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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

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • 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

  • 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