dc.contributor.author |
GUPTA, ARVIND K. |
en_US |
dc.contributor.author |
Nagarkar, Sanjog S. |
en_US |
dc.contributor.author |
BOOMISHANKAR, RAMAMOORTHY |
en_US |
dc.date.accessioned |
2019-02-14T05:01:22Z |
|
dc.date.available |
2019-02-14T05:01:22Z |
|
dc.date.issued |
2013-05 |
en_US |
dc.identifier.citation |
Dalton Transactions, 42(30), 10964-10970. |
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/123456789/1629 |
|
dc.identifier.uri |
https://doi.org/10.1039/C3DT51123E |
en_US |
dc.description.abstract |
Two polymorphic 2D-coordination polymers of composition [ZnL(HCO2)]∞ were synthesized from an in situ generated ligand [PO2(NH4Py)2]− (L−). The ligand L− was generated by a facile metal-assisted P–N bond hydrolysis reaction from the corresponding phosphonium salt 1, [P(NH4Py)4]Cl, or from the neutral phosphoric triamide 2, [PO(NH4Py)3]. The de-solvated sample of the polymer [ZnL(HCO2)]∞ features polar micropores and shows a type I isotherm for CO2 sorption whereas a type II behaviour was observed for N2. The vapour sorption isotherm of the de-solvated sample of [ZnL(HCO2)]∞ shows preferential adsorption of water vapour over aliphatic alcohols. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Royal Society of Chemistry |
en_US |
dc.subject |
Coordination polymer |
en_US |
dc.subject |
Aliphatic alcohols |
en_US |
dc.subject |
Polymorphic 2D-coordination |
en_US |
dc.subject |
Preferential adsorption of water vapour |
en_US |
dc.subject |
2013 |
en_US |
dc.title |
Zn(ii) coordination polymer of an in situ generated 4-pyridyl (4Py) attached bis(amido)phosphate ligand, [PO2(NH4Py)2]− showing preferential water uptake over aliphatic alcohols |
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 |