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DC Field | Value | Language |
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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 |
Appears in Collections: | JOURNAL ARTICLES |
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