Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2451
Full metadata record
DC FieldValueLanguage
dc.contributor.authorRAUT, RAVINDRA K.en_US
dc.contributor.authorMAJUMDAR, MOUMITAen_US
dc.date.accessioned2019-04-25T07:00:12Z
dc.date.available2019-04-25T07:00:12Z
dc.date.issued2019-05en_US
dc.identifier.citationJournal of Organometallic Chemistry, 887, 18-23.en_US
dc.identifier.issn0022-328Xen_US
dc.identifier.issn1872-8561en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2451-
dc.identifier.urihttps://doi.org/10.1016/j.jorganchem.2019.02.019en_US
dc.description.abstractAn acyclic flexible bis(α-iminopyridine) ligand has been employed for the stabilization of chlorostannyliumylidene and a tin(II) dication. The syntheses involve the abstraction of chloride from the tin dichloride precursor using trimethylsilyl trifluoromethane sulfonate. The apically disposed tin(II) dication exhibits electrophilic behaviour and undergoes transmetallation reaction with GeCl2.dioxane resulting in stabilizing the Ge(II) dication. All the compounds have been characterized by NMR techniques and single crystal X-ray crystallography.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectTin(II) (poly)cationen_US
dc.subjects-characteren_US
dc.subjectElectrophilicen_US
dc.subjectNucleophilicen_US
dc.subjectTransmetallationen_US
dc.subjectInert pair effecten_US
dc.subjectTOC-APR-2019en_US
dc.subject2019en_US
dc.titleA pyramidal Tin(II) dication and its reactivity studiesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleJournal of Organometallic Chemistryen_US
dc.publication.originofpublisherForeignen_US
Appears in Collections:JOURNAL ARTICLES

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.