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Coordination Trends in Alkali Metal Crown Ether Uranyl Halide Complexes: The Series [A(Crown)]2[UO2X4] Where A = Li, Na, K and X = Cl, Br

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TLDR
The Raman spectra reveal nu(U-O) values that correlate with expected trends and structural trends are discussed within the context of classical principles of hard-soft acid-base theory.
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Oxo ligand functionalization in the uranyl ion (UO22

TL;DR: A review of the chemistry of the two oxo ligands of the uranyl ion can be found in this article, where the authors explore the interaction of uranyl oxoxide ligands with Lewis acids, and outline attempts to selectively functionalize the oxo-ligands by chemical means.
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Extending the chemistry of the uranyl ion: Lewis acid coordination to a U=O oxygen.

TL;DR: Treatment of the thf adduct UO2(NCN)thf (NCN = [(Me3SiN)CPh(NSiMe3)]) (1) with 2 equiv of B(C6F5)3 provides UO{OB(C 6F5]3}( NCN)2 (2) the first example of a neutral uranyl complex exhibiting Lewis basic behavior.
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Selective oxo functionalization of the uranyl ion with 3d metal cations.

TL;DR: The linear uranyl dication [UO2]2+ can be bound in one of two coordination sites in the ditopic Pacman-shaped pyrrolic macrocyle H4L using Mn2+, Fe2+, or Co2+ cations in the second donor compartment.
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Isolation of Stable Organodysprosium(II) Complexes by Chemical Reduction of Dysprosium(III) Precursors

TL;DR: In this paper, the reduction of bis(tri-tert-butylcyclopentadienyl)dysprosium(III) complexes by potassium/graphite in the presence of a crown ether has been shown to yield structurally characterized divalent organolanthanide compounds.
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Inorganic Chemistry: Principles of Structure and Reactivity

TL;DR: In this article, inorganic chemistry principles of structure and reactivity are presented. But, they do not cover how to use these principles in the design of products, and they are not available in any type of product.
Journal ArticleDOI

Electronic Structure, Spectra, and Magnetic Properties of Oxycations. III. Ligation Effects on the Infrared Spectrum of the Uranyl Ion

TL;DR: In this paper, a series of uranyl complexes KxUO2Ly(NO3)2, where L is the variable ligand (or ligands), has been prepared; it has been shown that a ligand series may be defined using the antisymmetric stretching frequency of the uranyl entity, and this series exhibits a remarkable parallelism with the spectrochemical series defined by Δ in octahedral complexes of transition metals of the first and 2nd series.
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Aqueous uranium complexes. 2. Raman spectroscopic study of the complex formation of the dioxouranium(VI) ion with a variety of inorganic and organic ligands

TL;DR: In this article, a linear correlation between the frequency of the O=U=O symmetrical stretching vibration and the average number of ligands coordinated equatorially to the central uranium atom in the given species has been established for the above-mentioned ligands according to the following equation: [nu][sub 1] (cm[sup [minus]1]) = -A[bar n] + 870.
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