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Behavior of Ylides Containing N, O, and C Atoms as Hydrogen Bond Acceptors
Abstract
The hydrogen bond (HB) basicity of a series of ylides containing nitrogen, oxygen, or carbon as heavy atoms, as well as the influence of the formation of the HB complexes on their structure, has been studied. In addition, in this paper we propose the formation of some rather strong HBs (that could be considered low-barrier hydrogen bonds, LBHBs) between ylides and different neutral molecules. The ylides chosen for the study were H 3 N + −N - H, Me 3 N + −N - H, H 2 O + −N - H, Me 2 O + −N - H, H 2 O + −O -, Me 2 O + −O -, and Me 3 N + −C - H 2 . As HB donors, classical donors such as HF, HCN, and HCCH were used. The analysis of the protonation energies of the ylides and the optimized geometries, interaction energies, and characteristics of the electron density of the complexes shows that these ylides are very good HB acceptors, forming stable complexes even with weak HB donors. With strong donors, when the proton transfer did not take place, very strong HBs were formed with quite large interaction energies and very short HB distances which could be considered as LBHBs. Moreover, we have found that the sign of the Laplacian of the electron density at the bond critical point (∇ 2 ρ BCP ) and that of the energy density ( H BCP ) could characterize the strength of HBs. Thus, weak HBs ( E I < 12.0 kcal/mol) show both ∇ 2 ρ BCP and H BCP > 0, and medium HBs (12.0 < E I < 24.0 kcal/mol) show ∇ 2 ρ BCP > 0 and H BCP < 0, while strong HBs (and therefore LBHBs; E I > 24.0 kcal/mol) show both ∇ 2 ρ BCP and H BCP < 0.
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What Is the Covalency of Hydrogen Bonding?
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Metadata
- Authors
- Rozas, I., Alkorta, I., & Elguero, J.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2000-11-01
- Volume
- 122
- Issue
- 45
- Pages
- 11154-11161
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2089962804
- Cited by
- 1,732
- References
- 13
- FWCI
- 1.78
- Type
- journal article
- Language
- en
- Open access
- closed
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