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A Comparative Study of the CD and CH Stretching Spectral Regions of Typical Surfactants Systems Using VSFS: Orientation Analysis of theTerminal CH3 and CD3 Groups
KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface Chemistry.
KTH, School of Chemical Science and Engineering (CHE), Chemistry, Corrosion Science.ORCID iD: 0000-0003-2100-8864
2012 (English)In: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 116, 1080-1091 p.Article in journal (Refereed) Published
Abstract [en]

A systematic comparison between the vibrational spectra in the CD and CH stretching regions of four deuterated and perprotonated surfactants adsorbed at the liquid/vapor interface has been carried out using vibrational sum frequency spectroscopy (VSFS). Bulk IR and polarized Raman spectra of hexane and its deuterated analogue have also been obtained for reference. Due to differences in the Fermi resonances, the relative positions and intensities of the spectral features, including conformational order indicators vary between the CD and CH regions. The commonly used sum frequency (SF) order indicator for perprotonated molecules, which involves the amplitude ratio of the symmetric CH3 r(+)/ symmetric CH2 d(+) bands is not directly transposable to the CD region. Instead, the ratio between the asymmetric CH3 r(-)/ antisymmetric CD2 d(-) bands is proposed as a more suitable alternative. Using as a starting point the SF spectra from the upright all-trans monolayer of dodecanol and its deuterated analogue, the theoretically modeling of the terminal methyl group orientation has been critically evaluated. The orientational analysis in the CD region gives significantly more reliable and consistent results, mainly because of the relative simplicity in unambiguously resolving the concerned peaks in the SF spectra.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2012. Vol. 116, 1080-1091 p.
National Category
Physical Chemistry Other Chemistry Topics
URN: urn:nbn:se:kth:diva-71133DOI: 10.1021/jp210013gISI: 000298978700133ScopusID: 2-s2.0-84855874458OAI: diva2:486604
Swedish Research Council
QC 20120228Available from: 2012-01-30 Created: 2012-01-30 Last updated: 2012-02-28Bibliographically approved

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Tyrode, EricHedberg, Jonas
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