Abstract
The reaction of the NHC–disilicon(0) complex [(IAr)Si=Si(IAr)] (1, IAr=:C{N(Ar)C(H)}2, Ar=2,6-iPr2C6H3) with two equiv of elemental Te in toluene at room temperature for three days afforded a mixture of the first dimeric NHC–silicon monotelluride [(IAr)Si=Te]2 (2) and its isomeric complex [(IAr)Si(μ-Te)Si(IAr)=Te] (3). When the same reaction was performed for ten days, only 3 was isolated from the reaction mixture. Compound 1 reacted with four equiv of elemental Te in toluene for four weeks, which proceeded through the formation of 2, 3 and the NHC–disilicon tritelluride complex [{(IAr)Si(=Te)}2Te] (5-Te), to form the dimeric NHC–silicon ditelluride [(IAr)Si(=Te)(μ-Te)]2 (4). The reactions are in line with theoretical mechanistic studies for the formation of 4. Compound 3 reacted with one equiv of elemental sulfur in toluene to form the first NHC–disilicon sulfur ditelluride complex [{(IAr)Si(=Te)}2S] (5-S).
Original language | English |
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Pages (from-to) | 11565-11569 |
Number of pages | 5 |
Journal | Angewandte Chemie - International Edition |
Volume | 56 |
Issue number | 38 |
DOIs | |
Publication status | Published - Sept 11 2017 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
ASJC Scopus Subject Areas
- Catalysis
- General Chemistry
Keywords
- carbenes
- low-valent homologues
- silicon
- sulfur
- tellurium