We report the single-crystal synthesis of a chlorine-centered bimetallic cluster, Cl@Ag22 Au6 (4-TBBT)28 (PPh4 ), which bears a quatrefoil-structured Cl@Ag22 (SR)16 core studded by six Au(SR)2 staples showing a quasi Td symmetry. This cluster bears 28 metal atoms and 28 ligands, with a chlorine atom hosted in the center of the metallic Ag22 Au6 core. Single-crystal analysis shows that this cluster possesses essentially a different bonding nature compared with other monolayer-protected metal clusters (MPCs) or traditional metal-sulfur complexes. We fully dissect the structure evolution in forming such a chlorine-centered cluster. Interestingly, this cluster, Cl@Ag22 Au6 (4-TBBT)28 (PPh4 ), displays a fluorescence emission at 570 nm and supports the solid emission with a minor red shift at 574 nm. On the other hand, we have tested the nonlinear optical property and observed unambiguous nonlinear optical property with a normal valley-shaped transmittance curve corresponding to reverse saturated absorption (RSA) of the cluster.
Keywords: Cl@Ag22(SR)16; Metal cluster; bimetallic cluster; chlorine centre; photoluminescence.
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