is a rich source of high-value plant secondary metabolites that have been used in the treatment of various ailments since ancient times. Herein, we report the conversion of bulk Ag ions into highly potent organometallic Ag nanostructures (OM-Ag-NS) using extract as a phytochelating agent for the first time. Analysis by X-ray diffraction (XRD) of OM-Ag-NS revealed that they are of a hybrid nature and include pure Ag crystal planes and Ag-organic-complex crystal planes. An investigation by scanning electron microscopy (SEM) of the NS revealed the rough nanocube-like morphology of OM-Ag-NS with an average particle size of 32 nm. Ultra-performance liquid chromatography-diode array detector (UPLC-DAD) and Fourier transform infrared (FTIR) spectroscopy of extract and the residue validated the utilization of phytochelating compounds in the synthesis process of OM-Ag-NS. Thermogravimetric analysis (TGA) supplemented the findings of UPLC-DAD and showed the thermal loss of the organic capping agent around OM-Ag-NS between 300 and 320 °C. NanoDrop-ultraviolet and visible (UV) spectroscopic analysis showed that the tailored bandgap energy of OM-Ag-NS was 2.82 eV. Moreover, compared with chemically stabilized Ag nanostructures (CS-Ag-NS), OM-Ag-NS exhibited promising performance against highly virulent multidrug-resistant (NDM-1) and (KPC). Our current findings suggest that is a top candidate for tailoring the potential of NS towards various biological activities.
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http://dx.doi.org/10.1039/c8ra05655b | DOI Listing |
Sci Rep
December 2024
Department of Mathematical Sciences, Faculty of Science, Somali National University, Mogadishu Campus, Mogadishu, Somalia.
Phthalocyanine derivative nanostructures are highly organized organometallic structures that exhibit two-dimensional polymeric phthalocyanine frameworks. We analyze phthalocyanine using the Zagreb-type indices, which offer important insights into the topological characteristics of the molecular structure. Furthermore, we use Pearson correlation analysis to examine the degree of relationship between various structural features and qualities.
View Article and Find Full Text PDFLangmuir
December 2024
Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources and International Innovation Center for Forest Chemicals and Materials, Nanjing Forestry University, Nanjing 210037, China.
This study reports the development of an innovative electrochemical sensor based on organometallic framework nanostructures for detecting valganciclovir (VLCV). VLCV is employed in the treatment of cytomegalovirus retinitis in AIDS patients. Rational design of nanoarchitectures for electroactive materials is a crucial approach for boosting their electrocatalytic performance.
View Article and Find Full Text PDFJ Phys Chem Lett
December 2024
Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Joint International Research Laboratory of Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123, P. R. China.
Alkali element doping has significant physical implications for two-dimensional materials, primarily by tuning the electronic structure and carrier concentration. It can enhance interface electronic interactions, providing opportunities for effective charge transfer at metal-organic interfaces. In this work, we investigated the effects of gradually increasing the level of K doping on the lattice structure and electronic properties of an organometallic coordinated Kagome lattice on a Ag(111) surface.
View Article and Find Full Text PDFBeilstein J Nanotechnol
November 2024
Department of Chemistry, Johns Hopkins University, Baltimore, MD, 21218, USA.
Ion beam-induced deposition (IBID) using Pt(CO)Cl and Pt(CO)Br as precursors has been studied with ultrahigh-vacuum (UHV) surface science techniques to provide insights into the elementary reaction steps involved in deposition, complemented by analysis of deposits formed under steady-state conditions. X-ray photoelectron spectroscopy (XPS) and mass spectrometry data from monolayer thick films of Pt(CO)Cl and Pt(CO)Br exposed to 3 keV Ar, He, and H ions indicate that deposition is initiated by the desorption of both CO ligands, a process ascribed to momentum transfer from the incident ion to adsorbed precursor molecules. This precursor decomposition step is accompanied by a decrease in the oxidation state of the Pt(II) atoms and, in IBID, represents the elementary reaction step that converts the molecular precursor into an involatile PtX species.
View Article and Find Full Text PDFAdv Mater
November 2024
Center for Ordered Materials, Organometallics and Catalysis (COMOC), Department of Chemistry, Ghent University, Krijgslaan 281-S3, Ghent, 9000, Belgium.
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