Structurally precise metal nanoclusters with a facile synthetic process and high catalytic performance have been long pursued. These atomically precise nanocatalysts are regarded as model systems to study structure-performance relationships, surface coordination chemistry, and the reaction mechanism of heterogeneous metal catalysts. Nevertheless, the research on silver-based nanoclusters for driving chemical transformations is sluggish in comparison to gold counterparts. Herein, we report the one-step synthesis of Pt/Ag alloy nanoclusters of [PtAg 9 (C 18 H 12 Br 3 P) 7 Cl 3 ](C 18 H 12 Br 3 P), which are highly active in catalysing cycloaddition reactions of CO 2 and epoxides. The cluster was obtained in a rather simple way with the reduction of silver and platinum salts in the presence of ligands in one pot. The molecular structure of the titled cluster describes the protection of the Pt-centred Ag 9 crown by the shell of phosphine ligands and halides. Its electronic structure, as revealed by density function theoretical calculations, adopts a superatomic geometry with 1S 2 1P 6 configuration. Interestingly, the cluster displays high activity in the formation of cyclic carbonates from CO 2 under mind conditions.
Keyphrases
- sensitive detection
- quantum dots
- highly efficient
- energy transfer
- fluorescent probe
- label free
- gold nanoparticles
- visible light
- silver nanoparticles
- density functional theory
- ionic liquid
- molecular dynamics
- high resolution
- molecularly imprinted
- mass spectrometry
- reduced graphene oxide
- metal organic framework
- monte carlo