About: Ionic Liquids Catalysis for Carbon Dioxide Conversion With Nucleophiles

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scientific article published on 08 October 2018

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у 2018 (uk) im Oktober 2018 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'ochobre de 2018 (ast) scientific article published on 08 October 2018 (en)
publication date	wds:Q57817424-D41F0155-665C-4605-AA4D-F92B4B65FE05
publication date	2018-10-08 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57817424-137B5ABB-AADB-4FDE-8CEB-7EDB104A71FB
language of work or name	English
cites work	wds:Q57817424-04B25348-F70F-4347-ACD6-D70A7B8D472F wds:Q57817424-094F9B09-9481-46E9-BA6A-3E5959F06F60 wds:Q57817424-0DAE7D54-539A-4B8B-A9A2-80F0BF420465 wds:Q57817424-1DE22226-29E8-41F3-8EEF-C51F400AE8F8 wds:Q57817424-22E29299-C98E-4CDB-85C9-5294968AD7B3 wds:Q57817424-35271334-A325-4187-9B15-51F3B1B58B17 wds:Q57817424-3CC89528-13DF-42FD-A3C2-4D660CBBF3A9 wds:Q57817424-51F4D9A0-2A78-4F8B-B286-7EE8A7AD8898 wds:Q57817424-5377B221-C2EE-4203-8278-98D344A7D955 wds:Q57817424-5730F159-2B6B-40B1-81EC-34E076EFCC7A wds:Q57817424-615C2898-43F0-4540-9B5E-6673CAC0C9C7 wds:Q57817424-6BB83729-0334-4CB5-BF16-2AEFCA27F5B0 wds:Q57817424-6E2E1C95-BEB0-4DCE-8070-512C6BAABBEF wds:Q57817424-74155DA5-6D91-4B80-B2CA-56F44C44A0E4 wds:Q57817424-7C238B3C-7E18-421E-8D69-E5A9AFBA24B8 wds:Q57817424-823378F3-A1EE-4D2B-89E7-CE3237E2FFA4 wds:Q57817424-8D402B31-C9D2-4A28-B4CA-5D1FA07C07CF wds:Q57817424-9C80EB95-CF75-4E2D-AF92-D889670B1320 wds:Q57817424-9D7678DB-C638-4868-9B00-BD626BD6EA24 wds:Q57817424-B2D8A641-DF40-4B4F-BC55-16C36F610358 wds:Q57817424-BE657DEC-8F2B-467D-956C-C9BAA511356B wds:Q57817424-C1EA3F2C-E549-4AE5-8163-04542DA5CBED wds:Q57817424-C4FD9F4A-9F69-4F97-A5D7-D8EE44DAB0FA wds:Q57817424-C5672342-8805-4B47-B940-9F0A03E3083A wds:Q57817424-D89AEB22-0705-4756-B8BA-79BA44E1DE90 wds:Q57817424-E511B955-BDDD-4EC5-9E9D-F3DD9213B5E1 wds:Q57817424-ED528039-6406-4AA1-8BF2-70F15995B591
cites work	Tuning the basicity of ionic liquids for efficient synthesis of alkylidene carbonates from CO2 at atmospheric pressure Gas solubility in ionic liquids. Hydrogenation of carbon dioxide is promoted by a task-specific ionic liquid. A bifunctional tungstate catalyst for chemical fixation of CO2 at atmospheric pressure A protic ionic liquid catalyzes CO₂ conversion at atmospheric pressure and room temperature: synthesis of quinazoline-2,4(1H,3H)-diones Equimolar CO(2) absorption by anion-functionalized ionic liquids Using carbon dioxide as a building block in organic synthesis Catalysis for the valorization of exhaust carbon: from CO2 to chemicals, materials, and fuels. technological use of CO2. Tuning the Basicity of Ionic Liquids for Equimolar CO2 Capture Transformation of atmospheric CO2 catalyzed by protic ionic liquids: efficient synthesis of 2-oxazolidinones CO(2) capture by a task-specific ionic liquid Ionic liquids and dense carbon dioxide: a beneficial biphasic system for catalysis Active chemisorption sites in functionalized ionic liquids for carbon capture Alternatives to phosgene and carbon monoxide: synthesis of symmetric urea derivatives with carbon dioxide in ionic liquids Efficient [WO4](2-)-catalyzed chemical fixation of carbon dioxide with 2-aminobenzonitriles to quinazoline-2,4(1H,3H)-diones Are Ionic Liquids