From an environmental perspective, silver recovery through a green process is imperative. In this work, a green supramolecular separation process of Ag has been developed by using a highly charged anionic Ti4L6 (L = embonate) cage as the extractant. Such a Ti4L6 cage has unique selectivity toward [Ag(NH3)2]+ ions, because only linear [Ag(NH3)2]+ ions can be trapped into the windows of the Ti4L6 cage, which is demonstrated by single-crystal X-ray diffraction analysis. To further illustrate the efficiency and mechanism of the herein constructed silver separation method, three co-crystals of the Ti4L6 cage with various [Ag(NH3)2]+ ions were prepared and structurally characterized, annotating the stepwise recognition of [Ag(NH3)2]+ ions by the Ti4L6 extractant. However, it failed to trap larger tetrahedral [Zn(NH3)4]2+ and quadrilateral [Pb(NH3)4]2+ ions under the same reaction conditions, indicating that configuration matching contributes to the high selectivity of the above-mentioned silver separation procedure. More interestingly, Ag nanoparticles with high yield could be obtained by the reduction of the [Ag(NH3)2]&Ti4L6 extracts with hydrazine hydrate (N2H4·H2O), and the Ti4L6 cages can be readily recycled through recrystallization. This discovery offers a green supramolecular procedure for silver recovery with coordination cages as efficient and recyclable extractants.
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http://dx.doi.org/10.1039/d0dt03214j | DOI Listing |
J Colloid Interface Sci
May 2024
College of Chemical and Material Engineering, Quzhou University, Quzhou, Zhejiang, 324000, China. Electronic address:
Novel two-dimensional MXene with unique optical and electrical properties has become a new focus in the field of sensing. In particular, their metallic conductivity, good biocompatibility and high anchoring ability to biomaterials make them attractive candidates. Despite such remarkable properties, there are certain limitations, such as low oxidative stability.
View Article and Find Full Text PDFChem Sci
September 2020
Department of Chemistry, University of North Texas 1155 Union Circle #305070 Denton Texas 76203 USA
An efficient strategy for designing charge-transfer complexes using coinage metal cyclic trinuclear complexes (CTCs) is described herein. Due to opposite quadrupolar electrostatic contributions from metal ions and ligand substituents, [Au(μ-Pz-(i-CH))]·[Ag(μ-Tz-(-CF))] (Pz = pyrazolate, Tz = triazolate) has been obtained and its structure verified by single crystal X-ray diffraction - representing the 1 crystallographically-verified stacked adduct of monovalent coinage metal CTCs. Abundant supramolecular interactions with aggregate covalent bonding strength arise from a combination of M-M' (Au → Ag), metal-π, π-π interactions and hydrogen bonding in this charge-transfer complex, according to density functional theory analyses, yielding a computed binding energy of 66 kcal mol between the two trimer moieties - a large value for intermolecular interactions between adjacent d centres (nearly doubling the value for a recently-claimed Au(i) → Cu(i) polar-covalent bond: , 2017, , E5042) - which becomes 87 kcal mol with benzene stacking.
View Article and Find Full Text PDFCarbohydr Polym
June 2021
Tianjin Key Laboratory of Pulp and Paper, Tianjin University of Science and Technology, No. 29, 13th Street, TEDA, Tianjin 300457, PR China. Electronic address:
The laccase/TEMPO system was employed to oxidise the C6 primary hydroxyl group on the chitosan (CS) to form a carboxyl group to obtain oxidised chitosan (C-COS). The silver-oxidised chitosan complex(C-COS-Ag) was prepared by reacting C-COS with silver nitrate, then C-COS-Ag and cotton fibres were subjected to a reaction to prepare bacteriostatic fibres. FT-IR and XPS analysis showed that: Ag and C-COS were combined in these forms: Ag, [Ag(NH)] OH, -COOAg, and AgO.
View Article and Find Full Text PDFInorg Chem
March 2021
Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, Magyar Tudósok krt 2, Budapest H-1117, Hungary.
Two monoclinic polymorphs of [Ag(NH)]MnO containing a unique coordination mode of permanganate ions were prepared, and the high-temperature polymorph was used as a precursor to synthesize pure AgMnO. The hydrogen bonds between the permanganate ions and the hydrogen atoms of ammonia were detected by IR spectroscopy and single-crystal X-ray diffraction. Under thermal decomposition, these hydrogen bonds induced a solid-phase quasi-intramolecular redox reaction between the [Ag(NH)] cation and MnO anion even before losing the ammonia ligand or permanganate oxygen atom.
View Article and Find Full Text PDFInt J Mol Sci
December 2020
Department of Physical Chemistry, Institute of Chemical Sciences, Maria Curie-Sklodowska University, 3 Sq. Maria Curie-Sklodowska, 20-031 Lublin, Poland.
In this work, ultra-small and stable silver nanoparticles (AgNP) on chitosan biopolymer (BP/AgP) were prepared by in situ reduction of the diamminesilver(I) complex ([Ag(NH)]) to create a biostatic membrane system. The small AgNP (3 nm) as a stable source of silver ions, their crystal form, and homogeneous distribution in the whole solid membrane were confirmed by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The X-ray photoelectron spectroscopy (XPS) and Auger analysis were applied to investigate the elemental composition, concentration, and chemical state of surface atoms.
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