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Author Spotlight: Experimental Approaches for the Synthesis of Low-Valent Metal-Organic Frameworks from Multitopic Phosphine Linkers
Published on: May 12, 2023
Engineering Highly Reduced Molybdenum Polyoxometalates via the Incorporation of d and f Block Metal Ions
Eduard Garrido Ribó1, Nicola L Bell1, De-Liang Long1
1School of Chemistry, The University of Glasgow, Glasgow, G12 8QQ, UK.
Abstract:
The assembly of nanoscale polyoxometalate (POM) clusters has been dominated by the highly reduced icosahedral {Mo132 } "browns" and the toroidal {Mo154 } "blues" which are 45 % and 18 % reduced, respectively. We hypothesised that there is space for a greater diversity of structures in this immediate reduction zone. Here we show it is possible to make highly reduced mix-valence POMs by presenting new classes of polyoxomolybdates: [MoV 52 MoVI 12 H26 O200 ]42- {Mo64 } and [MoV 40 MoVI 30 H30 O215 ]20- {Mo70 }, 81 % and 57 % reduced, respectively. The {Mo64 } cluster archetype has a super-cube structure and is composed of five different types of building blocks, each arranged in overlayed Archimedean or Platonic polyhedra. The {Mo70 } cluster comprises five tripodal {MoV 6 } and five tetrahedral {MoV 2 MoVI 2 } building blocks alternatively linked to form a loop with a pentagonal star topology. We also show how the reaction yielding the {Mo64 } super-cube can be used in the enrichment of lanthanides which exploit the differences in selectivity in the self-assembly of the polyoxometalates.
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