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Homocoupling of CO and isocyanide mediated by a C,C '-bis(silylenyl)-substituted ortho-carborane
Authors: Xiong Yun | Yao Shenglai | Szilvasi Tibor | Růžička Aleš | Driess Matthias
Year: 2020
Type of publication: článek v odborném periodiku
Name of source: Chemical Communications
Publisher name: Royal Society of Chemistry
Place: Cambridge
Page from-to: 747-750
Titles:
Language Name Abstract Keywords
cze Homokopulace CO a isokyanidu zprostředkovaná C, C '-bis (silylenyl) -substituovaným ortokarboranem Neočekávaná reaktivita bis-silylenu [(LSi:) C] (2) B (10) H (10) 1 {L = PhC (tBuN) (2)} na oxid uhelnatý a 2,6- uvádí se dimethylfenylisokyanid. Zatímco reakce 1 s CO vede selektivně k novému přímému spojení a produktu štěpení CO 2 ze dvou molekul 1 a čtyř molekul CO, reakce 1 s 2,6-dimethylfenylisokyanidem poskytuje pouze molární 1: 2 spojovací produkt 3 hlava-ocas s vazbou SiC. Homokopulace; substituovaný ortokarboranem; isokyanid
eng Homocoupling of CO and isocyanide mediated by a C,C '-bis(silylenyl)-substituted ortho-carborane The unexpected reactivity of the o-carborane supported bis-silylene [(LSi:)C](2)B(10)H(10)1 {L= PhC(tBuN)(2)} towards carbon monoxide and 2,6-dimethylphenyl isocyanide is reported. While the reaction of 1 with CO leads selectively to the novel head-to-head coupling and C-O cleavage product 2 from two molecules 1 and four molecules CO, the reaction of 1 with 2,6-dimethylphenyl isocyanide affords solely the 1 : 2 molar head-to-tail coupling product 3 with a SiC bond. 2-coordinate; silylene; isonitriles; activation; monoxide; elements