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Orbital hybridisation

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This article is about hybridisation in valence bond theory. For s-p mixing, see molecular orbital diagram.

In chemistry, orbital hybridisation (or hybridization) is the concept of mixing atomic orbitals into new hybrid orbitals (with different energies, shapes, etc., than the component atomic orbitals) suitable for the pairing of electrons to form chemical bonds in valence bond theory. Hybrid orbitals are very useful in the explanation of molecular geometry and atomic bonding properties and are symmetrically disposed in space. Although sometimes taught together with the valence shell electron-pair repulsion (VSEPR) theory, valence bond and hybridisation are in fact not related to the VSEPR model.[1]

History

Chemist Linus Pauling first developed the hybridisation theory in 1931 to explain the structure of simple molecules such as methane (CH4) using atomic orbitals.[2] Pauling pointed out that a carbon atom forms four bonds by using one s and three p orbitals, so that "it might be inferred" that a carbon atom would form three bonds at right angles (using p orbitals) and a fourth weaker bond using the s orbital in some arbitrary direction. In reality, methane has four bonds of equivalent strength separated by the tetrahedral bond angle of 109.5°. Pauling explained this by supposing that in the presence of four hydrogen atoms, the s and p orbitals form four equivalent combinations or hybrid orbitals, each denoted by sp3 to indicate its composition, which are directed along the four C-H bonds.[3] This concept was developed for such simple chemical systems, but the approach was later applied more widely, and today it is considered an effective heuristic for rationalising the structures of organic compounds. It gives a simple orbital picture equivalent to Lewis structures. Hybridisation theory finds its use mainly in organic chemistry, one of the most compelling examples being Baldwin's rules.

Atomic orbitals

Main article: Atomic orbital

Orbitals are a model representation of the behaviour of electrons within molecules. In the case of simple hybridisation, this approximation is based on atomic orbitals, similar to those obtained for the hydrogen atom, the only neutral atom for which the Schrödinger equation can be solved exactly. In heavier atoms, such as carbon, nitrogen, and oxygen, the atomic orbitals used are the 2s and 2p orbitals, similar to excited state orbitals for hydrogen.

Overview

Hybrid orbitals are assumed to be mixtures of atomic orbitals, superimposed on each other in various proportions. For example, in methane, the C hybrid orbital which forms each carbon–hydrogen bond consists of 25% s character and 75% p character and is thus described as sp3 (read as s-p-three) hybridised. Quantum mechanics describes this hybrid as an sp3 wavefunction of the form N(s + √3pσ), where N is a normalisation constant (here 1/2) and pσ is a p orbital directed along the C-H axis to form a sigma bond. The ratio of coefficients (denoted λ in general) is √3 in this example. Since the electron density associated with an orbital is proportional to the square of the wavefunction, the ratio of p-character to s-character is λ2 = 3. The p character or the weight of the p component is N2λ2 = 3/4.

The amount of p character or s character, which is decided mainly by orbital hybridisation, can be used to reliably predict molecular properties such as acidity or basicity.[4]

Two possible representations

Main article: Sigma-pi and equivalent-orbital models

Molecules with multiple bonds or multiple lone pairs can have orbitals represented in terms of sigma and pi symmetry or equivalent orbitals. The sigma and pi representation of Erich Hückel is the more common one compared to the equivalent orbital representation of Linus Pauling. The two have mathematically equivalent total many-electron wave functions, and are related by a unitary transformation of the set of occupied molecular orbitals.

Types of hybridisation

sp3

Four sp3 orbitals.

Hybridisation describes the bonding atoms from an atom's point of view. For a tetrahedrally coordinated carbon (e.g., methane CH4), the carbon should have 4 orbitals with the correct symmetry to bond to the 4 hydrogen atoms.

Carbon's ground state configuration is 1s2 2s2 2p2 or more easily read:

C ↑↓ ↑↓ ↑ ↑  
1s 2s 2p 2p 2p

The carbon atom can use its two singly occupied p-type orbitals, to form two covalent bonds with two hydrogen atoms, yielding the singlet methylene CH2, the simplest carbene. The carbon atom can also bond to four hydrogen atoms by an excitation of an electron from the doubly occupied 2s orbital to the empty 2p orbital, producing four singly occupied orbitals.

