|کد مقاله||کد نشریه||سال انتشار||مقاله انگلیسی||ترجمه فارسی||نسخه تمام متن|
|1324925||1499928||2012||7 صفحه PDF||سفارش دهید||دانلود رایگان|
A very easy method is described for direct phosphorylation of silica gel to afford silica diphenylphosphinite (SDPP). This new phosphorylated silica contains higher amounts of P(III) moiety compared to the method based on the sol-gel technique. The phosphorylated silica reacts with Pd(II) to produce nano Pd(0)/SDPP which was characterized by different techniques. The obtained nano Pd(0) catalyst exhibited excellent reactivity and stability in the Mizoroki–Heck and Suzuki–Miyaura cross-coupling reactions with different aryl iodides and bromides. This heterogeneous catalyst can be easily recovered and reused in several runs.
A very easy method is described for the direct phosphorylation of silica gel to afford silica diphenylphosphinite (SDPP). This phosphorylated silica reacts with Pd(II) to produce nano Pd(0)/SDPP catalyst and is applied for the Mizoroki–Heck and Suzuki–Miyaura coupling reactions.Figure optionsDownload as PowerPoint slideHighlights
► Direct phosphorylation of activated silica gel.
► An easy method for the preparation of phosphorylated silica support (SDPP).
► A suitable catalyst in Mizoroki–Heck and Suzuki–Miyaura reactions.
► The recoverable and reusable heterogeneous catalyst in several runs.
Journal: Journal of Organometallic Chemistry - Volumes 708–709, 15 June 2012, Pages 118–124