Franke S, Rosenzweig M, Heinemann FW, Meyer K (2015)
Publication Language: English
Publication Status: Published
Publication Type: Journal article, Original article
Publication year: 2015
Publisher: Royal Society of Chemistry
Book Volume: 6
Pages Range: 275-282
DOI: 10.1039/c4sc02602k
We report the syntheses, electronic properties, and molecular structures of a series of mono-and dinuclear uranium(IV) hydrochalcogenido complexes supported by the sterically demanding but very flexible, single N-anchored tris(aryloxide) ligand ((ArO)-Ar-Ad)(3)N)(3-). The mononuclear complexes [(((ArO)-Ar-Ad)(3)N)U(DME)(EH)] (E = S, Se, Te) can be obtained from the reaction of the uranium(III) starting material [(((ArO)-Ar-Ad)(3)N)U-III(DME)] in DME via reduction of H2E and the elimination of 0.5 equivalents of H-2. The dinuclear complexes [{(((ArO)-Ar-Ad)(3)N)U}(2)(mu-EH)(2)] can be obtained by dissolving their mononuclear counterparts in non-coordinating solvents such as benzene. In order to facilitate the work with the highly toxic gases, we created concentrated THF solutions that can be handled using simple glovebox techniques and can be stored at -35 degrees C for several weeks.
APA:
Franke, S., Rosenzweig, M., Heinemann, F.W., & Meyer, K. (2015). Reactivity of uranium(III) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(IV) hydrochalcogenido complexes. Chemical Science, 6, 275-282. https://doi.org/10.1039/c4sc02602k
MLA:
Franke, Sebastian, et al. "Reactivity of uranium(III) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(IV) hydrochalcogenido complexes." Chemical Science 6 (2015): 275-282.
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