C* ↑↓ ↑ ↑ ↑ ↑
1s 2s 2p 2p 2p

The energy released by formation of two additional bonds more than compensates for the excitation energy required, energetically favouring the formation of four C-H bonds.

Quantum mechanically, the lowest energy is obtained if the four bonds are equivalent, which requires that they are formed from equivalent orbitals on the carbon. A set of four equivalent orbitals can be obtained that are linear combinations of the valence-shell (core orbitals are almost never involved in bonding) s and p wave functions,[5] which are the four sp3 hybrids.

C* ↑↓ ↑ ↑ ↑ ↑
1s sp3 sp3 sp3 sp3

In CH4, four sp3 hybrid orbitals are overlapped by hydrogen 1s orbitals, yielding four σ (sigma) bonds (that is, four single covalent bonds) of equal length and strength.

A schematic presentation of hybrid orbitals overlapping hydrogen orbitals translates into Methane's tetrahedral shape

sp2

Three sp2 orbitals.
Ethene structure

Other carbon compounds and other molecules may be explained in a similar way. For example, ethene (C2H4) has a double bond between the carbons.

For this molecule, carbon sp2 hybridises, because one π (pi) bond is required for the double bond between the carbons and only three σ bonds are formed per carbon atom. In sp2 hybridisation the 2s orbital is mixed with only two of the three available 2p orbitals,

C* ↑↓ ↑ ↑ ↑ ↑
1s sp2 sp2 sp2 2p

forming a total of three sp2 orbitals with one remaining p orbital. In ethylene (ethene) the two carbon atoms form a σ bond by overlapping one sp2 orbital from each carbon atom. The π bond between the carbon atoms perpendicular to the molecular plane is formed by 2p–2p overlap. Each carbon atom forms two covalent bonds with hydrogen by s–sp2 overlap all with 120° angles. The hydrogen–carbon bonds are all of equal strength and length, in agreement with experimental data.

sp

Two sp orbitals

The chemical bonding in compounds such as alkynes with triple bonds is explained by sp hybridisation. In this model, the 2s orbital is mixed with only one of the three p orbitals,

C* ↑↓ ↑ ↑ ↑ ↑
1s sp sp 2p 2p

resulting in two sp orbitals and two remaining p orbitals. The chemical bonding in acetylene (ethyne) (C2H2) consists of sp–sp overlap between the two carbon atoms forming a σ bond and two additional π bonds formed by p–p overlap. Each carbon also bonds to hydrogen in a σ s–sp overlap at 180° angles.

Hybridisation and molecule shape

Hybridisation helps to explain molecule shape, since the angles between bonds are (approximately) equal to the angles between hybrid orbitals, as explained above for the tetrahedral geometry of methane. As another example, the three sp2 hybrid orbitals are at angles of 120° to each other, so this hybridisation favours trigonal planar molecular geometry with bond angles of 120°. Other examples are given in the table below.

Classification Main group Transition metal[6][7]
AX2
  • Linear (180°)
  • sp hybridisation
  • E.g., CO2
  • Bent (90°)
  • sd hybridisation
  • E.g., VO2+
AX3
AX4
AX5
  • Irregular shape (65.9°, 114.1°)
  • sd4 hybridisation
AX6

Hybridisation of hypervalent molecules

Main article: Hypervalent molecule

Valence shell expansion

Hybridisation is often presented for main group AX5 and above, as well as for many transition metal complexes, using the hybridisation scheme first proposed by Pauling.

Classification Main group
AX5
AX6
AX7
Classification Transition metal[8]
AX4
AX6
  • Octahedral (90°)
  • d2sp3 hybridisation
  • E.g., Mo(CO)6
Note: AX5 and AX7 have variable molecular shapes[9][10]

In this notation, d orbitals of main group atoms are listed after the s and p orbitals since they have the same principal quantum number (n), while d orbitals of transition metals are listed first since the s and p orbitals have a higher n. Thus for AX6 molecules, sp3d2 hybridisation in the S atom involves 3s, 3p and 3d orbitals, while d2sp3 for Mo involves 4d, 5s and 5p orbitals.

