Publications by authors named "Jiashan Mi"

Article Synopsis
  • - Rare-earth elements (REEs) are important in various materials, and developing solid adsorbents for their capture could help recycle REE-rich magnets and electronics cost-effectively.
  • - Covalent organic frameworks (COFs) have a high surface area and potential for REE adsorption, but their use is limited due to their poor lifespan in acidic conditions and challenges in ligand incorporation.
  • - A new approach using the Ugi multicomponent reaction to modify imine-based COFs has produced a diglycolic acid-functionalized COF that significantly increases REE adsorption capacity, making it a promising candidate for efficient and recyclable REE capture.
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Two hydrogen-bonded crosslinked organic frameworks (HOFs) were synthesized free radical reactions utilizing butadiene and isoprene as crosslinkers. These HOFs exhibit high crystallinity, enabling detailed structural characterization single-crystal X-ray diffraction analysis. Subsequently, one of the olefin-rich HOFs was converted to a hydroxylated framework through hydroboration-oxidation while maintaining the high crystallinity.

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Crystallization is a widely used purification technique in the manufacture of active pharmaceutical ingredients (APIs) and precursor molecules. However, when impurities and desired compounds have similar molecular structures, separation by crystallization may become challenging. In such cases, some impurities may form crystalline solid solutions with the desired product during recrystallization.

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Solid-state nuclear magnetic resonance (ssNMR) spectroscopy has found increasing application as a method for quantification and structure determination of solid forms (polymorphs) of organic solids and active pharmaceutical ingredients (APIs). However, ssNMR spectroscopy suffers from low sensitivity and resolution, making it challenging to detect dilute solid forms that may be present after recrystallization or reaction with co-formers. Cousin (S.

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The library of imine-linked covalent organic frameworks (COFs) has grown significantly over the last two decades, featuring a variety of morphologies, pore sizes, and applications. An array of synthetic methods has been developed to expand the scope of the COF functionalities; however, most of these methods were designed to introduce functional scaffolds tailored to a specific application. Having a general approach to diversify COFs via late-stage incorporation of functional group handles would greatly facilitate the transformation of these materials into platforms for a variety of useful applications.

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