TRANSITION-METAL POLYHYDRIDE COMPLEXES - A THEORETICAL VIEW Academic Article uri icon

abstract

  • The factors governing the stabilities of classical and non-classical isomers in transition metal polyhydride complexes are summarized in this review. Diagonal lines in the Periodic Table, which divide the classical (left-hand side of the line) and non-classical (right-hand side of the line) isomers, were defined for neutral (through Ru and Ir) and cationic (between Tc/Ru and Os/Ir) complexes with only phosphine ligands. The carbonyl ligand was found to stabilize significantly the non-classical isomers due to its strong -accepting ability. The strong ""- and ""-donating ability of the Cp ligand makes most of its polyhydride complexes adopt classical structures. In this review, we also discuss some unique structural features in several types of polyhydride complex, such as the orientation of 2-H2; ligands in non-classical structures and the distortions in the "four-legged piano-stool" complexes (MHnL4-nCp) and the pseudo-pentagonal-bipyramidal complexes (MHnL6-nCp). 1994.

published proceedings

  • COORDINATION CHEMISTRY REVIEWS

altmetric score

  • 3

author list (cited authors)

  • LIN, Z. Y., & HALL, M. B.

citation count

  • 98

complete list of authors

  • LIN, ZY||HALL, MB

publication date

  • November 1994