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Ligand Substitutions Influence Gold Cluster Size and Fragmentation Pathways

Scientists at PNNL used synthesis in solution and high-resolution mass spectrometry to show that the substitution of diphosphine ligands dramatically affects the size and fragmentation pathways of gold clusters. This research overturns assumptions about cluster synthesis and provides insight into designing materials for energy storage and chemical manufacturing.

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Ligand Substitutions Influence Gold Cluster Size and Fragmentation Pathways

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  1. Minor Substitution Provides Insight into Designing Materials for Energy Storage and Chemical Manufacturing Using a combination of synthesis in solution and high-resolution mass spectrometry, scientists at PNNL demonstrated that the substitution of diphosphine ligands (top: cyclohexane; bottom: phenyl) dramatically influences the size and fragmentation pathways of otherwise identical gold clusters. Johnson GE, T Priest, and J Laskin. 2013. ChemPlusChem 78:1033-1039. DOI: 10.1002/cplu.201300134 Work was performed at EMSL Scientific Achievement Proved that changes at the phosphorus centers of diphenylphosphine ligands alter the size of gold clusters synthesized in solution and the fragmentation pathways of otherwise identical clusters. Significance and Impact Overturns assumptions about the influence of substitutions in cluster synthesis, a key process for building tailored materials. Research Details • Synthesized gold clusters capped with diphosphine ligands; prepared 2 solutions that differed only in the ligands used. • Electrosprayed liquids into mass spectrometer, creating positively charged ions in a gaseous stream. • Clusters synthesized using the phenyl-based ligand contained predominantly 11 gold atoms; clusters prepared using the cyclohexane-based ligand contained 9 gold atoms. • Gold clusters with the phenyl-containing ligand fragmented through the loss of gold atoms as well as activation of the phosphorus-carbon bonds of the ligands. Gold clusters with the cyclohexane ligands exhibited far less activation of the ligand.

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