Mixed-linker synthesis of L-histidine@zeolitic imidazole framework-8 on amyloid nanofibrils-modified polyacrylonitrile membrane with high separation and antifouling properties

Bells and Whistles on Fertilizers: Molecular Hands to Hang Nanoporous Foliar Fertilizer Reservoirs

“…41 However, in the histidine MOF N 1s spectra, peaks at 398.5, 399.9, and 400.7 eV are attributed to the pyridinic, pyrrolinic, and quaternary nitrogen species, respectively (Figure S3). 42 ζ-Potential and DLS Size Measurement. The zeta potential and DLS of the prepared MOFs were assessed in water, which indicates their solubility (Figure 1c).…”

“… 41 However, in the histidine MOF N 1s spectra, peaks at 398.5, 399.9, and 400.7 eV are attributed to the pyridinic, pyrrolinic, and quaternary nitrogen species, respectively ( Figure S3 ). 42 …”

Preparation of imidazole-modified paper membrane for selective extraction of gallic acid and its structural and functional analogues from Pomegranate Peel

“…27 For integration with functional membranes, several forms have been developed through outstanding approaches in materials science, such as the derivatives of IM, 28 IM-based ionic liquids, 29 polymers containing IM, 30 and IM-type metal–organic frameworks (MOFs). 31 To regulate selectivity, IM as a functional monomer, alone or combined with other chemical groups, can be used for the adsorption or sensing of antibiotics, 32,33 pesticides, 33 salicylic acid, 34 or metal ions. 35 For further enhancement, the application of molecularly imprinted polymers (MIPs), 36–40 especially using IM-type functional monomers and template-induced cavities, 41 can achieve tailor-made selectivity towards a target compound or a class of compounds.…”