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Enantiopure Polyradical Tetrahedral Pd12L6 Cages

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dc.contributor.author RAJASEKAR, PRABHAKARAN en_US
dc.contributor.author Swain, Abinash en_US
dc.contributor.author Rajaraman, Gopalan en_US
dc.contributor.author BOOMISHANKAR, RAMAMOORTHY en_US
dc.date.accessioned 2021-06-11T04:37:27Z
dc.date.available 2021-06-11T04:37:27Z
dc.date.issued 2021-07 en_US
dc.identifier.citation Chemistry—A European Journal, 27(39), 10012-10015. en_US
dc.identifier.issn 0947-6539 en_US
dc.identifier.issn 1521-3765 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5930
dc.identifier.uri https://doi.org/10.1002/chem.202101239 en_US
dc.description.abstract The synthesis of cages with a polyradical framework remains a challenging task. Herein is reported an enantiomeric pair of quinoid-bridged polyradical tetrahedral palladium(II) cages that are stabilized by an unusual dianionic diradical form (dhbq..2−). These cages have been characterized by electron paramagnetic resonance and UV-visible spectroscopy, squid magnetometry and mass spectrometry. Single-crystal-derived X-ray investigations of the iso-structural cages built on fluoranilate linkers confirm the tetrahedral structure of the obtained radical cages. Theoretical calculations showed that the diradical state of the dhbq anions is more stable than the usual monoradical state. A weak ferromagnetic exchange between adjacent radical centers was observed in DFT studies. en_US
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.subject Cages en_US
dc.subject Chirality en_US
dc.subject Palladium en_US
dc.subject P-N ligands en_US
dc.subject Radicals en_US
dc.subject 2021-JUN-WEEK2 en_US
dc.subject TOC-JUN-2021 en_US
dc.subject 2021 en_US
dc.title Enantiopure Polyradical Tetrahedral Pd12L6 Cages en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Chemistry—A European Journal en_US
dc.publication.originofpublisher Foreign en_US


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