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Activity and stability studies of H-transfer reduction reactions of aldehydes and ketones over aluminium isopropoxide heterogenised catalysts

Aluminium isopropoxide Al(O(i)Pr)(3) immobilised on various mesoporous supports (SiO(2), TiO(2) and γ-Al(2)O(3)) was tested for H-transfer reductions of various aldehydes and ketones in the presence of 2-propanol as a sacrificial agent. The heterogenised catalysts were characterised by N(2) physisor...

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Autores principales: Muhammad, Atika, Ismaila, Ammaru, Usman, Bashir Jelani, Di Carmine, Graziano, D'Agostino, Carmine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706686/
https://www.ncbi.nlm.nih.gov/pubmed/36544994
http://dx.doi.org/10.1039/d2ra06437e
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author Muhammad, Atika
Ismaila, Ammaru
Usman, Bashir Jelani
Di Carmine, Graziano
D'Agostino, Carmine
author_facet Muhammad, Atika
Ismaila, Ammaru
Usman, Bashir Jelani
Di Carmine, Graziano
D'Agostino, Carmine
author_sort Muhammad, Atika
collection PubMed
description Aluminium isopropoxide Al(O(i)Pr)(3) immobilised on various mesoporous supports (SiO(2), TiO(2) and γ-Al(2)O(3)) was tested for H-transfer reductions of various aldehydes and ketones in the presence of 2-propanol as a sacrificial agent. The heterogenised catalysts were characterised by N(2) physisorption, XRD, SEM-EDX, FTIR and ICP-OES. The characterisation results show a successful grafting of the homogeneous aluminium isopropoxide catalyst, covalently bound to the solid surface, with high dispersion over the mesoporous supports. The heterogenised catalysts show an excellent catalytic activity with high selectivity towards the desired alcohol product, with performances that are comparable with those of the homogeneous Al(O(i)Pr)(3) catalyst. Al(O(i)Pr)(3) grafted on SiO(2) shows higher activity compared to γ-Al(2)O(3) and TiO(2) supported catalysts. The catalysts remain very active after 5 cycles of reuse and no leached Al(O(i)Pr)(3) was found in the reaction mixture, hence showing an excellent stability. The work reported here shows that it is possible to effectively immobilise catalytic functions, usually working in the homogeneous phase, over solid supports, with the resulting heterogenised catalysts keeping the same catalytic activity of the homogeneous counterpart and excellent stability, and with the advantage of being able to recycle and reuse them, without loss of catalytic materials.
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spelling pubmed-97066862022-12-20 Activity and stability studies of H-transfer reduction reactions of aldehydes and ketones over aluminium isopropoxide heterogenised catalysts Muhammad, Atika Ismaila, Ammaru Usman, Bashir Jelani Di Carmine, Graziano D'Agostino, Carmine RSC Adv Chemistry Aluminium isopropoxide Al(O(i)Pr)(3) immobilised on various mesoporous supports (SiO(2), TiO(2) and γ-Al(2)O(3)) was tested for H-transfer reductions of various aldehydes and ketones in the presence of 2-propanol as a sacrificial agent. The heterogenised catalysts were characterised by N(2) physisorption, XRD, SEM-EDX, FTIR and ICP-OES. The characterisation results show a successful grafting of the homogeneous aluminium isopropoxide catalyst, covalently bound to the solid surface, with high dispersion over the mesoporous supports. The heterogenised catalysts show an excellent catalytic activity with high selectivity towards the desired alcohol product, with performances that are comparable with those of the homogeneous Al(O(i)Pr)(3) catalyst. Al(O(i)Pr)(3) grafted on SiO(2) shows higher activity compared to γ-Al(2)O(3) and TiO(2) supported catalysts. The catalysts remain very active after 5 cycles of reuse and no leached Al(O(i)Pr)(3) was found in the reaction mixture, hence showing an excellent stability. The work reported here shows that it is possible to effectively immobilise catalytic functions, usually working in the homogeneous phase, over solid supports, with the resulting heterogenised catalysts keeping the same catalytic activity of the homogeneous counterpart and excellent stability, and with the advantage of being able to recycle and reuse them, without loss of catalytic materials. The Royal Society of Chemistry 2022-11-29 /pmc/articles/PMC9706686/ /pubmed/36544994 http://dx.doi.org/10.1039/d2ra06437e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Muhammad, Atika
Ismaila, Ammaru
Usman, Bashir Jelani
Di Carmine, Graziano
D'Agostino, Carmine
Activity and stability studies of H-transfer reduction reactions of aldehydes and ketones over aluminium isopropoxide heterogenised catalysts
title Activity and stability studies of H-transfer reduction reactions of aldehydes and ketones over aluminium isopropoxide heterogenised catalysts
title_full Activity and stability studies of H-transfer reduction reactions of aldehydes and ketones over aluminium isopropoxide heterogenised catalysts
title_fullStr Activity and stability studies of H-transfer reduction reactions of aldehydes and ketones over aluminium isopropoxide heterogenised catalysts
title_full_unstemmed Activity and stability studies of H-transfer reduction reactions of aldehydes and ketones over aluminium isopropoxide heterogenised catalysts
title_short Activity and stability studies of H-transfer reduction reactions of aldehydes and ketones over aluminium isopropoxide heterogenised catalysts
title_sort activity and stability studies of h-transfer reduction reactions of aldehydes and ketones over aluminium isopropoxide heterogenised catalysts
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706686/
https://www.ncbi.nlm.nih.gov/pubmed/36544994
http://dx.doi.org/10.1039/d2ra06437e
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