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稀土元素的循环利用:从电子垃圾到立体选择性催化反应

Recycling of Rare Earth Elements: From E-Waste to Stereoselective Catalytic Reactions.

作者信息

Donato Emanuela, Medici Fabrizio, Chiroli Valerio, Puglisi Alessandra, Rogoli Clemens, Fröhlich Peter, Bertau Martin, Zanoni Giuseppe, Benaglia Maurizio

机构信息

Dipartimento di Chimica, Università degli Studi di Milano, Via C. Golgi 19, 20133, Milano, Italy.

Institute of Chemical Technology, TU Bergakademie Freiberg, Lessingstr. 45, 09599, Freiberg, Germany.

出版信息

ChemSusChem. 2025 Feb 1;18(3):e202401787. doi: 10.1002/cssc.202401787. Epub 2024 Oct 30.

Abstract

Raw mixtures of Rare Earths Elements, REE, recovered by E-waste, were used as catalysts to promote the (stereoselective) synthesis of highly valuable compounds. YO, the major species that is recovered by the E-waste, can be easily converted into the catalytically active Y(OTf) that is able to efficiently promote the Michael addition of indoles to benzylidene malonates and the stereoselective Diels-Alder cycloaddition between cyclopentadiene and 4-(S)-3 acryloyl 4-tert-butyl 2-oxazolidinone. Additionally, the raw mixtures were immobilissed onto silica and used to construct packed reactors, resulting in values for Productivity and Space-Time Yields that were significantly higher than those of the corresponding batch conversions. Notably, the prepared cartridge employed in the model Michael reaction maintained its catalytic efficiency for more than 4 days of continuous running.

摘要

通过电子垃圾回收得到的稀土元素(REE)的原始混合物被用作催化剂,以促进高价值化合物的(立体选择性)合成。氧化钇(YO)是通过电子垃圾回收的主要物质,它可以很容易地转化为具有催化活性的三氟甲磺酸钇(Y(OTf)),这种物质能够有效地促进吲哚与亚苄基丙二酸酯的迈克尔加成反应,以及环戊二烯与4-(S)-3-丙烯酰基-4-叔丁基-2-恶唑烷酮之间的立体选择性狄尔斯-阿尔德环加成反应。此外,将原始混合物固定在硅胶上,并用于构建填充反应器,其生产率和时空产率的值显著高于相应的间歇转化反应。值得注意的是,用于模型迈克尔反应的制备好的柱在连续运行超过4天的时间里仍保持其催化效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fa/11789994/4c3bb6ffeaa2/CSSC-18-e202401787-g010.jpg

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