Resum
Calculations performed using both density functional theory (DFT) and the modified coupled-pair functional (MCPF) approach show that FeC5H6+ is more stable than HFeC5H5+ by about 10 kcal/mol. The ground state of FeC5H6+ is a quartet state derived from the 3d7 occupation of Fe+. For HFeC5H5+, the MCPF approach yields a sextet ground state while DFT yields a quartet; however, these two states are close in energy at both levels of theory. © 1995.
Idioma original | Anglès |
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Pàgines (de-a) | 526-532 |
Revista | Chemical Physics Letters |
Volum | 240 |
Número | 5-6 |
DOIs | |
Estat de la publicació | Publicada - 7 de jul. 1995 |