Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2731
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dc.contributor.authorSwamy, V. S. V. S. N.en_US
dc.contributor.authorYadav, Sandeepen_US
dc.contributor.authorPAL, SHIVen_US
dc.contributor.authorDas, Tamalen_US
dc.contributor.authorVanka, Kumaren_US
dc.contributor.authorSen, Sakya S.en_US
dc.date.accessioned2019-04-29T10:16:52Z
dc.date.available2019-04-29T10:16:52Z
dc.date.issued2016-05en_US
dc.identifier.citationChemical Communications, 50(52), 7890-7892.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2731-
dc.identifier.urihttps://doi.org/10.1039/C6CC03789Een_US
dc.description.abstractHerein, we introduce isocyanide as a ligand in main group chemistry and describe the facile isolation of a Ge(II) dication. The reaction of 2,6-dimethylphenylisocyanide with GeCl2 leads to the formation of a Ge(II) dication with two [GeCl3]− molecules as counter anions. The dicationic Ge(II) center is bound to four isocyanide ligands and also holds a lone pair of electrons. DFT calculations reveal that the dication is stabilized only by σ-donation from the four isocyanide ligands. Natural population analysis gives a charge of +0.74 on the Ge(II) center, indicating that the positive charge is shared by the isocyanide substituents.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectFacile accessen_US
dc.subjectDicationen_US
dc.subjectIsocyanidesen_US
dc.subjectPale yellow crystalsen_US
dc.subjectNBO analysisen_US
dc.subjectNon-metallic cationsen_US
dc.subject2016en_US
dc.titleFacile access to a Ge(II) dication stabilized by isocyanidesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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