Electron counting
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Electron counting is a formalism used for classifying compounds and for explaining or predicting electronic structure and bonding. Many rules in chemistry rely on electron-counting:
- Octet rule for main group elements, especially the lighter ones such as carbon, nitrogen, and oxygen,
- Eighteen electron rule in inorganic chemistry and organometallic chemistry of transition metals,
- The 32-electron rule, an extension of the 18-electron rule relevant to derivatives of the lanthanide and actinide elements,
- Polyhedral skeletal electron pair theory for cluster compounds, including transition metals and main group elements such as boron including Wade's rules for polyhedral cluster compounds, including transition metals and main group elements and mixtures thereof.
Counting rules
Two styles of electron counting are popular and both give the same result. The neutral counting approach is usually considered easier but the "ionic counting" approach rewards the user with a knowledge of oxidation states, which can be valuable. One can check one's calculation by counting employing both approaches.
Neutral counting
- Locate the central atom on the periodic table and determine the number of its valence electrons. One counts valence electrons for main group elements differently from transition metals.
- E.g. in group 2: B, C, N, O, and F have 3, 4, 5, 6, and 7 valence electrons, respectively.
- E.g. in group 3: K, Ca, Ti, V, Cr, Fe, Ni have 1, 2, 4, 5, 6, 8, 10 valence electrons respectively.
Ionic counting
- Calculate the number of electrons of the element, assuming an oxidation state
- e.g. for a Fe2+ has 6 electrons
- S2- has 8 electrons
Electrons donated by common fragments
| Ligand | Electrons contributed (neutral counting) | Electrons contributed (ionic counting) |
|---|---|---|
| X | 1 | 2 (X-; X = F, Cl, Br, I) |
| H | 1 | 2 (H-) |
| O | 2 | 4(O2-) |
| N | 3 | 6 (N3-) |
| NR3 | 2 | 2 (NR3; R = H, alkyl, aryl) |
| CR2 | 2 | 4 (CR22-) |
| Ethylene | 2 | 2 (C2H4) |
| cyclopentadienyl | 5 | 6(C5H5-) |
| benzene | 6 | 6 (C6H6) |
\"Special cases\"
The numbers of electrons "donated" by some ligands depends on the geometry of the metal-ligand ensemble. Perhaps the most famous example of this complication is the M-NO entity. When this grouping is linear, the NO ligand is considered to be a three-electon ligand. When the M-NO subunit is strongly bent at N, the NO is treated as a pseudohalide and is thus a one electron (in the neutral counting approach). The situation is not very different from the η-3 vs. η-1 allyl. Another unusual ligand from the electron counting perspective is sulfur dioxide.Examples of electron counting
- CH4, for the central C
- neutral counting: C contributes 4 electrons, each H radical contributes one each: 4+4(1) = 8 valence electrons
- ionic counting: C4- contributes 8 electrons, each proton contributes 0 each: 8 + 4(0) = 8 electrons.
- Similar for H:
- neutral counting: H contributes 1 electron, the C contributes 1 electron (the other 3 electrons of C are for the other 3 hydrogens in the molecule): 1 + 1(1) = 2 valence electrons.
- ionic counting: H contributes 0 electrons (H+), C4- contributes 2 electrons (per H), 0 + 1(2) = 2 valence electrons
- conclusion: Methane follows the octet-rule for carbon, and the duet rule for hydrogen, and hence is expected to be a stable molecule (as we see from daily life)
- H2S, for the central S
- SCl2, for the central S
- SF6, for the central S
- TiCl4, for the central Ti
- Ferrocene, (C5H5)2Fe, for the central Fe:
please note: these examples show the methods of electron counting, they are a formulism, and don't have anything to do with real life chemical transformations. Most of the 'fragments' mentioned above do not exist as such; they cannot be kept in a bottle: e.g. the neutral C, the tetraanionic C, the neutral Ti, and the tetracationic Ti are not free species, they are always bound to something, for neutral C, it is commonly found in graphite, charcoal, diamond (sharing electrons with the neighboring carbons), as for Ti which can be found as its metal (where it shares its electrons with neighboring Ti atoms!), C4- and Ti4+ 'exist' only with appropriate counterions (with which they probably share electrons). So these formulisms are only used to predict stabilities or properties of compounds!
See also
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