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• W2894402857 abstract "Abstract Despite fundamental importance, the experimental characterization of the hydrogen bond network, particularly in multicomponent protic solutions, remains a challenge. Although recent work has experimentally validated that the oxygen K‐edge X‐ray absorption spectra is sensitive to local hydrogen bond patterns in pure water and aqueous alcohol solutions, the generality of this observation is unknown—as is the sensitivity to the electronic structure of the alcohol cosolvent. In this work, we investigate the electronic structure of water solvated alcohol model geometries using energy specific time‐dependent density functional theory to calculate oxygen K‐edge X‐ray excitations. We find that the geometry of dangling hydrogen bonds in pure water is the main contributor to the pre‐edge feature seen in the X‐ray absorption spectra, agreeing with previous experimental and theoretical work. We then extend this result to solvated alcohol systems and observe a similar phenomenon, yet importantly, the increase of electron donation from alkyl chains to the alcohol OH group directly correlates to the strength of the core excitation on the dangling hydrogen bond model geometry. This trend arises from a stronger transition dipole moment due to electron localization on the OH group." @default.
• W2894402857 created "2018-10-05" @default.
• W2894402857 creator A5043778112 @default.
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• W2894402857 date "2018-09-22" @default.
• W2894402857 modified "2023-10-14" @default.
• W2894402857 title "X‐ray absorption signatures of hydrogen‐bond structure in water–alcohol solutions" @default.
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• W2894402857 doi "https://doi.org/10.1002/qua.25802" @default.
• W2894402857 hasPublicationYear "2018" @default.
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