Journal
DALTON TRANSACTIONS
Volume 50, Issue 35, Pages 12079-12082Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1dt02747f
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Funding
- JSPS KAKENHI [JP17K05814, JP21J22572]
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The use of alkylene-bridged bis-N-heterocyclic carbene ligands enhances the reactivity of the Pt3S2 core in a triplatinum complex. Despite the potential reaction between an Ag(i) ion and the Pt-Pt bond, steric hindrance results in coordination of one sulfide ligand to the Ag(i) ion.
Alkylene-bridged bis-N-heterocyclic carbene ligands working as strong sigma-donors enhance the reactivity of the Pt3S2 core in a triplatinum complex. Although an Ag(i) ion possibly reacts with the Pt-Pt bond, one of the sulfide ligands coordinates to an Ag(i) ion due to the steric hindrance of the ligands.
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