Orbital hybridisation

In chemistry, 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. 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 in order 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 however, 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.

Atomic orbitals

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 normalization 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

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:

The carbon atom can utilize 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.

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 be 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.

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.

translates into

sp²

Three sp² orbitals.

Ethene structure

Other carbon based 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,

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 two sp² orbitals and each carbon atom forms two covalent bonds with hydrogen by s–sp² overlap all with 120° angles. The π bond between the carbon atoms perpendicular to the molecular plane is formed by 2p–2p overlap. 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,

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.

Hybridisation of hypervalent molecules

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.

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 hybridization in bonding in hypervalent compounds of second-row 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 centers, 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 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 d^mspⁿ resonance structures.

Classification	Main group	Transition metal
AX2		Linear (180°)
AX3		Trigonal planar (120°)
AX4		Square planar (90°)
AX5	Trigonal bipyramidal (90°, 120°)	Trigonal bipyramidal or Square pyramidal[9]
AX6	Octahedral (90°)	Octahedral (90°)
AX7	Pentagonal bipyramidal (90°, 72°)	Pentagonal bipyramidal, Capped octahedral or Capped trigonal prismatic[7][10]

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 sp^2.5 are also readily described.

The hybridisation of bond orbitals is determined by Bent's rule: "Atomic s character concentrates in orbitals directed toward 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 sp^4[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
• Monocoordinate
  • One isovalent hybrid bond orbitals
  • E.g., CO, SO, HF

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 utilizing 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°)
	Square planar equator (two p orbitals)		Square pyramidal (AX5E1) (90°, 90°)	Square planar (AX4E2) (90°)
	Pentagonal planar equator (two p orbitals)		Pentagonal pyramidal (AX6E1) (90°, 72°)	Pentagonal planar (AX5E2) (72°)

Hybridisation defects

Hybridisation of s and p orbitals to form effective sp^x 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 analyzed by considering localized molecular orbitals, for example using natural localized 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 localized hybrids, quantum mechanics requires that the (in this case ionized) wavefunction obey the symmetry of the molecule which implies resonance in valence bond theory. For example, in methane, the ionized 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 ionized state and the ground state would be an ionization 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 localized molecular orbitals, which can be formed from the delocalized 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 delocalized orbital description for ground state total energy and electron density, as well as the molecular geometry that corresponds to the minimum total energy value.

See also

• Bent's rule (effect of ligand electronegativity)
• Linear combination of atomic orbitals molecular orbital method
• MO diagrams
• Ligand field theory
• Crystal field theory
• Isovalent hybridization

References

External links

• Covalent Bonds and Molecular Structure
• Hybridisation flash movie
• Hybrid orbital 3D preview program in OpenGL
• Understanding Concepts: Molecular Orbitals
• General Chemistry tutorial on orbital hybridization