Imido-P(V) trianion supported enantiopure neutral tetrahedral Pd(II) cages

RAJASEKAR, PRABHAKARAN; Pandey, Swechchha; CHUGH, JEETENDER; BOOMISHANKAR, RAMAMOORTHY; PAITHANKAR, HARSHAD; Steiner, Alexander

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dc.contributor.author	RAJASEKAR, PRABHAKARAN	en_US
dc.contributor.author	Pandey, Swechchha	en_US
dc.contributor.author	PAITHANKAR, HARSHAD	en_US
dc.contributor.author	CHUGH, JEETENDER	en_US
dc.contributor.author	Steiner, Alexander	en_US
dc.contributor.author	BOOMISHANKAR, RAMAMOORTHY	en_US
dc.date.accessioned	2019-09-09T11:36:44Z
dc.date.available	2019-09-09T11:36:44Z
dc.date.issued	2018-01	en_US
dc.identifier.citation	Chemical Communications, 54(15), 1873-1876.	en_US
dc.identifier.issn	1359-7345	en_US
dc.identifier.issn	1364-548X	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3987
dc.identifier.uri	https://doi.org/10.1039/C8CC00207J	en_US
dc.description.abstract	Charge-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.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Imido-P(V)	en_US
dc.subject	Trianion	en_US
dc.subject	Supported enantiopure	en_US
dc.subject	Neutral tetrahedral Pd(II) cages	en_US
dc.subject	2018	en_US
dc.title	Imido-P(V) trianion supported enantiopure neutral tetrahedral Pd(II) cages	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Chemical Communications	en_US
dc.publication.originofpublisher	Foreign	en_US