Asma Ghazzy

The extreme hydration, small ionic size, and high charge density of Be ²⁺ ions make their recovery from hazardous industrial sludge a challenge, raising environmental concerns.

Ferrocene derivatives represent a transformative class of molecular sensors, combining exceptional electrochemical stability with tunable redox characteristics that enable precise detection across diverse analytical challenges in environmental, medical, and industrial applications. This comprehensive review examines the expanding applications of ferrocene‐based sensors (FBSs) across critical analytical domains. In environmental monitoring, these sensors achieve remarkable specificity for heavy metals and pesticides, with detection limits reaching nanomolar concentrations, thereby advancing pollution control strategies and ecosystem protection initiatives. In the medical field, FBSs detect biomarkers in biological fluids for early disease diagnosis, including the identification of enzymes and proteins crucial for understanding biological processes. They play a vital role in industrial monitoring by detecting volatile organic compounds (VOCs) to maintain workplace safety and environmental compliance. Furthermore, FBSs are applied to food safety by detecting contaminants, thereby safeguarding public health. These applications highlight the potential of FBSs as innovative tools for advancing sustainability, green chemistry, and eco‐friendly technologies.

The rapidly growing concern over the hazardous impact of phthalates on the environment and public health has led to a critical need for alternative and environmentally friendly plastics. Plasticizers developed from natural materials represent one possible solution. This paper explores four types of renewable feedstocks (sorbitol/polyols, glycerin, cardanol from cashew nutshell liquid, and limonene from citrus peels) as sources for developing alternative plasticizer systems. Key areas explored include the type of feedstock utilized, the methods used for extracting or processing the feedstocks, the nature of the chemical modification processes (e.g., esterification, epoxidation, etherification, or reactive grafting) applied to generate the respective plasticizers, and the resultant physical and mechanical properties. The performance of each plasticizer system in polymers such as PVC, PLA, and polysaccharide-based bioplastics is evaluated, alongside the compatibility with biological tissues, toxicological properties, biodegradability, and chemical migration into food simulants. The feasibility of each family of plasticizers is also assessed from an economic perspective, including availability of the feedstocks, economies of scale associated with large-volume production, and competitive pricing relative to established petroleum-derived plasticizers. Overall, sorbitol/polyol and glycerin derivative families have reached a level of maturity that provides a good balance of processability, food-contact safety, and biodegradability. Cardanol-based systems provide an attractive option where aromatic functional groups and combined plasticization–stabilization effects are needed. Limonene-derived plasticizer systems appear promising for use in PLA, but their broader utility may be limited by volatility, strong odors, and susceptibility to oxidation. Common issues identified across all four families include chemical migration into food products, regulatory approval, and the need for detailed life-cycle assessments.

Iron oxide nanozymes (IONzymes) have become fundamental components in various analyte detection methodologies such as colorimetric, electrochemistry, fluorescence and luminescence. Their tunability, stability and the possibility of modification, alongside their ability to mimic the catalytic properties of natural enzymes like peroxidase, render them invaluable in analytical chemistry. This review explores the diverse applications of IONzymes across analytical chemistry, with a particular highlighting on their roles in different detection techniques and their potential in biomedical and diagnostic applications. This information would be valuable for researchers and practitioners in the fields of analytical chemistry, biochemistry, biotechnology and materials science who are interested in applying IONzymes in their work. In essence, this review article on iron oxide nanozymes in analytical chemistry would serve as a valuable resource for researchers, educators and industry professionals, offering insights, guidance and inspiration for further study and application of this promising class of nanomaterials.

Complexes tris((1-ferrocenyl-1H-1,2,3-triazol-4-yl)methyl)amine (3), bis((1-ferrocenyl-1H-1,2,3-triazol-4-yl)methyl)amine (6), bis((1-ferrocenyl-1H-1,2,3-triazol-4-yl)methyl)ether (7), and 1-ferrocenyl-1H-1,2,3-triazol-4-yl)methanamine (9) were synthesized using the copper-catalyzed click reaction. Complexes 3, 6, 7, and 9 were characterized using NMR (¹H and ¹³{¹H}) and IR spectroscopy, elemental analysis, and mass spectrometry. Structures of 3, 7, and 9 in the solid state were determined using single-crystal X-ray diffraction. It was found that the triazole rings were planar and slightly twisted with respect to the cyclopentadienyl groups attached to them. Chains and 3D network structures were observed due to the presence of π⋯π and C–H⋯N interactions between the cyclopentadienyl and triazole ligands. A reversible redox behavior of the Fc groups between 239 and 257 mV with multicycle stability was characteristic for all the compounds, revealing that the electrochemically generated species Fc⁺ remained soluble in dichloromethane. Electrochemical sensor tests demonstrated the applicability of all the complexes to enhance the quantification sensing behavior of the screen-printed carbon electrode (SPCE) toward Cd²⁺, Pb²⁺, and Cu²⁺ ions.

