Valence shell electron pair repulsion (VSEPR) theory (/ˈvɛspər, vəˈsɛpər/ VESP-ər,^[1]: 410 və-SEP-ər^[2]) is a model used in chemistry to predict the geometry of individual molecules from the number of electron pairs surrounding their central atoms.^[3] It is also named the Gillespie-Nyholm theory after its two main developers, Ronald Gillespie and Ronald Nyholm.

The premise of VSEPR is that the valence electron pairs surrounding an atom tend to repel each other. The greater the repulsion, the higher in energy (less stable) the molecule is. Therefore, the VSEPR-predicted molecular geometry of a molecule is the one that has as little of this repulsion as possible. Gillespie has emphasized that the electron-electron repulsion due to the Pauli exclusion principle is more important in determining molecular geometry than the electrostatic repulsion.^[4]

The insights of VSEPR theory are derived from topological analysis of the electron density of molecules. Such quantum chemical topology (QCT) methods include the electron localization function (ELF) and the quantum theory of atoms in molecules (AIM or QTAIM).^[4][5]

The idea of a correlation between molecular geometry and number of valence electron pairs (both shared and unshared pairs) was originally proposed in 1939 by Ryutaro Tsuchida in Japan,^[6] and was independently presented in a Bakerian Lecture in 1940 by Nevil Sidgwick and Herbert Powell of the University of Oxford.^[7] In 1957, Ronald Gillespie and Ronald Sydney Nyholm of University College London refined this concept into a more detailed theory, capable of choosing between various alternative geometries.^[8][9]

VSEPR theory is used to predict the arrangement of electron pairs around central atoms in molecules, especially simple and symmetric molecules. A central atom is defined in this theory as an atom which is bonded to two or more other atoms, while a terminal atom is bonded to only one other atom.^[1]: 398 For example in the molecule methyl isocyanate (H₃C-N=C=O), the two carbons and one nitrogen are central atoms, and the three hydrogens and one oxygen are terminal atoms.^[1]: 416 The geometry of the central atoms and their non-bonding electron pairs in turn determine the geometry of the larger whole molecule.

The number of electron pairs in the valence shell of a central atom is determined after drawing the Lewis structure of the molecule, and expanding it to show all bonding groups and lone pairs of electrons.^{[1]: 410–417} In VSEPR theory, a double bond or triple bond is treated as a single bonding group.^[1] The sum of the number of atoms bonded to a central atom and the number of lone pairs formed by its nonbonding valence electrons is known as the central atom's steric number.

The electron pairs (or groups if multiple bonds are present) are assumed to lie on the surface of a sphere centered on the central atom and tend to occupy positions that minimize their mutual repulsions by maximizing the distance between them.^{[1]: 410–417 [10]} The number of electron pairs (or groups), therefore, determines the overall geometry that they will adopt. For example, when there are two electron pairs surrounding the central atom, their mutual repulsion is minimal when they lie at opposite poles of the sphere. Therefore, the central atom is predicted to adopt a linear geometry. If there are 3 electron pairs surrounding the central atom, their repulsion is minimized by placing them at the vertices of an equilateral triangle centered on the atom. Therefore, the predicted geometry is trigonal. Likewise, for 4 electron pairs, the optimal arrangement is tetrahedral.^{[1]: 410–417}

As a tool in predicting the geometry adopted with a given number of electron pairs, an often used physical demonstration of the principle of minimal electron pair repulsion utilizes inflated balloons. Through handling, balloons acquire a slight surface electrostatic charge that results in the adoption of roughly the same geometries when they are tied together at their stems as the corresponding number of electron pairs. For example, five balloons tied together adopt the trigonal bipyramidal geometry, just as do the five bonding pairs of a PCl₅ molecule.

