2010
DOI: 10.1063/1.3511705
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Erratum: “Observation of buried water molecules in phospholipid membranes by surface sum-frequency generation spectroscopy” [J. Chem. Phys. 131, 161107 (2009)]

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Cited by 40 publications
(44 citation statements)
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“…[38][39][40][41] Due to lipid headgroup-water electrostatics, water OH chromophores on average point upwards near negatively charged interfaces and point downwards near positively charged interfaces, resulting respectively in positive and negative SFG spectra. 20,24,42,43 The SFG spectrum for water at a zwitterionic interface is similar to the anionic case, indicating average upward orientation of OH chromophores. However, the peak height of the spectrum depends on lipid headgroup-water hydrogen bonding as well as the ionic strength of the solution.…”
Section: Introductionmentioning
confidence: 75%
“…[38][39][40][41] Due to lipid headgroup-water electrostatics, water OH chromophores on average point upwards near negatively charged interfaces and point downwards near positively charged interfaces, resulting respectively in positive and negative SFG spectra. 20,24,42,43 The SFG spectrum for water at a zwitterionic interface is similar to the anionic case, indicating average upward orientation of OH chromophores. However, the peak height of the spectrum depends on lipid headgroup-water hydrogen bonding as well as the ionic strength of the solution.…”
Section: Introductionmentioning
confidence: 75%
“…Based on our earlier experiments [54,55], we found that surfactant anions can be detected on the surface with both their C H and S O stretch modes (that have comparable SF cross-sections) from concentrations in the order of 5-10 M (on d 34 -hexadecane droplets in D 2 O as used in this study). Since the SF cross section for the C H modes is comparable to that of the O D modes [56], we may expect changes in the SF signal at comparable concentrations, i.e. from pD ∼9.…”
Section: Ph Dependence and The Origin Of The Interfacial Chargementioning
confidence: 98%
“…In such cases, polar orientation of interfacial water molecules underneath a zwitterionic lipid monolayer is difficult to determine with conventional SFVS. Sovago et al tried to do so for interfacial water under DPPC and DPPE monolayers by applying the maximum entropy analysis to the measured SF intensity spectra, and concluded that the average polar orientations of water molecules under DPPC and DPPE monolayers were the same as that under a positively charged lipid monolayer [119]. However, recent phase-sensitive SFVS measurement found that they are the same as that under a negatively charged lipid monolayer [120].…”
Section: Effect Of Adsorbed Ions At Interfacesmentioning
confidence: 99%