Superparamagnetic nanoparticles for asymmetric catalysis—a perfect match

Literature Information

Publication Date 2011-01-31
DOI 10.1039/C0CY00069H
Impact Factor 6.119
Authors

Kalluri V. S. Ranganath, Frank Glorius


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Abstract

The aim of this perspective is to highlight the potential application of (superpara)magnetic nanoparticles in asymmetric catalysis. The unique combination of high enantioselectivity and enhanced reactivity combined with its recyclability and ease of separation makes this chiral nanotechnology one of the most promising strategies for the formation of enantiomerically enriched compounds on an industrial scale. This perspective focuses on the most representative examples of this young and emerging research field and highlights recent achievements and future prospects of magnetic nanoparticles in asymmetric catalysis.

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Catalysis Science & Technology

Catalysis Science & Technology
CiteScore: 5.91
Self-citation Rate: 4.5%
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Catalysis Science & Technology is committed to publishing research reporting high-quality, cutting-edge developments across the catalysis community at large. The journal places equal focus on publications from the heterogeneous, homogeneous, thermo-, electro-, photo-, organo- and biocatalysis communities. Works published in the journal feature a balanced mix of fundamental, technology-oriented, experimental, computational, digital and data-driven original research, thus appealing to catalysis practitioners in both academic and industrial environments. Original research articles published in the journal must demonstrate new catalytic discoveries and/or methodological advances that represent a significant advance on previously published work, from the molecular to the process scales. We welcome rigorous research in a wide range of timely or emerging applications related to the environment, health, energy and materials. Catalysis Science & Technology publishes Communications, Articles, Reviews and Perspectives. More details regarding manuscript types may be found in the Information for Authors section.

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