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2-Methylimidazole Copper Iminodiacetates for the Adsorption of Oxygen and Catalytic Oxidation of Cyclohexane

The mixed-ligand copper(II) iminodiacetates [Cu(ida)(2-mim)(H(2)O)(2)]·H(2)O (1), [Cu(ida)(2-mim)(2)]·2H(2)O (2), [Cu(ida)(2-mim)(H(2)O)](n)·4.5nH(2)O (3), and [Cu(2)(ida)(2)(2-mim)(2)](n)·nH(2)O (4) (H(2)ida = iminodiacetic acid, 2-mim = 2-methylimidazole) were obtained from neutral or alkaline sol...

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Autores principales: Chen, Xi, An, Dong-Li, Zhan, Xin-Qi, Zhou, Zhao-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7143979/
https://www.ncbi.nlm.nih.gov/pubmed/32178320
http://dx.doi.org/10.3390/molecules25061286
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author Chen, Xi
An, Dong-Li
Zhan, Xin-Qi
Zhou, Zhao-Hui
author_facet Chen, Xi
An, Dong-Li
Zhan, Xin-Qi
Zhou, Zhao-Hui
author_sort Chen, Xi
collection PubMed
description The mixed-ligand copper(II) iminodiacetates [Cu(ida)(2-mim)(H(2)O)(2)]·H(2)O (1), [Cu(ida)(2-mim)(2)]·2H(2)O (2), [Cu(ida)(2-mim)(H(2)O)](n)·4.5nH(2)O (3), and [Cu(2)(ida)(2)(2-mim)(2)](n)·nH(2)O (4) (H(2)ida = iminodiacetic acid, 2-mim = 2-methylimidazole) were obtained from neutral or alkaline solutions at different temperatures. The novel complex 4 contains very small holes with diameters of 2.9 Å, which can adsorb O(2) selectively and reversibly between 1.89 to 29.90 bars, compared with the different gases of N(2), H(2), CO(2), and CH(4). This complex is stable up to 150 °C based on thermal analyses and XRD patterns. The four complexes show catalytic activities that facilitate the conversion of cyclohexane to cyclohexanol and cyclohexanone with hydrogen peroxide in a solution. The total conversion is 31% for 4.
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spelling pubmed-71439792020-04-13 2-Methylimidazole Copper Iminodiacetates for the Adsorption of Oxygen and Catalytic Oxidation of Cyclohexane Chen, Xi An, Dong-Li Zhan, Xin-Qi Zhou, Zhao-Hui Molecules Article The mixed-ligand copper(II) iminodiacetates [Cu(ida)(2-mim)(H(2)O)(2)]·H(2)O (1), [Cu(ida)(2-mim)(2)]·2H(2)O (2), [Cu(ida)(2-mim)(H(2)O)](n)·4.5nH(2)O (3), and [Cu(2)(ida)(2)(2-mim)(2)](n)·nH(2)O (4) (H(2)ida = iminodiacetic acid, 2-mim = 2-methylimidazole) were obtained from neutral or alkaline solutions at different temperatures. The novel complex 4 contains very small holes with diameters of 2.9 Å, which can adsorb O(2) selectively and reversibly between 1.89 to 29.90 bars, compared with the different gases of N(2), H(2), CO(2), and CH(4). This complex is stable up to 150 °C based on thermal analyses and XRD patterns. The four complexes show catalytic activities that facilitate the conversion of cyclohexane to cyclohexanol and cyclohexanone with hydrogen peroxide in a solution. The total conversion is 31% for 4. MDPI 2020-03-12 /pmc/articles/PMC7143979/ /pubmed/32178320 http://dx.doi.org/10.3390/molecules25061286 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Xi
An, Dong-Li
Zhan, Xin-Qi
Zhou, Zhao-Hui
2-Methylimidazole Copper Iminodiacetates for the Adsorption of Oxygen and Catalytic Oxidation of Cyclohexane
title 2-Methylimidazole Copper Iminodiacetates for the Adsorption of Oxygen and Catalytic Oxidation of Cyclohexane
title_full 2-Methylimidazole Copper Iminodiacetates for the Adsorption of Oxygen and Catalytic Oxidation of Cyclohexane
title_fullStr 2-Methylimidazole Copper Iminodiacetates for the Adsorption of Oxygen and Catalytic Oxidation of Cyclohexane
title_full_unstemmed 2-Methylimidazole Copper Iminodiacetates for the Adsorption of Oxygen and Catalytic Oxidation of Cyclohexane
title_short 2-Methylimidazole Copper Iminodiacetates for the Adsorption of Oxygen and Catalytic Oxidation of Cyclohexane
title_sort 2-methylimidazole copper iminodiacetates for the adsorption of oxygen and catalytic oxidation of cyclohexane
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7143979/
https://www.ncbi.nlm.nih.gov/pubmed/32178320
http://dx.doi.org/10.3390/molecules25061286
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