Modulation of benzene or naphthalene binding to palladium cluster sites by the backside-ligand effect.

Abstract

The backside-ligand modulation strategy to enhance the substrate binding property of Pd clusters is reported. The benzene or naphthalene binding ability of Pd3 or Pd4 clusters is enhanced significantly by the backside cyclooctatetraene ligand, leading to the formation of the first solution-stable benzene- or naphthalene Pd clusters. The present results imply that the ligand design of the metal clusters, especially for the backside ligand of the metal cluster site, is crucial to acquire a desired reactivity of metal clusters.