Titanocene phosphinidenes react with terminal alkynes in formal [2 + 2] cycloadditions to give unsaturated [C2PTi] metallcycles. Diphosphene complexes in combination with aryl-substituted alkynes rea...

Aromaticity is a fundamental concept traditionally used to explain the structure, stability, and reactivity of cyclic organic compounds. Heavier analogs have also been investigated for their aromatic ...

Phosphaalkkenes are an underrepresented class of phosphorus-based ligands that hold great potential for the stabilisation of low-valent transition metal and main group fragments. We present the synthe...

[K@crypt-222][TeCN] was synthesized from KCN, Te, and crypt-222 in acetone. We discuss fundamental properties of [TeCN]−: Single crystal X-ray diffraction, nuclear magnetic resonance (13C, 15N, 125Te...

The dinuclear title compound [(Cp2Zr)2(µ-Me)(µ-C2Ph)] 5 was prepared from a zirconocene alkynyl methyl complex and Rosenthal’s zirconocene source [Cp2Zr(py)(h2-Me3SiC2SiMe3)] in a formal comproportio....

Cyanophosphides of the general form [RPCN]− can be viewed as cyanide adducts of phosphinidenes and are phosphorus species in the (+1)-oxidation state. We have recently reported on the stable cyanophosphide [DippTerPCN]K (DippTer = 2,6-Dipp2C6H3, Dipp = 2,6-iPrC6H3) and now investigate its reactions with ECln (E = Ge, n = 2; E = P, As, n = 3) in either salt metathesis or base-assisted dehydrohalogenation reactions. In the case of GeCl2, salt metathesis with [DippTerPCN]K afforded the dimer of a chlorogermylene [DippTerP(CN)GeCl]2. When only 0.5 equiv of GeCl2 was used, the diphosphanylgermylene [DippTerP(CN)]2Ge was generated in solution. With ECl3 (E = P, As), facile cyanophosphide transfer was achieved from DippTerP(H)CN in NEt3-assisted dehydrohalogenation, giving diphosphanes or arsaphosphanes of the type DippTerP(CN)ECl2 (E = P, As), respectively.