Contrary evidence

In 1990, Magnusson published a seminal work definitively excluding the role of d-orbital hybridisation in bonding in hypervalent compounds of second-row (period 3) elements, ending a point of contention and confusion. Part of the confusion originates from the fact that d-functions are essential in the basis sets used to describe these compounds (or else unreasonably high energies and distorted geometries result). Also, the contribution of the d-function to the molecular wavefunction is large. These facts were incorrectly interpreted to mean that d-orbitals must be involved in bonding.[11][12]

For transition metal centres, the d and s orbitals are the primary valence orbitals, which are only weakly supplemented by the p orbitals.[13] The question of whether the p orbitals actually participate in bonding has not been definitively resolved, but all studies indicate they play a minor role.

Resonance

In light of computational chemistry, a better treatment would be to invoke sigma bond resonance in addition to hybridisation, which implies that each resonance structure has its own hybridisation scheme. For main group compounds, all resonance structures must obey the octet (8-electron) rule. For transition metal compounds, the resonance structures that obey the duodectet (12-electron) rule[14] suffice to describe bonding, with optional inclusion of dmspn resonance structures.

Classification Main group
AX5 Trigonal bipyramidal (90°, 120°)
AX6 Octahedral (90°)
AX7 Pentagonal bipyramidal (90°, 72°)
Classification Transition metal[6]
AX4 Square planar (90°)
File:Tetra plat.svg
AX6 Octahedral (90°)
File:Hexa moly.svg
Note: AX5 and AX7 have variable molecular shapes[9][10]

Isovalent hybridisation

Main article: Isovalent hybridisation

Although ideal hybrid orbitals can be useful, in reality most bonds require orbitals of intermediate character. This requires an extension to include flexible weightings of atomic orbitals of each type (s, p, d) and allows for a quantitative depiction of bond formation when the molecular geometry deviates from ideal bond angles. The amount of p-character is not restricted to integer values; i.e., hybridisations like sp2.5 are also readily described.

The hybridisation of bond orbitals is determined by Bent's rule: "Atomic s character concentrates in orbitals directed towards electropositive substituents".

Molecules with lone pairs

For molecules with lone pairs, the bonding orbitals are isovalent hybrids. For example, the two bond-forming hybrid orbitals of oxygen in water can be described as sp4[15] to give the interorbital angle of 104.5°. This means that they have 20% s character and 80% p character and does not imply that a hybrid orbital is formed from one s and four p orbitals on oxygen since the 2p subshell of oxygen only contains three p orbitals. The shapes of molecules with lone pairs are:

  • Trigonal pyramidal
    • Three isovalent hybrid bond orbitals
    • E.g., NH3
  • Bent
    • Two isovalent hybrid bond orbitals
    • E.g., SO2, H2O

In such cases, there are two mathematically equivalent ways of representing lone pairs. They can be represented by orbitals of sigma and pi symmetry similar to molecular orbital theory or by equivalent orbitals similar to VSEPR theory.

Hypervalent molecules

For hypervalent molecules with lone pairs, the bonding scheme can be split into a hypervalent component and a component consisting of isovalent bonding hybrids. The hypervalent component consists of resonating bonds using p orbitals. The table below shows how each shape is related to the two components and their respective descriptions.

Number of isovalent bonding hybrids (marked in red)
Two One –
Hypervalent component Linear axis
(one p orbital) 		Seesaw (AX4E1) (90°, 180°, >90°) T-shaped (AX3E2) (90°, 180°) Linear (AX2E3) (180°)
File:Tetra sulf.svg File:Tri chlo.svg File:Di xeno.svg
Square planar equator
(two p orbitals) 		Square pyramidal (AX5E1) (90°, 90°) Square planar (AX4E2) (90°)
File:Penta chlo.svg File:Tetra xeno.svg
Pentagonal planar equator
(two p orbitals) 		Pentagonal pyramidal (AX6E1) (90°, 72°) Pentagonal planar (AX5E2) (72°)
File:Hexa xeno.svg File:Penta xeno.svg

