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Instant and quantitative epoxidation of styrene under ambient conditions over a nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized SBA-15

Nickel(ii)dibenzotetramethyltetraaza[14]annulene complex (Nitmtaa) was synthetized and immobilized on post amino-functionalized SBA-15 (N-SBA-15) to obtain a stable and reusable nanocatalyst named as Nitmtaa@N-SBA-15. Here (3-aminopropyl)triethoxysilane (APTES) was first grafted on the surface SBA-1...

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Autores principales: Abboud, Mohamed, Al-Zaqri, Nabil, Sahlabji, Taher, Eissa, Murad, Mubarak, Ahmed T., Bel-Hadj-Tahar, Radhouane, Alsalme, Ali, Alharthi, Fahad A., Alsyahi, Amjad, Hamdy, Mohamed S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056905/
https://www.ncbi.nlm.nih.gov/pubmed/35515658
http://dx.doi.org/10.1039/d0ra07244c
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author Abboud, Mohamed
Al-Zaqri, Nabil
Sahlabji, Taher
Eissa, Murad
Mubarak, Ahmed T.
Bel-Hadj-Tahar, Radhouane
Alsalme, Ali
Alharthi, Fahad A.
Alsyahi, Amjad
Hamdy, Mohamed S.
author_facet Abboud, Mohamed
Al-Zaqri, Nabil
Sahlabji, Taher
Eissa, Murad
Mubarak, Ahmed T.
Bel-Hadj-Tahar, Radhouane
Alsalme, Ali
Alharthi, Fahad A.
Alsyahi, Amjad
Hamdy, Mohamed S.
author_sort Abboud, Mohamed
collection PubMed
description Nickel(ii)dibenzotetramethyltetraaza[14]annulene complex (Nitmtaa) was synthetized and immobilized on post amino-functionalized SBA-15 (N-SBA-15) to obtain a stable and reusable nanocatalyst named as Nitmtaa@N-SBA-15. Here (3-aminopropyl)triethoxysilane (APTES) was first grafted on the surface SBA-15, then Nitmtaa was added and coordinated on the silica surface via APTES amine groups. The structure and morphology, and thermal stability of the prepared nanocatalyst was investigated using SEM, HR-TEM, BET, FT-IR, powder XRD, and TGA. HR-TEM and XRD results revealed a high dispersion of Nitmtaa on the SBA-15 surface. The catalytic activity of this nanocatalyst was evaluated in the epoxidation of styrene, under ambient conditions, using meta-chloroperoxybenzoic acid (m-CPBA) as the oxygen donor. This nanocatalyst showed an immediate and quantitative epoxidation of styrene with high turn-over-frequency ∼31.58 s(−1). Moreover, the superior catalytic activity and high stability of Nitmtaa@N-SBA-15 could be maintained after four successive cycles. A possible reaction mechanism is also proposed.
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spelling pubmed-90569052022-05-04 Instant and quantitative epoxidation of styrene under ambient conditions over a nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized SBA-15 Abboud, Mohamed Al-Zaqri, Nabil Sahlabji, Taher Eissa, Murad Mubarak, Ahmed T. Bel-Hadj-Tahar, Radhouane Alsalme, Ali Alharthi, Fahad A. Alsyahi, Amjad Hamdy, Mohamed S. RSC Adv Chemistry Nickel(ii)dibenzotetramethyltetraaza[14]annulene complex (Nitmtaa) was synthetized and immobilized on post amino-functionalized SBA-15 (N-SBA-15) to obtain a stable and reusable nanocatalyst named as Nitmtaa@N-SBA-15. Here (3-aminopropyl)triethoxysilane (APTES) was first grafted on the surface SBA-15, then Nitmtaa was added and coordinated on the silica surface via APTES amine groups. The structure and morphology, and thermal stability of the prepared nanocatalyst was investigated using SEM, HR-TEM, BET, FT-IR, powder XRD, and TGA. HR-TEM and XRD results revealed a high dispersion of Nitmtaa on the SBA-15 surface. The catalytic activity of this nanocatalyst was evaluated in the epoxidation of styrene, under ambient conditions, using meta-chloroperoxybenzoic acid (m-CPBA) as the oxygen donor. This nanocatalyst showed an immediate and quantitative epoxidation of styrene with high turn-over-frequency ∼31.58 s(−1). Moreover, the superior catalytic activity and high stability of Nitmtaa@N-SBA-15 could be maintained after four successive cycles. A possible reaction mechanism is also proposed. The Royal Society of Chemistry 2020-09-24 /pmc/articles/PMC9056905/ /pubmed/35515658 http://dx.doi.org/10.1039/d0ra07244c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Abboud, Mohamed
Al-Zaqri, Nabil
Sahlabji, Taher
Eissa, Murad
Mubarak, Ahmed T.
Bel-Hadj-Tahar, Radhouane
Alsalme, Ali
Alharthi, Fahad A.
Alsyahi, Amjad
Hamdy, Mohamed S.
Instant and quantitative epoxidation of styrene under ambient conditions over a nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized SBA-15
title Instant and quantitative epoxidation of styrene under ambient conditions over a nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized SBA-15
title_full Instant and quantitative epoxidation of styrene under ambient conditions over a nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized SBA-15
title_fullStr Instant and quantitative epoxidation of styrene under ambient conditions over a nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized SBA-15
title_full_unstemmed Instant and quantitative epoxidation of styrene under ambient conditions over a nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized SBA-15
title_short Instant and quantitative epoxidation of styrene under ambient conditions over a nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized SBA-15
title_sort instant and quantitative epoxidation of styrene under ambient conditions over a nickel(ii)dibenzotetramethyltetraaza[14]annulene complex immobilized on amino-functionalized sba-15
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056905/
https://www.ncbi.nlm.nih.gov/pubmed/35515658
http://dx.doi.org/10.1039/d0ra07244c
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