Thiacalix[4]arene-Protected Silver Nanoclusters Encapsulating Different Two-Electron Superatom Oligomers.

The subvalent silver kernel represents the nascent state of silver cluster formation, yet the growth mechanism has long been elusive. Herein, two silver nanoclusters ( Ag30 and Ag34 ) coprotected by TC4A 4- (H 4 TC4A = p - tert -butylthiacalix[4]arene) and TBPMT - (TBPMTH = 4- tert -butylbenzenemethanethiol) containing 6e and 4e silver kernels are synthesized and characterized. The trimer of the 2e superatom Ag 14 kernel in Ag30 is built from a central Ag 6 octahedron sandwiched by two orthogonally oriented Ag 5 trigonal bipyramids through sharing vertexes, whereas a double-octahedral Ag 10 kernel in Ag34 is a dimer of 2e superatoms. They manifest disparate polyhedron fusion growth patterns at the beginning of the silver cluster formation. Their excellent solution stabilities are contributed by the multisite and multidentate coordination fashion of TC4A 4- and the special valence electron structures. This work demonstrates the precise control of silver kernel growth by the solvent strategy and lays a foundation for silver nanocluster application in photothermal conversion.