Hybridisation defects

Hybridisation of s and p orbitals to form effective spx hybrids requires that they have comparable radial extent. While 2p orbitals are on average less than 10% larger than 2s, in part attributable to the lack of a radial node in 2p orbitals, 3p orbitals which have one radial node, exceed the 3s orbitals by 20–33%.[16] The difference in extent of s and p orbitals increases further down a group. The hybridisation of atoms in chemical bonds can be analysed by considering localised molecular orbitals, for example using natural localised molecular orbitals in a natural bond orbital (NBO) scheme. In methane, CH4, the calculated p/s ratio is approximately 3 consistent with "ideal" sp3 hybridisation, whereas for silane, SiH4, the p/s ratio is closer to 2. A similar trend is seen for the other 2p elements. Substitution of fluorine for hydrogen further decreases the p/s ratio.[17] The 2p elements exhibit near ideal hybridisation with orthogonal hybrid orbitals. For heavier p block elements this assumption of orthogonality cannot be justified. These deviations from the ideal hybridisation were termed hybridisation defects by Kutzelnigg.[18]

Photoelectron spectra

One misconception concerning orbital hybridisation is that it incorrectly predicts the ultraviolet photoelectron spectra of many molecules. While this is true if Koopmans' theorem is applied to localised hybrids, quantum mechanics requires that the (in this case ionised) wavefunction obey the symmetry of the molecule which implies resonance in valence bond theory. For example, in methane, the ionised states (CH4+) can be constructed out of four resonance structures attributing the ejected electron to each of the four sp3 orbitals. A linear combination of these four structures, conserving the number of structures, leads to a triply degenerate T2 state and a A1 state.[19] The difference in energy between each ionised state and the ground state would be an ionisation energy, which yields two values in agreement with experiment.

Hybridisation theory vs. molecular orbital theory

Hybridisation theory is an integral part of organic chemistry and in general discussed together with molecular orbital theory. For drawing reaction mechanisms sometimes a classical bonding picture is needed with two atoms sharing two electrons.[20] Predicting bond angles in methane with MO theory is not straightforward. Hybridisation theory explains bonding in alkenes[21] and methane.[22]

Bonding orbitals formed from hybrid atomic orbitals may be considered as localised molecular orbitals, which can be formed from the delocalised orbitals of molecular orbital theory by an appropriate mathematical transformation. For molecules with a closed electron shell in the ground state, this transformation of the orbitals leaves the total many-electron wave function unchanged. The hybrid orbital description of the ground state is therefore equivalent to the delocalised orbital description for ground state total energy and electron density, as well as the molecular geometry that corresponds to the minimum total energy value. Weinhold and Landis describe the proper (symmetry appropriate) use of the orbital hybridization concept within the context of natural bond orbitals, a localized orbital theory containing modernized analogs of classical (valence bond/Lewis structure) bonding pairs and lone pairs.[23] For the hydrogen fluoride molecule, for example, two F lone pairs are essentially unhybridized p orbitals, while the other is an sp hydrid orbital. An analogous consideration applies to water (one O lone pair is in a pure p orbital, another is in an spx hybrid orbital).

