A 66‐Nuclear All‐Alkynyl Protected Peanut‐Shaped Silver(I)/Copper(I) Heterometallic Nanocluster: Intermediate in Copper‐Catalyzed Alkyne‐Azide Cycloaddition

Abstract Ligand‐protected heterometallic nanoclusters in contrast to homo‐metal counterparts show more broad applications due to the synergistic effect of hetero‐metals but their controllable syntheses remain a challenge. Among heterometallic nanoclusters, monovalent Ag‐Cu compounds are rarely explored due to much difference of Ag(I) and Cu(I) such as atom radius, coordination habits, and redox potential. Encouraged by copper‐catalyzed alkyne‐azide cycloaddition (CuAAC) reaction, comproportionation reaction of Cu(II)X 2 and Cu(0) in the presence of (PhC≡CAg) n complex and molybdate generated a core‐shell peanut‐shaped 66‐nuclear Ag(I)‐Cu(I) heterometallic nanocluster, [(Mo 4 O 16 ) 2 @Cu 12 Ag 54 (PhC≡C) 50 ] (referred to as Ag 54 Cu 12 ). The structure and composition of Ag‐Cu heterometallic nanocluster are fully characterized. X‐ray single crystal diffraction reveals that Ag 54 Cu 12 has a peanut‐shaped silver(I)/copper(I) heterometallic nanocage protected by fifty phenylacetylene ligands in µ 3 –modes and encapsulated two mutually twisted tetramolybdates. Heterometallic nanocage contains a 54‐Ag‐atom outer ellipsoid silver cage decorated by 12 copper inside wall. Nanosized Ag 54 Cu 12 is a n ‐type narrow‐band‐gap semiconductor with a good photocurrent response. Preliminary experiments demonstrates that Ag 54 Cu 12 itself and activated carbon supported Ag 54 Cu 12 /C are effective catalysts for 1,3‐dipole cycloaddition between alkynes and azides at ambient conditions. The work provides not only a new synthetic route toward Ag(I)‐Cu(I) nanoclusters but also an important heterometallic intermediate in CuAAC catalytic reaction.