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Hydrogen Bond Networks in Binary Mixtures of Water and Organic Solvents

[Image: see text] We here present an approach for the optical in situ characterization of hydrogen bond networks (HBNs) in binary mixtures of water and organic solvents (OSs), such as methanol, ethanol, and acetonitrile. HBNs are characterized based on (i) the analysis of experimental molar Raman sp...

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Autores principales: Stehle, Simon, Braeuer, Andreas Siegfried
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539547/
https://www.ncbi.nlm.nih.gov/pubmed/31046274
http://dx.doi.org/10.1021/acs.jpcb.9b02829
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author Stehle, Simon
Braeuer, Andreas Siegfried
author_facet Stehle, Simon
Braeuer, Andreas Siegfried
author_sort Stehle, Simon
collection PubMed
description [Image: see text] We here present an approach for the optical in situ characterization of hydrogen bond networks (HBNs) in binary mixtures of water and organic solvents (OSs), such as methanol, ethanol, and acetonitrile. HBNs are characterized based on (i) the analysis of experimental molar Raman spectra of the mixture, (ii) partial molar Raman spectra of the mixture constituents, and (iii) computed ideal molar Raman spectra of the mixture. Especially, the consideration of the partial molar Raman spectra provides insights into the development of hydrogen bonds of molecules of one species with their neighbors. The obtained Raman spectra are evaluated with respect to the centroid of the symmetric stretching vibration Raman signal of water and to the hydroxyl stretching vibration of alcohols. We show the influence of composition and temperature on the development of the HBN of the mixtures, the HBN of water, and the HBN of the OS molecules.
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spelling pubmed-65395472019-05-30 Hydrogen Bond Networks in Binary Mixtures of Water and Organic Solvents Stehle, Simon Braeuer, Andreas Siegfried J Phys Chem B [Image: see text] We here present an approach for the optical in situ characterization of hydrogen bond networks (HBNs) in binary mixtures of water and organic solvents (OSs), such as methanol, ethanol, and acetonitrile. HBNs are characterized based on (i) the analysis of experimental molar Raman spectra of the mixture, (ii) partial molar Raman spectra of the mixture constituents, and (iii) computed ideal molar Raman spectra of the mixture. Especially, the consideration of the partial molar Raman spectra provides insights into the development of hydrogen bonds of molecules of one species with their neighbors. The obtained Raman spectra are evaluated with respect to the centroid of the symmetric stretching vibration Raman signal of water and to the hydroxyl stretching vibration of alcohols. We show the influence of composition and temperature on the development of the HBN of the mixtures, the HBN of water, and the HBN of the OS molecules. American Chemical Society 2019-05-02 2019-05-23 /pmc/articles/PMC6539547/ /pubmed/31046274 http://dx.doi.org/10.1021/acs.jpcb.9b02829 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Stehle, Simon
Braeuer, Andreas Siegfried
Hydrogen Bond Networks in Binary Mixtures of Water and Organic Solvents
title Hydrogen Bond Networks in Binary Mixtures of Water and Organic Solvents
title_full Hydrogen Bond Networks in Binary Mixtures of Water and Organic Solvents
title_fullStr Hydrogen Bond Networks in Binary Mixtures of Water and Organic Solvents
title_full_unstemmed Hydrogen Bond Networks in Binary Mixtures of Water and Organic Solvents
title_short Hydrogen Bond Networks in Binary Mixtures of Water and Organic Solvents
title_sort hydrogen bond networks in binary mixtures of water and organic solvents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539547/
https://www.ncbi.nlm.nih.gov/pubmed/31046274
http://dx.doi.org/10.1021/acs.jpcb.9b02829
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