The 18-electron rule is a rule used primarily for predicting and rationalizing formulae for stable metal complexes, especially organometallic compounds. The rule is based on the fact that the valence shells of transition metals consist of nine valence orbitals (one s orbital, three p orbitals and five d orbitals), which collectively can accommodate 18 electrons as either bonding or nonbonding electron pairs. This means that, the combination of these nine atomic orbitals with ligand orbitals creates nine molecular orbitals that are either metal-ligand bonding or non-bonding. When a metal complex has 18 valence electrons, it is said to have achieved the same electron configuration as the noble gas in the period. The rule and its exceptions are similar to the application of the octet rule to main group elements. The rule is not helpful for complexes of metals that are not transition metals, and interesting or useful transition metal complexes will violate the rule because of the consequences deviating from the rule bears on reactivity. The rule was first proposed by American chemist Irving Langmuir in 1921.
- 1 Applicability of the 18-electron rule
- 2 Exceptions to the 18-electron rule
- 3 See also
- 4 References
- 5 Further reading
Applicability of the 18-electron rule
Ligands in a complex determine the applicability of the 18-electron rule. In general, complexes that obey the rule are composed at least partly of π-acceptor ligands (also known as π-acids). This kind of ligand exerts a very strong ligand field, which lowers the energies of the resultant molecular orbitals and thus favorably occupied. Typical ligands include olefins, phosphines, and CO. Complexes of π-acids typically feature metal in a low-oxidation state. The relationship between oxidation state and the nature of the ligands is rationalized within the framework of π backbonding.
Consequences for reactivity
Compounds that obey the 18-electron rule are typically "exchange inert". Examples include [Co(NH3)6]Cl3, Mo(CO)6, and [Fe(CN)6]4−. In such cases, in general ligand exchange occurs via dissociative substitution mechanisms, wherein the rate of reaction is determined by the rate of dissociation of a ligand. On the other hand, 18-electron compounds can be highly reactive toward electrophiles such as protons, and such reactions are associative in mechanism, being acid-base reactions.
Current computational findings suggest valence p-orbitals on the metal participate in metal-ligand bonding, albeit weakly. Some new theoretical treatments do not count the metal p-orbitals in metal-ligand bonding, although these orbitals are still included as polarization functions. This results in a duodectet (12-electron) rule for one s-orbital and five d-orbitals only, but the modified rule has yet to be adopted by the general chemistry community.
Exceptions to the 18-electron rule
π-donor or σ-donor ligands with small interactions with the metal orbitals lead to a weak ligand field which increases the energies of t2g orbitals. These molecular orbitals become non-bonding or weakly anti-bonding orbitals (small Δoct). Therefore, addition or removal of electron has little effect on complex stability. In this case, there is no restriction on the number of d-electrons and complexes with 12–22 electrons are possible. Small Δoct makes filling eg* possible (>18 e−) and π-donor ligands can make t2g antibonding (<18 e−). These types of ligand are located in the low-to-medium part of the spectrochemical series. For example: [TiF6]2− (Ti(IV), d0, 12 e−), [Co(NH3)6]3+ (Co(III), d6, 18 e−), [Cu(OH2)6]2+ (Cu(II), d9, 21 e−).
An important class of complexes that violate the 18e rule are the 16-electron complexes with metal d8 configurations. All high-spin d8 metal ions are octahedral (or tetrahedral), but the low-spin d8 metal ions are all square planar. Important examples of square-planar low-spin d8 metal Ions are Rh(I), Ir(I), Ni(II), Pd(II), and Pt(II). At picture below is shown the splitting of the d subshell in low-spin square-planar complexes. Examples are especially prevalent for derivatives of the cobalt and nickel triads. Such compounds are typically square-planar. The most famous example is Vaska's complex (IrCl(CO)(PPh3)2), [PtCl4]2−, and Zeise's salt [PtCl3(η2-C2H4)]−. In such complexes, the dz2 orbital is doubly occupied and nonbonding.
Many catalytic cycles operate via complexes that alternate between 18-electron and square-planar 16-electron configurations. Examples include Monsanto acetic acid synthesis, hydrogenations, hydroformylations, olefin isomerizations, and some alkene polymerizations.
