Ming-Xing Li

Single‐Chain Magnetic Behavior in a Hetero‐Tri‐Spin Complex Mediated by Supramolecular Interactions with TCNQF.− Radicals

The self-assembly of organic TCNQF˙⁻ radicals (2-fluoro-7,7,8,8-tetracyano-p-quinodimethane) and the anisotropic [Tb(valpn)Cu](3+) dinuclear cations produced a single-chain magnet (SCM) involving stacking interactions of TCNQF˙⁻ radicals (H2valpn is the Schiff base from the condensation of o-vanillin with 1,3-diaminopropane). Static and dynamic magnetic characterizations reveal that the effective energy barrier for the reversal of the magnetization in this hetero-tri-spin SCM is significantly larger than the barrier of the isolated single-molecule magnet based on the {TbCu} dinuclear core.

Alkaline Earth Guests in Polyoxopalladate Chemistry: From Nanocube to Nanostar via an Open‐Shell Structure

The three novel, discrete palladium(II)-oxo clusters [CaPd12O8(PhAsO3)8](6-) (CaPd12), [SrPd12O6(OH)3(PhAsO3)6(OAc)3](4-) (SrPd12), and [BaPd15O10(PhAsO3)10](8-) (BaPd15) encapsulating alkaline earth metal ions were prepared and fully characterized by a multitude of solution and solid-state physicochemical techniques. We have discovered a structure-directing template effect induced by the respective size of the alkaline earth guest ion, which determines the detailed condensation arrangement of the peripheral Pd(II)-oxo shell. The unprecedented SrPd12 with an open-shell type structure is of particular importance and reflects a successful strategy for deliberate design of new structural classes of polyoxo-noble-metalates. Furthermore, the unusual acetate-water ligand exchange phenomenon renders SrPd12 as a promising candidate for noble-metal-based catalysis.

Tetra-Antimony(III)-Bridged 18-Tungsto-2-Arsenates(V), [(LSbIII)4(A-α-AsVW9O34)2]10– (L = Ph, OH): Turning Bioactivity On and Off by Ligand Substitution

Two tetra-antimony(III)-bridged, sandwich-type 18-tungsto-2-arsenates(V), [(LSb(III))4(A-α-As(V)W9O34)2](10-) (L = Ph (1), OH (2)), were prepared and fully characterized in the solid state and in solution. Both polyanions are stable in aqueous physiological medium for at least 24 h (at concentrations ≥2.5 × 10(-6) M). Despite the presence of an isostructural tetra-antimony(III) motif in 1 and 2, distinctly different antibacterial activity was observed for both polyanions. The minimum inhibitory concentrations (MIC) of 1 (7.8-62.5 μg/mL) is lower than for any other organoantimony(III)-containing polyoxometalate reported to date.

CCDC 1481631: Experimental Crystal Structure Determination

Related Article: Zhao-Xi Wang, Lin-Fei Wu, Xuan Zhang, Feifei Xing, Ming-Xing Li|2016|Dalton Trans.|45|19500|doi:10.1039/C6DT04010A