Literature DB >> 29105716

Hydrogen bonds, and σ-hole and π-hole bonds - mechanisms protecting doublet and octet electron structures.

Sławomir J Grabowski1.   

Abstract

The hydrogen bond interaction and σ-hole and π-hole bonds are steered by the same mechanisms. There is electron charge transfer from the Lewis base to the Lewis acid unit, and further, for various interactions the same mechanisms try to protect the former electronic structure of the Lewis acid centre. The increase of the polarization of bonds to this centre seems to be the common effect. In the case of the A-HB hydrogen bond it is the increase of the polarization of the A-H bond connected with the outflow of the electron charge from the H-atom to the A-centre. For other interactions the outflow of electron charge from the Lewis acid centre is also observed. These electron charge shifts try to protect the doublet/octet structure of the acidic centre. The extremely strong interaction is often equivalent to the formation of new covalent bonds or it may lead to chemical reactions. Numerous interactions may be treated as the preliminary stages of chemical reactions: hydrogen bond - proton transfer, dihydrogen bond - molecular hydrogen release, tetrel bond - SN2 reaction, etc.

Entities:  

Year:  2017        PMID: 29105716     DOI: 10.1039/c7cp06393h

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  12 in total

1.  Hydrogen bonds and other interactions as a response to protect doublet/octet electron structure.

Authors:  Sławomir J Grabowski
Journal:  J Mol Model       Date:  2018-01-08       Impact factor: 1.810

2.  New Type of Halogen Bond: Multivalent Halogen Interacting with π- and σ-Electrons.

Authors:  Sławomir J Grabowski
Journal:  Molecules       Date:  2017-12-05       Impact factor: 4.411

3.  Crystallographic and Computational Characterization of Methyl Tetrel Bonding in S-Adenosylmethionine-Dependent Methyltransferases.

Authors:  Raymond C Trievel; Steve Scheiner
Journal:  Molecules       Date:  2018-11-13       Impact factor: 4.411

Review 4.  Hydrogen Bond and Other Lewis Acid-Lewis Base Interactions as Preliminary Stages of Chemical Reactions.

Authors:  Sławomir J Grabowski
Journal:  Molecules       Date:  2020-10-13       Impact factor: 4.411

5.  Molecular Hydrogen as a Lewis Base in Hydrogen Bonds and Other Interactions.

Authors:  Sławomir J Grabowski
Journal:  Molecules       Date:  2020-07-20       Impact factor: 4.411

6.  The Nature of Triel Bonds, a Case of B and Al Centres Bonded with Electron Rich Sites.

Authors:  Sławomir J Grabowski
Journal:  Molecules       Date:  2020-06-11       Impact factor: 4.411

7.  Comparative Strengths of Tetrel, Pnicogen, Chalcogen, and Halogen Bonds and Contributing Factors.

Authors:  Wenbo Dong; Qingzhong Li; Steve Scheiner
Journal:  Molecules       Date:  2018-07-10       Impact factor: 4.411

8.  Tetrel Bonds with π-Electrons Acting as Lewis Bases-Theoretical Results and Experimental Evidences.

Authors:  Sławomir J Grabowski
Journal:  Molecules       Date:  2018-05-15       Impact factor: 4.411

9.  Comparison between Tetrel Bonded Complexes Stabilized by σ and π Hole Interactions.

Authors:  Wiktor Zierkiewicz; Mariusz Michalczyk; Steve Scheiner
Journal:  Molecules       Date:  2018-06-11       Impact factor: 4.411

10.  Quantitative Assessment of Tetrel Bonding Utilizing Vibrational Spectroscopy.

Authors:  Daniel Sethio; Vytor Oliveira; Elfi Kraka
Journal:  Molecules       Date:  2018-10-25       Impact factor: 4.411

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