Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10264
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dc.contributor.authorGHOSH, MOUSHAKHIen_US
dc.contributor.authorPANWARIA, PRAKASHen_US
dc.contributor.authorTothadi, Srinuen_US
dc.contributor.authorKHAN, SHABANAen_US
dc.date.accessioned2025-07-07T10:32:08Z-
dc.date.available2025-07-07T10:32:08Z-
dc.date.issued2025-01en_US
dc.identifier.citationInorganic Chemistry, 64(02), 1110–1123.en_US
dc.identifier.issn0020-1669en_US
dc.identifier.issn1520-510Xen_US
dc.identifier.urihttps://doi.org/10.1021/acs.inorgchem.4c04703en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10264-
dc.description.abstractHerein, we report the isolation of pyridine moiety-functionalized SiNSi pincer-based bis-silylene ligand (1) and its reactivity toward various halide precursors (X = Br and I) of group 13 elements (M = Al, Ga, and In). This gave us straightforward access to the SiNSi pincer-coordinated group 13 cations (2–7). These complexes are duly characterized by single-crystal X-ray diffraction studies, multinuclear magnetic resonance spectroscopy (1H, 13C, and 29Si), and high-resolution mass spectrometry techniques. Their electronic properties were further analyzed with the help of quantum chemical calculations.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectAnionsen_US
dc.subjectAromatic compoundsen_US
dc.subjectHydrocarbonsen_US
dc.subjectMathematical methodsen_US
dc.subjectMolecular structureen_US
dc.subject2025en_US
dc.titleAccess to Bis-Silylene-Stabilized Group 13 Cationsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleInorganic Chemistryen_US
dc.publication.originofpublisherForeignen_US
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