Halide-free deep eutectic solvents constructed from natural compounds for converting carbon dioxide to cyclic carbonate
Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO 2 and epoxides, with a TOF of 645 h −1 . The DFT calculation result was in good agreement with the experiment result, indicating that the ring closur...
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Published in | Chemical communications (Cambridge, England) Vol. 61; no. 16; pp. 3391 - 3394 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Royal Soc Chemistry
18.02.2025
Royal Society of Chemistry |
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Abstract | Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO
2
and epoxides, with a TOF of 645 h
−1
. The DFT calculation result was in good agreement with the experiment result, indicating that the ring closure process was the rate-determining step.
Halide-free deep eutectic solvents (DESs) constructed from natural compounds were used to efficiently transform CO
2
into cyclic carbonates. |
---|---|
AbstractList | Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO
2
and epoxides, with a TOF of 645 h
−1
. The DFT calculation result was in good agreement with the experiment result, indicating that the ring closure process was the rate-determining step.
Halide-free deep eutectic solvents (DESs) constructed from natural compounds were used to efficiently transform CO
2
into cyclic carbonates. Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO 2 and epoxides, with a TOF of 645 h −1 . The DFT calculation result was in good agreement with the experiment result, indicating that the ring closure process was the rate-determining step. Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO and epoxides, with a TOF of 645 h . The DFT calculation result was in good agreement with the experiment result, indicating that the ring closure process was the rate-determining step. Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO2 and epoxides, with a TOF of 645 h-1. The DFT calculation result was in good agreement with the experiment result, indicating that the ring closure process was the rate-determining step.Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO2 and epoxides, with a TOF of 645 h-1. The DFT calculation result was in good agreement with the experiment result, indicating that the ring closure process was the rate-determining step. Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO2 and epoxides, with a TOF of 645 h−1. The DFT calculation result was in good agreement with the experiment result, indicating that the ring closure process was the rate-determining step. Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO2 and epoxides, with a TOF of 645 h-1. The DFT calculation result was in good agreement with the experiment result, indicating that the ring closure process was the rate-determining step. |
Author | Chu, Dan-Dan Zhou, Jie Yu, Wen-Wang Meng, Xiang-Guang Li, Wen Ma, Xian-Jian |
AuthorAffiliation | College of Chemistry Key Laboratory of Green Chemistry and Technology Ministry of Education Sichuan University |
AuthorAffiliation_xml | – name: Sichuan University – name: College of Chemistry – name: Key Laboratory of Green Chemistry and Technology Ministry of Education |
Author_xml | – sequence: 1 givenname: Wen-Wang surname: Yu fullname: Yu, Wen-Wang – sequence: 2 givenname: Xiang-Guang surname: Meng fullname: Meng, Xiang-Guang – sequence: 3 givenname: Wen surname: Li fullname: Li, Wen – sequence: 4 givenname: Jie surname: Zhou fullname: Zhou, Jie – sequence: 5 givenname: Xian-Jian surname: Ma fullname: Ma, Xian-Jian – sequence: 6 givenname: Dan-Dan surname: Chu fullname: Chu, Dan-Dan |
