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https://hdl.handle.net/10356/105214
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chan, Yuk-Chi | en |
dc.contributor.author | Li, Yongxin | en |
dc.contributor.author | Ganguly, Rakesh | en |
dc.contributor.author | So, Cheuk-Wai | en |
dc.date.accessioned | 2015-06-18T04:43:06Z | en |
dc.date.accessioned | 2019-12-06T21:47:34Z | - |
dc.date.available | 2015-06-18T04:43:06Z | en |
dc.date.available | 2019-12-06T21:47:34Z | - |
dc.date.copyright | 2015 | en |
dc.date.issued | 2015 | en |
dc.identifier.citation | Chan, Y.-C., Li, Y., Ganguly, R., & So, C.-W. (2015). Acyclic amido-containing silanechalcogenones. European journal of inorganic chemistry, 2015(23), 3821-3824. | en |
dc.identifier.issn | 1434-1948 | en |
dc.identifier.uri | https://hdl.handle.net/10356/105214 | - |
dc.description.abstract | Reactions of the amidinate-stabilized silicon(II) bis(trimethylsilyl)amide [LSiN(SiMe3)2], {L = PhC(NtBu)2, 1} with a stiochiometric amount of elemental sulfur, selenium and tellurium afforded the first stable silanechalcogenones comprising an acyclic amido substituent [L{N(SiMe3)2}Si=E] {E = S (2), Se (3) or Te (4)}. All compounds were characterized by X-ray crystallography and multinuclear NMR spectroscopy. The results illustrate that these compounds possess some silicon–chalcogen double bond character. | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | European journal of inorganic chemistry | en |
dc.rights | © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | en |
dc.subject | DRNTU::Science::Chemistry::Inorganic chemistry::Analysis | en |
dc.title | Acyclic amido-containing silanechalcogenones | en |
dc.type | Journal Article | en |
dc.contributor.school | School of Physical and Mathematical Sciences | en |
dc.identifier.doi | 10.1002/ejic.201500108 | en |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
Appears in Collections: | SPMS Journal Articles |
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