Tunable laser photodissociation spectroscopy measurements and photofragment imaging experiments are employed to investigate the dissociation energy of the Fe(benzene) ion-molecule complex. Additional spectroscopy measurements determine the dissociation energy of Fe(benzene). The dissociation energies for Fe(benzene) determined from the threshold for the appearance of the Fe fragment (48.4 ± 0.2 kcal/mol) and photofragment imaging (≤49.3 ± 3.2 kcal/mol) agree nicely with each other and with the value determined previously by collision-induced dissociation (49.5 ± 2.9 kcal/mol), but they are lower than the values produced by computational chemistry at the density functional theory level using different functionals recommended for transition-metal chemistry. The threshold measurement for Fe(benzene) (43.0 ± 0.2 kcal/mol) likewise agrees with the value (44.7 ± 3.8 kcal/mol) from previous collision-induced dissociation measurements.
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http://dx.doi.org/10.1021/acs.jpca.3c00735 | DOI Listing |
J Phys Chem A
December 2024
Department of Chemistry, University of Georgia, Athens, Georgia 30602, United States.
Tunable laser photodissociation spectroscopy and photofragment imaging experiments are employed to investigate the spectroscopy and dissociation dynamics of the Mg(benzene) ion-molecule complex. When excited with ultraviolet radiation, Mg(benzene) photodissociates efficiently, producing both Mg and benzene fragments, with branching ratios depending on the wavelength. The wavelength dependence of these processes are similar, with intense resonances at 330 and 241 nm and weaker features at 290 and 258 nm.
View Article and Find Full Text PDFJ Phys Chem A
October 2024
Departamento de Química Física, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, 28040 Madrid, Spain.
J Phys Chem A
July 2024
State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, CAS, Dalian 116023, P. R. China.
Under irradiation of a vacuum ultraviolet (VUV) photon, methane dissociates and yields multiple fragments. This photochemical behavior is not only of fundamental importance but also with wide-ranging implications in several branches of science. Despite that and numerous previous investigations, the product channel branching is still under debate, and the underlying dissociation mechanisms remain elusive.
View Article and Find Full Text PDFJ Phys Chem A
April 2024
Hangzhou Institute of Advanced Studies, Zhejiang Normal University, 1108 Gengwen Road, Hangzhou 311231, Zhejiang, P. R. China.
The wavelength-dependent dynamics of the O(D) channel, formed by photoexcitation of CO to the Δ state at 143.53-153.03 nm, is investigated by using the time-sliced velocity-mapped ion imaging method.
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