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Cites_doi | 10.1038/s41467-019-13638-9 10.1021/acs.chemrev.0c00883 10.1039/d2gc02517e 10.1016/j.jcou.2020.101302 10.1007/s10311-022-01470-5 10.1039/d2gc02146c 10.1016/j.cej.2022.138715 10.3390/molecules27249006 10.1016/j.mcat.2023.113812 10.1039/c7ta08629f 10.1016/j.gee.2019.03.002 10.2174/0122133461255437230930182648 10.1021/sc500096j 10.1002/cctc.202201373 10.1039/c2cs35178a 10.1016/j.jcou.2023.102659 10.1016/j.cogsc.2020.04.002 10.1021/acs.inorgchem.3c01899 10.1021/acssuschemeng.2c03210 10.1039/D2GC02517E 10.1039/D2GC02146C 10.1039/C7TA08629F |
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References | Manka, D (WOS:000903235200001) 2022; 27 Werlinger, F (WOS:001166075100001) 2024; 79 Qin, H (WOS:000516829700004) 2020; 5 Kleij, AW (WOS:000570249200014) 2020; 24 Mogale, R (WOS:001164535600001) 2024; 554 Bragato, N (WOS:000928649000001) 2023; 15 Zhang, QH (WOS:000309544700015) 2012; 41 Zhi, YF (WOS:000419188300008) 2018; 6 Singh, G (WOS:001042134500001) 2023; 62 Vagnoni, M (WOS:000599716100006) 2020; 42 Ai, L (WOS:000818609500001) 2022; 20 Zhang, WW (WOS:000851446000002) 2023; 451 Terazzi, C (WOS:000864715000001) 2022 Paiva, A (WOS:000335547600001) 2014; 2 Yu, W (WOS:000700878800003) 2021; 121 Rostami, A (WOS:000851574800001) 2022; 24 Esteves, H (WOS:001185301800004) 2024; 11 Ye, RP (WOS:000503207700001) 2019; 10 Zhang, AJ (WOS:000848862900001) 2022; 24 Ye (D4CC06282E/cit1/1) 2019; 10 Kleij (D4CC06282E/cit16/1) 2020; 24 Vagnoni (D4CC06282E/cit6/1) 2020; 42 Terazzi (D4CC06282E/cit17/1) 2022; 10 Zhi (D4CC06282E/cit10/1) 2018; 6 Ai (D4CC06282E/cit2/1) 2022; 20 Yu (D4CC06282E/cit4/1) 2021; 121 Singh (D4CC06282E/cit11/1) 2023; 62 Mogale (D4CC06282E/cit5/1) 2024; 554 Esteves (D4CC06282E/cit3/1) 2024; 11 Qin (D4CC06282E/cit13/1) 2020; 5 Paiva (D4CC06282E/cit14/1) 2014; 2 Zhang (D4CC06282E/cit9/1) 2023; 451 Manka (D4CC06282E/cit15/1) 2022; 27 Zhang (D4CC06282E/cit19/1) 2022; 24 Zhang (D4CC06282E/cit12/1) 2012; 41 Rostami (D4CC06282E/cit18/1) 2022; 24 Bragato (D4CC06282E/cit8/1) 2023; 15 Werlinger (D4CC06282E/cit7/1) 2024; 79 |
References_xml | – volume: 10 start-page: ARTN 5698 year: 2019 ident: WOS:000503207700001 article-title: CO2 hydrogenation to high-value products via heterogeneous catalysis publication-title: NATURE COMMUNICATIONS doi: 10.1038/s41467-019-13638-9 – volume: 121 start-page: 10865 year: 2021 ident: WOS:000700878800003 article-title: Aliphatic Polycarbonates from Cyclic Carbonate Monomers and Their Application as Biomaterials publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.0c00883 – volume: 24 start-page: 7194 year: 2022 ident: WOS:000848862900001 article-title: Imidazolium-based ionic liquids containing multipoint hydrogen bond donors as bifunctional organocatalysts for efficient cooperative conversion of CO2 to cyclic carbonates publication-title: GREEN CHEMISTRY doi: 10.1039/d2gc02517e – volume: 42 start-page: ARTN 101302 year: 2020 ident: WOS:000599716100006 article-title: Choline-based eutectic mixtures as catalysts for effective synthesis of cyclic carbonates from epoxides and CO2 publication-title: JOURNAL OF CO2 UTILIZATION doi: 10.1016/j.jcou.2020.101302 – volume: 20 start-page: 3555 year: 2022 ident: WOS:000818609500001 article-title: Carbon dioxide electroreduction into formic acid and ethylene: a review publication-title: