Im Jahr 2025 waren aller guten Dinge der Hauptgruppenchemie drei: ein dreifach geladenes Triborattrianion, ein Molekül mit linearer Al3-Einheit, das dritte Erdalkalimetall, das Stickstoff bindet, ein ...

Im Jahr 2025 waren aller guten Dinge der Hauptgruppenchemie drei: ein dreifach geladenes Triborattrianion, ein Molekül mit linearer Al3-Einheit, das dritte Erdalkalimetall, das Stickstoff bindet, ein ...

Here, we report a breakthrough study in catalytic alkene isomerisation using crown ether-supported alkali metal phosphides in which the activity increases sequentially and significantly as Group One ...

When the cationic, octahedral terminal nitrido complex of Mo(VI) supported by a diborate pentadentate ligand is generated in the absence of trapping nucleophiles, it activates the C(sp2)–H bonds of si...

A rare silicon(IV)-based azo compound featuring a Si─N═N─Si linkage was synthesized via the direct reaction of an organoazide with a silaiminyl–silylene precursor. This compound undergoes an unusual ...

The reaction of [K(thf)0.33][Co(η4-cod)2] (E; cod = 1,5-cyclooctadiene) with 0.5 equiv of MgCl2 led to the isolation of the magnesium dicobalt complex Mg[Co(η4-cod)2]2 (1). Complex 1 forms a tight ionic complex in the solid state and in toluene solution due to electrostatic interactions between the Mg2+ cation and the [Co(η4-cod)2]− anions. The complex is a successful precatalyst for the hydrogenation of sterically challenging tri- and tetra-substituted alkenes, surpassing the catalytic capabilities of related alkali metal and β-diketiminate magnesium complexes.

Previous studies have hinted at the similarities of Mn(II) and Mg alkyl complexes. Advancing this field, here we present a comparative study of tetra(n-butyl) lithium manganate(II) and magnesiate. Com...

The alkaline earth metals are notorious for their tendency to form ionic compounds of their dications. In recent years, however, chemists have found ways to kinetically skirt around the edges of these...