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  Highly crystalline poly(heptazine imides) by mechanochemical synthesis for photooxidation of various organic substrates using an intriguing electron acceptor – Elemental sulfur

Savateev, A., Dontsova, D., Kurpil, B., & Antonietti, M. (2017). Highly crystalline poly(heptazine imides) by mechanochemical synthesis for photooxidation of various organic substrates using an intriguing electron acceptor – Elemental sulfur. Journal of Catalysis, 350, 203-211. doi:10.1016/j.jcat.2017.02.029.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-002D-3D54-F Version Permalink: http://hdl.handle.net/21.11116/0000-0004-194A-E
Genre: Journal Article

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Savateev, Aleksandr1, Author              
Dontsova, Dariya2, Author              
Kurpil, Bogdan1, Author              
Antonietti, Markus3, Author              
Affiliations:
1Aleksandr Savateev, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_2421702              
2Dariya Dontsova, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1933288              
3Markus Antonietti, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863321              

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 Abstract: Low-defect potassium poly(heptazine imide) (PHIK-BM) was engineered for application in photocatalytic oxidation of organic substrates. Mechanochemical pretreatment of a mixture of 5-aminotetrazole in LiCl/KCl eutectics using high-energy ball milling afforded a highly homogeneous mixture that, upon sequential thermolysis at 600 °C, gave nanosized particles of PHIK–BM. The photocatalytic activity of the free-standing PHIK–BM plates was assessed in the oxidation of benzyl alcohol to benzaldehyde under visible light irradiation using elemental sulfur as an electron acceptor. Both quantitative conversion (gt;99) of benzyl alcohol and selectivity (gt;98) with respect to benzaldehyde were achieved. The developed method was extended to aliphatic alcohol oxidation coupled with multicomponent Hantzsch 1,4-dihydropyridine synthesis. These 1,4-dihydropyridines were also photocatalytically oxidized by PHIK–BM to the corresponding substituted pyridines, with very good yields and under mild metal-free conditions.

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 Dates: 2017
 Publication Status: Published in print
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 Identifiers: DOI: 10.1016/j.jcat.2017.02.029
BibTex Citekey: Savateev2017203
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Title: Journal of Catalysis
Source Genre: Journal
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Publ. Info: Amsterdam : Elsevier
Pages: - Volume / Issue: 350 Sequence Number: - Start / End Page: 203 - 211 Identifier: ISSN: 0021-9517