ENVIRONMENTAL CHEMISTRY LETTERS doi: 10.1007/s10311-022-01470-5 – volume: 24 start-page: 9069 year: 2022 ident: WOS:000851574800001 article-title: 2-Picolinic acid as a naturally occurring hydrogen bond donor for the preparation of cyclic carbonates from terminal/internal epoxides and CO2 publication-title: GREEN CHEMISTRY doi: 10.1039/d2gc02146c – volume: 451 start-page: ARTN 138715 year: 2023 ident: WOS:000851446000002 article-title: Rational design of Lewis acid-base bifunctional nanopolymers with high performance on CO2/epoxide cycloaddition without a cocatalyst publication-title: CHEMICAL ENGINEERING JOURNAL doi: 10.1016/j.cej.2022.138715 – volume: 27 start-page: ARTN 9006 year: 2022 ident: WOS:000903235200001 article-title: Deep Eutectic Solvents as Catalysts for Cyclic Carbonates Synthesis from CO2 and Epoxides publication-title: MOLECULES doi: 10.3390/molecules27249006 – volume: 554 start-page: ARTN 113812 year: 2024 ident: WOS:001164535600001 article-title: Highly efficient DES-based catalytic systems for carbon dioxide utilization via cycloaddition with epoxide substrates publication-title: MOLECULAR CATALYSIS doi: 10.1016/j.mcat.2023.113812 – volume: 6 start-page: 374 year: 2018 ident: WOS:000419188300008 article-title: Covalent organic frameworks: efficient, metal-free, heterogeneous organocatalysts for chemical fixation of CO2 under mild conditions publication-title: JOURNAL OF MATERIALS CHEMISTRY A doi: 10.1039/c7ta08629f – volume: 5 start-page: 8 year: 2020 ident: WOS:000516829700004 article-title: Overview of acidic deep eutectic solvents on synthesis, properties and applications publication-title: GREEN ENERGY & ENVIRONMENT doi: 10.1016/j.gee.2019.03.002 – volume: 11 start-page: 87 year: 2024 ident: WOS:001185301800004 article-title: Organocatalysis for the Chemical Fixation of Carbon Dioxide to Synthesise N-Heterocycles publication-title: CURRENT GREEN CHEMISTRY doi: 10.2174/0122133461255437230930182648 – volume: 2 start-page: 1063 year: 2014 ident: WOS:000335547600001 article-title: Natural Deep Eutectic Solvents - Solvents for the 21st Century publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING doi: 10.1021/sc500096j – volume: 15 year: 2023 ident: WOS:000928649000001 article-title: Dihydroxybenzene-derived ILs as Halide-Free, Single-component Organocatalysts for CO2 Insertion Reactions publication-title: CHEMCATCHEM doi: 10.1002/cctc.202201373 – volume: 41 start-page: 7108 year: 2012 ident: WOS:000309544700015 article-title: Deep eutectic solvents: syntheses, properties and applications publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c2cs35178a – volume: 79 start-page: ARTN 102659 year: 2024 ident: WOS:001166075100001 article-title: Turning waste into resources. Efficient synthesis of biopolyurethanes from used cooking oils and CO2 publication-title: JOURNAL OF CO2 UTILIZATION doi: 10.1016/j.jcou.2023.102659 – volume: 24 start-page: 72 year: 2020 ident: WOS:000570249200014 article-title: Advancing halide-free catalytic synthesis of CO2-based heterocycles publication-title: CURRENT OPINION IN GREEN AND SUSTAINABLE CHEMISTRY doi: 10.1016/j.cogsc.2020.04.002 – volume: 62 start-page: 13058 year: 2023 ident: WOS:001042134500001 article-title: Fe(III)-Anchored Porphyrin-Based Nanoporous Covalent Organic Frameworks for Green Synthesis of Cyclic Carbonates from Olefins and CO2 under Atmospheric Pressure Conditions publication-title: INORGANIC CHEMISTRY doi: 10.1021/acs.inorgchem.3c01899 – year: 2022 ident: WOS:000864715000001 article-title: Synthesis