Isolation of Potassium Bis(amido)diazadipnictogenide Salts
The reaction of Zintl phases K<sub>3</sub>As<sub>7</sub> and K<sub>3</sub>P<sub>7</sub> were investigated with 1-azido-4-bromobenzene (4-BrC<sub>6</sub>H<sub>4</sub>N<sub>3</sub>) and found to yield potassium salts of substituted diazadipnictogen rings (general molecular fragment {(RN)<sub>2</sub>Pn<sub>2</sub>}; Pn = P, As). In the case of the arsenic derivatives, amido-(imino)-arsenide persists in solution and bis-(amido)-diazadiarsenide persists in the solid state. These two species can be considered to share a monomer-dimer relationship, accessible by alteration between the solid and solution states, whereas in the case of K<sub>3</sub>P<sub>7</sub>, our crystallographic and spectroscopic studies are consistent with the formation of a bisamido-(bisimino)-diazadiphosphenide, the "dimeric" form, persisting in both the solid and solution phase. Subsequent reactivity studies with amido-(imino)-arsenide show that it can act as a source of amide anion, giving a carbonate and a thiourea derivative when investigated with CO<sub>2</sub> and CS<sub>2</sub>, respectively.
Authors
- Meera Mehta
- Reece Lister-Roberts
Institutions
- Mansfield University (US)
- University of Manchester (GB)
- University of Oxford (GB)
Publication Details
- Journal
- Organometallics
- Published
- 2026-01-26
- DOI
- https://doi.org/10.1021/acs.organomet.5c00493
- Primary Topic
- Synthesis and characterization of novel inorganic/organometallic compounds
- Type
- article
- Field-Weighted Citation Impact
- 0.00