Synthetic and Structural Chemistry of Uranyl-Amidoxime Complexes: Technological Implications
نویسندگان
چکیده
Resource shortage is a major problem in our world. Nuclear energy green and because of this its high density, it has been attracting more attention during the last few decades. Uranium valuable nuclear fuel used majority power plants. More than one thousand times uranium exists oceans, at very low concentrations, present terrestrial ores. As demand for generation increases year-on-year, access to reserve paramount importance security. Water-insoluble polymeric materials functionalized with amidoxime group are technically feasible platform extracting uranium, form {UO2}2+, from seawater, which also contains various concentrations other competing metal ions, including vanadium (V). An in-depth understanding coordination modes binding strength uranyl ions key parameter improving extraction efficiency selectivity. Very limited information on complexation {UO2}2+ amidoximes was available before 2012. However, significant advances have made decade. This report reviews solid-state chemistry (alone or within ligands potential donor sites) ion, while sporadic solution theoretical studies given. Comparative briefly described. Eight different neutral singly deprotonated groups identified structures complexes. Particular emphasis given describing reactivity open-chain glutardiamidoxime, closed-ring glutarimidedioxime glutarimidoxioxime moieties, as side chains sorbents, towards moiety. The technological implications some observed outlined. It believed that X-ray crystallography small uranyl-amidoxime molecules may help build an interactions seawater amidoxime-functionalized polymers improve their recovery capacity selectivity, leading efficient extractants. challenges scientists working structural elucidation complexes review six sections 95 references.
منابع مشابه
Surface-grafted Europium and Erbium Complexes of the 12-Tungstosilicate Heteropolyoxometalate: A Synthetic and Structural Investigations
The hydrothermal synthesis of two new inorganic-organic hybrid materials in which PDA (PDA = 1,10-phenanthroline-2,9-dicarboxylate) is connected to a well-defined Keggin-type polyoxometalate anion (POM) and a Ln(III) cation (POM = [SiW12O40]4−; Ln = Eu3+ (1), Er3+ (2)), are reported. These hybrids are characterized by elemental analyses, IR spectra and single-crystal X-ray diffraction. Single-c...
متن کاملUranyl sequestration: synthesis and structural characterization of uranyl complexes with a tetradentate methylterephthalamide ligand.
Uranyl complexes of a bis(methylterephthalamide) ligand (LH(4)) have been synthesized and characterized by X-ray crystallography. The structure is an unexpected [Me(4)N](8)[L(UO(2))](4) tetramer, formed via coordination of the two MeTAM units of L to two uranyl moieties. Addition of KOH to the tetramer gave the corresponding monomeric uranyl methoxide species [Me(4)N]K(2)[LUO(2)(OMe)].
متن کاملSynthetic, structural and magnetic implications of introducing 2,2'-dipyridylamide to sodium-ferrate complexes.
Using a transamination approach to access novel Fe(ii) complexes, this study presents the synthesis, X-ray crystallographic and magnetic characterisation of a series of new iron complexes containing the multifunctional 2,2-dipyridylamide (DPA) ligand using iron bis(amide) [{Fe(HMDS)2}2] and sodium ferrate [{NaFe(HMDS)3}∞] (1) as precursors (HMDS = 1,1,1,3,3,3-hexamethyldisilazide). Reactions of...
متن کاملTwo alternative approaches to access mixed hydride-amido zinc complexes: synthetic, structural and solution implications.
Using bis(amide) Zn(HMDS)2 (HMDS = 1,1,1,3,3,3-hexamethyldisilazide) as a precursor, this study explores the synthesis of N-heterocyclic carbene stabilized mixed amido-hydride zinc complexes using two alternative hydride sources, namely dimethylamine borane (DMAB) and phenylsilane PhSiH3. Hydride-rich zinc cluster Zn4(HMDS)2H6·2IPr () (IPr = 1,3-bis(2,6-di-isopropylphenyl)imidazol-2-ylidene), w...
متن کاملSynthesis and structural chemistry of non-cyclopentadienyl organolanthanide complexes.
ion upon treatment with B(C6F5)3 in THF to generate the cationic species [(MAC)Y(CH2SiMe3)][B(C6F5)3(CH2SiMe3)]. However, this salt was found to be highly unstable and could not be isolated as a pure material.97 Fryzuk et al. have developed a remarkable organoyttrium chemistry around the phosphorus-containing macrocycle syn-{P2N2} ({P2N2} ) [PhP(CH2SiMe2NSiMe2CH2)2PPh]). The starting material w...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Chemistry
سال: 2023
ISSN: ['2624-8549']
DOI: https://doi.org/10.3390/chemistry5020097