Metallic bonding

Section: 3 Chemical Bonding  |  Syllabus: Cambridge AS Level Chemistry (9701)

Metallic Bonding

Metallic Bonding The electrostatic attraction between positively charged metal ions (cations) and a sea of delocalised electrons.

When metal atoms pack together in a solid, their outer (valence) electrons leave their parent atoms and become free to move throughout the entire metallic lattice. This creates:

Figure 3.14: Metallic Bonding

(Regular array of positive metal ions (circles with + symbol) in a lattice. Between and around them, randomly scattered small dots representing delocalised electrons. Label: "sea of delocalised electrons" and "positive metal ions". Arrows showing electrostatic attraction between ions and electrons.)

Factors Affecting Strength of Metallic Bonding

Metal Delocalised e⁻ per atom Melting point / °C Trend
Na198Melting point increases across Period 3 as metallic bonding strengthens
Mg2650
Al3660

Properties Explained by Metallic Bonding

Key Point

Metallic bonding is non-directional - the electrostatic attraction acts equally in all directions. This is why metals are malleable: layers of ions can slip without the bond breaking completely, unlike ionic or covalent lattices.

Relative Strength of Bonding Types

In general, the three primary bonding types are all significantly stronger than intermolecular forces:

Bonding Type Typical strength Example
Covalent (triple bond)~200–1000 kJ mol⁻¹N≡N (940 kJ mol⁻¹)
Ionic~600–3000 kJ mol⁻¹ (lattice)MgO
MetallicModerate to very strongAl, Fe, W
Hydrogen bonding~10–40 kJ mol⁻¹H₂O···H₂O
Permanent dipole–dipole~2–20 kJ mol⁻¹HCl···HCl
id–id (London dispersion)~0.1–10 kJ mol⁻¹Noble gases, alkanes
Exam Tip

The syllabus requires you to state that ionic, covalent and metallic bonding are in general stronger than intermolecular forces. This explains why molecular substances (e.g. Cl₂, HCl) have much lower melting/boiling points than ionic or metallic solids.

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