Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2694
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dc.contributor.authorDESAI, AAMOD V.en_US
dc.contributor.authorManna, Biplaben_US
dc.contributor.authorKarmakar, Avisheken_US
dc.contributor.authorSahu, Amiten_US
dc.contributor.authorGHOSH, SUJIT K.en_US
dc.date.accessioned2019-04-29T10:15:08Z
dc.date.available2019-04-29T10:15:08Z
dc.date.issued2016-06en_US
dc.identifier.citationAngewandte Chemie International Edition, 55(27), 7811-7815.en_US
dc.identifier.issn1433-7851en_US
dc.identifier.issn1521-3773en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2694-
dc.identifier.urihttps://doi.org/10.1002/anie.201600185en_US
dc.description.abstractA three‐dimensional water‐stable cationic metal–organic framework (MOF) pillared by a neutral ligand and with NiII metal nodes has been synthesized employing a rational design approach. Owing to the ordered arrangement of the uncoordinated tetrahedral sulfate (SO42−) ions in the channels, the compound has been employed for aqueous‐phase ion‐exchange applications. The compound exhibits rapid and colorimetric aqueous‐phase capture of environmentally toxic oxoanions (with similar geometries) in a selective manner. This system is the first example of a MOF‐based system which absorbs both dichromate (Cr2O72−) and permanganate (MnO4−) ions, with the latter acting as a model for the radioactive contaminant pertechnetate (TcO4−).en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectWater-Stable Cationicen_US
dc.subjectMetal Organic Frameworken_US
dc.subjectDual Adsorbent of Oxoanion Pollutantsen_US
dc.subjectSequestration of toxicen_US
dc.subject2016en_US
dc.titleA Water‐Stable Cationic Metal–Organic Framework as a Dual Adsorbent of Oxoanion Pollutantsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleAngewandte Chemie International Editionen_US
dc.publication.originofpublisherForeignen_US
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