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使用嵌入FeCo/石墨壳纳米晶体的高效且可回收的介孔二氧化硅球与各种亲核化合物进行炔丙基取代反应。

Propargylic substitution reactions with various nucleophilic compounds using efficient and recyclable mesoporous silica spheres embedded with FeCo/graphitic shell nanocrystals.

作者信息

Jang Seongwan, Kim A Young, Seo Won Seok, Park Kang Hyun

机构信息

Department of Chemistry and Chemistry Institute for Functional Materials, Pusan National University, Busan, 609-735 South Korea.

Department of Chemistry, Sogang University, Seoul, 121-742 South Korea.

出版信息

Nanoscale Res Lett. 2015 Jan 23;10:2. doi: 10.1186/1556-276X-10-2. eCollection 2015.

Abstract

Phosphomolybdic acid (PMA, H3PMo12O40) functioned as a catalyst for reactions of secondary propargylic alcohols and nucleophiles. Highly stable and magnetically recyclable mesoporous silica spheres (MMS) embedded with FeCo-graphitic carbon shell nanocrystals (FeCo/GC@MSS) were fabricated by a modified Stöber process and chemical vapor deposition (CVD) method. The FeCo/GC@MSS were loaded with phosphomolybdic acid (PMA@FeCo/GC@MSS), and their catalytic activity was investigated. Propargylic reactions of 1,3-diphenyl-2-propyn-1-ol with a wide range of nucleophiles bearing activating substituents were catalyzed under mild conditions. It was found that the MMS possess mesoporosities and have enough inner space to load FeCo and phosphomolybdic acid. The FeCo/GC@MSS were found to be chemically stable against acid etching and oxidation. This suggests that the nanocrystals can be used as a support for an acid catalyst. Moreover, the magnetic property of the nanocrystals enabled the facile separation of catalysts from the products.

摘要

磷钼酸(PMA,H3PMo12O40)作为仲炔丙醇与亲核试剂反应的催化剂。通过改进的Stöber法和化学气相沉积(CVD)法制备了负载有FeCo-石墨碳壳纳米晶体(FeCo/GC@MSS)的高稳定性且可磁回收的介孔二氧化硅球(MMS)。将磷钼酸负载到FeCo/GC@MSS上(PMA@FeCo/GC@MSS),并对其催化活性进行了研究。在温和条件下催化了1,3-二苯基-2-丙炔-1-醇与一系列带有活化取代基的亲核试剂的炔丙基反应。发现MMS具有介孔结构且有足够的内部空间来负载FeCo和磷钼酸。发现FeCo/GC@MSS对酸蚀刻和氧化具有化学稳定性。这表明该纳米晶体可作为酸催化剂的载体。此外,纳米晶体的磁性使得催化剂能够从产物中轻松分离出来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afda/4385110/865e4494ace1/11671_2014_2426_Fig2_HTML.jpg

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