2020
DOI: 10.1016/j.cej.2020.124652
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Efficient CO2 enrichment and fixation by engineering micropores of multifunctional hypercrosslinked ionic polymers

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Cited by 114 publications
(62 citation statements)
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“…It is known that the imidazoline group has two nitrogen species, the imine-like (–N ) and amine-like (–NH–). 51 The N 1s spectral signal was deconvoluted into three peaks ( Fig. 5(b) ) representing the two nitrogen atoms with different chemical positions, which were ascribed to the imidazole moiety.…”
Section: Resultsmentioning
confidence: 99%
“…It is known that the imidazoline group has two nitrogen species, the imine-like (–N ) and amine-like (–NH–). 51 The N 1s spectral signal was deconvoluted into three peaks ( Fig. 5(b) ) representing the two nitrogen atoms with different chemical positions, which were ascribed to the imidazole moiety.…”
Section: Resultsmentioning
confidence: 99%
“…[18,[26][27][28] One efficient way is to utilize the unique advantages of ionic hyper-crosslinked polymers due to their large surface area, versatile architectures, and diverse ionic building blocks. [29,30] Wang et al synthesized imidazolium-functionalized hyper-crosslinked polymers (HCPs) using a series of benzylimidazole salts as the (charged) ionic monomers and a,a 0 -dibromo-p-xylene as a (neutral) crosslinking agent. [31] The connection between the phenyl ring and the imidazolium cation facilitated a hyper-crosslinking reaction through FeCl 3 -catalyzed Friedel-Crafts alkylation.…”
Section: Functionalized Ionic Polymers For Co 2 Conversionmentioning
confidence: 99%
“…sulfite group. [29] The better performance of the hydroxyl-tethered ionic polymer is attributed to the formation of medium-strength hydrogen bonds, which is an important pre-requisite for epoxide activation and ring opening. [29] By increasing the number of adjacent hydrogen-bond donors, the catalytic activity of the ionic polymer can be increased.…”
Section: Functionalized Ionic Polymers For Co 2 Conversionmentioning
confidence: 99%
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