Abstract

Group 15 triphenyl compounds with coordination ability such as triphenylamine (NPh3) and triphenylphosphine (PPh3) have been widely investigated for the construction of functional porous organic materials. In this work, a SbPh3-based organic molecular cage (Sb-cage) was unprecedently synthesized. The spatial configuration of Sb-cage was precisely analyzed by single crystal X-ray diffraction, showing a trigonal–bipyramidal [2 + 3] assembly. Sb-cage was employed to the mediated growth of palladium nanoparticles (PdNPs) with an average diameter of 0.70 nm. As-synthesized utrafine PdNPs exhibits good catalytic activity in Suzuki-Miyaura coupling reaction between aryl halides and phenylboronic acid, where the PdNPs could grow up in situ to a stable size distribution of 1.71 ± 0.30 nm. Furthermore, the advantages of the trigonal bipyramidal configuration in the stabilization of metal nanoparticles during the catalytic reaction cycles were demonstrated via the control experiments on SbPh3-based unclosed semicage.

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