See also

References

  1. ^ Gillespie, R.J. (2004), "Teaching molecular geometry with the VSEPR model", Journal of Chemical Education, 81 (3): 298–304, Bibcode:2004JChEd..81..298G, doi:10.1021/ed081p298
  2. ^ Pauling, L. (1931), "The nature of the chemical bond. Application of results obtained from the quantum mechanics and from a theory of paramagnetic susceptibility to the structure of molecules", Journal of the American Chemical Society, 53 (4): 1367–1400, doi:10.1021/ja01355a027
  3. ^ L. Pauling The Nature of the Chemical Bond (3rd ed., Oxford University Press 1960) p.111–120.
  4. ^ "Acids and Bases". Orgo Made Simple. Retrieved 23 June 2015.
  5. ^ McMurray, J. (1995). Chemistry Annotated Instructors Edition (4th ed.). Prentice Hall. p. 272. ISBN 978-0-131-40221-8
  6. ^ a b Weinhold, Frank; Landis, Clark R. (2005). Valency and bonding: A Natural Bond Orbital Donor-Acceptor Perspective. Cambridge: Cambridge University Press. pp. 367, 381–383, 570–572. ISBN 978-0-521-83128-4.
  7. ^ Kaupp, Martin (2001). ""Non-VSEPR" Structures and Bonding in d(0) Systems". Angew Chem Int Ed Engl. 40 (1): 3534–3565. doi:10.1002/1521-3773(20011001)40:19<3534::AID-ANIE3534>3.0.CO;2-#.
  8. ^ Jean, Yves (2005). Molecular Orbitals of Transition Metal Complexes. Oxford: Oxford University Press. pp. 37–76. ISBN 978-0-19-151369-5.
  9. ^ a b Angelo R. Rossi; Roald. Hoffmann (1975). "Transition metal pentacoordination". Inorganic Chemistry. 14 (2): 365–374. doi:10.1021/ic50144a032.
  10. ^ a b Roald. Hoffmann; Barbara F. Beier; Earl L. Muetterties; Angelo R. Rossi (1977). "Seven-coordination. A molecular orbital exploration of structure, stereochemistry, and reaction dynamics". Inorganic Chemistry. 16 (3): 511–522. doi:10.1021/ic50169a002.
  11. ^ E. Magnusson. Hypercoordinate molecules of second-row elements: d functions or d orbitals? J. Am. Chem. Soc. 1990, 112, 7940–7951. doi:10.1021/ja00178a014
  12. ^ David L. Cooper; Terry P. Cunningham; Joseph Gerratt; Peter B. Karadakov; Mario Raimondi (1994). "Chemical Bonding to Hypercoordinate Second-Row Atoms: d Orbital Participation versus Democracy". Journal of the American Chemical Society. 116 (10): 4414–4426. doi:10.1021/ja00089a033.
  13. ^ Frenking, Gernot; Shaik, Sason, eds. (May 2014). "Chapter 7: Chemical bonding in Transition Metal Compounds". The Chemical Bond: Chemical Bonding Across the Periodic Table. Wiley -VCH. ISBN 978-3-527-33315-8.
  14. ^ C. R. Landis; F. Weinhold (2007). "Valence and extra-valence orbitals in main group and transition metal bonding". Journal of Computational Chemistry. 28 (1): 198–203. doi:10.1002/jcc.20492.
  15. ^ Frenking, Gernot; Shaik, Sason, eds. (2014). "Chapter 3: The NBO View of Chemical Bonding". The Chemical Bond: Fundamental Aspects of Chemical Bonding. John Wiley & Sons. ISBN 978-3-527-66471-9.
  16. ^ Kaupp, Martin (2007). "The role of radial nodes of atomic orbitals for chemical bonding and the periodic table". Journal of Computational Chemistry. 28 (1): 320–325. doi:10.1002/jcc.20522. ISSN 0192-8651.
  17. ^ Kaupp, Martin (2014) [1st. Pub. 2014]. "Chapter 1: Chemical bonding of main group elements". In Frenking, Gernod; Shaik, Sason (eds.). The Chemical Bond: Chemical Bonding Across the Periodic Table. Wiley-VCH. ISBN 978-1-234-56789-7. {{cite book}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
  18. ^ Kutzelnigg, W. (August 1988). "Orthogonal and non-orthogonal hybrids". Journal of Molecular Structure: THEOCHEM. 169: 403–419. doi:10.1016/0166-1280(88)80273-2.  – via ScienceDirect (Subscription may be required or content may be available in libraries.)
  19. ^ Sason S. Shaik; Phillipe C. Hiberty (2008). A Chemist's Guide to Valence Bond Theory. New Jersey: Wiley-Interscience. ISBN 978-0-470-03735-5.
  20. ^ Clayden, Jonathan; Greeves, Nick; Warren, Stuart; Wothers, Peter (2001). Organic Chemistry (1st ed.). Oxford University Press. p. 105. ISBN 978-0-19-850346-0.
  21. ^ Organic Chemistry, Third Edition Marye Anne Fox James K. Whitesell 2003 ISBN 978-0-7637-3586-9
  22. ^ Organic Chemistry 3rd Ed. 2001 Paula Yurkanis Bruice ISBN 978-0-130-17858-9
  23. ^ Weinhold, Frank; Landis, Clark R. (2012). Discovering Chemistry with Natural Bond Orbitals. Hoboken, N.J.: Wiley. pp. 67–68. ISBN 978-1-118-11996-9.
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