Controlling Complexation Behavior of Early Lanthanides via the Subtle Interplay of their Lewis Acidity with the Chemical Stability of 5,5'-(Azobis)tetrazolide

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Weinberger, P.; Giester, G.; Steinhauser, G.: Controlling Complexation Behavior of Early Lanthanides via the Subtle Interplay of their Lewis Acidity with the Chemical Stability of 5,5'-(Azobis)tetrazolide. In: Zeitschrift für Anorganische und Allgemeine Chemie (ZAAC) - Journal of Inorganic and General Chemistry (Formerly: Zeitschrift für anorganische Chemie) 646 (2020), Nr. 23-24, S. 1882-1885. DOI: https://doi.org/10.1002/zaac.202000384

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Abstract: 
Two novel nitrogen-rich lanthanide compounds of 5,5'-(azo bis)tetrazolide (ZT) were synthesized and structurally characterized. The dinuclear, isostructural compounds [Ce2(ZT)2CO3(H2O)12] · 4 H2O (1) and [Pr2(ZT)2CO3(H2O)12]·4H2O (2) were synthesized via two independent routes. Compound 1 was obtained after partial Lewis acidic decomposition of ZT by CeIV in aqueous solution of (NH4)2Ce(NO3)6 and Na2ZT. Compound 2 was obtained by crystallization from aqueous solutions of Pr(NO3)3, Na2ZT, and Na2CO3. By X-ray diffraction analysis at 200 K, it was found that the trivalent lanthanide cations are bridged by a bidentate carbonato ligand and each cation is further coordinated by six H2O ligands and one ZT ligand thus being ninefold coordinated.
License of this version: CC BY 4.0 Unported
Document Type: Article
Publishing status: publishedVersion
Issue Date: 2020
Appears in Collections:Fakultät für Mathematik und Physik

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2 image of flag of Indonesia Indonesia 1 25.00%
3 image of flag of Germany Germany 1 25.00%
4 image of flag of China China 1 25.00%

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