dc.contributor.author |
GUPTA, ARVIND K. |
en_US |
dc.contributor.author |
Chipem, Francis A. S. |
en_US |
dc.contributor.author |
BOOMISHANKAR, RAMAMOORTHY |
en_US |
dc.date.accessioned |
2019-07-23T11:08:49Z |
|
dc.date.available |
2019-07-23T11:08:49Z |
|
dc.date.issued |
2012-01 |
en_US |
dc.identifier.citation |
Dalton Transactions, 41 (6), 1848-1853. |
en_US |
dc.identifier.issn |
1477-9226 |
en_US |
dc.identifier.issn |
1477-9234 |
en_US |
dc.identifier.uri |
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3631 |
|
dc.identifier.uri |
https://doi.org/10.1039/C1DT12004B |
en_US |
dc.description.abstract |
A new phosphine imine 3, [P(Npy)(NHpy)3] (py = 2-pyridyl), was synthesized from the phosphonium salt 1, [P(NHpy)4]Cl. Subsequent reaction of 1 or 3 with AgClO4 lead to an unprecedented penta-nuclear Ag(I) complex 4 stabilized by two [P(Npy)2(NHpy)2]− anions [L]−. The packing diagram of 4 shows an interesting channel structure which contains solvated molecules of methanol and toluene. The diimine ligand [L]−, which represents the N-analogue of a phosphinate ion (H2PO4−), was obtained in situ under the mild reaction conditions in the absence of a base. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Royal Society of Chemistry |
en_US |
dc.subject |
A 2-pyridyl |
en_US |
dc.subject |
Phosphine imine |
en_US |
dc.subject |
Phosphine imine |
en_US |
dc.subject |
N-analogues of common phosphorus |
en_US |
dc.subject |
Crystallography |
en_US |
dc.subject |
Theoretical calculations |
en_US |
dc.subject |
2012 |
en_US |
dc.title |
A 2-pyridyl (py) attached phosphine imine [P(Npy)(NHpy)3] and an imido phosphinate ion [P(Npy)2(NHpy)2]− in its Ag(i) complex |
en_US |
dc.type |
Article |
en_US |
dc.contributor.department |
Dept. of Chemistry |
en_US |
dc.identifier.sourcetitle |
Dalton Transactions |
en_US |
dc.publication.originofpublisher |
Foreign |
en_US |