2023
DOI: 10.1016/j.cattod.2023.114296
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Acetalization of glycerol with acetone over UAV-59 catalyst: Mild reaction conditions and enhanced selectivity

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Cited by 3 publications
(6 citation statements)
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“…Such as been previously speculated, and a proposed mechanism can be seen in Figure 7, in this case specifically for a Brönsted acid catalyst [18]. In general, the reaction is kickstarted when the catalyst interacts with the carbonyl of the substrate, either by protonation or coordination with a metal site (for Brönsted and Lewis acids, respectively) [35,41,42,55]. This interaction forms a protonated intermediate structure that, when interacting with the hydroxyl groups in glycerol, originates a hemiketal/hemicetal.…”
Section: Catalystmentioning
confidence: 53%
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“…Such as been previously speculated, and a proposed mechanism can be seen in Figure 7, in this case specifically for a Brönsted acid catalyst [18]. In general, the reaction is kickstarted when the catalyst interacts with the carbonyl of the substrate, either by protonation or coordination with a metal site (for Brönsted and Lewis acids, respectively) [35,41,42,55]. This interaction forms a protonated intermediate structure that, when interacting with the hydroxyl groups in glycerol, originates a hemiketal/hemicetal.…”
Section: Catalystmentioning
confidence: 53%
“…Catalyst recycling was evaluated for ten consecutive cycles, with MOF-808 (Hf) demonstrating high stability [35]. Santos-Vieira et al reported the preparation of a coordination polymer (UAV-59), constituted by Gd 3+ cations and nitrilo(trimethylphosphonic acid) [55]. This catalyst was applied to acetalization reactions, at 55 °C, obtaining a glycerol conversion of 94%, with simultaneous high solketal selectivity (97%).…”
Section: Heterogeneous Catalysts For Glycerol Conversionmentioning
confidence: 99%
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“…According to previous speculation, a proposed mechanism can be seen in Figure 7, in this case specifically for a Brönsted acid catalyst [19]. In general, the reaction is kickstarted when the catalyst interacts with the carbonyl of the substrate, either by protonation or coordination with a metal site (for Brönsted and Lewis acids, respectively) [40,46,47,60]. This interaction forms a protonated intermediate structure that, when interacting with the hydroxyl groups in glycerol, originates a hemiketal/hemiacetal.…”
Section: Catalystmentioning
confidence: 81%
“…Catalyst recycling was evaluated for ten consecutive cycles, with MOF-808 (Hf) demonstrating high stability [40]. Santos-Vieira et al reported the preparation of a coordination polymer (UAV-59), constituted by Gd 3+ cations and nitrile (trimethylphosphonic acid) [60]. This catalyst was applied to acetalization reactions, at 55 • C, obtaining a glycerol conversion of 94%, with simultaneous high solketal selectivity (97%).…”
Section: Heterogeneous Catalysts For Glycerol Acetalizationmentioning
confidence: 99%