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dc.contributor.authorRAJASEKAR, PRABHAKARANen_US
dc.contributor.authorPandey, Swechchhaen_US
dc.contributor.authorPAITHANKAR, HARSHADen_US
dc.contributor.authorCHUGH, JEETENDERen_US
dc.contributor.authorSteiner, Alexanderen_US
dc.contributor.authorBOOMISHANKAR, RAMAMOORTHYen_US
dc.date.accessioned2019-09-09T11:36:44Z
dc.date.available2019-09-09T11:36:44Z
dc.date.issued2018-01en_US
dc.identifier.citationChemical Communications, 54(15), 1873-1876.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3987-
dc.identifier.urihttps://doi.org/10.1039/C8CC00207Jen_US
dc.description.abstractCharge-neutral chiral hosts are attractive due to their ability to recognize a wide range of guest functionalities and support enantioselective processes. However, reports on such charge-neutral cages are very scarce in the literature. Here, we report an enantiomeric pair of tetrahedral Pd(II) cages built from chiral tris(imido)phosphate trianions and oxalate linkers, which exhibit enantioselective separation capabilities for epichlorohydrin, β-butyrolactone, and 3-methyl- and 3-ethyl cyclopentanone.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectImido-P(V)en_US
dc.subjectTrianionen_US
dc.subjectSupported enantiopureen_US
dc.subjectNeutral tetrahedral Pd(II) cagesen_US
dc.subject2018en_US
dc.titleImido-P(V) trianion supported enantiopure neutral tetrahedral Pd(II) cagesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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