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DC Field | Value | Language |
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dc.contributor.author | GHOSH, MOUSHAKHI | en_US |
dc.contributor.author | PANWARIA, PRAKASH | en_US |
dc.contributor.author | Tothadi, Srinu | en_US |
dc.contributor.author | KHAN, SHABANA | en_US |
dc.date.accessioned | 2025-07-07T10:32:08Z | - |
dc.date.available | 2025-07-07T10:32:08Z | - |
dc.date.issued | 2025-01 | en_US |
dc.identifier.citation | Inorganic Chemistry, 64(02), 1110–1123. | en_US |
dc.identifier.issn | 0020-1669 | en_US |
dc.identifier.issn | 1520-510X | en_US |
dc.identifier.uri | https://doi.org/10.1021/acs.inorgchem.4c04703 | en_US |
dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10264 | - |
dc.description.abstract | Herein, 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.iso | en | en_US |
dc.publisher | American Chemical Society | en_US |
dc.subject | Anions | en_US |
dc.subject | Aromatic compounds | en_US |
dc.subject | Hydrocarbons | en_US |
dc.subject | Mathematical methods | en_US |
dc.subject | Molecular structure | en_US |
dc.subject | 2025 | en_US |
dc.title | Access to Bis-Silylene-Stabilized Group 13 Cations | en_US |
dc.type | Article | en_US |
dc.contributor.department | Dept. of Chemistry | en_US |
dc.identifier.sourcetitle | Inorganic Chemistry | en_US |
dc.publication.originofpublisher | Foreign | en_US |
Appears in Collections: | JOURNAL ARTICLES |
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