A novel cerium-based metal-organic framework supported Pd catalyst for semi-hydrogenation of phenylacetylene.

Phenylacetylene is a detrimental impurity in the polymerisation of styrene, capable of poisoning catalysts even at ppm levels and significantly degrading the quality of polystyrene. The semi-hydrogenation of phenylacetylene to styrene instead of ethylbenzene is, therefore, an important industrial process. We report a novel cerium(iv)-based metal-organic framework (denoted as Ce-bptc), which comprises {Ce} clusters bridged by biphenyl-3,3',5,5'-tetracarboxylate linkers. Ce-bptc serves as an ideal support for palladium nanoparticles and the Pd@Ce-bptc catalyst demonstrates excellent catalytic performance for semi-hydrogenation of phenylacetylene, achieving a selectivity of 93% towards styrene on full conversion under ambient conditions with excellent reusability. synchrotron X-ray powder diffraction and electron paramagnetic resonance spectroscopy reveal the binding domains of phenylacetylene within Ce-bptc, and details of the reaction mechanism are discussed.