Through space J FH spin–spin coupling constant transmission pathways in 2-(trifluoromethyl)thiophenol: formation of unusual stabilizing bifurcated CF⋯HS and CF⋯SH interactions
Given its importance and the possibility of organic F to participate in hydrogen bonds (H-bonds), the understanding of its behavior as a H-bond acceptor with different donors is crucial. The interest in organofluorine compounds and the works related to the study of the participation of this atom in...
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Published in | Physical chemistry chemical physics : PCCP Vol. 23; no. 15; pp. 9080 - 9088 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
22.04.2021
|
Online Access | Get full text |
ISSN | 1463-9076 1463-9084 |
DOI | 10.1039/D0CP05887D |
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Summary: | Given its importance and the possibility of organic F to participate in hydrogen bonds (H-bonds), the understanding of its behavior as a H-bond acceptor with different donors is crucial. The interest in organofluorine compounds and the works related to the study of the participation of this atom in non-covalent interactions is constantly growing. Following recent studies in this subject, we evaluated the existence of two bifurcated intramolecular interactions, a bifurcated CF⋯HS H-bond in the
cis
conformer of 2-trifluoromethylthiophenol and an unusual, bifurcated CF⋯SH interaction in the
trans
conformer. The
J
FH
spin–spin coupling constant (SSCC) was evaluated for 2-trifluoromethylthiophenol both experimentally by
1
H and
19
F NMR and theoretically using the natural bond orbitals (NBO), the quantum theory of atoms in molecules (QTAIM) and the non-covalent interactions (NCI) framework. Although both interactions are crucial for the stabilization of the conformer geometries, the observed positive
J
FH
spin–spin coupling constant (SSCC) is mainly resultant from the
trans
conformer, which has a large calculated positive SSCC, and is transmitted through steric interactions involving the F lone pairs and the σ
SH
bonding orbital. |
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ISSN: | 1463-9076 1463-9084 |
DOI: | 10.1039/D0CP05887D |