Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2393
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dc.contributor.authorKHAN, SHABANAen_US
dc.contributor.authorRoesky, Herbert W.en_US
dc.date.accessioned2019-03-26T10:01:04Z
dc.date.available2019-03-26T10:01:04Z
dc.date.issued2019-02en_US
dc.identifier.citationChemistry—A European Journal, 25(7), 1636-1648.en_US
dc.identifier.issn0947-6539en_US
dc.identifier.issn1521-3765en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2393
dc.identifier.urihttps://doi.org/10.1002/chem.201801672en_US
dc.description.abstractThe isolation of stable carbenes, such as N‐heterocyclic carbenes, cyclic alkyl amino carbenes, and abnormal N‐heterocyclic carbenes, has encouraged synthetic chemists to use them as neutral ligands for stabilizing unusual compounds with main group elements. In this Minireview, an overview is provided of the recent developments in the chemistry of carbene‐stabilized silicon halides, in which the silicon atoms are in low oxidation state. The structural diversities emanating from the differences in the HOMO–LUMO gaps of various carbenes will also be discussed.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectAbnormal N-heterocyclic carbenesen_US
dc.subjectCyclic alkyl amino carbenesen_US
dc.subjectHalidesen_US
dc.subjectN-heterocyclic carbenesen_US
dc.subjectSiliconen_US
dc.subjectSilyleneen_US
dc.subjectTOC-MAR-2019en_US
dc.subject2019en_US
dc.titleCarbene-Stabilized Exceptional Silicon Halidesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemistry—A European Journalen_US
dc.publication.originofpublisherForeignen_US
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