Affiliation:
1. School of Chemistry and Chemical Engineering State Key Laboratory of Crystal Materials Shandong University Ji'nan 250100 P. R. China
2. Computational Physics Laboratory Tampere University 33014 Tampere Finland
3. Department of Physics Norwegian University of Science and Technology 7491 Trondheim Norway
4. Department of Chemistry Bilkent University Ankara 06800 Turkey
Abstract
AbstractPolyoxometalates (POMs) represent crucial intermediates in the formation of insoluble metal oxides from soluble metal ions, however, the rapid hydrolysis‐condensation kinetics of MoVI or WVI makes the direct characterization of coexisted molecular species in a given medium extremely difficult. Silver nanoclusters have shown versatile capacity to encapsulate diverse POMs, which provides an alternative scene to appreciate landscape of POMs in atomic precision. Here, we report a thiacalix[4]arene protected silver nanocluster (Ag72b) that simultaneously encapsulates three kinds of molybdates (MoO42−, Mo6O228− and Mo7O258−) in situ transformed from classic Lindqvist Mo6O192−, providing more deep understanding on the structural diversity and condensation growth route of POMs in solution. Ag72b is the first silver nanocluster trapping so many kinds of molybdates, which in turn exert collective template effect to aggregate silver atoms into a nanocluster. The post‐reaction of Ag72b with AgOAc or PhCOOAg produces a discrete Ag24 nanocluster (Ag24a) or an Ag28 nanocluster based 1D chain structure (Ag28a), respectively. Moreover, the post‐synthesized Ag28a can be utilized as potential ignition material for further application. This work not only provides an important model for unlocking dynamic features of POMs at atom‐precise level but also pioneers a promising approach to synthesize silver nanoclusters from known to unknown.