RESUMEN
A series of low-valent Group 14-15 compounds were obtained starting from [(Dipp2 NacNac)MCl] (M=Ge-Pb) (I-III) (Dipp2 NacNac=HC{C(Me)N(Dipp)}2 ) and M'E(SiMe3 )2 (M'=Li, E=As; M'=K, E=Sb, Bi) (IV-VI). In the course of this investigations we were able to fully characterize all permutations except Pb-Bi for compounds of the composition [(Dipp2 NacNac)ME(SiMe3 )2 ] (1E : M=Ge, 2E : M=Sn, 3E : M=Pb). Thus, we report the first low valent tetrelene with Sn-Bi bond. All isolated compounds, were examined by NMR spectroscopy, IR spectroscopy and except compound 1As by X-ray structure analysis. Moreover, were examined UV-Vis spectroscopy and investigated the reactivity of these compounds towards different substrates in more detail. Starting with the compound [(Dipp2 NacNac)SnAs(SiMe3 )2 ] (2As ), the reaction with red selenium yields [(Dipp2 NacNac)Sn-Se-As(SiMe3 )2 ] (4) which exhibits a Sn-Se-As chain.
RESUMEN
Reaction of the cesium antimonide complex [Cs(18C6)2][SbH2] (1, 18C6 = 18-crown-6 ether) with the triamidoamine actinide separated ion pairs [An(TrenTIPS)(L)][BPh4] (TrenTIPS = {N(CH2CH2NSiiPr3)3}3-; An/L = Th/DME (2Th); U/THF (2U)) affords the triactinide undeca-antimontriide Zintl clusters [{An(TrenTIPS)}3(µ3-Sb11)] (An = Th (3Th), U (3U)) by dehydrocoupling. Clusters 3Th and 3U provide two new examples of the Sb113- Zintl trianion and are unprecedented examples of molecular Sb113- being coordinated to anything since all previous reports featured isolated Sb113- Zintl trianions in separated ion quadruple formulations with noncoordinating cations. Quantum chemical calculations describe dominant ionic An-Sb interactions in 3Th and 3U, though the data suggest that the latter exhibits slightly more covalent An-Sb linkages than the former. Complexes 3Th and 3U have been characterized by single crystal X-ray diffraction, NMR, IR, and UV/vis/NIR spectroscopies, elemental analysis, and quantum chemical calculations.
RESUMEN
Alkali metal dihydrogen-antimonides [M(L)x SbH2 ], short: alkali metal antimonides (M=Li, Na, K, Rb, Cs; 1: L=pmdta; 2: L=crown-ether), were prepared from stibine and n-Butyllithium, M(hmds) (hmds=hexamethyldisilazane) or MOtBu, respectively. We developed a generally applicable synthesis route for these compounds and the obtained compounds were examined on their stability depending on the alkali metal and stabilizing additives used, whereby the use of appropriate crown-ethers allowed their isolation and characterization at room temperature. Moreover, the 1,4-dioxane adduct [Na(dioxane)x SbH2 ] was the appropriate starting compound for the synthesis of the first primary silylstibane (Me3 Si)3 SiSbH2 (3) which was characterized by NMR and IR spectroscopy. Reaction of 3 with (Dipp2 NacNac)Ga (Dipp2 NacNac=HC{C(Me)N(Dipp)}2 ; Dipp=2,6-iPr2 C6 H3 ) resulted in the formation of (Dipp2 NacNac)GaH(SbHSi(SiMe3 )3 ) (4) which was furthermore characterized by single crystal x-ray diffraction.
RESUMEN
There is continued burgeoning interest in metal-metal multiple bonding to further our understanding of chemical bonding across the periodic table. However, although polar covalent metal-metal multiple bonding is well known for the d and p blocks, it is relatively underdeveloped for actinides. Homometallic examples are found in spectroscopic or fullerene-confined species, and heterometallic variants exhibiting a polar covalent σ bond supplemented by up to two dative π bonds are more prevalent. Hence, securing polar covalent actinide double and triple metal-metal bonds under normal experimental conditions has been a fundamental target. Here we exploit the protonolysis and dehydrocoupling chemistry of the parent dihydrogen-antimonide anion, to report one-, two- and three-fold thorium-antimony bonds, thus introducing polar covalent actinide-metal multiple bonding under normal experimental conditions between some of the heaviest ions in the periodic table with little or no bulky-substituent protection at the antimony centre. This provides fundamental insights into heavy element multiple bonding, in particular the tension between orbital-energy-driven and overlap-driven covalency for the actinides in a relativistic regime.
RESUMEN
Multiple interpnictogen compounds with covalent single bonds between a diarylbismuth fragment and all lighter pnictogens were prepared from the corresponding diarylhalido bismuthanes. The aminobismuthanes Ph2BiNMe2 (1) and Mes2BiNMe2 (2) (Mes = 2,4,6-trimethylphenyl-) have been obtained via a salt metathesis reaction and compound 2 was successfully reacted with tBuNH2 in a condensation reaction to yield Mes2BiNHtBu (3). The bismuthanyl phosphanes Ar2BiPtBu2 (Ar = Ph: 4 and Ar = Mes: 5) and arsanes Ar2BiAstBu2 (Ar = Ph: 8 and Ar = Mes: 9) were also obtained via salt metathesis. Through a trimethylsilyl halide abstraction reaction of the diaryl halido bismuthanes and EtBu(SiMe3)2 (E = P and As), the bismuthanyl phosphanes Ar2BiPtBu(SiMe3) (Ar = Ph: 6; Ar = Mes: 7) and the arsanes Ar2BiAstBu(SiMe3) (Ar = Ph: 10; Ar = Mes: 11) have been prepared. Bismuthanyl stibanes were accessed via a condensation reaction of Mes2SbH with 1 or 2, respectively. The compound Ph2BiSbMes2 (12), which has different substituents at the bismuth and antimony atoms, was isolated and fully characterised. In contrast, the isolation of Mes2BiSbMes2 (13) was not possible due to a dynamic equilibrium with Mes4Bi2 and Mes4Sb2 which was investigated via low-temperature 1H-NMR spectroscopy in solution. The isolated compounds with a single bond between bismuth and the heavy pnictogens arsenic and antimony are rare examples of their kind. All isolated compounds (1-12) were characterised by NMR and IR spectroscopy, mass spectrometry, elemental analysis and single crystal X-ray diffraction.