Publications by authors named "Norah Alsadun"

For the modified progression of organo-oxidative reactions of alcohols, a monometallic copper(II) diarylhydrazone complex (CuONLCl) was constructed through the coordination of an arylhydrazone ligand (HONL) with a copper(II) ion. Its chemical structure was validated by alternative spectroscopic approaches. The heterogeneity of CuONLCl was constructed through successful surface covering of highly paramagnetic FeO/TiO nanoparticles (as CuONLCl@FeO/TiO).

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A highly sensitive and stable nonenzymatic glucose biosensor has been developed via composite materials composed of CuO and graphene oxide (GO)/carbon nanotube (CNT) nanohybrid (CuO/GO/CNTs). Copper oxide nanoparticle(NP)-modified CNTs were stacked via graphene sheets and synthesized through hydrothermal method, providing a larger surface area with boosted catalytic activity for efficient mass and electron passage, respectively. Scanning electron microscopy (SEM) and energy-dispersive x-ray (EDX) spectroscopy have been used to investigate the morphology and composition of as-prepared nanohybrids, whereas x-ray diffraction (XRD) patterns provide information about the crystal structure and lattice parameters.

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Here, the fundamental requirements are described for understanding and using topology tools in the design of porous materials, emphasizing the relationships between nets, metal-organic framework (MOF) structures, nodes, and building blocks. Common design approaches are discussed, highlighting prerequisites for the rational design of MOFs, such as those with simple pcu topology through the molecular building block approach, or axial-to-axial pillaring. The importance of highly connected nets and building units is emphasized for achieving structural predictability.

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Rational design of intricate multicomponent reticular structures is often hindered by the lack of suitable blueprint nets. We established the merged-net approach, proffering optimal balance between designability and complexity, as a systematic solution for the rational assembly of multicomponent structures. In this work, by methodically mapping node-net relationships among 53 basic edge-transitive nets, we conceived a signature net map to identify merging net pairs, resulting in the enumeration of 53 merged nets.

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In aqueous and solid media, 2-HP-β/γ-CD inclusion complexes with poly aromatic hydrocarbon (PAH) Phenanthrene (PHN), Anthracene (ANT), Benz(a)pyrene (BaP), and Fluoranthene (FLT) were investigated for the first time. The inclusion complexes were characterized and investigated using fluorescence and HNMR spectroscopy. The most prevalent complexes consisting of both guests and hosts were those with a 1:1 guest-to-host ratio.

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Proton activity in electrolytes plays a crucial role in deciding the electrochemical performance of aqueous batteries. On the one hand, it can influence the capacity and rate performance of host materials because of the high redox activity of protons. On the other hand, it can also cause a severe hydrogen evolution reaction (HER) when the protons are aggregated near the electrode/electrolyte interface.

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In spite of massive progress in oil-water separation, attributable to the use of advanced materials, the separation process faces challenges such as low permeance and fouling problems. Therefore, superwettable materials used in several fields are considered potential candidates for oily wastewater treatment. Metal-organic frameworks (MOFs) are receiving more and more interest in various separation applications due to their wide potential applications.

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Membrane technology, regarded as an environmentally friendly and sustainable approach, offers great potential to address the large energy penalty associated with the energy-intensive propylene/propane separation. Quest for molecular sieving membranes for this important separation is of tremendous interest. Here, a fluorinated metal-organic framework (MOF) material, known as KAUST-7 (KAUST: King Abdullah University of Science and Technology) with well-defined narrow 1D channels that can effectively discriminate propylene from propane based on a size-sieving mechanism, is successfully incorporated into a polyimide matrix to fabricate molecular sieving mixed matrix membranes (MMMs).

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The ongoing global industrialization along with the notable world population growth is projected to challenge the global environment as well as pose greater pressure on water and food needs. Foreseeably, an improved irrigation management system is essential and the quest for refined chemical sensors for soil-moisture monitoring is of tremendous importance. Nevertheless, the persisting challenge is to design and construct stable materials with the requisite sensitivity, selectivity, and high performance.

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Mixed-matrix membranes (MMMs) based on luminescent metal-organic frameworks (MOFs) and emissive polymers with the combination of their unique advantages have great potential in separation science, sensing, and light-harvesting applications. Here, we demonstrate MMMs for the field of high-speed visible-light communication (VLC) using a very efficient energy transfer strategy at the interface between a MOF and an emissive polymer. Our steady-state and ultrafast time-resolved experiments, supported by high-level density functional theory calculations, revealed that efficient and ultrafast energy transfer from the luminescent MOF to the luminescent polymer can be achieved.

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Herein we report novel mesoporous zirconium-based metal-organic frameworks (MOFs) with zeolitic sodalite () topology. Zr-ZMOF-1 and -2 are constructed based on a novel cantellation design strategy. Distinctly, organic linkers are judiciously designed in order to promote the deployment of the 12-coordinated Zr hexanuclear molecular building block (MBB) as a tetrahedral secondary building unit, a prerequisite for zeolite-like nets.

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Herein, we report a new light-harvesting mixed-ligand Zr(IV)-based metal-organic framework (MOF),with underlying topology, encompassing the [Zr(μ-O)(μ-OH)(OC-)] cluster and an equimolar mixture of thiadiazole- and benzimidazole-functionalized ligands. The successful integration of ligands with similar structural features but with notable chemical distinction afforded the attainment of a highly efficient energy transfer (ET). Notably, the very strong spectral overlap between the emission spectrum of benzimidazole (energy donor) and the absorption spectrum of thiadiazole (energy acceptor) provided an ideal platform to achieve very rapid (picosecond time scale) and highly efficient energy transfer (around 90% efficiency), as evidenced by time-resolved spectroscopy.

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