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Special Issue: Intramolecular Hydrogen Bonding 2017
 
 
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Correction to Molecules 2017, 22(3), 423.
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Correction

Correction: Mishra, S.K. and Suryaprakash, N. Intramolecular Hydrogen Bonding Involving Organic Fluorine: NMR Investigations Corroborated by DFT-Based Theoretical Calculations: Molecules 2017, 22, 423

by
Sandeep Kumar Mishra
and
N. Suryaprakash
*
NMR Research Centre, Solid State and Structural Chemistry Unit, Indian Institute of Science, Bangalore 560012, India
*
Author to whom correspondence should be addressed.
Molecules 2019, 24(10), 2000; https://doi.org/10.3390/molecules24102000
Submission received: 14 March 2019 / Accepted: 23 April 2019 / Published: 24 May 2019
(This article belongs to the Special Issue Intramolecular Hydrogen Bonding 2017)
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Versions Notes
The authors wish to make the following corrections to their paper [1]. The authors regret that in the above-mentioned paper, Figure 2 and the associated text were adapted without attribution from “Molecular Interactions (Noncovalent Interactions) and the Behaviors of Biological Macromolecules” by Loren Dean Williams [2]. The authors sincerely thank Prof. Loren Dean Williams for bringing this to our attention.

References

  1. Mishra, S.K.; Suryaprakash, N. Intramolecular Hydrogen Bonding Involving Organic Fluorine: NMR Investigations Corroborated by DFT-Based Theoretical Calculations. Molecules 2017, 22, 423. [Google Scholar] [CrossRef] [PubMed]
  2. Williams, L.D. Molecular Interactions (Noncovalent Interactions) and the Behaviors of Biological Macromolecules. Available online: http://ww2.chemistry.gatech.edu/~lw26/structure/molecular_interactions/mol_int.html (accessed on 26 February 2019).
Molecules 24 02000 g001 550
Figure 2. The pictorial illustration of hydrogen bond interaction, where HB acceptor/donor can be an F, O, N, or S atom in the molecule. Electron polarization and exposure of a positive proton on either side are shown schematically.
Figure 2. The pictorial illustration of hydrogen bond interaction, where HB acceptor/donor can be an F, O, N, or S atom in the molecule. Electron polarization and exposure of a positive proton on either side are shown schematically.
Molecules 24 02000 g001

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MDPI and ACS Style

Mishra, S.K.; Suryaprakash, N. Correction: Mishra, S.K. and Suryaprakash, N. Intramolecular Hydrogen Bonding Involving Organic Fluorine: NMR Investigations Corroborated by DFT-Based Theoretical Calculations: Molecules 2017, 22, 423. Molecules 2019, 24, 2000. https://doi.org/10.3390/molecules24102000

AMA Style

Mishra SK, Suryaprakash N. Correction: Mishra, S.K. and Suryaprakash, N. Intramolecular Hydrogen Bonding Involving Organic Fluorine: NMR Investigations Corroborated by DFT-Based Theoretical Calculations: Molecules 2017, 22, 423. Molecules. 2019; 24(10):2000. https://doi.org/10.3390/molecules24102000

Chicago/Turabian Style

Mishra, Sandeep Kumar, and N. Suryaprakash. 2019. "Correction: Mishra, S.K. and Suryaprakash, N. Intramolecular Hydrogen Bonding Involving Organic Fluorine: NMR Investigations Corroborated by DFT-Based Theoretical Calculations: Molecules 2017, 22, 423" Molecules 24, no. 10: 2000. https://doi.org/10.3390/molecules24102000

APA Style

Mishra, S. K., & Suryaprakash, N. (2019). Correction: Mishra, S.K. and Suryaprakash, N. Intramolecular Hydrogen Bonding Involving Organic Fluorine: NMR Investigations Corroborated by DFT-Based Theoretical Calculations: Molecules 2017, 22, 423. Molecules, 24(10), 2000. https://doi.org/10.3390/molecules24102000

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