Coordination polymer-forming liquid Cu(2-isopropylimidazolate).

The structure of the melt state of one-dimensional (1D) coordination polymer crystal Cu(isopropylimidazolate) (melting temperature = 143 °C) was characterized by DSC, variable temperature PXRD, solid-state NMR (SSNMR), viscoelastic measurements, XAS, and DFT-AIMD calculations. These analyses suggested "coordination polymer-forming liquid" formation with preserved coordination bonds above . Variable chain configurations and moderate cohesive interaction in adjacent chains are the keys to the rarely observed polymer-forming liquid.

Hydroxylation of UiO-66 Metal-Organic Frameworks for High Arsenic(III) Removal Efficiency.

Zirconium clusters of UiO-66 have been hydroxylated with NaOH to generate strong binding sites for As(III) species in wastewater treatment. Hydroxylated UiO-66 provides high adsorption capacity over a wide range of pH from 1 to 10 with a maximum uptake of 204 mg g, which is significantly enhanced compared to those of pristine UiO-66, acid-modulated UiO-66, and other adsorbents for use in a wide pH range of treatment processes. The local structure of hydroxylated sites and As(III) adsorption mechanism are determined by extended X-ray absorption fine structure combined with density functional theory calculations.

Processable UiO-66 Metal-Organic Framework Fluid Gel and Electrical Conductivity of Its Nanofilm with Sub-100 nm Thickness.

Zr-based UiO-66 metal-organic framework (MOF) is one of the most studied MOFs with a wide range of potential applications. While UiO-66 is typically synthesized as a microcrystalline solid, we employ a particle downsizing strategy to synthesize UiO-66 as fluid gel with unique rheological properties, which allows the solution-based processing as sub-100 nm films and enhances the electrical conductivity of its pristine structure. Film thicknesses ranging from 40 to 150 nm could be achieved by controlling the spin-coating parameters.

Incorporation of Al Sites on Brønsted Acid Metal-Organic Frameworks for Glucose-to-Hydroxylmethylfurfural Transformation.

5-hydroxylmethylfurfural (HMF) is a bio-based chemical that can be prepared from natural abundant glucose by using combined Brønsted-Lewis acid catalysts. In this work, Al catalytic site has been grafted on Brønsted metal-organic frameworks (MOFs) to enhance Brønsted-Lewis acidity of MOF catalysts for a one-pot glucose-to-HMF transformation. The uniform porous structure of zirconium-based MOFs allows the optimization of both acid strength and density of acid sites in MOF-based catalysts by incorporating the desired amount of Al catalytic sites at the organic linker.

Metalloporphyrin-Based Metal-Organic Frameworks on Flexible Carbon Paper for Electrocatalytic Nitrite Oxidation.

Deposition of redox-active metal-organic frameworks (MOFs) as thin films on conductive substrates is of great importance to improve their electrochemical performance and durability. In this work, a series of metalloporphyrinic MOF crystals was successfully deposited as thin films on carbon fiber paper (CFP) substrates, which is an alternative to rigid glass substrates. The specific dimensions of the obtained films could be adjusted easily by simple cutting.