Acyclic amido-containing silanechalcogenones
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),...
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Main Authors: | , , , |
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Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2015
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Subjects: | |
Online Access: | https://hdl.handle.net/10356/105214 http://hdl.handle.net/10220/25963 http://dx.doi.org/10.1002/ejic.201500108 |
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Institution: | Nanyang Technological University |
Language: | English |
Summary: | 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. |
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