In theoretical chemistry, the charge-shift bond is a proposed new class of chemical bonds that sits alongside the three familiar families of covalent, ionic, and metallic bonds where electrons are shared or transferred respectively.[1][2] The charge shift bond derives its stability from the resonance of ionic forms rather than the covalent sharing of electrons which are often depicted as having electron density between the bonded atoms. A feature of the charge shift bond is that the predicted electron density between the bonded atoms is low. It has long been known from experiment that the accumulation of electric charge between the bonded atoms is not necessarily a feature of covalent bonds.[3]

An example where charge shift bonding has been used to explain the low electron density found experimentally is in the central bond between the inverted tetrahedral carbon atoms in [1.1.1]propellanes. Theoretical calculations on a range of molecules have indicated that a charge shift bond is present, a striking example being fluorine, F2, which is normally described as having a typical covalent bond.[2] The charge shift bond (CSB) has also been shown to exist at the cation-anion interface of protic ionic liquids (PILs).[4] The authors have also shown how CSB character in PILs correlates with their physicochemical properties.

Valence bond description

The valence bond view of chemical bonding that owes much to the work of Pauling is familiar to many, if not all, chemists. The basis of Pauling's description of the chemical bond is that an electron pair bond involves the mixing, resonance, of one covalent and two ionic structures. In bonds between two atoms of the same element, homonuclear bonds, Pauling assumed that the ionic structures make no appreciable contribution to the overall bonding. This assumption followed on from published calculations for the hydrogen molecule in 1933 by Weinbaum and by James and Coolidge[5] that showed that the contribution of ionic forms amounted to only a small percentage of the H−H bond energy. For heteronuclear bonds, A−X, Pauling estimated the covalent contribution to the bond dissociation energy as being the mean of the bond dissociation energies of homonuclear A−A and X−X bonds. The difference between the mean and the observed bond energy was assumed to be due to the ionic contribution. The calculation for HCl is shown below.[5]

Actual H−H Actual Cl−Cl H−Clcov Covalent bond energy H−Cl,
arithmetic mean (H−H) and (Cl−Cl)		 H−Clact
Actual H−Cl		 "Ionic contribution"
H−Clact – H−Clcov
Bond dissociation energy(kcal mol−1) 103.5 57.8 80.6 102.7 22.1

The ionic contribution to the overall bond dissociation energy was attributed to the difference in electronegativity between the A and X, and these differences were the starting point for Pauling's calculation of the individual electronegativities of the elements. The proponents of charge shift bond bonding re−examined the validity of Pauling's assumption that ionic forms make no appreciable contribution to the overall bond dissociation energies of homonuclear bonds. What they found using modern valence bond methods was that in some cases the contribution of ionic forms was significant, the most striking example being F2, fluorine, where their calculations indicate that the bond energy of the F−F bond is due wholly to the ionic contribution.[2]

Calculated bond energies

The contribution of ionic resonance structures has been termed the charge−shift resonance energy, REcs, and values have been calculated for a number of single bonds, some of which are shown below:[2]

Covalent contribution
kcal mol−1		 REcs
kcal mol−1		 % REcs
contribution
H−H 95.8 9.2 8.8
Li−Li 18.2 2.8 13.1
H3C−CH3 63.9 27.2 30.2
H2N−NH2 22.8 43.8 65.7
HO−OH –7.1 56.9 114.3
F−F –28.4 62.2 183.9
Cl−Cl –9.4 48.7 124.1
H−F 33.2 90.8 73.2
H−Cl 57.1 34.9 37.9
H3C−Cl 34.0 45.9 57.4
H3Si−Cl 37.0 65.1 63.8

The results show that for homonuclear bonds the charge shift resonance energy can be significant, and for F2 and Cl2 show it is the attractive component whereas the covalent contribution is repulsive. The reduced density along the bond axis density is apparent using ELF, electron localization function, a tool for determining electron density.[2][6]

The bridge bond in a propellane

The bridge bond (inverted bond between the bridgehead atoms which is common to the three cycles) in a substituted [1.1.1]propellane has been examined experimentally.[7] A theoretical study on [1.1.1]propellane has shown that it has a significant REcs stabilisation energy.[8]

Factors causing charge shift bonding

Analysis of a number of compounds where charge shift resonance energy is significant shows that in many cases elements with high electronegativities are involved and these have smaller orbitals and are lone pair rich. Factors that reduce the covalent contribution to the bond energy include poor overlap of bonding orbitals, and the lone pair bond weakening effect where repulsion due to the Pauli exclusion principle is the main factor.[2] There is no correlation between the charge−shift resonance energy REcs and the difference between the electronegativities of the bonded atoms as might be expected from the Pauling bonding model, however there is a global correlation between REcs and the sum of their electronegativities which can be accounted for in part by the lone pair bond weakening effect.[2] The charge-shift nature of the inverted bond in [1.1.1]propellanes has been ascribed to the Pauli repulsion due to the adjacent "wing" bonds destabilising of the covalent contribution.