Steric number

The steric number of a central atom in a molecule is the number of atoms bonded to that central atom, called its coordination number, plus the number of lone pairs of valence electrons on the central atom.^[11] In the molecule SF₄, for example, the central sulfur atom has four ligands; the coordination number of sulfur is four. In addition to the four ligands, sulfur also has one lone pair in this molecule. Thus, the steric number is 4 + 1 = 5.

The "AXE method" of electron counting is commonly used when applying the VSEPR theory. The electron pairs around a central atom are represented by a formula AX_mE_n, where A represents the central atom and always has an implied subscript one. Each X represents a ligand (an atom bonded to A). Each E represents a lone pair of electrons on the central atom.^{[1]: 410–417} The total number of X and E is known as the steric number. For example in a molecule AX₃E₂, the atom A has a steric number of 5.

When the substituent (X) atoms are not all the same, the geometry is still approximately valid, but the bond angles may be slightly different from the ones where all the outside atoms are the same. For example, the double-bond carbons in alkenes like C₂H₄ are AX₃E₀, but the bond angles are not all exactly 120°. Likewise, SOCl₂ is AX₃E₁, but because the X substituents are not identical, the X–A–X angles are not all equal.

Based on the steric number and distribution of Xs and Es, VSEPR theory makes the predictions in the following tables.

Main-group elements

For main-group elements, there are stereochemically active lone pairs E whose number can vary between 0 to 3. Note that the geometries are named according to the atomic positions only and not the electron arrangement. For example, the description of AX₂E₁ as a bent molecule means that the three atoms AX₂ are not in one straight line, although the lone pair helps to determine the geometry.

More information Steric number, Molecular geometry 0 lone pairs ...

Steric number	Molecular geometry[12] 0 lone pairs	Molecular geometry[1]: 413–414  1 lone pair	Molecular geometry[1]: 413–414  2 lone pairs	Molecular geometry[1]: 413–414  3 lone pairs
2	Linear
3	Trigonal planar	Bent
4	Tetrahedral	Trigonal pyramidal	Bent
5	Trigonal bipyramidal	Seesaw	T-shaped	Linear
6	Octahedral	Square pyramidal	Square planar
7	Pentagonal bipyramidal	Pentagonal pyramidal	Pentagonal planar
8	Square antiprismatic

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More information Molecule type, Molecular Shape: 413–414 ...

Molecule type	Molecular Shape[1]: 413–414	Electron Arrangement[1]: 413–414  including lone pairs, shown in yellow	Geometry[1]: 413–414  excluding lone pairs	Examples
AX2E0	Linear			BeCl2,[3] CO2[10]
AX2E1	Bent			NO− 2,[3] SO2,[1]: 413–414  O3,[3] CCl2
AX2E2	Bent			H2O,[1]: 413–414  OF2[13]: 448
AX2E3	Linear			XeF2,[1]: 413–414  I− 3,[13]: 483  XeCl2
AX3E0	Trigonal planar			BF3,[1]: 413–414  CO2− 3,[13]: 368  CH 2O, NO− 3,[3] SO3[10]
AX3E1	Trigonal pyramidal			NH3,[1]: 413–414  PCl3[13]: 407
AX3E2	T-shaped			ClF3,[1]: 413–414  BrF3[13]: 481
AX4E0	Tetrahedral			CH4,[1]: 413–414  PO3− 4, SO2− 4,[10] ClO− 4,[3] XeO4[13]: 499
AX4E1	Seesaw or disphenoidal			SF4[1]: 413–414 [13]: 45
AX4E2	Square planar			XeF4[1]: 413–414
AX5E0	Trigonal bipyramidal			PCl5,[1]: 413–414  PF5, [1]: 413–414
AX5E1	Square pyramidal			ClF5,[13]: 481  BrF5,[1]: 413–414  XeOF4[10]
AX5E2	Pentagonal planar			XeF− 5[13]: 498
AX6E0	Octahedral			SF6[1]: 413–414
AX6E1	Pentagonal pyramidal			XeOF− 5,[14] IOF2− 5[14]
AX7E0	Pentagonal bipyramidal[10]			IF7[10]
AX8E0	Square antiprismatic[10]			IF− 8, XeF82- in (NO)2XeF8

