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dc.contributor.authorDASGUPTA, RAJARSHIen_US
dc.contributor.authorKHAN, SHABANAen_US
dc.date.accessioned2021-02-10T04:39:54Z-
dc.date.available2021-02-10T04:39:54Z-
dc.date.issued2020en_US
dc.identifier.citationAdvances in Organometallic Chemistry, 74, 105-152.en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5638-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0065305520300149?via%3Dihuben_US
dc.description.abstractRecent years have witnessed a tremendous growth in the area of heavier tetrelylenes, e.g., silylenes, germylenes and stannylenes. However, germylenes and stannylenes are quite different from their lighter congeners in terms of their electronic properties and orbital participation. Owing to their electronic differences these heavier tetrelylenes have unique bonding scenario which provides interesting reactivity patterns. Herein, we have summarized a detailed discussion on the synthesis, reactivity and catalytic application of the germylenes and stannylenes.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectN-heterocylic germyleneen_US
dc.subjectN-heterocyclic stannyleneen_US
dc.subjectSmall molecule activationen_US
dc.subjectHydroborationen_US
dc.subjectCyanosilylationen_US
dc.subject2020en_US
dc.titleN-heterocyclic germylenes and stannylenes: Synthesis, reactivity and catalytic application in a nutshellen_US
dc.typeBook chapteren_US
dc.contributor.departmentDept. of Chemistryen_US
dc.title.bookAdvances in Organometallic Chemistryen_US
dc.identifier.doihttps://doi.org/10.1016/bs.adomc.2020.04.001en_US
dc.identifier.sourcetitleAdvances in Organometallic Chemistryen_US
dc.publication.originofpublisherForeignen_US
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