کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1320792 | 1499849 | 2015 | 5 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Rhodium(I) and iridium(I) imidazo[1,5-a]pyridine-1-ylalkylalkoxy complexes: Synthesis, characterization and application as catalysts for hydrosilylation of alkynes Rhodium(I) and iridium(I) imidazo[1,5-a]pyridine-1-ylalkylalkoxy complexes: Synthesis, characterization and application as catalysts for hydrosilylation of alkynes](/preview/png/1320792.png)
• Rh(I) and Ir(I) complexes bearing imidazo[1,5-a]pyridine-1-ylalkyl alcohol as chelating NˆO-monoanionic ligands have been prepared.
• Their spectroscopic properties and structures were determined based on IR and NMR spectra and X-ray analyses.
• The Rh(I) complexes were used as catalysts for the E-selective hydrosilylation of alkynes.
Rh(I) and Ir(I) complexes bearing imidazo[1,5-a]pyridine-1-ylalkyl alcohol as chelating NˆO-monoanionic ligands were prepared as thermally stable compounds. Their spectroscopic properties and structures were determined based on IR and NMR spectra and X-ray analyses. The Rh(I) complexes were used as catalysts for the hydrosilylation of alkynes. The catalytic activities of the complexes were highly influenced by the substituents on their aromatic rings. Highly E-selective formation of vinylsilanes was achieved at higher temperatures for longer reaction times.
Rh(I) and Ir(I) complexes bearing imidazo[1,5-a]pyridine-1-ylalkyl alcohol as chelating NˆO-monoanionic ligands were prepared as thermally stable compounds. Their spectroscopic properties and structures were determined based on IR and NMR spectra and X-ray analyses. The Rh(I) complexes were used as catalysts for the hydrosilylation of alkynes. The catalytic activities of the complexes were highly influenced by the substituents on their aromatic rings. Highly E-selective formation of vinylsilanes was achieved at higher temperatures for longer reaction times.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 794, 1 October 2015, Pages 76–80