Gold nanoparticles (AuNPs) can be prepared from the reduction of Au(III) with cyclodextrins acting as both, reducing and capping agent. It has been stated that a basic medium (pH=9-12) is a mandatory condition to achieve such reduction. We demonstrated, for the first time, the reduction of Au(III) by a crosslinked β-cyclodextrin-epichlorohydrin polymer (βCDP) in acid medium (pH ∼3). The coordination of Au(III) to the βCD in βCDP polymer required a βCD:[AuCl] ratio of 4:1. The same ratio was necessary to achieve a 50% of the reduction of Au(III) to Au within the first 24h of reaction. During this initial time, the reaction showed a concentration-dependent reduction rate while for longer times the reduction rate was diffusion-dependent. An overall mechanism to explain this dependency has been proposed. The C NMR spectrum identified the oxidation of the COH groups to carboxylic ones by recording a signal at 175.6ppm. Gold nanoparticles cores (AuNPs) with a diameter of 34.2±7.7nm, determined by Transmission Electron Microscopy (TEM), was prepared by refluxing HAuCl in an aqueous solution of βCDP. The AuNPs core was capped by dimers of the βCDP polymer as determined by Dynamic Light Scattering measurements.
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http://dx.doi.org/10.1016/j.carbpol.2017.08.013 | DOI Listing |
Langmuir
January 2025
College of Optoelectronic Materials and Technology, Jianghan University, Wuhan, Hubei 430056, People's Republic of China.
Adsorption is an efficient and highly selective method for gold recovery. Introducing rich N/S organic groups to combine with metal-organic frameworks (MOFs) as adsorbents is regarded as a practical and efficient approach to enhance gold recovery. Herein, a MOF (zirconium isothiocyanatobenzenedicarboxylate MOF, UiO-66-NCS) was designed to combine with amidinothiourea (AT) to form UiO-66-AT (zirconium amidothiourea-benzenedicarboxylate MOF) for efficient and rapid adsorption.
View Article and Find Full Text PDFPharmaceutics
December 2024
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, 1649-003 Lisboa, Portugal.
The therapeutic management of melanoma, the most aggressive form of skin cancer, remains challenging. In the search for more effective therapeutic options, metal-based complexes are being investigated for their anticancer properties. Cisplatin was the first clinically approved platinum-based drug and, based on its success, other metals (e.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
MOE Key Laboratory of Resource Chemistry and Shanghai Key Laboratory of Rare Earth Functional Material, Shanghai Normal University, Shanghai, 200234, China.
The use of precious metals (PMs) in many areas, such as printed circuit boards, catalysts, and target drugs, is increasing due to their unique physical and chemical properties, but their recovery remains a great challenge in terms of zero-valent PMs as the final product. We report a highly hydrophilic carbon dot (CD) as a reductant (electron donor), in which the defects in CD served as efficient active sites for zero-valent PMs recovery with an electron-donating capacity of ~1.7 mmol g.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, LiuFang Campus, No.206, Guanggu 1st road, Donghu New & High Technology Development Zone, Wuhan 430205, Hubei Province, PR China. Electronic address:
This study aims to prepare a monodisperse catalyst with a space-confined strategy, employing cellulose beads (CBs) as a carrier. Amino functionalized cellulose beads (ACBs) were prepared by grafting polyethyleneimine into the space of CBs via glutaraldehyde cross-linking. The in-situ reduction method was successfully employed to confine monodisperse ultrasmall gold nanoparticles (AuNPs) within the amino functionalized cellulose beads (AuNPs@ACBs) matrix.
View Article and Find Full Text PDFACS Macro Lett
November 2024
Department of Chemistry and Biochemistry, University of California, Los Angeles, Los Angeles, California 90095, United States.
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