Novel bi- and trinuclear gallium halides and hydrides with acyclic and bicyclic guanidinate substituents: synthesis and reactivity

We report on the synthesis and characterization of new molecular Ga halides and hydrides with acyclic guanidinate substituents with bicyclic guanidinate substituents. Acyclic guanidinates were found to adopt terminal bonding modes like in the dimeric GaII compound [(iPr2N)C(NiPr)2GaI]2. In contrast,...

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Hauptverfasser: Rudolf, Daniel Thomas (VerfasserIn) , Kaifer, Elisabeth (VerfasserIn) , Himmel, Hans-Jörg (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 27 August 2010
In: European journal of inorganic chemistry
Year: 2010, Heft: 31, Pages: 4952-4961
ISSN:1099-0682
DOI:10.1002/ejic.201000598
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/ejic.201000598
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ejic.201000598
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Verfasserangaben:Daniel Rudolf, Elisabeth Kaifer and Hans-Jörg Himmel
Beschreibung
Zusammenfassung:We report on the synthesis and characterization of new molecular Ga halides and hydrides with acyclic guanidinate substituents with bicyclic guanidinate substituents. Acyclic guanidinates were found to adopt terminal bonding modes like in the dimeric GaII compound [(iPr2N)C(NiPr)2GaI]2. In contrast, bicyclic guanidinates prefer bridging bonding modes. Hence, the reaction between Me3N·GaH3 and htbo (1,4,6-triazabicyclo[3.3.0]oct-4-ene) affords the binuclear GaIII hydride [H2Ga(μ-tbo)]2. This new hydride turned out to be unstable in solution at 25 °C, dihydrogen is slowly eliminated. In the solid state, however, the hydride is stable up to 80 °C. The thermodynamic properties of this and similar dehydrogenation reactions were studied my means of quantum chemical calculations. With Ga2H5(μ3-O)(μ-tbn)2 and Ga2H5(μ3-O)(μ-hpp)2, two new hydrides were synthesized which can be regarded as the first hydrolysis intermediates of binuclear Ga hydrides with bridging guanidinate substituents.
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Beschreibung:Online Resource
ISSN:1099-0682
DOI:10.1002/ejic.201000598