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Insights into the Interaction between Amylose-Rich Corn Starch and Maleic Anhydride in Imidazolium Chloride-Based Ionic Liquids AITranslate

University of Toronto; University of Toronto; University of Toronto
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Publisher: ACS
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Abstract AITranslate

Starch maleates with a high degree of maleic anhydride (MA) substitutions (DS) are in-demand for producing advanced composites. High-DS maleates are synthesized in imidazolium chloride-based ionic liquids because they could sustain starch-MA esterification, the precise mechanism of which, however, is largely unknown. In this study, we mapped chemical shifts of imidazolium cations before and after MA was added to each of the three starch-[C2mim]Cl, starch-[Amim]Cl, and starch-[C4mim]Cl systems. [C4mim]+ and [Amim]+ cations were observed to form substantial H-bonds with hydroxyls of starch. These hydroxyls could further associate with MA, liberating the bound cations. The liberated [Amim]+ cations, unlike [C4mim]+ cations, could readily donate their C2–H protons to activated MA, providing high-DS maleates (DSNMR ≈ 0.1, DStitration ≈ 1.20). The insights gained from this study would benefit the development of maleates from a wide range of biopolymers and expedite the screening of ionic liquids with varying cation–anion combinations for high-DS maleate synthesis.

KeyWords AITranslate

anhydroglucose unit (AGU) 1butyl3methylimidazolium chloride ([C4mim]Cl) 1ethyl3methylimidazolium chloride ([C2mim]Cl) Show More
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DOI:https://doi.org/10.1021/acsapm.2c01917

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Citation Information:

Starch maleates with a high degree of maleic anhydride (MA) substitutions (DS) are in-demand for producing advanced composites. High-DS maleates are synthesized in imidazolium chloride-based ionic liquids because they could sustain starch-MA esterification, the precise mechanism of which, however, is largely unknown. In this study, we mapped chemical shifts of imidazolium cations before and after MA was added to each of the three starch-[C2mim]Cl, starch-[Amim]Cl, and starch-[C4mim]Cl systems. [C4mim]+ and [Amim]+ cations were observed to form substantial H-bonds with hydroxyls of starch. These hydroxyls could further associate with MA, liberating the bound cations. The liberated [Amim]+ cations, unlike [C4mim]+ cations, could readily donate their C2–H protons to activated MA, providing high-DS maleates (DSNMR ≈ 0.1, DStitration ≈ 1.20). The insights gained from this study would benefit the development of maleates from a wide range of biopolymers and expedite the screening of ionic liquids with varying cation–anion combinations for high-DS maleate synthesis.

quote

GB/T 7714-2015 [1] Shrestha Roy Goswami, Sen Wang, Ning Yan. ACS Applied Polymer Materials, 2023(5). DOI:10.1021/acsapm.2c01917.
MLA [1] Shrestha Roy Goswami, et al., ACS Applied Polymer Materials, no. 5, 2023, https://doi.org/10.1021/acsapm.2c01917.
APA [1] Shrestha Roy Goswami, Sen Wang, & Ning Yan. (2023). ACS Applied Polymer Materials(5). https://doi.org/10.1021/acsapm.2c01917
IEEE [1] Shrestha Roy Goswami, Sen Wang, and Ning Yan, ACS Applied Polymer Materials, no. 5, 2023, doi: 10.1021/acsapm.2c01917. keywords: {anhydroglucose unit (AGU);1butyl3methylimidazolium chloride ([C4mim]Cl);1ethyl3methylimidazolium chloride ([C2mim]Cl);Show More}