Startseite Naturwissenschaften Recyclable magnetically retrievable nanocatalysts for C–heteroatom bond formation reactions
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Recyclable magnetically retrievable nanocatalysts for C–heteroatom bond formation reactions

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Veröffentlicht/Copyright: 13. Mai 2022
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Abstract

During recent years, magnetic separation has proven to be a highly indispensable and sustainable tool for facile separation of catalysts from the reaction medium with the aid of only an external magnetic force that precludes the requirement of energy intensive, solvent based centrifugation or filtration techniques. Extensive research in the area of catalysis has clearly divulged that while designing any catalyst, the foremost features that need to be paid due attention to include high activity, ready recoverability and good reusability. Fortunately, the magnetic nanocatalysts involving a superparamagnetic core material that could comprise of iron oxides such as magnetite, maghemite or hematite or mixed ferrites (CoFe2O4, CuFe2O4) have offered bright prospects of designing the ideal catalysts by proving their efficacy as strong support material that could be further engineered with various tools of nanotechnology and efficiently catalyze various C–heterobond formation reactions. This chapter provides succinct overview of all the approaches utilized for fabricating different types of magnetic nanoparticles and strategies adopted for imparting them durability. The prime forte however remains to exclusively showcase the applications of the various types of magnetic nanocatalysts in C–O, C–N, C–S and miscellaneous (C–Se, C–Te) bond formation reactions which are anticipated to benefit the synthetic community on a broad spectrum by helping them rationalize and analyze the key features that need to be taken into account, while developing these magical nanostructured catalytic systems for boosting the green bond formation reactions/transformations.


Corresponding author: Rakesh Kumar Sharma, Green Chemistry Network Centre, Department of Chemistry, University of Delhi, Delhi-110007, India, E-mail:

Funding source: University of Delhi

Award Identifier / Grant number: TAR/2021/000201

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: We would like to thank Faculty Research Programme Grant – IoE, University of Delhi for providing the financial assistance. We would also like to thank SERB for providing fund to Dr. Prashant Kumar under the scheme of Teacher Associateship for Research Excellence (TARE) (file number TAR/2021/000201).

  3. Conflict of interest statement: The authors declare no conflicts of interest regarding this article.

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/psr-2021-0101).


Received: 2022-02-22
Accepted: 2022-04-09
Published Online: 2022-05-13

© 2022 Walter de Gruyter GmbH, Berlin/Boston

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