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- W2008200767 abstract "Density functional calculations have been carried out to determine the structure and bonding for ruthenium porphyrin and carbonyl diyl complexes (CO)4Ru−EHeq (1a−e), (CO)4Ru−EHax (2a−e), (Por)Ru−EH (3a−e), and for (Por)Ru−E(trip) (4a−e, trip = 2,4,6-triisopropylphenyl) with E being a group 13 element (E = B−Tl). Subsequent natural bond orbital (NBO) analyses have been applied to examine in detail the Ru−E bonding situation and the influence of the porphyrin ligand. The calculations reveal high Ru−E (E = B−Tl) bond dissociation energies, especially for the ruthenium boron bonds in 3a and 4a. The NBO analyses show E−Ru π-back-bonding is most significant in the case of boron. The influence of the porphyrin ligand on this π-back-bonding interaction is similar to the one demonstrated for carbonyl ligands; however, the σ-donation from E to Ru is stronger in the case of the porphyrin ligand." @default.
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- W2008200767 date "2002-10-24" @default.
- W2008200767 modified "2023-10-18" @default.
- W2008200767 title "Theoretical Investigations into Transition Metal−Group 13 Element Bonding: Comparison between Ruthenium Porphyrin and Ruthenium Carbonyl Diyl Compounds" @default.
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- W2008200767 doi "https://doi.org/10.1021/om020530z" @default.
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