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Transition metals (Kepert model)

The lone pairs on transition metal atoms are usually stereochemically inactive, meaning that their presence does not change the molecular geometry. For example, the hexaaquo complexes M(H₂O)₆ are all octahedral for M = V³⁺, Mn³⁺, Co³⁺, Ni²⁺ and Zn²⁺, despite the fact that the electronic configurations of the central metal ion are d², d⁴, d⁶, d⁸ and d¹⁰ respectively.^[13]: 542 The Kepert model ignores all lone pairs on transition metal atoms, so that the geometry around all such atoms corresponds to the VSEPR geometry for AX_n with 0 lone pairs E.^{[15][13]: 542} This is often written ML_n, where M = metal and L = ligand. The Kepert model predicts the following geometries for coordination numbers of 2 through 9:

More information Molecule type, Shape ...

Molecule type	Shape	Geometry	Examples
ML2	Linear		HgCl2[3]
ML3	Trigonal planar
ML4	Tetrahedral		NiCl2− 4
ML5	Trigonal bipyramidal		Fe(CO) 5
	Square pyramidal		MnCl52−
ML6	Octahedral		WCl6[13]: 659
ML7	Pentagonal bipyramidal[10]		ZrF3− 7
	Capped octahedral		MoF− 7
	Capped trigonal prismatic		TaF2− 7
ML8	Square antiprismatic[10]		ReF− 8
	Dodecahedral		Mo(CN)4− 8
	Bicapped trigonal prismatic		ZrF4− 8
ML9	Tricapped trigonal prismatic		ReH2− 9[13]: 254
	Capped square antiprismatic

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The methane molecule (CH₄) is tetrahedral because there are four pairs of electrons. The four hydrogen atoms are positioned at the vertices of a tetrahedron, and the bond angle is cos⁻¹(−1⁄3) ≈ 109° 28′.^[16][17] This is referred to as an AX₄ type of molecule. As mentioned above, A represents the central atom and X represents an outer atom.^{[1]: 410–417}

The ammonia molecule (NH₃) has three pairs of electrons involved in bonding, but there is a lone pair of electrons on the nitrogen atom.^{[1]: 392–393} It is not bonded with another atom; however, it influences the overall shape through repulsions. As in methane above, there are four regions of electron density. Therefore, the overall orientation of the regions of electron density is tetrahedral. On the other hand, there are only three outer atoms. This is referred to as an AX₃E type molecule because the lone pair is represented by an E.^{[1]: 410–417} By definition, the molecular shape or geometry describes the geometric arrangement of the atomic nuclei only, which is trigonal-pyramidal for NH₃.^{[1]: 410–417}

Steric numbers of 7 or greater are possible, but are less common. The steric number of 7 occurs in iodine heptafluoride (IF₇); the base geometry for a steric number of 7 is pentagonal bipyramidal.^[10] The most common geometry for a steric number of 8 is a square antiprismatic geometry.^[18]: 1165 Examples of this include the octacyanomolybdate (Mo(CN)⁴⁻
₈) and octafluorozirconate (ZrF⁴⁻
₈) anions.^[18]: 1165 The nonahydridorhenate ion (ReH²⁻
₉) in potassium nonahydridorhenate is a rare example of a compound with a steric number of 9, which has a tricapped trigonal prismatic geometry.^{[13]: 254 [18]}

Steric numbers beyond 9 are very rare, and it is not clear what geometry is generally favoured.^[19] Possible geometries for steric numbers of 10, 11, 12, or 14 are bicapped square antiprismatic (or bicapped dodecadeltahedral), octadecahedral, icosahedral, and bicapped hexagonal antiprismatic, respectively. No compounds with steric numbers this high involving monodentate ligands exist, and those involving multidentate ligands can often be analysed more simply as complexes with lower steric numbers when some multidentate ligands are treated as a unit.^{[18]: 1165, 1721}

There are groups of compounds where VSEPR fails to predict the correct geometry.