Experimental evidence for charge-shift bonds

The interpretation of experimentally determined electron density in molecules often uses AIM theory. In this the electron density between the atomic nuclei along the bond path are calculated, and the bond critical point where the density is at a minimum is determined. The factors that determine the type of chemical bond are the Laplacian and the electron density at the bond critical point. At the bond critical point a typical covalent bond has significant density and a large negative Laplacian. In contrast a "closed shell" interaction as in an ionic bond has a small electron density and a positive Laplacian.[2] A charge shift bond is expected to have a positive or small Laplacian. Only a limited number of experimental determinations have been made, compounds with bonds with a positive Laplacian are the N–N bond in solid N2O4,[9][10] and the (Mg−Mg)2+ diatomic structure.[11][disputed – discuss]

References

  1. ^ Sini, Gjergji; Maitre, Philippe; Hiberty, Philippe C.; Shaik, Sason S. (1991). "Covalent, ionic and resonating single bonds". Journal of Molecular Structure: THEOCHEM. 229: 163–188. doi:10.1016/0166-1280(91)90144-9. ISSN 0166-1280.
  2. ^ a b c d e f g h Shaik, Sason; Danovitch, David; Wei, Wu & Hiberty, Phillippe.C. (2014) [1st. Pub. 2014]. "Chapter 5: The Valence Bond Perspective of the Chemical Bond". In Frenking, Gernod & Shaik, Sason (eds.). The Chemical Bond. Wiley-VCH.
  3. ^ Dunitz, Jack D.; Seiler, Paul (1983). "The absence of bonding electron density in certain covalent bonds as revealed by x-ray analysis". Journal of the American Chemical Society. 105 (24): 7056–7058. doi:10.1021/ja00362a007. ISSN 0002-7863.
  4. ^ Patil, Amol Baliram; Bhanage, Bhalchandra Mahadeo (2016). "Modern ab initio valence bond theory calculations reveal charge shift bonding in protic ionic liquids". Physical Chemistry Chemical Physics. 18: 15783–15790. doi:10.1039/C6CP02819E.
  5. ^ a b The Nature of the Chemical bond, L. Pauling, 1940, 2d edition, pp. 49−59, Oxford University Press
  6. ^ Shaik, Sason; Danovich, David; Silvi, Bernard; Lauvergnat, David L.; Hiberty, Philippe C. (2005). "Charge−Shift Bonding—A Class of Electron-Pair Bonds That Emerges from Valence Bond Theory and Is Supported by the Electron Localization Function Approach". Chemistry: A European Journal. 11 (21): 6358–6371. doi:10.1002/chem.200500265. ISSN 0947-6539. PMID 16086335.
  7. ^ Messerschmidt, Marc; Scheins, Stephan; Grubert, Lutz; Pätzel, Michael; Szeimies, Günter; Paulmann, Carsten; Luger, Peter (2005). "Electron Density and Bonding at Inverted Carbon Atoms: An Experimental Study of a [1.1.1]Propellane Derivative". Angewandte Chemie International Edition. 44 (25): 3925–3928. doi:10.1002/anie.200500169. ISSN 1433-7851.
  8. ^ Shaik, Sason; Danovich, David; Wu, Wei; Hiberty, Philippe C. (2009). "Charge-shift bonding and its manifestations in chemistry". Nature Chemistry. 1 (6): 443–449. Bibcode:2009NatCh...1..443S. doi:10.1038/nchem.327. ISSN 1755-4330.
  9. ^ Messerschmidt, Marc; Wagner, Armin; Wong, Ming Wah; Luger, Peter (2002). "Atomic Properties of N2O4 Based on Its Experimental Charge Density". Journal of the American Chemical Society. 124 (5): 732–733. doi:10.1021/ja011802c. ISSN 0002-7863.
  10. ^ Tsirelson, Vladimir G.; Shishkina, Anastasia V.; Stash, Adam I.; Parsons, Simon (2009). "The experimental and theoretical QTAIMC study of the atomic and molecular interactions in dinitrogen tetroxide" (PDF). Acta Crystallographica Section B. 65 (5): 647–658. doi:10.1107/S0108768109028821. hdl:20.500.11820/5fa0a31e-7a10-466e-a0f3-239f685217e6. ISSN 0108-7681.
  11. ^ Platts, James A.; Overgaard, Jacob; Jones, Cameron; Iversen, Bo B.; Stasch, Andreas (2011). "First Experimental Characterization of a Non-nuclear Attractor in a Dimeric Magnesium(I) Compound". The Journal of Physical Chemistry A. 115 (2): 194–200. Bibcode:2011JPCA..115..194P. doi:10.1021/jp109547w. ISSN 1089-5639. PMID 21158464.
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