Iron oxide nanozymes, which are magnetic nanoparticles with enzymatic properties, are explored, including their robust production techniques and diverse applications in the fields of biomedicine and environmental science.

There has been a new approach in the development of antibacterials in order to enhance the antibacterial potential. The nanoparticles are tagged on to the surface of other metals or metal oxides and polymers to achieve nanocomposites. These have shown significant antibacterial properties when compared to nanoparticles. In this article we explore the antibacterial potentials of metal-based and metal–polymer-based nanocomposites, various techniques which are involved in the synthesis of the metal–polymer, nanocomposites, mechanisms of action, and their advantages, disadvantages, and applications.

Treatment of 3,4-(ClC(O))₂-^cC₄H₂S (1) with [FcCH₂OLi] (2-Li) (Fc = Fe(η⁵-C₅H₅)(η⁵-C₅H₄)) in a 1:2 ratio gave 3,4-(FcCH₂OC(O))₂-^cC₄H₂S (3). Compound 3 decomposes in solution during crystallization to produce FcCH₂OH (2) along with 3,4-thiophenedicarboxylic anhydride (4). The cyclic voltammogram of 3 exhibits a reversible ferrocene-related redox couple (E_1/2 = 108 mV, vs. Cp₂Fe/Cp₂Fe⁺) using [NⁿBu₄] [B(C₆F₅)₄] as the supporting electrolyte. DFT calculations reveal that the energy values of the LUMO orbitals of 3 (3,4-thiophene core) show 1 eV higher energies than that one of 2,5-(FcCH₂OC(O))₂-^cC₄H₂S (5), both compounds’ HOMO orbitals are close to each other. Compound 4 was characterized by single X-ray structure analysis. It forms a band-type structure based on intermolecular O1···S1 interactions being parallel to (110) and (1–10) in the solid state, while electrostatic C···O interactions between the C=O functionalities of adjacent molecules connect both 3D-networks. Hirshfeld surface analysis was used to gain more insight into the intermolecular interactions in 4, the enrichment ratios (E) suggest that O···H, S···S, and O···C are the most favored intermolecular interactions, as shown by E values above 1.20. The relevance of the weak O···H, O···O, and O···C contacts in stabilizing the molecular structure of 4 was highlighted by the interaction energies between molecular pairs.

Here, we report a visible light-induced-trimetallic catalyst (Cu_0.5Zn_0.5Fe₂O₄) prepared through green synthesis using Tilia plant extract. These nanomaterials were characterized for structural and morphological studies using powder x-ray diffraction (P-XRD), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). The spinel crystalline material was ~34 nm. In benign reaction conditions, the prepared photocatalyst oxidized various benzylic alcohols with excellent yield and selectivity toward aldehyde with 99% and 98%; respectively. Aromatic and aliphatic alcohols (such as furfuryl alcohol and 1-octanol) were photo-catalytically oxidized using Cu_0.5Zn_0.5Fe₂O₄, LED light, H₂O₂ as oxidant, 2 h reaction time and ambient temperature. The advantages of the catalyst were found in terms of reduced catalyst loading, activating catalyst using visible light in mild conditions, high conversion of the starting material and the recyclability up to 5 times without loss of the selectivity. Thus, our study offers a potential pathway for the photocatalytic nanomaterial, which will contribute to the advancement of photocatalysis studies.

Here, we report on a phyto-mediated bimetallic (NiFe₂O₄) preparation using a Boswellia carterii extract, which was characterized by XRD, FT-IR, TGA, electron microscopy, magnetic spectroscopy, and Mössbauer spectroscopy measurements. The prepared nano-catalysts were tested for oxidation of lignin monomer molecules—vanillyl alcohol and cinnamyl alcohol. In comparison with previously reported methods, the nano NiFe₂O₄ catalysts showed high photocatalytic activity and selectivity, under visible light irradiation with a nitroxy radical initiator (2,2,6,6-tetramethylpiperidinyloxy or 2,2,6,6-tetramethylpiperidine 1-oxyl; TEMPO) at room temperature and aerobic conditions. The multifold advantages of the catalyst both in terms of reduced catalyst loading and ambient temperature conditions were manifested by higher conversion of the starting material.