Some AX₆E₁ and AX₈E₁ molecules

Some AX₆E₁ molecules, e.g. xenon hexafluoride (XeF₆) and the Te(IV) and Bi(III) anions, TeCl²⁻
₆, TeBr²⁻
₆, BiCl³⁻
₆, BiBr³⁻
₆ and BiI³⁻
₆, are octahedral, rather than pentagonal pyramids, and the lone pair does not affect the geometry to the degree predicted by VSEPR.^[26] Similarly, the octafluoroxenate ion (XeF²⁻
₈) in nitrosonium octafluoroxenate(VI)^{[13]: 498 [27][28]} is a square antiprism with minimal distortion, despite having a lone pair. One rationalization is that steric crowding of the ligands allows little or no room for the non-bonding lone pair;^[24] another rationalization is the inert-pair effect.^[13]: 214

Complexes with strong d-contribution

Some transition metal complexes with low d electron count have unusual geometries, which can be ascribed to d subshell bonding interaction.^[29] Gillespie found that this interaction produces bonding pairs that also occupy the respective antipodal points (ligand opposed) of the sphere.^[30][4] This phenomenon is an electronic effect resulting from the bilobed shape of the underlying sd^x hybrid orbitals.^[31][32] The repulsion of these bonding pairs leads to a different set of shapes.

More information Molecule type, Shape ...

Molecule type	Shape	Geometry	Examples
ML2	Bent		TiO2[29]
ML3	Trigonal pyramidal		CrO3[33]
ML4	Tetrahedral		TiCl4[13]: 598–599
ML5	Square pyramidal		Ta(CH3)5[34]
ML6	C3v Trigonal prismatic		W(CH3)6[35]

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The gas phase structures of the triatomic halides of the heavier members of group 2, (i.e., calcium, strontium and barium halides, MX₂), are not linear as predicted but are bent, (approximate X–M–X angles: CaF₂, 145°; SrF₂, 120°; BaF₂, 108°; SrCl₂, 130°; BaCl₂, 115°; BaBr₂, 115°; BaI₂, 105°).^[36] It has been proposed by Gillespie that this is also caused by bonding interaction of the ligands with the d subshell of the metal atom, thus influencing the molecular geometry.^[24][37]

The VSEPR theory can be extended to molecules with an odd number of electrons by treating the unpaired electron as a "half electron pair"—for example, Gillespie and Nyholm^{[8]: 364–365} suggested that the decrease in the bond angle in the series NO⁺
₂ (180°), NO₂ (134°), NO⁻
₂ (115°) indicates that a given set of bonding electron pairs exert a weaker repulsion on a single non-bonding electron than on a pair of non-bonding electrons. In effect, they considered nitrogen dioxide as an AX₂E_0.5 molecule, with a geometry intermediate between NO⁺
₂ and NO⁻
₂. Similarly, chlorine dioxide (ClO₂) is an AX₂E_1.5 molecule, with a geometry intermediate between ClO⁺
₂ and ClO⁻
₂.^{[citation needed]}

Finally, the methyl radical (CH₃) is predicted to be trigonal pyramidal like the methyl anion (CH⁻
₃), but with a larger bond angle (as in the trigonal planar methyl cation (CH⁺
₃)). However, in this case, the VSEPR prediction is not quite true, as CH₃ is actually planar, although its distortion to a pyramidal geometry requires very little energy.^[41]

• Bent's rule (effect of ligand electronegativity)
• Comparison of software for molecular mechanics modeling
• Linear combination of atomic orbitals
• Molecular geometry
• Molecular modelling
• Molecular Orbital Theory (MOT)
• Thomson problem
• Valence Bond Theory (VBT)
• Valency interaction formula