Magnetic field controlled C60-TEMPO catalyst for the oxidation of alcohols. (21st January 2020)
- Record Type:
- Journal Article
- Title:
- Magnetic field controlled C60-TEMPO catalyst for the oxidation of alcohols. (21st January 2020)
- Main Title:
- Magnetic field controlled C60-TEMPO catalyst for the oxidation of alcohols
- Authors:
- Piotrowski, Piotr
Żukrowski, Jan
Kaim, Andrzej - Abstract:
- Abstract : TEMPO functionalized C60 fullerene phosphonic acid was grafted onto the surface of magnetic IONPs. The resulting catalyst was employed in oxidation of various primary and secondary alcohols to their corresponding aldehyde or ketone analogues. Abstract : TEMPO functionalized C60 fullerene bearing phosphonic acid anchoring group was successfully synthesized and characterized using cyclic voltammetry and the following spectroscopic techniques: ESI-MS, NMR, ESR, and FT-IR. The obtained fullerene derivative was grafted onto the surface of oleic acid stabilized magnetic iron oxide nanoparticles using the ligand exchange reaction. The resulting nanocomposite material was characterized by means of TEM, EDX, XPS, Mössbauer spectroscopy, and TGA. Subsequently, the obtained catalyst was employed for the selective oxidation of various primary and secondary alcohols to their corresponding aldehyde or ketone analogues and its activity was examined. The results showed high activity of the described catalyst; the reported procedure enables the oxidation of selected alcohols with chemoselectivity and good yields at mild conditions. Moreover, the magnetic properties of the presented catalyst allow easy control and removal of the catalyst using external magnetic field. High stability of the catalyst along with a simple removal method and no disposal problems, and allowing multiple reuse without noticeable loss of efficiency demonstrates the potential value of the reported catalystAbstract : TEMPO functionalized C60 fullerene phosphonic acid was grafted onto the surface of magnetic IONPs. The resulting catalyst was employed in oxidation of various primary and secondary alcohols to their corresponding aldehyde or ketone analogues. Abstract : TEMPO functionalized C60 fullerene bearing phosphonic acid anchoring group was successfully synthesized and characterized using cyclic voltammetry and the following spectroscopic techniques: ESI-MS, NMR, ESR, and FT-IR. The obtained fullerene derivative was grafted onto the surface of oleic acid stabilized magnetic iron oxide nanoparticles using the ligand exchange reaction. The resulting nanocomposite material was characterized by means of TEM, EDX, XPS, Mössbauer spectroscopy, and TGA. Subsequently, the obtained catalyst was employed for the selective oxidation of various primary and secondary alcohols to their corresponding aldehyde or ketone analogues and its activity was examined. The results showed high activity of the described catalyst; the reported procedure enables the oxidation of selected alcohols with chemoselectivity and good yields at mild conditions. Moreover, the magnetic properties of the presented catalyst allow easy control and removal of the catalyst using external magnetic field. High stability of the catalyst along with a simple removal method and no disposal problems, and allowing multiple reuse without noticeable loss of efficiency demonstrates the potential value of the reported catalyst in the application of primary and secondary alcohol oxidation. … (more)
- Is Part Of:
- New journal of chemistry. Volume 44:Number 5(2020)
- Journal:
- New journal of chemistry
- Issue:
- Volume 44:Number 5(2020)
- Issue Display:
- Volume 44, Issue 5 (2020)
- Year:
- 2020
- Volume:
- 44
- Issue:
- 5
- Issue Sort Value:
- 2020-0044-0005-0000
- Page Start:
- 1971
- Page End:
- 1978
- Publication Date:
- 2020-01-21
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c9nj05567c ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12660.xml