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- W2949457268 startingPage "83" @default.
- W2949457268 abstract "Abstract The chloroamide complexes U(NEt2)4−xClx (x=1, 2) were obtained by comproportionation of UCl4 and U(NEt2)4. The novel protonolysis reaction of a metal–amide bond with an acidic ammonium salt proved to be an efficient and convenient synthesis of cationic compounds. Thus were synthesized a series of metallo-organic and organometallic uranium cations in the oxidation states +3, +4, +5. The cationic amide compounds were valuable precursors of new derivatives, as they reacted with anionic reagents, acidic substrates and unsaturated molecules to give the addition, substitution and insertion products; in particular, such reactions were useful for the synthesis of monocyclooctatetraene uranium compounds. The dialkyl amide ligand was found able to stabilize the +5 oxidation state of uranium; neutral and cationic uranium(V) complexes were obtained by oxidation of their corresponding anionic and neutral U(IV) precursors." @default.
- W2949457268 created "2019-06-27" @default.
- W2949457268 creator A5022761172 @default.
- W2949457268 creator A5079733641 @default.
- W2949457268 date "1998-12-01" @default.
- W2949457268 modified "2023-10-18" @default.
- W2949457268 title "New advances in the chemistry of uranium amide compounds" @default.
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