Size and Origins of Long-Range Orientational Water Correlations in Dilute Aqueous Salt Solutions
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F17%3A00474220" target="_blank" >RIV/61388955:_____/17:00474220 - isvavai.cz</a>
Alternative codes found
RIV/61388963:_____/17:00474220
Result on the web
<a href="http://dx.doi.org/10.1021/acs.jpclett.7b00727" target="_blank" >http://dx.doi.org/10.1021/acs.jpclett.7b00727</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acs.jpclett.7b00727" target="_blank" >10.1021/acs.jpclett.7b00727</a>
Alternative languages
Result language
angličtina
Original language name
Size and Origins of Long-Range Orientational Water Correlations in Dilute Aqueous Salt Solutions
Original language description
Long-range ordering of water around solutes has been repeatedly invoked as the key to its biological function. Recently, it has been shown that in an 8 mM aqueous NaCl solution the orientational correlation between water molecules extends beyond 8 nm. This was interpreted as arising from ion-induced long-range effects on the water collective hydrogen-bond interactions. Each ion was suggested to affect >10 000 water molecules, leading to a picture involving nanoscopic „ordered domains“. Using molecular dynamics simulations, we show that the very small long-range tail in the correlation function is caused primarily by pairs of water molecules belonging to different ions´ hydration shells and can be made to practically disappear by rearranging the ionic positions. This means that the ion induced water orientational ordering in millimolar salt solutions cannot be separated from ion ion interaction effects, for which the Debye-Hiickel screening length shrinks to less than 1 nm at physiological ionic strengths.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10403 - Physical chemistry
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Physical Chemistry Letters
ISSN
1948-7185
e-ISSN
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Volume of the periodical
8
Issue of the periodical within the volume
9
Country of publishing house
US - UNITED STATES
Number of pages
5
Pages from-to
2031-2035
UT code for WoS article
000400885600018
EID of the result in the Scopus database
2-s2.0-85018785153