| Literature DB >> 32212190 |
Maxim Bykov1,2,3, Stella Chariton4, Elena Bykova3, Saiana Khandarkhaeva2, Timofey Fedotenko5, Alena V Ponomareva6, Johan Tidholm7, Ferenc Tasnádi7, Igor A Abrikosov7, Pavel Sedmak8, Vitali Prakapenka4, Michael Hanfland8, Hanns-Peter Liermann9, Mohammad Mahmood1, Alexander F Goncharov3, Natalia Dubrovinskaia5,7, Leonid Dubrovinsky2.
Abstract
Polynitrides are intrinsically thermodynamically unstable at ambient conditions and require peculiar synthetic approaches. Now, a one-step synthesis of metal-inorganic frameworks Hf4 N20 ⋅N2 , WN8 ⋅N2 , and Os5 N28 ⋅3 N2 via direct reactions between elements in a diamond anvil cell at pressures exceeding 100 GPa is reported. The porous frameworks (Hf4 N20 , WN8 , and Os5 N28 ) are built from transition-metal atoms linked either by polymeric polydiazenediyl (polyacetylene-like) nitrogen chains or through dinitrogen units. Triply bound dinitrogen molecules occupy channels of these frameworks. Owing to conjugated polydiazenediyl chains, these compounds exhibit metallic properties. The high-pressure reaction between Hf and N2 also leads to a non-centrosymmetric polynitride Hf2 N11 that features double-helix catena-poly[tetraz-1-ene-1,4-diyl] nitrogen chains [-N-N-N=N-]∞ .Entities:
Keywords: high-pressure synthesis; inclusion compounds; inorganic double helix; metal-inorganic frameworks; polynitrides
Year: 2020 PMID: 32212190 DOI: 10.1002/anie.202002487
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336