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  • 1
    In: Physical Chemistry Chemical Physics, Royal Society of Chemistry (RSC), Vol. 25, No. 33 ( 2023), p. 22089-22102
    Abstract: Vibrational spectroscopy in supersonic jet expansions is a powerful tool to assess molecular aggregates in close to ideal conditions for the benchmarking of quantum chemical approaches. The low temperatures achieved as well as the absence of environment effects allow for a direct comparison between computed and experimental spectra. This provides potential benchmarking data which can be revisited to hone different computational techniques, and it allows for the critical analysis of procedures under the setting of a blind challenge. In the latter case, the final result is unknown to modellers, providing an unbiased testing opportunity for quantum chemical models. In this work, we present the spectroscopic and computational results for the first HyDRA blind challenge. The latter deals with the prediction of water donor stretching vibrations in monohydrates of organic molecules. This edition features a test set of 10 systems. Experimental water donor OH vibrational wavenumbers for the vacuum-isolated monohydrates of formaldehyde, tetrahydrofuran, pyridine, tetrahydrothiophene, trifluoroethanol, methyl lactate, dimethylimidazolidinone, cyclooctanone, trifluoroacetophenone and 1-phenylcyclohexane- cis -1,2-diol are provided. The results of the challenge show promising predictive properties in both purely quantum mechanical approaches as well as regression and other machine learning strategies.
    Type of Medium: Online Resource
    ISSN: 1463-9076 , 1463-9084
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 1476283-3
    detail.hit.zdb_id: 1476244-4
    detail.hit.zdb_id: 1460656-2
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2022
    In:  Physical Chemistry Chemical Physics Vol. 24, No. 43 ( 2022), p. 26449-26457
    In: Physical Chemistry Chemical Physics, Royal Society of Chemistry (RSC), Vol. 24, No. 43 ( 2022), p. 26449-26457
    Abstract: When formic acid and 2,2,2-trifluoroethanol are co-expanded through a slit nozzle into vacuum, a single dominant, hinge-like 1 : 1 complex is formed in significant amounts and its two OH stretching fundamentals separated by 100 cm −1 can be unambiguously assigned by a combination of infrared absorption and Raman scattering. Quantum chemical calculations at different levels reproduce this finding in a satisfactory way and suggest that in-phase (Raman-sensitive and lower wavenumber) OH stretch excitation more or less along the concerted degenerate proton transfer coordinate in the hydrogen-bonded ring stays below the barrier for this concerted exchange. Anharmonic calculations indicate only weak intensity sharing with dark states coming into reach due to the hydrogen bond downshift of the OH stretching vibration. This well-behaved system sets the stage for acid combinations with more basic alcohols, where the in-phase OH stretching vibration is more difficult to detect, possibly due to fast intra-complex vibrational dynamics. It thus provides a benchmark point from which one can explore the evolution of vibrational resonances when the acidic proton meets a more electron-rich alcoholic oxygen.
    Type of Medium: Online Resource
    ISSN: 1463-9076 , 1463-9084
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 1476283-3
    detail.hit.zdb_id: 1476244-4
    detail.hit.zdb_id: 1460656-2
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
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