Controllable synthesis of hollow mesoporous organosilica nanoparticles with pyridine-2,6-bis-imidazolium frameworks for CO conversion

A series of hard-template-derived hollow mesoporous organosilica nanoparticles (HMONs) with pyridine-2,6-bis-imidazolium frameworks have been described for the first time. As a part of the investigation, to evaluate the effects of the hard template nature, the Si/CTAB and organosilica/TEOS molar rat...

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Veröffentlicht in:Nanoscale 2024-09, Vol.16 (36), p.16977-16989
Hauptverfasser: Anvarian-Asl, Ghazale, Joudian, Sadegh, Todisco, Stefano, Mastrorilli, Pietro, Khorasani, Mojtaba
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container_end_page 16989
container_issue 36
container_start_page 16977
container_title Nanoscale
container_volume 16
creator Anvarian-Asl, Ghazale
Joudian, Sadegh
Todisco, Stefano
Mastrorilli, Pietro
Khorasani, Mojtaba
description A series of hard-template-derived hollow mesoporous organosilica nanoparticles (HMONs) with pyridine-2,6-bis-imidazolium frameworks have been described for the first time. As a part of the investigation, to evaluate the effects of the hard template nature, the Si/CTAB and organosilica/TEOS molar ratios, and the stepwise addition of precursors, four reaction conditions denoted as methods A-D were designed. In the presence of polystyrene latex as a hard template, the HMONs that we wished to synthesize were not yielded with a Si/CTAB molar ratio of 3 (method A), but we could synthesize the desired HMONs with a Si/CTAB molar ratio of 9 and an organosilica : TEOS ratio of 1 : 99 (method B). The ratio of organosilica to TEOS could be improved up to 2.5 : 97.5 if the precursor additions are made in a stepwise manner rather than by simultaneous additions (method C). Using sSiO 2 as a hard template, a yolk-shell morphology was observed by adopting a Si/CTAB molar ratio of 3 (method D). The HMONs were modified by iodide ions and their activity was explored toward the coupling of CO 2 with epoxides. Among the catalysts, I-HMON-L-C-2.5 exhibited excellent results under mild reaction conditions. Well-oriented pore sizes and short channel length facilitated easy mass transfer from one side and the integration of the interior hollow regions of the catalyst particles from the other side improved the CO 2 retention time around pores where the imidazolium organocatalysts were located, which made I-HMON-L-C-2.5 an effective catalyst for title CO 2 utilization. The catalyst was reused at least six times without exhibiting any changes in its activity. HMONs can also be used as solid CNC ligands for the preparation of copper catalysts for the click reaction between phenyl acetylene and benzyl azide. The effects of a hard template, stepwise addition of precursors, and Si/CTAB and organosilica/TEOS molar ratios have been systematically studied during the synthesis of hollow mesoporous organosilica nanoparticles with pyridine-bis-imidazolium units.
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As a part of the investigation, to evaluate the effects of the hard template nature, the Si/CTAB and organosilica/TEOS molar ratios, and the stepwise addition of precursors, four reaction conditions denoted as methods A-D were designed. In the presence of polystyrene latex as a hard template, the HMONs that we wished to synthesize were not yielded with a Si/CTAB molar ratio of 3 (method A), but we could synthesize the desired HMONs with a Si/CTAB molar ratio of 9 and an organosilica : TEOS ratio of 1 : 99 (method B). The ratio of organosilica to TEOS could be improved up to 2.5 : 97.5 if the precursor additions are made in a stepwise manner rather than by simultaneous additions (method C). Using sSiO 2 as a hard template, a yolk-shell morphology was observed by adopting a Si/CTAB molar ratio of 3 (method D). The HMONs were modified by iodide ions and their activity was explored toward the coupling of CO 2 with epoxides. Among the catalysts, I-HMON-L-C-2.5 exhibited excellent results under mild reaction conditions. Well-oriented pore sizes and short channel length facilitated easy mass transfer from one side and the integration of the interior hollow regions of the catalyst particles from the other side improved the CO 2 retention time around pores where the imidazolium organocatalysts were located, which made I-HMON-L-C-2.5 an effective catalyst for title CO 2 utilization. The catalyst was reused at least six times without exhibiting any changes in its activity. HMONs can also be used as solid CNC ligands for the preparation of copper catalysts for the click reaction between phenyl acetylene and benzyl azide. 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Among the catalysts, I-HMON-L-C-2.5 exhibited excellent results under mild reaction conditions. Well-oriented pore sizes and short channel length facilitated easy mass transfer from one side and the integration of the interior hollow regions of the catalyst particles from the other side improved the CO 2 retention time around pores where the imidazolium organocatalysts were located, which made I-HMON-L-C-2.5 an effective catalyst for title CO 2 utilization. The catalyst was reused at least six times without exhibiting any changes in its activity. HMONs can also be used as solid CNC ligands for the preparation of copper catalysts for the click reaction between phenyl acetylene and benzyl azide. 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As a part of the investigation, to evaluate the effects of the hard template nature, the Si/CTAB and organosilica/TEOS molar ratios, and the stepwise addition of precursors, four reaction conditions denoted as methods A-D were designed. In the presence of polystyrene latex as a hard template, the HMONs that we wished to synthesize were not yielded with a Si/CTAB molar ratio of 3 (method A), but we could synthesize the desired HMONs with a Si/CTAB molar ratio of 9 and an organosilica : TEOS ratio of 1 : 99 (method B). The ratio of organosilica to TEOS could be improved up to 2.5 : 97.5 if the precursor additions are made in a stepwise manner rather than by simultaneous additions (method C). Using sSiO 2 as a hard template, a yolk-shell morphology was observed by adopting a Si/CTAB molar ratio of 3 (method D). The HMONs were modified by iodide ions and their activity was explored toward the coupling of CO 2 with epoxides. Among the catalysts, I-HMON-L-C-2.5 exhibited excellent results under mild reaction conditions. Well-oriented pore sizes and short channel length facilitated easy mass transfer from one side and the integration of the interior hollow regions of the catalyst particles from the other side improved the CO 2 retention time around pores where the imidazolium organocatalysts were located, which made I-HMON-L-C-2.5 an effective catalyst for title CO 2 utilization. The catalyst was reused at least six times without exhibiting any changes in its activity. HMONs can also be used as solid CNC ligands for the preparation of copper catalysts for the click reaction between phenyl acetylene and benzyl azide. The effects of a hard template, stepwise addition of precursors, and Si/CTAB and organosilica/TEOS molar ratios have been systematically studied during the synthesis of hollow mesoporous organosilica nanoparticles with pyridine-bis-imidazolium units.</abstract><doi>10.1039/d4nr02144d</doi><tpages>13</tpages></addata></record>
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