A Spectroscopic Overview of Intramolecular Hydrogen Bonds of NH…O,S,N Type

Hansen, Poul Erik

doi:10.3390/molecules26092409

Cited by 27 publications

(11 citation statements)

References 108 publications

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“…The dependences of 1 H and 13 C chemical shifts on hydrogen bonding have been extensively studied. They agree with dependences obtained for other experimental and empirical parameters [ 18 , 19 , 20 , 21 , 22 ]. More about the application of these and other correlations can be found elsewhere [ 23 , 24 , 25 , 26 ].…”

Section: Introductionsupporting

confidence: 89%

Modeling of the Response of Hydrogen Bond Properties on an External Electric Field: Geometry, NMR Chemical Shift, Spin-Spin Scalar Coupling

Shenderovich

Denisov

2021

Molecules

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The response of the geometric and NMR properties of molecular systems to an external electric field has been studied theoretically in a wide field range. It has been shown that this adduct under field approach can be used to model the geometric and spectral changes experienced by molecular systems in polar media if the system in question has one and only one bond, the polarizability of which significantly exceeds the polarizability of other bonds. If this requirement is met, then it becomes possible to model even extreme cases, for example, proton dissociation in hydrogen halides. This requirement is fulfilled for many complexes with one hydrogen bond. For such complexes, this approach can be used to facilitate a detailed analysis of spectral changes associated with geometric changes in the hydrogen bond. For example, in hydrogen-bonded complexes of isocyanide C≡15N-1H⋯X, 1J(15N1H) depends exclusively on the N-H distance, while δ(15N) is also slightly influenced by the nature of X.

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Section: Introductionsupporting

confidence: 89%

Modeling of the Response of Hydrogen Bond Properties on an External Electric Field: Geometry, NMR Chemical Shift, Spin-Spin Scalar Coupling

Shenderovich

Denisov

2021

Molecules

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“…It is well known that hydrogen-bonded linkages play major roles in a variety of areas in chemistry and molecular biology, and the investigation of such linkages by spectroscopic procedures is a subject of current interest [1]. Historically, IR absorption spectroscopy has been the most important spectroscopic tool in the investigation of hydrogen-bonded systems, typically involving OH•••O and NH•••O linkages [2][3][4].…”

Section: Introductionmentioning

confidence: 99%

NH Stretching Frequencies of Intramolecularly Hydrogen-Bonded Systems: An Experimental and Theoretical Study

et al. 2021

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The vibrational NH stretching transitions in secondary amines with intramolecular NH···O hydrogen bonds were investigated by experimental and theoretical methods, considering a large number of compounds and covering a wide range of stretching wavenumbers. The assignment of the NH stretching transitions in the experimental IR spectra was, in several instances, supported by measurement of the corresponding ND wavenumbers and by correlation with the observed NH proton chemical shifts. The observed wavenumbers were correlated with theoretical wavenumbers predicted with B3LYP density functional theory, using the basis sets 6-311++G(d,p) and 6-31G(d) and considering the harmonic as well as the anharmonic VPT2 approximation. Excellent correlations were established between observed wavenumbers and calculated harmonic values. However, the correlations were non-linear, in contrast to the results of previous investigations of the corresponding OH···O systems. The anharmonic VPT2 wavenumbers were found to be linearly related to the corresponding harmonic values. The results provide correlation equations for the prediction of NH stretching bands on the basis of standard B3LYP/6-311++G(d,p) and B3LYP/6-31G(d) harmonic analyses, with standard deviations close to 38 cm−1. This is significant because the full anharmonic VPT2 analysis tends to be impractical for large molecules, requiring orders of magnitude more computing time than the harmonic analysis.

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“…Hydrogen bond energies and the less well-defined hydrogen bond strength is clearly very important for molecular properties [65]. One way of getting a qualitative idea is the monitor isotope effects in solvents of different polarity.…”

Section: Hydrogen Bond Energymentioning

confidence: 99%

Isotope Effects on Chemical Shifts in the Study of Hydrogen Bonds in Small Molecules

Hansen

2022

Molecules

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This review is giving a short introduction to the techniques used to investigate isotope effects on NMR chemical shifts. The review is discussing how isotope effects on chemical shifts can be used to elucidate the importance of either intra- or intermolecular hydrogen bonding in ionic liquids, of ammonium ions in a confined space, how isotope effects can help define dimers, trimers, etc., how isotope effects can lead to structural parameters such as distances and give information about ion pairing. Tautomerism is by advantage investigated by isotope effects on chemical shifts both in symmetric and asymmetric systems. The relationship between hydrogen bond energies and two-bond deuterium isotope effects on chemical shifts is described. Finally, theoretical calculations to obtain isotope effects on chemical shifts are looked into.

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A Spectroscopic Overview of Intramolecular Hydrogen Bonds of NH…O,S,N Type

Cited by 27 publications

References 108 publications

Modeling of the Response of Hydrogen Bond Properties on an External Electric Field: Geometry, NMR Chemical Shift, Spin-Spin Scalar Coupling

Modeling of the Response of Hydrogen Bond Properties on an External Electric Field: Geometry, NMR Chemical Shift, Spin-Spin Scalar Coupling

NH Stretching Frequencies of Intramolecularly Hydrogen-Bonded Systems: An Experimental and Theoretical Study

Isotope Effects on Chemical Shifts in the Study of Hydrogen Bonds in Small Molecules

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