of Cyclic Carbonates Catalyzed by CaI2-Et3N and Studies on Their Biocatalytic Kinetic Resolution publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING doi: 10.1021/acssuschemeng.2c03210 – volume: 2 start-page: 1063 year: 2014 ident: D4CC06282E/cit14/1 publication-title: ACS Sustainable Chem. Eng. doi: 10.1021/sc500096j – volume: 24 start-page: 7194 year: 2022 ident: D4CC06282E/cit19/1 publication-title: Green Chem. doi: 10.1039/D2GC02517E – volume: 24 start-page: 72 year: 2020 ident: D4CC06282E/cit16/1 publication-title: Curr. Opin. Green Sustainable Chem. doi: 10.1016/j.cogsc.2020.04.002 – volume: 24 start-page: 9069 year: 2022 ident: D4CC06282E/cit18/1 publication-title: Green Chem. doi: 10.1039/D2GC02146C – volume: 41 start-page: 7108 year: 2012 ident: D4CC06282E/cit12/1 publication-title: Chem. Soc. Rev. doi: 10.1039/c2cs35178a – volume: 10 start-page: 13335 issue: 40 year: 2022 ident: D4CC06282E/cit17/1 publication-title: ACS Sustainable Chem. Eng. doi: 10.1021/acssuschemeng.2c03210 – volume: 11 start-page: 87 year: 2024 ident: D4CC06282E/cit3/1 publication-title: Current Green Chem. doi: 10.2174/0122133461255437230930182648 – volume: 554 start-page: 113812 year: 2024 ident: D4CC06282E/cit5/1 publication-title: Mol. Catal. doi: 10.1016/j.mcat.2023.113812 – volume: 5 start-page: 8 year: 2020 ident: D4CC06282E/cit13/1 publication-title: Green Energy Environ. doi: 10.1016/j.gee.2019.03.002 – volume: 15 start-page: e202201373 year: 2023 ident: D4CC06282E/cit8/1 publication-title: ChemCatChem doi: 10.1002/cctc.202201373 – volume: 121 start-page: 10865 year: 2021 ident: D4CC06282E/cit4/1 publication-title: Chem. Rev. doi: 10.1021/acs.chemrev.0c00883 – volume: 42 start-page: 101302 year: 2020 ident: D4CC06282E/cit6/1 publication-title: J. CO2 Util. doi: 10.1016/j.jcou.2020.101302 – volume: 6 start-page: 374 year: 2018 ident: D4CC06282E/cit10/1 publication-title: J. Mater. Chem. A doi: 10.1039/C7TA08629F – volume: 451 start-page: 138715 year: 2023 ident: D4CC06282E/cit9/1 publication-title: Chem. Eng. J. doi: 10.1016/j.cej.2022.138715 – volume: 62 start-page: 13058 year: 2023 ident: D4CC06282E/cit11/1 publication-title: Inorg. Chem. doi: 10.1021/acs.inorgchem.3c01899 – volume: 79 start-page: 102659 year: 2024 ident: D4CC06282E/cit7/1 publication-title: J. CO2 Util. doi: 10.1016/j.jcou.2023.102659 – volume: 27 start-page: 9006 year: 2022 ident: D4CC06282E/cit15/1 publication-title: Molecules doi: 10.3390/molecules27249006 – volume: 20 start-page: 3555 year: 2022 ident: D4CC06282E/cit2/1 publication-title: Environ. Chem. Lett. doi: 10.1007/s10311-022-01470-5 – volume: 10 start-page: 5698 year: 2019 ident: D4CC06282E/cit1/1 publication-title: Nat. Commun. doi: 10.1038/s41467-019-13638-9 |
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Snippet | Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO
2
and... Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO2 and... Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO 2 and... Halide-free deep eutectic solvents (DESs) derived from natural biological compounds were used to gently catalyze the cycloaddition reaction between CO and... |
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SubjectTerms | Carbon dioxide Chemistry Chemistry, Multidisciplinary Cycloaddition Eutectic reactions Physical Sciences Science & Technology Solvents |
Title | Halide-free deep eutectic solvents constructed from natural compounds for converting carbon dioxide to cyclic carbonate |
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