The hydrothermal synthesis of zinc oxide (ZnO) particles from zinc acetylacetonate monohydrate in "pure" aqueous solution and in aqueous NaOH solution at 90 °C is reported. The structural and morphological properties of ZnO particles were investigated by powder X-ray diffraction, X-ray absorption spectroscopy (XAS), field emission scanning electron microscopy, and transmission electron microscopy. The effect of NaOH on the growth mechanism and photocatalytic performance of hierarchical ZnO structures was investigated. The experimental findings, supported by results of quantum chemical calculations at the level of density functional theory, were used to propose the mechanism of nucleation and preferential growth of finely tuned hollow and nonhollow ZnO structures and their effects on the photocatalytic activity. The calculations indicate that the process of ZnO nucleation in "pure" aqueous solution mainly proceeds by the reaction of small monomers, while tetramers play a crucial role in aqueous NaOH solution. Both the preferred ZnO nanostructure and microstructure growth processes are driven by O-H···O hydrogen bonds as controlling elements. The calculated values of the interaction indicate a stronger interaction via O-H···O hydrogen bonds in "pure" aqueous media ( = -11.73 kcal mol) compared to those obtained in aqueous NaOH solution ( = -8.41 kcal mol). The specific structural motif of the (ZnO-HO) dodecamers with calculated negative Δ* free release energy indicates that the formation of anisotropic nanocrystalline ZnO with the -axis as the primary growth direction is spontaneous and accelerated exclusively in "pure" aqueous solution, whereas it is an unfavorable endergonic process in aqueous NaOH solution (Δ* > 0). Efforts have been made to determine the photocatalytic efficiency of the ZnO samples based on the XAS measurements. ZnO particles obtained in "pure" aqueous solution show the highest photocatalytic activity due to the presence of a larger amount of oxygen vacancies.
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http://dx.doi.org/10.1021/acs.inorgchem.1c03905 | DOI Listing |
Int J Nanomedicine
January 2025
Division of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, 72079, USA.
Poor aqueous solubility and bioavailability limit the translation of new drug candidates into clinical applications. Nanocrystal formulations offer a promising approach for improving the dissolution rate and saturation solubility. These formulations are applicable for various routes of administration, with each presenting unique opportunities and challenges posed by the physiological barriers.
View Article and Find Full Text PDFLangmuir
January 2025
School of Advanced Engineering, Kogakuin University, Tokyo 192-0015, Japan.
Arsenocholine-containing methacrylate (MTAsB) inspired by marine organisms was synthesized by the reaction of 2-bromoethyl methacrylate and trimethylarsine to investigate its polymerization behavior and the fundamental properties of the resulting polymer. Controlled radical polymerization of MTAsB proceeded in the presence of a copper catalyst and imidazolium chloride at 60 °C for 8 h to give a water-soluble polycation with a 94% yield. The smaller amount of nonfreezing water and intermediate water of poly(MTAsB) was observed compared with that of the ammonium-containing polycations.
View Article and Find Full Text PDFMacromol Rapid Commun
January 2025
Qingdao Innovation and Development Center, Harbin Engineering University, Qingdao, 266000, China.
Hydrogels are flexible materials characterized by a 3D network structure, which possess high water content and adjustable physicochemical properties. They have found widespread applications in tissue engineering, electronic skin, drug delivery, flexible sensors, and photothermal therapy. However, hydrogel networks often exhibit swelling behavior in aqueous environments, which can result in structural degradation and a loss of gel performance.
View Article and Find Full Text PDFJ Phys Chem B
January 2025
Molecular Modeling Laboratory, Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721302, India.
It is widely believed that the aggregation of amyloid β (Aβ) peptides into soluble oligomers is the root cause behind Alzheimer's disease. In this study, we have performed room-temperature molecular dynamics (MD) simulations of aggregated Aβ oligomers of different sizes (pentamer (O(5)), decamer (O(10)), and hexadecamer (O(16))) in binary aqueous solutions containing 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIM][BF]) ionic liquid (IL). Investigations have been carried out to obtain a microscopic understanding of the effects of the IL on the dynamic environment around the exterior surfaces and within the confined nanocores of the oligomers.
View Article and Find Full Text PDFCurr Org Synth
January 2025
Laboratoire de Chimie Organique (LR17ES08), Faculté des Sciences de Sfax, University of Sfax, Route de Soukra Km 3.5, BP 1171, 3000, Sfax, Tunisia.
Aim And Objective: It is well established that 4H-pyran derivatives hold a significant position in synthetic organic chemistry due to their diverse biological and pharmacological properties. This work aims to introduce a novel synthetic pathway for highly functionalized 4H-pyran derivatives, achieved through a 1,4-Michael addition followed by a cascade cyclization. This reaction is catalyzed by LiOH·H2O under ultrasonic irradiation in water, offering an efficient and environmentally friendly approach.
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