Literature DB >> 22095853

1hJFH coupling in 2-fluorophenol revisited: is intramolecular hydrogen bond responsible for this long-range coupling?

Rodrigo A Cormanich1, Marilua A Moreira, Matheus P Freitas, Teodorico C Ramalho, Cléber P A Anconi, Roberto Rittner, Rubén H Contreras, Cláudio F Tormena.   

Abstract

The present study shows that a hydrogen bond between the OH group and the fluorine atom is not involved in the (1h)J(FH) spin-spin coupling transmission either for 4-bromo-2-fluorophenol or 2-fluorophenol. In fact, according to a quantum theory of atoms in molecules analysis, no bond critical point is found between O-H and F moieties. The nature of the transmission mechanism of the Fermi contact term of the (1h)J(FH) spin-spin coupling is studied by analyzing canonical molecular orbitals (see J. Phys. Chem. A 2010, 114, 1044), and it is observed that virtual orbitals play only a quite minor role in its transmission. This is typical of a Fermi contact term transmitted mainly through exchange interactions owing to the overlap of proximate electronic clouds; therefore, it is suggested to identify them as (nTS)J(FH) coupling where n stands for the number of formal bonds separating the coupling nuclei. In the cases studied in this work is n = 4. Results presented in this work could provide an interesting rationalization for different experimental signs known in the current literature for proximate J(FH) couplings.
Copyright © 2011 John Wiley & Sons, Ltd.

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Year:  2011        PMID: 22095853     DOI: 10.1002/mrc.2838

Source DB:  PubMed          Journal:  Magn Reson Chem        ISSN: 0749-1581            Impact factor:   2.447


  5 in total

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Authors:  Fátima M P de Rezende; Marilua A Moreira; Rodrigo A Cormanich; Matheus P Freitas
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2.  QSAR Study of N-Myristoyltransferase Inhibitors of Antimalarial Agents.

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Journal:  Molecules       Date:  2018-09-13       Impact factor: 4.411

3.  Retention of strong intramolecular hydrogen bonds in high polarity solvents in binaphthalene-benzamide derivatives: extensive NMR studies.

Authors:  Arun Kumar Patel; Sandeep Kumar Mishra; Kiran Krishnamurthy; N Suryaprakash
Journal:  RSC Adv       Date:  2019-10-14       Impact factor: 4.036

4.  An unexpected and significantly lower hydrogen-bond-donating capacity of fluorohydrins compared to nonfluorinated alcohols.

Authors:  Jérôme Graton; Zhong Wang; Anne-Marie Brossard; Daniela Gonçalves Monteiro; Jean-Yves Le Questel; Bruno Linclau
Journal:  Angew Chem Int Ed Engl       Date:  2012-05-10       Impact factor: 15.336

5.  Conformational analysis and intramolecular interactions in monosubstituted phenylboranes and phenylboronic acids.

Authors:  Josué M Silla; Rodrigo A Cormanich; Roberto Rittner; Matheus P Freitas
Journal:  Beilstein J Org Chem       Date:  2013-06-11       Impact factor: 2.883

  5 in total

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