首页> 外文期刊>Applied Organometallic Chemistry >Ru~(III)(OTf)SalophenCH2-NHSiO2-Fe: an efficient and magnetically recoverable catalyst for trimethylsilylation of alcohols and phenols with hexamethyldisilazane
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Ru~(III)(OTf)SalophenCH2-NHSiO2-Fe: an efficient and magnetically recoverable catalyst for trimethylsilylation of alcohols and phenols with hexamethyldisilazane

机译:Ru〜(III)(OTf)SalophenCH2-NHSiO2-Fe:一种高效且可磁回收的醇和酚与六甲基二硅氮烷的三甲基硅烷化催化剂

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摘要

Efficient trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMOS) catalyzed by ruthenium(III) complex of chloromethylated Salophen supported on nanomagnetic materials is reported. First, the iron nanomagnets were silica coated, functionalized with amine and then ruthenium CM-Salophen was successfully bonded to their surface. The catalyst, Ru~(III)(OTf) SalophenCH2-NHSiO2-Fe, was characterized by elemental analysis, FT-lR and UV-visible spectroscopic techniques, transmission electron microscopy and inductively coupled plasma (ICP). The Ru~(III)(OTf)SalophenCH2-NHSiO2-Fe catalyzed trimethylsilylation of primary and secondary alcohols as well as phenols, and the corresponding TMS ethers were obtained in high yields and short reaction times at room temperature. This new heterogenized trimethylsilylation catalyst is easily recovered with a magnet and showed no appreciable loss of activity even after five consecutive runs.
机译:报道了在纳米磁性材料上负载的氯甲基化Salophen的钌(III)络合物催化的六甲基二硅氮烷(HMOS)对醇和酚的三甲基甲硅烷基化反应。首先,将铁纳米磁铁涂有二氧化硅,用胺官能化,然后将CM-沙洛芬钌成功地键合到它们的表面。通过元素分析,FT-1R和紫外可见光谱技术,透射电子显微镜和电感耦合等离子体(ICP)对催化剂Ru〜(III)(OTf)SalophenCH2-NHSiO2-Fe进行了表征。 Ru〜(III)(OTf)SalophenCH2-NHSiO2-Fe催化伯醇和仲醇以及苯酚的三甲基硅烷化反应,并在室温下以高收率和短反应时间获得了相应的TMS醚。这种新的杂化三甲基甲硅烷基化催化剂很容易用磁铁回收,即使连续运行五次也没有明显的活性损失。

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