Other violations can be classified according to the kinds of ligands on the metal center.
Bulky ligands can preclude the approach of the full complement of ligands that would allow the metal to achieve the 18 electron configuration. Examples:
- Ti(neopentyl)4 (8 e−)
- Cp*2Ti(C2H4) (16 e−)
- V(CO)6 (17 e−)
- Cp*Cr(CO)3 (17 e−)
- Pt(PtBu3)2 (14 e−)
- Co(norbornyl)4 (13 e−)
- [FeCp2]+ (17 e−)
Sometimes such complexes engage in agostic interactions with the hydrocarbon framework of the bulky ligand. For example:
- W(CO)3[P(C6H11)3]2 has 16 e− but has a short bonding contact between one C–H bond and the W center.
- Cp(PMe3)V(CHCMe3) (14 e−, diamagnetic) has a short V–H bond with the 'alkylidene-H', so the description of the compound is somewhere between Cp(PMe3)V(CHCMe3) and Cp(PMe3)V(H)(CCMe3).
High-spin metal complexes have singly occupied orbitals and may not have any empty orbitals into which ligands could donate electron density. In general, there are few or no π-acidic ligands in the complex. These singly occupied orbitals can combine with the singly occupied orbitals of radical ligands (e.g., oxygen), or addition of a strong field ligand can cause electron-pairing, thus creating a vacant orbital that it can donate into. Examples:
- CrCl3(THF)3 (15 e−)
- [Mn(H2O)6]2+ (17 e−)
- [Cu(H2O)6]2+ (21 e−, see comments below)
- [CrO4]2− (16 e−)
- Mo(=NR)2Cl2 (12 e−)
In the latter case, there is substantial donation of the nitrogen lone pairs to the Mo (so the compound could also be described as a 16 e− compound). This can be seen from the short Mo–N bond length, and from the angle Mo–N–C(R), which is nearly 180°. Counter-examples:
- trans-WO2(Me2PCH2CH2PMe2)2 (18 e−)
- Cp*ReO3 (18 e−)
In these cases, the M=O bonds are "pure" double bonds (i.e., no donation of the lone pairs of the oxygen to the metal), as reflected in the relatively long bond distances.
Ligands where the coordinating atom bear nonbonding lone pairs often stabilize unsaturated complexes. Metal amides and alkoxides often violate the 18e rule.
Combinations of effects
The above factors can sometimes combine. Examples include
- Cp*VOCl2 (14 e−)
- TiCl4 (8 e−)
Higher electron counts
Some complexes have more than 18 electrons. Examples:
Often, cases where complexes have more than 18 valence electrons are attributed to electrostatic forces – the metal attracts ligands to itself to try to counterbalance its positive charge, and the number of electrons it ends up with is unimportant. In the case of the metallocenes, the chelating nature of the cyclopentadienyl ligand stabilizes its bonding to the metal. Somewhat satisfying are the two following observations: cobaltocene is a strong electron donor, readily forming the 18-electron cobaltocenium cation; and nickelocene tends to react with substrates to give 18-electron complexes, e.g. CpNiCl(PR3) and free CpH.
In the case of nickelocene, the extra two electrons are in orbitals which are weakly metal-carbon antibonding, this is why it often participates in reactions where the M–C bonds are broken and the electron count of the metal changes to 18.
- Langmuir, I. (1921). "Types of Valence". Science. 54 (1386): 59–67. Bibcode:1921Sci....54...59L. doi:10.1126/science.54.1386.59.
- Jensen, William B. (2005). "The Origin of the 18-Electron Rule". J. Chem. Educ. 82 (1): 28. doi:10.1021/ed082p28.
- 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.
- Landis, C. R.; Weinhold, F. (2007). "Valence and extra-valence orbitals in main group and transition metal bonding". J. Comput. Chem. 28 (1): 198–203. doi:10.1002/jcc.20492.
- Girolami, Gregory; Rauchfuss, Thomas; Angelici, Robert (1999). "Experiment 20". Synthesis and Technique in Inorganic Chemistry. Sausalito, California: University Science Books. ISBN 978-0-935702-48-4.