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One-pot mechanochemical synthesis was demonstrated to be an efficient strategy to synthesize host-guest POM⊂rho-ZIF complexes (POM = polyoxometalate; rho-ZIF = zeolitic imidazolate framework with rho topology) with high crystallinity. In this work, the metastable rho-ZIF with large interior cavities and windows was used as host matrix for encapsulating and immobilizing bulky guest molecules with high loading efficiency and chemical stability. As novel catalysts, POM⊂rho-ZIF complexes were found effective for the selective oxidation of a series of sulfides to sulfoxides. Moreover, the heterogeneity of these composite catalysts was confirmed by leaching tests, and they can be recycled at least four times without significant loss of activity.

We report macroscopic evidence of the liquidlike nature of surface-tethered poly(dimethylsiloxane) (PDMS) brushes by studying their adhesion to ice. Whereas ice permanently detaches from solid surfaces when subjected to sufficient shear, commonly referred to as the material's ice adhesion strength, adhered ice instead slides over PDMS brushes indefinitely. When additionally methylated, we observe Couette-like flow of the PDMS brushes between the ice and silicon surface. PDMS brush ice adhesion displays a shear-rate-dependent shear stress, rheological behavior reminiscent of liquids, and is affected by ice velocity, temperature, and brush thickness, following scaling laws akin to liquid PDMS films. This liquidlike nature allows ice to detach solely by self-weight, yielding an ice adhesion strength of 0.3 kPa, 1000 times less than a low surface energy, perfluorinated monolayer. The methylated PDMS brushes also display omniphobicity, repelling essentially all liquids with vanishingly small contact angle hysteresis. Methylation results in significantly higher contact angles than previously reported, nonmethylated brushes, especially for polar liquids of both high and low surface tension.

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