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Isolation of Potassium Bis(amido)diazadipnictogenide Salts

Abstract:
The reaction of Zintl phases K3As7 and K3P7 were investigated with 1-azido-4-bromobenzene (4-BrC6H4N3) and found to yield potassium salts of substituted diazadipnictogen rings (general molecular fragment {(RN)2Pn2}; 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 K3P7, 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 CO2 and CS2, respectively.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1021/acs.organomet.5c00493

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry
Role:
Author
ORCID:
0000-0001-9277-7586
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry
Role:
Author
ORCID:
0000-0002-6833-5574


More from this funder
Funder identifier:
https://ror.org/0439y7842
Grant:
EP/Y037391/1


Publisher:
American Chemical Society
Journal:
Organometallics More from this journal
Volume:
45
Issue:
3
Pages:
253-258
Publication date:
2026-01-26
Acceptance date:
2026-01-23
DOI:
EISSN:
1520-6041
ISSN:
0276-7333


Language:
English
Keywords:
Pubs id:
2378013
Local pid:
pubs:2378013
Source identifiers:
3744653
Deposit date:
2026-02-10
ARK identifier:
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