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Role of water in complexation of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6) with Li(+) and K(+) in hydrophobic 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ionic liquid

Complexation characteristics of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6, 18C6) with Li(+) and K(+) in a hydrophobic ionic liquid of 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide under dry and humid conditions at 298.2 K were studied by (1)H and (13)C NMR chemical shifts. T...

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Autores principales: Umecky, Tatsuya, Takamuku, Toshiyuki, Kanzaki, Ryo, Takagi, Masaya, Kawai, Eiji, Matsumoto, Tomoya, Funazukuri, Toshitaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190452/
https://www.ncbi.nlm.nih.gov/pubmed/25328427
http://dx.doi.org/10.1007/s10847-014-0427-1
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author Umecky, Tatsuya
Takamuku, Toshiyuki
Kanzaki, Ryo
Takagi, Masaya
Kawai, Eiji
Matsumoto, Tomoya
Funazukuri, Toshitaka
author_facet Umecky, Tatsuya
Takamuku, Toshiyuki
Kanzaki, Ryo
Takagi, Masaya
Kawai, Eiji
Matsumoto, Tomoya
Funazukuri, Toshitaka
author_sort Umecky, Tatsuya
collection PubMed
description Complexation characteristics of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6, 18C6) with Li(+) and K(+) in a hydrophobic ionic liquid of 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide under dry and humid conditions at 298.2 K were studied by (1)H and (13)C NMR chemical shifts. The comparison of the (1)H and (13)C chemical shifts of 18C6 molecule between the dry and humid IL solutions without the alkali metal ions showed that uncomplexed 18C6 molecules are solvated by water molecules in the humid ionic liquid solution. The changes in the (1)H and (13)C chemical shifts of 18C6 ligand molecule with the increases in the Li(+) and K(+) concentrations revealed that in both dry and humid ionic liquid solutions 18C6 molecule forms 1:1 complexes with Li(+) and K(+). The (1)H NMR data of water molecules in the humid ionic liquid solutions demonstrated that water molecules interact with Li(+)-18C6 complexes and free Li(+), but do not with K(+)-18C6 complexes and free K(+). The mechanisms of the formation of the Li(+) and K(+) complexes in the humid ionic liquid solution are different from each other due to the differences in the complex-water interactions.
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spelling pubmed-41904522014-10-15 Role of water in complexation of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6) with Li(+) and K(+) in hydrophobic 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ionic liquid Umecky, Tatsuya Takamuku, Toshiyuki Kanzaki, Ryo Takagi, Masaya Kawai, Eiji Matsumoto, Tomoya Funazukuri, Toshitaka J Incl Phenom Macrocycl Chem Original Article Complexation characteristics of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6, 18C6) with Li(+) and K(+) in a hydrophobic ionic liquid of 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide under dry and humid conditions at 298.2 K were studied by (1)H and (13)C NMR chemical shifts. The comparison of the (1)H and (13)C chemical shifts of 18C6 molecule between the dry and humid IL solutions without the alkali metal ions showed that uncomplexed 18C6 molecules are solvated by water molecules in the humid ionic liquid solution. The changes in the (1)H and (13)C chemical shifts of 18C6 ligand molecule with the increases in the Li(+) and K(+) concentrations revealed that in both dry and humid ionic liquid solutions 18C6 molecule forms 1:1 complexes with Li(+) and K(+). The (1)H NMR data of water molecules in the humid ionic liquid solutions demonstrated that water molecules interact with Li(+)-18C6 complexes and free Li(+), but do not with K(+)-18C6 complexes and free K(+). The mechanisms of the formation of the Li(+) and K(+) complexes in the humid ionic liquid solution are different from each other due to the differences in the complex-water interactions. Springer Netherlands 2014-06-10 2014 /pmc/articles/PMC4190452/ /pubmed/25328427 http://dx.doi.org/10.1007/s10847-014-0427-1 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Umecky, Tatsuya
Takamuku, Toshiyuki
Kanzaki, Ryo
Takagi, Masaya
Kawai, Eiji
Matsumoto, Tomoya
Funazukuri, Toshitaka
Role of water in complexation of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6) with Li(+) and K(+) in hydrophobic 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ionic liquid
title Role of water in complexation of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6) with Li(+) and K(+) in hydrophobic 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ionic liquid
title_full Role of water in complexation of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6) with Li(+) and K(+) in hydrophobic 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ionic liquid
title_fullStr Role of water in complexation of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6) with Li(+) and K(+) in hydrophobic 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ionic liquid
title_full_unstemmed Role of water in complexation of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6) with Li(+) and K(+) in hydrophobic 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ionic liquid
title_short Role of water in complexation of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6) with Li(+) and K(+) in hydrophobic 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ionic liquid
title_sort role of water in complexation of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6) with li(+) and k(+) in hydrophobic 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ionic liquid
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190452/
https://www.ncbi.nlm.nih.gov/pubmed/25328427
http://dx.doi.org/10.1007/s10847-014-0427-1
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