A Robust Magnetically Recoverable Nickel Nanocatalyst for Sustainable α-Olefination of Nitriles Using Primary Alcohols

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The paper studies synthesis and catalytic performance of a magnetically recoverable nickel nanocatalyst for the α-olefination of nitriles using primary alcohols, using a benzyl alcohol derivative and benzyl cyanide derivative under refluxing toluene with KOt-Bu. The authors design Fe3O4@SiO2 as a magnetic support, functionalize it with epichlorohydrin and ortho-phenylenediamine, load nickel to form Fe3O4@SiO2/EP/OPDA@Ni, and confirm fabrication with X-ray diffraction, TEM, EDS, and vibrating-sample magnetometry. They report that the catalyst can be separated by an external magnetic field and remains reusable with only minor activity loss over at least five consecutive cycles. A major caveat explicitly stated is that the work is a preprint and has not been peer reviewed. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract A novel nickel nanocatalyst with a magnetic core was designed and synthesized through a multi-step procedure. First, an iron oxide core was synthesized (Fe 3 O 4 ), then coated with a silica layer (Fe 3 O 4 @SiO 2 ). The catalyst support was further functionalized using epichlorohydrin (EP) and ortho -phenylenediamine (OPDA) (Fe 3 O 4 @SiO 2 /EP/OPDA), and finally, nickel was loaded onto the structure to obtain the finished catalyst (Fe 3 O 4 @SiO 2 /EP/OPDA@Ni). Its successful fabrication was confirmed by various characterization techniques, including X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and vibrating-sample magnetometry. The nanocatalyst was then effectively applied in the α-olefination of nitriles using primary alcohols through the reaction of a benzyl alcohol derivative with a benzyl cyanide derivative in refluxing toluene, using KO t -Bu as the base. The catalyst could be easily separated from the reaction mixture by applying an external magnetic field. It was also reusable, retaining its activity with only a minor loss over at least five consecutive cycles.
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A Robust Magnetically Recoverable Nickel Nanocatalyst for Sustainable α-Olefination of Nitriles Using Primary Alcohols | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Research Article A Robust Magnetically Recoverable Nickel Nanocatalyst for Sustainable α-Olefination of Nitriles Using Primary Alcohols Effat Vatankhah, Hossein Eshghi, Ali Shiri This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-9324654/v1 This work is licensed under a CC BY 4.0 License Status: Under Revision Version 1 posted 11 You are reading this latest preprint version Abstract A novel nickel nanocatalyst with a magnetic core was designed and synthesized through a multi-step procedure. First, an iron oxide core was synthesized (Fe 3 O 4 ), then coated with a silica layer (Fe 3 O 4 @SiO 2 ). The catalyst support was further functionalized using epichlorohydrin (EP) and ortho -phenylenediamine (OPDA) (Fe 3 O 4 @SiO 2 /EP/OPDA), and finally, nickel was loaded onto the structure to obtain the finished catalyst (Fe 3 O 4 @SiO 2 /EP/OPDA@Ni). Its successful fabrication was confirmed by various characterization techniques, including X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and vibrating-sample magnetometry. The nanocatalyst was then effectively applied in the α-olefination of nitriles using primary alcohols through the reaction of a benzyl alcohol derivative with a benzyl cyanide derivative in refluxing toluene, using KO t -Bu as the base. The catalyst could be easily separated from the reaction mixture by applying an external magnetic field. It was also reusable, retaining its activity with only a minor loss over at least five consecutive cycles. Nickel nanocatalyst Benzyl cyanide Benzyl alcohol α-olefination reaction Full Text Additional Declarations No competing interests reported. Supplementary Files SupportingInformation.pdf Cite Share Download PDF Status: Under Revision Version 1 posted Editorial decision: Revision requested 03 May, 2026 Reviews received at journal 03 May, 2026 Reviews received at journal 02 May, 2026 Reviews received at journal 22 Apr, 2026 Reviewers agreed at journal 08 Apr, 2026 Reviewers agreed at journal 08 Apr, 2026 Reviewers agreed at journal 08 Apr, 2026 Reviewers invited by journal 08 Apr, 2026 Editor assigned by journal 08 Apr, 2026 Submission checks completed at journal 07 Apr, 2026 First submitted to journal 05 Apr, 2026 You are reading this latest preprint version Research Square lets you share your work early, gain feedback from the community, and start making changes to your manuscript prior to peer review in a journal. As a division of Research Square Company, we’re committed to making research communication faster, fairer, and more useful. We do this by developing innovative software and high quality services for the global research community. Our growing team is made up of researchers and industry professionals working together to solve the most critical problems facing scientific publishing. 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