Chemically Stable? Computer-Assisted Design of Ionic Liquids for Efficient Synthesis of 3(2H)-Furanones: A Domino Reaction Triggered by CO2. Highly efficient and reversible SO2 capture by tunable azole-based ionic liquids through multiple-site chemical absorption Green chemistry: reversible nonpolar-to-polar solvent Periodic Mesoporous Organosilica with a Basic Urea-Derived Framework for Enhanced Carbon Dioxide Capture and Conversion Under Mild Conditions Azole-Anion-Based Aprotic Ionic Liquids: Functional Solvents for Atmospheric CO2 Transformation into Various Heterocyclic Compounds Synthesis of Asymmetrical Organic Carbonates using CO2 as a Feedstock in AgCl/Ionic Liquid System at Ambient Conditions Ionic liquid as an efficient promoting medium for fixation of CO2: clean synthesis of alpha-methylene cyclic carbonates from CO2 and propargyl alcohols catalyzed by metal salts under mild conditions Task-specific ionic liquid and CO2-cocatalysed efficient hydration of propargylic alcohols to α-hydroxy ketones. Highly Efficient Nitric Oxide Capture by Azole-Based Ionic Liquids through Multiple-Site Absorption. Ionic liquid as an efficient promoting medium for fixation of carbon dioxide: a clean method for the synthesis of 5-methylene-1,3-oxazolidin-2-ones from propargylic alcohols, amines, and carbon dioxide catalyzed by Cu(I) under mild conditions. Ab initio calculations of the interaction between CO2 and the acetate ion
author name string	wds:Q57817424-836F7434-C225-4466-84E5-712FB647248F wds:Q57817424-AC136ABB-00A3-472D-B92D-4BD4AD736118 wds:Q57817424-CA6A67B2-018D-41EE-A05D-A873ACC8EB31
author name string	Hong-Chen Fu Liang-Nian He Shu-Mei Xia
rdfs:label	Ionic Liquids Catalysis for Carbon Dioxide Conversion With Nucleophiles (en) Ionic Liquids Catalysis for Carbon Dioxide Conversion With Nucleophiles (nl)
skos:prefLabel	Ionic Liquids Catalysis for Carbon Dioxide Conversion With Nucleophiles (en) Ionic Liquids Catalysis for Carbon Dioxide Conversion With Nucleophiles (nl)
name	Ionic Liquids Catalysis for Carbon Dioxide Conversion With Nucleophiles (en) Ionic Liquids Catalysis for Carbon Dioxide Conversion With Nucleophiles (nl)
author	wds:Q57817424-3573626B-1C49-44CE-8456-E31B7EB8BD31
author	Kaihong Chen
title	wds:Q57817424-DE9296DE-C8BC-4B17-8A74-BEEF599261AE
title	Ionic Liquids Catalysis for Carbon Dioxide Conversion With Nucleophiles (en)
page(s)	wds:Q57817424-F64F875F-1877-41E5-863C-95DA14FC0C88
page(s)	462
instance of	wds:Q57817424-F12364FE-B8F6-435F-A20F-64401AD4539C
instance of	scholarly article
main subject	wds:Q57817424-D8819C07-7BEA-4CAF-BECE-296F45F37890
main subject	general chemistry
PubMed ID	wds:Q57817424-36417B37-49D4-4854-B017-B1A0F7AFFE54
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30349815
PubMed ID	30349815
published in	wds:Q57817424-10BF5985-F827-43C7-9DC4-6E769EFF080B
published in	Frontiers in Chemistry
volume	wds:Q57817424-7AB410D3-ED16-4CFF-86A6-A062792650D8
volume	6
DOI	wds:Q57817424-99C9B7EF-CE92-459F-86A4-C357C63C8CB7
DOI	http://dx.doi.org/10.3389/FCHEM.2018.00462
DOI	10.3389/FCHEM.2018.00462
copyright license	wds:Q57817424-cec80ce4-509f-417a-82a9-876217cdb7a2
copyright status	wds:Q57817424-10d546d3-b3f0-425c-b992-1f53bda787bb
copyright license	Creative Commons Attribution 4.0 International
copyright status	copyrighted

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