2016
DOI: 10.1039/c6cp03857c
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Local, solvation pressures and conformational changes in ethylenediamine aqueous solutions probed using Raman spectroscopy

Abstract: Raman spectra of 1,2-ethylenediamine (EDA) in aqueous solutions are used to demonstrate that EDA molecules experience an anti-gauche conformational change resulting from the interactions with water. The observed Raman shift reveals a compressive (hydrophobic) effect of water on both methylene and amino groups of EDA. Raman spectra of EDA at high pressures are used as reference to quantify the intermolecular EDA-HO interactions in terms of local pressures. These results are compared with macroscopic solvation p… Show more

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Cited by 8 publications
(3 citation statements)
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References 26 publications
(24 reference statements)
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“…Since this increase in gauche conformers was found to be pressure-independent, we can conclude that water molecules do not play a significant role in the molecular arrangement of the alkane chains in the bulk. Similar studies on ethylenediamine 69 as well as on dimethoxyethane and dimethoxymethane 70 have shown an opposite effect. By applying Raman spectroscopy, both Caćeres et al 69 and Wada et al 70 revealed an increase of gauche conformers by increasing the water concentration.…”
Section: ■ Introductionmentioning
confidence: 57%
See 1 more Smart Citation
“…Since this increase in gauche conformers was found to be pressure-independent, we can conclude that water molecules do not play a significant role in the molecular arrangement of the alkane chains in the bulk. Similar studies on ethylenediamine 69 as well as on dimethoxyethane and dimethoxymethane 70 have shown an opposite effect. By applying Raman spectroscopy, both Caćeres et al 69 and Wada et al 70 revealed an increase of gauche conformers by increasing the water concentration.…”
Section: ■ Introductionmentioning
confidence: 57%
“…Similar studies on ethylenediamine 69 as well as on dimethoxyethane and dimethoxymethane 70 have shown an opposite effect. By applying Raman spectroscopy, both Caćeres et al 69 and Wada et al 70 revealed an increase of gauche conformers by increasing the water concentration. The absent influence of water molecules on the observed alkane−alkane contacts can be explained by the water spreading in the alkane-rich liquid phase during the solvation process combined with its low solubility, 30 which hinders the formation of hydrogen bonds.…”
Section: ■ Introductionmentioning
confidence: 57%
“…[ 29 ] Furthermore, we previously demonstrated that the extent of these molecular interactions can be quantified in terms of local pressure by using Raman spectra of a given molecule at high pressure as a reference. [ 30,31 ]…”
Section: Resultsmentioning
confidence: 99%