 nm

We employ ultrafast mid-infrared transient absorption spectroscopy to probe the rapid loss of carbonyl ligands from gas-phase nickel tetracarbonyl following ultraviolet photoexcitation at 261 nm. Here, nickel tetracarbonyl undergoes prompt dissociation to produce nickel tricarbonyl in a singlet exci...

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Bibliographic Details
Published in:The Journal of chemical physics 2022-04, Vol.156 (14), p.144306-144306
Main Authors: Cole-Filipiak, Neil C., Troß, Jan, Schrader, Paul, McCaslin, Laura M., Ramasesha, Krupa
Format: Article
Language:eng
Subjects:
Absorption spectroscopy
Anharmonicity
Carbon monoxide
Carbonyls
Clusters
Density functional theory
Equations of motion
Excitation
Infrared spectroscopy
Nickel
Nickel carbonyl
Photodissociation
Photoexcitation
Potential energy
Spectrum analysis
Spin-orbit interactions
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Summary:We employ ultrafast mid-infrared transient absorption spectroscopy to probe the rapid loss of carbonyl ligands from gas-phase nickel tetracarbonyl following ultraviolet photoexcitation at 261 nm. Here, nickel tetracarbonyl undergoes prompt dissociation to produce nickel tricarbonyl in a singlet excited state; this electronically excited tricarbonyl loses another CO group over tens of picoseconds. Our results also suggest the presence of a parallel, concerted dissociation mechanism to produce nickel dicarbonyl in a triplet excited state, which likely dissociates to nickel monocarbonyl. Mechanisms for the formation of these photoproducts in multiple electronic excited states are theoretically predicted with one-dimensional cuts through the potential energy surfaces and computation of spin–orbit coupling constants using equation of motion coupled cluster methods (EOM-CC) and coupled cluster theory with single and double excitations (CCSD). Bond dissociation energies are calculated with CCSD, and anharmonic frequencies of ground and excited state species are computed using density functional theory (DFT) and time-dependent density functional theory (TD-DFT).
ISSN:0021-9606
1089-7690