Abstract
We report the gas-phase synthesis of stable 20-electron carbonyl anion complexes of group 3 transition metals, TM(CO)8− (TM=Sc, Y, La), which are studied by mass-selected infrared (IR) photodissociation spectroscopy. The experimentally observed species, which are the first octacarbonyl anionic complexes of a TM, are identified by comparison of the measured and calculated IR spectra. Quantum chemical calculations show that the molecules have a cubic (Oh) equilibrium geometry and a singlet (1A1g) electronic ground state. The 20-electron systems TM(CO)8− are energetically stable toward loss of one CO ligand, yielding the 18-electron complexes TM(CO)7− in the 1A1 electronic ground state; these exhibit a capped octahedral structure with C3v symmetry. Analysis of the electronic structure of TM(CO)8− reveals that there is one occupied valence molecular orbital with a2u symmetry, which is formed only by ligand orbitals without a contribution from the metal atomic orbitals. The adducts of TM(CO)8− fulfill the 18-electron rule when only those valence electrons that occupy metal–ligand bonding orbitals are considered.
Original language | English |
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Pages (from-to) | 6236-6241 |
Number of pages | 6 |
Journal | Angewandte Chemie - International Edition |
Volume | 57 |
Issue number | 21 |
DOIs | |
State | Published - 22 May 2018 |
Keywords
- 18-electron rule
- DFT calculations
- bonding analysis
- carbonyl complexes
- photodissociation spectroscopy