Ligand effects in transition metal dihydrogen complexes: A theoretical study

Stefan Dapprich, Gernot Frenking

科研成果: 期刊稿件文章同行评审

66 引用 (Scopus)

摘要

Ab initio calculations at the MP2 and CCSD(T) level of theory using effective core potentials for the heavy atoms have been carried out in order to investigate systematically the trans influence of different ligands L upon H2 coordination in the dihydrogen complexes ML(CO)4-(H2) (M = Cr, Mo, W; L = CO, SiO, CS, CN-, NC-, NO+, N2, H-, F-, Cl-, PH3). The optimized geometries and the theoretically predicted M-H2 bond dissociation energies are reported. The ligands L are characterized in terms of their donor and acceptor capability using the CDA partitioning scheme. Strong σ-donor ligands in the trans position enhance the M-H2 bonding, while strong π-acceptors weaken the M-H2 bond. There is a good correlation between the calculated acceptor strength of L and the distance r(H-H) and the M-(H2) bond dissociation energy De, respectively. Finally, the dihydrogen complexes are compared with the related classical hydrides ML(CO)4(H)2.

源语言英语
页(从-至)4547-4551
页数5
期刊Organometallics
15
21
出版状态已出版 - 15 10月 1996
已对外发布

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